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WO2022128369A1 - Composition - Google Patents

Composition Download PDF

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Publication number
WO2022128369A1
WO2022128369A1 PCT/EP2021/082737 EP2021082737W WO2022128369A1 WO 2022128369 A1 WO2022128369 A1 WO 2022128369A1 EP 2021082737 W EP2021082737 W EP 2021082737W WO 2022128369 A1 WO2022128369 A1 WO 2022128369A1
Authority
WO
WIPO (PCT)
Prior art keywords
alkyl
composition according
composition
water
anionic surfactant
Prior art date
Application number
PCT/EP2021/082737
Other languages
English (en)
Inventor
Sarmistha BISWAS
Rachana SANKAR
Original Assignee
Unilever Ip Holdings B.V.
Unilever Global Ip Limited
Conopco, Inc., D/B/A Unilever
HAZRA, Swarnaditya
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unilever Ip Holdings B.V., Unilever Global Ip Limited, Conopco, Inc., D/B/A Unilever, HAZRA, Swarnaditya filed Critical Unilever Ip Holdings B.V.
Publication of WO2022128369A1 publication Critical patent/WO2022128369A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • C11D1/146—Sulfuric acid esters
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/83—Mixtures of non-ionic with anionic compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2068—Ethers
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2075—Carboxylic acids-salts thereof
    • C11D3/2079—Monocarboxylic acids-salts thereof
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2093—Esters; Carbonates
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/22—Carbohydrates or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/43—Solvents

Definitions

  • the present invention relates to a highly concentrated liquid laundry or liquid dishwash composition.
  • a concentrated isotropic liquid detergent composition comprising less than 5% water, anionic surfactant, non-ionic surfactant and up to 20 % wt. non-aqueous solvent, wherein the anionic surfactant is alkyl ether sulphate and/or linear alkyl benzene sulphonate.
  • non-aqueous solvents are able to provide appropriate physical performance characteristics in the context of laundry and dishwash detergents whether composition which can be used to form a wash liquor in the normal manner, concentrated formulations which can be diluted by the consumer to form liquid detergent compositions or unit dose formulations which are typically packaged in water dissoluble films.
  • Preferred solvents include:
  • -glycol ethers e.g. diethylene glycol alkyl ether (esp. diethylene butyl ether), dipropylene glycol alkyl ether, especially dipropylene dimethyl ether)
  • diethylene glycol alkyl ether esp. diethylene butyl ether
  • dipropylene glycol alkyl ether especially dipropylene dimethyl ether
  • alkyl esters e.g. alkyl levulinate, preferably where alkyl is C1-C4 and most preferably where alkyl is ethyl; alkyl octanoate, preferably where alkyl is C1-C4 and most preferably where alkyl is methyl and alkyl soyate, preferably where alkyl is C1-C4 and most preferably where alkyl is methyl).
  • alkyl esters are ethyl levulinate, methyl soyate and methyl octanoate.
  • alkyl amides e.g. N, N-dimethyl alkenamide, more preferably N, N-dimethyl decenamide.
  • Preferred solvents include those with a Hansen Solubility Parameter D between 15 and 17; a P value between 5 and 10 and a H value between 6 and 23.
  • the solvent is present at from 1 to 20% wt. of the composition, more preferably from 1.5 to 15% wt. and especially preferably from 2 to 10% wt. of the composition.
  • the alkyl ether sulphate anionic surfactant comprises a monoisopropylamine (MIPA) and/or triisopropanolamine (TIPA) counterion.
  • MIPA monoisopropylamine
  • TIPA triisopropanolamine
  • the MIPA and/or TIPA non-soap anionic surfactant comprises from 50 to 100% wt. of the anionic surfactant, more preferably from 75% to 100% and more preferably from 90 to 100% wt. of the non-soap anionic surfactant present.
  • the anionic surfactant with a MIPA and/or TIPA counterion is a C10-18 alkyl ether sulphate. Most preferably, it is a C12 based alkyl ether sulphate. The most preferred is MIPA LES, a C12 alkyl ether sulphate with MIPA counterion.
  • Weight proportions are calculated for the protonated form of the appropriate surfactant.
  • the composition is visually clear.
  • visually clear means that the composition when diluted 1 part premix in 3 parts water is less than 20 NTU.
  • the composition comprises non-ionic surfactant.
  • the composition comprises from 10 to 80% wt. non-ionic surfactant based on the total weight of composition, more preferably from 30 to 60% wt. non-ionic surfactant by weight of the composition.
  • surfactant in the context of particulate detergent formulations denotes a surfactant which provides a detersive (i.e. cleaning) effect to dishwash compositions or laundry compositions which are used as part of a domestic laundering process.
  • the non-ionic surfactant comprises a secondary alcohol ethoxylate.
  • the secondary alcohol ethoxylate comprises an alkyl chain with a secondary ethoxylate joined thereto.
  • the secondary ethoxylate comprises from 2 to 20 EO groups, preferably from 5 to 12 and most preferably 9 EO groups.
  • the alkyl chain preferably comprises from 8 to 22 carbons, more preferably from 10 to 14 and most preferably 12.
  • the alkyl chain is preferably saturated.
  • the secondary alcohol ethoxylate is according to the following formula (I):
  • a preferred secondary alcohol ethoxylate is Tergitol 15-S 9 ex Dow.
  • the secondary alcohol ethoxylate is present at from 10 to 100% wt. of the total non-ionic surfactant, more preferably from 12% by wt. of the total non-ionic surfactant.
  • non-ionics the polyoxyalkylene compounds which have a variety of block and heteric (random) structures.
  • they can comprise a single block of alkylene oxide, or they can be diblock alkoxylates or triblock alkoxylates.
  • the blocks can be all ethylene oxide or all propylene oxide, or the blocks can contain a heteric mixture of alkylene oxides.
  • Examples of such materials include Cs to C22 alkyl phenol ethoxylates with an average of from 5 to 25 moles of ethylene oxide per mole of alkyl phenol; and aliphatic alcohol ethoxylates such as Cs to Cis primary or secondary linear or branched alcohol ethoxylates with an average of from 2 to 40 moles of ethylene oxide per mole of alcohol.
  • a preferred class of nonionic surfactant (additional to the secondary alcohol ethoxylate) for use in the invention includes aliphatic C12 to C15 primary linear alcohol ethoxylates with an average of from 3 to 20, more preferably from 5 to 10 moles of ethylene oxide per mole of alcohol.
  • the alcohol ethoxylate may be provided in a single raw material component or by way of a mixture of components.
  • a further class of non-ionic surfactants include the alkyl poly glycosides.
  • the composition comprises an anionic surfactant.
  • Non-soap anionic surfactants for use in the invention are typically salts of organic sulfates and sulfonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term “alkyl” being used to include the alkyl portion of higher acyl radicals. Examples of such materials include alkyl sulfates, C12-C14 alkyl ether sulfates, alkaryl sulfonates, alpha-olefin sulfonates and mixtures thereof.
  • the alkyl radicals preferably contain from 10 to 18 carbon atoms and may be unsaturated.
  • the C12-C14 alkyl ether sulfates may contain from one to ten ethylene oxide or propylene oxide units per molecule, and preferably contain one to three ethylene oxide units per molecule.
  • C12-C14 alkyl ether sulfates having a straight or branched chain alkyl group having 12 to 14 carbon atoms and containing an average of 1 to 3EO units per molecule.
  • a preferred example is sodium lauryl ether sulfate (SLES) in which the predominantly C12 lauryl alkyl group has been ethoxylated with an average of 3EO units per molecule.
  • the C12-C14 alkyl ether sulphate may be provided in a single raw material component or by way of a mixture of components.
  • the counterion for any of the anionic surfactants used in the compositions described herein is principally a monoisopropylamine (MIPA) and/or Triisopropanolamine (TIPA), but others are additionally available. These include alkali metals such as sodium or potassium; or an ammoniacal counterion such as ammonium, monoethanolamine, (MEA), diethanolamine (DEA) or triethanolamine (TEA). Mixtures of such counterions may also be employed.
  • MIPA monoisopropylamine
  • TIPA Triisopropanolamine
  • alkali metals such as sodium or potassium
  • an ammoniacal counterion such as ammonium, monoethanolamine, (MEA), diethanolamine (DEA) or triethanolamine (TEA). Mixtures of such counterions may also be employed.
  • compositions according to the invention may preferably include alkylbenzene sulfonates, particularly linear alkylbenzene sulfonates (LAS) with an alkyl chain length of from 10 to 18 carbon atoms.
  • LAS linear alkylbenzene sulfonates
  • Commercial LAS is a mixture of closely related isomers and homologues alkyl chain homologues, each containing an aromatic ring sulfonated at the “para" position and attached to a linear alkyl chain at any position except the terminal carbons.
  • the linear alkyl chain typically has a chain length of from 11 to 15 carbon atoms, with the predominant materials having a chain length of about C12.
  • Each alkyl chain homologue consists of a mixture of all the possible sulfophenyl isomers except for the 1 -phenyl isomer.
  • LAS is normally formulated into compositions in acid (i.e. HLAS) form and then at least partially neutralized in-situ.
  • alkyl sulfate surfactant may be used, such as non-ethoxylated primary and secondary alkyl sulphates with an alkyl chain length of from 10 to 18.
  • the composition comprises an anionic surfactant.
  • the composition comprises from 10 to 80% wt. anionic surfactant based on the total weight of composition, more preferably from 30 to 60% wt. anionic surfactant by weight of the composition.
  • composition is a dishwash composition it preferably comprises a fatty amide.
  • Suitable fatty amides include cocoamidopropyl betaine (CAPB), coco amido propyl amine oxide (CAPAO), cocodiethanol amide (CDEA) and cocomonoethanol amide (CMEA).
  • Most preferred amphoteric surfactant is cocoamidopropyl betaine.
  • the fatty amide is present at from 0.1 to 10% wt. of the composition.
  • Suitable fatty acids for laundry liquid compositions in the context of this invention include aliphatic carboxylic acids of formula RCOOH, where R is a linear or branched alkyl or alkenyl chain containing from 6 to 24, more preferably 10 to 22, most preferably from 12 to 18 carbon atoms and 0 or 1 double bond.
  • R is a linear or branched alkyl or alkenyl chain containing from 6 to 24, more preferably 10 to 22, most preferably from 12 to 18 carbon atoms and 0 or 1 double bond.
  • saturated C 12-18 fatty acids such as lauric acid, myristic acid, palmitic acid or stearic acid
  • fatty acid mixtures in which 50 to 100% (by weight based on the total weight of the mixture) consists of saturated C12-18 fatty acids.
  • Such mixtures may typically be derived from natural fats and/or optionally hydrogenated natural oils (such as coconut oil, palm kernel oil or tallow).
  • the fatty acids may be present in the form of their sodium, potassium or ammonium salts and/or in the form of soluble salts of organic bases, such as mono-, di- or triethanolamine. Mixtures of any of the above described materials may also be used.
  • Fatty acids and/or their salts when included, may be present in an amount ranging from about 0.25 to 5%, more preferably from 0.5 to 5%, most preferably from 0.75 to 4% (by weight based on the total weight of the composition).
  • fatty acids and/or their salts are not included in the level of surfactant or in the level of builder.
  • a composition of the invention may incorporate non-aqueous carriers such as hydrotropes, cosolvents and phase stabilizers.
  • non-aqueous carriers such as hydrotropes, cosolvents and phase stabilizers.
  • Such materials are typically low molecular weight, water-soluble or water-miscible organic liquids such as C1 to C5 monohydric alcohols (such as ethanol and n- or i- propanol); C2 to C6 diols (such as monopropylene glycol and dipropylene glycol); C3 to C9 triols (such as glycerol); polyethylene glycols having a weight average molecular weight (M w ) ranging from about 200 to 600; C1 to C3 alkanolamines such as mono-, di- and triethanolamines; and alkyl aryl sulfonates having up to 3 carbon atoms in the lower alkyl group (such as the sodium and potassium xylene, toluene, eth
  • Non-aqueous carriers when included, may be present in an amount ranging from 0.1 to 20%, preferably from 2 to 15%, and more preferably from 10 to 14% (by weight based on the total weight of the composition).
  • the level of hydrotrope used is linked to the level of surfactant and it is desirable to use hydrotrope level to manage the viscosity in such compositions.
  • the preferred hydrotropes are monopropylene glycol and glycerol.
  • the composition comprises less than 5% water.
  • free water water which is added to the composition and does not include water which is added along with a further raw material in which it is incorporated.
  • surfactants are commercially available as aqueous solutions or suspensions of surfactants.
  • the composition comprises less than 1 % wt. water.
  • Water-Soluble Film Compositions are particularly preferred.
  • composition according to the invention is a unit dose composition it is preferably contained within a pouch formed by a water dissoluble film.
  • Such water-soluble film compositions, optional ingredients for use therein, and methods of making the same are well known in the art, whether being used for making relatively thin water-soluble films (e.g., as pouch materials) or otherwise.
  • the water-soluble film includes a water dissoluble material.
  • Preferred such materials include polyvinyl alcohol (PVOH), including homopolymers thereof (e.g., including substantially only vinyl alcohol and vinyl acetate monomer units) and copolymers thereof (e.g., including one or more other monomer units in addition to vinyl alcohol and vinyl acetate units).
  • PVOH is a synthetic resin generally prepared by the alcoholysis, usually termed hydrolysis or saponification, of polyvinyl acetate. Fully hydrolyzed PVOH, wherein virtually all the acetate groups have been converted to alcohol groups, is a strongly hydrogen-bonded, highly crystalline polymer which dissolves only in hot water- greater than about 140 degrees Fahrenheit (60 degrees C).
  • PVOH polymer If a sufficient number of acetate groups are allowed to remain after the hydrolysis of polyvinyl acetate, the PVOH polymer then being known as partially hydrolyzed, it is more weakly hydrogen-bonded and less crystalline and is soluble in cold water- less than about 50 degrees Fahrenheit (10 degrees C).
  • An intermediate cold or hot water soluble film can include, for example, intermediate partially- hydrolyzed PVOH (e.g., with degrees of hydrolysis of about 94 percent to about 98 percent), and is readily soluble only in warm water- e.g., rapid dissolution at temperatures of about 40 degrees centigrade and greater. Both fully and partially hydrolyzed PVOH types are commonly referred to as PVOH homopolymers although the partially hydrolyzed type is technically a vinyl alcohol- vinyl acetate copolymer.
  • the degree of hydrolysis (DH) of the PVOH polymers and PVOH copolymers included in the water- soluble films of the present disclosure can be in a range of about 75 percent to about 99 percent (e.g., about 79 percent to about 92 percent, about 86.5 percent to about 89 percent, or about 88 percent, such as for cold-water soluble compositions; about 90 percent to about 99 percent, about 92 percent to about 99 percent, or about 95 percent to about 99 percent).
  • DH degree of hydrolysis
  • the degree of hydrolysis of the PVOH can be chosen such that the water- solubility of the polymer is temperature dependent, and thus the solubility of a film made from the polymer, any compatibilizer polymer, and additional ingredients is also influenced.
  • the film is cold water-soluble.
  • a cold water-soluble film, soluble in water at a temperature of less than 10 degrees centigrade can include PVOH with a degree of hydrolysis in a range of about 75 percent to about 90 percent, or in a range of about 80 percent to about 90 percent, or in a range of about 85 percent to about 90 percent.
  • the film is hot water-soluble.
  • a hot water- soluble film, soluble in water at a temperature of at least about 60 degrees centigrade can include PVOH with a degree of hydrolysis of at least about 98 percent.
  • water soluble polymers for use in addition to the PVOH polymers and PVOH copolymers in the blend can include, but are not limited to modified polyvinyl alcohols, polyacrylates, water-soluble acrylate copolymers, polyvinyl pyrrolidone, polyethyleneimine, pullulan, water-soluble natural polymers including, but not limited to, guar gum, gum Acacia, xanthan gum, carrageenan, and starch, water-soluble polymer derivatives including, but not limited to, modified starches, ethoxylated starch, and hydroxypropylated starch, copolymers of the forgoing and combinations of any of the foregoing.
  • water-soluble polymers can include polyalkylene oxides, polyacrylamides, polyacrylic acids and salts thereof, celluloses, cellulose ethers, cellulose esters, cellulose amides, polyvinyl acetates, polycarboxylic acids and salts thereof, polyaminoacids, polyamides, gelatines, methylcelluloses, carboxymethylcelluloses and salts thereof, dextrins, ethylcelluloses, hydroxyethyl celluloses, hydroxypropyl methylcelluloses, maltodextrins, and polymethacrylates.
  • Such water- soluble polymers, whether PVOH or otherwise are commercially available from a variety of sources. Any of the foregoing water-soluble polymers are generally suitable for use as film-forming polymers.
  • the water- soluble film can include copolymers and/or blends of the foregoing resins.
  • the water-soluble polymers can be included in the film in an amount in a range of about 30 weight percent or 50 weight percent to about 90 weight percent or 95 weight percent, for example.
  • the weight ratio of the amount of all water-soluble polymers as compared to the combined amount of all plasticizers, compatibilizing agents, and secondary additives can be in a range of about 0.5 to about 18, about 0.5 to about 15, about 0.5 to about 9, about 0.5 to about 5, about 1 to 3, or about 1 to 2, for example.
  • the specific amounts of plasticizers and other non-polymer component can be selected in a particular embodiment based on an intended application of the water-soluble film to adjust film flexibility and to impart processing benefits in view of desired mechanical film properties.
  • Water-soluble polymers for use in the film described herein can be characterized by a viscosity in a range of about 3.0 to about 27.0 cP, about 4.0 to about 24.0 cP, about 4.0 to about 23.0 cP, about 4.0 cP to about 15 cP, or about 6.0 to about 10.0 cP, for example.
  • the viscosity of a polymer is determined by measuring a freshly made solution using a Brookfield LV type viscometer with UL adapter as described in British Standard EN IS0 15023-2:2006 Annex E Brookfield Test method.
  • the viscosity of a water-soluble polymer is correlated with the weight- average molecular weig ht (W) of the same polymer, and often the viscosity is used as a proxy for Mw.
  • the weight- average molecular weight of the water- soluble polymers can be in a range of about 30,000 to about 175,000, or about 30,000 to about 100,000, or about 55,000 to about 80,000, for example.
  • the water-soluble film can contain other auxiliary agents and processing agents, such as, but not limited to, plasticizers, plasticizer compatibilizers, surfactants, lubricants, release agents, fillers, extenders, cross-linking agents, antiblocking agents, antioxidants, detackifying agents, antifoams, nanoparticles such as layered silicate-type nanoclays (e.g., sodium montmorillonite), bleaching agents (e.g., sodium metabisulfite, sodium bisulfite or others), aversive agents such as bitterants (e.g., denatonium salts such as denatonium benzoate, denatonium saccharide, and denatonium chloride; sucrose octaacetate; quinine; flavonoids such as quercetin and naringen; and quassinoids such as quassin and brucine) and pungents (e.g., capsaicin, piperine, allyl isothiocyanate, and resinferatoxi
  • Embodiments including plasticizers are preferred.
  • the amount of such agents can be up to about 50 wt. , 20 wt percent, 15 wt percent, 10 wt percent, 5 weight percent, 4 wt percent and/or at least 0.01 weight percent, 0.1 wt percent, 1 wt percent, or 5 wt, individually or collectively.
  • the plasticizer can include, but is not limited to, glycerin, diglycerin, sorbitol, ethylene glycol, diethylene glycol, triethylene glycol, dipropylene glycol, tetraethylene glycol, propylene glycol, polyethylene glycols up to 400 MW, neopentyl glycol, trimethylolpropane, polyether polyols, sorbitol, 2-methyl-l,3-propanediol, ethanolamines, and a mixture thereof.
  • a preferred plasticizer is glycerin, sorbitol, triethyleneglycol, propylene glycol, diproyplene glycol, 2-methyl-l,3-propanediol, trimethylolpropane, or a combination thereof.
  • the total amount of the plasticizer can be in a range of about 10 weight percent to about 40 wt. , or about 15 weight percent to about 35 wt. , or about 20 weight percent to about 30 wt., for example about 25 wt., based on total film weight.
  • glycerin can be used in an amount of about 5 wt percent to about 30 wt, or 5 wt percent to about 20 wt, e.g., about 13 wt percent.
  • dipropylene glycol can be used in an amount of about 1 weight percent to about 20 wt., or about 3 weight percent to about 10 wt., for example 6 weight percent.
  • sorbitol can be used in an amount of about 1 wt percent to about 20 wt, or about 2 wt percent to about 10 wt, e.g., about 5 wt percent.
  • the specific amounts of plasticizers can be selected in a particular embodiment based on desired film flexibility and processability features of the water-soluble film. At low plasticizer levels, films may become brittle, difficult to process, or prone to breaking. At elevated plasticizer levels, films may be too soft, weak, or difficult to process for a desired use.
  • the composition comprises a taste aversive such as denatonium benzoate and/or a pungent agent such as capsaicin.
  • composition is a unit dosed composition of from 4 to 12ml and contained within a water dissoluble pouch as described above.
  • a composition may also contain one or more cosurfactants (such as amphoteric (zwitterionic) and/or cationic surfactants) in addition to the non-soap anionic and/or non-ionic detersive surfactants described above.
  • cosurfactants such as amphoteric (zwitterionic) and/or cationic surfactants
  • Specific cationic surfactants include Cs to Cis alkyl dimethyl ammonium halides and derivatives thereof in which one or two hydroxyethyl groups replace one or two of the methyl groups, and mixtures thereof.
  • Cationic surfactant when included, may be present in an amount ranging from 0.1 to 5% (by weight based on the total weight of the premix composition).
  • amphoteric (zwitterionic) surfactants include alkyl amine oxides, alkyl betaines, alkyl amidopropyl betaines, alkyl sulphobetaines (sultaines), alkyl glycinates, alkyl carboxyglycinates, alkyl amphoacetates, alkyl amphopropionates, alkylamphoglycinates, alkyl amidopropyl hydroxysultaines, acyl taurates and acyl glutamates, having alkyl radicals containing from about 8 to about 22 carbon atoms, the term “alkyl” being used to include the alkyl portion of higher acyl radicals.
  • Amphoteric (zwitterionic) surfactant when included, may be present in an amount ranging from 0.1 to 5% (by weight based on the total weight of the composition).
  • a composition may also contain one or more chelating agents fortransition metal ions. Such chelating agents may also have calcium and magnesium chelation capacity, but preferentially bind heavy metal ions such as iron, manganese and copper. Such chelating agents may help to improve the stability of the composition and protect for example against transition metal catalyzed decomposition of certain ingredients.
  • Suitable transition metal ion chelating agents include phosphonates, in acid and/or salt form.
  • alkali metal e.g. sodium and potassium
  • alkanolammonium salts are preferred.
  • Specific examples of such materials include aminotris(methylene phosphonic acid) (ATMP), 1-hydroxyethylidene diphosphonic acid (HEDP) and diethylenetriamine penta(methylene phosphonic acid (DTPMP) and their respective sodium or potassium salts.
  • HEDP is preferred. Mixtures of any of the above described materials may also be used.
  • Transition metal ion chelating agents when included, may be present in an amount ranging from about 0.1 to about 10%, preferably from about 0.1 to about 3% (by weight based on the total weight of the composition). Mixtures of any of the above described materials may also be used.
  • a composition may also comprise an effective amount of one or more enzyme selected from the group comprising, pectate lyase, protease, amylase, cellulase, lipase, mannanase and mixtures thereof.
  • the enzymes are preferably present with corresponding enzyme stabilizers.
  • a composition may contain further optional ingredients to enhance performance and/or consumer acceptability.
  • additional optional ingredients include foam control agents, preservatives (e.g. bactericides), fluorescers and pearlisers.
  • preservatives e.g. bactericides
  • fluorescers e.g. bactericides
  • pearlisers e.g. bactericides
  • Each of these ingredients will be present in an amount effective to accomplish its purpose.
  • these optional ingredients are included individually at an amount of up to 5% (by weight based on the total weight of the composition).
  • a composition of the invention may be packaged as unit dose in polymeric film soluble in the wash water.
  • a composition of the invention may be supplied in multidose plastics packs with a top or bottom closure.
  • a dosing measure may be supplied with the pack either as a part of the cap or as an integrated system.
  • a method for forming a dishwash or laundry liquid composition by taking a composition as described herein and adding from 3 to 100 parts of water to one part of composition and mixing.
  • the resulting laundry or dishwash liquid composition is stable and may be kept by the consumer until ready for use as a liquid detergent composition.
  • a packaged product comprising a composition as described herein.

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Abstract

La composition détergente liquide isotrope concentrée comprend moins de 5 % d'eau, un tensioactif anionique, un tensioactif non ionique et jusqu'à 20 % en poids de solvant non aqueux, le tensioactif anionique étant un sulfate d'alkyl éther et/ou un alkylbenzène sulfonate linéaire.
PCT/EP2021/082737 2020-12-14 2021-11-24 Composition WO2022128369A1 (fr)

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IN202021054416 2020-12-14
IN202021054416 2020-12-14
EP21153183.5 2021-01-25
EP21153183 2021-01-25

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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001010993A1 (fr) * 1999-08-10 2001-02-15 The Procter & Gamble Company Compositions detergentes comportant des hydrotropes
WO2002053695A2 (fr) * 2001-01-05 2002-07-11 Henkel Kommanditgesellschaft Auf Aktien Portion d'agent de lavage, d'agent de rinçage ou d'agent de nettoyage contenant des tensioactifs
US20030100468A1 (en) * 1997-12-19 2003-05-29 The Procter & Gamble Company Nonaqueous, particulate-containing liquid detergent compositions with alkyl benzene sulfonate surfactant
US20060247146A1 (en) * 2005-04-22 2006-11-02 Robert Greenberg Colloidal cleaning system
US20100041577A1 (en) * 2008-08-14 2010-02-18 Melaleuca, Inc. Ultra Concentrated Liquid Laundry Detergent
US20160067661A1 (en) * 2013-04-24 2016-03-10 Clariant International Ltd. Benzyl Alcohol Alkoxylates As Solubilizers For Aqueous Surfactant Solutions
CN111088121A (zh) * 2020-01-09 2020-05-01 广州市加茜亚化妆品有限公司 一种含醇醚溶剂的洗衣凝珠及其制备方法
WO2020214996A1 (fr) * 2019-04-18 2020-10-22 Pilot Chemical Corp. Compositions tensioactives concentrées liquides

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030100468A1 (en) * 1997-12-19 2003-05-29 The Procter & Gamble Company Nonaqueous, particulate-containing liquid detergent compositions with alkyl benzene sulfonate surfactant
WO2001010993A1 (fr) * 1999-08-10 2001-02-15 The Procter & Gamble Company Compositions detergentes comportant des hydrotropes
WO2002053695A2 (fr) * 2001-01-05 2002-07-11 Henkel Kommanditgesellschaft Auf Aktien Portion d'agent de lavage, d'agent de rinçage ou d'agent de nettoyage contenant des tensioactifs
US20060247146A1 (en) * 2005-04-22 2006-11-02 Robert Greenberg Colloidal cleaning system
US20100041577A1 (en) * 2008-08-14 2010-02-18 Melaleuca, Inc. Ultra Concentrated Liquid Laundry Detergent
US20160067661A1 (en) * 2013-04-24 2016-03-10 Clariant International Ltd. Benzyl Alcohol Alkoxylates As Solubilizers For Aqueous Surfactant Solutions
WO2020214996A1 (fr) * 2019-04-18 2020-10-22 Pilot Chemical Corp. Compositions tensioactives concentrées liquides
CN111088121A (zh) * 2020-01-09 2020-05-01 广州市加茜亚化妆品有限公司 一种含醇醚溶剂的洗衣凝珠及其制备方法

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