Process for manufacturing a detergent portion unit
Patent Information
- Application Number
- EP2023701631
- Authority / Receiving Office
- EP · EP
- Patent Type
- Applications
- Current Assignee / Owner
- Priority Date
- 2022-04-13
- Filing Date
- 2023-01-18
- Publication Date
- 2025-02-19
- Estimated Expiration
- 2043-01-18
AI Technical Summary
Existing detergent packaging materials are hygroscopic, leading to adhesion issues and reduced mechanical stability, which complicates the production of quickly soluble detergent portion units that are both efficient and sustainable.
A method involving a dimensionally stable gel body formed by mixing surfactant and gelling agent compositions within a mold, using a dynamic mixing device to create a surfactant-containing and gelling agent-containing mixture that solidifies into a gel body with enhanced mechanical stability and dissolution properties.
The method produces detergent portion units with high product and storage stability, reduced packaging usage, and improved handling and performance, suitable for both textile laundry and cleaning hard surfaces, while maintaining a visually appealing and haptic appealing form.
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Abstract
Description
[0001] .Method for producing a detergent portion unit'
[0002] The present invention relates to a process for producing a detergent portion unit comprising a gel body.
[0003] The packaging and distribution of detergents and cleaning agents are constantly evolving. For some time now, a key focus has been on convenient dosing of detergents and cleaning agents by the consumer and simplifying the steps required to carry out a washing or cleaning process. One technical solution is pre-portioned detergents or cleaning agents, for example, water-soluble containers with one or more compartments for powdered or liquid detergents or cleaning agents. Another technical solution is detergent tablets, which can be designed as single- or multi-phase products.
[0004] To produce the water-soluble containers, water-soluble polymers are typically formed into receiving chambers, which are then filled with a detergent or cleaning agent and finally sealed. The receiving chambers can be produced, for example, from water-soluble polymer films using a deep-drawing process. In an alternative process, a water-soluble polymer is formed into a receiving container using injection molding.
[0005] The water-soluble packaging material used to package the filled detergent portion units is generally hygroscopic. The water absorption capacity and tendency of the packaging material during production, packaging, storage, and subsequent use by the consumer can lead to portion units adhering to the surfaces of machines or packaging materials and preventing optimal conveyance, or to adjacent portion units sticking together, for example, in shared outer packaging. To prevent this tendency of the water-soluble portion units to adhere, it is possible to modify their surface properties by applying a powder. Powdering the water-soluble detergent portion units, in turn, requires an additional process step.
[0006] The water-soluble packaging materials used generally do not have any washing or cleaning properties, and therefore do not contribute to the product's effectiveness. Reducing the proportion of packaging in the total weight of the detergent portion units would therefore not result in any loss of performance and would be welcome for reasons of sustainability and cost-effectiveness.
[0007] Finally, the washing performance achieved by the detergent dosage unit is directly related to its dissolution properties. Especially in view of the increasing use of cold-wash processes, it is preferable to keep the thickness of the water-soluble film material contained in the detergent dosage unit as low as possible in order to accelerate the dissolution process. However, reducing the thickness of the surrounding film material simultaneously results in reduced mechanical stability of the dosage units. Overcoming this apparent dichotomy between mechanical stability and dissolution rate using water-soluble film-packaged detergent dosage units remains a relevant consideration in the development of water-soluble detergent dosage units.
[0008] An alternative to the previously described sachets is offered by detergent tablets, although sufficient mechanical stability and a high dissolution rate are incompatible in a similar way to the case of sachets.
[0009] An alternative to fully compressed detergent tablets is offered by multiphase detergent portion units, for example in the form of core tablets, which, in addition to a tableted body, also contain wax or gel phases. For example, European patent EP 1 032 642 B1 describes detergent tablets comprising a compressed phase and a non-compressed gel phase, and processes for their production.
[0010] Against the background of the previously described prior art, the application was based on the objective of providing efficient processes for the production of rapidly dissolving detergent portion units that offer high product and storage stability, are easy to package using minimal packaging materials, and appeal to consumers through their appealing olfactory, visual, and tactile qualities. The detergent portion units should offer high product performance and be easy and safe to handle for the consumer.
[0011] A first subject matter of the application is a process for producing a detergent portion unit, comprising a) a dimensionally stable gel body, comprising the steps of: i) providing a first flowable surfactant-containing composition; ii) providing a second flowable gel-forming agent-containing composition different from the first flowable composition; iii) feeding the first and second flowable compositions to a mold; iv) introducing the first and second flowable compositions into the mold; v) mixing the first and second flowable compositions in the mold by means of a dynamic mixing device to form a surfactant-containing and gel-forming agent-containing mixture; vi) allowing the surfactant-containing and gel-forming agent-containing mixture to solidify in the mold to form a dimensionally stable gel body.
[0012] The term "detergent portion unit" describes a packaging containing a measured portion of a detergent or cleaning agent. Detergent portion units therefore refer to packaging for both textile washing and packaging for cleaning hard surfaces such as ceramics, glass, metal, or tiles. The detergent portion unit preferably has a weight of 14 g to 42 g, preferably 18 g to 38 g, and in particular 20 g to 34 g.
[0013] The detergent portion unit comprises a gel body. The detergent portion unit can consist of the gel body. In this case, the gel body preferably has a weight of 14 g to 42 g, preferably 18 g to 38 g, in particular 20 g to 34 g. If the detergent portion unit comprises further components in addition to the gel body, the weight of the gel body is preferably 10 g to 28 g, preferably 12 g to 23 g, and in particular 15 g to 20 g.
[0014] Gel bodies are bodies that exhibit elastic deformation behavior under the application of force. Bodies are considered dimensionally stable if they have an intrinsic shape stability that enables them to assume a non-disintegrating spatial shape under normal conditions of production, storage, transport, and handling by the consumer. This spatial shape does not change under these conditions even over a prolonged period, preferably 4 weeks, more preferably 8 weeks, and especially 32 weeks. This means that under the normal conditions of production, storage, transport, and handling by the consumer, they remain in the spatial-geometric shape determined by production, i.e., they do not melt.
[0015] The spatial shape of the gel body is fundamentally freely selectable; its side surfaces can be convex, concave, or flat, for example. However, certain spatial configurations have proven particularly advantageous in terms of manufacturability, storage, and use of the gel bodies.
[0016] In correspondingly advantageous detergent portion units, the gel body has a flat underside whose largest diagonal is greater than the height of the gel body. These bodies are not only easy to produce, for example by means of a casting process, they can also be packaged easily and in a space-saving manner and are suitable for dosing via the dosing or dispensing chambers of electronic cleaning appliances. It is preferred if the gel body has a flat underside whose largest diagonal is more than 1.5 times, preferably more than 2 times the height of the gel body. For manufacturability, for example with regard to demolding the gel body from a casting mold, it has proven advantageous if the underside of the gel body has no corners. Preferred gel bodies are therefore characterized by oval undersides or alternatively by ellipsoidal or round, preferably round, undersides.Corresponding gel bodies with a non-square bottom are also preferred by many consumers due to their appearance. Therefore, gel bodies with a bottom and a top connected by a cylindrical surface are preferred.
[0017] Advantages in terms of space utilization during production and packaging are realized by angular undersides. If, for example, the gel bodies are cast in the form of sheets, which are subsequently cut into gel bodies, angular undersides are advantageous because such gel bodies can be cut without creating any residue and can be packaged in a space-saving manner. In an alternative embodiment, preferred gel bodies therefore have angular undersides, in particular triangular, square, or hexagonal undersides. For further processing or packaging, it can be advantageous if the gel body has a angular underside with rounded corners.
[0018] With regard to the production, packaging and use of the detergent portion units, it has also proven advantageous if the gel bodies have an upper side that is plane-parallel to the underside.
[0019] In a first preferred geometric embodiment, the gel body has a bottom side and a top side which have the same geometric shape, wherein the bottom side and the top side have the same surface area. Corresponding gel bodies can, as already described above, be produced in a simple manner, for example by casting sheets and subsequently cutting the sheets into individual gel bodies. Moreover, these gel bodies can be spatially aligned more easily in any subsequent process steps, during packaging or use by the user due to the geometric identity of the bottom and top sides than gel bodies with a lower body symmetry. This applies in particular to gel bodies which simultaneously have a top side that is plane-parallel to the bottom side.Examples of such gel bodies are circular cylinders, elliptical cylinders, parallelepipeds, rhombohedrons, straight or oblique prisms, cuboids, or cubes. The group of circular cylinders and elliptical cylinders includes vertical circular cylinders and elliptical cylinders, as well as oblique circular cylinders and elliptical cylinders. Due to their ease of manufacture by singulation from a sheet, gel bodies in the form of vertical circular cylinders, vertical elliptical cylinders, straight prisms, straight cuboids, or cubes are preferred. In an alternative embodiment, the gel body has a bottom and a top side that have the same geometric shape, with the bottom and top sides having different surface areas. Such gel bodies may be preferred due to their attractive appearance or their optimized fit, coupled with their comparatively simple manufacture.Examples of such gel bodies are circular cylinders or elliptical cylinders with a convex or concave bottom and a flat top. Other examples are truncated cones or truncated pyramids.
[0020] In summary, preferred subject matters of the application can be characterized as detergent portion units comprising a gel body with a bottom side and a top side, wherein the area of the top side is 80 to 100%, preferably 90 to 100% and in particular 98 to 100% of the bottom side.
[0021] The process is particularly suitable for the manufacture of gel bodies with a high surfactant content. In preferred embodiments, the first flowable surfactant-containing composition contains, based on its total weight, 30 to 70 wt.%, preferably 40 to 60 wt.%, and in particular 45 to 55 wt.% surfactant.
[0022] For the producibility and subsequent dissolving power of the gel bodies, it has proven advantageous if they contain 15 to 35 wt.%, preferably 20 to 30 wt.%, of an aqueous-organic solvent. The aqueous-organic solvent of the gel body is preferably introduced via the first and second flowable compositions. Thus, it is preferred if the second flowable gel-forming agent-containing composition also contains an organic solvent. Particularly preferred flowable gel-forming agent-containing compositions contain gel-forming agent and organic solvent in a total weight proportion above 50 wt.%, preferably above 70 wt.%, and in particular above 90 wt.%.
[0023] Preferred gel bodies also contain dye.
[0024] Preferred gel bodies are transparent. "Transparent" refers to gel bodies that exhibit a transmission above 50%, preferably above 60%, and especially above 80% in the wavelength range from 410 to 800 nm at at least one wavelength, preferably at 600 nm. Transmission is determined using VIS spectrometry at a sample temperature of 20°C and a cuvette length of 10 mm.
[0025] For the production and subsequent storage and transport properties of the gel bodies, it has proven advantageous to use low-molecular-weight gel formers with a molar mass of up to 2000 g / mol in the gel body, with their weight fraction of the total weight of the gel body preferably being less than 5 wt.%, preferably 0.1 to 5 wt.%, and particularly preferably 0.1 to 2.5 wt.%. Furthermore, the advantages of the process according to the invention are particularly evident in the processing of these low-molecular-weight gel formers with their specific gelling properties.
[0026] In a preferred embodiment, the low-molecular-weight gelling agent has a water solubility of less than 0.1 g / L (20°C). The solubility of the organic gelling agent is determined at 20°C in double-distilled, demineralized water.
[0027] Furthermore, gel formers are preferably suitable which have a structure containing at least one hydrocarbon structural unit having 6 to 20 carbon atoms (preferably at least one carbocyclic, aromatic structural unit) and additionally an organic structural unit covalently bonded to the aforementioned hydrocarbon unit, which has at least two groups selected from -OH, -NH-, or mixtures thereof.
[0028] Particularly preferred gel bodies are characterized in that said gel bodies contain at least one benzylidene alditol compound of the formula (GB-I) as gelling agent where a covalent single bond between an oxygen atom of the alditol
[0029] basic structure and the intended residue, n stands for 0 or 1, preferably for 1, m stands for 0 or 1, preferably for 1,
[0030] R 1 , R 2 and R 3independently of one another represents a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a cyano group, a nitro group, an amino group, a carboxyl group, a hydroxy group, a -C(=O)-NH-NH2 group, a -NH-C(=O)-(C2-C4 alkyl) group, a C1-C4 alkoxy group, a C1-C4 alkoxy-C2-C4 alkyl group, two of the radicals together with the residual molecule form a 5- or 6-membered ring,
[0031] R 4 , R 5 and R 6 independently of one another represent a hydrogen atom, a halogen atom, a Ci-C4 alkyl group, a cyano group, a nitro group, an amino group, a carboxyl group, a hydroxy group, a -C(=O)-NH-NH2 group, a -NH-C(=O)-(C2-C4 alkyl) group, a Ci-C4 alkoxy group, a Ci-C4 alkoxy-C2-C4 alkyl group, two of the radicals together with the residual molecule form a 5- or 6-membered ring.
[0032] Due to the stereochemistry of the alditols, it should be noted that both the said benzylidene alditols in the L-configuration or in the D-configuration, or a mixture of both, are suitable according to the invention. Due to their natural availability, the benzylidene alditol compounds in the D-configuration are preferably used according to the invention. It has been found to be preferred if the alditol backbone of the benzylidene alditol compound according to formula (GB-I) contained in the shaped body is derived from D-glucitol, D-mannitol, D-arabinitol, D-ribitol, D-xylitol, L-glucitol, L-mannitol, L-arabinitol, L-ribitol, or L-xylitol.
[0033] Particularly preferred are those gel bodies which are characterized in that R 1 , R 2 , R 3 , R 4 , R 5 and R 6according to the benzylidene alditol compound of the formula (GB-I), independently of one another, represents a hydrogen atom, methyl, ethyl, chlorine, fluorine or methoxy, preferably a hydrogen atom. n according to the benzylidene alditol compound of the formula (GB-I) preferably represents 1. m according to the benzylidene alditol compound of the formula (GB-I) preferably represents 1.
[0034] Most preferably, the gel body contains as benzylidene alditol compound of formula (GB-I) at least one compound of formula (GB-11) where R 1 , R 2 , R 3 , R 4 , R 5 and R 6 as defined in formula (I). Most preferably, according to formula (GB-11) R 1 , R 2 , R 3 , R 4 , R 5 and R 6 independently of one another represent a hydrogen atom, methyl, ethyl, chlorine, fluorine or methoxy, preferably a hydrogen atom.
[0035] Most preferably, the benzylidene alditol compound of formula (GB-I) is selected from 1,3:2,4-di-G-benzylidene-D-sorbitol; 1,3:2,4-di-O-(p-methylbenzylidene)-D-sorbitol; 1,3:2,4-di-O-(p-chlorobenzylidene)-D-sorbitol; 1,3:2,4-di-O-(2,4-dimethylbenzylidene)-D-sorbitol; 1,3:2,4-di-O-(p-ethylbenzylidene)-D-sorbitol; 1,3:2,4-di-O-(3,4-dimethylbenzylidene)-D-sorbitol or mixtures thereof. Preferred gel bodies contain at least one 2,5-diketopiperazine compound of formula (GB-II) as a gelling agent. wherein
[0036] R 1 , R 2 , R 3 and R 4independently of one another represent a hydrogen atom, a hydroxy group, a (Ci-Ce)-alkyl group, a (C2-Ce)-alkenyl group, a (C2-C6)-acyl group, a (C2-C6)-acyloxy group, a (Ci-Ce)-alkoxy group, an amino group, a (C2-C6)-acylamino group, a (Ci-C6)-alkylaminocarbonyl group, an aryl group, an aroyl group, an aroyloxy group, an aryloxy group, an aryl-(Ci-C4)-alkyloxy group, an aryl-(Ci-C3)-alkyl group, a heteroaryl group, a heteroaryl-(Ci-C3)-alkyl group, a (C1-C4)-hydroxyalkyl group, a (Ci-C4)-aminoalkyl group, a carboxy-(Ci-C3)-alkyl group, where at least two of the radicals R 1 to R 4 together with the remaining molecule can form a 5 or 6-membered ring,
[0037] R 5represents a hydrogen atom, a linear (Ci to Ce) alkyl group, a branched (C3 to C10) alkyl group, a (C3 to C6) cycloalkyl group, a (C2-C8) alkenyl group, a (C2-C6) alkynyl group, a (Ci-C4) hydroxyalkyl group, a (Ci-C4) alkoxy-(Ci-C4) alkyl group, a (C1-C4) acyloxy-(Ci-C4) alkyl group, an aryloxy-(Ci-C4) alkyl group, a G-(aryl-(Ci-C4) alkyl)oxy-(Ci-C4) alkyl group, a (Ci-C4) alkylsulfanyl-(Ci-C4) alkyl group, an aryl group, an aryl-(Ci-C3) alkyl group, a heteroaryl group, a Heteroaryl-(Ci-C3)-alkyl group, a (C1-C4)-hydroxyalkyl group, a (Ci-C4)-aminoalkyl group, an N-(Ci-C4)-alkylamino-(Ci-C4)-alkyl group, an N,N-(Ci-C4)-dialkylamino-(Ci-C4)-alkyl group, an N-(C2-C8)-acylamino-(Ci-C4)-alkyl group, an N-(C2-C8)-acyl-N-(Ci-C4)-alkylamino-(Ci-C4)-alkyl group, an N-(C2-C8)-aroyl-N-(Ci-C4)-alkylamino-(Ci-C4)-alkyl group, an N,N-(C2-C8)-diacylamino-(Ci-C4)-alkyl group,an N-(aryl-(Ci-C4)-alkyl)amino-(Ci-C4)-alkyl group, an N,N-di(aryl-(Ci-C4)-alkyl)amino-(Ci-C4)-alkyl group, a (Ci-C4)-carboxyalkyl group, a (Ci-C4)-alkoxycarbonyl-(Ci-Cs)-alkyl group, a (Ci-C4)-acyloxy-(Ci-Cs)-alkyl group, a guanidino-(Ci-Cs)-alkyl group, an aminocarbonyl-(Ci-C4)-alkyl group, an N-(Ci-C4)-alkylaminocarbonyl-(Ci-C4)-alkyl group, an N,N-di((Ci-C4)-alkyl)aminocarbonyl-(Ci-C4)-alkyl group, an N-(C2-C8)-acylaminocarbonyl-(Ci- C4)-alkyl group, an N,N-(C2-C8)-diacylaminocarbonyl-(Ci-C4)-alkyl group, an N-(C2-C8)-acyl-N-(Ci-C4)-alkylaminocarbonyl-(Ci-C4)-alkyl group, an N-(aryl-(Ci-C4)-alkyl)aminocarbonyl-(Ci-C4)-alkyl group, an N-(aryl-(Ci-C4)-alkyl)-N-(Ci-C6)-alkylaminocarbonyl-(Ci-C4)-alkyl group or an N,N-di(aryl-(Ci-C4)-alkyl)aminocarbonyl-(Ci-C4)-alkyl group. It is preferred according to the invention if R, 3 and R 4 according to formula (GB-II) represents a hydrogen atom. It is particularly preferred according to the invention if R2 , R 3 and R 4 according to formula (GB-II) represents a hydrogen atom. Therefore, very particularly preferred shaped bodies according to the invention contain at least one 2,5-diketopiperazine compound according to formula (GB-IIa) where R 1 and R 5 as defined under formula (GB-II) (vide supra).
[0038] It has been found to be preferable if the residue R 1 according to formula (GB-II) and according to formula (GB-IIa) in the para-position of the phenyl ring. Therefore, for the purposes of the present invention, preferred shaped bodies according to the invention are those which contain at least one 2,5-diketopiperazine compound according to formula (GB-IIb), where R 1 and R 5as previously defined under formula (GB-II) (vide supra). The numbers 3 and 6 positioned on the ring atoms in formula (GB-IIb) merely mark positions 3 and 6 of the diketopiperazine ring for illustrative purposes, as they are generally used within the scope of the invention for the naming of all 2,5-diketopiperazines according to the invention.
[0039] The 2,5-diketopiperazine compounds of formula (GB-II) have chiral centers at least at the carbon atoms of positions 3 and 6 of the 2,5-diketopiperazine ring. The numbering of ring positions 3 and 6 was illustrated by way of example in formula (GB-IIb). The 2,5-diketopiperazine compound of formula (GB-II) of the compositions according to the invention is preferably, based on the stereochemistry of the carbon atoms at positions 3 and 6 of the 2,5-diketopiperazine ring, the configurational isomer 3S,6S, 3R,6S, 3S,6R, 3R,6R or mixtures thereof, particularly preferably 3S,6S.
[0040] Preferred gel bodies contain at least one 2,5-diketopiperazine compound of the formula (GB-II) as a gelling agent, selected from 3-benzyl-6-carboxyethyl-2,5-diketopiperazine, 3-benzyl-6-carboxymethyl-2,5-diketopiperazine, 3-benzyl-6-(p-hydroxybenzyl)-2,5-diketopiperazine, 3-benzyl-6-isopropyl-2,5-diketopiperazine, 3-benzyl-6-(4-aminobutyl)-2,5-diketopiperazine, 3,6-di(benzyl)-2,5-diketopiperazine, 3,6-di(p-hydroxybenzyl)-2,5-diketopiperazine, 3,6-di(p-(benzyloxy)benzyl)-2,5-diketopiperazine, 3-Benzyl-6-(4-imidazolyl)methyl-2,5-diketopiperazine, 3-benzyl-6-methyl-2,5-diketopiperazine, 3-benzyl-6-(2-(benzyloxycarbonyl)ethyl)-2,5-diketopiperazine, or mixtures thereof. Compounds with the aforementioned configurational isomers are preferred for selection.
[0041] It is also possible for the gel bodies according to the invention to contain as gelling agents a) at least one diarylamidocystin compound of the formula (GB-III) wherein
[0042] X + independently represents a hydrogen atom or an equivalent of a cation,
[0043] R 1 , R 2 , R 3 and R 4 independently of one another represent a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 alkoxy group, a C2-C4 hydroxyalkyl group, a hydroxyl group, an amino group, an N-(C1-C4 alkyl)amino group, an N,N-di(C1-C4 alkyl)amino group, an N-(C2-C4 hydroxyalkyl)amino group, an N,N-di(C2-C4 hydroxyalkyl)amino group or R 1 with R 2 or R 3 with R 4 forms a 5- or 6-membered fused ring, which in turn can be substituted by at least one group selected from the group consisting of Ci-C4 alkyl group, Ci-C4 alkoxy group, C2-C4 hydroxyalkyl group, hydroxyl group, amino group, N-(Ci-C4 alkyl)amino group, N,N-di(Ci-C4 alkyl)amino group, N-(C2-C4 hydroxyalkyl)amino group, N,N-di(C2-C4 hydroxyalkyl)amino group.
[0044] Each of the stereocenters contained in the compound of formula (GB-III) can independently represent the L- or D-stereoisomer. According to the invention, it is preferred if said cystine compound of formula (GB-III) is derived from the L-stereoisomer of cysteine.
[0045] Said gel bodies may contain at least one compound of formula (GB-III) in which R 1 , R 2 , R 3 and R 4 independently of one another represent a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 alkoxy group, a C2-C4 hydroxyalkyl group, a hydroxyl group, or R 1 with R 2 or R 3 with R 4forms a 5- or 6-membered fused ring, which in turn may be substituted by at least one group selected from the group consisting of Ci-C4 alkyl group, Ci-C4 alkoxy group, C2-C4 hydroxyalkyl group, or hydroxyl group. Shaped bodies which are particularly suitable as diarylamidocystine compounds of the formula (GB-III) N,N'-dibenzoylcystine (R 1 = R 2 = R 3 = R 4 = hydrogen atom; X + = independently of one another represent hydrogen atom or an equivalent of a cation), in particular N,N'-dibenzoyl-L-cystine.
[0046] The N-(C8-C24)-hydrocarbylglyconamide compounds suitable as gel formers a) preferably have the formula (GB-IV) where n is 2 to 4, preferably 3 or 4, especially 4;
[0047] R 1is selected from hydrogen, C1-C16 alkyl radicals, C1-C3 hydroxy or methoxyalkyl radicals, preferably C1-C3 alkyl, hydroxyalkyl or methoxyalkyl radicals, particularly preferably methyl;
[0048] R 2 is selected from Cs-C24 alkyl radicals, Cs-C24 monoalkenyl radicals, C8-C24 dialkenyl radicals, C8-C24 trialkenyl radicals, C8-C24 hydroxyalkyl radicals, C8-C24 hydroxyalkenyl radicals, C1-C3 hydroxyalkyl radicals or methoxy-Ci-Cs alkyl radicals, preferably Cs-Os alkyl radicals and mixtures thereof, more preferably Cs, C10, C12, C14, s and Os alkyl radicals and mixtures thereof, most preferably C12 and C14 alkyl radicals or a mixture thereof.
[0049] In particularly preferred embodiments, the radical is HO-CH2-(CHOH) n -C- one of a
[0050] II
[0051] O
[0052] Glycuronic acid, in particular the glycuronic acid of a hexose (n=4), derived residue. Glucuronic acid is particularly preferred here. R 1 is preferably H or a short-chain alkyl radical, especially methyl. R 2 is preferably a long-chain alkyl radical, for example a Cs-s alkyl radical.
[0053] Compounds of the formula (GB-IV1) are therefore particularly preferred. where R 2 has the meanings given for formula (GB-IV).
[0054] In a particularly preferred embodiment, the at least one low-molecular-weight gelling agent of the second flowable gelling agent-containing composition is selected from the group consisting of cyclic dipeptides, cyclic dipeptide derivatives, and dibenzylidene sorbitols. Due to its technical effect, the at least one gelling agent of the second flowable gelling agent-containing composition is particularly preferred to be dibenzylidene sorbitol (DBS). In step iii) of the process, the first and second flowable compositions are fed to the mold. In one embodiment of the process, the first flowable composition and the second flowable composition are fed to the mold in the same line. This process is characterized by a reduced apparatus structure.With this process, a partial mixing of the first and second flowable compositions can already occur in the feed line leading to the mold. The disadvantages of this process are reduced control of the gelling process and, in the event of a production interruption, increased cleaning effort before restarting the production equipment.
[0055] For the latter reasons, it is preferable to supply the first flowable composition and the second flowable composition to the mold in separate lines.
[0056] Materials known to those skilled in the art for the manufacture of casting molds are suitable for manufacturing the mold, for example, materials from the group of metals, polymers, or rubbers. Materials from the group of silicones have proven particularly suitable for molding the gel body from the mold.
[0057] In step iv) of the process, the first and second flowable compositions are introduced into the mold. In one embodiment of the process, the first flowable composition and the second flowable composition are introduced into the mold by means of a common injector. As in the case of the previously described common feed line, this process is characterized by a reduced apparatus structure. In addition, in this case too, a partial mixing of the first and second flowable compositions can already take place in the common injector. The disadvantages of this process, however, are, albeit to a lesser extent than in the case of the common feed line, reduced control of the gelation process and, in the event of a production interruption, increased cleaning effort before the production equipment is restarted.
[0058] For the latter reasons, it is preferred to introduce the first flowable composition and the second flowable composition into the mold by means of separate injectors.
[0059] An injector refers to a device suitable for introducing a flowable composition into a mold. The injector is, for example, a filling nozzle or a nozzle. In a preferred process variant, the first flowable composition and the second flowable composition are introduced into the mold simultaneously in step iv). This procedure improves the desired mixing of the two compositions due to turbulent flow.
[0060] The process according to the invention is particularly suitable for processes in which flowable compositions are mixed in widely differing weight proportions. Thus, in the process according to the invention, the first flowable composition and the second flowable composition are preferably mixed in the mold in a weight ratio of 50:1 to 5:1, preferably 35:1 to 8:1.
[0061] The introduction of the first flowable composition and the second flowable composition into the mold is preferably carried out at a filling rate of 1 ml / s to 25 ml / s.
[0062] For process efficiency, it has also proven advantageous if the dynamic mixing device is lowered before the first flowable composition and the second flowable composition are introduced into the mold. It is particularly preferred to introduce the first flowable composition and the second flowable composition into the active area of the mixing element of the dynamic mixing device.
[0063] Impeller mixers, for example, can be used as mixers. Preferred mixing devices have a gear as the mixing element. The use of a dynamic mixing device, which comprises two intermeshing gears as the mixing element, is particularly preferred. An appropriate arrangement of the mixing elements not only enables the homogeneous mixing of the two flowable compositions but also ensures uninterrupted cleaning of the two gears used as the mixing element.
[0064] The mixing element preferably fills only 1 to 10 vol.%, more preferably 2 to 8 vol.%, of the internal volume of the mold. It is preferably placed at the center of the volume of the mold. Furthermore, positioning the mixing element close to the bottom of the mold is preferred, as this allows the mixing element's effect on the two compositions to begin early.
[0065] To assist the mixing process, the mixing element and the mold can be moved relative to one another in step v). Such a relative movement can be achieved by moving the mixing element, the mold, or the movement of the mixing element and mold. The mixing of the two compositions in the mold can be improved by means of the relative movement. A preferred process variant that is technically easy to implement provides for the mixing element to be moved in the mold in step v). The movement can take place in the mold in a horizontal or vertical or horizontal and vertical direction. In the case of a horizontal movement, the direction of movement of the mixing element is parallel to the opening surface of the mold; in the case of a vertical movement, the direction of movement is orthogonal to this surface.
[0066] Alternatively, or in conjunction with the movement of the mixing element, the mold can be moved in step v). A corresponding relative movement can result, for example, from transporting the mold on a conveyor belt or from a vibrating movement of the mold. The mold can also move horizontally, vertically, or both horizontally and vertically. During a horizontal movement, the direction of movement of the mold is parallel to its opening surface; during a vertical movement, the direction of movement is orthogonal to this surface.
[0067] The mixing of the first flowable composition and the second flowable composition in step v) is preferably carried out over a period of 1 to 20 seconds, preferably 2 to 10 seconds.
[0068] In step vi) of the process, the surfactant- and gel-forming agent-containing mixture solidifies in the mold, forming a dimensionally stable gel. To accelerate the solidification process, the surfactant- and gel-forming agent-containing mixture can be cooled in step vi). Cooling preferably takes place under defined climatic conditions, where, in addition to the temperature, the humidity in the process chamber is also controlled and regulated.
[0069] Finally, the dimensionally stable gel body can be removed from the mold.
[0070] For the production of detergent portion units which comprise further components in addition to the gel body, a procedure in which the gel body is combined with a prefabricated molded body is suitable.
[0071] In a first preferred procedure, the mold into which the first and second flowable preparations are introduced in step iv) is partially filled with a prefabricated molded body. The prefabricated molded body preferably covers at least partially, particularly preferably completely, the bottom surface of the mold into which the first and second flowable preparations are introduced in step iv).
[0072] In an alternative procedure, or in conjunction with the procedure described above, a second preferred procedure, the surfactant-containing and gelling agent-containing mixture is covered with a prefabricated molded body before, during, or after solidification in step vi). It is preferred that the surface of the surfactant-containing and gelling agent-containing mixture visible in the mold be completely covered with a prefabricated molded body.
[0073] If the surfactant-containing and gelling agent-containing mixture is introduced into the mold onto a first prefabricated molded body and the side opposite the side covered with the first prefabricated molded body is covered with a second prefabricated molded body, a sandwich-like detergent portion unit is obtained which is particularly advantageous in terms of handling and appearance.
[0074] A particularly preferred process variant for producing a detergent portion unit, comprising a) a dimensionally stable gel body b) two shaped bodies, comprises the steps: i) providing a first flowable surfactant-containing composition; ii) providing a second flowable gel-forming agent-containing composition different from the first flowable composition; iii) feeding the first and second flowable compositions to a mold; iv) introducing the first and second flowable compositions into the mold, the bottom surface of which is at least partially covered with a first prefabricated shaped body; v) mixing the first and second flowable compositions in the mold by means of a dynamic mixing device to form a surfactant-containing and gel-forming agent-containing mixture;vi) covering the side of the dimensionally stable gel body opposite the side covered with the first prefabricated shaped body with a second prefabricated shaped body; vii) allowing the surfactant-containing and gelling agent-containing mixture to solidify in the mold to form a dimensionally stable gel body; viii) removing the gel body from the mold to form a detergent portion unit comprising a gel body and the first and second prefabricated shaped bodies;
[0075] Preferred molded bodies fill 5 to 45 vol.%, preferably 10 to 25 vol.% of the mold.
[0076] The molded body can be manufactured in a variety of ways. The use of cast bodies has proven to be a technically simpler method. The production of the molded body by casting processes has the advantage of allowing the production of a wide variety of geometries. The cast bodies are preferably solidified melts. Due to their ease of large-scale production, compressed bodies, especially tablets, are particularly preferred as molded bodies.
[0077] Regardless of the process used for its production, the shaped body preferably has a breaking strength of 50 N to 300 N, in particular 50 N to 150 N. This breaking strength ensures, on the one hand, sufficient stability of the shaped body during production, transport, and handling by the consumer, and, on the other hand, satisfactory dissolution behavior of the shaped body in an aqueous liquor. The hardness of the shaped body is measured by deformation until fracture, whereby the force acts on the side surfaces of the shaped body and the maximum force it can withstand is determined. A tablet testing device from Sotax, for example, is suitable for determining the hardness of the shaped body.
[0078] Preferred molded bodies have a print.
[0079] If the gel body is combined with a molded body as described above, the dimensionally stable gel body, partially covered by a molded body, is finally removed from the mold. The gel body and the molded body are preferably adhesively bonded to each other.
[0080] In a preferred embodiment of the detergent portion units, the shaped body also contributes to the washing and cleaning action. Corresponding detergent portion units comprise a shaped body that contains, based on its total weight, more than 40% by weight, preferably more than 60% by weight, particularly preferably more than 80% by weight of washing or cleaning active ingredient.
[0081] The first group of active washing or cleaning ingredients integrated into the molded body are fragrances. Their incorporation into the molded body ensures a perceptible fragrance experience for the consumer, which cannot be achieved to the same extent when the fragrances are incorporated into the gel body.
[0082] Another group of washing or cleaning-active ingredients preferably incorporated into the coating substance are the builders, in particular citrates, zeolites, silicates, and carbonates, particularly preferably citrates and zeolites. The weight fraction of these active substances in the total weight of the coating substance is preferably 5 to 60 wt.%, in particular 10 to 50 wt. Particularly preferred are coating substances which, based on their total weight, contain 5 to 60 wt.%, in particular 10 to 50 wt.% citrate and / or zeolite. These active substances not only contribute to the intended washing and cleaning action, but also improve the contour sharpness and durability of the printed image when the molded body surface is printed.
[0083] For the sharpness of the contours and durability of the printed image, the use of active ingredients from the group of polymeric detergent or cleaning agents, preferably from the group of celluloses and cellulose derivatives and anionic or non-ionic aromatic polyesters, preferably from the group of celluloses, microcrystalline celluloses and carboxymethylcelluloses, and anionic or non-ionic aromatic polyesters, is also advantageous. The weight proportion of these cellulose-based active ingredients to the total weight of the coating substance is preferably 2 to 50% by weight.
[0084] The composition of some preferred detergent portion units can be found in the following tables (data in wt.% based on the total weight of the gel body or the coating substance unless otherwise stated).
[0085] In summary, this application provides, among other things, the following items:
[0086] 1. A method for producing a detergent portion unit, comprising a) a dimensionally stable gel body, comprising the steps of: i) providing a first flowable surfactant-containing composition; ii) providing a second flowable gel-forming agent-containing composition different from the first flowable composition; iii) feeding the first and second flowable compositions to a mold; iv) introducing the first and second flowable compositions into the mold; v) mixing the first and second flowable compositions in the mold by means of a dynamic mixing device to form a surfactant-containing and gel-forming agent-containing mixture; vi) allowing the surfactant-containing and gel-forming agent-containing mixture to solidify in the mold to form a dimensionally stable gel body.
[0087] 2. Process according to point 1, wherein the gel body has a weight of 14 g to 42 g, preferably of 18 g to 38 g, in particular of 20 g to 34 g.
[0088] 3. Method according to one of the preceding points, wherein the gel body has a flat bottom whose largest diagonal is greater than the height of the gel body.
[0089] 4. Method according to one of the preceding points, wherein the gel body has a flat underside whose largest diagonal is more than 1.5 times, preferably more than 2 times the height of the gel body.
[0090] 5. Method according to one of the preceding points, wherein the gel body has an oval underside.
[0091] 6. Method according to one of the preceding points, wherein the gel body has an ellipsoidal or round, preferably a round, bottom.
[0092] 7. Method according to one of the preceding points, wherein the gel body has a square underside.
[0093] 8. Method according to one of the preceding points, wherein the gel body has a triangular, square or hexagonal bottom.
[0094] 9. Method according to one of the preceding points, wherein the gel body has a square bottom with rounded corners.
[0095] 10. The method according to any one of the preceding points, wherein the gel body has a top side that is plane-parallel to the bottom side. 11. The method according to any one of the preceding points, wherein the gel body has a bottom side and a top side that have the same geometric shape, and wherein the bottom side and the top side have the same surface area.
[0096] 12. Method according to one of the preceding points, wherein the gel body has a bottom side and a top side which have the same geometric shape and wherein the bottom side and the top side have different surface sizes.
[0097] 13. Method according to one of the preceding points, wherein the gel body has a bottom side and a top side which are connected to one another by a cylindrical outer surface.
[0098] 14. Method according to one of the preceding points, wherein the gel body has a bottom side and a top side and the area of the bottom side is 80 to 100%, preferably 90 to 100% and in particular 98 to 100% of the top side.
[0099] 15. A method according to any one of the preceding points, wherein the first flowable composition and the second flowable composition are fed to the mold in separate lines.
[0100] 16. Method according to one of the preceding points, wherein the mold is made of a material from the group of metals, polymers or rubbers.
[0101] 17. Method according to one of the preceding points, wherein the mold is made of a material from the group of silicones.
[0102] 18. Method according to one of the preceding points, wherein the first flowable composition and the second flowable composition are introduced into the mold by means of a common injector.
[0103] 19. Method according to one of the preceding points, wherein the first flowable composition and the second flowable composition are introduced into the mold by means of separate injectors.
[0104] 20. The method according to any one of the preceding points, wherein the first flowable composition and the second flowable composition are introduced into the mold simultaneously. 21. The method according to any one of the preceding points, wherein the first flowable composition and the second flowable composition are mixed in the mold in a weight ratio of 50:1 to 5:1, preferably 35:1 to 8:1.
[0105] 22. A method according to any one of the preceding points, wherein the first flowable composition and the second flowable composition are introduced into the mold at a filling rate of 1 ml / s to 25 ml / s.
[0106] 23. A method according to any one of the preceding points, wherein the mixing element of the dynamic mixing device is lowered before introducing the first flowable composition and the second flowable composition into the mold.
[0107] 24. Method according to one of the preceding points, wherein the first flowable composition and the second flowable composition are introduced into the active region of the mixing element of the dynamic mixing device.
[0108] 25. Method according to one of the preceding points, wherein the dynamic mixing device comprises a gear as the mixing element.
[0109] 26. Method according to one of the preceding points, wherein the dynamic mixing device comprises two intermeshing gears as the mixing element.
[0110] 27. Method according to one of the preceding points, wherein the mixing element fills 1 to 10 vol.%, preferably 2 to 8 vol.% of the internal volume of the mold.
[0111] 28. Method according to one of the preceding points, wherein the mixing element of the dynamic mixing device is located in the volume center of the mold.
[0112] 29. Method according to one of the preceding points, wherein in step v) the mixing element and the mold are moved relative to each other.
[0113] 30. Method according to one of the preceding points, wherein in step v) the mixing element is moved in the mold.
[0114] 31. Method according to one of the preceding points, wherein in step v) the mixing element is moved in the mold in a horizontal and / or vertical direction.
[0115] 32. Method according to any one of the preceding points, wherein in step v) the mold is moved. 33. Method according to any one of the preceding points, wherein in step v) the mold is moved in a horizontal and / or vertical direction.
[0116] 34. Method according to one of the preceding points, wherein the mixing of the first flowable composition and the second flowable composition in step v) takes place over a period of 1 to 20 seconds, preferably 2 to 10 seconds.
[0117] 35. Process according to any one of the preceding points, wherein the surfactant-containing and gelling agent-containing mixture is cooled in step vi).
[0118] 36. Method according to one of the preceding points, wherein the dimensionally stable gel body is removed from the mold following step vi).
[0119] 37. A process according to any one of the preceding points, wherein the mold into which the first and second flowable preparations are introduced in step iv) is partially filled with a prefabricated molded body.
[0120] 38. The method according to item 37, wherein the bottom surface of the mold into which the first and second flowable preparations are introduced in step iv) is at least partially, preferably completely, covered with a prefabricated molded body.
[0121] 39. Process according to one of the preceding points, wherein the surfactant-containing and gelling agent-containing mixture is covered with a prefabricated shaped body before, during or after solidification in step vi).
[0122] 40. Process according to item 39, wherein the surface of the surfactant-containing and gelling agent-containing mixture is completely covered with a prefabricated shaped body.
[0123] 41. Process according to one of items 37 to 40, wherein the prefabricated shaped body fills 5 to 45 vol.%, preferably 10 to 25 vol.% of the mold.
[0124] 42. Method according to one of items 37 to 41, wherein the shaped body is in the form of a cast body.
[0125] 43. Process according to one of items 37 to 41, wherein the shaped body is in the form of a pressed body, preferably a tablet.
[0126] 44. The method according to any one of items 37 to 43, wherein the molded body has a breaking strength of 30 N to 300 N, preferably of 50 N to 150 N. 45. The method according to any one of items 37 to 44, wherein the molded body has a print.
[0127] 46. A process according to any one of items 37 to 45, wherein the dimensionally stable gel body partially covered by a shaped body is removed from the mold following step vi).
[0128] 47. Process according to one of the preceding points, wherein the first flowable surfactant-containing composition contains, based on its total weight, 30 to 70 wt.%, preferably 40 to 60 wt.% and in particular 45 to 55 wt.% surfactant.
[0129] 48. Process according to one of the preceding points, wherein the dimensionally stable gel body contains, based on its total weight, 15 to 35% by weight, preferably 20 to 30% by weight of an aqueous-organic solvent.
[0130] 49. Process according to one of the preceding points, wherein the second flowable gelling agent-containing composition contains low molecular weight gelling agent with a molar mass of up to 2000 g / mol, wherein its weight proportion of the total weight of the gel body is preferably less than 5 wt.%, preferably 0.1 to 5 wt.%, particularly preferably 0.1 to 2.5 wt.%.
[0131] 50. Process according to one of the preceding points, wherein the second flowable gelling agent-containing composition contains low molecular weight gelling agent selected from the group of cyclic dipeptides, cyclic dipeptide derivatives and dibenzylidene sorbitols.
[0132] 51. A process according to any one of the preceding points, wherein the second flowable gelling agent-containing composition contains dibenzylidene sorbitol as low molecular weight gelling agent.
[0133] 52. The method according to any one of the preceding items, wherein the second flowable gelling agent-containing composition further contains an organic solvent.
[0134] 53. Process according to one of the preceding points, wherein the second flowable gelling agent-containing composition contains gelling agent and organic solvent in a total weight proportion above 50 wt.%, preferably above 70 wt.% and in particular above 90 wt.%.
[0135] 54. Process according to any one of items 37 to 53, wherein the shaped body contains, based on its total weight, more than 40% by weight, preferably more than 60% by weight, particularly preferably more than 80% by weight of washing or cleaning active ingredient.
[0136] 55. The process according to any one of items 37 to 54, wherein the shaped body contains a washing or cleaning active ingredient from the group of fragrances. 56. The process according to any one of items 37 to 55, wherein the shaped body contains a washing or cleaning active ingredient from the group of builders, in particular at least one active ingredient from the group of citrates, zeolites, silicates, and carbonates, preferably from the group of citrates and zeolites.
[0137] 57. Process according to any one of items 37 to 56, wherein the shaped body contains a polymeric washing or cleaning-active ingredient, preferably a polymeric washing or cleaning-active ingredient from the group of celluloses and cellulose derivatives and from the group of anionic or non-ionic aromatic polyesters, preferably from the group of celluloses, microcrystalline celluloses and carboxymethylcelluloses and from the group of anionic or non-ionic aromatic polyesters.
[0138] 58. Method according to one of items 37 to 57, wherein the gel body and the shaped body are adhesively bonded to one another.
Claims
Patent claims 1. A method for producing a detergent portion unit, comprising: a) a dimensionally stable gel body, comprising the steps of: i) providing a first free-flowing surfactant-containing composition; ii) providing a second free-flowing gelling agent-containing composition, different from the first free-flowing composition; iii) feeding the first and second free-flowing compositions to a mold; iv) introducing the first and second free-flowing compositions into the mold; v) mixing the first and second free-flowing compositions in the mold by means of a dynamic mixing device to form a surfactant-containing and gelling agent-containing mixture; vi) allowing the surfactant-containing and gelling agent-containing mixture to solidify in the mold to form a dimensionally stable gel body.
2. The method of claim 1, wherein the first flowable composition and the second flowable composition are introduced into the mold by means of a common injector.
3. Method according to one of the preceding claims, wherein the first flowable composition and the second flowable composition are introduced into the mold by means of separate injectors.
4. Method according to one of the preceding claims, wherein the first flowable composition and the second flowable composition are mixed in the form in a weight ratio of 50:1 to 5:1, preferably from 35:1 to 8:
1.
5. Method according to one of the preceding claims, wherein the dynamic mixing device comprises two intermeshing gears as the mixing element.
6. Method according to one of the preceding claims, wherein in step v) the mixing element and the mold are moved relative to each other.
7. Method according to one of the preceding claims, wherein the mixing of the first flowable composition and the second flowable composition in step v) takes place over a period of 1 to 20 seconds, preferably 2 to 10 seconds.
8. Method according to one of the preceding claims, wherein the mold into which the first and second flowable preparations are introduced in step iv) is partially filled with a pre-made molded body.
9. Method according to one of the preceding claims, wherein the first free-flowing surfactant-containing composition contains, based on its total weight, 30 to 70 wt.%, preferably 40 to 60 wt.% and particularly 45 to 55 wt.% surfactant.
10. Method according to one of the preceding claims, wherein the second flowable gelling agent-containing composition contains low molecular weight gelling agent with a molar mass of up to 2000 g / mol, wherein the weight fraction of which is preferably less than 5 wt.%, preferably 0.1 to 5 wt.%, particularly preferably 0.1 to 2.5 wt.%.