EP0095205B1 - Fettsäure enthaltende Detergenszusammensetzungen - Google Patents

Fettsäure enthaltende Detergenszusammensetzungen Download PDF

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Publication number
EP0095205B1
EP0095205B1 EP83200688A EP83200688A EP0095205B1 EP 0095205 B1 EP0095205 B1 EP 0095205B1 EP 83200688 A EP83200688 A EP 83200688A EP 83200688 A EP83200688 A EP 83200688A EP 0095205 B1 EP0095205 B1 EP 0095205B1
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Prior art keywords
alkyl
weight
carbon atoms
composition
group
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French (fr)
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EP0095205A1 (de
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Jean-Luc Henri Marie Wertz
Pierre Charles Emile Goffinet
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Procter and Gamble Co
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Procter and Gamble Co
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    • 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
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • 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
    • C11D1/42Amino alcohols or amino ethers
    • C11D1/44Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines
    • 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
    • C11D1/62Quaternary ammonium compounds
    • 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
    • C11D1/65Mixtures of anionic with cationic compounds
    • 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
    • C11D1/75Amino oxides
    • 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
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3711Polyacetal carboxylates
    • 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
    • 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
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • 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
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
    • 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
    • C11D1/28Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/40Monoamines or polyamines; Salts thereof

Definitions

  • the present invention relates to detergent compositions, preferably liquid detergents, containing an anionic synthetic surfactant, a cosurfactant selected from the group consisting of certain quaternary ammonium, diquaternary ammonium, amine and diamine surfactants, and a fatty acid.
  • the compositions herein have a molar ratio of the anionic synthetic surfactant to the cosurfactant of at least 1 and are formulated to provide an initial pH of from about 6.0 to about 8.5 at a concentration of from about 0.1 % to about 2% by weight in water at 20°C.
  • the compositions provide both superior greasy/oily soil removal and good builder/pH sensitive soil removal at the near-neutral wash pH.
  • the compositions have a pH of from about 6.0 to 7.5.
  • the present invention encompasses detergent compositions comprising:
  • the detergent compositions herein contain an anionic synthetic surfactant, a cosurfactant selected from certain quaternary ammonium diquaternary ammonium, amine and diamine surfactants, and a fatty acid material.
  • the compositions can be in any form, including granules, liquids, tablets or pastes. However, liquid compositions are highly preferred since the compositions herein are especially effective when applied directly to soils and stains in a pretreatment step.
  • compositions herein must have a molar ratio of the anionic synthetic surfactant to the cosurfactant of at least one, preferably from about 2:1 to about 20:1, and are formulated to provide an initial pH of from about 6.0 to about 8.5 at a concentration of from about 0.1 % to about 2% by weight in water at 20°C. It has been found that the addition of the cosurfactant to the fatty acid containing detergents herein provides important greasy/oily soil removal benefits only at the near-neutral wash pH.
  • the wash pH is preferably from about 7.0 to about 8.5, more preferably from about 7.5 to about 8.0.
  • the cosurfactant and anionic surfactant herein form complexes which enhance packing of the surfactants at the oil/water interface, thereby lowering interfacial tension and improving detergency.
  • the amine and diamine surfactants would be at least partially protonated at the near-neutral pH and thus can form charges species capable of complexing with the anionic surfactant).
  • the fatty acid component exists in a chemical form which is optimal for effective detergency. At too low a pH, the non-dissociated form of the acid is ineffective. It is also believed that the higher pH's (i.e., above about 8.5) affect the interaction of the fatty acid with the cosurfactant and water hardness and result in the formation of undesirable species at the oil/water interface which reduce detergency performance.
  • the detergent compositions herein contain from about 2% to about 60% by weight of an anionic synthetic surfactant, or mixtures thereof.
  • the anionic surfactant preferably represents from about 5% to about 40%, and more preferably from about 10% to about 20%, by weight of the detergent composition.
  • Anionic surfactants useful herein are disclosed in U.S. Patent 4,285,841, Barrat et al, issued August 25, 1981, and in U.S. Patent 3,919,678, Laughlin et al, issued December 30, 1975.
  • Useful anionic surfactants include the water-soluble salts, particularly the alkali metal, ammonium and alkylolammonium (e.g., monoethanolammonium or triethanolammonium) salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from about 10 to about 20 carbon atoms and a sulfonic acid or sulfuric acid ester group. (Included in the term “alkyl” is the alkyl portion of aryl groups).
  • alkyl sulfates especially those obtained by sulfating the higher alcohols (C 8 -C, e carbon atoms) such as those produced by reducing the glycerides of tallow or coconut oil; and the alkylbenzene sulfonates in which the alkyl group contains from about 9 to about 15 carbon atoms, in straight chain or branched chain configuration, e.g., those of the type described in United States Patents 2,220,099 and 2,477,383.
  • linear straight chain alkylbenzene sulfoantes in which the average number of carbon atoms in the alkyl group is from about 11 to 14.
  • anionic surfactants herein are the water-soluble salts of: paraffin sulfonates containing from about 8 to about 24 (preferably about 12 to 18) carbon atoms; alkyl glyceryl ether sulfonates, especially those ethers of C s - 18 alcohols (e.g., those derived from tallow and coconut oil); alkyl phenol ethylene oxide ether sulfates containing from about 1 to about 4 units of ethylene oxide per molecule and from about 8 to about 12 carbon atoms in the alkyl group; and alkyl ethylene oxide ether sulfates containing about 1 to about 4 units of ethylene oxide per molecule and from about 10 to about 20 carbon atoms in the alkyl group.
  • Other useful anionic surfactants herein include the water-soluble salts of esters of a-sulfonated fatty acids containing from about 6 to 20 carbon atoms in the fatty acid group and from about 1 to 10 carbon atoms in the ester group; water-soluble salts of 2 - acyloxy - alkane - 1 - sulfonic acids containing from about 2 to 9 carbon atoms in the acyl group and from about 9 to about 23 carbon atoms in the alkane moiety; water-soluble salts of olefin sulfonates containing from about 12 to 24 carbon atoms; and ⁇ -alkyloxy alkane sulfonates containing from about 1 to 3 carbon atoms in the alkyl group and from about 8 to 20 carbon atoms in the alkane moiety.
  • Particularly preferred anionic surfactants herein are the alkyl sulfates of the formula wherein R is an alkyl chain having from about 8 to about 18 carbon atoms, saturated or unsaturated, and the longest linear portion of the alkyl chain is 15 carbon atoms or less on the average, M is a cation which makes the compound water-soluble, especially an alkali metal, ammonium or substituted ammonium cation, and x is from 0 to about 4.
  • Most preferred are the non-ethoxylated C 12 - 15 primary and secondary alkyl sulfates. Under cold water washing conditions, i.e., less than about 65°F (18.3°C), it is preferred that there be a mixture of such alkyl sulfates.
  • alkyl sulfates with the above-described alkylbenzene sulfonates, paraffin sulfonates, alkyl glyceryl ether sulfonates and esters of a a-sulfonated fatty acids, particularly with the C11-13 linear alkylbenzene sulfonates, are also preferred.
  • compositions herein also contain from about 0.25% to about 12%, preferably from about 0.5% to about 8%, more preferably from about 1% to about 4%, by weight of a cosurfactant selected from the group of certain quaternary ammonium, diquaternary ammonium, amine and diamine surfactants.
  • a cosurfactant selected from the group of certain quaternary ammonium, diquaternary ammonium, amine and diamine surfactants.
  • the quaternary ammonium surfactants are particularly preferred.
  • the quaternary ammonium surfactants herein are of the formula: wherein R 2 is an alkyl or alkyl benzyl group having from about 8 to about 18 carbon atoms in the alkyl chain; each R 3 is selected from the group consisting of -CH 2 CH 2 -, -CH 2 CH(CH 3 )-, -CH 2 CH(CH 2 OH)-, -CH 2 CH 2 CH 2 -, and mixtures thereof; each R 4 is selected from the group consisting of C 1 - 4 alkyl, C 1 - 4 hydroxyalkyl, benzyl, ring structures formed by joining the two R 4 groups, wherein R 6 is any hexose or hexose polymer having a molecular weight less than about 1000, and hydrogen when y is not 0; R 5 is the same as R or is an alkyl chain wherein the total number of carbon atoms or R 2 plus R 5 is not more than about 18; each y is from 0 to about 10 and
  • alkyl quaternary ammonium surfactants especially the mono-long chain alkyl surfactants described in the above formula when R 5 is selected from the same groups as R 4 .
  • the most preferred quaternary ammonium surfactants are the chloride, bromide and methylsulfate C 8 - 16 alkyl trimethylammonium salts, C S - 16 alkyl di(hydroxyethyl)methylammonium salts, the C 8-16 alkyl hydroxyethyldimethylammonium salts, and C 8-16 alkyloxypropyl trimethylammonium salts.
  • decyl trimethylammonium methylsulfate lauryl trimethylammonium chloride, myristyl trimethylammonium bromide and coconut trimethylammonium chloride and methylsulfate are particularly preferred.
  • the C 8-10 alkyltrimethyl ammonium surfactants are particularly preferred since they have a lower Kraft boundary and, therefore, a lower crystallization temperature than the longer alkyl chain quaternary ammonium surfactants herein.
  • Diquaternary ammonium surfactants herein are of the formula: wherein the R 2 , R 3 , R 4 , R 5 , y and X substituents are as defined above for the quaternary ammonium surfactants. These substituents are also preferably selected to provide diquaternary ammonium surfactants corresponding to the preferred quaternary ammonium surfactants. Particularly preferred are the C 8-16 alkyl pentamethylethylenediammonium chloride, bromide and methylsulfate salts.
  • Amine surfactants useful herein are of the formula: wherein the R 2 , R 3 , R 4 , R 5 and y substituents are as defined above for the quaternary ammonium surfactants. Particularly preferred are the C 12 - 16 alkyl dimethyl amines.
  • Diamine surfactants herein are of the formula: wherein the R Z , R 3 , R 4 , R 5 and y substituents are as defined above. Preferred are the C 12 - 16 alkyl trimethylethylene diamines.
  • compositions of the present invention contain from about 5% to about 40%, preferably from about 7% to about 30%, most preferably from about 10% to about 20%, by weight of a fatty acid containing from about 10 to about 22 carbon atoms.
  • the fatty acid can also contain from about 1 to about 10 ethylene oxide units in the hydrocarbon chain.
  • Suitable fatty acids are saturated and/or unsaturated and can be obtained from natural sources such as plant or animal esters (e.g., palm kernel oil, palm oil, coconut oil, babassu oil, safflower oil, tall oil, castor oil, tallow and fish oils, grease, and mixtures thereof) or synthetically prepared (e.g., via the oxidation of petroleum or by hydrogenation of carbon monooxide via the Fisher-Tropsch process).
  • suitable saturated fatty acids for use in the compositions of this invention include capric, lauric, myristic, palmitic, stearic, arachidic and behenic acid.
  • Suitable unsaturated fatty acid species include: palmitoleic, oleic, linoleic, linolenic and ricinoleic acid.
  • preferred fatty acids are saturated C 10 -C 14 (coconut) fatty acids, from about 5:1 to 1:1 (preferably about 3:1) weight ratio mixtures of lauric and myristic acid, and mixtures of the above lauric/myristic blends with oleic acid at a weight ratio of about 4:1 to 1:4 mixed lauric/myristic:oleic.
  • compositions of the present invention also preferably contain up to about 30%, preferably from about 1% to about 20%, more preferably from about 5% to about 15%, by weight of an ethoxylated nonionic surfactant.
  • ethoxylated alcohols and ethoxylated alkyl phenols of the formula R(OC 2 H 4 ) n OH, wherein R is selected from the group consisting of aliphatic hydrocarbon radicals containing from about 8 to about 15 carbon atoms and alkyl phenyl radicals in which the alkyl groups contain from about 8 to about 12 carbon atoms, n is from about 3 to about 9, and said nonionic surfactant has an HLB (hydrophile- lipophile balance) value of from about 10 to about 13.
  • HLB hydrophile- lipophile balance
  • Particularly preferred are ethoxylated alcohols having an average of from about 10 to about 15 carbon atoms in the alcohol and an average degree of ethoxylation of from about 3 to about 8 moles of ethylene oxide per mole of alcohol.
  • compositions herein also preferably contain up to about 40%, more preferably from about 1% to about 30%, by weight of a detergent builder material. While all manner of detergent builders known in the art can be used in the present compositions, the type and level of builder must be selected such that the final composition has an initial pH of from about 6.0 to about 8.5 at a concentration of from about 0.1 % to about 1 % by weight in water at 20°C. Detergent builders are described in U.S. Patent 4,321,165, Smith et al, issued March 23, 1982. In the preferred liquid detergent compositions herein, the builder preferably represents from about 1% to about 20%, more preferably from about 3% to about 10%, by weight of the composition. Preferred builders for use in liquid detergents herein are described in U.S. Patent 4,284,532, Leikhim et al, issued August 18, 1981. A particularly preferred builder is citric acid.
  • liquid detergents herein are the neutralizing agents, buffering agents, phase regulants, hydrotropes, enzymes, enzyme stabilizing agents, polyacids, suds regulants, opacifiers, antioxidants, bactericides, dyes, perfumes, and brighteners described in the U.S. Patent 4,285,841, Barrat et al, issued August 25, 1981.
  • Preferred neutralizing agents for use herein are organic bases, especially triethanolamine and monoethanolamine, which result in better detergency performance than inorganic bases such as sodium and potassium hydroxides.
  • Particularly preferred compositions herein contain from about 0.1% to about 2% by weight of detersive enzymes, especially the amylases, proteases, and mixtures thereof, of the type well known to detergent formulators.
  • Composition A a commercially available heavy-duty liquid detergent
  • Composition B containing, by weight, 6.2% sodium C 13 linear alkylbenzene sulfonate, 9.4% sodium C 14 - 16 alkyl sulfate, 10.0% C, 2 - 13 alcohol polyethoxylate (6.5), 10.0% coconut fatty acid, 5.0% oleic fatty acid, 15.0% citric acid, 0.3% diethylenetriame pentamethylene phosphonic acid, 0.23% brightener, 1.0% protease enzyme, enough monoethanolamine to achieve the desired pH and the balance, to 100% water; Composition C, which was B plus 2.7% by weight of C 12 alkyl trimethylammonium chloride; or Composition D, which was B plus 2.7% by weight of C 12 - 16 alkyl dimethyl amine oxide.
  • the wash pH was about 7.3 for Composition A and about 7.4 for B, C and D.
  • the wash water temperature was 95°F (35°C) and the water hardness was 86 mg/l (5 grains/gallon) (3:1 Ca -+ :Mg + ++ ).
  • the swatches were then dried and each set was round robin comparison graded against its counterparts to determine relative soil removal provided by the detergent compositions.
  • a grading scale of -4 to 4 was used, with -4 indicating much less soil removal, 0 indicating no difference and 4 indicating much more soil removal.
  • the results for each composition were then averaged and Composition A was assigned a relative value of 0.
  • composition C of the present invention containing quaternary ammonium cosurfactant, provides important advantages on greasy/oil soils and also on grass and clay (on PC) relative to Composition B at wash pH's of 7.4. However, these advantages are substantially eliminated at wash pH's of 9.5.
  • the present invention also encompasses a method for laundering fabrics comprising contacting said fabrics with an aqueous solution having a pH of from about 6.0 to about 8.5 at 20°C and containing at least about 0.1% by weight of the compositions herein.
  • Liquid detergent compositions of the present invention are as follows.
  • Composition A was prepared by adding the components, with continuous mixing, in the following order: alcohol polyethoxylate; monoethanolamine; premix of coconutalkyl sulfuric acid paste (containing propanediol, triethanolamine, coconutalkyl sulfuric acid, water and minors) and monoethanolamine- neutralized alkylbenzene sulfonic acid; premix of toluene sulfonate and water; citric acid; alkyl trimethylammonium chloride; premix of fatty acids; phosphonic acid; acetic acid; premix of dye, brightener, formate, ethanol and water; adjust pH to about 8.1 with monoethanolamine or water; protease enzyme; amylase enzyme; and perfume.
  • the product obtained was a clear liquid.
  • Composition B was obtained by mixing the components.
  • compositions of the present invention are obtained when the alkyl trimethylammonium halides in the above compositions are replaced with coconutalkyl trimethylammonium chloride, decyl trimethylammonium methylsulfate, lauryl di(hydroxyethyl) methylammonium chloride, decyloxypropyl trimethylammonium chloride, lauryl pentamethylethylenediammonium chloride, lauryl diethanolamine or coconutalkyl trimethylethylene diamine.
  • compositions herein are obtained when, in the above compositions, the C 13 linear alkylbenzene sulfonic acid is replaced with coconutalkyl sulfuric acid or C 14 - 15 alkyl sulfuric acid, and when the coconutalkyl sulfuric acid is replaced with C 14 - 15 alkyl ethoxy (1 avg) sulfuric acid.
  • compositions of the present invention are also obtained when the lauric/myristic/oleic fatty acid mixture in the above compositions is replaced with coconut fatty acid or a 3:1 weight ratio mixture of lauric and myristic acid.
  • Granular detergents of the present invention can be obtained by spray-drying the above compositions and admixing heat-sensitive materials such as the enzymes.

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Claims (13)

1. Eine Detergenszusammensetzung, enthaltend:
(a) 2 Gew.-% bis 60 Gew.-% eines anionischen, synthetischen oberflächenaktiven Mittels;
(b) 0,25 Gew.-% bis 12 Gew.-% eines co-oberflächenaktiven Mittels, ausgewählt aus der aus:
(i) quaternären Ammonium-oberflächenaktiven Mitteln mit der Formel:
Figure imgb0019
worin R2 eine Alkyl- oder Alkylbenzylgruppe mit 8 bis 18 Kohlenstoffatomen in der Alkylkette ist; jeder Rest R3 aus der Gruppe ausgewählt ist, die aus -CH2CHz-, -CH2CH(CH3)-, -CH2CH(CH2OH)-, -CH2CH2CH2-, und Mischungen davon, besteht; jeder Rest R4 aus der Gruppe ausgewählt ist, die aus Wasserstoff (vorausgesetzt, daß y nicht Null ist), C1-4-Alkyl, Cl-4-Hydroxyalkyl, Benzyl, Ringstrukturen, die durch Verbindung der zwei R4-Gruppen gebildet werden, und
Figure imgb0020
wobei R6 irgendeine Hexose oder irgendein Hexosepolymer mit einem Molekulargewicht bis zu 1000 ist, besteht; R5 die gleiche Bedeutung hat wie R4, oder eine Alkylkette ist, wobei die Gesamtzahl von Kohlenstoffatomen von RZ plus R5 nicht höher als 18 ist; jedes Symbol y 0 bis 10 darstellt, und die Summe der y-Werte 0 bis 15 beträgt; und X irgendein verträgliches Anion ist;
(ii) diquaternären Ammonium-oberflächenaktiven Mitteln mit der Formel:
Figure imgb0021
worin R2, R3, R4, R5, y und X wie oben definiert sind;
(iii) Amin-oberflächenaktiven Mitteln mit der Formel
Figure imgb0022
worin R2, R3, R4, R5 und y wie oben definiert sind; und
(iv) Diamin-oberflächenaktiven Mitteln mit der Formel:
Figure imgb0023
worin R2, R3, R4, R5 und y wie oben definiert sind; bestehenden Gruppe; und
(c) 5 Gew.-% bis 40 Gew.-% einer Fettsäure, die 10 bis 22 Kohlenstoffatome und 0 bis 10 Ethylenoxideinheiten in der Kohlenwasserstoffkette enthält, wobei die Zusammensetzung ein Molverhältnis des anionischen, synthetischen oberflächenaktiven Mittels zu dem co-oberflächenaktiven Mittel von wenigstens 1 aufweist und so formuliert ist, daß sich bei einer Konzentration von etwa 0,1 Gew.-% bis etwa 2 Gew.-% in Wasser bei 20°C ein Anfangs-pH von etwa 6,0 bis etwa 8,5 ergibt.
2. Die Zusammensetzung des Anspruchs 1, wobei das anionische oberflächenaktive Mittel ein Alkylsulfat der Formel
Figure imgb0024
umfaßt, worin R eine Alkylkette mit 8 bis 18 Kohlenstoffatomen, die gesättigt oder ungesättigt ist, bedeutet, wobei der längste lineare Abschnitt der Alkylkette im Durchschnitt 15 Kohlenstoffatome oder weniger aufweist, M ein die Verbindung wasserlöslich machendes Kation ist und x 0 bis 4 bedeutet.
3. Die Zusammensetzung des Anspruchs 2, wobei in dem Alkylsulfat-oberflächenaktiven Mittel R eine etwa 12 bis 15 Kohlenstoffatome enthaltende Alkylgruppe ist, x 0 ist und M ein Alkalimetall-, Ammonium-oder substituiertes Ammoniumkation ist.
4. Die Zusammensetzung des Anspruchs 3, wobei das anionische oberflächenaktive Mittel zusätzlich ein wasserlösliches Salz eines Alkylbenzolsulfonats, Paraffinsulfonats, Alkylglycerylethersulfonats oder eines Esters einer a-sulfonierten Fettsäure enthält.
5. Die Zusammensetzung des Anspruchs 3, wobei das anionische oberflächenaktive Mittel zusätzlich ein Alkalimetall-, Ammonium- oder substituiertes Ammoniumsalz eines linearen Alkylbenzolsulfonats mit einem Gehalt von 11 bis 13 Kohlenstoffatomen in der Alkylkette umfaßt.
6. Die Zusammensetzung des Anspruchs 1, wobei das co-oberflächenaktive Mittel aus der Gruppe ausgewählt ist, die aus den Chlorid-, Bromid- und Methylsulfat - C8-16 - alkyltrimethylammoniumsalzen, - C8-16 - alkyldi(hydroxyethyl)methylammoniumsalzen, - C8-16 - alkylhydroxyethyldimethylammoniumsalzen und - C8-16 - alkyloxypropyltrimethylammoniumsalzen besteht.
7. Die Zusammensetzungen des Anspruchs 6, wobei das co-oberflächenaktiven Mittel Decyltrimethylammoniummethylsulfat, Lauryltrimethylammoniumchlorid, Myristyltrimethylammoniumbromid und Kokosnußalkyltrimethylammoniumchlorid und -methylsulfat ist.
8. Die Zusammensetzungen des Anspruchs 1, wobei die Fettsäure ein 10 bis 14 Kohlenstoffatome enthaltendes Material, oder Mischungen davon, umfaßt.
9. Die Zusammensetzungen des Anspruchs 3, wobei das co-oberflächenaktive Mittel aus der Gruppe ausgewählt ist, die aus den Chlorid-, Bromid- und Methylsulfat -C8-16 - alkyltrimethylammoniumsalzen, - CS-16 - alkyldi(hydroxyethyl)methylammoniumsalzen, - C8-16 - alkylhydroxyethyldimethylammoniumsalzen und - C8-16 - alkyloxypropyltrimethylammoniumsalzen besteht, und die Fettsäure ein 10 bis 14 Kohlenstoffatome enthaltendes Material, oder Mischungen davon, umfaßt.
10. Eine flüssige Detergenszusammensetzung nach Anspruch 9, enthaltend 10 Gew.-% bis 20 Gew.-% des anionischen, synthetischen oberflächenaktiven Mittels, 1 Gew.-% bis 4 Gew.-% des co-oberflächenaktiven Mittels und 10 Gew.-% bis 20 Gew.-% der Fettsäure.
11. Die Zusammensetzung des Anspruchs 10, welche zusätzlich 0,1 Gew.-% bis 2 Gew.-% eines zur Verwendung in Detergenszusammensetzungen geeigneten Enzyms enthält, das aus der aus Amylasen, Proteasen, und Mischungen davon, bestehenden Gruppe ausgewählt ist.
12. Die Zusammensetzung des Anspruchs 11, welche zusätzlich 3 Gew.-% bis 10 Gew.-% Zitronensäure enthält.
13. Ein Verfahren zum Waschen von Textilien, umfassend das Inkontaktbringen der genannten Textilien mit einer wässerigen Lösung, die einen pH-Wert von 6,0 bis 8,5 bei 20°C aufweist und wenigstens 0,1 Gew.-% der Zusammensetzung des Anspruchs 1 enthält.
EP83200688A 1982-05-24 1983-05-16 Fettsäure enthaltende Detergenszusammensetzungen Expired EP0095205B1 (de)

Priority Applications (1)

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AT83200688T ATE22920T1 (de) 1982-05-24 1983-05-16 Fettsaeure enthaltende detergenszusammensetzungen.

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US38098882A 1982-05-24 1982-05-24
US380988 1982-05-24

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EP0095205B1 true EP0095205B1 (de) 1986-10-15

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JP (1) JPS5925894A (de)
AT (1) ATE22920T1 (de)
AU (1) AU559791B2 (de)
CA (1) CA1208519A (de)
DE (1) DE3366958D1 (de)
FI (1) FI73727C (de)
GR (1) GR78820B (de)
IE (1) IE55427B1 (de)
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US4747977A (en) * 1984-11-09 1988-05-31 The Procter & Gamble Company Ethanol-free liquid laundry detergent compositions
SE8603087L (sv) * 1985-07-25 1987-01-26 Colgate Palmolive Co Textilmjukgorande och antistatisk detergentkomposition
SE8604714L (sv) * 1985-11-15 1987-05-16 Colgate Palmolive Co Detergentkomposition med forbettrad formaga att avlegsna oljig smuts
DE3614825A1 (de) * 1986-05-02 1987-11-05 Henkel Kgaa Verwendung von alkylaminopolyglykolethern als schaumdrueckende zusaetze in schaumarmen reinigungsmitteln
US4704221A (en) * 1986-10-22 1987-11-03 The Procter & Gamble Company Granular detergents which contain high levels of anionic surfactant that forms a middle-phase, surface treated with a water soluble cationic surfactant
EP0495554A1 (de) * 1991-01-16 1992-07-22 The Procter & Gamble Company Waschmittelzusammensetzungen mit hochaktiven Cellulasen und quaternären Ammoniumverbindungen
WO1995020025A1 (en) * 1994-01-25 1995-07-27 The Procter & Gamble Company Low sudsing detergent compositions containing long chain amine oxide and branched alkyl carboxylates
ES2132631T5 (es) * 1994-01-25 2011-02-17 THE PROCTER & GAMBLE COMPANY Composiciones detergentes líquidas o gelificadas para lavar vajillas de acción poco severa y alta jabonadura que contienen óxidos de aminas de cadena larga.
US5466394A (en) * 1994-04-25 1995-11-14 The Procter & Gamble Co. Stable, aqueous laundry detergent composition having improved softening properties
WO1995029217A1 (en) * 1994-04-25 1995-11-02 The Procter & Gamble Company Stable, aqueous laundry detergent composition having improved softening properties
WO1995030734A1 (en) * 1994-05-10 1995-11-16 The Procter & Gamble Company Heavy duty liquid laundry detergent composition containing anionic and amine oxide surfactants and fatty acid
AU3824195A (en) * 1995-09-29 1997-04-17 Procter & Gamble Company, The Liquid laundry detergents containing selected quaternary ammonium compounds
AR003724A1 (es) * 1995-09-29 1998-09-09 Procter & Gamble Composicion detergente liquida estructurada de lavanderia, para trabajo duro, que comprende surfactantes anionicos y cationicos.
US6017874A (en) * 1995-09-29 2000-01-25 The Procter & Gamble Company Liquid laundry detergents containing selected quaternary ammonium compounds
AR003725A1 (es) * 1995-09-29 1998-09-09 Procter & Gamble Composiciones detergentes liquidas que contienen una amina, un alquilsulfato y un surfactante anionico adicional.
WO1997012022A1 (en) * 1995-09-29 1997-04-03 The Procter & Gamble Company Stable aqueous laundry detergent compositions comprising quaternary surfactants and amine oxides and having improved suspension properties
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MA25183A1 (fr) * 1996-05-17 2001-07-02 Arthur Jacques Kami Christiaan Compositions detergentes
DE19626620A1 (de) * 1996-07-03 1998-01-08 Clariant Gmbh Enzymhaltige Waschmittelformulierung
CA2268772C (en) * 1996-10-18 2008-12-09 The Procter & Gamble Company Detergent compositions comprising an amylolytic enzyme and a cationic surfactant
BR9713320A (pt) * 1996-10-18 2000-01-25 Procter & Gamble Composições de detergente
AR017744A1 (es) * 1999-02-08 2001-09-12 Procter & Gamble Glicoles polimericos y dioles para composiciones detergentes mejoradas para el lavado de vajilla
JP5396707B2 (ja) * 2007-11-07 2014-01-22 ライオンハイジーン株式会社 洗浄剤組成物
EP2083067A1 (de) 2008-01-25 2009-07-29 Basf Aktiengesellschaft Verwendung von organischen Komplexbildnern und/oder polymeren carbonsäuregruppenhaltigen Verbindungen in einer flüssigen Wasch- oder Reinigungsmittelzusammensetzung
US20120324655A1 (en) 2011-06-23 2012-12-27 Nalini Chawla Product for pre-treatment and laundering of stained fabric
JP6052777B2 (ja) * 2012-12-26 2016-12-27 花王株式会社 液体洗浄剤組成物

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EP0002084A1 (de) * 1977-11-17 1979-05-30 THE PROCTER & GAMBLE COMPANY Körnige Reinigungsmittelgemische zur besseren Entfernung von schmierigen Flecken
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US4397776A (en) * 1981-03-17 1983-08-09 The Procter & Gamble Company Liquid detergent compositions containing alpha-amine oxide surfactants

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IE831206L (en) 1983-11-24
FI831832A0 (fi) 1983-05-23
FI73727B (fi) 1987-07-31
DE3366958D1 (en) 1986-11-20
FI831832L (fi) 1983-11-25
IE55427B1 (en) 1990-09-12
AU1488883A (en) 1983-12-01
CA1208519A (en) 1986-07-29
FI73727C (fi) 1987-11-09
EP0095205A1 (de) 1983-11-30
JPS5925894A (ja) 1984-02-09
AU559791B2 (en) 1987-03-19
JPH0477038B2 (de) 1992-12-07
MX162610A (es) 1991-05-31
GR78820B (de) 1984-10-02
ATE22920T1 (de) 1986-11-15

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