Premixes containing alkyl polyglycosides for use in preparing liquid detergent formulations - Patents.com
Patent Information
- Application Number
- JP2024502010
- Authority / Receiving Office
- JP · JP
- Patent Type
- Applications
- Current Assignee / Owner
- Priority Date
- 2021-07-16
- Filing Date
- 2022-07-06
- Publication Date
- 2025-07-10
- Estimated Expiration
- Not applicable · inactive patent
AI Technical Summary
Commercially available alkyl polyglycosides with longer alkyl chains exhibit high viscosity and crystallization issues at low temperatures, making them difficult to handle and store, and increasing their concentration leads to undesirable properties like cloudiness and opacity.
A premix comprising alkyl polyglycosides with specific hydrotropes and solvents, such as sodium cumene sulfonate in water, reduces viscosity and prevents crystallization, maintaining stability even at low temperatures.
The premix achieves low viscosity and prevents crystallization over extended periods, facilitating handling and storage without the need for reheating or excessive dilution, ensuring uniform product quality.
Abstract
Description
[Technical field]
[0001] The present invention relates to a premix comprising an alkyl polyglycoside, a hydrotrope and a solvent, where the alkyl polyglycoside has an alkyl chain of 10 to 16 carbon atoms, the hydrotrope is preferably sodium cumene sulfonate and the solvent is preferably water. [Background technology]
[0002] Sugar surfactants, such as alkyl polyglycosides, are distinguished by excellent cleaning properties and high ecotoxicity compatibility.For this reason, these classes of nonionic surfactants are becoming more and more important.They are commonly used in the formulation of liquid and powder detergents, such as, for example, laundry detergents and dishwashing detergents and hair shampoos.
[0003] Typically, commercially available alkyl polyglycosides are 10 -C 16 For alkyl polyglycosides with longer alkyl chain lengths, such as alkyl polyglycosides, about 40% to up to 50% and C8-C 10 In the case of alkyl polyglycosides with shorter alkyl chain lengths, such as C, C10, C20, C30, C40, C50, C60, C70, C80, C90, C100, C120, C140, C160, C180, C200, C300, C400, C500, C60, C70, C80, C90, C120, C140, C160, C180, C160, C180, C200, C16 ... 10 -C 16 Increasing the active level of alkyl polyglycosides can cause undesirable high viscosity of the product at low temperatures, making it difficult to handle in cold or winter conditions. Most notably, 10 -C 16 Certain alkyl polyglycosides, such as alkyl polyglycosides, exhibit unacceptably high viscosities at low temperatures when transported, such as by injection or pumping. In addition, the higher alkyl (C 10 -C 16) polyglycosides, due to their supersaturated state, tend to crystallize during storage below 30°C. 10 -C 16 Alkyl polyglycosides become cloudy, i.e., cloudy and opaque in appearance, as the solids contained therein exceed their supersaturation state, which is a highly undesirable phenomenon and makes it difficult to achieve uniform product quality. To solve this problem, 10 -C 16 The alkyl polyglycoside solution must be heated to resolvate the crystals and reduce the viscosity, which makes the process expensive and time consuming, or the use of C8-C 10 However, this solution required a high concentration of low alkyl chain polyglycosides (>20%) to achieve the desired properties. Therefore, the C 10 -C 16 It is possible to reduce the viscosity and prevent the solid crystallization without excessively diluting the alkyl polyglycoside with other ingredients, C 10 -C 16 It remains a challenge to obtain an alkyl polyglycoside composition containing an alkyl polyglycoside. 10 -C 16 Compositions containing alkyl polyglycoside solutions can facilitate processes in preparing cleaning formulations containing alkyl polyglycosides. Summary of the Invention [Means for solving the problem]
[0004] In accordance with the present invention, it has been surprisingly discovered that a premix comprising an alkyl polyglycoside, at least one hydrotrope and a solvent can overcome the aforementioned difficulties.
[0005] In one aspect, the present invention relates to a premix comprising an alkyl polyglycoside, at least one hydrotrope, and at least one solvent, In this case, the alkyl polyglycoside has the formula: C n H 2n+1 O(CH 10 O5) x Characterized by H, In the formula, n is an integer of 8 to 18, preferably 8 to 16, and more preferably 10 to 16. x is 1 to 3, preferably 1.1 to about 2.7, and more preferably 1.2 to 2; at least one hydrotrope is selected from the group consisting of sodium cumene sulfonate, sodium xylene sulfonate, sodium toluene sulfonate, dioctyl sodium sulfosuccinate, alkyl naphthalene sulfonates and dihexyl sodium sulfosuccinate, preferably the hydrotrope is sodium cumene sulfonate; - at least one solvent comprises water and optionally at least one water-miscible organic solvent, preferably the solvent is essentially water, more preferably water.
[0006] The premixes of the present invention are useful in a wide range of products, particularly detergent products such as liquid and / or granular laundry detergent formulations, dishwashing detergent compositions and the like.
[0007] Thus, in a further aspect, the present invention provides a premix for use in the preparation of a liquid detergent formulation, preferably a liquid laundry detergent formulation or a liquid dishwashing detergent formulation.
[0008] In another aspect, the present invention provides a method for preparing a liquid laundry detergent formulation or a liquid dishwashing detergent formulation comprising one step of adding a premix as defined herein to the formulation, the method comprising mixing the premix of the present invention at any time during the preparation of the final / finished composition, i.e. at the very beginning as the first addition or at the very end as the last addition and / or at any time in between.
[0009] In yet another aspect, the present invention relates to the use of a premix as defined herein for preparing a liquid laundry detergent formulation or a liquid dishwashing detergent formulation.
[0010] Surprisingly and unexpectedly, the inventors have discovered that the premix of the present invention is capable of reducing the viscosity even at very low temperatures and of eliminating the tendency of alkyl polyglycosides to crystallize during prolonged storage under ambient conditions or even at very low temperatures, thus making it possible to achieve the above mentioned objectives. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0011] Throughout this specification, including the claims, the terms "comprising one" or "comprising a" should be understood as being synonymous with the term "comprising at least one," unless otherwise specified, and the term "between" should be understood to be inclusive of the limits.
[0012] The indefinite articles "a", "an" and "the" are used to refer to one or to more than one (ie, to at least one) of the grammatical object of the article.
[0013] The term "and / or" encompasses the meaning of "and", "or" as well as all other possible combinations of the components to which this term is associated.
[0014] It should be noted that when specifying any range of concentrations, weight ratios or amounts, any particular upper concentration, weight ratio or amount may be associated with any particular lower concentration, weight ratio or amount limit, respectively.
[0015] The term "essentially" as used herein refers within the meaning of the present invention to a majority, for example a concentration of greater than 95%, or a concentration of greater than 98%.
[0016] The term "premix" or "premix" as used herein refers to a mixture of ingredients designed to be mixed with other ingredients to form a finished or final composition, such as liquid laundry detergent and liquid dishwashing detergent. The "premix" itself may be a commodity and can be sold for subsequent mixing with other ingredients at a remote location to obtain a finished composition.
[0017] As used herein, the abbreviation APG stands for alkyl polyglycoside.
[0018] Throughout this specification, "alkyl polyglucoside" is used to include alkyl polyglycosides due to the change in stereochemistry of the sugar moiety during the preparation reaction.
[0019] All percentages, ratios and proportions herein are by weight unless otherwise specified.
[0020] "Viscosity" is measured using a Brookfield Viscometer Model DV2T LVT equipped with a Thermosel System. To assess stability, the viscosity of the systems is measured during storage at 20°C.
[0021] As used herein, "pumpable" refers to a viscosity of less than about 10000 mPas, preferably less than about 3000 mPas. The term "about" as used herein means within the meaning of the present invention, plus or minus 5%, preferably plus or minus 2%, inclusive of the exact number.
[0022] The present invention relates to a premix comprising an alkyl polyglycoside, at least one hydrotrope and at least one solvent, In this case, the alkyl polyglycoside has the formula C n H 2n+1 O(CH 10 O5) x Characterized by H, During the ceremony, n is an integer of 8 to 18, preferably 8 to 16, more preferably 10 to 16, and x is an integer of 1 to 3, preferably 1.1 to about 2.7, more preferably 1.2 to 2; at least one hydrotrope is selected from the group consisting of sodium cumene sulfonate, sodium xylene sulfonate, sodium toluene sulfonate, dioctyl sodium sulfosuccinate, alkyl naphthalene sulfonates and dihexyl sodium sulfosuccinate, preferably the hydrotrope is sodium cumene sulfonate; - at least one solvent comprises water and optionally at least one water-miscible organic solvent, preferably the solvent is essentially water, more preferably water.
[0023] According to any one of the embodiments of the present invention, the premix comprises alkyl groups of 10 to 16 carbon atoms (i.e., C 100 to C 200) in the range of 60% to about 100%, preferably 70%, 75%, 80%, 85%, 90%, 95% or 98% to 100% by weight of the total weight of alkyl polyglycosides, and any value between "60" and "100". 10 -C 16 Alkyl polyglycosides having the following structure:
[0024] According to any one of the embodiments of the present invention, the premix comprises an alkyl polyglycoside and a hydrotrope in a weight ratio of alkyl polyglycoside to hydrotrope of 30 / 70 to 90 / 10, preferably 70 / 30 to 85 / 15, more preferably 75 / 25 to 80 / 20, and preferably the alkyl polyglycoside has an alkyl group of 10 to 16 carbon atoms (i.e., C 10 -C 16 alkyl polyglycosides).
[0025] According to any one of the embodiments of the present invention, the premix may optionally include at least one water-miscible organic solvent, such as methanol, ethanol, propanol, isopropanol, glycerol, propylene glycol, ethylene glycol, 1,2-propanediol, sorbitol, or mixtures thereof.
[0026] According to any one of the embodiments of the present invention, the premix comprises a solvent in an amount of 40% to 90%, preferably 45% to 65%, of the total weight of the premix.
[0027] According to any one of the embodiments of the present invention, the premix has a pour point of -10°C to 5°C, preferably -10°C to 0°C, more preferably -10°C to -3°C.
[0028] The premix of the present invention is suitable for use in a wide range of detergent products.The premix of the present invention is particularly suitable for use in liquid laundry detergent and liquid dishwashing detergent.In such applications, the premix is mixed with one or more components to form a final / finished composition, and such mixing can be carried out at any time during the preparation of the final / finished composition, i.e., at the very beginning as the first addition, or at the very end as the last addition, and / or at any time in between.
[0029] Finished composition The premix of the present invention is suitable for use in a wide range of detergent products.The premix of the present invention is particularly suitable for use in liquid laundry detergents and liquid dishwashing detergents.In such applications, the premix is mixed with one or more components selected from anionic, cationic, nonionic, zwitterionic, amphoteric surfactants, fatty acids, citric acid and other builders, chelating agents, bleaching agents and bleach activators, enzymes, suds suppressors, organic solvents including ethanol, 1,2-propanediol, soil removal polymers, and other ingredients known to be useful in such detergents.
[0030] Liquid detergents are suitably formulated by adding the premix, surfactant component of the present invention to water and then adding the other ingredients with agitation.
[0031] The liquid detergent may comprise one or more components selected from anionic, nonionic, cationic, zwitterionic, amphoteric surfactants. Preferably, the liquid detergent comprises 5 to 70% by weight, in particular 15 to 55% by weight, more in particular 25 to 45% by weight, of at least one such surfactant.
[0032] A wide variety of anionic surfactants are useful in the present invention. Useful anionic surfactants include alkyl aryl sulfonates, alkyl sulfonates, alkyl sulfates, alkyl ether sulfates, alkyl phosphates, amine oxides, isethionates, C8-C 30 These include fatty acid soaps, taurines, betaines, sulfobetaines, and mixtures thereof. Suitable anionic surfactants are, for example, sulfates of (fatty) alcohols having 8 to 22, preferably 10 to 18, carbon atoms, in particular C9C 11 -Alcohol sulfate, C 12 C 14 -Alcohol sulfate, C 12 -C 18 -Alcohol sulfate, lauryl sulfate, cetyl sulfate, myristyl sulfate, palmityl sulfate, stearyl sulfate, and tallow fat alcohol sulfate, sulfated alkoxylated C8-C 22 -alcohols (alkyl ether sulfates): compounds of this type are, for example, first C8-C 22 -alcohol, preferably C 10 -C 18 -Alcohols, such as fatty alcohols, are prepared by alkoxylation followed by sulfation of the alkoxylation product. Alkoxylation can involve the use of ethylene oxide, linear C8-C 20 - Alkylbenzene sulfonates (LAS), preferably linear C9-C 13-Alkylbenzenesulfonates and -alkyltoluenesulfonates, alkanesulfonates, especially C8-C 24 -Alkanesulfonates, preferably C 10 -C 18 -Alkanesulfonates, fatty acid ester sulfonates of formula RCH(SOM)COR, where R is C6-C 20 -Alkyl, preferably C-C 16 -alkyl, R2 is C1-C4-alkyl, preferably methyl or ethyl, M is hydrogen, a water-soluble cation, for example an alkali metal cation or an ammonium ion, and it is preferred to use olefin sulfonates, isethionates, in particular acyl isethionates, and N-acyltaurates, N-acylsarcosinates, sulfosuccinates (mono- or diesters of sulfosuccinates) and alkyl succinates, organic phosphate esters, in particular mixtures of mono- and diester phosphates of hydroxyl-terminated alkoxide condensates and their salts, having 8 to 22, preferably 12 to 18, carbon atoms. These include, for example, alkoxylated C8-C 22 -Polyoxyalkylated alkylaryl phosphate esters, C8-C based on alcohol or alkoxylated phenol derivatives 24 - soaps such as the sodium and potassium salts of carboxylic acids. The anionic surfactants are preferably added to the detergent in the form of a salt. Suitable salts are, for example, alkali metal salts such as sodium, potassium and lithium salts, and ammonium salts such as hydroxyethylammonium, di(hydroxyethyl)ammonium and tri(hydroxyethyl)ammonium salts.
[0033] A wide range of nonionic surfactants are useful in the present invention. Nonionic surfactants are generally the product of the reaction of polyoxyalkylene compounds, i.e., alkylene oxides such as ethylene oxide or propylene oxide or mixtures thereof, with starter molecules that contain active hydrogen atoms that react with the alkylene oxide. Such starter molecules include alcohols, amines, carboxylic acids, amides, and mercaptans. When the starter molecule is an alcohol, the reaction product is known as an alcohol alkoxylate. Polyoxyalkylene compounds can have a variety of block and heterostructures. For example, they can include a single block of alkylene oxide, or they can be diblock or triblock alkoxylates. Within the block structure, the blocks can be all ethylene oxide or all propylene oxide, or the blocks can include heteromixtures of alkylene oxides. Preferred nonionic surfactants are selected from the class of alcohol ethoxylates, which are alcohol alkoxylates in which the alkylene oxide is ethylene oxide. The alcohols used to produce the alcohol alkoxylates and preferred ethoxylates of the present invention are generally those having from 6 to 18 carbon atoms. Suitable surfactants are those having 7 ethylene oxide units and a single C 12 -C 15 Such surfactants are known to those skilled in the art under various names. For example, 12 - 15 7 mole ethoxylate of alcohol, or 7 mole ethylene oxide adduct, or C 12 -C 15 7 mole ethoxylate of alcohol, or C 12 -C 15 and the like. All such nomenclature conventions are used interchangeably herein as well as in the art.
[0034] The liquid detergent may further comprise a cationic surfactant. Suitable cationic surfactants include C7-C 25 -Alkylamines, N,N-dimethyl-N-(C7-C 25 -hydroxyalkyl)ammonium salts, mono- and di-(C7-C 25 -alkyl)dimethylammonium compounds, ester quats, especially C8-C 22 -Quaternary esterified mono-, di- and trialkanolamines esterified with carboxylic acids and quaternary ammonium imidazolines.
[0035] The liquid detergent may further comprise amphoteric and / or zwitterionic surfactants.Suitable amphoteric surfactants are derivatives of aliphatic or heterocyclic secondary and tertiary amines, the aliphatic group preferably having 8-18 carbon atoms, at least one group containing one or more anionic water-soluble groups, such as one or more carboxylate, sulfonate, sulfate, phosphate or phosphonate groups.Examples of suitable amphoteric surfactants are 3-(alkylamino)propionates, (alkylamino)acetates, 3-(dialkylamino)propionates and (dialkylamino)acetates, in which at least one alkyl group preferably contains 8-18 carbon atoms, [(2-acylaminoethyl)(2-hydroxyethyl)amino]acetates, in which the acyl group preferably contains 8-18 carbon atoms, (alkylamino)propanesulfonates, in which the alkyl group preferably contains 8-18 carbon atoms. Suitable zwitterionic surfactants are, for example: amine oxides, in particular alkyldimethylamine oxides and alkyldiethylamine oxides, in which the alkyl group preferably contains from 8 to 18 carbon atoms, betaines, in particular carbobetaines, sulfobetaines, phosphobetaines, cocoamidopropylbetaines.
[0036] The detergent composition of the present invention may also contain one or more conventional additives found in liquid laundry detergents or other aqueous detergent compositions. Such additives are known to those skilled in the art and include, for example: anti-redeposition agents, bleaching agents, builders such as sodium sulfate or sodium carbonate, buffers such as borax, defoamers, enzymes, brighteners, enzyme stabilizers, solvents such as ethanol or glycerol, hydrotropes such as sodium xylene sulfonate, preservatives, softeners such as quaternary ammonium salts, formulation aids such as sorbitol, fragrances, dyes, and colorants. The types of additives used and the levels of additives in the formulation will be selected by the skilled formulator to produce a composition with the desired cleaning power and other properties.
[0037] The present invention further relates to a method for preparing a liquid laundry detergent formulation or a liquid dishwashing detergent formulation (i.e., as a "final / finished composition", respectively) which comprises one step of adding a premix of the present invention to the formulation. Such a method includes mixing a premix of the present invention at any time during the preparation of the final / finished composition, i.e., at the very beginning as the first addition, or at the very end as the last addition, and / or at any time in between.
[0038] The present invention also relates to the use of a premix of the present invention for preparing a liquid laundry detergent formulation or a liquid dishwashing detergent formulation.
[0039] The following examples are provided to illustrate the invention, but are not intended to limit it. EXAMPLES
[0040] Materials and Measurements (APG-1): a C 2 O 4 having a DP of about 1.4, commercially available from BASF 10 -C 16 Alkyl polyglucosides 50-53% (active matter by weight)
[0041] (APG-2): C8-C with a DP of about 1.5 commercially available from BASF 10 Alkyl polyglucosides 62-65% (by weight of active substance).
[0042] (APG-3): 2-ethylhexyl alkyl polyglucosides 60-65% (by weight of active substance). The synthesis of 2-ethylhexyl alkyl polyglucosides is described in patent application WO 2020 / 169632.
[0043] (APG-4): about 65% (by weight active matter) C4 alkyl polyglucoside having a DP of about 1.4 commercially available from BASF.
[0044] Sodium cumene sulfonate: MICOLIN SCS40 approximately 40% (by weight active matter) supplied by Miwon.
[0045] Premix General Procedures and Settings The premixing process was carried out by setting up an overhead mechanical stirrer (RW 20 Digital from IKA) and a water bath (HWS-26 from Yiheng Technology Co. Ltd).
[0046] All the raw materials of the premix were preheated in an oven (Binder FD 115) at 40°C for at least 1 hour to ensure thorough homogenization. The preheated alkyl polyglycoside was then pre-charged into a vessel whose temperature was controlled by a water bath. Stirring was started at a speed of 100 rpm to 500 rpm, and the hydrotrope and / or solvent were dosed into the vessel stepwise within a specific time period. After dosing, stirring was maintained for 0.5 to 3 hours to obtain the final premix.
[0047] Premix Stability Testing The prepared premixes were filled into glass bottles and tested at various temperatures. Then the bottles containing the premix samples were separately placed into constant temperature stability test chambers (BPHS-060A, Yiheng Technology Co. Ltd.) at 5°C, 10°C, 20°C, and 30°C.
[0048] The viscosity of the premix samples was checked by a viscometer (Brookfield DV2T LVT) equipped with a temperature cycler (Brookfield TC-550MC) and visual observation was made to see if crystallization had occurred. The viscosity and crystallization status were then tracked and recorded until crystallization occurred or for up to 12 weeks.
[0049] Pour Point Measurement Pour point is a physical property of a chemical that indicates the feasibility of handling the chemical at various temperatures. It was measured by an automatic cloud and pour point tester (HCP 852 from WALTER HERZOG GmbH) according to ASTM D5950.
[0050] Experimental Tests and Data 1.C with sodium cumene sulfonate 10 -C 16 Stability test of premixes containing APG (APG-1) Following the general procedure and setup of the premix, 145.45 g of APG-1 (50-53% aqueous solution) was mixed with 54.55 g of sodium cumene sulfonate (40% aqueous solution). (Alkyl polyglycoside used: APG-1, commercially available from BASF).
[0051] The premix process was carried out according to the method for determining apparent viscosity as specified in ISO 2555 using a four-blade propeller stirrer (IKA R 1342) at a stirring speed of 300 rpm and in a water bath at 45° C. for 30 min.
[0052] After stability testing of the premixes, the viscosity and crystallization state were tracked and recorded, and the results are shown in Table 1.
[0053] [Table 1]
[0054] The results show that the premix containing APG-1 and an aqueous solution of sodium cumene sulfonate can be easily handled even when the temperature is below 5°C and is stable between 5°C and 30°C for at least 12 weeks without crystallization. The viscosity was always below 300 mPa.s from 5°C to 30°C, so no reheating was required. Therefore, it can be easily handled during transportation, storage, and loading / unloading.
[0055] 2. C with Various Solvents 10 -C 16 Stability test of premixes containing APG (APG-1) Following the general procedure and setup of the premix, APG-1 (50-53% aqueous solution) and various solvents were mixed (alkyl polyglycoside: APG-1 commercially available from BASF).
[0056] The premix process was carried out according to the method for determining apparent viscosity specified in ISO 2555 using a four-blade propeller stirrer (IKA R 1342) at a stirring speed of 300 rpm and in a water bath at 45° C. for 30 min.
[0057] After stability testing of the premixes, the viscosity and crystallization state were tracked and recorded, and the results are shown in Table 2.
[0058] [Table 2]
[0059] Premixes of water and organic solvents commonly used in liquid laundry and dishwashing detergent formulations are 10 -C 16Although the viscosity of APG can be significantly reduced, this still does not prevent crystallization at low temperatures, especially at 5°C.
[0060] 3. C4-C as a hydrotrope 10 C with alkyl polyglucosides 10 -C 16 Stability testing of premixes containing alkyl polyglucosides Following the general procedure and setup of the premix, alkyl polyglycosides were mixed in aqueous solution with or without hydrotrope (alkyl polyglycosides: APG-1 commercially available from BASF).
[0061] The premix process was carried out according to the method for determining apparent viscosity specified in ISO 2555 using a four-blade propeller stirrer (IKA R 1342) at a stirring speed of 300 rpm and in a water bath at 45° C. for 30 min.
[0062] After stability testing of the premixes, the viscosity and crystallization state were tracked and recorded, and the results are shown in Table 3.
[0063] [Table 3]
[0064] C8-C 10 Low alkyl chain polyglycosides such as alkyl polyglucosides are easy to handle and have the C 10 -C 16 It can also be used as a hydrotrope by premixing with alkyl polyglucosides, however high concentrations of low alkyl chain polyglucosides (>20%) are required to achieve the desired properties.
[0065] For example, Premix-6 contains 20% C8-C 10 Alkyl polyglucosides were included, which inhibited crystallization, but the viscosity was still too high at 5°C. 10Alkyl polyglucosides predominated at the 35% dosage level, resulting in both crystallization inhibition and low viscosity. However, C8-C 10 Excessive dilution with alkyl polyglycosides results in C 10 -C 16 This can lead to a significant loss of performance provided by the alkyl polyglycosides.
[0066] In addition, even shorter chain APGs, specifically about 10% C4-C8 alkyl polyglucosides, are also 10 -C 16 Alkyl polyglucoside (C 10 -C 16 APG was premixed with Premix-8 and Premix-9) at a dilution of less than 20%. However, the premixes were not stable at 5°C for more than one month and crystallization was inhibited.
[0067] The results are shown in Table 1. 10 -C 16 This illustrates that premixes containing APG have more desirable stability performance than other premixes containing hydrotropes other than SCS.
[0068] 4. Various weight ratios of C 10 -C 16 Stability study of premixes containing APG (APG-1) and sodium cumene sulfonate Following the general procedure and setup of the premix, alkyl polyglycosides and sodium cumene sulfonate were premixed in an aqueous solution (alkyl polyglycosides: APG-1, commercially available from BASF).
[0069] The premix process was carried out according to the method for determining apparent viscosity specified in ISO 2555, using a four-blade propeller stirrer (IKA R1342) at a stirring speed of 300 rpm and under a water bath at 45° C. for 30 min.
[0070] After stability testing of the premixes, the crystallization status was recorded and the results are shown in Table 4.
[0071] [Table 4]
[0072] The results are shown in Table 1. 10 -C 16 It is shown that the premix containing APG and sodium cumene sulfonate demonstrates excellent stability performance without the appearance of crystals even over a period of more than three months.
Claims
1. A premix comprising an alkyl polyglycoside, at least one hydrotrope, and at least one solvent, - The alkyl polyglycoside has the formula: C n H 2n+1 O(C 6 H 10 O 5 ) x characterized by H, wherein n is an integer from 8 to 18, preferably from 8 to 16, more preferably from 10 to 16, and x is from 1 to 3, preferably from 1.1 to about 2.7, more preferably from 1.2 to 2, - The at least one hydrotrope is selected from the group consisting of sodium cumenesulfonate, sodium xylenesulfonate, sodium toluenesulfonate, dioctyl sodium sulfosuccinate, alkylnaphthalenesulfonate, and dihexyl sodium sulfosuccinate, and preferably, the hydrotrope is sodium cumenesulfonate, - The at least one solvent comprises water and optionally at least one water-miscible organic solvent, and preferably, the solvent is essentially only water, more preferably water, premix.
2. The alkyl polyglycoside having an alkyl group of 10 to 16 carbon atoms is present in the range of 60% to about 100%, preferably 70%, 75%, 80%, 85%, 90%, 95% or 98% to 100% by weight of the total weight of the alkyl polyglycoside, the premix according to claim 1.
3. The weight ratio of the alkyl polyglycoside to the hydrotrope is from 30 / 70 to 90 / 10, preferably from 70 / 30 to 85 / 15, more preferably from 75 / 25 to 80 / 20, and preferably, the alkyl polyglycoside has an alkyl group of 10 to 16 carbon atoms, the premix according to claim 1.
4. The at least one water-miscible organic solvent is selected from methanol, ethanol, propanol, isopropanol, glycerol, propylene glycol, ethylene glycol, 1,2-propanediol, sorbitol, and any mixture thereof, the premix according to claim 1.
5. The solvent is present in an amount of 40% to 90%, preferably 45% to 65% by weight of the total weight of the premix, the premix according to claim 1.
6. - Having a pour point of -10°C to 5°C, preferably -10°C to 0°C, more preferably -10°C to -3°C, the premix according to claim 1.
7. A liquid detergent formulation obtained by mixing the premix according to any one of claims 1 to 6 with at least one component selected from anionic, cationic, nonionic, zwitterionic, amphoteric surfactants, fatty acids, citric acid and / or other builders, chelating agents, bleaching agents and bleach activators, enzymes, foam inhibitors, ethanol, an organic solvent containing 1,2-propanediol, and soil removal polymers.
8. The liquid detergent formulation according to claim 7, which is a liquid detergent formulation or a liquid dishwashing formulation.
9. A method for preparing a liquid laundry detergent formulation or a liquid dishwashing detergent formulation, comprising the step of adding the premix according to any one of claims 1 to 6 to the formulation at the start, after completion, or at any point during the preparation of the formulation.
10. Use of the premix according to any one of claims 1 to 6 for preparing a liquid laundry detergent formulation or a liquid dishwashing detergent formulation.