EP0241073B1 - Liquid detergents containing anionic surfactant, succinate builder and fatty acid - Google Patents

Liquid detergents containing anionic surfactant, succinate builder and fatty acid Download PDF

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Publication number
EP0241073B1
EP0241073B1 EP87200529A EP87200529A EP0241073B1 EP 0241073 B1 EP0241073 B1 EP 0241073B1 EP 87200529 A EP87200529 A EP 87200529A EP 87200529 A EP87200529 A EP 87200529A EP 0241073 B1 EP0241073 B1 EP 0241073B1
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EP
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Prior art keywords
composition
fatty acid
succinate
alkyl
surfactant
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EP87200529A
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German (de)
French (fr)
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EP0241073A2 (en
EP0241073A3 (en
EP0241073B2 (en
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Stanton L. Boyer
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Procter and Gamble Co
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Procter and Gamble Co
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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
    • C11D1/02Anionic compounds
    • C11D1/37Mixtures of compounds all of which are anionic
    • 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
    • C11D1/04Carboxylic acids or salts thereof
    • 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
    • C11D1/04Carboxylic acids or salts thereof
    • C11D1/08Polycarboxylic acids containing no nitrogen or sulfur
    • 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
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0026Low foaming or foam regulating compositions
    • 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
    • C11D1/123Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
    • 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
    • C11D1/29Sulfates 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
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • 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

Definitions

  • the present invention relates to liquid detergent compositions, preferably heavy-duty liquid detergents, containing an anionic synthetic surfactant and a builder system comprising a C 12 -C 14 alkyl or alkenyl succinic acid or salt thereof (hereinafter referred to as a "succinate”) and a C 12 -C 14 fatty acid or salt thereof (hereinafter referred to as a "fatty acid”) in a molar ratio (calculated on an acid basis) of succinate to fatty acid of from 0,8 to 2,4.
  • succinate and fatty acid mixture surprisingly provides a minimum of sudsing in otherwise high sudsing detergents containing a significant amount of anionic synthetic surfactant
  • Example 10 is a low-sudsing detergent containing 2% dodecyl benzene sulfonate, 6% of an 80:20 mixture of tallow:coconut soap, and 6% disodium hexadecane- 1, 2-dicarboxylate. This results in a molar ratio of dicarboxylate to C 12 -C 14 fatty acid of about 2,7.
  • Examples D-M contain 0-1% LAS, 5.5-6% nonenyl succinic anhydride and 1,2-3% coconut fatty acid. The lowest ratio of suctinate to fatty acid present is about 1,7.
  • U.S Patent 3,776,851, Cheng, issued December 4,1973, discloses detergents containing 5-70% tetrahydroxysuccinic acid builders.
  • Example 4 contains 20% tetrahydroxysuccinic acid and 1.8% 80:20 tallow:coconut soap as a suds suppressor.
  • the present Invention relates to a liquid detergent composition comprising, by weight:
  • the detergent compositions of the present invention contain anionic synthetic surfactant and succinate and fatty acid builders in a molar ratio (calculated on an acid basis) of succinate to fatty acid of from 0.8 to 2.4, preferably from 0.9 to 1.8, more preferably from 1.0 to 1.4.
  • the succinate and fatty acid provide a minimum of suds in otherwise high sudsing detergents containing a signifitant amount (e.g., greater than 10% by weight) of anionic synthetic surfactant This is particularly surprising given that one would have expected that sudsing would gradually increase with increasing levels of succinate and decrease with increasing levels of fatty acid.
  • the detergent compositions herein contain from 10% to 50%, preferably from 13% to 40%, more preferably from 16% to 30%, by weight, on an acid basis, of an anionic synthetic surfactant
  • Anionic synthetic surfactants 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 alkylolamrranium (e. g., monoethanolammonium or triethanolammonium) salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from 8 to 20 carbon atoms and a sulfonic acid or sulfuric acid ester group.
  • water-soluble salts particularly the alkali metal, ammonium and alkylolamrranium (e. g., monoethanolammonium or triethanolammonium) salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from 8 to 20 carbon atoms and a sulfonic acid or sulfuric acid ester group.
  • alkyl is the alkyl portion of aryl groups.
  • alkyl sulfates especially those obtained by sulfating the higher alcohols (C 8 -C 18 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 9 to 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.
  • anionic sunfactants herein are the water-soluble salts of: paraffin sulfonates containing from 8 to 24 (preferably 12 to 18 ) carbon atoms; alkyl glyceryl ether sulfonates, especially those ethers of C a - 18 alcohols (e.g., those derived from tallow and coconut oil); alkyl phenol ethylene oxide ether sulfates containing from 1 to 4 units of ethylene oxide per molecule and from 8 to 12 carbon atoms in the alkyl group; and alkyl ethylene oxide ether sulfates containing 1 to 4 units of ethylene oxide per molecule and from 10 to 20 carbon atoms in the alkyl group.
  • Other useful anionic surfactants herein include the water-soluble salts of esters of alpha-sulfonated fatty acids containing from 6 to 20 carbon atoms in the fatty acid group and from 1 to 10 carbon atoms in the ester group; water-soluble salts of 2-acyloxy-alkane-1-sulfonic acids containing from 2 to 9 carbon atoms in the acyl group and from 9 to 23 carbon atoms in the alkane moiety; water-soluble salts of olefin sulfonates containing from 12 to 24 carbon atoms; and beta-alkyloxy alkane sulfonates containing from 1 to 3 carbon atoms in the alkyl group and from 8 to 20 carbon atoms in the alkane moiety.
  • Preferred anionic surfactants herein are the alkyl sulfates of the formula
  • anionic surfactants are the linear straight chain alkylbenzene sulfonates in which the average number of carbon atoms in the alkyl group is from 12 to 13, and the C 12 -1 5 alcohol sulfates containing from 0 to 3 ethylene oxide units, as described above. Also preferred are mixtures of these surfactants in a weight ratio of from 3:1 to 1:3, preferably from 2:1 to 1:2. These anionics form hardness, preferably magnesium, surfactants that are particularly effective at lowering interfacial tension and removing greasy/oily soils.
  • the detergent compositions herein also contain from 2% to 25%, preferably from 3% to 20%, more pref- erablyfrom 5% to 15%, by weight of a succinate builder of the general formula R-CH (COOH)CH 2 (COOH), wherein R is C 12 -C 14 alkyl or alkenyl group.
  • succinate builders are preferably used in the form of their water-soluble salts, including the sodium, potassium, ammonium and alkanolammonium salts (e.g., mono-, di-, or tri-ethanolammonium).
  • succinate builders include: lauryl succinate, myristyl succinate, 2-dodecenyl succinate (preferred) and 2-tetradecenyl succinate.
  • compositions of the present invention further contain from 1 % to 15%, preferably from 2% to 10%, more preferably from 3% to 6%, by weight of a C 12 -C 14 fatty acid, or salt thereof.
  • Suitable fatty acids can be obtained from natural sources such as plant or animal esters (e.g., palm kemel oil, palm oil and coconut oil) or synthetically prepared (e.g., via the oxidation of petroleum or by hydrogenation of carbon monoxide via the Fisher-Tropsch process).
  • suitable fatty acids for use in the compositions of this invention include lauric, myristic, coconut and palm kernel fatty acid.
  • Preferred are saturated coconut fatty acids, from 5:1 to 1:1 (preferably about 3:1) weight ratio mixtures of lauric and myristic acid, and palm kernel fatty acid.
  • the succinate and fatty acid builders herein are calcium-selective builders, which means they preferentially control calcium ion in the wash solution, rather than magnesium or other hardness ions. It is believed that these calcium-selective builders adequately control wash water hardness, preventing excessive interactions with the anionic surfactant herein and with soils, while allowing sufficient free hardness to complex some of the anionic surfactant to produce a hardness surfactant (such as magnesium linear alkylbenzene sulfonate) that is highly effective at removing greasy and oily soils. Such hardness-surfactants pack at the oil/water interface where they lower interfacial tension and enhance removal of greasy/oily soils.
  • a hardness surfactant such as magnesium linear alkylbenzene sulfonate
  • the liquid detergent compositions herein can optionally contain any of the auxiliary ingredients known for use in detergent compositions. These include cosurfactants, cobuilders, neutralizing agents, buffering agents, phase regulants, solvents, hydrotropes, enzymes, enzyme stabilizing agents, polyacids, suds regulants, opacifiers, antioxidants, bactericides, dyes, perfumes, and brighteners, such as those described in U.S. Patent 4,285,841, Barrat et al, issued August 25, 1981.
  • compositions herein include those described in U.S. Patent 4,561,998, Wertz et al, issued December 31, 1985, and U.S. Patent 4,507,219, Hughes, issued March 26, 1985.
  • compositions herein preferably contain from 1% to 20%, more preferably from 3% to 15%, most preferably from 5% to 10%, by weight of an ethoxylated nonionic surfactant of the formula R 1 (OC 2 H 4 ) n OH, wherein R 1 is a C 10 -C 16 alkyl group (preferred) or a C s -C 12 alkyl phenyl group, n is from 3 to 9, and said nonionic surfactants has an HLB (hydrophile-lipophile balance) of from 9 to 13, preferably from 10 to 13.
  • HLB hydrophile-lipophile balance
  • ethoxylated nonionic surfactants suspend hardness-surfactants in the wash water solution. They are used a a level high enough to prevent extessive precipitation of hardness-surfactants at the oil/water interface (which makes soil removal more difficult), but low enough to allow for the desired adsorption and packing at the interface.
  • compositions herein can be formulated to have a pH of from 7,5 to 12, more preferably from 8 to 11.
  • Certain preferred compositions herein are alkaline compositions that are particularly useful in combination with peroxyacid bleach compositions, which generally have a pH of from 2 to 5 for best bleach stability.
  • Such alkaline compositions have a pH of from 9 to 12, preferably from 9,5 to 11.5, more preferably from 10 to 11. They preferably contain from 2% to 15%, more preferably from 4% to 10%, by weight of monoethanolamine.
  • the com- binat i on of such an alkaline composition and peroxyacid bleach preferably delivers a wash water pH of from 7.8 to 9, preferably from 7.9 to 8.5, which is desired for good bleaching performance, a minimum of fabric yellowing, and a minimum of bleach decomposition by the monoethanolamine.
  • composition was prepared by adding the components to a mixing tank in the order listed with continuous mixing.
  • the above composition is preferably used in combination with the following liquid diperoxyacid bleach composition.
  • the liquid bleach composition was prepared by high shear mixing of the components in an Eppen- bach mixer while in an ice bath.
  • the DPDA and water were added to the mixer before turning the mixer on.
  • the suds suppressor was added to minimize foaming while mixing and to minimize air entrapment in the finished composition.
  • the other components were added in the order listed at the indicated times after turning on the mixer.
  • the pH of the composition was determined to be 3.20 at 20°C. After 4 hr. 10 min., the pH was again determined to be 3.20 at 20°C and the mixer was turned off.
  • the composition was a stable suspension of the ingredients and had a viscosity of about 350 mPa-s at about 20°C.
  • the DPDA had an average particle size of about 2-5 ⁇ m.
  • the compositions are preferably used in a volume ratio of detergent composition to liquid bleach of about 5.5:1.
  • the detergent composition is designed for a usage level of about 0,55 cups in a typical U.S. laundering process. This delivers a concentration of product in the wash water of about 0,22% by weight. Usage of about 0.1 cups (i.e., about 25 ml) of the liquid bleach delivers about 10 ppm of available oxygen to the wash water.
  • the detergent composition and liquid bleach are preferably simultaneously codispersed from a dual compartment bottle at a volume ratio of detergent to bleach of about 5.5:1.
  • the mixture of the succinate and fatty acid builders in the above detergent composition is preferred because it causes less fabric yellowing and measuring cup residue than an all fatty acid formula when used with the above liquid bleach.
  • compositions of the invention which can be prepared by adding the components to a mixing tank in the order listed with continuous mixing, are as follows.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
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Abstract

Liquid detergent compositions containing anionic synthetic surfactant, C12-C14 alkyl or alkenyl succinate builder and C12-C14 fatty acid, in a molar ratio of succinate to fatty acid of from about 0.8 to about 2.4, provide a minimum of suds in otherwise high sudsing compositions.

Description

    Technical Field
  • The present invention relates to liquid detergent compositions, preferably heavy-duty liquid detergents, containing an anionic synthetic surfactant and a builder system comprising a C12-C14 alkyl or alkenyl succinic acid or salt thereof (hereinafter referred to as a "succinate") and a C12-C14 fatty acid or salt thereof (hereinafter referred to as a "fatty acid") in a molar ratio (calculated on an acid basis) of succinate to fatty acid of from 0,8 to 2,4. Within this range, the succinate and fatty acid mixture surprisingly provides a minimum of sudsing in otherwise high sudsing detergents containing a significant amount of anionic synthetic surfactant
  • Background Art
  • British Patent 1, 293, 753, Evans et al, published October25,1972, discloses dicarboxylate builders, indud- ing alkyl and alkenyl succinates, Example 10 is a low-sudsing detergent containing 2% dodecyl benzene sulfonate, 6% of an 80:20 mixture of tallow:coconut soap, and 6% disodium hexadecane- 1, 2-dicarboxylate. This results in a molar ratio of dicarboxylate to C12-C14 fatty acid of about 2,7.
  • European Patent Application 28,850, van der Griend, published May 20, 1981, discloses liquid detergents containing nonionic surfactant, a small amount of C10-C15 alkylbenzene sulfonate, builder and CrC12 alkyl or alkenyl succinate as a hydrotrope. Examples D-M contain 0-1% LAS, 5.5-6% nonenyl succinic anhydride and 1,2-3% coconut fatty acid. The lowest ratio of suctinate to fatty acid present is about 1,7.
  • U.S Patent 3,776,851, Cheng, issued December 4,1973, discloses detergents containing 5-70% tetrahydroxysuccinic acid builders. Example 4 contains 20% tetrahydroxysuccinic acid and 1.8% 80:20 tallow:coconut soap as a suds suppressor.
  • U.S. Patent 3,707,511, Lamberti et al, issued December 26, 1972, discloses that C10-C16 alkyl or alkenyl succinates are useful as suds boosters and stabilizers for detergents, particularly those containing alkylaryl sulfonates. There are no examples of compositions containing succinate and fatty acid.
  • Summary of the Invention
  • The present Invention relates to a liquid detergent composition comprising, by weight:
    • (a) from 10% to 50% of an anionic synthetic surfactant;
    • (b) from 2% to 25% of a C12-C14 alkyl or alkenyl succinic acid, or salt thereof; and
    • (c) from 1% to 15% of a C12-C14 fatty acid, or salt thereof;
      the molar ratio of (b) to (c), on an acid basis, being from 0.8 to 2.4.
    Detailed Description of the Invention
  • The detergent compositions of the present invention contain anionic synthetic surfactant and succinate and fatty acid builders in a molar ratio (calculated on an acid basis) of succinate to fatty acid of from 0.8 to 2.4, preferably from 0.9 to 1.8, more preferably from 1.0 to 1.4. Within these ratios, the succinate and fatty acid provide a minimum of suds in otherwise high sudsing detergents containing a signifitant amount (e.g., greater than 10% by weight) of anionic synthetic surfactant This is particularly surprising given that one would have expected that sudsing would gradually increase with increasing levels of succinate and decrease with increasing levels of fatty acid.
  • Anionic Synthetic Surfactant
  • The detergent compositions herein contain from 10% to 50%, preferably from 13% to 40%, more preferably from 16% to 30%, by weight, on an acid basis, of an anionic synthetic surfactant Anionic synthetic surfactants 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 alkylolamrranium (e. g., monoethanolammonium or triethanolammonium) salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from 8 to 20 carbon atoms and a sulfonic acid or sulfuric acid ester group. (Included in the term "alkyl" is the alkyl portion of aryl groups.) Examples of this group of synthetic surfactants are the alkyl sulfates, especially those obtained by sulfating the higher alcohols (C8-C18 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 9 to 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.
  • Other anionic sunfactants herein are the water-soluble salts of: paraffin sulfonates containing from 8 to 24 (preferably 12 to 18 ) carbon atoms; alkyl glyceryl ether sulfonates, especially those ethers of Ca-18 alcohols (e.g., those derived from tallow and coconut oil); alkyl phenol ethylene oxide ether sulfates containing from 1 to 4 units of ethylene oxide per molecule and from 8 to 12 carbon atoms in the alkyl group; and alkyl ethylene oxide ether sulfates containing 1 to 4 units of ethylene oxide per molecule and from 10 to 20 carbon atoms in the alkyl group.
  • Other useful anionic surfactants herein include the water-soluble salts of esters of alpha-sulfonated fatty acids containing from 6 to 20 carbon atoms in the fatty acid group and from 1 to 10 carbon atoms in the ester group; water-soluble salts of 2-acyloxy-alkane-1-sulfonic acids containing from 2 to 9 carbon atoms in the acyl group and from 9 to 23 carbon atoms in the alkane moiety; water-soluble salts of olefin sulfonates containing from 12 to 24 carbon atoms; and beta-alkyloxy alkane sulfonates containing from 1 to 3 carbon atoms in the alkyl group and from 8 to 20 carbon atoms in the alkane moiety.
  • Preferred anionic surfactants herein are the alkyl sulfates of the formula
    • RO{C2H40)XS03-M+
      wherein R is an alkyl chain having from 12 to 18 carbon atoms, saturated or unsaturated, 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 4. Preferably, R is a C12-C16 alkyl or hydroxyalkyl group, especially a C12-C15 alkyl, and x is from 0 to 3.
  • Highly preferred anionic surfactants are the linear straight chain alkylbenzene sulfonates in which the average number of carbon atoms in the alkyl group is from 12 to 13, and the C12-15 alcohol sulfates containing from 0 to 3 ethylene oxide units, as described above. Also preferred are mixtures of these surfactants in a weight ratio of from 3:1 to 1:3, preferably from 2:1 to 1:2. These anionics form hardness, preferably magnesium, surfactants that are particularly effective at lowering interfacial tension and removing greasy/oily soils.
  • Succinate Builder
  • The detergent compositions herein also contain from 2% to 25%, preferably from 3% to 20%, more pref- erablyfrom 5% to 15%, by weight of a succinate builder of the general formula R-CH (COOH)CH2(COOH), wherein R is C12-C14 alkyl or alkenyl group.
  • These succinate builders are preferably used in the form of their water-soluble salts, including the sodium, potassium, ammonium and alkanolammonium salts (e.g., mono-, di-, or tri-ethanolammonium).
  • Specifc examples of succinate builders include: lauryl succinate, myristyl succinate, 2-dodecenyl succinate (preferred) and 2-tetradecenyl succinate.
  • Fatty Acid
  • The compositions of the present invention further contain from 1 % to 15%, preferably from 2% to 10%, more preferably from 3% to 6%, by weight of a C12-C14 fatty acid, or salt thereof.
  • Suitable fatty acids can be obtained from natural sources such as plant or animal esters (e.g., palm kemel oil, palm oil and coconut oil) or synthetically prepared (e.g., via the oxidation of petroleum or by hydrogenation of carbon monoxide via the Fisher-Tropsch process). Examples of suitable fatty acids for use in the compositions of this invention include lauric, myristic, coconut and palm kernel fatty acid. Preferred are saturated coconut fatty acids, from 5:1 to 1:1 (preferably about 3:1) weight ratio mixtures of lauric and myristic acid, and palm kernel fatty acid.
  • The succinate and fatty acid builders herein are calcium-selective builders, which means they preferentially control calcium ion in the wash solution, rather than magnesium or other hardness ions. It is believed that these calcium-selective builders adequately control wash water hardness, preventing excessive interactions with the anionic surfactant herein and with soils, while allowing sufficient free hardness to complex some of the anionic surfactant to produce a hardness surfactant (such as magnesium linear alkylbenzene sulfonate) that is highly effective at removing greasy and oily soils. Such hardness-surfactants pack at the oil/water interface where they lower interfacial tension and enhance removal of greasy/oily soils.
  • The liquid detergent compositions herein can optionally contain any of the auxiliary ingredients known for use in detergent compositions. These include cosurfactants, cobuilders, neutralizing agents, buffering agents, phase regulants, solvents, hydrotropes, enzymes, enzyme stabilizing agents, polyacids, suds regulants, opacifiers, antioxidants, bactericides, dyes, perfumes, and brighteners, such as those described in U.S. Patent 4,285,841, Barrat et al, issued August 25, 1981.
  • Preferred compositions herein include those described in U.S. Patent 4,561,998, Wertz et al, issued December 31, 1985, and U.S. Patent 4,507,219, Hughes, issued March 26, 1985.
  • The compositions herein preferably contain from 1% to 20%, more preferably from 3% to 15%, most preferably from 5% to 10%, by weight of an ethoxylated nonionic surfactant of the formula R1(OC2H4)nOH, wherein R1 is a C10-C16 alkyl group (preferred) or a Cs-C12 alkyl phenyl group, n is from 3 to 9, and said nonionic surfactants has an HLB (hydrophile-lipophile balance) of from 9 to 13, preferably from 10 to 13. HLB is defined in detail in Nonionic Surfactants, by M.J. Schick, Marcel Dekker, Inc., 1966, pages 607-613. These ethoxylated nonionic surfactants suspend hardness-surfactants in the wash water solution. They are used a a level high enough to prevent extessive precipitation of hardness-surfactants at the oil/water interface (which makes soil removal more difficult), but low enough to allow for the desired adsorption and packing at the interface.
  • The compositions herein can be formulated to have a pH of from 7,5 to 12, more preferably from 8 to 11. Certain preferred compositions herein are alkaline compositions that are particularly useful in combination with peroxyacid bleach compositions, which generally have a pH of from 2 to 5 for best bleach stability. Such alkaline compositions have a pH of from 9 to 12, preferably from 9,5 to 11.5, more preferably from 10 to 11. They preferably contain from 2% to 15%, more preferably from 4% to 10%, by weight of monoethanolamine. The com- bination of such an alkaline composition and peroxyacid bleach preferably delivers a wash water pH of from 7.8 to 9, preferably from 7.9 to 8.5, which is desired for good bleaching performance, a minimum of fabric yellowing, and a minimum of bleach decomposition by the monoethanolamine.
  • The following examples illustrate the compositions of the present invention.
  • All parts, percentages and ratios used herein are by weight unless otherwise specified.
  • EXAMPLE I
  • The following composition was prepared by adding the components to a mixing tank in the order listed with continuous mixing.
    Figure imgb0001
  • The above composition is preferably used in combination with the following liquid diperoxyacid bleach composition. The liquid bleach composition was prepared by high shear mixing of the components in an Eppen- bach mixer while in an ice bath. The DPDA and water were added to the mixer before turning the mixer on. The suds suppressorwas added to minimize foaming while mixing and to minimize air entrapment in the finished composition. The other components were added in the order listed at the indicated times after turning on the mixer.
  • Figure imgb0002
  • After 3 hr. 30 min., the pH of the composition was determined to be 3.20 at 20°C. After 4 hr. 10 min., the pH was again determined to be 3.20 at 20°C and the mixer was turned off. The composition was a stable suspension of the ingredients and had a viscosity of about 350 mPa-s at about 20°C. The DPDA had an average particle size of about 2-5 µm.
  • The above describes the preferred process for making the composition since high shear mixing of the components in an ice bath, their order of addition and the approximate times of addition have all been found to be important to obtain the desired physical stability.
  • The compositions are preferably used in a volume ratio of detergent composition to liquid bleach of about 5.5:1. The detergent composition is designed for a usage level of about 0,55 cups in a typical U.S. laundering process. This delivers a concentration of product in the wash water of about 0,22% by weight. Usage of about 0.1 cups (i.e., about 25 ml) of the liquid bleach delivers about 10 ppm of available oxygen to the wash water. The detergent composition and liquid bleach are preferably simultaneously codispersed from a dual compartment bottle at a volume ratio of detergent to bleach of about 5.5:1.
  • The mixture of the succinate and fatty acid builders in the above detergent composition is preferred because it causes less fabric yellowing and measuring cup residue than an all fatty acid formula when used with the above liquid bleach.
  • EXAMPLE 11
  • Other compositions of the invention, which can be prepared by adding the components to a mixing tank in the order listed with continuous mixing, are as follows.
    Figure imgb0003

Claims (11)

1. A liquid detergent composition comprising, by weight:
(a) from 10% to 50% of an anionic synthetic surfactant;
(b) from 2% to 25% of a C12-C14 alkyl or alkenyl succinic acid, or salt thereof; and
(c) from 1% to 15% of a C12-C14 fatty acid, or salt thereof;
the molar ratio of (b) to (c), on an acid basis, being from 0.8 to 2.4.
2. The composition of Claim 1 wherein the molar ratio of (b) to (c), on an acid basis, is from 1.0 to 1.4.
3. The composition of Claim 1 wherein the anionic surfactant comprises a C12-C13 linear alkylbenzene sulfonate, a C12-C15 alcohol sulfate containing from 0 to 3 ethylene oxide units, or mixtures thereof.
4. The composition of Claim 1 wherein (b) is sodium 2-dodecenyl succinate.
5. The composition of Claim 1 comprising from 16% to 30% of an ionic synthetic surfactant, which comprises a C12-C13 linear alkylbenzene sulfonate, a C12-C15 alcohol sulfate containing from 0 to 3 ethylene oxide units, or mixtures thereof.
6. The composition of Claim 5 comprising from 5% to 15% of sodium 2-dodecenyl succinate and from 3% to 6% of C12-C14 fatty acid.
7. The composition of Claim 6 wherein the molar ratio of (b) to (c) is from 1.0 to 1.4.
8. The composition of Claim 1 having a pH of from 9.5 to 11.5.
9. The composition of Claim 7 having a pH of from 10 to 11.
10. The composition of Claim 9 comprising from 4% to 10% of monoethanolamine.
11. The composition of Claim 10 further comprising from 5% to 10% of an ethoxylated nonionic surfactant of the formula R1(OC2H4)nOH, wherein R1 is a C10-C16 alkyl group, and n is from 3 to 9, said surfactant having an HLB of from 9 to 13.
EP87200529A 1986-03-31 1987-03-23 Liquid detergents containing anionic surfactant, succinate builder and fatty acid Expired - Lifetime EP0241073B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT87200529T ATE69260T1 (en) 1986-03-31 1987-03-23 LIQUID DETERGENTS CONTAINING AN ANIONIC SURFACE ACTIVE AGENT, A Succinic Acid Builder SALT AND A FATTY ACID.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US84638286A 1986-03-31 1986-03-31
US846382 1986-03-31

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EP0241073A2 EP0241073A2 (en) 1987-10-14
EP0241073A3 EP0241073A3 (en) 1989-03-15
EP0241073B1 true EP0241073B1 (en) 1991-11-06
EP0241073B2 EP0241073B2 (en) 1995-03-08

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DE19540373A1 (en) * 1995-10-30 1997-05-07 Henkel Kgaa Ultrasonic cleaning and suitable cleaning agents
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US6352966B1 (en) 2000-05-19 2002-03-05 Albemarle Corporation Cleansing bars
EP2130897B1 (en) * 2008-06-02 2011-08-31 The Procter & Gamble Company Surfactant concentrate
JP2011213992A (en) * 2010-03-15 2011-10-27 Kao Corp Liquid detergent composition
JP2013076054A (en) * 2011-09-15 2013-04-25 Kao Corp Liquid detergent composition
WO2016196555A1 (en) * 2015-06-02 2016-12-08 Stepan Company Cold-water cleaning method
PL3101101T3 (en) * 2015-06-05 2018-06-29 The Procter & Gamble Company Compacted liquid laundry detergent composition
US11879110B2 (en) 2019-11-27 2024-01-23 The Procter & Gamble Company Alkylbenzenesulfonate surfactants

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CA1332137C (en) 1994-09-27
GB2188645A (en) 1987-10-07
ATE69260T1 (en) 1991-11-15
JPH07113120B2 (en) 1995-12-06
AU612317B2 (en) 1991-07-11
HK50294A (en) 1994-05-27
EP0241073A2 (en) 1987-10-14
EP0241073A3 (en) 1989-03-15
MX169254B (en) 1993-06-28
IE870815L (en) 1987-09-30
DE3774312D1 (en) 1991-12-12
AU7078187A (en) 1987-10-08
JPS63397A (en) 1988-01-05
KR870009007A (en) 1987-10-22
KR950004927B1 (en) 1995-05-16
NZ219812A (en) 1989-06-28
IE60012B1 (en) 1994-05-18
EP0241073B2 (en) 1995-03-08
GB8707572D0 (en) 1987-05-07
GR3003069T3 (en) 1993-02-17

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