Dissolvable and dispersable PVA cleaning sheet

Abstract

The described invention is a water dissolvable PVA sheet used for bleaching, car cleaning, and fragrance.

Description

[0001] APPLICATION FOR LETTERS PATENT TITLE: DISSOLVABLE AND DISPERSABLE PVA CLEANING SHEET FIELD OF THE INVENTION This invention relates to a product in the form of a dissolvable or dispersible sheet containing polyvinyl alcohol and various cleaning compositions and methods for a wide range of applications. BACKGROUND OF THE INVENTION This invention relates to a product in the form of a dissolvable or dispersible sheet that can provide bleaching, car cleaning, and or fragrance. Accordingly there remains a need for a cleaning sheet that doesn’t require any of these many types of ingredients added separately or added together.

[0002] SUMMARY OF THE INVENTION The invention relates to a dissolvable or dispersible bleach sheet and a manufacturing method thereof that can effectively deliver the full bleaching power of bleach. In the present invention, a bleach sheet includes a water dissolvable film or water dispersible film, one or more bleaching agents, one or more bleaching activator, and one or more pH increasing agents used to deliver a dissolvable or dispersible bleach sheet. The present invention is a dissolvable or dispersible bleach sheet manufactured using a water dissolvable film or a water dispersible film, prepared by removing a solvent from a solution containing a film-forming water dissolvable polymer or a film forming water-dispersible polymer. It is characterized by providing a dissolvable or dispersible bleach sheet in which an active ingredient for bleaching doesn’t negatively interact with the bleach sheet composition and wherein said bleaching effect is delivered by adding the bleach sheet to water or water-based compositions. The bleaching agent may be in a form that is fully dissolved, partially dissolved, or not dissolved in the final manufacturing form of the bleach sheet. If the bleaching agent is not dissolved in the composition, it reduces the potential to negatively interact with the bleach sheet during and after manufacturing. The active ingredient for bleaching may be in a granular form and distributed in the bleach sheet. Various coatings will be disclosed to prevent the dissolution of the bleach granules during the manufacturing of the bleach sheet. Said bleach sheet can be prepared as a solution formed by mixing a water dissolvable polymer for film formation or a water dispersible polymer for film formation but is not limited to the production method. Any form in which the bleaching component is included in the film may be included in the above. The invention also relates to a flexible car cleaning sheet based on a combination of polyvinyl alcohol, a cleaning composition, and a composition of perfume and / or fragrances, and ingredients consisting of thickening agents, polymers such as starch, cellulose, and other ingredients that when dried, produce a composition that remains solid and flexible when dried, and produces a CCS that remains solid and flexible when dry and then dissolves completely in water. Once the composition is mixed in proper ratios, it forms a liquid that is poured onto a drying plate and after drying results in a flexible CCS that can be used in a wide range of applications. When wet or when in contact with water, said composition dissolves completely and releases all of its active ingredients which may include surfactants, chelating agents, dyes, fabric softeners, bleaching agents, enzymes, perfumes, fragrances and perfume microcapsules. The invention also relates to a water dissolvable fragrance sheet and specifically a water dissolvable fragrance sheet containing various compositions that can add or remove odor molecules. Said composition may contain perfume or fragrance or compositions that are known to remove odors which have negative impact. Said invention may also be based on various methods to produce water dissolvable fragrance sheet for a wide range of applications. The described invention is based on a flexible polyvinyl alcohol (PVA) and comprises several other components that are designed to create a consumer product that delivers or remove odors on a combination thereof, in a wide range of applications.

[0003] BRIEF DESCRIPTION OF THE FIGURES FIGURE 1 is an illustration of a non-limiting embodiment of a homogenizer assembly, component feeds, and drum dryer assembly according to the invention. FIGURE 2 is an illustration of a non-limiting embodiment in a perspective view showing the dimensions of a water dissolvable PVA sheet according to the invention. FIGURE 3 is a photo representation of a top view of a non-limiting embodiment showing ruler dimensions of a water dissolvable PVA sheet according to the invention. FIGURE 4 is a photo representation of a side view of a non-limiting embodiment showing ruler dimensions of a water dissolvable PVA sheet according to the invention. FIGURE 5 is a flow chart illustration of a non-limiting embodiment of a method of manufacturing a water dissolvable PVA sheet using a homogenizer assembly, a supply for component feeds, and a drum dryer assembly according to the invention. FIGURE 6 is a perspective illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive and a sheet winding assembly according to the invention. FIGURE 7 is a perspective illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive according to the invention. FIGURE 8 is a perspective illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive and steam inlet according to the invention. FIGURE 9 is an side view illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive, a steam inlet, and applicator roller tray according to the invention. FIGURE 10 is an end view illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive, motor, and sheet winding assembly according to the invention. FIGURE 11 is a top view illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive, motor, and sheet winding assembly according to the invention. FIGURE 12 is a cut-away view illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive, motor, dryer drum, roller tray, roller, and steam delivery conduit according to the invention. FIGURE 13 is an perspective illustration of a non-limiting embodiment of an applicator roller tray, and roller assembly according to the invention. FIGURE 14 is an perspective illustration of a non-limiting embodiment of an applicator roller tray, and roller assembly according to the invention. FIGURE 15 is an perspective illustration of a non-limiting embodiment of a tray raising / lowering assembly according to the invention. FIGURE 16 is a side view illustration of a non-limiting embodiment of a tray raising / lowering assembly according to the invention. FIGURE 17 is an perspective illustration of a non-limiting embodiment of an applicator tray, roller, and tray raising / lowering assembly according to the invention. FIGURE 18 is an perspective illustration of a non-limiting embodiment of a (sheet) feed leveling roller assembly according to the invention. FIGURE 19 is a detail illustration of a non-limiting embodiment of a leveling adjustment mechanism for the (sheet) feed leveling roller assembly according to the invention.

[0004] DETAILED DESCRIPTION OF THE INVENTION Bleach Sheet Preferred Embodiments It has been demonstrated that a bleaching composition can be prepared in sheet form that is dissolvable or dispersible in water. These bleach sheet compositions include the combination of a water dissolvable film or water dispersible film forming sheet combined with a bleaching agent. An example of beaching may be percarbonate or perborate or a combination thereof. Said bleaching agent may be in the form of a granule. Said bleaching agent granule may further be encapsulated to protect the bleaching agent during manufacturing and storage. Additionally, a pH modifier may be added to increase the generation of oxygen bleach when using said bleaching agents. Furthermore, a bleach activator such as NOBS or TAED or a combination thereof may be added to the dissolvable or dispersible bleach sheet to form peracid which increases the bleaching performance of said bleach sheet. Currently, dissolvable and dispersible polymer films are widely used in laundry applications, but also in personal care products such as pharmaceuticals and cosmetics, and household products such as household goods. Dissolvable laundry detergent sheets which comprise of mixing active ingredients for laundry such as a detergent into a water-soluble polymer film-forming composition are available today. Dissolvable sheets are used in laundry and other applications. Dissolvable laundry sheets, which contain a laundry detergent formula, are made from synthetic film forming polymers such as Polyvinyl Alcohol (PVA). Natural polymers used in the formulation of film include starches, gums, and cellulose. These dissolvable sheets are pre-measured laundry detergent sheets that dissolves in water and acts as a cleaning composition. A thickening agent such as starch may be added to said composition to produce a sheet that remains solid and flexible upon drying. However, if the laundry detergent comprises bleach, the bleach may be activated in a filmforming water-soluble polymer during or after manufacturing of said bleach sheet, the composition becomes unstable and the active ingredients for washing will be damaged or even destroyed. As a result, the problem associated with the stabilization of bleach in the bleach sheet composition and the manufacturing of said bleach sheet needs to be resolved for the ability to deliver the full effect of bleach in a dissolvable or dispersible bleach sheet. Bleach is a strong and effective disinfectant. Bleaches are commonly found in two forms: chlorine bleaches, which are some forms of hypochlorite, and oxygen bleaches based on primary ingredients, such as peroxides, percarbonate, perborates, etc. Chlorine bleach comes in liquid and powder form. Chlorine bleach contains sodium hypochlorite diluted in water. This type of bleach is very powerful. Chlorine bleach has a whitening and brightening effect on white fabric. It disinfects laundry but it is not safe on colored fabric and certain synthetic fabric. Chlorine bleach can lead to splotchy fading and even to holes and damage to the fabric. Chlorine bleaches have the advantages of lower cost and have a high level of bleaching power. However, chlorine bleach can damage some colors and fabrics and the bleach must be added to the wash water in dilute amounts. These compositions have not been usable in the space of water-soluble films as they are too oxidative and will not only damage the clothing but also the polymer film matrix. There have been attempts to utilize these chlorine bleaches in soluble sheets but due to its strong oxidative power, there are no such chlorine bleach sheets on the market today. There are also other items that have bleaching power and can act as bleaching agents. One of the common uses of bleach is laundry as it removes stains from clothing, but it also removes color from clothes. Oxygen beach is another form of bleach that is safe for use on most fabrics and is sometime referred to as color safe bleach or all-fabric bleach. Unlike chlorine bleach, this type of bleach does not typically remove color or patterns from the fabrics. There are 3 types of oxygen bleaches on the market. These are Hydrogen Peroxide that is liquid and Sodium Percarbonate and Sodium Perborate, that are powders which may be made from a natural plant derivative product. Once the percarbonate or perborate are exposed to water it releases oxygen and produces hydrogen peroxide, resulting in a much more effective and safer bleach than chlorine bleach. Oxygen bleach can also be used to disinfect, deodorize smells, and even reducing or killing microorganisms. Powdered oxygen bleach can be mixed with soda ash, which is sodium carbonate, to increase the pH of the solution and thus it increases the amount of hydrogen peroxide generated upon combining these ingredients. The addition of a bleach activator such as NOBS (Sodium nonaoyloxybenzenesulfonate) or TAED (Tetraacetylethylenediamine) or a combination thereof, which significantly increase the bleaching power of the composition. The preferable ratio of bleach activator to sodium percarbonate or sodium persulfate is from 1 :4 to 1 :1 and preferably 1 :3 to 1 :2 weight to weight ratio. Bleach activators react with hydrogen peroxide to form peroxy acids or peracids. Peroxy acids or peracids are more active than bleaches at lower temperature (<60C) but are typically too active to be stored in their active form in situ. Several common items can also be used as bleaching agents. While they may not be as tough as chlorine bleach, they still are capable of fading or discoloring fabrics. There are natural solutions, such as lemon juice that can sit on clothes in the sun and result in a bleaching effect. Vinegar can act as a mild bleach for some clothing. Hydrogen peroxide can also be used on colorfast fabric as if it were oxygen bleach. The problem to be solved in the present invention is to provide a dissolvable or dispersible bleach sheet and a manufacturing method thereof that can effectively deliver the full bleaching power of bleach. Said bleaching performance may be improved by increasing the pH of the composition. The pH of the composition in water needs to be alkaline with a pH greater than 9 and preferably greater than 10 and even more preferably greater than 11 for the bleach composition to produce oxygen bleach. Furthermore, even higher bleaching can be achieved by combining a bleaching activator with the active ingredients of said composition. The addition of a bleach activator such as NOBS or TAED may significantly increase the bleach effect and bleaching at lower temperatures. In order to solve the problems when combining bleach with a dissolvable or dispersible bleach sheet, the bleach granules may be coated and not dissolved until the bleach sheet is fully dissolved or fully dispersed in the water used during the application. Additionally, the bleach component or bleach granules may be introduced between two sheets and pressed together into a single bleach sheet. In the present invention, any one or more components selected from the group consisting of a water dissolvable film or water dispersible film, one or more bleaching agent, one or more bleaching activator, and one or more pH increasing agent may be used to deliver a dissolvable or dispersible bleach sheet. The present invention is a dissolvable or dispersible bleach sheet manufactured using a water dissolvable film or a water dispersible film, prepared by removing a solvent from a solution containing a film-forming water dissolvable polymer or a film forming water-dispersible polymer. It is characterized by providing a dissolvable or dispersible bleach sheet in which an active ingredient for bleaching doesn’t negatively interact with the bleach sheet composition and wherein said bleaching effect is delivered by adding the bleach sheet to water or water-based compositions. The bleaching agent may be in a form that is fully dissolved, partially dissolved, or not dissolved in the final manufacturing form of the bleach sheet. If the bleaching agent is not dissolved in the composition, it reduces the potential to negatively interact with the bleach sheet during and after manufacturing. The active ingredient for bleaching may be in a granular form and distributed in the bleach sheet. Various coatings will be disclosed to prevent the dissolution of the bleach granules during the manufacturing of the bleach sheet. Said bleach sheet can be prepared as a solution formed by mixing a water dissolvable polymer for film formation or a water dispersible polymer for film formation but is not limited to the production method. Any form in which the bleaching component is included in the film may be included in the above. In a preferred embodiment, the invention provides a bleach composition in the form of a drum-dried water soluble sheet, comprising: a water dissolvable polymer film having a bleaching agent, a bleach activator, a pH modifier, and water 1-5% by weight, wherein the polymer is 10-20 % by weight selected from the group consisting of polyvinyl alcohol, starch, and hydroxypropylcellulose, wherein the bleaching agent is 1- 60% by weight, wherein the bleach activator is 1-40% by weight, wherein the pH modifier is 1-70% by weight, wherein all percentages total 100. Any of the non-limiting embodiments may include wherein the polymer is polyvinyl alcohol. Any of the non-limiting embodiments may include wherein the bleaching agent is selected from the group consisting of sodium hypochlorite, sodium percarbonate, and sodium perborate. Any of the non-limiting embodiments may include wherein the bleach activator is selected from the group consisting of nonanoyloxybenzenesulfonate (NOBS), tetraacetylethylenediamine (TAED), lauryloxybenzenesulfonate (SDBS), benzoylcaprolactam (BzCL), 4-nitro Benzoylcaprolactam, 3- chlorobenzoylcaprolactam, benzoyloxybenzenesulfonate (BOBS), nonanoyloxybenzenesulfonate (NOBS), phenyl benzoate (PhBz), decanoyloxybenzenesulfonate (C 10 -OBS) , Benzoylvalerolactam (BZVL), octanoyloxybenzenesulfonate (C 8 -OBS), a perhydrolyzable ester, and a combination thereof. Any of the non-limiting embodiments may include wherein the pH modifying is selected from the group consisting of sodium carbonate, sodium bicarbonate, sodium hydroxide, sodium silicate and a combination thereof. Any of the non-limiting embodiments may include wherein the bleaching agent is an encapsulated dry particulate bleaching agent. Any of the non-limiting embodiments may include wherein the bleaching agent is an encapsulated dry particulate bleaching agent, and the bleaching agent is selected from the group consisting of sodium hypochlorite, sodium percarbonate, and sodium perborate, sodium dichloroisocyanurate dihydrate, sodium dichloroisocyanurate, potassium dichloroisocyanurate dihydrate, potassium dichloroisocyanurate, sodium perborate monohydrate, sodium perborate tetrahydrate and a combination thereof. Any of the non-limiting embodiments may include wherein the bleaching agent is an encapsulated dry particulate bleaching agent, and the bleaching agent is selected from the group consisting of sodium hypochlorite, sodium percarbonate, and sodium perborate, sodium dichloroisocyanurate dihydrate, sodium dichloroisocyanurate, potassium dichloroisocyanurate dihydrate, potassium dichloroisocyanurate, sodium perborate monohydrate, sodium perborate tetrahydrate and a combination thereof, and wherein the encapsulant is selected from the group consisting of sulfate, carbonate, carbohydrate, starch, maltodextrin dextrin, sucrose, cellulose, agar, carrageenan, wax, paraffin, diglyceride, gluten, casein, albumin, peptide, sodium alginate, gum arabic, chitosan, carboxymethylcellulose, pectin, shellac, and a combination thereof. Any of the non-limiting embodiments may include a surfactant selected from the group consisting of sodium lauryl sulfate, sodium dioctyl sulfosuccinate, linear alkyl benzene sulfonate, alpha olefin sulfonate, xylene sulfonate and a combination thereof. Any of the non-limiting embodiments may include glycerin 1 to 10% by weight. Any of the non-limiting embodiments may include a builder agent selected from the group consisting of citrate, citric acid, trisodium phosphate, zeolite, carbonate, phosphonate, and lime, in the amount of 1 to 10% by weight. Any of the non-limiting embodiments may include a chelating agent selected from the group consisting of EDTA, MGDA, DTPA, GLDA, and HEDP, and a combination thereof 0.1 to 1% by weight. Any of the non-limiting embodiments may include a fabric softener. Any of the non-limiting embodiments may include wherein starch is 10 - 60% by weight, said starch selected from the group consisting of corn, wheat, potato, rice, or tapioca starch and a combination thereof. Any of the non-limiting embodiments may include wherein the sheet comprises a perforated weakened tear-line. Any of the non-limiting embodiments may include wherein the sheet comprises one or more layers, and where the layers are the same or a different composition. Any of the non-limiting embodiments may include wherein said polyvinyl alcohol film includes a water dissolvable co-polymer of ethylene oxide, or a water dissolvable copolymer of propylene oxide or a combination thereof. Any of the non-limiting embodiments may include a surfactant such as an anionic surfactant, a cationic surfactant, a nonionic surfactant or a amphoteric surfactant or a combination thereof, and a binding agent, wherein the polyvinyl alcohol, surfactant, binding agent, water, or a combination thereof, are mixed and dried to form the water dissolvable bleach sheet. In another preferred embodiment, the invention provides a method for producing a water dissolvable bleach sheet, the steps comprising: (i) dissolving polyvinyl alcohol in water to form an aqueous PVA solution; (ii) mixing a bleaching agent, a bleach activator, a pH modifier to the aqueous PVA solution, and optionally one or more of a surfactant, a builder, a binding agent, and a chelating agent to form a paste; (iii) delivering the paste to a drum dryer to form a water dissolvable bleach sheet. Any of the non-limiting embodiments may include trimming the water dissolvable bleach sheet to a form 1.5-2.0 mm thick, 50-127 mm wide, and 76-203 mm long. Any of the non-limiting embodiments may include wherein the polyvinyl alcohol, water, bleaching agent, bleach activator, and pH modifier are mixed in a single homogenizer tank, wherein the homogenizer tank is heated using steam, wherein the drum dryer comprises a heated drying drum having a drive system and a mirror finish, said drying drum mounted over a bottom applicator roller assembly having a bottom feed tray with a bottom feed applicator roller disposed therein, the bottom fed tray having a inlet for receiving the paste, the bottom feed applicator roller in operative contact with paste in the bottom feed tray, wherein rotational engagement between the drying drum and the bottom feed applicator roller forms a water dissolvable bleach sheet. Any of the non-limiting embodiments may include surface spraying the water dissolvable bleach sheet with a surface agent selected from the group consisting of a bleaching agent, a bleach particle, a pH modifying agent, a bleach activator, a surfactant, a builder, a binding agent, a chelating agent, a fragrance, and a combination of one or more thereof. In another preferred embodiment, the invention provides a water dissolvable bleach sheet, comprising: a plurality of layers of a polymeric matrix of an aqueous polymer film, the polymer 10-20 % mass ratio selected from the group consisting of polyvinyl alcohol, starch, and hydroxypropylcellulose, blended with a bleaching agent, a bleach activator, and a pH modifier, wherein the aqueous polymer film, bleaching agent, bleach activator, and pH modifier are mixed together, and dried to form a water dissolvable bleach sheet. Any of the non-limiting embodiments herein may include a surfactant 1-5 %, a builder 0.1 - 5 %, a binding agent 0.1-5 %, an optional chelating agent 0.1-5 %, and water 50 - 97.6%, by weight. Any of the non-limiting embodiments herein may include wherein the aqueous polymer film layer is 50-100 urn and wherein the sheet is a laminate having 500 - 5000 layers, wherein the water dissolvable bleach sheet starts to dissolve in contact with an excess of water in less than 60 seconds. Any of the non-limiting embodiments herein may include wherein the laminate comprises biaxial layers, wherein the laminate layers are oriented as a weave, mesh, twill, satin or basket pattern, wherein the laminate is reinforced with a plurality of fibers selected from water dissolvable polymer fibers, wool fibers, cotton fibers, or hemp fibers, or wherein the laminate is reinforced with a plurality of fibers selected from water dissolvable polymer fibers, wool fibers, cotton fibers, hemp fibers, and the fibers are oriented as a weave, mesh, twill, satin or basket. Any of the non-limiting embodiments herein may include wherein the sheet is a continuous sheet having a perforated weakened tear-line to provide separate individual sheets, or wherein the sheet is mounted on a cleaning mitt, cleaning glove, or cleaning sponge. Any of the non-limiting embodiments herein may include wherein one or more of the layers is a hydrogel stiffener layer of polyvinyl alcohol, polysaccharide, or gelatin. Any of the non-limiting embodiments herein may include wherein said polyvinyl alcohol film includes a water dissolvable co-polymer of ethylene oxide, or a water dissolvable co-polymer of propylene oxide or a combination thereof. Any of the non-limiting embodiments herein may include: a surfactant such as an anionic surfactant, a cationic surfactant, a nonionic surfactant or a amphoteric surfactant or a combination thereof, and a binding agent, wherein the polyvinyl alcohol, surfactant, binding agent, water, or a combination thereof, are mixed and dried to form the water dissolvable bleach sheet. Any of the non-limiting embodiments herein may include: wherein the surfactant constitutes between 5 to 50% by weight; wherein the sheet is 3 - 10% water by weight compared to the total weight of the water dissolvable bleach sheet; wherein the composition comprises at least of 0.5% to 12% copolymer by weight compared to the total weight of the water dissolvable bleach sheet; wherein the anionic surfactant composition consists of at least 5% to 40% anionic surfactant by weight compared to the total weight of the water dissolvable bleach sheet; wherein the cationic surfactant composition consists of at least 5% to 40% cationic surfactant by weight compared to the total weight of the water dissolvable bleach sheet; wherein the non-ionic surfactant composition consists of at least 5% to 40% non-ionic surfactant by weight compared to the total weight of the water dissolvable bleach sheet; wherein the amphoteric surfactant composition consists of at least 5% to 40% amphoteric surfactant by weight compared to the total weight of the water dissolvable bleach sheet; or wherein said surfactant is selected from the group consisting of sulfate, sulfonate and a mixture thereof; or wherein the anionic surfactant is selected from the group of sodium dodecylbenzene sulfonate, sodium laureth sulfate or a combination thereof. Any of the non-limiting embodiments herein may include: a chelating agent selected from the group of EDTA, MGDA, DTPA, zeolite, phosphonate, citric acid, citrate, and a mixture thereof; a fragrance in the amount of 0 to 2% by weight; a bleaching agent is selected from the group consisting of calcium hypochlorite, sodium hypochlorite, sodium percarbonate, sodium perborate, sodium persulfate, tetrasodium pyrophosphate, urea peroxide and a combination thereof; or a fabric softener agent is selected from the group of quaternary ammonium cations / salts, cetrimonium bromide, quaternary ammonium chloride, polydimethylsiloxane, silicone, or a mixture thereof. Any of the non-limiting embodiments herein may include: wherein the polymer matrix includes a copolymer of ethylene oxide, propylene oxide or a combination thereof; or wherein the polymer matrix comprises a copolymer in the range of 0.5% to 10% of the co-polymer by weight. Any of the non-limiting embodiments herein may include: wherein the polymer matrix is a hydrogel comprising at least 50% water by weight. In another preferred embodiment, the invention provides a method for producing a water dissolvable bleach sheet, the steps comprising: (i) dissolving 5000 parts of dissolvable polymer in 20000 parts of water; (ii) mixing at 70 °C 2000 parts binder, 10 parts emulsifier, 40 parts of softening agent and 5 parts of silicone oil to the polyvinyl alcohol solution; (iii) applying the mixture to a substrate form at a depth of 50 - 100 urn and drying at a temperature of 120 °C to form a polymer film; (iv) surface treating the polymer film with a bleaching mixture to form a bleaching film, the bleaching mixture comprising a bleaching agent, a bleaching activator, and a pH modifier (v) layering the bleaching film to form a bleaching sheet having a depth from 750 - 7500 urn (micrometers), and optionally trimming and rolling to obtain a finished bleaching sheet. Any of the non-limiting methods herein may include the step of surface treating the polymer film with surfactant 1-5 %, a builder 0.1 - 5 %, a binding agent 0.1-5 %, or a chelating agent 0.1-5 %. Any of the non-limiting methods herein may include the step of including one or more layers of a hydrogel made from polyvinyl alcohol, polysaccharide, or gelatin, the hydrogel made by a process selected from reacting with a cross-linking agent (glutaraldehyde), applying a freeze-thaw cycle, or annealing. Any of the non-limiting methods herein may include the step of orienting the laminate layers as a weave, mesh, twill, satin or basket. Any of the non-limiting methods herein may include the step of applying to the laminate a plurality of reinforcement fibers selected from water dissolvable polymer fibers, wool fibers, cotton fibers, hemp fibers. Any of the non-limiting methods herein may include the step of applying to the laminate a plurality of reinforcement fibers selected from water dissolvable polymer fibers, wool fibers, cotton fibers, hemp fibers, and orienting the fibers as a weave, mesh, twill, satin or basket pattern. Any of the non-limiting methods herein may include the step of applying to a continuous sheet a perforated weakened tear-line to provide separate individual sheets. Any of the non-limiting embodiments herein may include: wherein the polymer comprises polyvinyl alcohol. Any of the non-limiting embodiments herein may include: a dispersing agent selected from the group consisting of inorganic dispersant or organic dispersant or a combination thereof. Any of the non-limiting embodiments herein may include: bleaching agent is encapsulated such that the bleaching agent is not incompatible with the dissolvable bleach sheet composition and has no adverse effect on said dissolvable bleach sheet composition. Any of the non-limiting embodiments herein may include: wherein the bleaching agent constitutes between 1 % and 60% weight to weight and preferably 2% to 50% and even more preferably 5 to 40% weight to weight ratio of the bleach sheet. Any of the non-limiting embodiments herein may include: wherein the bleaching agent comprises hypochlorite and preferably sodium hypochlorite. Any of the non-limiting embodiments herein may include: wherein the bleaching agent comprises percarbonate and preferably sodium percarbonate. Any of the non-limiting embodiments herein may include: wherein the bleaching agent comprises perborate and preferably sodium perborate. Any of the non-limiting embodiments herein may include: a dry particulate bleaching compound selected from the group consisting of sodium dichloroisocyanurate dihydrate, sodium dichloroisocyanurate, potassium dichloroisocyanurate dihydrate, potassium dichloroisocyanurate, sodium perborate monohydrate, sodium perborate tetrahydrate and sodium percarbonate or a combination thereof. Any of the non-limiting embodiments herein may include: wherein the bleaching agent comprises an encapsulant that coats the dry particulate bleaching agent. Any of the non-limiting embodiments herein may include: wherein the bleaching agent is encapsulated with the pH modifier agent in such a way that the pH modifier results in even greater bleaching effect than if the bleaching agent and the pH modifiers were added separately rather than encapsulated with said pH modifier. Any of the non-limiting embodiments herein may include:wherein the encapsulant used to coat the bleaching agent comprises of a coating such as sulfate, carbonate, carbohydrate, starch, maltodextrin dextrin, sucrose, cellulose, agar, carrageenan, wax, paraffin, diglyceride, gluten, casein, albumin, peptide, sodium alginate, gum arabic, chitosan, carboxymethylcellulose, pectin and shellac or a combination thereof. Any of the non-limiting embodiments herein may include:wherein the bleach activator is selected from NOBS, TAED, LOBS, BODA or a combination thereof. Any of the non-limiting embodiments herein may include: a bleach activator which is added between 1 to 40% and preferably 2 to 30% and more preferably between 3 to 20% weight to weight of the sheet. Any of the non-limiting embodiments herein may include: wherein the film forming composition constitutes between 1% to 30%, and preferably 5% to 25% and more preferably between 10% and 20% weight to weight of the sheet. Any of the non-limiting embodiments herein may include: a starch added between 10% and 60% weight to weight ratio of the dissolvable bleach sheet and comprises one or more of corn, wheat, potato, rice, or tapioca starch or a combination thereof. Any of the non-limiting embodiments herein may include: wherein water constitutes between 0 and 10% and preferably 2 to 8% and more preferably 3 to 6% weight to weight of the sheet. Any of the non-limiting embodiments herein may include: a humectant such as but not limited to glycerin which is added between 1 to 10% and preferably 2 to 8% and more preferably 3 to 6% weight to weight ratio of the dissolvable bleach sheet. Any of the non-limiting embodiments herein may include: pH modifier is selected from sodium carbonate, sodium bicarbonate, sodium hydroxide, or soda ash or a combination thereof. Any of the non-limiting embodiments herein may include: pH modifier constitutes between 1 % and 70% weight to weight and preferably 5% to 60% and even more preferably 10 to 50% weight to weight ratio of the dissolvable bleach sheet. Any of the non-limiting embodiments herein may include: a builder agent such as but not limited to citrate, citric acid, sodium triphosphate, zeolite, carbonate, phosphonate, and lime, in the amount of 0 to 10%, or preferably 1 to 8 % or even more preferably 2 to 7% weight to weight ratio of the dissolvable bleach sheet. Any of the non-limiting embodiments herein may include: a chelating agent selected from the group consisting of EDTA, MGDA, DTPA, GLDA, and HEDP, or a combination thereof in the amount of 0 to 1% of the sheet. Any of the non-limiting embodiments herein may include: a surfactant is selected from the group of anionic, nonionic or amphoteric surfactant or a mixture thereof. Any of the non-limiting embodiments herein may include: a solubilizer selected from the group consisting of sodium carbonate, sodium phosphate, sodium bicarbonate, sodium pyrophosphate, sodium tripolyphosphate, sodium borate, sodium citrate, sodium silicate, sodium hydroxide, sodium sulfate, zeolite or a combination thereof. Any of the non-limiting embodiments herein may include: wherein the bleaching agent is incorporated into a bleach sheet composition. Any of the non-limiting embodiments herein may include: wherein the bleaching agent is incorporated in between one or more bleach sheets. Any of the non-limiting embodiments herein may include: wherein the bleaching agent is dissolved in the bleach sheet composition. Any of the non-limiting embodiments herein may include: wherein the bleaching agent is not dissolved in the bleach sheet composition. Any of the non-limiting embodiments herein may include: wherein the bleaching agent dispersed in the bleach sheet composition. Any of the non-limiting embodiments herein may include: wherein the pH of the bleach sheet is above pH 9 and preferably above pH of 10 and even more preferably above pH of 11 . Any of the non-limiting embodiments herein may include: a dispersing agent used to increase the solubility of the film forming composition during manufacturing. Any of the non-limiting embodiments herein may include: a perfume or perfume micro-capsule or a combination thereof. Any of the non-limiting embodiments herein may include: wherein the polymer is not soluble in water but is dispersible in water such as a cellulose based extract. Any of the non-limiting embodiments herein may include: a dispersing agent selected from the group consisting of inorganic dispersant or organic dispersant or a combination thereof. Any of the non-limiting embodiments herein may include: a dry particulate bleaching compound selected from the group consisting of sodium dichloroisocyanurate dihydrate, sodium dichloroisocyanurate, potassium dichloroisocyanurate dihydrate, potassium dichloroisocyanurate, sodium perborate monohydrate, sodium perborate tetrahydrate and sodium percarbonate or a combination thereof. Any of the non-limiting embodiments herein may include: wherein the surfactant is selected from the group consisting of sodium lauryl sulfate, sodium dioctyl sulfosuccinate, linear alkyl benzene sulfonate, alpha olefin sulfonate, xylene sulfonate or a combination thereof. Referring now to the FIGURES, FIGURE 1 is an illustration of a non-limiting embodiment of a homogenizer assembly, component feeds, and drum dryer assembly according to the invention. Fig. 1 shows water supply at 70-90°C for delivery to the homogenizer tank via pumped delivery pipe with a control valve. The homogenizer tank includes a mixing paddle connected to electric motors. The PVA supply delivers polyvinyl alcohol to the homogenizer tank via pumped or gravity fed conduit for dissolving in the water. Component feeds A, B, C are delivered via pumped conduit to the homogenizer tank, and steam feed 70-120°C. In the present invention the polyvinyl alcohol, water, bleaching agent, bleach activator, and pH modifier are mixed in a single homogenizer tank, and the homogenizer tank is heated using steam. The PVA paste is pumped to the drum dryer assembly and delivered to a bottom feed tray having a bottom feed applicator roller disposed therein. The drum dryer comprises a heated drying drum having a drive system and a mirror finish, said drying drum mounted over a bottom applicator roller assembly having a bottom feed tray with a bottom feed applicator roller disposed therein, the bottom fed tray having a inlet for receiving the paste, the bottom feed applicator roller in operative contact with paste in the bottom feed tray, wherein rotational engagement between the drying drum and the bottom feed applicator roller forms a water dissolvable bleach sheet. Fig. 1 also shows optional the optional step of trimming the water dissolvable bleach sheet to a form 1.5-2.0 mm thick, 50-127 mm wide, and 76-203 mm long. In another non-limiting preferred embodiment, an additional step of surface spraying the water dissolvable bleach sheet with a surface agent selected from the group consisting of a bleaching agent, a bleach particle, a pH modifying agent, a bleach activator, a surfactant, a builder, a binding agent, a chelating agent, a fragrance, and a combination of one or more thereof. FIGURE 2 is an illustration of a non-limiting embodiment in a perspective view showing the dimensions of a water dissolvable PVA sheet according to the invention. FIGURE 3 is a photo representation of a top view of a non-limiting embodiment showing ruler dimensions of a water dissolvable PVA sheet according to the invention. FIGURE 4 is a photo representation of a side view of a non-limiting embodiment showing ruler dimensions of a water dissolvable PVA sheet according to the invention. FIGURE 5 is a flow chart illustration of a non-limiting embodiment of a method of manufacturing a water dissolvable PVA sheet using a homogenizer assembly, a supply for component feeds, and a drum dryer assembly according to the invention. FIGURE 6 is a perspective illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive and a sheet winding assembly. Fig. 6 shows drying drum gear system 9 with a motor having a variable frequency drive (VFD) gearbox pinion gear and main drum gear. Fig. 6 shows vapor outlet in canopy 10 with up / down movement scaffolding. Drying drum 1 is shown over the applicator tray and adjacent to the final product sheet guide roller 7. Final product sheet winding roller assembly 8 with drive system and VFD is shown in position to receive the dried sheet. FIGURE 7 is a perspective illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive. Fig. 7 shows drum / feed applicator roller 3B with a rotary joint for a steam inlet and condensate outlet for the drum. FIGURE 8 is a perspective illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive and steam inlet. Fig. 8 shows drum bearing support 2. Fig 8 also shows 3A rotary joint for a steam inlet for the drum. A bottom feed applicator roller 5 is shown having a drive system and VFD. A feed leveling roller 6 with a UCT bearing arrangement for level distance setting using feeler gauges is also shown. Bottom feed tray 4 is shown and contains nozzles with an electric ceramic heater. FIGURE 9 is an side view illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive, a steam inlet, and applicator roller tray. FIGURE 10 is an end view illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive, motor, and sheet winding assembly. FIGURE 11 is a top view illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive, motor, and sheet winding assembly. FIGURE 12 is a cut-away view illustration of a non-limiting embodiment of a drum dryer assembly showing a drum drive, motor, dryer drum, roller tray, roller, and steam delivery conduit. FIGURE 13 is an perspective illustration of a non-limiting embodiment of an applicator roller tray, and roller assembly. Fig. 13 shows applicator roller pipe with PFTE coating 5.2 as part of the applicator tray 5.1 . Drain 5.21 is shown at the bottom of the tray 5.1 and roller motor is shown with 5.7 gearbox mounting bracket, 5.8 gearbox, and motor 5.9. Tray flanges 5.3 and 5.4 are shown bordering tray 5.1 . Assembly lifting mechanism 5.5 is shown mounted on the tray lower surface. FIGURE 14 is an perspective illustration of a non-limiting embodiment of an applicator roller tray, and roller assembly. Fig. 14 shows overflow nozzle 5.22, drain / thermowell 5.23, and feed inlet 5.20 for paste. Applicator tray also shows a heater unit 5.10. Rotary union 5.19 connects the tray to the mount and / or the gear box 5.8. FIGURE 15 is an perspective illustration of a non-limiting embodiment of a tray raising / lowering assembly. Fig. 15 shows weld mount and section welded to the support structure. FIGURE 16 is a side view illustration of a non-limiting embodiment of a tray raising / lowering assembly. Fig. 16 shows 40 thread nut, ball, 12 thread nut, and studs attaching to section welded to the support structure. FIGURE 17 is an perspective illustration of a non-limiting embodiment of an applicator tray, roller, and tray raising / lowering assembly. FIGURE 18 is an perspective illustration of a non-limiting embodiment of a (sheet) feed leveling roller assembly. Fig. 18 shows feed leveling roller and inset detail K. FIGURE 19 is a detailed illustration of inset detail K which is a non-limiting embodiment of a leveling adjustment mechanism for the (sheet) feed leveling roller assembly having a UCT (take up) bearing and leveling adjustment with fine threading. A UCT bearing, also known as a take-up bearing, is a type of mounted bearing unit to support rotating shafts, where belt or chain tensioning and adjustment are required. UCT bearing accommodates movement and tensioning in the conveyor system, and can be adjusted to maintain proper belt or chain tension, which is important for preventing slippage and wear. DEFINITIONS The term "film" as used herein may be understood to mean a thin and flexible membrane or layer. The thickness is not particularly limited. The shape of the film is not particularly limited. The term "bleach sheet" as used herein may be understood as including a bleaching composition that is not activated in the film until said bleach sheet is being used and added to water to dissolve and / or disperse via its incorporation into a polymer film. Bleach sheets may include those formed by mixing a bleaching agent with a water dissolvable or water dispersible polymer film-forming composition. However, if the bleach granule is activated in a film-forming water dissolvable polymer or water dispersible during or after manufacturing of said bleach sheet, the composition becomes unstable and the active ingredient for bleaching may damage said bleach sheet. As a result, the problem associated with the stabilization of bleach in the bleach sheet composition and the manufacturing of said bleach sheet needs to be resolved for the ability to deliver the full effect of bleach in a dissolvable and / or dispersible bleach sheet. The “film” may be formed by completely drying a solution for preparing a film or a bleach film or may be in a semi-dried state. When the film is in a semi-dry state, it may mean a state in which the film maintains the shape of the film while containing some moisture in the film. For example, it may mean a state in which the moisture of the solution for manufacturing the film or bleach film is evaporated by 70% or more, preferably 80% or more, and even more preferably 90% or more. The term “sheet” as used herein refers to a film or bleach film in order to achieve the object of the present invention. The active ingredient for bleaching may mean preferably distributed in an undissolved state. The sheet of the present invention may include one bleach film and may be provided in the form of a single film or overlapping two or more films. When the sheet of the present invention includes two or more films, the bleaching composition may be incorporated between the two films. In another embodiment which consists of two or more films, at least one film is a bleach film. The term “bleaching agent” is any ingredient or composition that produces bleach. It may be in the form or conventional chlorine such as sodium hypochlorite bleach or the ingredients that forms some type of strong oxidizing chorine based composition such as but not limited to sodium dichloroisocyanurate. Also said “bleaching agent” may be in the form of oxygen bleach such as peroxide or the products that upon dissolution in water form hydrogen peroxide, such as but not limited to sodium percarbonate and sodium perborate. The term “dissolvable” or “soluble” as used wherein means that the composition, including the sheet, is soluble in water or somewhat soluble in water. Said soluble composition is preferably dissolved and solubilized homogenously in the water before the bleach sheet is made during production. The term “dispersible” as used wherein means the composition, including the sheet may not dissolve and may not be fully soluble in the water or completely insoluble in water, but will disperse in water. Said dispersible composition is preferably dispersed homogeneously in the water before the bleach sheet is made during production. The term “spherical1is a term including a shape that is not a perfect sphere shape. That is, the spherical cross section and / or the longitudinal section may be an ellipse rather than a perfect circle, and a regular or irregularly uneven shape is also included, not a smooth curved surface. The term “not dissolved state” means that the ingredient is 100 % not dissolved in the composition. It can be partially dissolved or completely not dissolved. The term "bleach stable" is meant that these materials must be sufficiently stable in the presence of oxygen bleaches so that they retain their aesthetics, physical, and chemical property. The term "builder" means a water softener which is capable of removing calcium and magnesium ions that are present in water. The bleach sheets of the present invention comprise a bleach stable film-forming water dissolvable or water dispersible polymer film which results in said bleach sheet form. An embodiment of the present invention comprises of a bleach sheet that is dissolvable or dispersible in water or other solvents. Said dissolvable or dispersible film is manufactured using bleaching components and a film-forming water dissolvable or water dispersible polymer, any one or more components selected from the group consisting of a bleach, a bleach activator and a pH modifier. These ingredients may be in a liquid form, a powder form, a granulated form or a combination thereof. In a preferred embodiment, a dissolvable bleach sheet according to a preferred embodiment of the present invention, may be achieved by: - Preparing a solution to produce a bleach film by dissolving a film-forming water- dissolvable polymer that can form a sheet: - Further adding a bleaching agent; - Further adding a pH modifying agent that can raise the pH above 9, 10 or 11 to maximize oxygen bleach formation: - Further adding a bleach activator to form a peracid that is even more effective at bleaching than oxygen bleach alone In yet another preferred embodiment, a dispersible bleach sheet according to a preferred embodiment of the present invention, may be achieved by: - Preparing a solution for the production of a bleach film by dissolving a film-forming water- dispersible polymer that can form a sheet: - Further adding a bleaching agent; Further adding a pH modifying agent that can raise the pH above 9, 10 or 11 to maximize oxygen bleach formation: - Further adding a bleach activator to form a peracid that is even more effective at bleaching than oxygen bleach alone. In another embodiment, during the film forming process the polymer chains aggregates and results in a film-forming water dissolvable or water dispersible polymer are released, and the active ingredients for bleach in a bleach form that is not dissolved between the polymer chains. Any one or more components selected from the group consisting of bleach activators can be added to increase the bleaching activity of the bleach sheet. In another embodiment, the present invention provides a sheet which contains the bleaching composition. These materials comprising the sheet must be bleach stable, film-forming, water dissolvable or dispersible polymers. Many water dissolvable or water dispersible sheet forming materials are not suitable for use in the present invention since it is known that these compositions will cross-link in the presence of an oxidizing agent to form a sheet that does not dissolve or disperse in water after manufacturing of said bleach sheet. Furthermore, since it is preferred that the particulate bleaching materials must be maintained in a substantially dry state, the composition of the sheet must be capable to be extruded in the form of bleach sheets, after all components have been mixed during manufacturing. Water dispersible films may offer advantages of preventing the bleaching particle from being activated during manufacturing. Furthermore, the film composition may tolerate the bleaching agent and not affected by the oxidizing power of the bleach composition in the bleach sheet. The content of the bleaching compound in said bleach sheet may include a bleaching composition comprising of but not limited to sodium percarbonate or sodium perborate. Said bleaching compound may be coated to prevent interaction with the film of the bleach sheet. Furthermore, said bleaching may be incorporated into the film by dissolution or dispersion. Suitable bleach stable water dissolvable or water dispersible film-forming polymers include but is not limited to PVA, Starch, Hydroxypropyl cellulose or other forms of cellulose. The composition of the bleach sheet should be sufficiently soluble in water or a non-aqueous solvent or should be sufficiently thermoplastic so that they can be formed into sheet form using known sheet forming methods such as extrusion. The compositions of the present invention can be formed by dissolving the bleach stable film- forming material in a suitable solvent such as methylene chloride, along with the bleaching agent. Another option is for the compositions of the present invention to be formed by dissolving the bleach stable film- forming material in an aqueous solvent such as water, along with the bleaching agent. The bleaching agent need not be soluble in the solvent but should be capable of being suspended along with the polymer. Other materials, such surfactants, may be added to improve the solubility or dispersibility if the bleach sheet. The film is then cast into sheet form and later cut up into the desired shape and size. If extrusion is to be utilized, it may not be possible to combine all the components of the present invention together at that time. In this method, the film-forming material may be extruded and the particulate bleaching composition, as well as other dry components may be dusted onto the hot surface of the film and adhere thereto. Alternatively, the above process can be utilized, and active bleaching agents can be covered with a second sheet of the same filmforming, water dissolvable or water dispersible polymer. In another embodiment, the bleaching agent or the bleach activator or a combination thereof may be added in the form of granules in order to add it in an undissolved state. Any one or more components selected from the bleach or bleach activator may be added in a “non-dissolved state', and the term “not dissolved state” means that the ingredient is 100 % not dissolved in the composition. In another embodiment, any one or more components selected from the group consisting of a bleach and a bleach activator may be added to the bleach film in an undissolved form, for example, in a granule form, which is then added to the bleach sheet. If it is contained in an undissolved form, the granules are not limited to any form. In another embodiment, the film-forming water-soluble polymer used in the bleach sheet may be selected from natural, semi-synthetic, and synthetic polymers or a combination thereof. Natural polymers may include but are not limited to gelatin, pectin, dextran, starch, chitosan, guar gum, xanthan gum, soy polysaccharide, gellan gum, maltodextrin, rosin collagen, agar, gum arabic, gum acacia, gum karaya, guar gum, carrageenan, and the like can be used. Semi-synthetic polymers, may include but are not limited to methyl cellulose, ethyl cellulose, hydroxyethyl cellulose, hydropropyl cellulose, sodium carboxy methyl cellulose, dextrin, carboxy methyl starch, dialdehyde starch, and the like may be used. Synthetic polymers may include but are not limited to polyvinyl alcohol, polyvinyl pyrrolidone, polyvinyl methacrylate, polyacrylic acid and salts thereof, polyethylene oxide, carboxy-containing acrylic resin, carboxy-containing polyester resin, water-soluble polyamide, water-soluble polyurethane, maltodextrin, and polydextrose may be used. A preferred example of the film-forming water-soluble polymer is polyvinyl alcohol (PVA) or PVA film (such as PVA film from Monosol or Kuraray). The film-forming water dissolvable polymer may be included in 5 to 80% by weight based on the total weight of the film or the bleach film after drying, and preferably 7 to 50% by weight, more preferably 10 to 20% by weight. When the content of the water- soluble polymer is less than 5% by weight, the tensile strength of the bleach sheet is too weak to form a film or a bleach film. When it is more than 80% by weight, the content of the active ingredient is relatively small. There is a problem in that the function of the film or the bleach film is deteriorated or the content of the bleaching agent or the total bleach composition resulting from the bleach activator. The coating of said bleaching agent can reduce the issues associated with the deterioration of the bleach film or the resulting bleach sheet. The film-forming water dispersible polymer may be included in 1 to 80% by weight based on the total weight of the film or the bleach film after drying, and preferably 2 to 50% by weight, more preferably 3 to 30% by weight. When the content of the water dispersible polymer is less than 5% by weight, the tensile strength of the bleach sheet is too weak to form a film or a bleach film. There is a problem in that the function of the film or the bleach film is deteriorated or the content of the bleaching agent or the total bleach composition resulting from the bleach activator. The coating of said bleaching agent can reduce the issues associated with the deterioration of the bleach film or the resulting bleach sheet. The 'water solubility' of the film-forming water dissolvable polymer in the bleach sheet according to the present invention may be defined as the following measurement conditions. After adding a certain amount of film (e.g. 10g) made of a film-forming polymer to 1 liter of water, stirring it on a magnetic stirrer set at a speed of 500 rpm for 10 minutes, and filtering the prepared film solution with a filter paper having a maximum pore size of 10 pm. Vacuum filtration may be needed to assist in the filtration process. Water is dried from the collected filtrate, and the weight of the residual material is measured. The residual weight is defined as a film-forming water- dissolvable polymer. Film-forming water-dispersible polymers also belong to the category of film-forming polymers in the present invention. When the film forming substrate is not 100% soluble in water, this referred to as a dispersible film. In this specification, the meaning of the term 'water dispersibility' is as follows. A certain amount of film (10g) was added to 1 L of water, stirred for 10 minutes on a magnetic stirrer set at a speed of 500 rpm, and the water dispersion was filtered through a 10 pm pore filter, and the filtered filter was dried. When the weight change is less than about 100%, or preferably less than 90%, or more preferably less than 80% of the weight of the initial film, it is defined as a water-dispersible film-forming polymer. The solvent used for preparing the bleach sheet according to the present invention comprises of water or a water based composition to dissolve the water-dissolvable polymer. The solvent used for preparing the bleach sheet according to the present invention comprises of water or a water based composition to disperse the water-dispersible polymer. In another embodiment the suitable bleach stable water dissolvable or water dispersible film forming polymers may be soluble in water or dispersible in water during manufacturing. In this embodiment, the bleaching composition may be soluble in water, partially soluble in water or insoluble in water. In this composition, the bleaching agent may be added during or after manufacturing the bleach sheet. Furthermore, the bleaching agent may be added by incorporating the bleach particles onto the bleach sheet by spraying, dusting or adding said bleaching agent directly onto the sheet or it may be incorporated in between two or more sheets. It has also been found that the combination of nanocellulose and a dispersing agent is very helpful in aiding dissolution of the sheet in the wash liquor and furthermore readily dissolve and / or disperse after said bleach sheet as been dried during manufacturing. Suitable dispersing agents include compounds such as surfactants. Other ingredients include. Furthermore, these materials often are personal care products as builders and also increase the bleaching of the overall system. In another embodiment the bleaching agent may use a bleach that results from the addition of an organic compound in water such as sodium dichloroisocyanurate dihydrate, sodium dichloroisocyanurate, potassium dichloroisocyanurate dihydrate, potassium dichloroisocyanurate, or a combination thereof. In another embodiment, the bleaching agent may use a bleach that results from the addition of an inorganic bleaching agents such as perborate (for example sodium perborate), percarbonate (for example, soda percarbonate), superphosphate, persulfate, persulfate perhydrate salt containing a silicate or a combination thereof. In another embodiment, the bleaching agent may use a bleach that results from the addition of an organic peroxy acid containing diacyl and tetraacyl peroxide or a combination thereof. In a preferred embodiment, the pH modifier in the present invention may be an alkaline ingredient and preferably is a carbonate (for example sodium carbonate), an hydroxide (for example sodium hydroxide), a silicate (for example sodium silicate) or a combination thereof. In another embodiment of the present invention the sheet comprises a pH modifying agent comprising but not limited to sodium carbonate, sodium bicarbonate, sodium hydroxide, sodium silicate or a combination thereof. Other pH modifiers that can raise the pH may be used. Its role is to increase the pH above 9, 10, or even above 11 . At higher pH, the bleaching agent such as percarbonate or perborate or a combination thereof increases the amount of oxygen bleach in said composition. In addition, the "bleach activator" in the present invention may be a bleach activator but is not limited to tetraacetylethylenediamine (TAED), benzoylcaprolactam (BzCL), 4-nitro Benzoylcaprolactam, 3- chlorobenzoylcaprolactam, benzoyloxybenzenesulfonate (BOBS), nonanoyloxybenzenesulfonate (NOBS), phenyl benzoate (PhBz), decanoyloxybenzenesulfonate (C 10 -OBS) , Benzoylvalerolactam (BZVL), octanoyloxybenzenesulfonate (C 8 -OBS) and any one selected from the group consisting of perhydrolyzable esters, or a combination thereof may be used. In a preferred embodiment of the present invention a peracid formed by the addition of a bleach activator comprising of but not limited to NOBS or TAED or a combination thereof. Other bleach activators may be used to increase the peracid level of the bleach sheet. In yet another embodiment a bleach and / or bleach activator is added in an undissolved form wherein most of the bleach and / or bleach activator is activated during actual bleaching, resulting in bleaching power compared to the case when added to a water dissolvable or water dispersible polymer solution. Preferably, in the present invention, when any one or more components selected from the group consisting of bleach, bleach activators and pH modifier are added as granules, in order not to dissolve in the film or the bleach film. In another embodiment the bleach granules may be coated with an inert coating or an active coating consisting of the pH modifier. In yet another embodiment, the bleach granule may be coated with the bleach activator. In yet another embodiment, the bleach activator may be coated with an inert coating or an active coating consisting of the pH modifier. In another embodiment, the granules or coated particles or a combination thereof are not limited to any form, that is, unless the component is dissolved in the manufactured bleach sheet, it is not limited to any form, and there is no particular limitation on its size. That is, the granule is a term that includes all those having irregular shapes and sizes, commonly referred to as particles, powders, granules, and the like. In yet another embodiment, the granules are a set of amorphous particles that do not have a specific shape, and in the present specification, a number of granules having different sizes are represented as average particle diameters. In another embodiment, the shape of the granules is not limited thereto, but may include, for example, a spherical type, a cylinder type, a splinter type, or a mixture of two or more types thereof. As used herein, the term "average particle diameter" means a particle size measured using a laser particle size analyzer. For reference, when measuring the particle size distribution, the diameter of the particle is an imaginary equivalent diameter. When one of the physical properties of the measured particle is similar to that of a sphere with a specific diameter, this diameter is called the equivalent diameter of the measured particle. The laser particle size analyzer uses the scattering properties to make an equivalent contrast, and the measured diameter is the equivalent scattering diameter. That is, the diameter of a fuselage sphere having the same scattering characteristics as the measured diameter is used to indicate the actual particle size. In another embodiment, the average particle diameter of the granules may be 1 to 2000 urn, preferably 10 to 500 urn, more preferably 50 to to 250 urn. In yet another embodiment, ingredients that can be applied in the form of granules may include, but are not limited to, builders, bleach, bleach activators, pH modifiers, sterilization / disinfectants, and fragrances. Therefore, any one or more components selected from the group consisting of the bleach, bleach activator, and pH modifier are added as granules, and if the granules are not dissolved after preparing a film or the bleach film, before drying, during drying or it can be added at any stage after drying. A preferred composition for the bleach sheets consists of water dissolvable or dispersible film polymer, a bleaching agent, a pH modifying agent, and a bleach activator. Another preferred composition of the present invention comprises of small amounts of materials such as a bleach stable perfume, or bleach stable perfume micro capsules or a combination thereof. The bleach sheet compositions of the present invention can be prepared by a number of conventional sheet-forming methods. One method comprises of casting a film into a mold and once the solvent is dried, a bleach sheet composition has been manufactured. The solvent for said bleach sheet may comprise of a non-aqueous liquid during manufacturing, wherein said non aqueous liquid is removed during manufacturing. Another method comprises of dissolving the film forming polymer in an aqueous solvent, wherein said aqueous liquid is removed during manufacturing. Another method for preparing the sheets of the present invention comprises extruding the film-forming composition into a sheet. This extruded sheet can be the film-forming polymer itself. This extruded film is then contacted with the dry bleaching agent. Another method for preparing said bleach sheet is to dissolve or disperse the bleaching composition into one or more sheet of film forming material. Another method for preparing said bleach sheet is to place the dry bleaching composition between one of more sheets of film-forming material. In another embodiment of the present invention, the bleach sheet may be manufactured by further comprising the step of further stacking the bleach film. After the distribution of an undissolved component of any one or more components selected from the group consisting of a film former, a pH modifier, a bleaching agent and a bleaching activator on one or both sides of the film, a bleach film is additionally added. It may include the step of laminating. The additionally laminated bleach film may be replaced with a film or a bleach film or a combination thereof. In yet another embodiment of the present invention, the step of adhering two films may be stacked by stacking each other or may be adhered after overlapping. Bonding may mean a form in which two sheets of films are attached to each other, and may be attached using an adhesive, heat, or ultrasonic waves, but the method of attaching is not particularly limited. The method of attaching the film to the film is particularly limited as long as it is possible to adhere the film so that any one or more components selected from the group consisting of bleach and bleach activators are present in an undissolved form between the film and the film. An embodiment of the present invention provides a bleach sheet manufactured by the method of manufacturing a bleach sheet of the present invention. Preferably, the manufacturing method may include a drying step, and the reaction conditions of the drying step vary depending on the process conditions and may consist of a drying drum. The temperature of the drying drum is 40 to 130°C, the drying time is 5 to 30 minutes, and the drying speed is 1 to 10 m / min of bleach sheet, and preferably the temperature of the drying furnace may be 60 to 120°C, and more preferably the drying temperature may be 70 to 110°C and more preferably 80 to 100°C. In another embodiment, a detergent component may be added to the bleach sheet composition. A generally widely used anionic surfactant, a nonionic surfactant, or an amphoteric surfactant, or a combination thereof may be mixed. It has been found that the inclusion of a small amount of surfactant into the composition aids in the dissolution of the sheet during the wash cycle. Suitable surfactants should be compatible with the other components of the composition of the present invention and should be stable in the presence of bleaching agents. The anionic surfactant may include but is not limited to carboxylate compounds such as soap, higher alcohols, higher alkyl esters, sulfuric ester salt compounds obtained by sulfated olefins, alkylbenzene sulfonates, and sulfate compounds including lauryl sulfate salts or a combination thereof. Key surfactants include but are not limited to Linear Alkyl Benzene Sulfonate (LAS), Sodium Lauryl Sulfate (SLS), Sodium Laureth Sulfate (SLES), Ammonium Lauryl Sulfate (ALS), Alcohol Ethoxylate (AE), Alcohol Ethoxysulfate (AES), Fatty Acid, Sodium Dodecyl Sulfate (SDS), Secondary Alkane Sulfonate (SAS), Methyl Ester Sulfonate, etc or a combination thereof. In addition, the nonionic surfactant may include but is not limited to polyoxyalkylene alkyl phenyl ether, polyoxyalkylene alkyl ether, polyoxyethylene polyoxypropylene block polymer, polyethylene glycol fatty acid ester, polyoxyethylene sorbitan fatty acid Esters, cocamido monomethylamine, cocamido dimethylamine, cocamido monoethylamine, fatty acid alkanolamine, amine oxide, alkyl polyglucoside, methyl polyethylene alkyl ether (methyl polyethylene alkyl ether) or sugar ether, and these may be used alone or a combination thereof. Preferably the nonionic is natural and not limited to yucca, saponin, coco glucoside, coco betaine, capryl glucoside, lauryl glucoside, or decyl glucoside or a combination therof. In addition, the amphoteric surfactant may include but is not limited to amine-oxide, Cocamidopropyl Betaine, Coco Betaine or a combination thereof. On the other hand, active ingredients for bleach, such as bleach, and bleach activators, are ingredients that react with water to express an effect and exhibit an effect of bleaching and are prepared by mixing with a film-forming water-soluble polymer or a film-forming water-dispersible sheet. As it dissolves in the process, its activity is expressed, and results in a bleaching effect that may decrease the solubility or dispersibility of the bleach sheet. Therefore, in order to solve the problem of deteriorating the performance of the bleach sheet that exhibits an effect by reacting with water in a water dissolvable polymer film or water dispersible film, an active ingredient for bleach prepared in the form of granules or coated bleaching agent and is applied to the composition for manufacturing a bleach sheet. That is, in the present invention, the active ingredient for bleaching prepared in the form of granules is mixed in a non-dissolved form between polymer chains of the bleach sheet or using encapsulated bleaching agent with an encapsulating composition that minimizes the degradation of the bleaching agent. That is, in the present invention, in a bleach sheet manufactured using a bleaching component and a film- forming water-dissolvable polymer or a water dispersible polymer, any one or more components selected from the group consisting of a builder, a bleach, and a bleach activator wherein their composition are granulated or encapsulated. It provides a bleach sheet, that is tolerant to the aggressive nature of the bleaching agent. Preferably, in the present invention, when any one or more components selected from the group consisting of bleach, bleach activators and pH modifiers are added as granules or coated particles or a combination thereof, in order not to dissolve or disperse the film, the bleaching ingredients may not be dissolved and may not be activated before washing. The moisture content is not limited to, but preferably may be about 20% by weight or less based on the total weight of the film, and preferably 10% by weight or less based on the total weight of the film. When the ingredients are mixed with a water dissolvable polymer or water dispersible solution when manufacturing a bleach sheet, their activity is expressed in the manufacturing process of the bleach sheet, and thus the performance cannot be exhibited when an actual product is used. And / or when separately added in a form that is not dissolved in the composition for manufacturing a bleach sheet, it was found that the performance of the above components can be fully exhibited, and the present invention was completed. In another embodiment, a builder component may be added to the bleach sheet composition. The term "builder" means a water softener. The builder is not limited to but refers to a substance that acts such as precipitating calcium or magnesium in hard water, removing it by ion exchange, or forming a chelate to block its function as an ion. That is, the builder is activated by reacting with water to express the above effect. The builder usable in the present invention may preferably be an alkali builder, but is not limited to sodium hydroxide, sodium carbonate, sodium hydrogen carbonate, sodium metasilicate, sodium alkali silicate, sodium neutral silicate, sodium tripolyphosphate, sodium pyrophosphate, Sodium borate, zeolite (sodium aluminosilicate), MEA (monoethanolamine, monoethanolamine), and TEA (triethanolamine, triethanolamine). It may be any one selected from the group consisting of, or a combination thereof. In general, when a builder is added to a water dissolvable polymer solution in powder form during the manufacturing process of a bleach sheet, as in the prior art, the builder is activated during the sheet manufacturing process by water contained in the water dissolvable or water dispersible polymer solution, thereby exerting a full effect during actual washing. It is difficult to do, and in the case of PVA, it is difficult to form a sheet due to gelation or salting out by reaction, and solubility may be deteriorated due to the bleaching agent. In order to solve this problem, the present invention uses a coating process to encapsulate the bleaching agent and thus prevent the immediate bleaching activation process. Said coating may comprise of the builder. In yet another embodiment, the bleaching agent doesn’t react negatively with the non-water dissolvable film and the water dispersible film is not affected by the bleaching agent and the resulting bleaching composition. In another embodiment, the "sterilization / disinfectant" may use components that can be generally used during bleaching, and is not limited thereto, but is not limited to sodium hypochlorite, hydrogen peroxide, urea peroxide, sodium diisocyanate (NaCI 3 (CON) 3 ) , Potassium sulfate ((KHSO 5 ) 2 KHSO 4 K 2 SO 4 ), calcium peroxide, sodium tripolyphosphate, sodium acid pyrophosphate, and the like can be used. When the component is prepared in the form of granules, it may be prepared in the form of granules by mixing a single component or two or more components. In another embodiment, a fabric softener, a dispersant, an emulsifier, etc. may be additionally added to the bleach sheet. More specifically, the bleach sheet according to the present invention may use a quaternary ammonium salt-based cationic surfactant as a fabric softener. For example, dialkyl dimethyl ammonium chloride, alkyl imidazolinium salt, dialkylamido quaternary ammonium salt and ester quat type, or a combination thereof may be added to the bleach sheet. In another embodiment, natural or synthetic cationic polymers may be used as the fabric softener component. For example, but not limited to, cationic guar such as guar hydroxypropyltrimonium chloride, hydroxypropyl guar hydroxypropyltrimonium chloride, cellulose (polyquaternium-10), polyquaternium series, dimethyl diallyl Ammonium chloride polymer, acrylamide-dimethyldiallylammonium copolymer, polyvinylpyrrolidone (PVP)-dimethylaminoethyl methacrylate copolymer, acrylic acid- dimethyldiallylammonium chloride copolymer, acrylamide-dimethylamino ethylmethacryl methyl chloride copolymer, a trimethylaminoethyl methacrylate polymer, or a combination thereof may be added to the bleach sheet. In another embodiment, a dispersant may be contained in the bleach sheet of the present invention. For example, a dispersant helps to uniformly mix a water- dissolvable polymer or stabilize a water dispersible polymer and an active ingredient such as a cationic surfactant, and the dispersant helps the water dispersibility of the active ingredient for bleaching when the film is dissolved or dispersed in water. The bleach sheet according to the present invention may use a nonionic surfactant as an emulsifier. For example, polyoxyalkylene alkyl phenyl ether, polyoxyalkylene alkyl ether, polyoxyethylene polyoxypropylene polymer, polyethylene glycol fatty acid ester, polyoxyethylene sorbitan fatty acid ester, or a combination thereof may be added to the bleach sheet. The content of the emulsifier may be 0 to 40% by weight based on the total weight of the film after drying, preferably 1 to 20% by weight, more preferably 1 to 10% by weight. The bleach sheet according to the present invention may be used by adding a bleach stable fragrance, a preservative, a stabilizer, a colorant or an antibacterial agent or a combination thereof in addition to the above components. The thickness of the bleach sheet according to the present invention is preferably 1 mm to 10 mm, and more preferably 1 .5 mm to 7 mm and even more preferably 2 mm to 5 mm. If the thickness of the dried bleach sheet is less than 1 mm, the active ingredient will be insufficient to produce enough bleaching using said bleach sheet. If the thickness of the dried bleach sheet exceeds 10 mm, the fast dissolution or fast dispersion properties will be reduced. The bleach sheet according to the present invention completely dissolves or completely disperses in water after the use is completed, and there is no need to remove the bleach sheet separately. That is, the water dissolvable polymer or the water dispersible polymer forming the matrix of the bleach sheet is dissolved or dispersed completely in water. In another embodiment, a bleach sheet having a multilayer structure in which one or more films or bleach films are stacked to form a multilayer structure. In another embodiment, there is provided a bleach sheet in which a film is prepared by using a film- forming water-dissolvable polymer or a film forming water dispersible film which is additionally laminated on one or both sides of the bleach sheet. The film-forming water-dissolvable or water dispersible polymer in which the active ingredient for bleaching is distributed between the polymer chains prepared according to the present invention is solidified in a film form, and in particular, from the group consisting of a bleach, a pH modifier, and a bleach activator prepared in a granular form. The bleach sheet containing any one or more selected ingredients provides excellent bleaching performance in the sheet form. The present invention also relates to a method of making a film containing a water soluble composition of polyvinyl alcohol (PVA), which is processed and may be extruded to produce filaments or fibers by converting the filaments and / or fibers and / or nonwoven webs into films. In another embodiment, the PVA is casted and formed into a film. Casting processes for making films, particularly water-soluble films, and / or films comprising water-soluble film forming materials (eg, polyvinyl alcohol) are known in the art. Such casting processes use a solvent and a solution of a film-forming material such as polyvinyl alcohol, which is deposited on and / or flowed over a casting surface such as a metal wheel, roller or belt. The solvent is then removed from the solution, for example by drying. Once the solvent is removed from the solution, a film formed from the filament forming material remains on the casting surface. The casting process for making films is known to be very time intensive since the solvent needs to be removed by drying. As used herein, “filament” means an elongated microparticle having a length that greatly exceeds its diameter, ie, a ratio of length to diameter of at least about 10. The filaments of the present invention can be spun from the filament forming composition via suitable spinning process operations, such as melt blowing and / or spun bonding. The filaments of the present invention may be single component and / or multicomponent. For example, the filament may comprise a bicomponent filament. The bicomponent filament may be in any form such as side-by-side, core and sheath, or sea-island type. The filaments of the present invention are 2 inches or more, and 3 inches or more, and 4 inches or more, and 6 inches or more. As used herein, an additive may include a plasticizer. Non-limiting examples of suitable plasticizers of the present invention include polyols, copolyols, polycarboxylic acids, polyesters, and dimethicone copolyols. Examples of useful polyols include glycerin, diglycerin, propylene glycol, ethylene glycol, butylene glycol, pentylene glycol, cyclohexanedimethanol, hexanediol, 2,2,4-trimethylpentane-1 ,3-diol, polyethylene glycol (200-600), sugar alcohols such as pentaerythritol, sorbitol, mannitol, lactitol and other mono- and polyhydric low molecular weight alcohols (eg C2-C8 alcohols); mono, di- and oligosaccharides such as fructose, Examples include, but are not limited to, glucose, sucrose, maltose, lactose, and higher fructose corn syrup solids, and dextrin, and ascorbic acid. In yet another example, the plasticizer includes glycerin and / or propylene glycol, and / or a glycerol derivative, such as propoxylated glycerol. In yet another embodiment, the plasticizer is selected from the group consisting of glycerin, ethylene glycol, polyethylene glycol, propylene glycol, glycidol, urea, sorbitol, xylitol, maltitol, saccharides, ethylene bisformamide, amino acids, and mixtures thereof. Is done. As used herein, an additive may include a crosslinking agent suitable for crosslinking one or more filament-forming materials present in the filaments of the present invention. In one example, the cross-linking agent includes a cross-linking agent that can cross-link the hydroxyl polymer together, for example, via the hydroxyl portion of the hydroxyl polymer. Non-limiting examples of suitable crosslinkers include imidazolidinone, polycarboxylic acids, and mixtures thereof. In one example, the cross-linking agent comprises a urea glyoxal adduct cross-linking agent, for example, a dihydroxy imidazolidinone such as dihydroxyethylene urea (“DHEU”). Crosslinking agents may be present in the filament forming composition of the present invention and / or in the filaments to control the solubility and / or dissolution of the filaments in a solvent such as a polar solvent. As used herein, an additive may include a rheology modifier such as a shear force modifier and / or an extension modifier. As used herein, an additive may include a visual signal agent wherein the additive may be used when the filament is exposed to the intended application conditions and / or when the active agent is released from the filament and / or when the morphology of the filament changes. To provide a visual signal, it includes one or more colors and / or dyes incorporated into the filaments of the present invention. As used herein, an additive may include one or more release agents and / or lubricants. Non-limiting examples of suitable release agents and / or lubricants include fatty acids, fatty acid salts, fatty alcohols, aliphatic esters, sulfonated fatty acid esters, aliphatic amine acetates, fatty acid amides, silicones, aminosilicones, fluoropolymers, and mixtures thereof. As used herein, the naturally occurring starch is generally consisting of a mixture of linear amylose and branched amylopectin polymers of D glucose units. Amylose is essentially a linear polymer of D-glucose linked by (1 ,4) -a-D bonds. Aminopectin is a highly branched polymer of (1 ,4) -a-D bonds and (1 ,6) -a-D-glucose units at branch points. Naturally occurring starch is typically a relatively high concentration of amylopectin, such as corn starch (64-80% amylopectin), waxy maize (93-100% amylopectin), rice (83-84% amylopectin), potato (About 78% amylopectin) and wheat (73-83% amylopectin). Although all starches are potentially useful herein, the present invention is most commonly practiced with high amylopectin natural starch derived from agricultural sources, which is an abundant source and can be easily supplemented and offers the advantage of being inexpensive. As used herein, the “starch” includes any naturally occurring unmodified starch, modified starch, synthetic starch, and mixtures thereof, and mixtures of amylose or amylopectin fractions, It may be modified by chemical, chemical, or biological processes, or combinations thereof. As used herein, the starch or starch mixture useful in the present invention is from about 20% to about 100%, more typically from about 40% to about 90%, even more typically. Having an amylopectin content from about 60 wt% to about 85 wt% starch or mixtures thereof. As used herein, suitable starches of natural origin include: corn starch, potato starch, sweet potato starch, wheat starch, sago palm starch, tapioca starch, rice starch, soybean starch, arrow root starch, amino starch, bracken starch, lotus starch, Nonlimiting examples include waxy corn starch and high amylose corn starch. Naturally occurring starches, particularly corn starch and wheat starch, are preferred starch polymers due to their economics and availability. As used herein, non-limiting examples of suitable surfactants include anionic surfactants, or cationic surfactants, or nonionic surfactants, or zwitterionic surfactants, or amphoteric surfactants, or a combination thereof. A co-surfactant may also be included in the filament. For example, for filaments designed for delivering cleaning benefits, the total surfactant concentration should be sufficient to provide cleaning including stain and / or odor removal, generally, in the range of about 0.5% to about 95%. In addition, surfactant systems comprising two or more surfactants designed for use in the bleach filaments are fully anionic surfactant systems, or a combination of two or more different anionic surfactants, or a mixture of different types of surfactant system, or a combination thereof. As used herein, a surfactant or a combination of surfactants may be linear or branched surfactants. As used herein suitable linear surfactants include those derived from agricultural chemical oils, such as coconut oil, palm kernel oil, soybean oil, or other vegetable oils. As used herein, the suitable anionic surfactants may include alkyl sulfates, alkyl ether sulfates, branched alkyl sulfates, branched alkyl alkoxylates, branched alkoxylate sulfates, medium chain branched alkyl allyl sulfonate, sulfated monoglyceride, sulfonated olefin, alkyl allyl sulfonate, primary or secondary alkane sulfonate, alkyl sulfosuccinate, acyl taurate, acyl isethionate, alkyl glyceryl ether sulfonate, sulfonated methyl ester, sulfonated fatty acid, alkyl phosphate, acyl glutamate, acrylic sarcosinate, alkyl sulfoacetate, acylated peptide, alkyl ether carboxylate, anionic fluorosurfactants, sodium lauroyl glutamate, or a combinations thereof. As used herein, the suitable alkyl sulfates and alkyl ether sulfates for use herein include materials having the corresponding formulas ROSO 3 M and RO

[0005] (C 2 H 4 O) x SO 3 M, wherein R Is an alkyl or alkenyl from about 8 to about 24 carbon atoms, x is 1-10, and M is a water-soluble cation such as ammonium, sodium, potassium, and triethanolamine. Other suitable anionic surfactants are MacCutcheon's “Detergents and Emulsifiers” (North American Edition (1986), Allred Publishing Corp.) and McCutcheon's “Functional Materials 92” (Natural Publishing Corp.). As used herein, anionic surfactants useful in the filaments of the present invention, C 9 -C 15 alkyl benzene sulfonates (LAS), C 8 -C 20 alkyl ether sulfates, such as alkyl poly (ethoxy) sulfates, C 8 ~ C 20 alkyl sulfates, and mixtures thereof. Other anionic surfactants may include methyl ester sulfonate (MES), methyl ester etchelate (MEE), sulfonated estolides, and mixtures thereof. As used herein, the anionic surfactant is a C n -C alkyl benzene sulfonate (“LAS”) and primary branched chain, and a random C 10 -C 20 alkyl sulfate (“AS”), formula CH3(CH2) x CHOSO3- M +) CH3and CH3(CH2)y(CHOSO3 - M +) C 10 ~C secondary of CH 2 CH 3 (2,3) alkyl sulfates (formula In which x and (y + 1) are integers of at least about 7, preferably about 9, and M is a water-solubilizing cation, in particular sodium, an unsaturated sulfate such as oleyl sulfate), C 10 -C a-sulfonated fatty acid esters, C 10 -C 18 sulfated alkyl polyglycosides, C 10 -C alkyl alkoxy sulfates ( "AExS") (the formula x is 1 to 30), and C 10 -C alkyl alkoxy Ruboxylates (eg containing 1-5 ethoxy units), medium chain branched alkyl sulfates as described in US Pat. Nos. 6,020,303 and 6,060,443; US Pat. No. 6,008, medium chain branched alkyl alkoxy sulfates (MLAS) as described in 181 and 6,020,303; as described in WO 99 / 05243, WO 99 / 05242, and WO 99 / 05244 Modified alkylbenzene sulfonate (MILAS); methyl ester sulfonate (MES); and alpha-olefin sulfonate (AOS). As used herein, other suitable anionic surfactants that can be used are alkyl ester sulfonate surfactants, including sulfonated linear esters of C 8 to C 20 carboxylic acids (ie fatty acids). The Other suitable anionic surfactants that can be used salts of soap, C8-C 22 primary or secondary alkane sulfonates (primary of secondary alkanesulfonates), C 8 ~C 24 olefin sulfonates, sulfonated polycarboxylic acids, C8- C 24 alkyl polyglycol ether sulfates (alkylpolyglycolethersulfates) (contain ethylene oxide up to 10 moles); alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleoyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, paraffin sulfonates, alkyl phosphates , isethionates, eg acyl isethionates, N-acyl taurates, alkyl succinates and sulfosuccinates, monoesters of sulfosuccinates (e.g. saturated and unsaturated C 12 -C monoesters) monoester, diester sulfosuccinates (e.g., saturated and unsaturated C 6 -C 12 diesters), and alkyl polysaccharide sulfates, such as alkyl polysaccharides sulfates, and alkyl polyethoxy carboxylates such as those of the formula RO(CH2CH2O) k -CH2COO-M + ( wherein R is a C8-C 22 alkyl, k is an integer of 0, M is a soluble salt-forming cation). As used herein, other suitable anionic surfactants are alkyl benzene sulphonic acid of C 10 -C 16, preferably an alkali metal salt of alkylbenzene sulfonic acid C n -C 14 As used herein, the suitable anionic surfactants are linear alkyl group is linear such as alkyl benzene sulfonates are known as “LAS”. Such surfactants and their preparation are described, for example, in US Pat. Nos. 2,220,099 and 2,477,383. In other examples, linear alkyl sulfonate or linear alkylbenzene sulfonate or liner alkyl benzene sulfonate. Car Cleaning Sheet Preferred Embodiments In a preferred embodiment, the invention provides a process for manufacturing a water dissolvable car cleaning sheet, comprising: (i) homogenizing at 85 °C in a high shear mixer an aqueous solution of polyvinyl alcohol, a surfactant, a builder, a binding agent, a chelating agent, and a car surface treatment ingredient, to form a PVA homogenate; (ii) casting the PVA homogenate as a wet film onto a heated stainless steel roller drum and dehydrating using steam heat to obtain a PVA film 1.5 - 2.0 mm thick; and (iii) optionally trimming the PVA film to form a single sheet size (2-5” wide and 3-8” length) of a water dissolvable car cleaning sheet. In another preferred embodiment, the invention provides a water dissolvable car cleaning sheet comprising polyvinyl alcohol 3 - 25 %, a surfactant 5 - 50 %, a builder 0.1 - 5 %, a binding agent 0.1 - 5 %, a chelating agent 0.1 - 5 %, a car surface treatment ingredient 0.1 - 5 %, and water 3 - 50%, by mass ratio, in a PVA film 1.5 - 2.0 mm thick; trimmed to form a single sheet size 2-5” wide and 3-8” length of a water dissolvable car cleaning sheet. Any of the preferred embodiments herein may include wherein the car surface treatment is a car interior cleaning treatment comprising sodium triphosphate, 2- butoxyethanol, and ethyl alcohol. Any of the preferred embodiments herein may include wherein the car surface treatment is a car exterior cleaning treatment comprising dimethicone, citral, polyethylene glycol (PEG-9), and sodium hydroxide. Any of the preferred embodiments herein may include wherein said binding agent is selected from the group consisting of: resin, wax, gum, accroides, candelilla, guar gum, gum Arabic, shellac, tragacanth, and a mixture of one or more thereof. Any of the preferred embodiments herein may include wherein the builder is selected from the group consisting of: citric acid, citrate, sodium carbonate, sodium silicate, polyphosphates, and a mixture of one or more thereof. Any of the preferred embodiments herein may include wherein the chelant is selected from the group consisting of EDTA, MGDA, DTPA, sodium gluconate or a mixture of one or more thereof. Any of the preferred embodiments herein may include wherein the aqueous solution includes a residue remover. Any of the preferred embodiments herein may include wherein said aqueous solution includes a water dissolvable co-polymer selected from the group consisting of ethylene oxide co-polymer, propylene oxide co-polymer, and a combination ethylene oxide-propylene oxide co-polymer. Any of the preferred embodiments herein may include wherein the water dissolvable car cleaning sheet is 3 - 10% water by weight. Any of the preferred embodiments herein may include wherein the water dissolvable car cleaning sheet comprises 0.5% to 12% of a copolymer by weight. Any of the preferred embodiments herein may include wherein the water dissolvable car cleaning sheet comprises 5% to 50% surfactant by weight, wherein the surfactant is selected from the group consisting of an anionic surfactant, a cationic surfactant, a non-ionic surfactant, and an amphoteric surfactant. Any of the preferred embodiments herein may include wherein the chelating agent is selected from the group of EDTA, MGDA, DTPA, zeolite, phosphonate, citric acid, citrate, and a mixture thereof. Any of the preferred embodiments herein may include the step of applying a waterbased fragrance 0.3% by weight to the water dissolvable car cleaning sheet using a sandwich roller. Any of the preferred embodiments herein may include wherein the aqueous solution includes a bleaching agent is selected from the group consisting of calcium hypochlorite, sodium hypochlorite, sodium percarbonate, sodium perborate, sodium persulfate, tetrasodium pyrophosphate, urea peroxide and a combination thereof. Any of the preferred embodiments herein may include wherein the aqueous solution includes a fabric softener agent is selected from the group of quaternary ammonium cations / salts, cetrimonium bromide, quaternary ammonium chloride, polydimethylsiloxane, silicone, and a mixture thereof. Any of the preferred embodiments herein may include wherein water dissolvable car cleaning sheet is a hydrogel comprising at least 50% water by weight. Any of the preferred embodiments herein may include wherein the anionic surfactant is selected from a group consisting of sulfate, sulfonate, sodium dodecylbenzene sulfonate, sodium laureth sulfate, and a combination thereof. Any of the preferred embodiments herein may include wherein the aqueous solution includes an anti-beading compound. Any of the preferred embodiments herein may include wherein the aqueous solution includes a cleaning grit selected from the group consisting of silicate, diatomaceous earth, silica particles, quartz particles, calcite particles, rottenstone, whiting, pumice, volcanic ash, marble particles, feldspar particles, copper particles, polymer particles, and metal particles. Any of the preferred embodiments herein may include wherein the sheet is mounted on a cleaning mitt, cleaning glove, or cleaning sponge. Any of the non-limiting embodiments herein may include wherein the sheet is manufactured as a laminate, or wherein the laminate comprises biaxial layers, or wherein the laminate layers are oriented as a weave, mesh, twill, satin or basket pattern. Any of the non-limiting embodiments herein may include wherein the sheet is reinforced with a plurality of fibers selected from water dissolvable polymer fibers, wool fibers, cotton fibers, or hemp fibers, or wherein the fibers are oriented as a weave, mesh, twill, satin or basket. Any of the non-limiting embodiments herein may include wherein the sheet is a continuous sheet having a perforated weakened tear-line to provide separate individual sheets, or wherein the sheet is mounted on a cleaning mitt, cleaning glove, or cleaning sponge. Any of the non-limiting embodiments herein may include wherein sheet is a hydrogel of polyvinyl alcohol, polysaccharide, or gelatin. Any of the non-limiting embodiments herein may include a water-repellent beading ingredient comprising a hydroxy-terminated polydimethylsiloxane in acetone and water. In another preferred embodiment, the invention provides a method for producing a water dissolvable car cleaning sheet, the steps comprising: (i) dissolving 5000 parts of polyvinyl alcohol in 20000 parts of water; (ii) mixing at 70 °C 2000 parts binder, 10 parts emulsifier, 40 parts of softening agent and 5 parts of silicone oil to the polyvinyl alcohol solution; (iii) applying the mixture to a substrate form at a depth of 50 - 100 urn and drying at a temperature of 120 °C to form a polyvinyl alcohol film; (iv) surface treating the polyvinyl alcohol film with a cleaning mixture to form a cleaning film, the cleaning mixture comprising a surfactant 1-5 %, a builder 0.1 - 5 %, a binding agent 0.1-5 %, a chelating agent 0.1-5 %, and a car surface treatment ingredient; (v) layering the cleaning film to form a cleaning sheet having a depth from 750 - 7500 urn (micrometers), and optionally trimming and rolling to obtain a finished cleaning sheet. Any of the non-limiting methods herein may include the step of including one or more layers of a hydrogel made from polyvinyl alcohol, polysaccharide, or gelatin, the hydrogel made by a process selected from reacting with a cross-linking agent (glutaraldehyde), applying a freeze-thaw cycle, or annealing. There are a wide range of compositions that can be used to develop a CCS that can be used to clean any of the exterior and / or interior of the car surfaces. In order to deliver the best possible car cleaning results, a single dissolvable PVA film sheet may be produced or a series of laminated dissolvable PVA film sheets may be developed to incorporate all of the desirable car cleaning tasks using said CCS composition. By using a CCS composition that is made of two or more sheets that overlap each other, a series of unique car cleaning benefits that can be first delivered with the first layer of the CCS composition and a secondary benefit can be achieved as the first layer of the CCS dissolves and then exposes the composition of the second layer to perform a different cleaning task than the first layer was designed to deliver. A third and perhaps even a fourth layer may be used to deliver a unique set of sequential car cleaning tasks that couldn’t be achieved with a single layered sheet of said CCS composition. One of the most common ingredients used for car cleaning and detailing is surfactant. Some of these surfactants include sodium Lauryl Sulfates, Linear Alkyl Benzene Sulfonic Acid, Sodium Lauryl Ether Sulfate, Coco Diethanolamine, Alkylpolyglucosides, Amine Oxides, and Betaines. Synergetic compositions of surfactants are sought to maximize foam and cleaning performance while minimizing the total amount of the overall surfactant fraction in the CCS. Other surface cleaners, all-purpose cleaners, car wash products and hand soap composition can be incorporated into the PVA substrate of the CCS to deliver maximum cleaning with or without the addition of water or other solvents. The total range of surfactant composition in the CCS ranges from approximately 0.1 % to more than approximately 35%, and preferably 3% to 25% and more preferably 5% to 20% in the CCS composition. The surfactants are incorporated into the PVA film and can be released as the PVA film dissolves. The CCS can be used directly onto the car surface or combined with the addition of water or other solvents to activate the surfactants in the CCS. Additionally, the CCS can be used after the car has been cleaned and used while the car is drying or is fully dried. In this step, the CCS can deliver different attributes as a conditioner. For this particular benefit, various ingredients such as cationic surfactants, various polymers and additional deposition from specific binding agents can collaborate towards the conditioning or treatment of the car surface that is targeted for said benefit such as fabric conditioning or exterior car surface conditioning such as urethane coating to deliver residual shine and protection from the external elements including but not limited to ingredients such as sun, oxidation, oil, dirt or a combination thereof. Additionally, the CCS can be used to protect the external surface of the car and can consist of waxes, clear coat, paint sealant, or any other external treatment designed to protect the external surface of the car. Some example applications include adding the fibrous matrix to the CCS to further add some form of mild abrasion to deliver buffing benefit to remove oxidative layers or remove small scratches on the paint. In some forms, the CCS may include the composition of small particle size of silica, alumina, calcified kaolin, hydrous kaolin, calcified alumina, calcified silica, Wollastonite, Clay bar, or a combination thereof. The abrasion from the smaller particles should be followed up with a CCS composition that consists of a step that will prevent exposure of the external car surface, once the treatment has been completed, and a protective coating should be applied to further protect the car surface from further damage. The present invention relates to a composition for forming fibers or forming a film of car cleaning composition. The CCS fiber may include a PVA composition and may be combined with a wide range of ingredients to deliver a wide range of consumer benefits. In yet another form, the present invention relates to a CCS that is fabricated from car cleaning fibers or extruded from car cleaning filaments that results in a woven or non-woven substrate depending on the targeted application. The described invention is based on a flexible poly-vinyl alcohol (PVA) and comprises several other components that are designed to create a consumer product that delivers car cleaning benefits in a wide range of applications. Said composition of the CCS may also be based on various methods to produce a CCS with a broad range of additional properties, either independently into a series of different CCS or via a combination of various properties that are incorporated into a single CCS that can be used to clean various car surfaces. The resulting CCS can be used to cover all the existing car cleaning applications today and even additional less typical properties such any of the existing external and internal car cleaning applications. This may be achieved via leaving a unique shine and protection of the car surface against the sun, oxidation, greasy residues, oily residue, clear coating, glass cleaning, glass protection, or a combination thereof. The CCS can essentially replace all the individual products that are currently sold on the market today in wet or dry forms. The CCS may be added to a bucket of water to wash the car surfaces or used directly to clean the exterior, or the interior or a combination thereof. The CCS may have a single layer or composed of a series of layers that can deliver sequential treatment that would otherwise require a multitude of different products rather than a single CCS to deliver the same or even better final car cleaning benefits. This invention provides a convenient and cost-effective method for delivering car cleaning and detailing using a completely new form consisting of a dissolvable sheet. The car cleaning and detailing ingredients are formed into fibers that may be interconnected into a fibrous matrix or simply dried into a film with different aesthetics, size and many other properties depending on the composition and purpose. The fibrous matrix of the car cleaning and detailing composition is made to be used as-is or can be activated when water or some other form of liquid is added to the CCS to form a car cleaning and detailing composition. Similar benefit can be achieved with a film like substrate as compared to that of a fiber like composition. Some examples include additional car conditioning materials and / or perfume and fragrance composition to further increase the benefit of the PVA based conditioning and scent delivery system. For car cleaning and detailing a CCS is a preferred form as it can deliver any of the car cleaning objectives. The car cleaning checklist for the exterior consists of a wide range of potential tasks depending on the surface for which the CCS is formulated. On painted surfaces the use can consist of washing the surface, removing bug and tar, oxidation removal, polish, protect, wax or seal that paint surface. For wheels, the CCS can wash the wheels, apply a protective coating, clean the wheel wells, and clean the brake calipers. On tires, the CCS can clean rubber and dress the tires. For window and glass, the CCS can clean the windshield, sunroof, side mirror, passenger windows, headlights, and taillights. For trim and molding, the CCS can clean the front bumper, the splash guards, the front grill and the rocker panels. Other miscellaneous applications for the CCS consist of cleaning the tailpipe, license plate, doorjambs and gas tank plate. For car cleaning and detailing a CCS is also a preferred form as it can deliver any of the interior car cleaning parts. On carpets and upholstery, the CCS can clean the floor mats, and the carpet. On dashboards, CCS can clean the dashboard, console area, passenger trim pieces, steering wheel, knobs, vents, glovebox, and set levers. On leather the CCS can clean and condition the leather. On windows and glass, the CCS can clean the windshield, sunroof, passenger windows, and console. On trunks, the CCS can clean the interior, the rain gutter, and the trunk lid. In another aspect, the present invention relates to a method of making a film containing a water soluble composition, optionally made from polyvinyl alcohol (PVA), which is processed and may be extruded to produce filaments or fibers by converting the filaments and / or fibers and / or nonwoven webs into films. In another embodiment, the PVA is casted and formed into a film. Casting processes for making films, particularly water-soluble films, and / or films comprising water-soluble film forming materials (eg, polyvinyl alcohol) are known in the art. Such casting processes use a solvent and a solution of a film-forming material such as polyvinyl alcohol, which is deposited on and / or flowed over a casting surface such as a metal wheel, roller or belt. The solvent is then removed from the solution, for example by drying. Once the solvent is removed from the solution, a film formed from the filament forming material remains on the casting surface. The casting process for making films is known to be very time intensive since the solvent needs to be removed by drying. Non-water soluble films and / or non-water soluble non-water soluble filament forming materials such as polypropylene, polyethylene, and thermotropic polymers (i.e., polymers that form liquid crystal melts) are, for example, water insoluble. Filaments of filament forming material have been made by spinning a web and then pressing the resulting web with heat into a film (often a porous film). However, such waterinsoluble films and / or films containing water-insoluble filament forming materials are not suitable for uses and / or products that require water-soluble films. Accordingly, films, particularly polar solvent soluble (e.g., water soluble) films, and / or polar solvent soluble filament forming materials, and / or difficulties of conventional film casting methods (specifically, solvents and film forming materials, and / or There is a need for a method of making a film comprising a water soluble filament forming material that avoids the fact that a film made from a casting solution containing a filament forming material is made at a low rate. The present invention creates a film, for example a polar solvent soluble film and / or a film containing a polar solvent soluble filament forming material, by converting a nonwoven web containing filaments and / or fibers comprising a polar solvent soluble filament forming material into a film. By satisfying the above requirements by providing a process to do so. In one embodiment of the present invention, a. Providing a nonwoven web comprising a plurality of filaments, the plurality of filaments comprising a polar solvent soluble filament forming material; b. Converting the nonwoven web to a film, and a process for making a film from the nonwoven web is provided. In another embodiment of the invention, a film made by the process according to the invention is provided. Accordingly, the present invention provides a process for making a film, a film made by such a process, and a unit volume product comprising such a film. Definitions As used herein, “filament” means an elongated microparticle having a length that greatly exceeds its diameter, ie, a ratio of length to diameter of at least about 10. The filaments of the present invention can be spun from the filament forming composition via suitable spinning process operations, such as melt blowing and / or spun bonding. The filaments of the present invention may be single component and / or multicomponent. For example, the filament may comprise a bicomponent filament. The bicomponent filament may be in any form such as side-by-side, core and sheath, or sea-island type. The filaments of the present invention are 2 inches or more, and 3 inches or more, and 4 inches or more, and 6 inches or more in length. As used herein, filaments are typically considered continuous or essentially nearly continuous. Filaments are relatively longer than fibers. Non-limiting examples of filaments include meltblown and / or spunbond filaments. As used herein, one or more fibers can be formed from the filaments of the present invention so that the filaments are cut to shorter lengths (e.g., less than 2 inches in length). Thus, in one embodiment, the present invention also comprises fibers comprising fibers made from the filaments of the present invention, such as one or more filament forming materials, and optionally one or more additives such as active agents. Including. Accordingly, references herein to the filaments of the present invention include fibers made from such filaments, unless otherwise noted. Fibers are typically considered discontinuous in nature relative to filaments that are considered to be essentially continuous. As used herein, “filament forming composition” means a composition suitable for making the filaments of the present invention, such as by melt blowing and / or spunbonding. Filament-forming compositions comprise one or more filament-forming materials that exhibit properties that make them suitable for spinning into filaments. In one example, the filament forming material comprises a polymer. In addition to the one or more filament forming materials, the filament forming composition may include one or more additives, such as one or more active agents. Furthermore, the filamentforming composition may comprise one or more polar solvents, such as water, in which one or more, for example all filament-forming materials and / or one or more, for example all active agents, which are further dissolved or dispersed or a combination thereof. As used herein, the filaments of the present invention are made from the filamentforming composition of the present invention has one or more additives, such as one or more active agents. The coating is such that it can be present in the filament rather than on the filament. The total concentration of filament forming material, and the total concentration of active agent present in the filament forming composition may be any suitable amount, as long as the filaments of the present invention are made therefrom. As used herein, one or more additives, such as an active agent, may be present in the filament and one or more additional additives, such as an active agent, may be present on the surface of the filament. In other embodiments, the filaments of the present invention may include one or more additives, such as an active agent, which are present in the filament when first made, but are subject to the conditions of the intended use of the filament, further resulting in a bloom on the surface of the filaments before and / or when exposed to air or other external conditions. As used herein, “filament-forming material” means a material such as a polymer or monomer that can produce a polymer that exhibits properties suitable for making filaments. In one example, the filament-forming material includes one or more substituted polymers, such as anionic, cationic, zwitterionic, and / or nonionic polymers. In other examples, the polymer may comprise a hydroxyl polymer, such as polyvinyl alcohol ("PVA"), and / or a polysaccharide, such as starch, and / or a starch derivative, such as ethoxylated starch, and / or acid diluted starch. In another example, the polymer may include polyethylene and / or terephthalate. In yet another embodiment, the filament forming material is a polar solvent soluble material. As used herein, “additive” means any material that is present in the filaments of the invention and is not a filament forming material. In one example, the additive includes an active agent. In other embodiments, the additive includes a processing aid. In yet another embodiment, the additive includes a filler. In one embodiment, the additive is present in the filament, and the absence of it in the filament does not cause the filament to lose its filament structure (i.e. , the absence of it causes the filament to be in its solid form. Including any material) that will not lose. In other embodiments, the additive, e.g., the active agent, includes a non-polymeric material. As used herein, the additive includes a plasticizer for the filament. Non-limiting examples of suitable plasticizers of the present invention include polyols, copolyols, polycarboxylic acids, polyesters, and dimethicone copolyols. Examples of useful polyols include glycerin, diglycerin, propylene glycol, ethylene glycol, butylene glycol, pentylene glycol, cyclohexanedimethanol, hexanediol, 2,2,4-trimethylpentane-1 ,3- diol, polyethylene glycol (m.w. 200-800), sugar alcohols such as pentaerythritol, sorbitol, mannitol, lactitol and other mono- and polyhydric low molecular weight alcohols (eg C2-C8 alcohols); mono, di- and oligosaccharides such as fructose, Examples include, but are not limited to, glucose, sucrose, maltose, lactose, and higher fructose corn syrup solids, and dextrin, and ascorbic acid. In yet another example, the plasticizer includes glycerin and / or propylene glycol, and / or a glycerol derivative, such as propoxylated glycerol. In yet another embodiment, the plasticizer is selected from the group consisting of glycerin, ethylene glycol, polyethylene glycol, propylene glycol, glycidol, urea, sorbitol, xylitol, maltitol, saccharides, ethylene bisformamide, amino acids, and mixtures thereof. Is done. As used herein,, the additive includes a crosslinking agent suitable for crosslinking one or more filament-forming materials present in the filaments of the present invention. In one example, the cross-linking agent includes a cross-linking agent that can cross-link the hydroxyl polymer together, for example, via the hydroxyl portion of the hydroxyl polymer. Non-limiting examples of suitable crosslinkers include imidazolidinone, polycarboxylic acids, and mixtures thereof. In one example, the cross-linking agent comprises a urea glyoxal adduct cross-linking agent, for example, a dihydroxy imidazolidinone such as dihydroxyethylene urea (“DHEU”). Crosslinking agents may be present in the filament forming composition of the present invention and / or in the filaments to control the solubility and / or dissolution of the filaments in a solvent such as a polar solvent. As used herein, the additive comprises a rheology modifier such as a shear force modifier and / or an extension modifier. Non-limiting examples of rheology modifiers include, but are not limited to, polyacrylamides, polyurethanes, and polyacrylates that can be used in the filaments of the present invention. Non-limiting examples of rheology modifiers are commercially available from Dow Chemical Company (Midland, Ml). As used herein,, the additive may be used when the filament is exposed to the intended application conditions and / or when the active agent is released from the filament and / or when the morphology of the filament changes. To provide a visual signal, it includes one or more colors and / or dyes incorporated into the filaments of the present invention. As used herein, the additive includes one or more release agents and / or lubricants. Non-limiting examples of suitable release agents and / or lubricants include fatty acids, fatty acid salts, fatty alcohols, aliphatic esters, sulfonated fatty acid esters, aliphatic amine acetates, fatty acid amides, silicones, aminosilicones, fluoropolymers, and mixtures thereof. In one embodiment, the release agent and / or lubricant is applied to the filament, in other words, after the filament is formed. In one example, one or more release agents / lubricants are applied to the filaments prior to collecting the filaments on the collection device to form a nonwoven. In other embodiments, one or more release agents / lubricants are applied to a nonwoven formed from the filaments of the present invention prior to contacting one or more nonwoven webs, such as a stack of nonwoven webs. In yet another embodiment, to facilitate removal of the filaments and / or nonwoven webs of the present invention and / or the layers of the filament / nonwoven webs of the present invention are adhered to each other, and further carelessly adhered. To avoid, the filaments and / or nonwovens comprising the filaments of the present invention may have one or more release agents / before the filaments and / or nonwovens contact the surface (such as the surface of an apparatus used in a processing system). Lubricant is applied. In one example, the release agent / lubricant includes particulates. As used herein, the additive includes one or more antiblocking agents and / or tack removers. Non-limiting examples of suitable antiblocking and / or detackifying agents include starch, starch derivatives, crosslinked polyvinylpyrrolidone, crosslinked cellulose, microcrystalline cellulose, silica, metal oxides, calcium carbonate, talc, mica, or a combination thereof. As used herein, “purpose application conditions” refers to the temperature, physical, chemical, and exposure to which the filaments of the invention are exposed when used for one or more of their design purposes. Means mechanical conditions. For example, if the filament and / or the nonwoven web comprising the filament is designed to be used in a washing machine for laundry care purposes, the condition of the intended use is any wash water during the laundry wash operation. Will include these temperatures, chemical, physical, and / or mechanical conditions present in the washing machine. In other examples, if the filament and / or the nonwoven web comprising the filament is designed to be used by humans as a shampoo for hair care purposes, the conditions for the intended use are during human hair shampooing. These temperatures, chemical, physical and / or mechanical conditions that exist will be included. Similarly, if the filament and / or the nonwoven web comprising the filament is designed to be used in a dishwashing operation by hand or by a dishwasher, the intended use condition is that the dishwashing water during the dishwashing operation is and / or these temperatures, chemical, physical, and / or mechanical conditions present in the dishwasher. As used herein, an “active agent” is used in the environment outside of a filament and / or a nonwoven web comprising the filament of the invention, e.g., the purpose of the filament and / or nonwoven web comprising the filament. By an additive that produces the intended effect when exposed to the conditions of use. In one example, the active agent is a surface, such as a hard surface (i.e., kitchen counter, bathtub, toilet, toilet bowl, sink, floor, wall, tooth, car, window, mirror, dish) and / or a soft surface (i.e., Fabrics, hair, skin, carpets, crops, plants). In other embodiments, the activator is a chemical reaction (i.e., foaming, foaming, coloring, increasing temperature, cooling, foaming, disinfection and / or purification, and / or chlorination, e.g., water purification, and / or water used in the disinfection and / or chlorination of water). In yet another embodiment, the active agent includes an additive that treats the environment (i.e., deodorizes, purifies, or aromas the air). In one example, the active agent is formed in situ, such as during the formation of a filament containing the active agent, e.g., the filament comprises a water soluble polymer (e.g., starch) and a surfactant (e.g., an anionic surfactant). However, they can create polymeric complexes, i.e., coacervates, that function as active agents used to treat the surface of the fabric. As used herein, “Treat”, with respect to surface treatment means that the active agent provides a benefit to the surface or environment. Treatment includes controlling and / or immediately improving the appearance of the surface or environment, cleanliness, tactile properties, residual treatment, purity, and / or feel. In one example, treatment relating to the treatment of the surface of exterior and / or interior of the car surface wherein the CCS is used to clean, shine, remove oxidation, soften leather or other surfaces in the interior of the vehicle. “Liquid processing active agent” as used herein means an active agent that provides benefits and / or improvements to a liquid when applied to a liquid such as water and / or alcohol. For example, chlorine and / or car cleaning materials are non-limiting examples of suitable liquid treatment activators. In other examples, clear coat activators, or other types of activator to trigger a benefit of the CCS are suitable for the filaments of the present invention. In addition, oil dispersants and / or oil scavengers are non-limiting examples of other suitable liquid treatment actives. As used herein, “industrial active agent” means an active agent that provides benefits within the article of manufacture. For example, glues and / or adhesives that provide a bond between two objects, pesticides, food and / or septic articles incorporated in insulators (e.g., housing insulators) Oxygen scavenging active agents incorporated into packages, insect repellents incorporated into articles used by humans to repel insects, and moisture scavengers incorporated into desiccants are present in the filaments of the present invention. Non-limiting examples of industrial activators obtained. “Weight ratio”, as used herein, refers to the weight of the additive, e.g., the filamentforming material on a dry weight basis in the filament to the active agent (g or %) in the filament on a dry weight basis. It means weight (g or %). The final concentration is expressed as weight percent (wt.%). As used herein, “hydroxyl polymer” includes any hydroxyl-containing polymer that can be incorporated into the filaments of the present invention, e.g., as a filament-forming material. In one example, the hydroxyl polymer of the present invention comprises greater than 10 wt% and / or greater than 20 wt.% and / or greater than 25 wt.% hydroxyl moieties. “Biodegradable” as used herein with respect to a material, such as a material, for example as a whole filament and / or as a polymer within a filament (e.g., filamentforming material), for example, at least of the initial filament and / or polymer. 5%, and / or 7%, and / or at least 10% according to OECD (1992) “Guideline for the Testing of Chemicals 301 B; Ready Biodegradability-CO 2 Evolution (Modified T) When measured, filaments and / or polymers can be converted to carbon dioxide in public solid waste composting facilities so that they are converted to carbon dioxide after 30 days. They can undergo a beauty / or biodegradable, and / or means that go through it. “Non-biodegradable” as used herein with reference to materials such as whole filaments and / or polymers within filaments (e.g. filament-forming material) filaments, e.g., at least 5% of the initial filaments and / or polymers. As measured after 30 days as measured according to OECD (1992) “Guideline for the Testing of Chemicals 301 B; Ready Biodegradability — CO 2 Evolution (Modified Storm Test) Test” incorporated herein. In particular, it means that the filament and / or polymer cannot undergo physical, chemical, thermal and / or biodegradation. “Non-thermoplastic” as used herein with respect to materials such as whole filaments and / or polymers within filaments (eg, filament-forming materials), filaments and / or polymers do not exhibit a melting point and / or softening point. This means that when there is no plasticizer such as water, glycerin, sorbitol, urea, it can flow under pressure. As used herein, “non-thermoplastic biodegradable filament” means a filament that exhibits biodegradable and non-thermoplastic properties as defined above. As used herein, “non-thermoplastic, non-biodegradable filament” means a filament that exhibits non-biodegradable and non-thermoplastic properties as defined above. “Thermoplastic” as used herein with respect to materials such as the entire filament and / or polymer within the filament (e.g., filament forming material), the filament and / or polymer has a melting point and / or softening point at a particular temperature. Which allows it to flow under pressure in the absence of a plasticizer. As used herein, “thermoplastic biodegradable filament” means a filament that exhibits biodegradable and thermoplastic properties as defined above. As used herein, “thermoplastic, non-biodegradable filament” means a filament that exhibits non-biodegradable and non-thermoplastic properties as defined above. As used herein, “non-cellulose containing” is less than 5% by weight and / or less than 3% by weight and / or less than 1% by weight and / or less than 0.1 % by weight. In addition, it means that weight percent cellulose polymer, cellulose derivative polymer and / or cellulose copolymer is present in the filament. In one example, “non- cellulose-containing” is less than 5% by weight and / or less than 3% by weight and / or less than 1% by weight and / or less than 0.1 % by weight and / or 0% by weight. As used herein, “polar solvent soluble material” means a material that is miscible in a polar solvent. In one example, the polar solvent soluble material is miscible in alcohol and / or water. In other words, the polar solvent soluble material forms a homogeneous solution that is stable at ambient conditions with a polar solvent, such as alcohol and / or water (no phase separation for more than 5 minutes after forming a homogeneous solution). As used herein, “alcohol soluble material” means a material that is miscible within the alcohol. In other words, it is a material that can form a homogeneous solution that is stable with alcohol at ambient conditions (it does not phase separate for more than 5 minutes after forming a homogeneous solution). As used herein, “water soluble material” means a material that is miscible in water. In other words, it is a material that can form a homogeneous solution that is stable with water (does not separate for more than 5 minutes after forming a homogeneous solution) at ambient conditions. As used herein, “nonpolar solvent soluble material” means a material that is miscible in a nonpolar solvent. In other words, a non-polar solvent soluble material is a material that can form a stable solution with a non-polar solvent (which does not phase separate for more than 5 minutes after forming a homogeneous solution). As used herein, “ambient conditions” means about 23 ° C. ± 2.2 ° C. (about 73 ° F. ± 4 ° F.) and 50% ± 10% relative humidity. As used herein, “weight average molecular weight” means gel penetration according to the procedure found in “Colloids and Surfaces A. Physico Chemical & Engineering Aspects” (Vol. 162, 2000, pg. 107-121). It means the weight average molecular weight determined using chromatography. As used herein with respect to a filament, “length” means the length along the longest axis from one end to the other end. If the filament is kinked, curved, or bent within it, the length is the length along the entire path of the filament. As used herein with respect to filaments, “diameter” is measured according to the diameter test method described herein. In one embodiment, the filaments of the invention are less than 100 pm and / or less than 75 pm and / or less than 50 pm and / or less than 25 pm and / or less than 20 pm and / or less than 15 pm and / or exhibit a diameter of less than 10 pm and / or less than 6 pm and / or greater than 1 pm and / or greater than 3 pm. As used herein, in yet another examples, incentive conditions may be present in the environment (e.g., water, etc.) when the filaments and / or nonwoven webs, and / or films of the present invention are added to water. In other words, nothing changes in water except for the fact that the filaments and / or nonwoven webs and / or films of the present invention have been added to water. As used herein with respect to filament morphological changes, "morphological change" means that the filament experiences a change in its physical structure. Nonlimiting examples of morphological changes for the filaments of the present invention include melting, melting, expanding, shrinking, shattering, rupturing, extending, shortening, and combinations thereof. The filaments of the present invention may lose their physical structure completely or substantially when exposed to the intended application conditions, their morphologies may change, or the filaments It can retain or substantially retain the physical structure. As used herein, “by weight on a dry filament basis” means that the filament is in a room conditioned at a temperature of 23 ° C. ± 2.2 ° C. (approximately 73 ° F. ± 4 ° F.) and a relative humidity of 50% ± 10% for 2 hours, It means the filament weight measured immediately after being adjusted. In one example, “by weight of dry filament base” refers to the weight of the filament based on the weight of the filament in moisture, eg, free water, as measured, for example, according to the moisture content testing method described herein. Less than 20% and / or less than 15% and / or less than 10% and / or less than 7% and / or less than 5% and / or less than 3% and / or less than 1 %. As used herein with respect to the total concentration of one or more active agents present in the filament, “total concentration” means the total weight or weight percent of all subject material (e.g., active agents). In other words, the filament comprises 50 wt% of perfume or fragrance on a dry filament basis. Optionally an additional 35 wt.% of anionic surfactant on a dry filament basis, 15 wt% nonionic surfactant on a dry filament basis, 10 wt.% chelating agent, and 5 wt.% perfume. So that the total concentration of active perfume or fragrance agent present in the filament is greater than 50% by weight on a dry filament basis. As used herein, a “web” is a collection of formed fibers and / or filaments (e.g., fibrous structures) and / or fibers and / or filaments of any attribute or origin associated with each other. It means a formed sheet (for example, a continuous filament). As used herein, the web is a sheet formed by a spinning process rather than a casting gloss. As used herein, a “nonwoven web” as defined for purposes of the present invention, and generally in the European Disposables and Nonwovens Association (EDANA), is a sheet of fibers and / or filaments (e.g., any means) or the like, continuous filaments of any quality or origin, etc., which can be joined together by any means except weaving or braiding. The felt obtained by wet milling is not a nonwoven web. As used herein, a nonwoven web according to the present invention refers to regularly arranged filaments within a structure to perform a function. As used herein, the nonwoven web of the present invention is in an arrangement that includes two or more and / or three or more filaments that are entangled within or otherwise associated with each other to form a nonwoven web. is there. As used herein the nonwoven web of the present invention may include one or more solid additives, such as particulates and / or fibers, in addition to the filaments of the present invention. As used herein, “microparticle” means a particulate material and / or powder. As used herein, the articles “a” and “an” as used herein, such as “an anionic surfactant” or “a fiber” are claimed. Alternatively, it is understood to mean one or more substances described. As used herein, the percentages and ratios are calculated by weight unless otherwise indicated. All percentages and ratios are calculated based on the total composition unless otherwise indicated. As used herein, unless otherwise stated, all concentrations of a component or composition relate to the activity level of that component or composition and exclude impurities that may be present in commercial sources, such as residual solvents or by-products. Is done. As used herein, the filament of the present invention comprises one or more filament forming materials. In addition to the filament forming material, the filament includes one or more active agents that are releasable from the filament, for example when exposed to the conditions of the intended application, and one or more filament forming materials present in the filament. The total concentration is less than 80% by weight on a dry filament basis, and the total concentration of one or more active agents present in the filament is provided above 20% by weight on a dry filament basis. As used herein, the CCS is produced from one or more filament-forming materials with or without one or more additives (deactivator additives) and then coated with one or more active agents. The filament in contact with is not within the scope of the present invention. However, one or more filament forming materials and filaments formed from one or more active agents, such as one or more filament forming materials with or without one or more inactive agents, and one filament formed from a mixture with the above active materials (i.e., the filament forming composition of the present invention) that are subsequently coated with one or more active agents are within the scope of the present invention. As used herein the filaments of the present invention include one or more filament forming materials and one or more active agents, wherein the total concentration of filament forming material present in the filaments is about 5 on a dry filament basis. The total concentration of active agent present in the total filament composition is from 50% to less than 50% by weight, or greater than 50% by weight and up to about 95% by weight on a dry filament basis. As used herein, the filaments of the present invention are about 100% by weight and / or greater than 95%, and / or greater than 90% and / or greater than 85% by weight and / or One or more filament-forming materials comprising more than 75% and / or more than 50% by weight. For example, the filament forming material may comprise polyvinyl alcohol and / or starch or starch derivatives. As used herein the filaments of the present invention include one or more filament forming materials and one or more active agents, wherein the total concentration of filament forming material present in the filaments is about dry filament basis. The total concentration of active agent present in the filaments, from 5% to less than 80% by weight, is greater than 20% by weight and up to about 95% by weight on a dry filament basis. As used herein, the filaments of the present invention are at least 10% and / or at least 15% and / or at least 20% and / or less than 80% and / or 75% by weight on a dry filament basis. Less than and / or less than 65% and / or less than 60% and / or less than 55% and / or less than 50% and / or less than 45% and / or less than 40%. As used herein, the filaments of the present invention are more than 20 wt.% and / or at least 35 wt.%, and / or at least 40 wt.%, and / or at least 50 wt.%, and / or at least 60 wt.%, and / or at least 65 wt.%, and / or less than 95 wt.%. As used herein, the filaments of the present invention are less than 90 wt%, or less than 85 wt.%, and / or less than 80 wt.%, less than 75 wt.%. The filaments of the present invention comprise greater than 80% by weight active agent on a dry filament basis. As used herein, the one or more filament forming materials and the active agent have a weight ratio of the total concentration of the filament forming material to the active agent of 4.0 or less, and / or 3.5 or less, and / or 3 0.0 or less and / or 2.5 or less and / or 2.0 or less and / or 1.85 or less and / or less than 1 .7 and / or less than 1 .6. And / or less than 1.5 and / or less than 1 .3 and / or less than 1.2 and / or less than 1 and / or less than 0.7 and / or less than 0.5 And / or less than 0.4 and / or less than 0.3 and I or more than 0.1 and / or more than 0.15 and / or more than 0.2 filaments exists within. As used herein, the filaments of the present invention comprise from about 10% and / or from about 15% to less than 80% filament-forming material (e.g., polyvinyl alcohol polymer and / or starch polymer) on a dry filament basis. And up to about 90% and / or up to about 85% by weight of additives (e.g., active agents) on a dry filament basis. The filament further comprises a plasticizer, such as glycerin, and / or a pH adjuster, such as citric acid. As used herein, the filaments of the present invention comprise from about 10% and / or from about 15% to less than 80% filament-forming material (eg, polyvinyl alcohol polymer and / or starch polymer) on a dry filament basis. And, based on dry filaments, greater than 20 wt.%, Up to about 90 wt.% And / or up to about 85 wt.% active agent, wherein the weight ratio of filament forming material to active agent is 40 wt.% or less. The filament further comprises a plasticizer, such as glycerin, and / or a pH adjuster, such as citric acid. As used herein, the filaments of the present invention comprise about 5% to less than 50% by weight filament forming material (e.g., polyvinyl alcohol polymer and / or starch polymer) on a dry filament basis and 50% on a dry filament basis. And up to about 95% by weight of additives, such as active agents (e.g., perfumes or fragrances or odor removing agents or odor reducing agents or a combination thereof). The filament further comprises a plasticizer, such as glycerin, and / or a pH adjuster, such as citric acid. As used herein, the filaments of the present invention have 0% to less than 20% and / or 0% to 15%, as measured according to the moisture content test method described herein. Less than 15% and / or more than 0% and less than 15% and / or more than 0% and less than 12% and / or more than 2% and less than 10wt.%. As used herein, the filaments of the present invention have from about 5 wt% to about 10 wt%, and / or from about 7 wt% to about 10 wt%, as measured according to the moisture content test method described herein. As used herein, the filament comprises one or more filament forming materials and enzymes, bleaches, builders, chelates that are releasable and / or released when the filament is exposed to the intended application conditions. And one or more active agents selected from the group consisting of these agents, and mixtures thereof. As used herein, the filaments are less than 95% and / or less than 90%, and / or less than 80%, and / or less than 50%, and / or less than 35%, and / or less, on a dry filament basis, and / or up to about 5% by weight and / or up to about 10% by weight and / or up to about 20% by weight of the total concentration of filament-forming material and more than 5% and / or 10% by weight on a dry filament basis. As used herein, the filaments are more than 20% and / or more than 35% and / or more than 50% and / or more than 65% and / or up to about 95% by weight of a total concentration of active agents selected from the group consisting of enzymes, bleaches, builders, chelating agents, and mixtures thereof. As used herein, the filaments of the present invention may contain active agents that may raise health and / or safety concerns when they are airborne. For example, the filament may be used to prevent enzymes in the filament from floating in the air. As used herein, the filaments of the present invention may be meltblown filaments. As used herein, the filaments of the present invention may be spunbond filaments. As used herein the filament may be a hollow filament before and / or after release of one or more of its active agents. As used herein, the filaments of the present invention may be hydrophilic or hydrophobic. The filaments may be surface treated and / or treated internally to alter the filament's inherent hydrophilic or hydrophobic properties. As used herein, the filament is less than 100 pm, and / or less than 75 pm, and / or less than 50 pm, and / or less than 25 pm, and / or less than 10 pm, as measured according to the diameter test method described herein. As used herein, the diameter of the filament may be less than 5 pm and / or less than 1 pm in diameter. As used herein, the filaments of the present invention exhibit a diameter of greater than 1 pm as measured according to the diameter test method described herein. The diameter of the filaments of the present invention may be used to control the release rate of one or more active agents present in the filament and / or the loss of and / or changing the physical structure of the filament. As used herein, the filament may contain two or more different active agents. As used herein, the filament includes two or more different active agents, the two or more different active agents being compatible with each other. As used herein he filament includes two or more different active agents, and the two or more different active agents are incompatible with each other. As used herein, the filament may include an active agent within the filament and an active agent on the outer surface of the filament, such as a coating on the filament. The active agent on the outer surface of the filament may be the same as or different from the active agent present in the filament. If different, the active agents may be compatible with each other or incompatible. As used herein, the filaments of the present invention do not contain preservatives, which for the purposes of the present invention are based on dry filaments, less than 2%, and / or less than 1%, and / or 0. Means less than 5% and / or less than 0.25% and / or 0% preservative. As used herein, the one or more active agents may be uniformly dispersed throughout the filament or may be substantially uniformly dispersed. As used herein, one or more active agents may be dispersed as separate regions within the filament. As used herein, the at least one active agent is uniformly or substantially uniformly dispersed throughout the filament, and at least the other active agent is dispersed as one or more separate regions within the filament. As used herein, at least one active agent is dispersed as one or more discrete regions within the filament, and the at least one other active agent is one or more from the first separate region within the filament. The filament may be used as a separate article. As used herein, the filament is a carrier substrate (eg, wipe, wash cloth, dryer sheet, fabric, garment, underwear, shine, protection from sun, moisture, dirt, etc.) and / or deposited thereon. As used herein, the plurality of filaments of the present invention are collected into and compressed into a film and thus released from the film when one or more filament forming materials and, for example, the film is exposed to the intended application conditions. It can be a film comprising one or more active agents that are possible. As used herein, the films of the present invention have a per sample less than than 100 seconds, and / or less than 80 seconds, and / or as measured according to the dissolution test methods described herein. It exhibits an average degradation time of less than 55 seconds and / or less than 50 seconds and / or less than 40 seconds and / or less than 30 seconds and / or 20 seconds / g (s / g). As used herein, the films of the present invention have a per sample less than 1000 seconds, and / or less than 900 seconds, and / or less than 800 seconds, and / or as measured according to the dissolution test methods described herein. Alternatively, it exhibits an average degradation time of less than 700 seconds and / or less than 600 seconds and / or less than 500 seconds / g (s / g). As used herein, the film of the present invention has a thickness greater than 0.01 mm and / or greater than 0.05 mm and / or 0.1 mm as measured by the thickness test method described herein. As used herein, the film of the present invention may be greater than and / or up to about 20 mm and / or up to about 10 mm and / or up to about 5 mm and / or up to about 2 mm and / or up to 0.5 mm and / or about 0. The film thickness may be up to 3 mm. As used herein, the filament-forming material is any suitable material, such as a polymer or monomer that can produce a polymer that exhibits properties suitable for making filaments, such as by a spinning process. As used herein, the filament forming material may comprise a polar solvent soluble material, such as an alcohol soluble material and / or a water soluble material. As used herein, the filament forming material may include a non-polar solvent soluble material. As used herein, the filament forming material may include a polar solvent soluble material and may not include a non-polar solvent soluble material (less than 5% by weight and / or 3% by weight on a dry filament basis). Less than and / or less than 1% by weight and / or 0% by weight). As used herein, the filament forming material may be a film forming material. In yet other embodiments, the filament-forming material may be synthetic or naturally derived, which may be chemically, enzymatically and / or physically modified. As used herein, the filament forming material is a polymer derived from acrylic monomers such as ethylenically unsaturated carboxylic acid monomers and ethylenically unsaturated monomers, polyvinyl alcohol, polyacrylates, polymethacrylates, Copolymers of acrylic acid and methyl acrylate, polyvinyl pyrrolidone, polyalkylene oxide, starch and starch derivatives, pullulan, gelatin, hydroxyl propyl methylcellulose, methylcellulose, and polymers selected from the group consisting of carboxymethylcellulose may be included. As used herein, the filament forming material is polyvinyl alcohol, polyvinyl alcohol derivative, starch, starch derivative, cellulose derivative, hemicellulose, hemicellulose derivative, protein, sodium alginate, hydroxypropylmethylcellulose, chitosan, chitosan derivative, polyethylene glycol, tetra It may include a polymer selected from the group consisting of methylene ether glycol, polyvinyl pyrrolidone, hydroxymethyl cellulose, hydroxyethyl cellulose, and mixtures thereof. As used herein, the filament-forming material comprises pullulan, hydroxypropylmethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, polyvinylpyrrolidone, carboxymethylcellulose, sodium alginate, xanthan gum, tragacanth gum, guar gum, acacia gum, gum arabic, polyacrylic acid, methyl Methacrylate copolymer, carboxyvinyl polymer, dextrin, pectin, chitin, levan, erucinane, collagen, gelatin, zein, gluten, soy protein, casein, polyvinyl alcohol, starch, starch derivative, hemicellulose, hemicellulose derivative, protein, chitosan, chitosan derivative, Polyethylene glycol, tetramethylene ether glycol, Mud carboxymethylcellulose, and comprises a polymer selected from the group consisting of mixtures. As used herein, the polar solvent-soluble materials include polar solvent-soluble polymers. The polar solvent soluble polymer may be synthetic or naturally derived and may be chemically and / or physically modified. As used herein, the polar solvent soluble polymer is at least about 10,000 g / mol, and / or at least about 20,000 g / mol, and / or at least 40,000 g / mol, and / or at least 80,000 g / mol, And / or at least about 100,000 g / mol, and / or at least 1 ,000,000 g / mol, and / or at least 3,000,000 g / mol, and / or at least 10,000,000 g / mol, and / or It exhibits a weight average molecular weight of at least 20,000,000 g / mol and / or up to about 40,000,000 g / mol and / or up to about 30,000,000 g / mol. As used herein, the polar solvent soluble polymer is selected from the group consisting of alcohol soluble polymers, water soluble polymers, and mixtures thereof. Non-limiting examples of water soluble polymers include water soluble hydroxyl polymers, water soluble thermoplastic polymers, water soluble degradable polymers, water soluble non biodegradable polymers, and mixtures thereof. As used herein, the water soluble polymer comprises polyvinyl alcohol. In other examples, the water soluble polymer comprises starch. In yet another embodiment, the water soluble polymer comprises polyvinyl alcohol and starch. As used herein, the solvent consists of a water-soluble hydroxyl polymers according to the present invention include polyols such as polyvinyl alcohol, polyvinyl alcohol derivatives, polyvinyl alcohol copolymers, starch, starch derivatives, starch copolymers, chitosan, chitosan derivatives , Chitosan copolymers, cellulose, cellulose derivatives, such as cellulose ether and ester derivatives, cellulose copolymers, hemicellulose, hemicellulose derivatives, hemicellulose copolymers, gums, arabinans, galactants, proteins and various other polysaccharides, and mixtures thereof . As used herein, the water soluble hydroxyl polymer of the present invention comprises a polysaccharide. As used herein, “polysaccharide” means natural polysaccharides and polysaccharide derivatives or modified polysaccharides. Suitable water soluble polysaccharides include, but are not limited to starch, starch derivatives, chitosan, chitosan derivatives, cellulose derivatives, hemicellulose, hemicellulose derivatives, gums, arabinans, galactans, and mixtures thereof. The water-soluble polysaccharide is from about 10,000 g / mole to about 40,000,000 g / mole and / or more than 100,000 g / mole and / or more than 1 ,000,000 g / mole. Alternatively, it may exhibit a weight average molecular weight of greater than 3,000,000 g / mol and / or greater than about 3,000,000 g / mol and up to about 40,000,000 g / mol. As used herein, the water-soluble polysaccharide may comprise non-cellulose and / or non-cellulose derivatives and / or non-cellulose copolymer water-soluble polysaccharides. Such non-cellulose soluble polysaccharides may be selected from the group consisting of starch, starch derivatives, chitosan, chitosan derivatives, hemicellulose derivatives, hemicellulose derivatives, gums, arabinans, galactans, and mixtures thereof. As used herein, the water soluble hydroxyl polymer of the present invention comprises a non-thermoplastic polymer. As used herein, the water-soluble hydroxyl polymer can be from about 10,000 g / mol to about 40,000,000 g / mol, and / or more than 100,000 g / mol, and / or more than 1 ,000,000 g / mol, and / or more than 3,000,000 g / mol and up to about 40,000,000 g / mol. Higher and lower molecular weight water-soluble hydroxyl polymers may be used in conjunction with hydroxyl polymers having a weight average molecular weight within a particular desired range. As used herein, the water soluble hydroxyl polymers may be selected from natural starch and include chemical and / or enzymatic modifications. As used herein, the water soluble hydroxyl polymer may be combined with native starch which can further be acid-thinned, hydroxyethylated, hydroxypropylated, and / or oxidized. As used herein, the water soluble hydroxyl polymer may comprise dent corn starch. As used herein, the naturally occurring starch is generally consisting of a mixture of linear amylose and branched amylopectin polymers of D glucose units. Amylose is essentially a linear polymer of D-glucose linked by (1 ,4) -a-D bonds. Aminopectin is a highly branched polymer of (1 ,4) -a-D bonds and (1 ,6) -a-D-glucose units at branch points. Naturally occurring starch is typically a relatively high concentration of amylopectin, such as corn starch (64-80% amylopectin), waxy maize (93-100% amylopectin), rice (83-84% amylopectin), potato (About 78% amylopectin) and wheat (73-83% amylopectin). Although all starches are potentially useful herein, the present invention is most commonly practiced with high amylopectin natural starch derived from agricultural sources, which is an abundant source and can be easily supplemented and offers the advantage of being inexpensive. As used herein, the “starch” includes any naturally occurring unmodified starch, modified starch, synthetic starch, and mixtures thereof, and mixtures of amylose or amylopectin fractions, It may be modified by chemical, chemical, or biological processes, or combinations thereof. As used herein, the unmodified or modified starch may depend on the desired end product. As used herein, the starch or starch mixture useful in the present invention is from about 20% to about 100%, more typically from about 40% to about 90%, even more typically. Having an amylopectin content from about 60 wt% to about 85 wt% starch or mixtures thereof. As used herein, suitable starches of natural origin include: corn starch, potato starch, sweet potato starch, wheat starch, sago palm starch, tapioca starch, rice starch, soybean starch, arrow root starch, amino starch, bracken starch, lotus starch, Nonlimiting examples include waxy corn starch and high amylose corn starch. Naturally occurring starches, particularly corn starch and wheat starch, are preferred starch polymers due to their economics and availability. As used herein, the polyvinyl alcohol herein can be grafted with other monomers to improve its properties. A wide range of monomers have been successfully grafted to polyvinyl alcohol. Non-limiting examples of such monomers include vinyl acetate, styrene, acrylamide, acrylic acid, 2-hydroxyethyl methacrylate, acrylonitrile, 1 ,3- butadiene, methyl methacrylate, methacrylic acid, maleic acid, itaconic acid, vinyl sulfonic acid. Sodium, sodium allyl sulfonate, sodium methyl allyl sulfonate, sodium phenyl allyl ether sulfonate, sodium phenyl methallyl ether sulfonate, 2-acrylamido- methyl propane sulfonic acid (AMPs), vinylidene chloride, vinyl chloride, vinyl amine, and acrylate esters. As used herein, the water soluble hydroxyl polymer is selected from the group consisting of polyvinyl alcohol, hydroxymethylcellulose, hydroxyethylcellulose, hydroxypropylmethylcellulose, and mixtures thereof. Non-limiting examples of suitable polyvinyl alcohols include those commercially available from Sekisui Specialty Chemicals America, LLC (Dallas, TX) under the trade name CELVOL®. Non-limiting examples of suitable hydroxypropyl methylcellulose include those commercially available from Dow Chemical Company (Midland, Ml) under the trademark METHOCEL®, including combinations with the hydroxypropyl methylcellulose described above. As used herein, the water-soluble thermoplastic polymers consists of examples of suitable water-soluble thermoplastic polymers include thermoplastic starch and / or starch derivatives, polylactic acid, polyhydroxyalkanoates, polycaprolactones, polyester amides, and certain polyesters or a combination thereof. As used herein, the water-soluble thermoplastic polymer of the present invention may be hydrophilic or hydrophobic. As used herein, the water soluble thermoplastic polymer may be surface treated and / or internally treated to alter the hydrophilic or hydrophobic properties inherent in the thermoplastic polymer. As used herein, the water soluble thermoplastic polymer may comprise a biodegradable polymer. Any suitable weight average molecular weight may be used for the thermoplastic polymer. For example, the weight average molecular weight of the thermoplastic polymer according to the present invention is greater than about 10,000 g / mole and / or greater than about 40,000 g / mole and / or greater than about 50,000 g / mole. And / or less than about 500,000 g / mole and / or less than about 400,000 g / mole and / or less than about 200,000 g / mole. As used herein, the non-polar solvent soluble materials include non-polar solvent soluble polymers. Non-limiting examples of suitable non-polar solvent soluble materials include cellulose, chitin, chitin derivatives, polyolefins, polyesters, copolymers thereof, and mixtures thereof. Non-limiting examples of polyolefins include polypropylene, polyethylene, and mixtures thereof. Non-limiting examples of polyesters include polyethylene terephthalate. As used herein, nonpolar solvent soluble materials may include non-biodegradable polymers such as polypropylene, polyethylene, and certain polyesters. Any suitable weight average molecular weight may be used for the thermoplastic polymer. For example, the weight average molecular weight of the thermoplastic polymer according to the present invention is greater than about 10,000 g / mole and / or greater than about 40,000 g / mole and / or greater than about 50,000 g / mole. And / or less than about 500,000 g / mole and / or less than about 400,000 g / mole and / or less than about 200,000 g / mole. As used herein, activators are a class of additives designed and intended to benefit something other than the filament itself, for example, benefiting the environment outside the filament. The active agent may be any suitable additive that produces the intended effect under the intended use of the filament. For example, the active agent may be a CCS that is designed to be added to water or other solvents to wash the vehicle. The active agent in the CCS may be used directly onto the car interior and / or exterior surface to deliver benefits that are typically achieved during the car cleaning process. As used herein, a CCS containing a conditioning agent, such as fabric care agents, fabric conditioning agents, fabric softeners, fabric anti-wrinkle agents, fabric care antistatic agents, fabric care stain removers, soil release agents, dispersants, foam inhibitors, foaming agents, antifoaming agents, fabric refreshing agents; hard surface care and / or conditioning agents, and abrasives; other cleaning and conditioning agents such as antibacterial agents, perfumes, bleaches (e.g. oxygen bleaching) , hydrogen peroxide, percarbonate bleach, perborate bleach, chlorine bleach), bleach activator, chelating agent, builder, lotion, whitening agent, air care agent, carpet care agent, dye transfer inhibitor, water softener, pH adjuster, enzyme, flocculant, foaming agent, preservative, cosmetic agent, makeup remover, foaming agent, adhesion aid, coacervate forming material, clay, thickener, latex, silica, desiccant or a combination thereof. As used herein, the composition may contain one or more classes of chemicals that may be useful for one or more of the active agents listed above. For example, a surfactant active may be useful for any number of the active agents described above. Similarly, bleach can be used in fabric care, hard surface cleaning, dishwashing, and even tooth whitening. Thus, those skilled in the art will appreciate that the active agent is selected based on the desired intended use of the filament and / or the nonwoven fabric made therefrom. As used herein, the filaments of the present invention and / or nonwovens made therefrom should be used for hair care and / or conditioning thereof, whereby one or more surfactants, such as foamable surfactants, Filaments and / or non-woven fabrics incorporating filaments can be selected to provide the desired benefits to the consumer when exposed to the intended application conditions. As used herein, the filaments of the invention and / or nonwovens made therefrom are designed or intended for use in the cleaning of the interior surface of the car such as the seats and any other porous surfaces inside the vehicle. The CCS may be used alone or in combination with water or other solvents. In order to achieve said car interior benefit, one or more suitable surfactants, or enzymes, or builders, or fragrances, or foam suppressors, or bleaching agents are desired when exposed to the intended use conditions of the filaments and / or nonwovens incorporating the filaments, an be chosen to provide consumers with the benefits. As used herein, the active agent comprises a non-surfactant. As used herein, the active agent comprises an inactive active agent, i.e., an active agent other than an ingestible active agent. As used herein, non-limiting examples of suitable surfactants include anionic surfactants, or cationic surfactants, or nonionic surfactants, or zwitterionic surfactants, or amphoteric surfactants, or a combination thereof. A co-surfactant may also be included in the filament. For example, for filaments designed for delivering cleaning benefits, the total surfactant concentration should be sufficient to provide cleaning including stain and / or odor removal, generally, in the range of about 0.5% to about 95%. In addition, surfactant systems comprising two or more surfactants designed for use in the car cleaning filaments are fully anionic surfactant systems, or a combination of two or more different anionic surfactants, or a mixture of different types of surfactant system, or a combination thereof. As used herein, a surfactant or a combination of surfactants may be linear or branched surfactants. As used herein suitable linear surfactants include those derived from agricultural chemical oils, such as coconut oil, palm kernel oil, soybean oil, or other vegetable oils. As used herein, the suitable anionic surfactants may include alkyl sulfates, alkyl ether sulfates, branched alkyl sulfates, branched alkyl alkoxylates, branched alkoxylate sulfates, medium chain branched alkyl allyl sulfonate, sulfated monoglyceride, sulfonated olefin, alkyl allyl sulfonate, primary or secondary alkane sulfonate, alkyl sulfosuccinate, acyl taurate, acyl isethionate, alkyl glyceryl ether sulfonate, sulfonated methyl ester, sulfonated fatty acid, alkyl phosphate, acyl glutamate, acrylic sarcosinate, alkyl sulfoacetate, acylated peptide, alkyl ether carboxylate, anionic fluorosurfactants, sodium lauroyl glutamate, or a combinations thereof. As used herein, the suitable alkyl sulfates and alkyl ether sulfates for use herein include materials having the corresponding formulas ROSO 3 M and RO

[0006] (C 2 H 4 O) x SO 3 M, wherein R Is an alkyl or alkenyl from about 8 to about 24 carbon atoms, x is 1-10, and M is a water-soluble cation such as ammonium, sodium, potassium, and triethanolamine. Other suitable anionic surfactants are MacCutcheon's “Detergents and Emulsifiers” (North American Edition (1986), Allred Publishing Corp.) and McCutcheon's “Functional Materials 92” (Natural Publishing Corp.). As used herein, anionic surfactants useful in the filaments of the present invention, C 9 -C 15 alkyl benzene sulfonates (LAS), C 8 -C 20 alkyl ether sulfates, such as alkyl poly (ethoxy) sulfates, C 8 ~ C 20 alkyl sulfates, and mixtures thereof. Other anionic surfactants may include methyl ester sulfonate (MES), methyl ester etchelate (MEE), sulfonated estolides, and mixtures thereof. As used herein, the anionic surfactant is a C n -C alkyl benzene sulfonate (“LAS”) and primary branched chain, and a random C 10 -C 20 alkyl sulfate (“AS”), formula CH3(CH2) x CHOSO3- M +) CH3and CH3(CH2)y(CHOSO3 - M +) C 10 ~C secondary of CH 2 CH 3 (2,3) alkyl sulfates (formula In which x and (y + 1) are integers of at least about 7, preferably about 9, and M is a water-solubilizing cation, in particular sodium, an unsaturated sulfate such as oleyl sulfate), C 10 -C a-sulfonated fatty acid esters, C 10 -C 18 sulfated alkyl polyglycosides, C 10 -C alkyl alkoxy sulfates ( "AExS") (the formula x is 1 to 30), and C 10 -C alkyl alkoxy Ruboxylates (eg containing 1-5 ethoxy units), medium chain branched alkyl sulfates as described in US Pat. Nos. 6,020,303 and 6,060,443; US Pat. No. 6,008, medium chain branched alkyl alkoxy sulfates (MLAS) as described in 181 and 6,020,303; as described in WO 99 / 05243, WO 99 / 05242, and WO 99 / 05244 Modified alkylbenzene sulfonate (MILAS); methyl ester sulfonate (MES); and alpha-olefin sulfonate (AOS). As used herein, other suitable anionic surfactants that can be used are alkyl ester sulfonate surfactants, including sulfonated linear esters of C 8 to C 20 carboxylic acids (ie fatty acids). The Other suitable anionic surfactants that can be used salts of soap, C8-C 22 primary or secondary alkane sulfonates (primary of secondary alkanesulfonates), C 8 ~C 24 olefin sulfonates, sulfonated polycarboxylic acids, C8- C 24 alkyl polyglycol ether sulfates (alkylpolyglycolethersulfates) (contain ethylene oxide up to 10 moles); alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleoyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, paraffin sulfonates, alkyl phosphates , isethionates, eg acyl isethionates, N-acyl taurates, alkyl succinates and sulfosuccinates, monoesters of sulfosuccinates (e.g. saturated and unsaturated C 12 -C monoesters) monoester, diester sulfosuccinates (e.g., saturated and unsaturated C 6 -C 12 diesters), and alkyl polysaccharide sulfates, such as alkyl polysaccharides sulfates, and alkyl polyethoxy carboxylates such as those of the formula RO(CH2CH2O) k -CH2COO-M + ( wherein R is a C8-C 22 alkyl, k is an integer of 0, M is a soluble salt-forming cation). As used herein, other suitable anionic surfactants are alkyl benzene sulphonic acid of C 10 -C 16, preferably an alkali metal salt of alkylbenzene sulfonic acid C n -C 14 As used herein, the suitable anionic surfactants are linear alkyl group is linear such as alkyl benzene sulfonates are known as “LAS”. Such surfactants and their preparation are described, for example, in US Pat. Nos. 2,220,099 and 2,477,383. In other examples, linear alkyl sulfonate or linear alkylbenzene sulfonate or liner alkyl benzene sulfonate. As used herein, the respect to filaments, “diameter” is measured according to the diameter test method described herein. In one embodiment, the filaments of the invention are less than 100 pm and / or less than 75 pm and / or less than 50 pm and / or less than 25 pm and / or less than 20 pm and / or less than 15 pm And / or exhibit a diameter of less than 10 pm and / or less than 6 pm and / or greater than 1 pm and / or greater than 3 pm. As used herein, an “incentive condition”, in one example, functions as a stimulus in the filament and changes (eg, loss or change in the physical structure of the filament, and / or additives such as activators) Means any activity or phenomenon that initiates or promotes the release of In other examples, incentive conditions may be present in the environment (eg, water, etc.) when the filaments and / or nonwoven webs, and / or films of the present invention are added to water. In other words, nothing changes in water except for the fact that the filaments and / or nonwoven webs and / or films of the present invention have been added to water. As used herein with respect to filament morphological changes, "morphological change" means that the filament experiences a change in its physical structure. Nonlimiting examples of morphological changes for the filaments of the present invention include melting, melting, expanding, shrinking, shattering, rupturing, extending, shortening, and combinations thereof. The filaments of the present invention may lose their physical structure completely or substantially when exposed to the intended application conditions, their morphologies may change, or the filaments It can retain or substantially retain the physical structure. “By weight on a dry filament basis” means that the filament is in a room conditioned at a temperature of 23 ° C. ± 2.2 ° C. (approximately 73 ° F. ± 4 ° F.) and a relative humidity of 50% ± 10% for 2 hours, It means the filament weight measured immediately after being adjusted. In one example, “by weight of dry filament base” refers to the weight of the filament based on the weight of the filament in moisture, eg, free water, as measured, for example, according to the moisture content testing method described herein. Less than 20% and / or less than 15% and / or less than 10% and / or less than 7% and / or less than 5% and / or less than 3% and / or up to 0% and / or 0 It means that it contains more than%. As used herein with respect to the total concentration of one or more active agents present in the filament, “total concentration” means the total weight or weight percent of all subject material (eg, active agents). In other words, the filament comprises 20 wt% of an anioinic surfactant on a dry filament basis, 15 wt% nonionic surfactant on a dry filament basis, 10 wt% chelating agent, and 2 wt% perfume. As used herein, a “web” is a collection of formed fibers and / or filaments (eg, fibrous structures) and / or fibers and / or filaments of any attribute or origin associated with each other. It means a formed sheet (for example, a continuous filament). In one embodiment, the web is a sheet formed by a spinning process rather than a castin gloss. As used herein, a “nonwoven web” as defined for purposes of the present invention, and generally in the European Disposables and Nonwovens Association (EDANA), is a sheet of fibers and / or filaments (eg, any means) Or the like, continuous filaments of any quality or origin, etc., which can be joined together by any means except weaving or braiding. The felt obtained by wet milling is not a nonwoven web. In one embodiment, a nonwoven web according to the present invention refers to regularly arranged filaments within a structure to perform a function. In one embodiment, the nonwoven web of the present invention is in an arrangement that includes two or more and / or three or more filaments that are entangled within or otherwise associated with each other to form a nonwoven web. is there. In one example, the nonwoven web of the present invention may include one or more solid additives, such as particulates and / or fibers, in addition to the filaments of the present invention. As used herein, “microparticle” means a particulate material and / or powder. As used herein, the articles “a” and “an” as used herein, such as “an anionic surfactant” or “a fiber” are claimed. Alternatively, it is understood to mean one or more substances described. All percentages and ratios are calculated by weight unless otherwise indicated. All percentages and ratios are calculated based on the total composition unless otherwise indicated. Unless otherwise stated, all concentrations of a component or composition relate to the activity level of that component or composition and exclude impurities that may be present in commercial sources, such as residual solvents or by-products. Is done. Filament The filament of the present invention comprises one or more filament forming materials. In addition to the filament forming material, the filament includes one or more active agents that are releasable from the filament, for example when exposed to the conditions of the intended application, and one or more filament forming materials present in the filament. The total concentration is less than 80% by weight on a dry filament basis, and the total concentration of one or more active agents present in the filament is provided above 20% by weight on a dry filament basis. Formed from one or more filament-forming materials with or without one or more additives (deactivator additives) and then coated with one or more active agents The filament in contact with is not within the scope of the present invention. However, one or more filament forming materials and filaments formed from one or more active agents, such as one or more filament forming materials with or without one or more inactive agents, and one Filaments formed from a mixture with the above active materials (ie, the filament forming composition of the present invention) that are subsequently coated with one or more active agents are within the scope of the present invention. In one embodiment, the filaments of the present invention include one or more filament forming materials and one or more active agents, wherein the total concentration of filament forming material present in the filaments is about 5 on a dry filament basis. The total concentration of active agent present in the filaments, from 50% to less than 50% by weight, is greater than 50% by weight and up to about 95% by weight on a dry filament basis. In one embodiment, the filaments of the present invention are about 100% by weight and / or greater than 95%, and / or greater than 90% and / or greater than 85% by weight and / or One or more filament-forming materials comprising more than 75% and / or more than 50% by weight. For example, the filament forming material may comprise polyvinyl alcohol and / or starch or starch derivatives. In other embodiments, the filaments of the present invention include one or more filament forming materials and one or more active agents, wherein the total concentration of filament forming material present in the filaments is about dry filament basis. The total concentration of active agent present in the filaments, from 5% to less than 80% by weight, is greater than 20% by weight and up to about 95% by weight on a dry filament basis. In one embodiment, the filaments of the present invention are at least 10% and / or at least 15% and / or at least 20% and / or less than 80% and / or 75% by weight on a dry filament basis. Less than and / or less than 65% and / or less than 60% and / or less than 55% and / or less than 50% and / or less than 45% and / or less than 40% More than 20% and / or at least 35%, and / or at least 40%, and / or at least 45%, and / or at least 50%, and / or at least 60 wt%, and / or at least 65 wt%, and / or less than 95 wt%, and / or less than 90 wt%, Beauty / or less than 85 wt%, and / or less than 80 wt%, including and / or an activator of less than 75 wt%, a. The filaments of the present invention comprise greater than 80% by weight active agent on a dry filament basis. In other embodiments, the one or more filament forming materials and the active agent have a weight ratio of the total concentration of the filament forming material to the active agent of 4.0 or less, and / or 3.5 or less, and / or 3 0.0 or less and / or 2.5 or less and / or 2.0 or less and / or 1.85 or less and / or less than 1.7 and / or less than 1.6. And / or less than 1.5 and / or less than 1.3 and / or less than 1.2 and / or less than 1 and / or less than 0.7 and / or less than 0.5 And / or less than 0.4 and / or less than 0.3 and / or more than 0.1 and / or more than 0.15 and / or more than 0.2 filaments exists within. In yet another embodiment, the filaments of the present invention comprise from about 10% and / or from about 15% to less than 80% filament-forming material (eg, polyvinyl alcohol polymer and / or starch polymer) on a dry filament basis. And up to about 90% and / or up to about 85% by weight of additives (eg active agents) on a dry filament basis. The filament further comprises a plasticizer, such as glycerin, and / or a pH adjuster, such as citric acid. In yet another embodiment, the filaments of the present invention comprise from about 10% and / or from about 15% to less than 80% filament-forming material (eg, polyvinyl alcohol polymer and / or starch polymer) on a dry filament basis). And, based on dry filaments, greater than 20 wt.%, Up to about 90 wt.% And / or up to about 85 wt.% active agent, wherein the weight ratio of filament forming material to active agent is 4. 0 or less. The filament further comprises a plasticizer, such as glycerin, and / or a pH adjuster, such as citric acid. In yet another embodiment, the filaments of the present invention comprise about 5% to less than 50% by weight filament forming material (eg, polyvinyl alcohol polymer and / or starch polymer) on a dry filament basis and 50% on a dry filament basis. And up to about 95% by weight of additives, such as active agents (eg, perfumes and / or fragrances). The filament further comprises a plasticizer, such as glycerin, and / or a pH adjuster, such as citric acid. In yet another embodiment of the present invention, the filaments of the present invention have 0% to less than 20% and / or 0% to 15%, as measured according to the moisture content test method described herein. Less than 15% and / or more than 0% and less than 15% and / or more than 0% and less than 12% and / or more than 2% and less than 10% and / or 4% Contains more than 8% by weight of water. In one example, the filaments of the present invention have from about 5 wt% to about 10 wt%, and / or from about 7 wt% to about 10 wt%, as measured according to the moisture content test method described herein. In yet another embodiment of the present invention, the filament comprises one or more filament forming materials and enzymes, bleaches, builders, chelates that are releasable and / or released when the filament is exposed to the intended application conditions. And one or more active agents selected from the group consisting of these agents, and mixtures thereof. In one example, the filaments are less than 95% and / or less than 90%, and / or less than 80%, and / or less than 50%, and / or less than 35%, and / or less, on a dry filament basis, and / or up to about 5% by weight and / or up to about 10% by weight and / or up to about 20% by weight of the total concentration of filament-forming material and more than 5% and / or 10% by weight on a dry filament basis. And / or more than 20% and / or more than 35% and / or more than 50% and / or more than 65% and / or up to about 95% and / or Up to about 90% by weight and / or up to about 80% by weight of a total concentration of active agents selected from the group consisting of builders, chelating agents, and mixtures thereof. In yet another embodiment of the present invention, the filaments of the present invention may contain active agents that may raise health and / or safety concerns when they are airborne. For example, the filament may be used to prevent enzymes in the filament from floating in the air. In one embodiment, the filaments of the present invention may be meltblown filaments. In other embodiments, the filaments of the present invention may be spunbond filaments. In other examples, the filament may be a hollow filament before and / or after release of one or more of its active agents. The filaments of the present invention may be hydrophilic or hydrophobic. The filaments may be surface treated and / or treated internally to alter the filament's inherent hydrophilic or hydrophobic properties. In one example, the filament is less than 100 pm, and / or less than 75 pm, and / or less than 50 pm, and / or less than 25 pm, and / or less than 10 pm, as measured according to the diameter test method described herein. And / or exhibit a diameter of less than 5 pm and / or less than 1 pm. In other examples, the filaments of the present invention exhibit a diameter of greater than 1 pm as measured according to the diameter test method described herein. The diameter of the filaments of the present invention may be used to control the release rate of one or more active agents present in the filament and / or the loss of and / or changing the physical structure of the filament. The filament may contain two or more different active agents. In one embodiment, the filament includes two or more different active agents, the two or more different active agents being compatible with each other. In other embodiments, the filament includes two or more different active agents, and the two or more different active agents are incompatible with each other. In one example, the filament may include an active agent within the filament and an active agent on the outer surface of the filament, such as a coating on the filament. The active agent on the outer surface of the filament may be the same as or different from the active agent present in the filament. If different, the active agents may be compatible with each other or incompatible. In one embodiment, the filaments of the present invention do not contain preservatives, which for the purposes of the present invention are based on dry filaments, less than 2%, and / or less than 1%, and / or 0. Means less than 5% and / or less than 0.25% and / or 0% preservative. In one example, the one or more active agents may be uniformly dispersed throughout the filament or may be substantially uniformly dispersed. In other examples, one or more active agents may be dispersed as separate regions within the filament. In yet other embodiments, the at least one active agent is uniformly or substantially uniformly dispersed throughout the filament, and at least the other active agent is dispersed as one or more separate regions within the filament. In yet other embodiments, the at least one active agent is dispersed as one or more discrete regions within the filament, and the at least one other active agent is one or more from the first separate region within the filament. The filament may be used as a separate article. In one embodiment, the filament is a carrier substrate (eg, wipe, paper towel, toilet paper, decorative paper, sanitary napkin, tampon, diaper, adult incontinence article, wash cloth, dryer sheet, laundry sheet, laundry Bar, dry cleaning sheet, mesh product, filter paper, fabric, garment, underwear, etc.) and / or deposited thereon. In addition, the plurality of filaments of the present invention are collected into and compressed into a film and thus released from the film when one or more filament forming materials and, for example, the film is exposed to the intended application conditions. It can be a film comprising one or more active agents that are possible. In one example, the films of the present invention have a per sample less than than 100 seconds, and / or less than 80 seconds, and / or as measured according to the dissolution test methods described herein. It exhibits an average degradation time of less than 55 seconds and / or less than 50 seconds and / or less than 40 seconds and / or less than 30 seconds and / or 20 seconds / g (s / g). In other examples, the films of the present invention have a per sample less than 1000 seconds, and / or less than 900 seconds, and / or less than 800 seconds, and / or as measured according to the dissolution test methods described herein. Alternatively, it exhibits an average degradation time of less than 700 seconds and / or less than 600 seconds and / or less than 500 seconds / g (s / g). In one example, the film of the present invention has a thickness greater than 0.01 mm and / or greater than 0.05 mm and / or 0.1 mm as measured by the thickness test method described herein. Greater than and / or up to about 20 mm and / or up to about 10 mm and / or up to about 5 mm and / or up to about 2 mm and / or up to 0.5 mm and / or about 0. The thickness may be up to 3 mm. The filament-forming material is any suitable material, such as a polymer or monomer that can produce a polymer that exhibits properties suitable for making filaments, such as by a spinning process. In one example, the filament forming material may comprise a polar solvent soluble material, such as an alcohol soluble material and / or a water soluble material. In other examples, the filament forming material may include a non-polar solvent soluble material. In yet other embodiments, the filament forming material may include a polar solvent soluble material and may not include a non-polar solvent soluble material (less than 5% by weight and / or 3% by weight on a dry filament basis). Less than and / or less than 1% by weight and / or 0% by weight). In yet another embodiment, the filament forming material may be a film forming material. In yet other embodiments, the filament-forming material may be synthetic or naturally derived, which may be chemically, enzymatically and / or physically modified. In yet another embodiment of the invention, the filament forming material is a polymer derived from acrylic monomers such as ethylenically unsaturated carboxylic acid monomers and ethylenically unsaturated monomers, polyvinyl alcohol, polyacrylates, polymethacrylates, Copolymers of acrylic acid and methyl acrylate, polyvinyl pyrrolidone, polyalkylene oxide, starch and starch derivatives, pullulan, gelatin, hydroxyl propyl methylcellulose, methylcellulose, and polymers selected from the group consisting of carboxymethylcellulose may be included. In yet another embodiment, the filament forming material is polyvinyl alcohol, polyvinyl alcohol derivative, starch, starch derivative, cellulose derivative, hemicellulose, hemicellulose derivative, protein, sodium alginate, hydroxypropylmethylcellulose, chitosan, chitosan derivative, polyethylene glycol, tetra It may include a polymer selected from the group consisting of methylene ether glycol, polyvinyl pyrrolidone, hydroxymethyl cellulose, hydroxyethyl cellulose, and mixtures thereof. In a further embodiment, the filament-forming material comprises pullulan, hydroxypropylmethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, polyvinylpyrrolidone, carboxymethylcellulose, sodium alginate, xanthan gum, tragacanth gum, guar gum, acacia gum, gum arabic, polyacrylic acid, methyl Methacrylate copolymer, carboxyvinyl polymer, dextrin, pectin, chitin, levan, erucinane, collagen, gelatin, zein, gluten, soy protein, casein, polyvinyl alcohol, starch, starch derivative, hemicellulose, hemicellulose derivative, protein, chitosan, chitosan derivative, Polyethylene glycol, tetramethylene ether glycol, Mud carboxymethylcellulose, and comprises a polymer selected from the group consisting of mixtures. Polar solvent-soluble materials Non-limiting examples of polar solvent-soluble materials include polar solvent-soluble polymers. The polar solvent soluble polymer may be synthetic or naturally derived and may be chemically and / or physically modified. In one example, the polar solvent soluble polymer is at least about 10,000 g / mol, and / or at least about 20,000 g / mol, and / or at least 40,000 g / mol, and / or at least 80,000 g / mol, And / or at least about 100,000 g / mol, and / or at least

[0007] 1 ,000,000 g / mol, and / or at least 3,000,000 g / mol, and / or at least 10,000,000 g / mol, and / or It exhibits a weight average molecular weight of at least 20,000,000 g / mol and / or up to about 40,000,000 g / mol and / or up to about 30,000,000 g / mol. In one example, the polar solvent soluble polymer is selected from the group consisting of alcohol soluble polymers, water soluble polymers, and mixtures thereof. Non-limiting examples of water soluble polymers include water soluble hydroxyl polymers, water soluble thermoplastic polymers, water soluble degradable polymers, water soluble non biodegradable polymers, and mixtures thereof. In one example, the water soluble polymer comprises polyvinyl alcohol. In other examples, the water soluble polymer comprises starch. In yet another embodiment, the water soluble polymer comprises polyvinyl alcohol and starch. In one example, the solvent consists of a water-soluble hydroxyl polymers according to the present invention include polyols such as polyvinyl alcohol, polyvinyl alcohol derivatives, polyvinyl alcohol copolymers, starch, starch derivatives, starch copolymers, chitosan, chitosan derivatives , Chitosan copolymers, cellulose, cellulose derivatives, such as cellulose ether and ester derivatives, cellulose copolymers, hemicellulose, hemicellulose derivatives, hemicellulose copolymers, gums, arabinans, galactants, proteins and various other polysaccharides, and mixtures thereof . In one embodiment, the water soluble hydroxyl polymer of the present invention comprises a polysaccharide. As used herein, “polysaccharide” means natural polysaccharides and polysaccharide derivatives or modified polysaccharides. Suitable water soluble polysaccharides include, but are not limited to starch, starch derivatives, chitosan, chitosan derivatives, cellulose derivatives, hemicellulose, hemicellulose derivatives, gums, arabinans, galactans, and mixtures thereof. The water-soluble polysaccharide is from about 10,000 g / mole to about 40,000,000 g / mole and / or more than 100,000 g / mole and / or more than 1 ,000,000 g / mole. Alternatively, it may exhibit a weight average molecular weight of greater than 3,000,000 g / mol and / or greater than about 3,000,000 g / mol and up to about 40,000,000 g / mol. The water-soluble polysaccharide may comprise non-cellulose and / or noncellulose derivatives and / or non-cellulose copolymer water-soluble polysaccharides. Such non-cellulose soluble polysaccharides may be selected from the group consisting of starch, starch derivatives, chitosan, chitosan derivatives, hemicellulose derivatives, hemicellulose derivatives, gums, arabinans, galactans, and mixtures thereof. In another embodiment, the water soluble hydroxyl polymer of the present invention comprises a non-thermoplastic polymer. The water-soluble hydroxyl polymer can be from about 10,000 g / mol to about 40,000,000 g / mol, and / or more than 100,000 g / mol, and / or more than 1 ,000,000 g / mol, and / or Alternatively, it may exhibit a weight average molecular weight of greater than 3,000,000 g / mol and / or greater than about 3,000,000 g / mol and up to about 40,000,000 g / mol. Higher and lower molecular weight water-soluble hydroxyl polymers may be used in conjunction with hydroxyl polymers having a weight average molecular weight within a particular desired range. Well known modifications of water soluble hydroxyl polymers such as natural starch include chemical and / or enzymatic modifications. For example, native starch can be acid-thinned, hydroxyethylated, hydroxyp ropy I ated, and / or oxidized. Further, the water soluble hydroxyl polymer may comprise dent corn starch. Naturally occurring starch is generally a mixture of linear amylose and branched amylopectin polymers of D glucose units. Amylose is essentially a linear polymer of D-glucose linked by (1 ,4) -a-D bonds. Aminopectin is a highly branched polymer of (1 ,4) -a-D bonds and (1 ,6) -a-D-glucose units at branch points. Naturally occurring starch is typically a relatively high concentration of amylopectin, such as corn starch (64-80% amylopectin), waxy maize (93-100% amylopectin), rice (83-84% amylopectin), potato (About 78% amylopectin) and wheat (73-83% amylopectin). Although all starches are potentially useful herein, the present invention is most commonly practiced with high amylopectin natural starch derived from agricultural sources, which is an abundant source and can be easily supplemented And offers the advantage of being inexpensive. As used herein, “starch” includes any naturally occurring unmodified starch, modified starch, synthetic starch, and mixtures thereof, and mixtures of amylose or amylopectin fractions, It may be modified by chemical, chemical, or biological processes, or combinations thereof. In the context of the present invention, the unmodified or modified starch may depend on the desired end product. In one embodiment of the present invention, the starch or starch mixture useful in the present invention is from about 20% to about 100%, more typically from about 40% to about 90%, even more typically. Having an amylopectin content from about 60 wt% to about 85 wt% starch or mixtures thereof. Suitable starches of natural origin include: corn starch, potato starch, sweet potato starch, wheat starch, sago palm starch, tapioca starch, rice starch, soybean starch, arrow root starch, amioca starch, bracken starch, lotus starch, Non-limiting examples include waxy corn starch and high amylose corn starch. Naturally occurring starches, particularly corn starch and wheat starch, are preferred starch polymers due to their economics and availability. The polyvinyl alcohol herein can be grafted with other monomers to improve its properties. A wide range of monomers have been successfully grafted to polyvinyl alcohol. Non-limiting examples of such monomers include vinyl acetate, styrene, acrylamide, acrylic acid, 2-hydroxyethyl methacrylate, acrylonitrile, 1 ,3-butadiene, methyl methacrylate, methacrylic acid, maleic acid, itaconic acid, vinyl sulfonic acid. Sodium, sodium allyl sulfonate, sodium methyl allyl sulfonate, sodium phenyl allyl ether sulfonate, sodium phenyl methallyl ether sulfonate, 2-acrylamido-methyl propane sulfonic acid (AMPs), vinylidene chloride, vinyl chloride, vinyl amine, and various Examples include acrylate esters. In one example, the water soluble hydroxyl polymer is selected from the group consisting of polyvinyl alcohol, hydroxymethylcellulose, hydroxyethylcellulose, hydroxypropylmethylcellulose, and mixtures thereof. Non-limiting examples of suitable polyvinyl alcohols include those commercially available from Sekisui Specialty Chemicals America, LLC (Dallas, TX) under the trade name CELVOL®. Non-limiting examples of suitable hydroxypropyl methylcellulose include those commercially available from Dow Chemical Company (Midland, Ml) under the trademark METHOCEL®, including combinations with the hydroxypropyl methylcellulose described above. . In yet another example, the water-soluble thermoplastic polymers consists of examples of suitable water-soluble thermoplastic polymers include thermoplastic starch and / or starch derivatives, polylactic acid, polyhydroxyalkanoates, polycaprolactones, polyester amides, and certain polyesters As well as mixtures thereof. The water-soluble thermoplastic polymer of the present invention may be hydrophilic or hydrophobic. The water soluble thermoplastic polymer may be surface treated and / or internally treated to alter the hydrophilic or hydrophobic properties inherent in the thermoplastic polymer. The water soluble thermoplastic polymer may comprise a biodegradable polymer. Any suitable weight average molecular weight may be used for the thermoplastic polymer. For example, the weight average molecular weight of the thermoplastic polymer according to the present invention is greater than about 10,000 g / mole and / or greater than about 40,000 g / mole and / or greater than about 50,000 g / mole. And / or less than about 500,000 g / mole and / or less than about 400,000 g / mole and / or less than about 200,000 g / mole. Non-polar solvent soluble material Non-limiting examples of non-polar solvent soluble materials include non-polar solvent soluble polymers. Non-limiting examples of suitable non-polar solvent soluble materials include cellulose, chitin, chitin derivatives, polyolefins, polyesters, copolymers thereof, and mixtures thereof. Nonlimiting examples of polyolefins include polypropylene, polyethylene, and mixtures thereof. Non-limiting examples of polyesters include polyethylene terephthalate. Nonpolar solvent soluble materials may include non-biodegradable polymers such as polypropylene, polyethylene, and certain polyesters. Any suitable weight average molecular weight may be used for the thermoplastic polymer. For example, the weight average molecular weight of the thermoplastic polymer according to the present invention is greater than about 10,000 g / mole and / or greater than about 40,000 g / mole and / or greater than about 50,000 g / mole. And / or less than about 500,000 g / mole and / or less than about 400,000 g / mole and / or less than about 200,000 g / mole. Activators are a class of additives designed and intended to benefit something other than the filament itself, for example, benefiting the environment outside the filament. The active agent may be any suitable additive that produces the intended effect under the intended use of the filament. For example, the active agent may be a personal cleansing and / or conditioning agent such as a hair care agent such as a shampoo and / or hair dye agent, a hair conditioning agent, a skin care agent, a sunscreen agent, and a skin conditioning agent; laundry care and / or conditioning Agents, such as fabric care agents, fabric conditioning agents, fabric softeners, fabric anti-wrinkle agents, fabric care antistatic agents, fabric care stain removers, soil release agents, dispersants, foam inhibitors, foaming agents, antifoaming agents , And fabric refreshing agents; hard surface care and / or conditioning agents, eg liquid and / or powder dishwashing agents (for dishwashing and / or automatic dishwashing for hand washing), and abrasives; other cleaning and And / or conditioning agents such as antibacterial agents, perfumes, bleaches (eg oxygen bleaching) , Hydrogen peroxide, percarbonate bleach, perborate bleach, chlorine bleach), bleach activator, chelating agent, builder, lotion, whitening agent, air care agent, carpet care agent, dye transfer inhibitor , Water softener, water softener, pH adjuster, enzyme, flocculant, foaming agent, preservative, cosmetic agent, makeup remover, foaming agent, adhesion aid, coacervate forming material, clay, thickener, latex, Silica, desiccant, odor inhibitor, antiperspirant, cooling agent, warming agent, absorbent gel, anti-inflammatory agent, dye, pigment, acid and base; liquid treatment active agent; agricultural active agent, industrial active agent, ingestion Possible active agents such as drugs, tooth whitening agents, tooth care agents, mouthwashes, periodontal gum care agents, edible agents, edible agents, vitamins, minerals, water treatment agents such as water purification and / or water disinfectants Selected from the group consisting of It may be. Non-limiting examples of suitable cosmetics, skin care agents, skin conditioning agents, hair care agents, and hair conditioning agents can be found in “CTFA Cosmetic Ingredient Handbook” (Second Edition, The Cosmetics, Toiletries, and Fragrance Assoc. 8 1992). One or more classes of chemicals may be useful for one or more of the active agents listed above. For example, a surfactant active may be useful for any number of the active agents described above. Similarly, bleach can be used in fabric care, hard surface cleaning, dishwashing, and even tooth whitening. Thus, those skilled in the art will appreciate that the active agent is selected based on the desired intended use of the filament and / or the nonwoven fabric made therefrom. For example, the filaments of the present invention and / or nonwovens made therefrom should be used for hair care and / or conditioning thereof, whereby one or more surfactants, such as foamable surfactants, Filaments and / or non-woven fabrics incorporating filaments can be selected to provide the desired benefits to the consumer when exposed to the intended application conditions. In one example, the filaments of the invention and / or nonwovens made therefrom are designed or intended for use in laundry of clothes in a laundry operation, and then one or more suitable surfactants, and Enzymes, and / or builders, and / or fragrances, and / or foam suppressors, and / or bleaching agents are desired when exposed to the intended use conditions of the filaments and / or nonwovens incorporating the filaments. Can be chosen to provide consumers with the benefits. In another embodiment, the filaments of the invention and / or nonwovens made therefrom are designed to be used in exterior or interior car washing operations, where the filaments are then washed a detergent composition may be included. As used herein “surfactants” includes non-limiting examples of suitable surfactants include anionic surfactants, cationic surfactants, nonionic surfactants, zwitterionic surfactants, and amphoteric surfactants. A co-surfactant may also be included in the filament. For example, for filaments designed for use as laundry detergents and / or dishwashing agents, the total surfactant concentration should be sufficient to provide cleaning including stain and / or odor removal. Generally in the range of about 0.5% to about 95%. In addition, surfactant systems comprising two or more surfactants designed for use in laundry detergent and / or dishwashing filaments are fully anionic surfactant systems, anionic and A mixture type surfactant system comprising a mixture of nonionic surfactants, or a mixture of nonionic-cationic surfactants may be included. Surfactants may be linear or branched herein. In one embodiment, suitable linear surfactants include those derived from agricultural chemical oils, such as coconut oil, palm kernel oil, soybean oil, or other vegetable oils. As used herein “anionic surfactants” includes non-limiting examples of suitable anionic surfactants include alkyl sulfates, alkyl ether sulfates, branched alkyl sulfates, branched alkyl alkoxylates, branched alkoxylate sulfates, medium Chain branched alkyl allyl sulfonate, sulfated monoglyceride, sulfonated olefin, alkyl allyl sulfonate, primary or secondary alkane sulfonate, alkyl sulfosuccinate, acyl taurate, acyl isethionate, alkyl glyceryl ether sulfonate, Sulfonated methyl ester, sulfonated fatty acid, alkyl phosphate, acyl glutamate, acrylic sarcosinate, alkyl sulfoacetate, acylated peptide, alkyl ether carboxylate, acyl. Examples include rulactylate, anionic fluorosurfactants, sodium lauroyl glutamate, and combinations thereof. Suitable alkyl sulfates and alkyl ether sulfates for use herein include materials having the corresponding formulas ROSO 3 M and RO (C 2 H 4 O)xSO 3 M, wherein R Is an alkyl or alkenyl from about 8 to about 24 carbon atoms, x is 1-10, and M is a water- soluble cation such as ammonium, sodium, potassium, and triethanolamine. Other suitable anionic surfactants are MacCutcheon's “Detergents and Emulsifiers” (North American Edition (1986), Allred Publishing Corp.) and McCutcheon's “Functional Materials 92” (Natural Publishing Corp.). )lt is described in. In one embodiment, anionic surfactants useful in the filaments of the present invention, C 9 -C 15 alkyl benzene sulfonates (LAS), C 8 -C 20 alkyl ether sulfates, such as alkyl poly (ethoxy) sulfates, C 8 ~ C 20 alkyl sulfates, and mixtures thereof. Other anionic surfactants include methyl ester sulfonate (MES), methyl ester etchelate (MEE), sulfonated estolides, and mixtures thereof. In other examples, the anionic surfactant is a C n -C alkyl benzene sulfonate (“LAS”) and primary branched chain, and a random C 10 -C 20 alkyl sulfate (“AS”), formula CH3(CH2)x(CHOSO3- M +) CH 3 and CH3(CH2)y( CHOSO3- M +) C 10 ~C 18 secondary of CH2CH 3 (2,3) alkyl sulfates (formula In which x and (y + 1 ) are integers of at least about 7, preferably about 9, and M is a water-solubilizing cation, in particular sodium, an unsaturated sulfate such as oleyl sulfate), C 10 -C a- sulfonated fatty acid esters, C 10 -C sulfated alkyl polyglycosides, C 10 -C alkyl alkoxy sulfates ( "AE x S") (the formula x is 1 to 30), and C 10 -C alkyl alkoxy Ruboxylates (eg containing 1-5 ethoxy units), medium chain branched alkyl sulfates as described in US Pat. Nos. 6,020,303 and 6,060,443; US Pat. No. 6,008, Medium chain branched alkyl alkoxy sulfates (MLAS) as described in 181 and 6,020,303; as described in WO 99 / 05243, WO 99 / 05242, and WO 99 / 05244 Modified alkylbenzene sulfonate (MILAS); methyl ester sulfonate (MES); and alpha-olefin sulfonate (AOS). Other suitable anionic surfactants that can be used are alkyl ester sulfonate surfactants, including sulfonated linear esters of C 8to C 20 carboxylic acids (ie fatty acids). The Other suitable anionic surfactants that can be used salts of soap, C 8 -

[0008] C 22 primary or secondary alkane sulfonates (primary of secondary alkanesulfonates), C 8 ~C 24 olefin sulfonates, sulfonated polycarboxylic acids, C 8 -C 24 alkyl polyglycol ether sulfates (alkylpolyglycolethersulfates) (contain ethylene oxide up to 10 moles); alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleoyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, paraffin sulfonates, alkyl phosphates , Isethinates, eg acyl isethionates, N-acyl taurates, alkyl succinates and sulfosuccinates, monoesters of sulfosuccinates (E.g. saturated and unsaturated C 12 - C 18 monoesters) monoester, diester sulfosuccinates (e.g., saturated and unsaturated C6-C 12 diesters), and alkyl polysaccharide sulfates, such as alkyl polysaccharides sulfates, and alkyl polyethoxy carboxylates such as those of the formula RO(CH2CH2O)k -CH 2 COO-M + ( wherein R is a C 8 -C 22 alkyl, k is an integer of 0, M is a soluble salt-forming cation). Other exemplary anionic surfactants are alkyl benzene sulphonic acid of C 10 -

[0009] C 16, preferably an alkali metal salt of alkylbenzene sulfonic acid C n -C 14 In one embodiment, the alkyl group is linear. Such linear alkyl benzene sulfonates are known as “LAS”. Such surfactants and their preparation are described, for example, in US Pat. Nos. 2,220,099 and 2,477,383. Referring now to the FIGURES, FIGURE 1 is an illustration of a non-limiting embodiment of a homogenizer assembly, component feeds, and drum dryer assembly according to the invention. Fig. 1 shows water supply at 70-90°C for delivery to the homogenizer tank via pumped delivery pipe with a control valve. The homogenizer tank includes a mixing paddle connected to electric motors. The PVA supply delivers polyvinyl alcohol to the homogenizer tank via pumped or gravity fed conduit for dissolving in the water. Component feeds A, B, C are delivered via pumped conduit to the homogenizer tank, and steam feed 70-120°C. In the present invention the polyvinyl alcohol, water, a surfactant, a builder, a binding agent, a chelating agent, and a car surface treatment ingredient, form a PVA homogenate by mixing in a single homogenizer tank, and the homogenizer tank is heated using steam. The PVA paste / homogenate is pumped to the drum dryer assembly and delivered to a bottom feed tray having a bottom feed applicator roller disposed therein. The drum dryer comprises a heated drying drum having a drive system and a mirror finish, said drying drum mounted over a bottom applicator roller assembly having a bottom feed tray with a bottom feed applicator roller disposed therein, the bottom fed tray having a inlet for receiving the paste, the bottom feed applicator roller in operative contact with paste in the bottom feed tray, wherein rotational engagement between the drying drum and the bottom feed applicator roller forms a water dissolvable car cleaning sheet. Fig. 1 also shows optional the optional step of trimming the water dissolvable car cleaning sheet to a form 1.5-2.0 mm thick, 50-127 mm wide, and 76-203 mm long. In another non-limiting preferred embodiment, an additional step of surface spraying the water dissolvable car cleaning sheet with a surface agent selected from the group consisting of a bleaching agent, a bleach particle, a pH modifying agent, a bleach activator, a surfactant, a builder, a binding agent, a chelating agent, a fragrance, and a combination of one or more thereof. Fragrance Sheet Preferred Embodiments In a non-limiting preferred embodiment, the invention provides a composition comprising PVA film combined with a perfume or fragrance, or a combination thereof to form a water dissolvable fragrance sheet. Any of the non-limiting embodiments may include wherein said water dissolvable fragrance sheet is used with the additional of an odor removing agent selected from the group consisting of Ozium, Lysol, Damprid, Lemon, BioKeen, or a combination thereof, or odor neutralizing agent, such as hydrogen peroxide, or baking soda, or vinegar, or charcoal, or a combination thereof Any of the non-limiting embodiments may include wherein said water dissolvable fragrance sheet is used during the laundry process and further added into the dryer after the washing process. Once the water dissolvable fragrance sheet has been transferred to the drying machine, said composition of the water dissolvable fragrance sheet will be coated onto the fiber of the garments and released over time with ingredients such as liquid softener, lubricants, fragrance coating ingredients or a combination thereof, to deliver a scent that can last from minutes to hours to days to even longer period of time. Any of the non-limiting embodiments may include wherein said composition contains ingredients such as laundry boosters selected from the group consisting of Lemon Juice, NaCI, Baking Soda, Alcohol, hydrogen peroxide, Vinegar, or a combination thereof, used to deodorize the odor of the laundry process Any of the non-limiting embodiments may include wherein said composition contains ingredients selected from the group consisting of Citronellol, Rose oil, Limonene, Essential oils, Sodium Bicarbonate or a combination thereof. Any of the non-limiting embodiments may include wherein said water dissolvable fragrance sheet contains ingredients selected from the group consisting of Clay, Bentonite Clay, Minerals, Pine, Wheat, Corn, Silica, Silica Gel, or a combination thereof. Any of the non-limiting embodiments may include wherein said composition contains ingredients selected from the group consisting of Essential oils, Sodium Bicarbonate, or a combination thereof. Any of the non-limiting embodiments may include wherein said composition contains ingredients selected from the group consisting of Disodium ethylenediaminetetraacetate dihydrate, Na2EDTA, DTPA, MGDA, EDTA or a combination thereof. Any of the non-limiting embodiments may include wherein said composition contains ingredients selected from the group consisting of Borax, Sodium Bicarbonate, Charcoal, Hypochlorite, hydrogen peroxide, vinegar, or a combination thereof. Any of the non-limiting embodiments may include wherein said composition contains ingredients selected from the group consisting of EpsonSalt, Sodium Bicarbonate, Bentonite Clay, hydrogen peroxide, vinegar, or a combination thereof. Any of the non-limiting embodiments may include wherein said composition contains ingredients selected from the group consisting of Essential oils, Lavender, Peppermint, Lemon, Bergamot, Ylang Ylang, Hydrosols, Resins, Carrier oils, Infused oils, Herbs, or a combination thereof. Any of the non-limiting embodiments may include wherein said composition contains ingredients selected from the group consisting of Perfume MicroCapsules or a combination of Perfume Micro Capsules, used for the delivery of a two-step odor release composition wherein one step is right out of the washer and / or dryer during the washing process and will also release scent after said washing and drying garment process. Any of the non-limiting embodiments may include wherein said composition contains water, starch, a surfactant, wherein the PVA, starch, surfactant and water are mixed and dried to form a water dissolvable fragrance sheet. Any of the non-limiting embodiments may include wherein the surfactant constitutes between 5 to 50% by weight of the total mixture, and wherein the water constitutes between 1 - 15% by weight of the total mixture. Any of the non-limiting embodiments may include a chelating agent selected from the group consisting of EDTA,MGDA, DTPA, zeolite, phosphonate, citric acid, citrate, or a mixture thereof. Any of the non-limiting embodiments may include a fragrance 0 to 2% by weight. Any of the non-limiting embodiments may include a brightening agent up to 1% by weight of the total mixture. Any of the non-limiting embodiments may include a bleaching agent selected from the group consisting of calcium hypochlorite, sodium hypochlorite, sodium percarbonate, sodium perborate, sodium persulfate, tetrasodium pyrophosphate, or urea peroxide or a combination thereof. Any of the non-limiting embodiments may include a fabric softener agent selected from the group consisting o fquaternary ammonium cations / salts, ceterinium bromide, quaternary ammonium chloride, polydimethylsiloxane, silicone, or a mixture thereof. Any of the non-limiting embodiments may include a perfume, a fragrance, a perfume micro capsule or a combination thereof. Any of the non-limiting embodiments may include a binding agent selected from the group consisting of a resin, a wax, a gum, accroides, candelilla, guar, gum Arabic, shellac, tragacanth, or a combination thereof. Any of the non-limiting embodiments may include (a) dissolving an oil phase perfume core material in a continuous phase of a polyvinyl alcohol matrix. Any of the non-limiting embodiments may include mixing into the PVA matrix scent absorbing ingredients selected form the group consisting of activated charcoal, beta cyclodextrins, odor absorbing fabrics which contains porous chambers, porous clays, waxes that can hold scents, lava rocks, felt pads, cardboard, and potpourri. Any of the non-limiting embodiments may include guar, gum Arabic, shellac, tragacanth, or a combination thereof. Any of the non-limiting embodiments may include an additional step of surface spraying the water dissolvable PVA sheet with a surface agent selected from the group consisting of a additional of an odor removing agent selected from the group consisting of Ozium, Lysol, Damprid, Lemon, BioKeen, or a combination thereof, or odor neutralizing agent, such as hydrogen peroxide, or baking soda, or vinegar, or charcoal, or a combination thereof, Any of the non-limiting embodiments may include laundry boosters selected from the group consisting of Lemon Juice, NaCI, Baking Soda, Alcohol, hydrogen peroxide, Vinegar, or a combination thereof, used to deodorize the odor of the laundry process, Citronellol, Rose oil, Limonene, Essential oils, Sodium Bicarbonate or a combination thereof, Clay, Bentonite Clay, Minerals, Pine, Wheat, Corn, Silica, Silica Gel, or a combination thereof, Essential oils, Sodium Bicarbonate, or a combination thereof, Disodium ethylenediaminetetraacetate dihydrate, Na2EDTA, DTPA, MGDA, EDTA or a combination thereof, Borax, Sodium Bicarbonate, Charcoal, Hypochlorite, hydrogen peroxide, vinegar, or a combination thereof, Epsom Salt, Sodium Bicarbonate, Bentonite Clay, hydrogen peroxide, vinegar, or a combination thereof, Essential oils, Lavender, Peppermint, Lemon, Bergamot, Ylang Ylang, Hydrosols, Resins, Carrier oils, Infused oils, Herbs, or a combination thereof, Perfume MicroCapsules or a combination of Perfume Micro Capsules, used for the delivery of a two-step odor release composition wherein one step is right out of the washer and / or dryer during the washing process and will also release scent after said washing and drying garment process, a chelating agent selected from the group consisting of EDTA,MGDA, DTPA, zeolite, phosphonate, citric acid, citrate, or a mixture thereof, a fragrance 0 to 2% by weight, a brightening agent up to 1% by weight of the total mixture, a bleaching agent selected from the group consisting of calcium hypochlorite, sodium hypochlorite, sodium percarbonate, sodium perborate, sodium persulfate, tetrasodium pyrophosphate, or urea peroxide or a combination thereof, a fabric softener agent selected from the group consisting o fquaternary ammonium cations / salts, ceterinium bromide, quaternary ammonium chloride, polydimethylsiloxane, silicone, or a mixture thereof, a perfume, a fragrance, a perfume micro capsule or a combination thereof, a binding agent selected from the group consisting of a resin, a wax, a gum, accroides, candelilla, guar, gum Arabic, shellac, tragacanth, or a combination thereof, and scent absorbing ingredients selected from the group consisting of activated charcoal, beta cyclodextrins, odor absorbing fabrics which contains porous chambers, porous clays, waxes that can hold scents, lava rocks, felt pads, cardboard, and potpourri. This invention provides a convenient and cost-effective method for delivering perfumes, or fragrances or odor removing technologies or odor neutralizing technologies or a combination thereof, using a completely new form consisting of a water dissolvable fragrance sheet. The water dissolvable fragrance sheet are formed into fibers that may be inter-connected into a fibrous matrix or simply dried into a film with different aesthetics, size and many other properties depending on the composition and purpose. The fibrous matrix of the perfumes or fragrances or odor removing agents or odor neutralizing agents or a combination thereof is made to be added to water, or some other liquid, to form an odorific compositions. Some examples include the additional of scent absorbing materials to further increases the benefit of the PVA based scent delivery system. The composition described herein can provide for a thorough water dissolvable fragrance sheet consisting of a composition that is convenient for the consumer to water dissolvable fragrance sheete in the wash machine and act as a fabric softening composition that can be provided in a composition with a plurality of particles that can deliver softening along with the odor benefit that consumer seek for long lasting signal of freshness over time. The ingredients in said composition can be provided in a package that is separate from the washing detergent composition for the machine wash. Having the odor composition separate from the wash can be beneficial since it allows the consumer to select the amount of perfumes or fragrances or odor removing agents or odor neutralizing agents or a combination thereof independent from the wash detergent product. This can give the consumer the opportunity to customize the amount of perfumes or fragrances or odor removing agents or odor neutralizing agents or a combination thereof used and thereby the amount of scent benefit they can achieve, which is a highly valuable consumer benefit. This is especially important for the segment of consumers that are scent seekers or desire an amount of residual scent that far exceeds the typical amount of scent that is delivered with the average detergent and fabric conditioner product that is sold on the market today. A water dissolvable fragrance sheet that is composed of ingredients that can easily be water dissolvable fragrance sheeted by consumers from a package that can be directly added into the wash or during the drying cycle that takes place after the washing machine process or can be added into the water dissolvable fragrance sheeting attachment of the washing machine or can be added directly into the drum of the wash machine, can be formulated into a dissolvable PVA sheet or similar dissolvable sheet composition. Said composition can have additional ingredients, other than the perfumes or fragrances or odor removing agents or odor neutralizing agents or a combination thereof such as quaternary ammonium compounds to contribute to the deposition of the odor ingredients and said quaternary ammonium compound increases the amount of ingredient that will deliver the perfume and / or fragrance to the garments in the wash or in the dryer cycle of the washing process. Perfumes and fragrances have up to 30% weight / weight (wt / wt) oil concentration but are typically used in lower level in different products. For the water dissolvable fragrance sheet the concentration of the perfume and / or perfumes range from less than 1% to more than 20% depending on the application. The perfumes or fragrances or odor removing agents or odor neutralizing agents, or a combination thereof are incorporated into the PVA film and can be released as the PVA film dissolves. Said perfumes or fragrances or odor removing agents or odor neutralizing agents, or a combination thereof can be added directly into the wash in a wash machine or in a wash basin. Additionally, it preferred to be added during the drying cycle of the washing process. The fragrance sheet is added to the dryer and during the drying cycle the moisture from the garment will slowly dissolve the PVA film comprised of the perfumes or fragrances or odor removing agents or odor neutralizing agents or a combination thereof scent will be transferred from the PVA film to the garments in the dryer. The scent will then remain on the garment from minutes to hours to days depending on the composition of the water dissolvable fragrance sheet. Some example applications include adding the fibrous matrix of water dissolvable fragrance sheet to laundry wash water and dish cleaning water. In some forms, the water dissolvable fragrance sheet may include color brighteners, bleaches, fabric softeners and anti-static materials, or any other ingredient that makes the fibrous matrix suitable for commerce, including any combination thereof. The present invention relates to a composition for forming fibers or forming a film of synthetic and / or natural perfumes or fragrances or odor removing agents or odor neutralizing agents, or a combination thereof perfumes and fragrances. In another example form, the present invention relates to an odor fiber that is composed of scent absorbing materials. The odor fiber may include a PVA composition and may be combined with a wide range of ingredients to deliver a wide range of consumer benefits. In yet another form, the present invention relates to a water dissolvable fragrance sheet that is fabricated from odor fibers or extruded from odor filaments that results in a woven or non-woven substrate depending on the targeted application. The present invention relates to a method of making a film containing a water-soluble composition, optionally made from polyvinyl alcohol (PVA), which is processed and may be extruded to produce filaments or fibers by converting the filaments and / or fibers and / or nonwoven webs into films. In another embodiment, the PVA is casted and formed into a film. Casting processes for making films, particularly water-soluble films, and / or films comprising water- soluble film forming materials (e.g., polyvinyl alcohol) are known in the art. Such casting processes use a solvent and a solution of a film-forming material such as polyvinyl alcohol, which is deposited on and / or flowed over a casting surface such as a metal wheel, roller, or belt. The solvent is then removed from the solution, for example by drying. Once the solvent is removed from the solution, a film formed from the filament forming material remains on the casting surface. The casting process for making films is known to be very time intensive since the solvent needs to be removed by drying. The resulting product consists of a water dissolvable fragrance sheet and may be cut to size depending on the application. Non-water soluble films and / or non-water soluble filament forming materials such as polypropylene, polyethylene, and thermotropic polymers (i.e., polymers that form liquid crystal melts) are, for example, water insoluble. Filaments of filament forming material have been made by spinning a web and then pressing the resulting web with heat into a film (often a porous film). However, such water-insoluble films and / or films containing water-insoluble filament forming materials are not suitable for uses and / or products that require water-soluble films. Accordingly, films, particularly polar solvent soluble (e.g., water soluble) films, and / or polar solvent soluble filament forming materials, and / or difficulties of conventional film casting methods (specifically, solvents and film forming materials, may result in the need for a method of making a film comprising a water soluble filament forming material that avoids the fact that a film made from a casting solution containing a filament forming material is made at a low rate. The present invention creates a film, for example a polar solvent soluble film and / or a film containing a polar solvent soluble filament forming material, by converting a nonwoven web containing filaments and / or fibers comprising a polar solvent soluble filament forming material into a film, which then is further converted to a water dissolvable fragrance sheet. By satisfying the above requirements by providing a process to do so. In one embodiment of the present invention, the water dissolvable fragrance sheet methos is providing a nonwoven web comprising a plurality of filaments, the plurality of filaments comprising a polar solvent soluble filament forming material. Said water dissolvable fragrance sheet method is further converting the nonwoven web to a film, and a process for making a film from the nonwoven web is provided. In another embodiment of the invention, a film made by the process according to the invention is provided. Accordingly, the present invention provides a process for making a film, a film made by such a process, and a unit volume product comprising such a film. The resulting product is a water dissolvable fragrance sheet. DEFINITIONS As used herein, “filament” means an elongated microparticle having a length that greatly exceeds its diameter, i.e., a ratio of length to diameter of at least about 10. The filaments of the present invention can be spun from the filament forming composition via suitable spinning process operations, such as melt blowing and / or spunbonding or a combination thereof. The filaments of the present invention may be single component and / or multicomponent. For example, the filament may comprise a bicomponent filament. The bicomponent filament may be in any form such as side-by-side, core and sheath, or sea-island type. The filaments of the present invention are 2 inches or more, and 3 inches or more, and 4 inches or more, and 6 inches or more of length. EMBODIMENTS As used herein, filaments are typically considered continuous or essentially nearly continuous. Filaments are relatively longer than fibers. Non-limiting examples of filaments include meltblown and / or spunbond filaments. As used herein, one or more fibers can be formed from the filaments of the present invention so that the filaments are cut to shorter lengths (e.g., less than 2 inches in length). Thus, in one embodiment, the present invention also comprises fibers comprising fibers made from the filaments of the present invention, such as one or more filament forming materials, and optionally one or more additives such as active agents. Including. Accordingly, references herein to the filaments of the present invention include fibers made from such filaments, unless otherwise noted. Fibers are typically considered discontinuous in nature relative to filaments that are considered to be essentially continuous. As used herein, “filament forming composition” means a composition suitable for making the filaments of the present invention, such as by melt blowing and / or spunbonding. Filament-forming compositions comprise one or more filament-forming materials that exhibit properties that make them suitable for spinning into filaments. In one example, the filament forming material comprises a polymer. In addition to the one or more filament forming materials, the filament forming composition may include one or more additives, such as one or more active agents. Furthermore, the filamentforming composition may comprise one or more polar solvents, such as water, in which one or more, for example all filament-forming materials and / or one or more, for example all active agents, which are further dissolved or dispersed or a combination thereof. As used herein, the filaments of the present invention are made from the filamentforming composition of the present invention has one or more additives, such as one or more active agents. The coating is such that it can be present in the filament rather than on the filament. The total concentration of filament forming material, and the total concentration of active agent present in the filament forming composition may be any suitable amount, as long as the filaments of the present invention are made therefrom. As used herein, one or more additives, such as an active agent, may be present in the filament and one or more additional additives, such as an active agent, may be present on the surface of the filament. In other embodiments, the filaments of the present invention may include one or more additives, such as an active agent, which are present in the filament when first made, but are subject to the conditions of the intended use of the filament, further resulting in a bloom on the surface of the filaments before and / or when exposed to air or other external conditions. As used herein, “filament-forming material” means a material such as a polymer or monomer that can produce a polymer that exhibits properties suitable for making filaments. In one example, the filament-forming material includes one or more substituted polymers, such as anionic, cationic, zwitterionic, and / or nonionic polymers. In other examples, the polymer may comprise a hydroxyl polymer, such as polyvinyl alcohol ("PVA"), and / or a polysaccharide, such as starch, and / or a starch derivative, such as ethoxylated starch, and / or acid diluted starch. In another example, the polymer may include polyethylene and / or terephthalate. In yet another embodiment, the filament forming material is a polar solvent soluble material. As used herein, “additive” means any material that is present in the filaments of the invention and is not a filament forming material. In one example, the additive includes an active agent. In other embodiments, the additive includes a processing aid. In yet another embodiment, the additive includes a filler. In one embodiment, the additive is present in the filament, and the absence of it in the filament does not cause the filament to lose its filament structure (i.e. , the absence of it causes the filament to be in its solid form. Including any material) that will not lose. In other embodiments, the additive, e.g., the active agent, includes a non-polymeric material. As used herein, the additive includes a plasticizer for the filament. Non-limiting examples of suitable plasticizers of the present invention include polyols, copolyols, polycarboxylic acids, polyesters, and dimethicone copolyols. Examples of useful polyols include glycerin, diglycerin, propylene glycol, ethylene glycol, butylene glycol, pentylene glycol, cyclohexanedimethanol, hexanediol, 2,2,4-trimethylpentane-1 ,3- diol, polyethylene glycol (200-600), sugar alcohols such as pentaerythritol, sorbitol, mannitol, lactitol and other mono- and polyhydric low molecular weight alcohols (eg C2-C8 alcohols); mono, di- and oligosaccharides such as fructose, Examples include, but are not limited to, glucose, sucrose, maltose, lactose, and higher fructose corn syrup solids, and dextrin, and ascorbic acid. In yet another example, the plasticizer includes glycerin and / or propylene glycol, and / or a glycerol derivative, such as propoxylated glycerol. In yet another embodiment, the plasticizer is selected from the group consisting of glycerin, ethylene glycol, polyethylene glycol, propylene glycol, glycidol, urea, sorbitol, xylitol, maltitol, saccharides, ethylene bisformamide, amino acids, and mixtures thereof. Is done. As used herein,, the additive includes a crosslinking agent suitable for crosslinking one or more filament-forming materials present in the filaments of the present invention. In one example, the cross-linking agent includes a cross- linking agent that can cross-link the hydroxyl polymer together, for example, via the hydroxyl portion of the hydroxyl polymer. Non-limiting examples of suitable crosslinkers include imidazolidinone, polycarboxylic acids, and mixtures thereof. In one example, the cross-linking agent comprises a urea glyoxal adduct cross-linking agent, for example, a dihydroxy imidazolidinone such as dihydroxyethylene urea (“DHEU”). Crosslinking agents may be present in the filament forming composition of the present invention and / or in the filaments to control the solubility and / or dissolution of the filaments in a solvent such as a polar solvent. As used herein,, the additive comprises a rheology modifier such as a shear force modifier and / or an extension modifier. Non-limiting examples of rheology modifiers include, but are not limited to, polyacrylamides, polyurethanes, and polyacrylates that can be used in the filaments of the present invention. Non-limiting examples of rheology modifiers are commercially available from Dow Chemical Company (Midland, Ml). As used herein,, the additive may be used when the filament is exposed to the intended application conditions and / or when the active agent is released from the filament and / or when the morphology of the filament changes. To provide a visual signal, it includes one or more colors and / or dyes incorporated into the filaments of the present invention. As used herein, the additive includes one or more release agents and / or lubricants. Non-limiting examples of suitable release agents and / or lubricants include fatty acids, fatty acid salts, fatty alcohols, aliphatic esters, sulfonated fatty acid esters, aliphatic amine acetates, fatty acid amides, silicones, aminosilicones, fluoropolymers, and mixtures thereof. In one embodiment, the release agent and / or lubricant is applied to the filament, in other words, after the filament is formed. In one example, one or more release agents / lubricants are applied to the filaments prior to collecting the filaments on the collection device to form a nonwoven. In other embodiments, one or more release agents / lubricants are applied to a nonwoven formed from the filaments of the present invention prior to contacting one or more nonwoven webs, such as a stack of nonwoven webs. In yet another embodiment, to facilitate removal of the filaments and / or nonwoven webs of the present invention and / or the layers of the filament / nonwoven webs of the present invention are adhered to each other, and further carelessly adhered. To avoid, the filaments and / or nonwovens comprising the filaments of the present invention may have one or more release agents / before the filaments and / or nonwovens contact the surface (such as the surface of an apparatus used in a processing system). Lubricant is applied. In one example, the release agent / lubricant includes particulates. As used herein,, the additive includes one or more antiblocking agents and / or tack removers. Non-limiting examples of suitable antiblocking and / or detackifying agents include starch, starch derivatives, crosslinked polyvinylpyrrolidone, crosslinked cellulose, microcrystalline cellulose, silica, metal oxides, calcium carbonate, talc, mica, or a combination thereof. As used herein, “purpose application conditions” refers to the temperature, physical, chemical, and exposure to which the filaments of the invention are exposed when used for one or more of their design purposes. Means mechanical conditions. For example, if the filament and / or the nonwoven web comprising the filament is designed to be used in a washing machine for laundry care purposes, the condition of the intended use is any wash water during the laundry wash operation. Will include these temperatures, chemical, physical, and / or mechanical conditions present in the washing machine. In other examples, if the filament and / or the nonwoven web comprising the filament is designed to be used by humans as a shampoo for hair care purposes, the conditions for the intended use are during human hair shampooing. These temperatures, chemical, physical and / or mechanical conditions that exist will be included. Similarly, if the filament and / or the nonwoven web comprising the filament is designed to be used in a dishwashing operation by hand or by a dishwasher, the intended use condition is that the dishwashing water during the dishwashing operation is and / or these temperatures, chemical, physical, and / or mechanical conditions present in the dishwasher. As used herein, an “active agent” is used in the environment outside of a filament and / or a nonwoven web comprising the filament of the invention, e.g., the purpose of the filament and / or nonwoven web comprising the filament. By an additive that produces the intended effect when exposed to the conditions of use. In one example, the active agent is a surface, such as a hard surface (i.e., kitchen counter, bathtub, toilet, toilet bowl, sink, floor, wall, tooth, car, window, mirror, dish) and / or a soft surface (i.e., Fabrics, hair, skin, carpets, crops, plants). In other embodiments, the activator is a chemical reaction (i.e., foaming, foaming, coloring, increasing temperature, cooling, foaming, disinfection and / or purification, and / or chlorination, e.g., water purification, and / or water used in the disinfection and / or chlorination of water). In yet another embodiment, the active agent includes an additive that treats the environment (i.e., deodorizes, purifies, or aromas the air). In one example, the active agent is formed in situ, such as during the formation of a filament containing the active agent, e.g., the filament comprises a water soluble polymer (e.g., starch) and a surfactant (e.g., an anionic surfactant). However, they can create polymeric complexes, i.e., coacervates, that function as active agents used to treat the surface of the fabric. As used herein, “Treat”, with respect to surface treatment means that the active agent provides a benefit to the surface or environment. Treatment includes controlling and / or immediately improving the appearance of the surface or environment, cleanliness, odor, purity, and / or feel. In one example, treatment relating to the treatment of the surface of keratinous tissue (e.g., skin and / or hair) means modulation of the superficial appearance and / or feel of keratinous tissue and / or instantaneous improvement. For example, “adjusting the condition of the skin, hair, or nails (keratinous tissue)” may increase the thickness of the skin, hair, or nails (e.g., skin condition) to reduce skin, hair, or nail atrophy. Construction of the epidermis and / or dermis and / or sub-dermal (e.g., subcutaneous fat or muscle) layer and, where applicable, construction of the stratum corneum of the nail and hair shaft), at the dermis-epidermal boundary Increased convolution (also known as interpapillary ridge), melanin or non-melanin changes in the skin, hair, or nail color under the eyes, spots (e.g., uneven red color due to rosacea, etc.). As used herein, treatment means removing odors from fabric articles (cloth, towels, linens, etc.) and / or hard surfaces (including counters and / sink, toilets, etc.). As used herein, “personal care active agent” means an active agent that can be applied to mammalian keratinous tissue that does not have undue undesirable efficacy. As used herein, “keratinous tissue” means a keratin-containing layer that is placed as the outermost protective covering of a mammal, including skin, hair, scalp, and nails. As used herein with respect to mammalian keratinous tissue, “beauty benefits” or “effects” include washing, sebum prevention, reducing the greasy and / or shiny appearance of skin and hair, dryness, Reduces itching and / or flakiness, skin pore size, exfoliation, reduction of desquamation, keratinous tissue appearance, conditioning, smoothing, skin deodorization and / or antiperspirant effect. “Cosmetics active agent” as used herein refers to an active agent capable of delivering one or more cosmetic effects. As used herein, “skin care active” means an active that provides an effect or improvement to the skin when applied to the skin. Skin care actives are useful not only for skin, but also when applied to hair, scalp, nails, and other mammalian keratinous tissues. As used herein, “hair care active agent” means an active agent that, when applied to mammalian hair, provides an effect and / or improvement on the hair. Non-limiting examples of effects and / or improvements on hair include flexibility, static control, hair repair, dandruff removal, dandruff resistance, hair color, shape retention, hair retention, and hair growth. As used herein, “fabric care active agent” means an active agent that, when applied to a fabric, provides a benefit and / or improvement to the fabric. Non-limiting examples of fabric benefits and / or improvements include addition of perfume and / or fragrance, removal of undesirable scents or smell, reduction of undesirable scent or smell, deodorant, wrinkle removal, color recovery, static control, wrinkle resistance, permanent press, wear reduction , Abrasion resistance, pill removal, pill resistance, dirt removal, dirt resistance (including dirt release), shape retention, shrinkage reduction, flexibility, fragrance, antibacterial, and antiviral. As used herein, “scent activator” refers to garments or fabrics when applied to fabrics made of materials such as cotton, polyester, poly-cotton, silk, synthetic polymers (e.g., lycra and related synthetic fibers, running gear etc.). This also applies to bedding sheets, blankets, wraps, towels. Means that it provides benefits and / or improvements to odor integrity of the sheet. Non-limiting examples of benefits and / or improvements to air surrounding. “Hard surface-active agent” as used herein refers to a floor, counter, sink, window, mirror when applied to a floor, counter, sink, window, mirror, shower, bathroom, and / or toilet. Active agent that benefits the shower, bathroom, and / or toilet. Non-limiting examples of benefits and / or improvements to floors, counters, sinks, windows, mirrors, showers, bathrooms, and / or toilets include mildew, un-pleasant smell, or other undesirable scent or smell from the hard surfaces. An “ingestible active agent” as used herein is defined by an animal, such as a mammal (such as a human), in the animal, mouth, nose, eyes, ears, pores, rectum, vagina, or other opening or by a wound (such as delivery of an active agent by a wound dressing) is meant an active agent suitable for ingestion and / or consumption. Non-limiting examples of ingestible active agents include feminine hygiene active agents, infant care active agents, oral care active agents, pharmaceutical active agents, vitamins, nutritional active agents (e.g., delivered in new food forms), pet care actives, and mixtures thereof. “Liquid processing active agent” as used herein means an active agent that provides benefits and / or improvements to a liquid when applied to a liquid such as water and / or alcohol. For example, chlorine and / or other swimming pool chemicals are nonlimiting examples of suitable liquid treatment activators. In other examples, water purification and / or water disinfecting activators, such as commercial water filtration and / or water treatment techniques, are suitable for the filaments of the present invention. In addition, oil dispersants and / or oil scavengers are non-limiting examples of other suitable liquid treatment actives. As used herein, “industrial active agent” means an active agent that provides benefits within the article of manufacture. For example, glues and / or adhesives that provide a bond between two objects, pesticides, food and / or septic articles incorporated in insulators (e.g., housing insulators) Oxygen scavenging active agents incorporated into packages, insect repellents incorporated into articles used by humans to repel insects, and moisture scavengers incorporated into desiccants are present in the filaments of the present invention. Non-limiting examples of industrial activators obtained. “Weight ratio”, as used herein, refers to the weight of the additive, e.g., the filamentforming material on a dry weight basis in the filament to the active agent (g or %) in the filament on a dry weight basis. It means weight (g or %). The final concentration is expressed as weight percent (wt.%). As used herein, “hydroxyl polymer” includes any hydroxyl-containing polymer that can be incorporated into the filaments of the present invention, e.g., as a filament-forming material. In one example, the hydroxyl polymer of the present invention comprises greater than 10 wt% and / or greater than 20 wt.% and / or greater than 25 wt.% hydroxyl moieties. “Biodegradable” as used herein with respect to a material, such as a material, for example as a whole filament and / or as a polymer within a filament (e.g., filamentforming material), for example, at least of the initial filament and / or polymer. 5%, and / or 7%, and / or at least 10% according to OECD (1992) “Guideline for the Testing of Chemicals 301 B; Ready Biodegradability-CO 2 Evolution (Modified T) When measured, filaments and / or polymers can be converted to carbon dioxide in public solid waste composting facilities so that they are converted to carbon dioxide after 30 days. They can undergo a beauty / or biodegradable, and / or means that go through it. “Non-biodegradable” as used herein with reference to materials such as whole filaments and / or polymers within filaments (e.g. filament-forming material) filaments, e.g., at least 5% of the initial filaments and / or polymers. As measured after 30 days as measured according to OECD (1992) “Guideline for the Testing of Chemicals 301 B; Ready Biodegradability — CO 2 Evolution (Modified Storm Test) Test” incorporated herein. In particular, it means that the filament and / or polymer cannot undergo physical, chemical, thermal and / or biodegradation. “Non-thermoplastic” as used herein with respect to materials such as whole filaments and / or polymers within filaments (eg, filament-forming materials), filaments and / or polymers do not exhibit a melting point and / or softening point. This means that when there is no plasticizer such as water, glycerin, sorbitol, urea, it can flow under pressure. As used herein, “non-thermoplastic biodegradable filament” means a filament that exhibits biodegradable and non- thermoplastic properties as defined above. As used herein, “non-thermoplastic, non-biodegradable filament” means a filament that exhibits non-biodegradable and non-thermoplastic properties as defined above. “Thermoplastic” as used herein with respect to materials such as the entire filament and / or polymer within the filament (e.g., filament forming material), the filament and / or polymer has a melting point and / or softening point at a particular temperature. Which allows it to flow under pressure in the absence of a plasticizer. As used herein, “thermoplastic biodegradable filament” means a filament that exhibits biodegradable and thermoplastic properties as defined above. As used herein, “thermoplastic, non-biodegradable filament” means a filament that exhibits non-biodegradable and non-thermoplastic properties as defined above. As used herein, “non-cellulose containing” is less than 5% by weight and / or less than 3% by weight and / or less than 1% by weight and / or less than 0.1 % by weight. In addition, it means that weight percent cellulose polymer, cellulose derivative polymer and / or cellulose copolymer is present in the filament. In one example, “non- cellulose- containing” is less than 5% by weight and / or less than 3% by weight and / or less than 1% by weight and / or less than 0.1 % by weight and / or 0% by weight. As used herein, “polar solvent soluble material” means a material that is miscible in a polar solvent. In one example, the polar solvent soluble material is miscible in alcohol and / or water. In other words, the polar solvent soluble material forms a homogeneous solution that is stable at ambient conditions with a polar solvent, such as alcohol and / or water (no phase separation for more than 5 minutes after forming a homogeneous solution). As used herein, “alcohol soluble material” means a material that is miscible within the alcohol. In other words, it is a material that can form a homogeneous solution that is stable with alcohol at ambient conditions (it does not phase separate for more than 5 minutes after forming a homogeneous solution). As used herein, “water soluble material” means a material that is miscible in water. In other words, it is a material that can form a homogeneous solution that is stable with water (does not separate for more than 5 minutes after forming a homogeneous solution) at ambient conditions. As used herein, “nonpolar solvent soluble material” means a material that is miscible in a nonpolar solvent. In other words, a non-polar solvent soluble material is a material that can form a stable solution with a non-polar solvent (which does not phase separate for more than 5 minutes after forming a homogeneous solution). As used herein, “ambient conditions” means about 23 ° C. ± 2.2 ° C. (about 73 ° F. ± 4 ° F.) and 50% ± 10% relative humidity. As used herein, “weight average molecular weight” means gel penetration according to the procedure found in “Colloids and Surfaces A. Physico Chemical & Engineering Aspects” (Vol. 162, 2000, pg. 107-121). It means the weight average molecular weight determined using chromatography. As used herein with respect to a filament, “length” means the length along the longest axis from one end to the other end. If the filament is kinked, curved, or bent within it, the length is the length along the entire path of the filament. As used herein with respect to filaments, “diameter” is measured according to the diameter test method described herein. In one embodiment, the filaments of the invention are less than 100 pm and / or less than 75 pm and / or less than 50 pm and / or less than 25 pm and / or less than 20 pm and / or less than 15 pm and / or exhibit a diameter of less than 10 m and / or less than 6 pm and / or greater than 1 pm and / or greater than 3 pm. As used herein, in yet another examples, incentive conditions may be present in the environment (e.g., water, etc.) when the filaments and / or nonwoven webs, and / or films of the present invention are added to water. In other words, nothing changes in water except for the fact that the filaments and / or nonwoven webs and / or films of the present invention have been added to water. As used herein with respect to filament morphological changes, "morphological change" means that the filament experiences a change in its physical structure. Nonlimiting examples of morphological changes for the filaments of the present invention include melting, melting, expanding, shrinking, shattering, rupturing, extending, shortening, and combinations thereof. The filaments of the present invention may lose their physical structure completely or substantially when exposed to the intended application conditions, their morphologies may change, or the filaments It can retain or substantially retain the physical structure. As used herein, “by weight on a dry filament basis” means that the filament is in a room conditioned at a temperature of 23 ° C. ± 2.2 ° C. (approximately 73 ° F. ± 4 ° F.) and a relative humidity of 50% ± 10% for 2 hours, It means the filament weight measured immediately after being adjusted. In one example, “by weight of dry filament base” refers to the weight of the filament based on the weight of the filament in moisture, eg, free water, as measured, for example, according to the moisture content testing method described herein. Less than 20% and / or less than 15% and / or less than 10% and / or less than 7% and / or less than 5% and / or less than 3% and / or less than 1 %. As used herein with respect to the total concentration of one or more active agents present in the filament, “total concentration” means the total weight or weight percent of all subject material (e.g., active agents). In other words, the filament comprises 50 wt% of perfume or fragrance on a dry filament basis. Optionally an additional 35 wt.% of anionic surfactant on a dry filament basis, 15 wt% nonionic surfactant on a dry filament basis, 10 wt.% chelating agent, and 5 wt.% perfume. So that the total concentration of active perfume or fragrance agent present in the filament is greater than 50% by weight on a dry filament basis. As used herein, a “web” is a collection of formed fibers and / or filaments (e.g., fibrous structures) and / or fibers and / or filaments of any attribute or origin associated with each other. It means a formed sheet (for example, a continuous filament). As used herein, the web is a sheet formed by a spinning process rather than a casting gloss. As used herein, a “nonwoven web” as defined for purposes of the present invention, and generally in the European Disposables and Nonwovens Association (EDANA), is a sheet of fibers and / or filaments (e.g., any means) or the like, continuous filaments of any quality or origin, etc., which can be joined together by any means except weaving or braiding. The felt obtained by wet milling is not a nonwoven web. As used herein, a nonwoven web according to the present invention refers to regularly arranged filaments within a structure to perform a function. As used herein, the nonwoven web of the present invention is in an arrangement that includes two or more and / or three or more filaments that are entangled within or otherwise associated with each other to form a nonwoven web. is there. As used herein the nonwoven web of the present invention may include one or more solid additives, such as particulates and / or fibers, in addition to the filaments of the present invention. As used herein, “microparticle” means a particulate material and / or powder. As used herein, the articles “a” and “an” as used herein, such as “an anionic surfactant” or “a fiber” are claimed. Alternatively, it is understood to mean one or more substances described. As used herein, the percentages and ratios are calculated by weight unless otherwise indicated. All percentages and ratios are calculated based on the total composition unless otherwise indicated. As used herein, unless otherwise stated, all concentrations of a component or composition relate to the activity level of that component or composition and exclude impurities that may be present in commercial sources, such as residual solvents or by-products. Is done. As used herein, the filament of the present invention comprises one or more filament forming materials. In addition to the filament forming material, the filament includes one or more active agents that are releasable from the filament, for example when exposed to the conditions of the intended application, and one or more filament forming materials present in the filament. The total concentration is less than 80% by weight on a dry filament basis, and the total concentration of one or more active agents present in the filament is provided above 20% by weight on a dry filament basis. As used herein, the water dissolvable fragrance sheet is produced from one or more filament-forming materials with or without one or more additives (deactivator additives) and then coated with one or more active agents. The filament in contact with is not within the scope of the present invention. However, one or more filament forming materials and filaments formed from one or more active agents, such as one or more filament forming materials with or without one or more inactive agents, and one filament formed from a mixture with the above active materials (i.e., the filament forming composition of the present invention) that are subsequently coated with one or more active agents are within the scope of the present invention. As used herein the filaments of the present invention include one or more filament forming materials and one or more active agents, wherein the total concentration of filament forming material present in the filaments is about 5 on a dry filament basis. The total concentration of active agent present in the total filament composition is from 50% to less than 50% by weight, or greater than 50% by weight and up to about 95% by weight on a dry filament basis. As used herein, the filaments of the present invention are about 100% by weight and / or greater than 95%, and / or greater than 90% and / or greater than 85% by weight and / or One or more filament-forming materials comprising more than 75% and / or more than 50% by weight. For example, the filament forming material may comprise polyvinyl alcohol and / or starch or starch derivatives. As used herein the filaments of the present invention include one or more filament forming materials and one or more active agents, wherein the total concentration of filament forming material present in the filaments is about dry filament basis. The total concentration of active agent present in the filaments, from 5% to less than 80% by weight, is greater than 20% by weight and up to about 95% by weight on a dry filament basis. As used herein, the filaments of the present invention are at least 10% and / or at least 15% and / or at least 20% and / or less than 80% and / or 75% by weight on a dry filament basis. Less than and / or less than 65% and / or less than 60% and / or less than 55% and / or less than 50% and / or less than 45% and / or less than 40%. As used herein, the filaments of the present invention are more than 20 wt.% and / or at least 35 wt.%, and / or at least 40 wt.%, and / or at least 50 wt.%, and / or at least 60 wt.%, and / or at least 65 wt.%, and / or less than 95 wt.%. As used herein, the filaments of the present invention are less than 90 wt%, or less than 85 wt.%, and / or less than 80 wt.%, less than 75 wt.%. The filaments of the present invention comprise greater than 80% by weight active agent on a dry filament basis. As used herein, the one or more filament forming materials and the active agent have a weight ratio of the total concentration of the filament forming material to the active agent of 4.0 or less, and / or 3.5 or less, and / or 3 0.0 or less and / or 2.5 or less and / or 2.0 or less and / or 1.85 or less and / or less than 1 .7 and / or less than 1 .6. And / or less than 1.5 and / or less than 1 .3 and / or less than 1.2 and / or less than 1 and / or less than 0.7 and / or less than 0.5 And / or less than 0.4 and / or less than 0.3 and / or more than 0.1 and / or more than 0.15 and / or more than 0.2 filaments exists within. As used herein, the filaments of the present invention comprise from about 10% and / or from about 15% to less than 80% filament-forming material (e.g., polyvinyl alcohol polymer and / or starch polymer) on a dry filament basis. And up to about 90% and / or up to about 85% by weight of additives (e.g., active agents) on a dry filament basis. The filament further comprises a plasticizer, such as glycerin, and / or a pH adjuster, such as citric acid. As used herein, the filaments of the present invention comprise from about 10% and / or from about 15% to less than 80% filament-forming material (eg, polyvinyl alcohol polymer and / or starch polymer) on a dry filament basis. And, based on dry filaments, greater than 20 wt.%, Up to about 90 wt.% And / or up to about 85 wt.% active agent, wherein the weight ratio of filament forming material to active agent is 40 wt.% or less. The filament further comprises a plasticizer, such as glycerin, and / or a pH adjuster, such as citric acid. As used herein, the filaments of the present invention comprise about 5% to less than 50% by weight filament forming material (e.g., polyvinyl alcohol polymer and / or starch polymer) on a dry filament basis and 50% on a dry filament basis. And up to about 95% by weight of additives, such as active agents (e.g., perfumes or fragrances or odor removing agents or odor reducing agents or a combination thereof). The filament further comprises a plasticizer, such as glycerin, and / or a pH adjuster, such as citric acid. As used herein, the filaments of the present invention have 0% to less than 20% and / or 0% to 15%, as measured according to the moisture content test method described herein. Less than 15% and / or more than 0% and less than 15% and / or more than 0% and less than 12% and / or more than 2% and less than 10wt.%. As used herein, the filaments of the present invention have from about 5 wt% to about 10 wt%, and / or from about 7 wt% to about 10 wt%, as measured according to the moisture content test method described herein. As used herein, the filament comprises one or more filament forming materials and enzymes, bleaches, builders, chelates that are releasable and / or released when the filament is exposed to the intended application conditions. And one or more active agents selected from the group consisting of these agents, and mixtures thereof. As used herein, the filaments are less than 95% and / or less than 90%, and / or less than 80%, and / or less than 50%, and / or less than 35%, and / or less, on a dry filament basis, and / or up to about 5% by weight and / or up to about 10% by weight and / or up to about 20% by weight of the total concentration of filament-forming material and more than 5% and / or 10% by weight on a dry filament basis. As used herein, the filaments are more than 20% and / or more than 35% and / or more than 50% and / or more than 65% and / or up to about 95% by weight of a total concentration of active agents selected from the group consisting of enzymes, bleaches, builders, chelating agents, and mixtures thereof. As used herein, the filaments of the present invention may contain active agents that may raise health and / or safety concerns when they are airborne. For example, the filament may be used to prevent enzymes in the filament from floating in the air. As used herein, the filaments of the present invention may be meltblown filaments. As used herein, the filaments of the present invention may be spunbond filaments. As used herein the filament may be a hollow filament before and / or after release of one or more of its active agents. As used herein, the filaments of the present invention may be hydrophilic or hydrophobic. The filaments may be surface treated and / or treated internally to alter the filament's inherent hydrophilic or hydrophobic properties. As used herein, the filament is less than 100 m, and / or less than 75 pm, and / or less than 50 pm, and / or less than 25 pm, and / or less than 10 pm, as measured according to the diameter test method described herein. As used herein, the diameter of the filament may be less than 5 pm and / or less than 1 pm in diameter. As used herein, the filaments of the present invention exhibit a diameter of greater than 1 pm as measured according to the diameter test method described herein. The diameter of the filaments of the present invention may be used to control the release rate of one or more active agents present in the filament and / or the loss of and / or changing the physical structure of the filament. As used herein, the filament may contain two or more different active agents. As used herein, the filament includes two or more different active agents, the two or more different active agents being compatible with each other. As used herein he filament includes two or more different active agents, and the two or more different active agents are incompatible with each other. As used herein, the filament may include an active agent within the filament and an active agent on the outer surface of the filament, such as a coating on the filament. The active agent on the outer surface of the filament may be the same as or different from the active agent present in the filament. If different, the active agents may be compatible with each other or incompatible. As used herein, the filaments of the present invention do not contain preservatives, which for the purposes of the present invention are based on dry filaments, less than 2%, and / or less than 1%, and / or 0. Means less than 5% and / or less than 0.25% and / or 0% preservative. As used herein, the one or more active agents may be uniformly dispersed throughout the filament or may be substantially uniformly dispersed. As used herein, one or more active agents may be dispersed as separate regions within the filament. As used herein, the at least one active agent is uniformly or substantially uniformly dispersed throughout the filament, and at least the other active agent is dispersed as one or more separate regions within the filament. As used herein, at least one active agent is dispersed as one or more discrete regions within the filament, and the at least one other active agent is one or more from the first separate region within the filament. The filament may be used as a separate article. As used herein, the filament is a carrier substrate (eg, wipe, paper towel, toilet paper, decorative paper, sanitary napkin, tampon, diaper, adult incontinence article, wash cloth, dryer sheet, laundry sheet, laundry bar, dry cleaning sheet, mesh product, filter paper, fabric, garment, underwear, etc.) and / or deposited thereon. As used herein, the plurality of filaments of the present invention are collected into and compressed into a film and thus released from the film when one or more filament forming materials and, for example, the film is exposed to the intended application conditions. It can be a film comprising one or more active agents that are possible. As used herein, the films of the present invention have a per sample less than than 100 seconds, and / or less than 80 seconds, and / or as measured according to the dissolution test methods described herein. It exhibits an average degradation time of less than 55 seconds and / or less than 50 seconds and / or less than 40 seconds and / or less than 30 seconds and / or 20 seconds / g (s / g). As used herein, the films of the present invention have a per sample less than 1000 seconds, and / or less than 900 seconds, and / or less than 800 seconds, and / or as measured according to the dissolution test methods described herein. Alternatively, it exhibits an average degradation time of less than 700 seconds and / or less than 600 seconds and / or less than 500 seconds / g (s / g). As used herein, the film of the present invention has a thickness greater than 0.01 mm and / or greater than 0.05 mm and / or 0.1 mm as measured by the thickness test method described herein. As used herein, the film of the present invention may be greater than and / or up to about 20 mm and / or up to about 10mmand / oruptoabout5mmand / oruptoabout2mmand / orupto0.5mmand / orabout0. Thefilm thickness may be up to 3 mm. As used herein, the filament-forming material is any suitable material, such as a polymer or monomer that can produce a polymer that exhibits properties suitable for making filaments, such as by a spinning process. As used herein, the filament forming material may comprise a polar solvent soluble material, such as an alcohol soluble material and / or a water soluble material. As used herein, the filament forming material may include a non-polar solvent soluble material. As used herein, the filament forming material may include a polar solvent soluble material and may not include a non- polar solvent soluble material (less than 5% by weight and / or 3% by weight on a dry filament basis). Less than and / or less than 1% by weight and / or 0% by weight). As used herein, the filament forming material may be a film forming material. In yet other embodiments, the filament- forming material may be synthetic or naturally derived, which may be chemically, enzymatically and / or physically modified. As used herein, the filament forming material is a polymer derived from acrylic monomers such as ethylenically unsaturated carboxylic acid monomers and ethylenically unsaturated monomers, polyvinyl alcohol, polyacrylates, polymethacrylates, Copolymers of acrylic acid and methyl acrylate, polyvinyl pyrrolidone, polyalkylene oxide, starch and starch derivatives, pullulan, gelatin, hydroxyl propyl methylcellulose, methylcellulose, and polymers selected from the group consisting of carboxymethylcellulose may be included. As used herein, the filament forming material is polyvinyl alcohol, polyvinyl alcohol derivative, starch, starch derivative, cellulose derivative, hemicellulose, hemicellulose derivative, protein, sodium alginate, hydroxypropylmethylcellulose, chitosan, chitosan derivative, polyethylene glycol, tetra It may include a polymer selected from the group consisting of methylene ether glycol, polyvinyl pyrrolidone, hydroxymethyl cellulose, hydroxyethyl cellulose, and mixtures thereof. As used herein, the filament-forming material comprises pullulan, hydroxypropylmethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, polyvinylpyrrolidone, carboxymethylcellulose, sodium alginate, xanthan gum, tragacanth gum, guar gum, acacia gum, gum arabic, polyacrylic acid, methyl Methacrylate copolymer, carboxyvinyl polymer, dextrin, pectin, chitin, levan, erucinane, collagen, gelatin, zein, gluten, soy protein, casein, polyvinyl alcohol, starch, starch derivative, hemicellulose, hemicellulose derivative, protein, chitosan, chitosan derivative, Polyethylene glycol, tetramethylene ether glycol, Mud carboxymethylcellulose, and comprises a polymer selected from the group consisting of mixtures. As used herein, the polar solvent-soluble materials include polar solvent-soluble polymers. The polar solvent soluble polymer may be synthetic or naturally derived and may be chemically and / or physically modified. As used herein, the polar solvent soluble polymer is at least about 10,000 g / mol, and / or at least about 20,000 g / mol, and / or at least 40,000 g / mol, and / or at least 80,000 g / mol, And / or at least about 100,000 g / mol, and / or at least 1 ,000,000 g / mol, and / or at least 3,000,000 g / mol, and / or at least 10,000,000 g / mol, and / or It exhibits a weight average molecular weight of at least 20,000,000 g / mol and / or up to about 40,000,000 g / mol and / or up to about 30,000,000 g / mol. As used herein, the polar solvent soluble polymer is selected from the group consisting of alcohol soluble polymers, water soluble polymers, and mixtures thereof. Non-limiting examples of water soluble polymers include water soluble hydroxyl polymers, water soluble thermoplastic polymers, water soluble degradable polymers, water soluble non biodegradable polymers, and mixtures thereof. As used herein, the water soluble polymer comprises polyvinyl alcohol. In other examples, the water soluble polymer comprises starch. In yet another embodiment, the water soluble polymer comprises polyvinyl alcohol and starch. As used herein, the solvent consists of a water-soluble hydroxyl polymers according to the present invention include polyols such as polyvinyl alcohol, polyvinyl alcohol derivatives, polyvinyl alcohol copolymers, starch, starch derivatives, starch copolymers, chitosan, chitosan derivatives , Chitosan copolymers, cellulose, cellulose derivatives, such as cellulose ether and ester derivatives, cellulose copolymers, hemicellulose, hemicellulose derivatives, hemicellulose copolymers, gums, arabinans, galactants, proteins and various other polysaccharides, and mixtures thereof . As used herein, the water soluble hydroxyl polymer of the present invention comprises a polysaccharide. As used herein, “polysaccharide” means natural polysaccharides and polysaccharide derivatives or modified polysaccharides. Suitable water soluble polysaccharides include, but are not limited to starch, starch derivatives, chitosan, chitosan derivatives, cellulose derivatives, hemicellulose, hemicellulose derivatives, gums, arabinans, galactans, and mixtures thereof. The water-soluble polysaccharide is from about 10,000 g / mole to about 40,000,000 g / mole and / or more than 100,000 g / mole and / or more than 1 ,000,000 g / mole. Alternatively, it may exhibit a weight average molecular weight of greater than 3,000,000 g / mol and / or greater than about 3,000,000 g / mol and up to about 40,000,000 g / mol. As used herein, the water-soluble polysaccharide may comprise non-cellulose and / or non-cellulose derivatives and / or non-cellulose copolymer water-soluble polysaccharides. Such non-cellulose soluble polysaccharides may be selected from the group consisting of starch, starch derivatives, chitosan, chitosan derivatives, hemicellulose derivatives, hemicellulose derivatives, gums, arabinans, galactans, and mixtures thereof. As used herein, the water soluble hydroxyl polymer of the present invention comprises a non-thermoplastic polymer. As used herein, the water-soluble hydroxyl polymer can be from about 10,000 g / mol to about 40,000,000 g / mol, and / or more than 100,000 g / mol, and / or more than

[0010] 1 ,000,000 g / mol, and / or more than 3,000,000 g / mol and up to about 40,000,000 g / mol. Higher and lower molecular weight water-soluble hydroxyl polymers may be used in conjunction with hydroxyl polymers having a weight average molecular weight within a particular desired range. As used herein, the water soluble hydroxyl polymers may be selected from natural starch and include chemical and / or enzymatic modifications. As used herein, the water soluble hydroxyl polymer may be combined with native starch which can further be acid- thinned, hydroxyethylated, hydroxyp ropy I ated, and / or oxidized. As used herein, the water soluble hydroxyl polymer may comprise dent corn starch. As used herein, the naturally occurring starch is generally consisting of a mixture of linear amylose and branched amylopectin polymers of D glucose units. Amylose is essentially a linear polymer of D-glucose linked by (1 ,4) -a-D bonds. Aminopectin is a highly branched polymer of (1 ,4) -a-D bonds and (1 ,6) -a-D-glucose units at branch points. Naturally occurring starch is typically a relatively high concentration of amylopectin, such as corn starch (64-80% amylopectin), waxy maize (93-100% amylopectin), rice (83-84% amylopectin), potato (About 78% amylopectin) and wheat (73-83% amylopectin). Although all starches are potentially useful herein, the present invention is most commonly practiced with high amylopectin natural starch derived from agricultural sources, which is an abundant source and can be easily supplemented and offers the advantage of being inexpensive. As used herein, the “starch” includes any naturally occurring unmodified starch, modified starch, synthetic starch, and mixtures thereof, and mixtures of amylose or amylopectin fractions, It may be modified by chemical, chemical, or biological processes, or combinations thereof. As used herein, the unmodified or modified starch may depend on the desired end product. As used herein, the starch or starch mixture useful in the present invention is from about 20% to about 100%, more typically from about 40% to about 90%, even more typically. Having an amylopectin content from about 60 wt% to about 85 wt% starch or mixtures thereof. As used herein, suitable starches of natural origin include: corn starch, potato starch, sweet potato starch, wheat starch, sago palm starch, tapioca starch, rice starch, soybean starch, arrow root starch, amino starch, bracken starch, lotus starch, Nonlimiting examples include waxy corn starch and high amylose corn starch. Naturally occurring starches, particularly corn starch and wheat starch, are preferred starch polymers due to their economics and availability. As used herein, the polyvinyl alcohol herein can be grafted with other monomers to improve its properties. A wide range of monomers have been successfully grafted to polyvinyl alcohol. Non-limiting examples of such monomers include vinyl acetate, styrene, acrylamide, acrylic acid, 2-hydroxyethyl methacrylate, acrylonitrile, 1 ,3- butadiene, methyl methacrylate, methacrylic acid, maleic acid, itaconic acid, vinyl sulfonic acid. Sodium, sodium allyl sulfonate, sodium methyl allyl sulfonate, sodium phenyl allyl ether sulfonate, sodium phenyl methallyl ether sulfonate, 2- acrylamido- methyl propane sulfonic acid (AMPs), vinylidene chloride, vinyl chloride, vinyl amine, and acrylate esters. As used herein, the water soluble hydroxyl polymer is selected from the group consisting of polyvinyl alcohol, hydroxymethylcellulose, hydroxyethylcellulose, hydroxypropylmethylcellulose, and mixtures thereof. Non-limiting examples of suitable polyvinyl alcohols include those commercially available from Sekisui Specialty Chemicals America, LLC (Dallas, TX) under the trade name CELVOL®. Non-limiting examples of suitable hydroxypropyl methylcellulose include those commercially available from Dow Chemical Company (Midland, Ml) under the trademark METHOCEL®, including combinations with the hydroxypropyl methylcellulose described above. . As used herein, the water-soluble thermoplastic polymers consists of examples of suitable water-soluble thermoplastic polymers include thermoplastic starch and / or starch derivatives, polylactic acid, polyhydroxyalkanoates, polycaprolactones, polyester amides, and certain polyesters or a combination thereof. As used herein, the water-soluble thermoplastic polymer of the present invention may be hydrophilic or hydrophobic. As used herein, the water soluble thermoplastic polymer may be surface treated and / or internally treated to alter the hydrophilic or hydrophobic properties inherent in the thermoplastic polymer. As used herein, the water soluble thermoplastic polymer may comprise a biodegradable polymer. Any suitable weight average molecular weight may be used for the thermoplastic polymer. For example, the weight average molecular weight of the thermoplastic polymer according to the present invention is greater than about 10,000 g / mole and / or greater than about 40,000 g / mole and / or greater than about 50,000 g / mole. And / or less than about 500,000 g / mole and / or less than about 400,000 g / mole and / or less than about 200,000 g / mole. As used herein, the non-polar solvent soluble materials include non-polar solvent soluble polymers. Non-limiting examples of suitable non-polar solvent soluble materials include cellulose, chitin, chitin derivatives, polyolefins, polyesters, copolymers thereof, and mixtures thereof. Non-limiting examples of polyolefins include polypropylene, polyethylene, and mixtures thereof. Non-limiting examples of polyesters include polyethylene terephthalate. As used herein, nonpolar solvent soluble materials may include non-biodegradable polymers such as polypropylene, polyethylene, and certain polyesters. Any suitable weight average molecular weight may be used for the thermoplastic polymer. For example, the weight average molecular weight of the thermoplastic polymer according to the present invention is greater than about 10,000 g / mole and / or greater than about 40,000 g / mole and / or greater than about 50,000 g / mole. And / or less than about 500,000 g / mole and / or less than about 400,000 g / mole and / or less than about 200,000 g / mole. As used herein, activators are a class of additives designed and intended to benefit something other than the filament itself, for example, benefiting the environment outside the filament. The active agent may be any suitable additive that produces the intended effect under the intended use of the filament. For example, the active agent may be a personal cleansing and conditioning agent such as a hair care agent such as a shampoo and / or hair dye agent, a hair conditioning agent, a skin care agent, a sunscreen agent, and a skin conditioning agent; laundry care and / or conditioning agents, such as fabric care agents, fabric conditioning agents, fabric softeners, fabric anti-wrinkle agents, fabric care antistatic agents, fabric care stain removers, soil release agents, dispersants, foam inhibitors, foaming agents, antifoaming agents, fabric refreshing agents; hard surface care and / or conditioning agents, e.g. liquid and / or powder dishwashing agents (for dishwashing or automatic dishwashing or hand dish washing), and abrasives; other cleaning and conditioning agents such as antibacterial agents, perfumes, bleaches (e.g. oxygen bleaching) , hydrogen peroxide, percarbonate bleach, perborate bleach, chlorine bleach), bleach activator, chelating agent, builder, lotion, whitening agent, air care agent, carpet care agent, dye transfer inhibitor, water softener, pH adjuster, enzyme, flocculant, foaming agent, preservative, cosmetic agent, makeup remover, foaming agent, adhesion aid, coacervate forming material, clay, thickener, latex, silica, desiccant, odor inhibitor, antiperspirant, cooling agent, warming agent, absorbent gel, anti-inflammatory agent, dye, pigment, acid and base, liquid treatment active agent, agricultural active agent, industrial active agent, ingestion, drugs, tooth whitening agents, tooth care agents, mouthwashes, periodontal gum care agents, edible agents, edible agents, vitamins, minerals, and water treatment agents such as water purification and / or water disinfectants. As used herein, the composition may contain one or more classes of chemicals that may be useful for one or more of the active agents listed above. For example, a surfactant active may be useful for any number of the active agents described above. Similarly, bleach can be used in fabric care, hard surface cleaning, dishwashing, and even tooth whitening. Thus, those skilled in the art will appreciate that the active agent is selected based on the desired intended use of the filament and / or the nonwoven fabric made therefrom. As used herein, the filaments of the present invention and / or nonwovens made therefrom should be used for hair care and / or conditioning thereof, whereby one or more surfactants, such as foamable surfactants, Filaments and / or non-woven fabrics incorporating filaments can be selected to provide the desired benefits to the consumer when exposed to the intended application conditions. As used herein, the filaments of the invention and / or nonwovens made therefrom are designed or intended for use in laundry of clothes in a laundry operation, and then one or more suitable surfactants, or enzymes, or builders, or fragrances, or foam suppressors, or bleaching agents are desired when exposed to the intended use conditions of the filaments and / or nonwovens incorporating the filaments. Can be chosen to provide consumers with the benefits. As used herein, the filaments of the invention and / or nonwovens made therefrom are designed to be used in washing fabrics in washing operations and / or washing dishes in dishwashing operations, wherein the filaments are then washed A detergent composition or dishwashing detergent composition may be included. As used herein, the active agent comprises a perfume active agent. As used herein, the active agent comprises a non-surfactant. As used herein, the active agent comprises an inactive active agent, i.e., an active agent other than an ingestible active agent. As used herein, non-limiting examples of suitable surfactants include anionic surfactants, or cationic surfactants, or nonionic surfactants, or zwitterionic surfactants, or amphoteric surfactants, or a combination thereof. A co-surfactant may also be included in the filament. For example, for filaments designed for use as laundry detergents and / or dishwashing agents, the total surfactant concentration should be sufficient to provide cleaning including stain and / or odor removal. Generally in the range of about 0.5% to about 95%. In addition, surfactant systems comprising two or more surfactants designed for use in laundry detergent and / or dishwashing filaments are fully anionic surfactant systems, or a combination of two or more different anionic surfactants, or a mixture of different types of surfactant system, or a combination thereof. As used herein, a surfactant or a combination of surfactants may be linear or branched surfactants. As used herein suitable linear surfactants include those derived from agricultural chemical oils, such as coconut oil, palm kernel oil, soybean oil, or other vegetable oils. As used herein, the suitable anionic surfactants may include alkyl sulfates, alkyl ether sulfates, branched alkyl sulfates, branched alkyl alkoxylates, branched alkoxylate sulfates, medium chain branched alkyl allyl sulfonate, sulfated monoglyceride, sulfonated olefin, alkyl allyl sulfonate, primary or secondary alkane sulfonate, alkyl sulfosuccinate, acyl taurate, acyl isethionate, alkyl glyceryl ether sulfonate, sulfonated methyl ester, sulfonated fatty acid, alkyl phosphate, acyl glutamate, acrylic sarcosinate, alkyl sulfoacetate, acylated peptide, alkyl ether carboxylate, anionic fluorosurfactants, sodium lauroyl glutamate, or a combinations thereof. As used herein, the suitable alkyl sulfates and alkyl ether sulfates for use herein include materials having the corresponding formulas ROSO 3 M and RO (C 2 H 4 O) x SO 3 M, wherein R Is an alkyl or alkenyl from about 8 to about 24 carbon atoms, x is 1-10, and M is a water-soluble cation such as ammonium, sodium, potassium, and triethanolamine. Other suitable anionic surfactants are MacCutcheon's “Detergents and Emulsifiers” (North American Edition (1986), Allred Publishing Corp.) and McCutcheon's “Functional Materials 92” (Natural Publishing Corp.). As used herein, anionic surfactants useful in the filaments of the present invention, C

[0011] 9 -C 15 alkyl benzene sulfonates (LAS), C 8 -C 20 alkyl ether sulfates, such as alkyl poly (ethoxy) sulfates, C 8 ~ C 20 alkyl sulfates, and mixtures thereof. Other anionic surfactants may include methyl ester sulfonate (MES), methyl ester etchelate (MEE), sulfonated estolides, and mixtures thereof. As used herein, the anionic surfactant is a C 11 -C 18 alkyl benzene sulfonate (“LAS”) and primary branched chain, andarandomCIO -C20 alkylsulfate(“AS”),formulaCH3. (CH2)x(CHOSO3-M+)CH3andCH3(CH2)y(CHOS03- M +) C 10 ~C 18 secondary of CH 2 CH 3 (2,3) alkyl sulfates (formula In which x and (y + 1) are integers of at least about 7, preferably about 9, and M is a watersolubilizing cation, in particular sodium, an unsaturated sulfate such as oleyl sulfate), C 10 -C 18 a-sulfonated fatty acid esters, C 10 -C 18 sulfated alkyl polyglycosides, C

[0012] 10 -C 18 alkyl alkoxy sulfates ( "AE X S") (the formula x is 1 to 30), and C 10 -C 18 alkyl alkoxy Ruboxylates (eg containing 1-5 ethoxy units), medium chain branched alkyl sulfates as described in US Pat. Nos. 6,020,303 and 6,060,443; US Pat. No. 6,008, medium chain branched alkyl alkoxy sulfates (MLAS) as described in 181 and 6,020,303; as described in WO 99 / 05243, WO 99 / 05242, and WO 99 / 05244 Modified alkylbenzene sulfonate (MILAS); methyl ester sulfonate (MES); and alpha-olefin sulfonate (AOS). As used herein, other suitable anionic surfactants that can be used are alkyl ester sulfonate surfactants, including sulfonated linear esters of C 8 to C 20 carboxylic acids (ie fatty acids). The Other suitable anionic surfactants that can be used salts of soap, C 8 -C 22 primary or secondary alkane sulfonates (primary of secondary alkanesulfonates), C 8 ~C 24 olefin sulfonates, sulfonated polycarboxylic acids, C 8 - C 24 alkyl polyglycol ether sulfates (alkylpolyglycolethersulfates) (contain ethylene oxide up to 10 moles); alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleoyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, paraffin sulfonates, alkyl phosphates , isethionates, eg acyl isethionates, N-acyl taurates, alkyl succinates and sulfosuccinates, monoesters of sulfosuccinates (e.g. saturated and unsaturated C 12 -C 18 monoesters) monoester, diester sulfosuccinates (e.g., saturated and unsaturated C 6 -C 12 diesters), and alkyl polysaccharide sulfates, such as alkyl polysaccharides sulfates, and alkyl polyethoxy carboxylates such as those of the formula RO (CH 2 CH 2 O) k -CH 2 COO-M + ( wherein R is a C 8 -C 22 alkyl, k is an integer of 0, M is a soluble salt-forming cation). As used herein, other suitable anionic surfactants are alkyl benzene sulphonic acid of C 10 -C 16, preferably an alkali metal salt of alkylbenzene sulfonic acid C 11 -C 14. As used herein, the suitable anionic surfactants are linear alkyl group is linear such as alkyl benzene sulfonates are known as “LAS”. Such surfactants and their preparation are described, for example, in US Pat. Nos. 2,220,099 and 2,477,383. In other examples, linear alkyl sulfonate or linear alkylbenzene sulfonate or liner alkyl benzene sulfonate. Referring now to the FIGURES, FIGURE 1 is an illustration of a non-limiting embodiment of a homogenizer assembly, component feeds, and drum dryer assembly according to the invention. Fig. 1 shows water supply at 70-90°C for delivery to the homogenizer tank via pumped delivery pipe with a control valve. The homogenizer tank includes a mixing paddle connected to electric motors. The PVA supply delivers polyvinyl alcohol to the homogenizer tank via pumped or gravity fed conduit for dissolving in the water. Component feeds A, B, C are delivered via pumped conduit to the homogenizer tank, and steam feed 70-120°C. In the present invention the polyvinyl alcohol, water, a fragrance, and optionally additional ingredients, form a PVA homogenate by mixing in a single homogenizer tank, and the homogenizer tank is heated using steam. The PVA paste / homogenate is pumped to the drum dryer assembly and delivered to a bottom feed tray having a bottom feed applicator roller disposed therein. The drum dryer comprises a heated drying drum having a drive system and a mirror finish, said drying drum mounted over a bottom applicator roller assembly having a bottom feed tray with a bottom feed applicator roller disposed therein, the bottom fed tray having a inlet for receiving the paste, the bottom feed applicator roller in operative contact with paste in the bottom feed tray, wherein rotational engagement between the drying drum and the bottom feed applicator roller forms a water dissolvable PVA fragrance sheet. Fig. 1 also shows optional the optional step of trimming the water dissolvable PVA fragrance sheet to a form 1.5-2.0 mm thick, 50-127 mm wide, and 76-203 mm long. In another non-limiting preferred embodiment, an additional step of surface spraying the water dissolvable PVA sheet with a surface agent selected from the group consisting of a additional of an odor removing agent selected from the group consisting of Ozium, Lysol, Damprid, Lemon, BioKeen, or a combination thereof, or odor neutralizing agent, such as hydrogen peroxide, or baking soda, or vinegar, or charcoal, or a combination thereof, laundry boosters selected from the group consisting of Lemon Juice, NaCI, Baking Soda, Alcohol, hydrogen peroxide, Vinegar, or a combination thereof, used to deodorize the odor of the laundry process, Citronellol, Rose oil, Limonene, Essential oils, Sodium Bicarbonate or a combination thereof, Clay, Bentonite Clay, Minerals, Pine, Wheat, Corn, Silica, Silica Gel, or a combination thereof, Essential oils, Sodium Bicarbonate, or a combination thereof, Disodium ethylenediaminetetraacetate dihydrate, Na2EDTA, DTPA, MGDA, EDTA or a combination thereof, Borax, Sodium Bicarbonate, Charcoal, Hypochlorite, hydrogen peroxide, vinegar, or a combination thereof, Epsom Salt, Sodium Bicarbonate, Bentonite Clay, hydrogen peroxide, vinegar, or a combination thereof, Essential oils, Lavender, Peppermint, Lemon, Bergamot, Ylang Ylang, Hydrosols, Resins, Carrier oils, Infused oils, Herbs, or a combination thereof, Perfume MicroCapsules or a combination of Perfume Micro Capsules, used for the delivery of a two-step odor release composition wherein one step is right out of the washer and / or dryer during the washing process and will also release scent after said washing and drying garment process, a chelating agent selected from the group consisting of EDTA, MGDA, DTPA, zeolite, phosphonate, citric acid, citrate, or a mixture thereof, a fragrance 0 to 2% by weight, a brightening agent up to 1 % by weight of the total mixture, a bleaching agent selected from the group consisting of calcium hypochlorite, sodium hypochlorite, sodium percarbonate, sodium perborate, sodium persulfate, tetrasodium pyrophosphate, or urea peroxide or a combination thereof, a fabric softener agent selected from the group consisting o fquaternary ammonium cations / salts, ceterinium bromide, quaternary ammonium chloride, polydimethylsiloxane, silicone, or a mixture thereof, a perfume, a fragrance, a perfume micro capsule or a combination thereof, a binding agent selected from the group consisting of a resin, a wax, a gum, accroides, candelilla, guar, gum Arabic, shellac, tragacanth, or a combination thereof, and scent absorbing ingredients selected from the group consisting of activated charcoal, beta cyclodextrins, odor absorbing fabrics which contains porous chambers, porous clays, waxes that can hold scents, lava rocks, felt pads, cardboard, and potpourri. TERMINOLOGY The terminology used herein is for the purpose of describing particular embodiments only and is not intended to limit the full scope of the claims. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art. Nothing in this disclosure is to be construed as an admission that the embodiments described in this disclosure are not entitled to antedate such disclosure by virtue of prior invention. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. With respect to the use of substantially any plural and / or singular terms herein, those having skill in the art can translate from the plural to the singular and / or from the singular to the plural as is appropriate to the context and / or application. The various singular / plural permutations may be expressly set forth herein for sake of clarity. In general, terms used herein, and especially in the appended claims (e.g., bodies of the appended claims) are generally intended as “open” terms (e.g., the term “including” should be interpreted as “including but not limited to,” the term “having” should be interpreted as “having at least,” etc.). Similarly, the terms “comprises” and / or “comprising,” when used in this specification, specify the presence of stated features, integers (or fractions thereof), steps, operations, elements, and / or components, but do not preclude the presence or addition of one or more other features, integers (or fractions thereof), steps, operations, elements, components, and / or groups thereof. As used in this document, the term “comprising” means “including, but not limited to.” As used herein the term “and / or” includes any and all combinations of one or more of the associated listed items. It should be understood that virtually any disjunctive word and / or phrase presenting two or more alternative terms, whether in the description, claims, or drawings, should be understood to contemplate the possibilities of including one of the terms, either of the terms, or both terms. For example, the phrase “A or B” will be understood to include the possibilities of “A” or “B” or “A and B.” All ranges disclosed herein also encompass any and all possible subranges and combinations of subranges thereof unless expressly stated otherwise. Any listed range should be recognized as sufficiently describing and enabling the same range being broken down into at least equal subparts unless expressly stated otherwise. As will be understood by one skilled in the art, a range includes each individual member. EQUIVALENTS Many modifications and variations can be made without departing from its spirit and scope, as will be apparent to those skilled in the art. Functionally equivalent methods and apparatuses within the scope of the disclosure, in addition to those enumerated herein, will be apparent to those skilled in the art from the foregoing descriptions. Such modifications and variations are intended to fall within the scope of the appended claims. The present disclosure is to be limited only by the terms of the appended claims, along with the full scope of equivalents to which such claims are entitled. It is to be understood that this disclosure is not limited to particular methods, reagents, compounds, compositions or biological systems, which can, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting. While various embodiments have been described above, it should be understood that they have been presented by way of example only, and not limitation. Where methods described above indicate certain events occurring in certain order, the ordering of certain events may be modified. Additionally, certain of the events may be performed concurrently in a parallel process when possible, as well as performed sequentially as described above. Where schematics and / or embodiments described above indicate certain components arranged in certain orientatio...

Claims

AMENDED CLAIMS received by the International Bureau on 30 April 2025 (30.04.2025)

1. A process for manufacturing a water dissolvable cleaning sheet, comprising the steps:(i) homogenizing in a high shear mixer at a temperature of 70-90 °C an aqueous solution of polyvinyl alcohol 3-25%, a surfactant 5-50%, a builder 0.1-5%, a binding agent 0.1-5%, a chelating agent 0.1-5%, and optionally one or more of a bleaching agent a car surface treatment ingredient, and a fragrance, to form a PVA homogenate;(ii) casting the PVA homogenate as a wet film onto a heated stainless steel roller drum having a drive system and a mirror finish and dehydrating at 70-120 °C using steam heat to obtain a water dissolvable cleaning sheet 1.5 - 2.0 mm thick, wherein said heated stainless steel roller drum is mounted over a bottom applicator roller assembly having a bottom feed tray with a bottom feed applicator roller disposed therein, the bottom feed tray having a inlet for receiving the PVA homogenate, the bottom feed applicator roller in operative contact with PVA homogenate in the bottom feed tray, wherein rotational engagement between the heated stainless steel roller drum and the bottom feed applicator roller forms the water dissolvable cleaning sheet ; and(iii) optionally trimming the water dissolvable cleaning sheet to form a single sheet size 50-127 mm wide and 76-203 mm length, all percentages by weight, all percentages total 100%.

2. The process according to claim 1 , wherein the surfactant is selected from the group consisting of sodium lauryl sulfate, sodium dioctyl sulfosuccinate, linear alkyl benzene sulfonate, alpha olefin sulfonate, xylene sulfonate and a combination thereof.

3. The process according to claim 1 , wherein the surfactant is selected from the group consisting of sodium lauryl sulfate, alpha olefin sulfonate, sodium dodecylbenzene sulfonate, sodium laureth sulfate, and a combination thereof.

4. The process according to claim 1 , wherein the builder agent is selected from the group consisting of citrate, citric acid,trisodium phosphate, zeolite, carbonate, phosphonate, and lime, in the amount of 1 to 10% by weight.

5. The process according to claim 1 , wherein the binder 1-10% is selected from resin, a wax, a gum, accroides, candelilla, guar, gum arabic, shellac, tragacanth, glycerin, or a combination thereof.

6. The process according to claim 1 , wherein the chelating agent is selected from the group consisting of EDTA, MGDA, DTPA, sodium gluconate, GLDA, zeolite, phosphonate, citric acid, citrate, and HEDP, and a combination thereof 0.1 to 1% by weight.

7. The process according to claim 1 , further comprising the step of applying to the water dissolvable cleaning sheet a perforated weakened tear-line.

8. The process according to claim 1 , further comprising the step of adding to the aqueous solution a bleaching agent wherein the bleaching agent is 1-40% and is selected from the group consisting of sodium hypochlorite, sodium percarbonate, and sodium perborate.

9. The process according to claim 7, further comprising the step of adding to the aqueous solution a bleach activator 1-40% and is selected from the group consisting of nonanoyloxybenzenesulfonate (NOBS), tetraacetylethylenediamine (TAED), lauryloxybenzenesulfonate (SDBS), benzoylcaprolactam (BzCL), 4-nitro Benzoylcaprolactam, 3- chlorobenzoylcaprolactam , benzoyloxybenzenesulfonate (BOBS), nonanoyloxybenzenesulfonate (NOBS), phenyl benzoate (PhBz), decanoyloxybenzenesulfonate (C 10 -OBS) , Benzoylvalerolactam (BZVL), octanoyloxybenzenesulfonate (C 8 -OBS), a perhydrolyzable ester, and a combination thereof.

10. The process according to claim 1 , further comprising the step of adding to the aqueous solution a bleaching agent wherein the bleaching agent is an encapsulated dry particulate bleaching agent, and the bleaching agent is selected from the group consisting of sodium hypochlorite, sodium percarbonate, and sodium perborate, sodium dichloroisocyanurate dihydrate, sodium dichloroisocyanurate, potassium dichloroisocyanuratedihydrate, potassium dichloroisocyanurate, sodium perborate monohydrate, sodium perborate tetrahydrate and a combination thereof, and wherein the encapsulant is selected from the group consisting of sulfate, carbonate, carbohydrate, starch, maltodextrin dextrin, sucrose, cellulose, agar, carrageenan, wax, paraffin, diglyceride, gluten, casein, albumin, peptide, sodium alginate, gum arabic, chitosan, carboxymethylcellulose, pectin, shellac, and a combination thereof.

11. The process according to claim 1 , further comprising the step of adding to the aqueous solution a car surface treatment 0.1 -5.0% is a car interior cleaning treatment or a car exterior cleaning treatment, the car interior cleaning treatment is selected from the group consisting of sodium triphosphate, 2- butoxyethanol, and ethyl alcohol, the car surface treatment is selected from the group consisting of dimethicone, citral, polyethylene glycol (PEG-9), and sodium hydroxide.

12. The process according to claim 1 , further comprising the step of adding to the aqueous solution an additional water dissolvable ingredient 10-60% selected from the group consisting of hydroxypropylcellulose, corn starch, wheat starch, potato starch, rice starch, tapioca starch, an ethylene oxide co-polymer, a propylene oxide co-polymer, an ethylene oxide-propylene oxide co-polymer, and a combination thereof.

13. The process according to claim 1 , further comprising the step of adding to the aqueous solution a pH modifier 1-70% to raise the pH above pH 9, wherein the pH modifier is selected from the group consisting of sodium carbonate, sodium bicarbonate, sodium hydroxide, sodium silicate and a combination thereof.

14. The process according to claim 1 , further comprising the step of adding to the aqueous solution a fabric softener or a residue remover, wherein the fabric softener is selected from the group of quaternary ammonium cations / salts, cetrimonium bromide, quaternary ammonium chloride, polydimethylsiloxane, silicone, and a mixture thereof.

15. The process according to claim 1 , further comprising the step of applying a water-based fragrance 0.3% by weight to the water dissolvable cleaning sheet using a sandwich roller.

16. The process according to claim 11 , further comprising the step of adding to the aqueous solution an anti-beading compound.

17. The process according to claim 11 , further comprising the step of adding to the aqueous solution a cleaning grit selected from the group consisting of silicate, diatomaceous earth, silica particles, quartz particles, calcite particles, rottenstone, whiting, pumice, volcanic ash, marble particles, feldspar particles, copper particles, polymer particles, and metal particles.

18. A water dissolvable cleaning sheet made according to the process of claim 1.

19. The water dissolvable cleaning sheet according to claim 18, wherein the water dissolvable cleaning sheet is removably mounted on an applicator unit selected from a cleaning mitt, a cleaning glove, a cleaning sponge, a handheld pad holder, and a long handled pad holder.

20. The process according to claim 15, further comprising the step of adding to the aqueous solution an odor removing or neutralizing agent selected from the group consisting of Ozium, Lysol, Damprid, lemon juice, BioKeen, hydrogen peroxide, baking soda, vinegar, charcoal, or a combination thereof.

21. The process according to claim 15, further comprising the step of adding to the aqueous solution an additional fragrance ingredient selected from the group consisting of citronellol, rose oil, limonene, an essential oil, pine oil, lavender, peppermint, lemon, bergamot, ylang ylang, a hydrosol, a resin, a carrier oil, an infused oil, an herb, or a combination thereof.

22. The process according to claim 1 , further comprising the step of adding to the aqueous solution a perfume micro capsule or a combination thereof.

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