GB2188645A - Liquid detergents containing anionic surfactant - Google Patents
Liquid detergents containing anionic surfactant Download PDFInfo
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- GB2188645A GB2188645A GB08707572A GB8707572A GB2188645A GB 2188645 A GB2188645 A GB 2188645A GB 08707572 A GB08707572 A GB 08707572A GB 8707572 A GB8707572 A GB 8707572A GB 2188645 A GB2188645 A GB 2188645A
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- composition
- succinate
- fatty acid
- alkyl
- acid
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/37—Mixtures of compounds all of which are anionic
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/08—Polycarboxylic acids containing no nitrogen or sulfur
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0026—Low foaming or foam regulating compositions
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/123—Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/75—Amino oxides
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
Abstract
Liquid detergent compositions containing anionic synthetic surfactant, C12-C14 alkyl or alkenyl succinate builder and C12-C14 fatty acid or soap, in a molar ratio of succinate to fatty acid or soap of from about 0.8 to about 2.4, provide a minimum of suds in otherwise high sudsing compositions.
Description
GB 2 188 645 A 1
SPECIFICATION
Liquid detergents containing anionic surfactant Technical field 5
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 about 0.8 to about 2.4. Within this range, the succinate and fatty acid mixture surprisingly provides a 10 minimum of sudsing in otherwise high sudsing detergents containing a significant amount of anionic synthetic surfactant.
Background art
British Patent 1,293,753, Evans eta], published October 25,1972, discloses dicarboxylate builders, including 15 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 ClZ-C14fatty 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 C1T-C15 alkylbenzene sulfonate, builder and C7-C12 alkyl or 20 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 succinate to fatty acid present is about 1.7.
U.S. Patent 3,776,851, Cheng, issued December 4,1973, discloses detergents containing 5-70% tetrahy droxysuccinic acid builders. Example 4 contains 20% tetra hydroxysuccin ic acid and 1.8% 80:20 tallow:coco nut soap as suds suppressor. 25 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 30
The present invention relates to a liquid detergent composition comprising, by weight:
(a) from about 10% to about 50% of an anionic synthetic surfactant; (b) from about 2% to about 25% of a C12-C14 alkyi or alkenyl succinic acid, or salt thereof; ar)d (c) from about 1 %to about 15% of a C12-C14 fatty acid, or salt thereof; the molar ratio of (b) to (c), on an acid basis, being from about 0.8to about 2.4. 35 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 about 0.8 to about 2.4, preferably from about 0.9 to about 1.8, more preferably from about 1.0 to about 1.4. Within these 40 ratios, the succinate and fatty acid provide a minimum of suds in otherwise high sudsing detergents containing a significant 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.
45 Anionic synthetic surfactapt The detergent co m positi ons h erei n contain from about 10% to a bout 50%, preferably from a bout 13% to about 40%, more preferably from about 16% to about 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 a], issued August 25,1981, and in U.S. Patent 3,919,678, Laughlin et ai, issued December 30,1975, both incorporated 50 herein by reference.
Useful anionic surfactants include the water-soluble salts, particularly the alkali metal, ammonium and alkyloammonium (e.g., monoethanolammonium or triethanolammonium) salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from about 8 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.) 55 Examples of this group of synthetic surfactants are the alkyl sulfates, especially those obtained by sulfating the higher alcohols (Cs-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 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. 60 Other 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 C8-18 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 the alkyl ethylene oxide ether sulfates containing about 1 to about 4 units of 65 2 GB 2 188 645 A 2 ethylene oxide per molecule and from about 10 to about 20 carbon atoms in the alkyl g roup.
Other useful anionic surfactants herein include the water-soluble salts of esters of alpha-sulfonated fatty acids containing from about 6to 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; 5 water-soluble salts of olefin sulfonates containing from about 12 to 24 carbon atoms; and beta-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.
Preferred anionic surfactants herein are the alkyl sulfates of the formula 10 RO(C21-140)xS03-M- wherein R is an alkyl chain having from about 12 to about 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 xis from 0 to about 4. Preferably, R is a C12-C16 alkyl or hydroxyalkyl group, especially 15 a C127C15 alkyl, and x is from about 0 to about 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 about 12 to about 13, and the C12-15 alcohol sulfates containing from 0 to about 3 ethylene oxide units, as described above. Also preferred are mixtures of these surfactants in a weight ratio of from about 3:1 to about 1:3, preferably from about 2:1 to about 1:2. 20 These anionics form hardness, preferably magnesium, surfactants that are particularly effective at lowering interfacial tension and removing greasyloily soils.
Succinate builder The detergent compositions herein also contain from about 2% to about 25%, preferably from about 3% to 25 about 20%, more preferably from about 5% to about 15%, by weight of a succinate builder of the general formula R-CH(C0OWC1-12(COOH), wherein R is C12-C14 alkyl or alkenyl group.
These succinate builders are preferably used in the form of their watersoluble salts, including the sodium, potassium, ammonium and alkanolammonium salts (e.g., mono-, di-, or tri- ethanolammonium).
Specific examples of succinate builders include: iauryl succinate, myristyl succinate, 2-dodecenyl succinate 30 (preferred) and 2-tetradecenyl succinate.
Fatty acid The co m positions of the p resent i nvention fu rth er conta i n from a bout 1 % to a bout 15%, preferably from 2% to a bout 10%, mo re preferably from about 3 % to a bout 6 %, by weig ht of a C12-C14 fatty aci, o r salt 35 thereof.
Suitable fatty acids can be obtained from natural sources such as plant or animal esters (e.g., palm kernel 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 40 saturated coconut fatty acids, from about 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 calciur-h-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 45 with the anionic surfactant herein and with soils, while allowing sufficient free hardness to complex some of the anionic surfactantto produce a hardness surfactant (such as magnesium linear alkylbenzene sulfonate) that is highly effective at removing greasy and oily soils. Such hardness- surfactants pack atthe oillwater interface where they lower interfacial tension and enhance removal of greasyloily soils.
The liquid detergent compositions herein can optionally contain any of the auxiliary ingredients known for 50 use in detergent compositions. These include cosurfactafits, 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, incorporated herein by reference.
Preferred compositions herein include those described in U.S. Patent 4, 561,998, Wertz et a], issued 55 December 31, 1985, and U.S. Patent 4,507,219, Hughes, issued March 26, 1985, both incorporated herein by reference.
The compositions herein preferably contain from about 1 % to about 20%, more preferably from about 3% to about 15%, most preferably from about 5% to about 10%, by weight of an ethoxylated nonionic surfactant of the formula R'(OC2H4)n0H, wherein R' is a C10-C1r, alkyl group (preferred) or a CS-C12 alkyl phenyl group, n 60 is from about 3 to about 9, and said nonionic surfactants has an HLB (hydrophile-lipophile balance) of from about 9 to about 13, preferably from about 10 to about 13. HLB is defined in detail in Nonionic Surfactants, by MJ. Schick, Marcel Dekker, Inc., 1966, pages 607-613, incorporated herein by reference. These ethoxylated nonionic surfactants suspend hardness-surfactants in the wash water solution. They are used at a level high enough to prevent excessive precipitation of hardness-surfactants at the oillwater interface (which makes soil 65 3 GB 2 188 645 A 3 removal more difficult), but low enough to allowforthe desired adsorption and packing atthe interface.
The compositions herein can be formulated to have a pH of from about 7.5 to about 12, more preferably from about 8 to about 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 about 2 to about 5 for best bleach stability. Such alkaline compositions have a pH of from about 9 to about 12, preferably 5 from about 9.5 to about 11.5, more preferably from about 10 to about 11. They preferably contain from about 2% to about 15%, more preferably from about 4% to about 10%, by weight of monoethanolarnine. The combination of such an alkaline composition and peroxyacid bleach preferably delivers a was'] water pH of from about 7.8 to about 9, preferably from about 7.9 to about 8.5, which is desired for good ble@ching 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 1 15
The following composition was prepared by adding the components to a mixing tank in the order listed with continuous mixing.
% wt. % wt. % Components Assay Product Stock 20 Sodium C1415 alkyl poly ethoxylate (2.25) sulfate 48.8 11.3 23.2' C13 linear alkylbenzene sulfonic acid 96.0 8.0 8.33 Sodium diethylenetriamine 25 pentaacetate 41.0 0.35 0.7 Propylene glycol 100.0 10.5 10.5 Monoetha nola mine 100.0 5.0 3.0 Brightener mix 100.0 - 6.2 12 C12-13 alcohol polyethoxy- 30 late (6.5) 100.0 9.0 7.0 Ethanol 92.0 10.48 7.3 Potassium hydroxide 45.0 2.48 5.51 Sodium hydroxide 50.0 2.94 5.88 Boric acid 100.0 1.25 1.25 35 Water - 5.65 Sodium 2-dodecenyl succinate 80.0 5.53 6.9 Cl 2-14 fatty acid 100.0 3.5 3.5 Citric acid 50.0 4.0 8.0 Calcium formate 10.0 0.12 1.2 40 TEPA-Ele,18- 80.0 3.0 3.75 pH trim to 10.5 - - - Protease enzyme (2,0 AU/g) 100.0 1.16 1.16 Arnylase enzyme (375 AM. Ulg) 100.0 0.16 0.16 Perfume 100.0 0.25 0.25 45 Dye 100.0 0.08 0.08 Water - to 100% 3.25 Paste also contains 16.2% ethanol and 35% water 2Contains 32.2% monoethanolamine, 32.2% water, 32.2% C12-13 50 alcohol polyethoxylate (6.5), and 3.36% of brightener.
Alcohol and monoethoxylated alcohol removed.
Tetraethylene pentaimine ethoylated with 15-18 moles (avg.) of ethylene oxide at each hydrogen site.
The above composition is preferably used in combination with the following liquid diperoxyacid bleach 55 composition. The liquid bleach composition was prepared by high shear mixing of the components in an Eppenbach mixer while in an ice bath. The DPDA and water 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. 60 4 GB 2 188 645 A 4 Grams wt. % Time 1. 1 2-Di peroxydodeca nedioic acid (DPDA) (26.68% active si u rry) 10,821.6 18.0 0 Water (additional) 1896 11.8 0 5 Suds suppressor 12.8 0.08 1 min.
C13 linear alkylbenze sulfonic acid (96% active) 417.8 2.5 3 min.
Sodium cumene sulfonate (50% active) 463.4 1.45 3 min. 10 Dipicolinicacid 1.6 0.01 3 min.
Sodium sulfate 641.6 4.0 1 hr.25 min.
Magnesium sulfate 1684.2 10.5 2 hr.10 min.
Sodium hydroxide (50% active) 104 0.32 3 hr.10 min. 15 Balance primarily water.
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 mixerwas turned off. The composition was a stable 20 suspension of the ingredients and had a viscosity of about 350 eps at about 20'C. The DPDA had an average particle size of about 2-5 microns.
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. 25 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 mi) 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 30 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.
35 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.
Components A 8 40 Sodium C14-15 alkyl poly ethoxylate (2.25) sulfate 12.7 8.1 Sodium C13 linear alkylbenzene sulfonate 8.5 3.9 Sodium diethylenetriamine pentaacetate 0.3 - 45 Propylene glycol 8.5 Monoethanolamine 2.0 5.4 C12-13 alcohol polyethoxy late (6.5) 5.0 C12-C16 alkyldimethylamine oxide 6.6 50 Ethanol 4.0 Sodium toluene sulfonate 8.0 Sodium 2-dodecenyl succinate 11.0 15.0 C12-14 fatty acid 7.0 7.0 Citric acid 4.0 2.0 55 Calcium formate 0.12 - Sodium formate 0.87 TEPA-E15-jj- 2.0 2.0 Protease enzyme (2.0 AU/g) 0.75 - Arnylase enzyme (375 AM, U/9) 0.16 60 Water and minors Balance to 100%
Claims (11)
- WHAT IS CLAIMED IS:GB 2 188 645 A 5 CLAIMS 1. A liquid detergent composition comprising, by weight:(a) from about 10% to about 50% of an anionic synthetic surfactant; (b) from about 2% to about 25% of a C12C14 alkyl or alkenyl succinic acid, or salt thereof; and 5 (c) from about 1 %to about 15% of a C12-C14 fatty acid, or salt thereof; the molar ratio of (b) to (c), on an acid basis, being from about 0.8 to about 2.4.
- 2. The composition of Claim 1 wherein the molar ratio of (b)to (c), on an acid basis, is from about 1.Oto about 1.4.
- 3. The composition of Claim 1 wherein the anionic su rfactant comprises a ClZ-C13 linear alkyl benzene 10 sulfonate, a C12-C15 alcohol sulfate containing from 0 to about 3 ethylene oxide units, or mixtures thereof.
- 4. The composition of Claim 1 wherein (b) is sodium 2-dedecenyl succinate.
- 5. The composition of Claim 1 comprising from about 16% to about 30% of anionic synthetic surfactant, which comprises a C12C13 linear alkylbenzene sulfonate, a Clz-C15 alcohol sulfate containing from 0 to about 3 ethylene oxide units, or mixtures thereof. 15
- 6. The composition of Claim 5 comprising from about 5% to about 15% of sodium 2-dodecenyl succinate and from about 3% to about 6% Of C12-C14 fatty acid.
- 7. The composition of Claim 6 wherein the molar ratio of (b) to (c) is from about 1.0 to about 1.4.
- 8. The composition of Claim 1 having a pH of from about 9.5to about 11.5.
- 9. The composition of Claim 7 having a pH of from about 10to about 11. 20
- 10. The composition of CLaim 9 comprising from about 4% to about 10% of monoethanolamine.
- 11. The composition of Claim 10 further comprising from about 5% to about 10% of an ethoxylated nonionic surfactant of the formula W(OC2H4)n01-1, wherein R' is a C10-C16 alkyl group, and n is from about 3 to about 9, said surfactant having an HLB of from about 9 to about 13.Printed for Her Majesty's Stationery Office by Croydon Printing Company (UK) Ltd, 8187, D8991685.Published by The Patent Office, 25 Southampton Buildings, London WC2A lAY, from which copies may be obtained.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US84638286A | 1986-03-31 | 1986-03-31 |
Publications (2)
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GB8707572D0 GB8707572D0 (en) | 1987-05-07 |
GB2188645A true GB2188645A (en) | 1987-10-07 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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GB08707572A Withdrawn GB2188645A (en) | 1986-03-31 | 1987-03-30 | Liquid detergents containing anionic surfactant |
Country Status (13)
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EP (1) | EP0241073B2 (en) |
JP (1) | JPH07113120B2 (en) |
KR (1) | KR950004927B1 (en) |
AT (1) | ATE69260T1 (en) |
AU (1) | AU612317B2 (en) |
CA (1) | CA1332137C (en) |
DE (1) | DE3774312D1 (en) |
GB (1) | GB2188645A (en) |
GR (1) | GR3003069T3 (en) |
HK (1) | HK50294A (en) |
IE (1) | IE60012B1 (en) |
MX (1) | MX169254B (en) |
NZ (1) | NZ219812A (en) |
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EP0976435A1 (en) * | 1998-07-29 | 2000-02-02 | Dow Corning Corporation | Foam control agents |
US6352966B1 (en) | 2000-05-19 | 2002-03-05 | Albemarle Corporation | Cleansing bars |
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JP2523341B2 (en) * | 1987-11-09 | 1996-08-07 | 花王株式会社 | Strongly alkaline aqueous solution of nonionic surfactant |
DE3834181A1 (en) * | 1988-10-07 | 1990-04-12 | Henkel Kgaa | LIQUID DETERGENT |
EP0430330A3 (en) * | 1989-11-24 | 1991-12-18 | The Procter & Gamble Company | Suspending liquid detergent compositions |
DE19540373A1 (en) * | 1995-10-30 | 1997-05-07 | Henkel Kgaa | Ultrasonic cleaning and suitable cleaning agents |
DE19635070A1 (en) * | 1996-08-30 | 1998-03-05 | Clariant Gmbh | Liquid bleach suspension |
US5972869A (en) * | 1996-12-17 | 1999-10-26 | Colgate-Palmolive Co | Mildly acidic laundry detergent composition providing improved protection of fine fabrics during washing and enhanced rinsing in hand wash |
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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---|---|---|---|---|
US2220099A (en) | 1934-01-10 | 1940-11-05 | Gen Aniline & Flim Corp | Sulphonic acids |
US2477383A (en) | 1946-12-26 | 1949-07-26 | California Research Corp | Sulfonated detergent and its method of preparation |
GB1215498A (en) | 1967-06-13 | 1970-12-09 | Unilever Ltd | Succinic acid derivatives and their use in detergent compositions |
DK130417A (en) * | 1968-08-08 | |||
GB1380390A (en) * | 1970-12-16 | 1975-01-15 | Unilever Ltd | Detergent compositions |
US3776851A (en) | 1972-09-25 | 1973-12-04 | Colgate Palmolive Co | Detergents containing tetrahydroxysuccinic acid and salts thereof |
US3919678A (en) | 1974-04-01 | 1975-11-11 | Telic Corp | Magnetic field generation apparatus |
DE3063434D1 (en) * | 1979-05-16 | 1983-07-07 | Procter & Gamble Europ | Highly concentrated fatty acid containing liquid detergent compositions |
EP0028850B1 (en) * | 1979-11-09 | 1983-04-20 | Unilever N.V. | Liquid detergent composition |
US4561998A (en) | 1982-05-24 | 1985-12-31 | The Procter & Gamble Company | Near-neutral pH detergents containing anionic surfactant, cosurfactant and fatty acid |
US4507219A (en) | 1983-08-12 | 1985-03-26 | The Proctor & Gamble Company | Stable liquid detergent compositions |
GB2179669B (en) * | 1985-08-15 | 1988-12-29 | Procter & Gamble | Built liquid detergents |
JP3470354B2 (en) * | 1993-07-21 | 2003-11-25 | 大同特殊鋼株式会社 | Dimension measuring device for heating traveling members |
-
1987
- 1987-03-23 DE DE8787200529T patent/DE3774312D1/en not_active Expired - Fee Related
- 1987-03-23 EP EP87200529A patent/EP0241073B2/en not_active Expired - Lifetime
- 1987-03-23 AT AT87200529T patent/ATE69260T1/en not_active IP Right Cessation
- 1987-03-30 IE IE81587A patent/IE60012B1/en not_active IP Right Cessation
- 1987-03-30 CA CA000533361A patent/CA1332137C/en not_active Expired - Fee Related
- 1987-03-30 NZ NZ219812A patent/NZ219812A/en unknown
- 1987-03-30 KR KR1019870002922A patent/KR950004927B1/en active IP Right Grant
- 1987-03-30 GB GB08707572A patent/GB2188645A/en not_active Withdrawn
- 1987-03-30 AU AU70781/87A patent/AU612317B2/en not_active Ceased
- 1987-03-31 MX MX005811A patent/MX169254B/en unknown
- 1987-03-31 JP JP62076555A patent/JPH07113120B2/en not_active Expired - Lifetime
-
1991
- 1991-11-07 GR GR91401150T patent/GR3003069T3/en unknown
-
1994
- 1994-05-19 HK HK50294A patent/HK50294A/en not_active IP Right Cessation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0976435A1 (en) * | 1998-07-29 | 2000-02-02 | Dow Corning Corporation | Foam control agents |
US6352966B1 (en) | 2000-05-19 | 2002-03-05 | Albemarle Corporation | Cleansing bars |
Also Published As
Publication number | Publication date |
---|---|
CA1332137C (en) | 1994-09-27 |
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 |
EP0241073B1 (en) | 1991-11-06 |
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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Legal Events
Date | Code | Title | Description |
---|---|---|---|
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |