WO1994001520A1 - Concentrated aqueous liquid detergent comprising polyvinylpyrrolidone - Google Patents

Concentrated aqueous liquid detergent comprising polyvinylpyrrolidone Download PDF

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Publication number
WO1994001520A1
WO1994001520A1 PCT/US1993/006086 US9306086W WO9401520A1 WO 1994001520 A1 WO1994001520 A1 WO 1994001520A1 US 9306086 W US9306086 W US 9306086W WO 9401520 A1 WO9401520 A1 WO 9401520A1
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WIPO (PCT)
Prior art keywords
weight
alkyl
composition according
polyvinylpyrrolidone
liquid detergent
Prior art date
Application number
PCT/US1993/006086
Other languages
French (fr)
Inventor
Serge Gabriel Pierre Roger Cauwberghs
Ivan Maurice Alfons Jan Herbots
Original Assignee
The Procter & Gamble Company
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Priority to JP6503360A priority Critical patent/JPH07508788A/en
Publication of WO1994001520A1 publication Critical patent/WO1994001520A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/83Mixtures of non-ionic with anionic compounds
    • C11D1/831Mixtures of non-ionic with anionic compounds of sulfonates with ethers of polyoxyalkylenes without phosphates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3769(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
    • C11D3/3776Heterocyclic compounds, e.g. lactam
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38618Protease or amylase in liquid compositions only
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38645Preparations containing enzymes, e.g. protease or amylase containing cellulase
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/525Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain two or more hydroxy groups per alkyl group, e.g. R3 being a reducing sugar rest

Definitions

  • the present invention relates to concentrated aqueous liquid detergent compositions containing polyvinyl ⁇ pyrrolidone, in which the anionic surfactant majorily consists of an alkyl ethoxy sulfate salt.
  • a new trend in the field of detergent compositions is the formulation of so-called concentrated detergents.
  • concentrated detergents In the context of liquid aqueous detergents, this refers to products comprising less water and a higher total amount of active ingredients.
  • the present invention is directed to liquid detergent compositions comprising an anionic surface-active agent, and from 2% to 35% by weight of the total composition of water, characterized in that the anionic surfactant contains at least 70%, preferably from 75% to 100% by weight of a water- soluble C 1:L _i 5 alkyl ethoxy sulfate salt containing an average per mole of from 1 to 9 ethoxy groups and that the composition comprises from 0.05% to 5% by weight of the total composition of polyvinylpyrrolidone.
  • compositions preferably contain less than 6% by weight of the total composition of alkyl benzene sulfonate salt or non-ethoxylated alkyl sulfate salt.
  • compositions according to the present invention are concentrated liquid detergents which comprise from 2% to 35% by weight of the total composition of water.
  • compositions according to the present invention comprise from 5% to 25% by weight of the total composition of water.
  • compositions according to the invention contain from 0.05% to 5% by weight of polyvinlypyrrolidone, preferably from 0.25% to 2%.
  • Preferred polyvinylpyrrolidone for use herein have a molecular weight of from 1000 to 100,000, preferably from 2500 to 30,000, most preferably from 5000 to 15,000.
  • compositions according to the present invention comprise a surfactant, and in particular an anionic surface active agent.
  • the anionic surfactant (hereafter meant as not including soaps) contains at least 70% by weight of said anionic surfactant, of a water soluble alkyl ethoxy sulfate salt containing an average of from 1 to 9 ethoxy groups per mole.
  • the C ⁇ -C ⁇ alkyl ethoxy sulfate salt herein comprises a primary alkyl ethoxy sulfate derived from the condensation product of a C 11 -C 15 alcohol with an average of up to 9 ethylene oxide groups.
  • C 13 -C 15 alkyl ethoxy sulfate with an average of two to three ethoxy groups per mole is preferred.
  • the C-L2-C- L 5 alcohol itself can be obtained from natural or synthetic sources.
  • C11- 15 alcohols, derived from natural fats, or Ziegler olefin build-up, or OXO synthesis can form suitable sources for the alkyl group.
  • synthetically derived materials include Dobanol 23 (RTM) sold by Shell Chemicals (UK) Ltd., Ethyl 24 sold by the Ethyl Corporation, a blend of C- j ⁇ -C- j ⁇ alcohols in the ratio 67%
  • C 13 33% C 15 sold under the trade name Lutensol by BASF GmbH and Synperonic (RTM) by ICI Ltd., and Lial 125 sold by Liquichimica Italiana.
  • Examples of naturally occurring materials from which the alcohols can be derived are coconut oil and palm kernel oil and the corresponding fatty acids.
  • the alkyl ethoxy sulfate salts are preferably present in the compositions herein at levels of from 75% to 100% by weight of the anionic surfactant system.
  • the anionic surfactant system may contain other types of surface-active agents, although in minor quantities; in particular, the present detergent compositions should contain less than 6% by weight of the total composition of alkyl benzene sulfonates and non-ethoxylated alkyl sulfates such as C3 . 2-14 primary alkyl sulfate salts;
  • anionic co-surfactants which may be present in minor quantities in the present compositions include C ⁇ -C ⁇ g s_ alkane sulfonates and alpha-sulphonated methyl fatty acid esters in which the fatty acid is derived from a Ci2 ⁇ i8 fatty source.
  • Suitable co-anionic surfactants suitable for the compositions herein are the alkali metal sarcosinates of formula
  • R is a C9-C17 linear or branched alkyl or alkenyl group
  • R* is a C1-C4 alkyl group
  • M is an alkali metal ion.
  • Preferred examples are the lauroyl, Cocoyl (C12-C-J . 4) myristyl and oleyl methyl sarcosinates in the form of their sodium salts.
  • compositions preferably also contain a nonionic surfactant in combination with the alkyl ethoxy sulfate salts herein;
  • Preferred nonionic surfactants for use herein are polyhydroxy fatty acid amides of the formula R 2 -C - N-Z,
  • R 1 wherein R 1 is H, C**- ⁇ hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl or a mixture thereof, R 2 is C 5 _ 3 i hydrocarbyl, and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyIs directly connected to the chain, or an alkoxylated derivative thereof.
  • R 1 is methyl
  • R 2 is a straight C- j ⁇ -is alkyl or alkenyl chain or mixtures thereof
  • Z is derived from a reducing sugar such as glucose, fructose, maltose, lactose, in a reductive amination reaction.
  • Nonionic surfactants suitable for use herein include those produced by condensing ethylene oxide with a hydrocarbon having a reactive hydrogen atom, e.g., a hydroxyl, carboxyl, or amido group, in the presence of an acidic or basic catalyst, and include compounds having the general formula RA(CH 2 CH 2 ⁇ )nH wherein R represents the hydrophobic moiety, A represents the group carrying the reactive hydrogen atom and n represents the average number of ethylene oxide moieties. R typically contains from about 8 to 22 carbon atoms. They can also be formed by the condensation of propylene oxide with a lower molecular weight compound. n usually varies from about 2 to about 24.
  • a preferred class of such nonionic ethoxylates is represented by the condensation product of a fatty alcohol having from 12 to 15 carbon atoms and from about 4 to 10 moles of ethylene oxide per mole or fatty alcohol.
  • Suitable species of this class of ethoxylates include : the condensation product of C 12 -C 15 oxo-alcohols and 3 to 9 moles
  • SUBSTITUTE SHEET of ethylene oxide per mole of alcohol the condensation product or narrow cut C- ⁇ -C*-* ⁇ oxo-alcohols and 3 to 9 moles of ethylene oxide per mole of fatty(oxo) alcohol; the condensation product of a narrow cut C 12 ⁇ C 13 fatty(oxo) alcohol and 6,5 moles of ethylene oxide per mole of fatty alcohol; and the condensation products of a C ⁇ o ⁇ c 14 coconut fatty alcohol with a degree of ethoxylation (moles EO/mole fatty alcohol) in the range from 4 to 8.
  • the fatty oxo alcohols while mainly linear can have, depending upon the processing conditions and raw material olefins, a certain degree of branching, particularly short chain such as methyl branching.
  • a degree of branching in the range from 15% to 50% (weight%) is frequently found in commercial oxo alcohols.
  • Another class of nonionic surfactants comprises alkyl polyglucoside compounds of general formula
  • RO(C n H 2n O) t Z x wherein Z is a moiety derived from glucose; R is a saturated hydrophobic alkyl group that contains from 12 to 18 carbon atoms; t is from 0 to 10 and n is 2 or 3; x is from 1.3 to 4, the compounds including less than 10% unreacted fatty alcohol and less than 50% short chain alkyl polyglucosides.
  • Compounds of this type and their use in detergent compositions are disclosed in EP-B 0 070 074, 0 070 077, 0 075 996 and 0 094 118.
  • the surfactant system herein may also contain types of surfactants other than anionic and nonionic species.
  • Suitable cationic surfactants include quaternary ammonium compounds of the formula R1R2R3 4N "1" where R ⁇ , R2 and R3 are methyl groups, and R4 is a C- ⁇ -lS alkyl group, or where R* ⁇ is an ethyl or hydroxy ethyl group, R 2 and R3 are methyl groups and R 4 is a C ⁇ 2 -15 alkyl group.
  • SUBSTITUTESHEET Zwitterionic surfactants include derivatives of aliphatic quaternary ammonium, phosphoniu , and sulfonium compounds in which the aliphatic moiety can be straight or branched chain and wherein one of the aliphatic substituents contains from about 8 to about 24 carbon atoms and another substituent contains, at least, an anionic water-solubilizing group.
  • Particularly preferred zwitterionic materials are the ethoxylated ammonium sulfonates and sulfates disclosed in U.S. Patents 3,925,262, Laughlin et al., issued December 9, 1975 and 3,929,678, Laughlin et al., issued December 30, 1975.
  • Semi-polar nonionic surfactants include water-soluble amine oxides containing one alkyl or hydroxy alkyl moiety of from about 8 to about 28 carbon atoms and two moieties selected from the group consisting of alkyl groups and hydroxy alkyl groups, containing from 1 to about 3 carbon atoms which can optionally be joined into ring structures.
  • the present concentrated detergent compositions typically contain from 25% to 45%, preferably 30% to 40% by weight of surfactant of which the weight ratio of anionic surfactant to nonionic surfactant is typically of 3:1 to 1:1, more preferably 2:1 to 1:1.
  • compositions according to the present invention may further comprise a builder.
  • a builder Any conventional builder system is suitable for use herein including polycarboxylates and fatty acids, materials such as ethylenediamine tetraacetate, metal ion sequestrants such as aminopolyphosphonates, particularly ethylenediamine tetramethylene phosphonic acid and diethylene triamine pentamethylenephosphonic acid.
  • phosphate builders can also be used herein.
  • Suitable polycarboxylates builders for use herein include citric acid, preferably in the form of a water-soluble salt, derivatives of succinic acid of the formula R- CH(COOH)CH 2 (COOH) wherein R is C 10 _ 2 o alkyl or alkenyl, preferably C 12 -i 6 , or wherein R can be substituted with hydroxyl, sulfo sulfoxyl or sulfone substituents.
  • Specific examples include lauryl succinate, myristyl succinate, palmityl succinate, 2-dodecenylsuccinate, 2-tetradecenyl succinate.
  • Succinate builders are preferably used in the form of their water-soluble salts, including sodium, potassium, ammonium, and alkanolammonium salts.
  • polycarboxylates are oxodisuccinates and mixtures of tartrate monosuccinic and tartrate disuccinic acid such as described in US 4,663,071.
  • Suitable fatty acid builders for use herein are saturated or unsaturated C 10 -i 8 fatty acids, as well as the corresponding soaps.
  • Preferred saturated species have from 12 to 16 carbon atoms in the alkyl chain.
  • the preferred unsaturated fatty acid is oleic acid.
  • a preferred builder system for use herein consists of a mixture of citric acid, fatty acids and succinic acid derivatives described hereinabove.
  • the builder system according to the present invention preferably represents from 5% to 35% by weight of the total composition.
  • compositions according to the invention preferably comprise enzymes.
  • Suitable enzymes for use herein are protease, lipases, cellulases, and a ylases and mixtures thereof.
  • compositions according to the present invention may still advantageously comprise an enzyme stabilizing system, although at reduced levels as compared to compositions where alkyl benzene sulfonate and/or non-ethoxylated alkyl sulfate salts are present in majority.
  • Any conventional enzyme stabilizing system is suitable for use herein, and preferred enzyme stabilizing systems are based on boric acid or derivatives thereof, 1, 2-propanediol, carboxylic acids such as formic acid/formate, and mixtures thereof.
  • anionic surfactant system of the present invention provides improved stability of enzymes such as cellulase in presence of a protease.
  • compositions herein can also advantageously contain a terephthalate-based soil release polymer at levels of from 0.05% to 2% of the total composition.
  • compositions herein can contain a series of further optional ingredients.
  • the like additives include solvents, alkanolamines, pH adjusting agents, suds regulants, opacifiers, agents to improve the machine compatibility in relation to enamel-coated surfaces, perfumes, dyes, bactericides, brighteners, softening agents and the like.

Abstract

The present invention relates to concentrated aqueous liquid detergent compositions containing polyvinylpyrrolidone, especially capable to provide superior color maintenance to the washed fabrics, in which the anionic surfactant majorily consists of an alkyl ethoxy sulfate salt.

Description

"Concentrated Aqueous Liquid Detergent Comprising Polyvinylpyrrolidone"
Technical Field
The present invention relates to concentrated aqueous liquid detergent compositions containing polyvinyl¬ pyrrolidone, in which the anionic surfactant majorily consists of an alkyl ethoxy sulfate salt.
Background of the invention
It is widely known in the art to use various polymers in liquid detergent compositions. The use of polyvinyl pyrrolidone in detergent compositions, mainly for fabric care properties, has been described for instance in EP 262 897, EP 327 927 and EP 203 486. These documents encompass the use of polyvinylpyrrolidone in liquid detergent compositions.
A new trend in the field of detergent compositions is the formulation of so-called concentrated detergents. In the context of liquid aqueous detergents, this refers to products comprising less water and a higher total amount of active ingredients.
SUBSTITUTE SHEET There is a need to provide concentrated detergent compositions which are able to provide superior color maintenance to the washed colored fabrics, that is compositions wherein polyvinylpyrrolidone provides an optimum efficiency as a dye transfer inhibitor agent.
It has now surprisingly been found that such an optimum efficiency of polyvinylpyrrolidone can be achieved in the present concentrated aqueous liquid detergent matrix, when the anionic surfactant in said matrix majorily consists of an alkyl ethoxy sulfate salt.
It has also been found that such a surfactant system improves stability of enzymes such as cellulase, in presence of protease.
Summary of the Invention
The present invention is directed to liquid detergent compositions comprising an anionic surface-active agent, and from 2% to 35% by weight of the total composition of water, characterized in that the anionic surfactant contains at least 70%, preferably from 75% to 100% by weight of a water- soluble C1:L_i5 alkyl ethoxy sulfate salt containing an average per mole of from 1 to 9 ethoxy groups and that the composition comprises from 0.05% to 5% by weight of the total composition of polyvinylpyrrolidone.
The compositions preferably contain less than 6% by weight of the total composition of alkyl benzene sulfonate salt or non-ethoxylated alkyl sulfate salt.
SUBSTITUTE SHEET Detailed Description of the Invention
The compositions according to the present invention are concentrated liquid detergents which comprise from 2% to 35% by weight of the total composition of water.
Preferred compositions according to the present invention comprise from 5% to 25% by weight of the total composition of water.
The compositions according to the invention contain from 0.05% to 5% by weight of polyvinlypyrrolidone, preferably from 0.25% to 2%. Preferred polyvinylpyrrolidone for use herein have a molecular weight of from 1000 to 100,000, preferably from 2500 to 30,000, most preferably from 5000 to 15,000.
The compositions according to the present invention comprise a surfactant, and in particular an anionic surface active agent.
In the compositions of the present invention, it is essential that the anionic surfactant (hereafter meant as not including soaps) contains at least 70% by weight of said anionic surfactant, of a water soluble
Figure imgf000005_0001
alkyl ethoxy sulfate salt containing an average of from 1 to 9 ethoxy groups per mole.
The C^-C^ alkyl ethoxy sulfate salt herein comprises a primary alkyl ethoxy sulfate derived from the condensation product of a C11-C15 alcohol with an average of up to 9 ethylene oxide groups. C13-C15 alkyl ethoxy sulfate with an average of two to three ethoxy groups per mole is preferred.
The C-L2-C-L5 alcohol itself can be obtained from natural or synthetic sources. Thus, C11- 15 alcohols, derived from natural fats, or Ziegler olefin build-up, or OXO synthesis can form suitable sources for the alkyl group. Examples of synthetically derived materials include Dobanol 23 (RTM) sold by Shell Chemicals (UK) Ltd., Ethyl 24 sold by the Ethyl Corporation, a blend of C-j^-C-j^ alcohols in the ratio 67%
C13 33% C15 sold under the trade name Lutensol by BASF GmbH and Synperonic (RTM) by ICI Ltd., and Lial 125 sold by Liquichimica Italiana. Examples of naturally occurring materials from which the alcohols can be derived are coconut oil and palm kernel oil and the corresponding fatty acids.
The alkyl ethoxy sulfate salts are preferably present in the compositions herein at levels of from 75% to 100% by weight of the anionic surfactant system. The anionic surfactant system may contain other types of surface-active agents, although in minor quantities; in particular, the present detergent compositions should contain less than 6% by weight of the total composition of alkyl benzene sulfonates and non-ethoxylated alkyl sulfates such as C3.2-14 primary alkyl sulfate salts;
Other anionic co-surfactants which may be present in minor quantities in the present compositions include C^-C^g s_ alkane sulfonates and alpha-sulphonated methyl fatty acid esters in which the fatty acid is derived from a Ci2~ i8 fatty source.
Other suitable co-anionic surfactants suitable for the compositions herein are the alkali metal sarcosinates of formula
R-CON (R) CH2COOM
wherein R is a C9-C17 linear or branched alkyl or alkenyl group, R* is a C1-C4 alkyl group and M is an alkali metal ion. Preferred examples are the lauroyl, Cocoyl (C12-C-J.4) myristyl and oleyl methyl sarcosinates in the form of their sodium salts.
SUBSTITUTE SHEET The present compositions preferably also contain a nonionic surfactant in combination with the alkyl ethoxy sulfate salts herein;
Preferred nonionic surfactants for use herein are polyhydroxy fatty acid amides of the formula R2-C - N-Z,
II I
O R1 wherein R1 is H, C**-^ hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl or a mixture thereof, R2 is C5_3i hydrocarbyl, and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyIs directly connected to the chain, or an alkoxylated derivative thereof. Preferably, R1 is methyl, R2 is a straight C-j^-is alkyl or alkenyl chain or mixtures thereof, and Z is derived from a reducing sugar such as glucose, fructose, maltose, lactose, in a reductive amination reaction. Preferred are C12 or C12-14 glucosamides.
Other preferred nonionic surfactants suitable for use herein include those produced by condensing ethylene oxide with a hydrocarbon having a reactive hydrogen atom, e.g., a hydroxyl, carboxyl, or amido group, in the presence of an acidic or basic catalyst, and include compounds having the general formula RA(CH2CH2θ)nH wherein R represents the hydrophobic moiety, A represents the group carrying the reactive hydrogen atom and n represents the average number of ethylene oxide moieties. R typically contains from about 8 to 22 carbon atoms. They can also be formed by the condensation of propylene oxide with a lower molecular weight compound. n usually varies from about 2 to about 24.
A preferred class of such nonionic ethoxylates is represented by the condensation product of a fatty alcohol having from 12 to 15 carbon atoms and from about 4 to 10 moles of ethylene oxide per mole or fatty alcohol. Suitable species of this class of ethoxylates include : the condensation product of C12-C15 oxo-alcohols and 3 to 9 moles
SUBSTITUTE SHEET of ethylene oxide per mole of alcohol; the condensation product or narrow cut C-^-C*-*^ oxo-alcohols and 3 to 9 moles of ethylene oxide per mole of fatty(oxo) alcohol; the condensation product of a narrow cut C12~C13 fatty(oxo) alcohol and 6,5 moles of ethylene oxide per mole of fatty alcohol; and the condensation products of a Cχo~c14 coconut fatty alcohol with a degree of ethoxylation (moles EO/mole fatty alcohol) in the range from 4 to 8. The fatty oxo alcohols while mainly linear can have, depending upon the processing conditions and raw material olefins, a certain degree of branching, particularly short chain such as methyl branching. A degree of branching in the range from 15% to 50% (weight%) is frequently found in commercial oxo alcohols.
Another class of nonionic surfactants comprises alkyl polyglucoside compounds of general formula
RO(CnH2nO)tZx wherein Z is a moiety derived from glucose; R is a saturated hydrophobic alkyl group that contains from 12 to 18 carbon atoms; t is from 0 to 10 and n is 2 or 3; x is from 1.3 to 4, the compounds including less than 10% unreacted fatty alcohol and less than 50% short chain alkyl polyglucosides. Compounds of this type and their use in detergent compositions are disclosed in EP-B 0 070 074, 0 070 077, 0 075 996 and 0 094 118.
The surfactant system herein may also contain types of surfactants other than anionic and nonionic species.
Suitable cationic surfactants include quaternary ammonium compounds of the formula R1R2R3 4N"1" where R^, R2 and R3 are methyl groups, and R4 is a C-^-lS alkyl group, or where R*^ is an ethyl or hydroxy ethyl group, R2 and R3 are methyl groups and R4 is a Cι2-15 alkyl group.
SUBSTITUTESHEET Zwitterionic surfactants include derivatives of aliphatic quaternary ammonium, phosphoniu , and sulfonium compounds in which the aliphatic moiety can be straight or branched chain and wherein one of the aliphatic substituents contains from about 8 to about 24 carbon atoms and another substituent contains, at least, an anionic water-solubilizing group. Particularly preferred zwitterionic materials are the ethoxylated ammonium sulfonates and sulfates disclosed in U.S. Patents 3,925,262, Laughlin et al., issued December 9, 1975 and 3,929,678, Laughlin et al., issued December 30, 1975.
Semi-polar nonionic surfactants include water-soluble amine oxides containing one alkyl or hydroxy alkyl moiety of from about 8 to about 28 carbon atoms and two moieties selected from the group consisting of alkyl groups and hydroxy alkyl groups, containing from 1 to about 3 carbon atoms which can optionally be joined into ring structures.
The present concentrated detergent compositions typically contain from 25% to 45%, preferably 30% to 40% by weight of surfactant of which the weight ratio of anionic surfactant to nonionic surfactant is typically of 3:1 to 1:1, more preferably 2:1 to 1:1.
The compositions according to the present invention may further comprise a builder. Any conventional builder system is suitable for use herein including polycarboxylates and fatty acids, materials such as ethylenediamine tetraacetate, metal ion sequestrants such as aminopolyphosphonates, particularly ethylenediamine tetramethylene phosphonic acid and diethylene triamine pentamethylenephosphonic acid. Though less preferred for obvious environmental reasons, phosphate builders can also be used herein.
SUBSTITUTE SHEET Suitable polycarboxylates builders for use herein include citric acid, preferably in the form of a water-soluble salt, derivatives of succinic acid of the formula R- CH(COOH)CH2 (COOH) wherein R is C10_2o alkyl or alkenyl, preferably C12-i6, or wherein R can be substituted with hydroxyl, sulfo sulfoxyl or sulfone substituents. Specific examples include lauryl succinate, myristyl succinate, palmityl succinate, 2-dodecenylsuccinate, 2-tetradecenyl succinate. Succinate builders are preferably used in the form of their water-soluble salts, including sodium, potassium, ammonium, and alkanolammonium salts.
Other suitable polycarboxylates are oxodisuccinates and mixtures of tartrate monosuccinic and tartrate disuccinic acid such as described in US 4,663,071.
Suitable fatty acid builders for use herein are saturated or unsaturated C10-i8 fatty acids, as well as the corresponding soaps. Preferred saturated species have from 12 to 16 carbon atoms in the alkyl chain. The preferred unsaturated fatty acid is oleic acid.
A preferred builder system for use herein consists of a mixture of citric acid, fatty acids and succinic acid derivatives described hereinabove. The builder system according to the present invention preferably represents from 5% to 35% by weight of the total composition.
The compositions according to the invention preferably comprise enzymes. Suitable enzymes for use herein are protease, lipases, cellulases, and a ylases and mixtures thereof.
SUBSTITUTE SHEET The compositions according to the present invention may still advantageously comprise an enzyme stabilizing system, although at reduced levels as compared to compositions where alkyl benzene sulfonate and/or non-ethoxylated alkyl sulfate salts are present in majority. Any conventional enzyme stabilizing system is suitable for use herein, and preferred enzyme stabilizing systems are based on boric acid or derivatives thereof, 1, 2-propanediol, carboxylic acids such as formic acid/formate, and mixtures thereof.
It has been found that the anionic surfactant system of the present invention provides improved stability of enzymes such as cellulase in presence of a protease.
The compositions herein can also advantageously contain a terephthalate-based soil release polymer at levels of from 0.05% to 2% of the total composition.
Such soil release polymers have been extensively described in the art, for instance in US 4,116,885, US 4,132,680, EP 185 427, EP 199 403, EP 241 985 and EP 241 984.
The compositions herein can contain a series of further optional ingredients. Examples of the like additives include solvents, alkanolamines, pH adjusting agents, suds regulants, opacifiers, agents to improve the machine compatibility in relation to enamel-coated surfaces, perfumes, dyes, bactericides, brighteners, softening agents and the like.
The present invention is further illustrated in the following examples.
BSTITUTE SHEET Examples
The following compositions were prepared
(weight % in formula) example 1 example 2
C13-15 Alkyl 3 ethoxylated sulfate 23 18 C13-15 alcohol 7 ethoxylated 6 5 C12-14 N-methyl glucosamide 9 9
Builders 16 17
Ethanol 2 2
1,2 Propane diol 13 10
Mono ethanolamine 13 13
Protease 1.8 0.8 Cellulase 0.15 0.15 Sodium Formate 1.0
Boric acid 2.5 2.0
Polyvinylpyrrolidone*
Water
Minors
Figure imgf000012_0001
* Molecular weight 5000 - 15000, marketed under name GAFTEX AE K15, by ISP
SUBSTITUTE SHEET

Claims

1. A liquid detergent composition comprising an anionic surface-active agent, and from 2% to 35% by weight of the total composition of water, characterized in that the anionic surfactant contains at least 70% by weight of said anionic surfactant of a water-soluble C11_15 alkyl ethoxy sulfate salt containing an average per mole of from 1 to 9 ethoxy groups, and that the composition comprises from 0.05% to 5% by weight of the total composition of polyvinylpyrrolidone.
2 A liquid detergent composition according to claim 1 which comprises from 5% to 25% by weight of the total composition of water.
3. A composition according to claims 1 or 2, which comprises from 0.25% to 2% by weight of the total composition of said polyvinylpyrrolidone.
4. A composition according to any of the preceding claims wherein said polyvinylpyrrolidone has a molecular weight of 5000 to 15000.
5. A composition according to any of the preceding claims wherein the anionic surfactant contains from 75% to 100% by weight of said anionic surfactant of said alkyl ethoxy sulfate salt.
6. A composition according to any of the preceding claims wherein the alkyl ethyxy sulfate salt is a C13-C15 alkyl ethoxy sulfate with an average of two to three ethoxy groups per mole.
7. A composition according to claims 5 or 6 which contains less than 6% by weight of alkyl benzene sulfonate salt or non-ethoxylated alkyl sulfate salt.
SUBSTITUTE SHEET
8. A composition according to any of the preceding claims wherein the surfactant also contains a nonionic surfactant in a weight ratio of anionic to nonionic of from 3:1 to 1:1.
9. A composition according to claim 8 wherein said nonionic surfactant comprises a C12 or C*L2-14 glucosamide.
10. A composition according to any of the preceding claims which contains a protease enzyme and a cellulase enzyme.
SUBSTITUTE SHEET
PCT/US1993/006086 1992-07-03 1993-06-28 Concentrated aqueous liquid detergent comprising polyvinylpyrrolidone WO1994001520A1 (en)

Priority Applications (1)

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JP6503360A JPH07508788A (en) 1992-07-03 1993-06-28 Concentrated aqueous liquid detergent containing polyvinylpyrrolidone

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP19920870098 EP0576778B1 (en) 1992-07-03 1992-07-03 Concentrated aqueous liquid detergent compositions
EP92870098.8 1992-07-03

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WO1994001520A1 true WO1994001520A1 (en) 1994-01-20

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JP (1) JPH07508788A (en)
CA (1) CA2139359A1 (en)
IE (1) IE930498A1 (en)
MX (1) MX9304037A (en)
TR (1) TR26910A (en)
WO (1) WO1994001520A1 (en)

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WO1995027028A1 (en) * 1994-03-31 1995-10-12 The Procter & Gamble Company Detergent composition
US5935922A (en) * 1994-03-31 1999-08-10 The Procter & Gamble Company Detergent composition containing zeolite map for washing a mixture of white and colored fabrics
US6211436B1 (en) * 1996-01-16 2001-04-03 Planttec Biotechnologie Gmbh Nucleic acid molecules from plants coding enzymes which participate in the starch synthesis
US9267095B2 (en) 2013-05-24 2016-02-23 The Procter & Gamble Company Low pH detergent composition comprising nonionic surfactants
US9840681B2 (en) 2013-05-24 2017-12-12 The Procter & Gamble Company Concentrated surfactant composition
US10519400B2 (en) 2013-05-24 2019-12-31 The Procter & Gamble Company Low PH detergent composition

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CA2191563A1 (en) * 1994-06-01 1995-12-07 Serge Gabriel Pierre Roger Cauwberghs Liquid detergent composition containing oleoyl sarcosinates and anionic surfactants
USH1513H (en) * 1994-06-01 1996-01-02 The Procter & Gamble Company Oleoyl sarcosinate with polyhydroxy fatty acid amides in cleaning products
WO1995033025A1 (en) * 1994-06-01 1995-12-07 The Procter & Gamble Company Oleoyl sarcosinate containing detergent compositions
USH1514H (en) * 1994-06-01 1996-01-02 The Procter & Gamble Company Detergent compositions with oleoyl sarcosinate and polymeric dispersing agent
EP0763084A1 (en) * 1994-06-01 1997-03-19 The Procter & Gamble Company Dye transfer inhibiting compositions containing oleoyl sarcosinate
US5798330A (en) * 1995-07-20 1998-08-25 Colgate-Palmolive Co Liquid cleaning compositions
US6025316A (en) * 1995-12-29 2000-02-15 Colgate-Palmolive Co. Detergent composition having improved cleaning power
EP0781837A1 (en) * 1995-12-29 1997-07-02 Colgate-Palmolive Company Detergent composition having improved cleaning power
DE19626338A1 (en) * 1996-07-01 1998-01-08 Vorwerk Co Interholding Carpet stain removers
US5880081A (en) * 1997-04-07 1999-03-09 Gopalkrishnan; Sridhar Concentrated built liquid detergents containing a dye-transfer inhibiting additive
AU1935799A (en) * 1997-12-29 1999-07-19 Colgate-Palmolive Company, The Detergent composition having improved cleaning power
JP2009507085A (en) * 2005-09-02 2009-02-19 ノボザイムス アクティーゼルスカブ Stabilization of concentrated liquid enzyme additives
GB0911294D0 (en) * 2009-06-30 2009-08-12 Reckitt Benckiser Nv Composition

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WO1995027028A1 (en) * 1994-03-31 1995-10-12 The Procter & Gamble Company Detergent composition
US5935922A (en) * 1994-03-31 1999-08-10 The Procter & Gamble Company Detergent composition containing zeolite map for washing a mixture of white and colored fabrics
US6211436B1 (en) * 1996-01-16 2001-04-03 Planttec Biotechnologie Gmbh Nucleic acid molecules from plants coding enzymes which participate in the starch synthesis
US9267095B2 (en) 2013-05-24 2016-02-23 The Procter & Gamble Company Low pH detergent composition comprising nonionic surfactants
US9840681B2 (en) 2013-05-24 2017-12-12 The Procter & Gamble Company Concentrated surfactant composition
US10519400B2 (en) 2013-05-24 2019-12-31 The Procter & Gamble Company Low PH detergent composition

Also Published As

Publication number Publication date
IE930498A1 (en) 1994-01-12
CA2139359A1 (en) 1994-01-20
JPH07508788A (en) 1995-09-28
EP0576778A1 (en) 1994-01-05
MX9304037A (en) 1994-05-31
EP0576778B1 (en) 1998-02-04
TR26910A (en) 1994-08-22

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