EP0108429A1 - Détergent granulaire contenant du pyrophosphate et un polymère de polyacrylate - Google Patents

Détergent granulaire contenant du pyrophosphate et un polymère de polyacrylate Download PDF

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Publication number
EP0108429A1
EP0108429A1 EP83201275A EP83201275A EP0108429A1 EP 0108429 A1 EP0108429 A1 EP 0108429A1 EP 83201275 A EP83201275 A EP 83201275A EP 83201275 A EP83201275 A EP 83201275A EP 0108429 A1 EP0108429 A1 EP 0108429A1
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EP
European Patent Office
Prior art keywords
weight
composition
pyrophosphate
polymer
silicate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Application number
EP83201275A
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German (de)
English (en)
Inventor
John Edward Morrow
Howard Austin Mills, Jr.
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Procter and Gamble Co
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Procter and Gamble Co
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Publication of EP0108429A1 publication Critical patent/EP0108429A1/fr
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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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • C11D3/3761(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in solid 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates

Definitions

  • the present Invention relates to granular detergents containing organic surfactant, pyrophosphate builder, low levels of alkali metal silicate, and a polyacrylate polymer.
  • the compositions herein are prepared by drying an aqueous slurry comprising the components. While the compositions are preferably substantially free of orthophosphates, they can contain minor amounts of such material provided the weight ratio of pyrophosphate to orthophosphate is at least about 5:1.
  • Pyrophosphates are known to be potentially more efficient builders than the tripolyphosphates commonly used in detergents due to their ability to remove more calcium and magnesium ions from the laundering solution per unit of P 2 O 5 . They do so, however, by precipitating these ions as insoluble phosphates (e.g., dicalcium pyrophosphate) whereas the tripolyphosphates retain them in solution as complex ions. These precipitates can build up on fabrics over a period of time and cause undesirable effects, such as greyness and harshness of feel, unless antirc- deposition agents are added to detergents containing pyrophosphates.
  • insoluble phosphates e.g., dicalcium pyrophosphate
  • antirc- deposition agents are added to detergents containing pyrophosphates.
  • Pyrophosphate-built granular detergents have often contained high levels (e.g., 10% by weight) of alkali metal silicates to provide optimum granule structure and processing. It is believed that when a crutcher mix containing silicate is spray-dried, the silicate dries to a tough film capable of cementing finely crystalline granule walls together. This results in granules having very desirable physical properties, i.e, crisp, durable and free-flowing granules. Silicates having lower SiO 2 to alkali metal oxide molar ratios (e.g., 1.6-2.0) are usually selected because they arc more water-soluble than the higher ratio silicates.
  • Silicates having lower SiO 2 to alkali metal oxide molar ratios e.g., 1.6-2.0
  • European patent application 82200458.6 discloses the use of film-forming polymers, Including polyacrylates, as structural aids to replace all or part of the silicate in low-phosphate granular detergents containing aluminosilicates.
  • the present invention encompasses a granular detergent composition comprising:
  • the granular detergent compositions of the present invention contain, as essential components, an organic surfactant, a pyrophosphate builder, an alkali metal silicate and a polyacrylate polymer.
  • the polyacrylate polymer acts as both a highly effective antiredeposition agent and structural aid, allowing for the formulation of granular detergents having desirable structure, solubility and whiteness maintenance characteristics.
  • the amount of orthophosphate in the compositions should be limited such that the weight ratio of pyrophosphate to orthophosphate Is at least about 5:1, preferably at least about 10:1, and more preferably at least about 20:1.
  • the compositions are most preferably substantially free of orthophosphates because they tend to form coarse precipitates which more readily deposit on fabrics than the pyrophosphate precipitates.
  • compositions herein are prepared by drying an aqueous slurry comprising the components.
  • the slurry generally contains from about 25% to about 50% water, whereas the dried granules initially contain from about 2% to about 10%, preferably from about 2% to about 5%, water.
  • the drying operation can be accomplished by any convenient means, such as by using spray-drying towers, both counter-current and co-current, fluid beds, flash-drying equipment, or industrial microwave or oven-drying equipment. These are more fully described in U.S. Patent 4,019,998, Benson et ai, issued April 26, 1977 (particularly from Column 14, line 19 to Column 15, line 9), incorporated herein by reference.
  • the granular detergents herein exhibit superior structure and physical properties because the polyacrylate polymer dries to a tough, non-sticky, non-hygroscopic film which cements the granule walls together much in the same manner as do the silicates.
  • the polymer film is readily water-soluble so that the granules quickly disintegrate in the laundering solution and leave little or no insoluble residue on fabrics.
  • the low level of silicate in the compositions contributes to the desired granule structure, and also aids processing and inhibits metal corrosion, without causing excessive insoluble silicate deposition.
  • the polyacrylate polymer Is also highly effective at suspending the insoluble dicalcium pyrophosphate salts, preventing their deposition and build-up on fabrics.
  • the detergent compositions herein contain from about 5% to about 50% by weight of an organic surfactant selected from the group consisting of anionic, nonionic, zwitterionic, ampholytic and cationic surfactants, and mixtures thereof.
  • the surfactant preferably represents from about 10% to about 30% by weight of the detergent composition.
  • Surfactants useful herein are listed in U.S. Patent 3,664,961, Norris, issued May 23, 1972, and in U.S. Patent 3,919,678, Laughiin, et ai, issued December 30, 1975, both incorporated herein by reference.
  • Useful cationic surfactants also include those described in U.S. Patent 4,222,905, Cockrell, issued September 16, 1980, and in U.S. Patent 4,239,659, Murphy, issued December 16, 1980, both incorporated herein by reference.
  • Water-soluble salts of the higher fatty acids are useful anionic surfactants in the compositions herein.
  • Soaps can be made by direct saponification of fats and oils or by the neutralization of free fatty acids.
  • Particularly useful are the sodium and potassium salts of the mixtures of fatty acids derived from coconut oil and tallow, i.e., sodium or potassium tallow and coconut soap.
  • Useful anionic surfactants also include the water-soluble salts, preferably the alkali metal, ammonium and substituted ammonium 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.
  • alkyl is the alkyl portion of acyl groups.
  • this group of synthetic surfactants are the sodium and potassium alkyl sulfates, especially those obtained by sulfating the higher alcohols (Ca-C18 carbon atoms) such as those produced by reducing the glycerides of tallow or coconut oil; and the sodium and potassium alkylbenzene sulfonates
  • 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 U.S. Patents 2,220,099 and 2,477,383.
  • Especially valuable are linear straight chain alkylbenzene sulfonates in which the average number of carbon atoms in the alkyl group is from about 11 to 13, abbreviated as C 11-13 LAS.
  • anionic surfactants herein are the sodium alkyl glyceryl ether sulfonates, especially those ethers of higher alcohols derived from tallow and coconut oil; sodium coconut oil fatty acid monoglyceride sulfonates and sulfates; sodium or potassium salts of alkyl phenol ethylene oxide ether sulfates containing from about 1 to about 10 units of ethylene oxide per molecule and from about 8 to about 12 carbon atoms in the alkyl group; and sodium or potassium salts of alkyl ethylene oxide ether sulfates containing about 1 to about 10 units of ethylene oxide per molecule and from about 10 to about 20 carbon atoms in the alkyl group.
  • Other useful anionic surfactants include the water-soluble salts of esters of alpha-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; alkyl ether sulfates containing from about 10 to 20 carbon atoms in the alkyl group and from about 1 to 30 moles of ethylene oxide; 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.
  • Water-soluble nonionic surfactants are also useful in the compositions of the invention.
  • Such nonionic materials include compounds produced by the condensation of alkylene oxide groups (hydrophilic in nature) with an organic hydrophobic compound, which may be aliphatic or alkyl aromatic in nature.
  • the length of the polyoxyalkylene group which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
  • Suitable nonionic surfactants include the polyethylene oxide condensates of alkyl phenols, e.g., the condensation products of alkyl phenols having an alkyl group containing from about 6 to 15 carbon atoms, in either a straight chain or branched chain configuration, with from about 3 to 12 moles of ethylene oxide per mole of alkyl phenol.
  • Preferred nonionics are the water-soluble condensation products of aliphatic alcohols containing from 8 to 22 carbon atoms, in either straight chain or branched configuration, with from 3 to 12 moles of ethylene oxide per mole of alcohol. Particularly preferred are the condensation products of alcohols having an alkyl group containing from about 9 to 15 carbon atoms with from about 4 to 8 moles of ethylene oxide per mole of alcohol.
  • Semi-polar nonionic surfactants useful herein include water-soluble amine oxides containing one alkyl moiety of from about 10 to 18 carbon atoms and two moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from 1 to 3 carbon atoms; water-soluble phosphine oxides containing one alkyl moiety of about 10 to 18 carbon atoms and two moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from about 1 to 3 carbon atoms; and water-soluble sulfoxides containing one alkyl moiety of from about 10 to 18 carbon atoms and a moiety selected from the group consisting of alkyl and hydroxyalkyl moieties of from about 1 to 3 carbon atoms.
  • Ampholytic surfactants include derivatives of aliphatic or aliphatic derivatives of heterocyclic secondary and tertiary amines in which the aliphatic moiety can be straight chain or branched and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and at least one aliphatic substituent contains an anionic water-solubilizing group.
  • Zwitterionic surfactants include derivatives of aliphatic quaternary ammonium; phosphonium, and sulfonium compounds in which one of the aliphatic substituents contains from about 8 to 18 carbon atoms.
  • Particularly preferred surfactants herein are anionic surfactants selected from the group consisting of the alkali metal salts. of C 11-13 alkylbenzene sulfonates, C 14-18 alkyl sulfates, C 14-18 alkyl linear polyethoxy sulfates containing from about 1 to about 4 moles of ethylene oxide, and mixtures thereof.
  • compositions of the present invention also contain from about 5% to about 80%, preferably from about 10% to about 70%, and most preferably from about 15% to about 60%, by weight of an alkali metal pyrophosphate builder.
  • Sodium and potassium, particularly sodium, pyrophosphates are preferred.
  • the pyrophosphate salts useful herein can be obtained commercially or can be formed by neutralization of the corresponding pyrophosphoric acids or acid salts.
  • the pyrophosphates can be anhydrous or hydrated, although anhydrous pyrophosphates in finely divided form are preferred for rapid dissolution in the wash.
  • Monosodium pyrophosphate and trisodium pyrophosphate also exist, the latter as the anhydrous form or the mono- or nona-hydrate.
  • the generic formula for the anhydrous forms of these compounds can be expressed as M x H y P 2 O 7 , where M is alkali metal and x and y are integers having the sum of 4.
  • compositions herein contain from about 0.5% to about 6%, preferably from about 1% to about 5%, more preferably from about 1.5% to about 4%, and most preferably from about 1.5% to about 3%, by weight of an alkali metal silicate having a molar ratio of SiO 2 to alkali metal oxide of from about 1.0 to about 3.2, preferably from about 1.6 to about 2.4.
  • Sodium silicate particularly having a molar ratio of from about 1.8 to about 2.2, is preferred.
  • the alkali metal silicates can be purchased In either liquid or granular form. Sllicate slurries can conveniently be used to avoid having to dissolve the dried form in the aqueous slurry (e.g., crutcher mix) of the components herein.
  • aqueous slurry e.g., crutcher mix
  • compositions of the present invention contain from about 0.1% to about 5%, preferably from about 0.3% to about 3%, and more preferably from about 0.5% to about 2%, by weight of a polyacrylate polymer soluble in an aqueous slurry comprising the essential components herein.
  • the polymer should have a molecular weight of from about 2 ,000 to about 200,000, preferably from about 25,000 to about 150,000, and more preferably from about 40,000 to about 100,000.
  • the polymer must be at least partially soluble in the slurry of the components for it to dry to a film capable of cementing the granule walls together as the slurry Is dried.
  • the polymer should be substantially soluble in the slurry, and it is preferably completely soluble in the slurry.
  • the slurry will generally be a strong electrolyte solution due to the presence of the pyrophosphate and silicate salts, and, when present, anionic surfactants and other neutral or alkaline salts, optimum solubility of the polymer is obtained when it is in the form of an at least partially neutralized alkali metal, ammonium or substituted ammonium (e.g., mono-, di- or triethanol ammonium) salt.
  • alkali metal, especially sodium, salts are most preferred.
  • Suitable polymers herein are the at least partially neutralized salts of homopolymers and copolymers of acrylic acid, hydroxyacrylic acid and methacrylic acid.
  • the copolymers can be formed of mixtures of these unsaturated carboxylic acids with or without other copolymerisable monomers, or they can be formed from single acids with other -copolymerisable monomers. In either case, the percentage by weight of the polymer units derived from the acids Is preferably greater than about 50%.
  • Suitable copolymerisable monomers include, for example, vinyl chloride, vinyl alcohol, furan, acrylonitrile, methacrylonitile, vinyl acetate, methyl acrylate, methyl methacrylate, styrene, alpha-methylstyrene, vinyl methyl ether, vinyl ethyl ether, vinyl propyl ether, acrylamide, ethylene, propylene and 3-butenoic acid.
  • Preferred polymers of the above group are salts of homopolymers of acrylic acid, hydroxyacrylic acid, or methacrylic acid, or copolymers of these acids containing at least about 80% by weight of units derived from the acid.
  • Particularly preferred is sodium polyacrylate, especially when it has an average molecular weight of from about 50,000 to about 70,000.
  • compositions of the present invention can be included in the compositions of the present invention. These include cobuilders, color speckles, bleaching agents and bleach activators, suds boosters or suds suppressors, anti-tarnish and anti-corrosion agents, soil release agents, dyes, fillers, optical brighteners, germicides, non-builder alkalinity sources, enzymes, enzyme-stabilizing agents, and perfumes.
  • Preferred cobuilders for use herein are disclosed in U.S. Patent 4,019,998, Benson et aI, issued April 26, 1977 (particularly from Column 11, line 40 to Column 13, line 5), incorporated herein by reference. Particularly preferred are the aluminosilicates, tripolyphosphates, carbonates and nitrilotriacetates, and mixtures thereof.
  • composition intended for usage at a level of 11 cups (129 g) in a normal capacity, top-loading washing machine, was prepared by spray-drying an aqueous crutcher-mix slurry of the components.
  • compositions of the present invention are obtained when the pyrophosphate in the above composition is replaced with a mixture of 21% pyrophosphate and 5% of either hydrated sodium aluminosilicate Zeolite A (avg. dia. 3 microns), sodium tripolyphosphate or sodium nitrilotriacetate, or when the silicate level is increased to 4%.
  • compositions herein are obtained when the polyacrylate is replaced with sodium polyhydroxyacrylate of m.w. 80,000, with a sodium polyacrylate polymer containing about 5-15% by weight of acrylamide and having a m.w. of about 20,000 or 40,000, or with sodium polyacrylate having a m.w. of 120,000.
  • compositions are obtained by drying an aqueous slurry comprising the essential components herein and alkali metal tripolyphosphates, wherein the weight ratio of pyrophosphate to tripolyphosphate is from about 50:1 to about 1:1, preferably from about 20:1 to about 2:1, and more preferably from about 10:1 to about 4:1.
  • the tripolyphosphate contributes to the formation of granules having very desirable structure and physical properties, including improved structural integrity and free-flowing characteristics, and reduced caking tendencies.
  • the tripolyphosphates also contribute to improved whiteness maintenance performance.
  • composition intended for usage at a level of 1 ⁇ 2 cup (51.9 g) in a normal capacity, top-loading washing machine, was prepared by spray-drying an aqueous crutcher-mix slurry of the components.
  • the dispersibility of the above granular composition can be improved by intimately mixing about 1% by weight of sodium polyacrylate of m.w. 2000 with the anionic surfactant paste prior to adding the balance of the components to the crutcher, as described in European patent application 82201390.0.
  • composition is prepared by first intimately mixing the 2000 m.w. polyacrylic acid with the anionic surfactant p ⁇ ste, and then spray-drying an aqueous crutcher-mix slurry of the components.
  • the base granules obtained are then admixed, at a level of 52.1 parts, with 41.3 parts of tetrasodium pyrophosphate, 5.2 parts of sodium carbonate, 0.6 parts of polyethylene glycol 6000, and minors to provide a finished granular detergent intended for usage at a level of 1 ⁇ 2 cup (51.9g) in a normal capacity, top-loading washing machine.

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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)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP83201275A 1982-09-07 1983-09-06 Détergent granulaire contenant du pyrophosphate et un polymère de polyacrylate Withdrawn EP0108429A1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US41509882A 1982-09-07 1982-09-07
US415098 1982-09-07
US44012582A 1982-11-08 1982-11-08
US440125 1982-11-08

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EP0108429A1 true EP0108429A1 (fr) 1984-05-16

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0179533A2 (fr) * 1984-10-26 1986-04-30 The Procter & Gamble Company Compositions détergentes granulaires séchées par pulvérisation et leur procédé de préparation
EP0208534A2 (fr) * 1985-07-09 1987-01-14 The Procter & Gamble Company Procédé de préparation de compositions détergentes granulaires séchées par atomisation
EP0221776A2 (fr) 1985-11-01 1987-05-13 Unilever Plc Compositions détergentes, parties constituantes et leurs procédés de préparation
EP0130639B1 (fr) * 1983-06-30 1987-09-23 THE PROCTER & GAMBLE COMPANY Compositions détergentes contenant du polyéthylène glycol et du polyacrylate
EP0282863A2 (fr) * 1987-03-14 1988-09-21 Henkel Kommanditgesellschaft auf Aktien Concentrés de nettoyage liquides alcalins
EP0289768A2 (fr) * 1987-05-06 1988-11-09 Degussa Aktiengesellschaft Agent de renforcement pour détergents sans phosphate
EP0323659A2 (fr) * 1987-12-11 1989-07-12 Unilever N.V. Procédé de préparation d'un produit détergent granulaire

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3579455A (en) * 1968-08-02 1971-05-18 Grace W R & Co Machine dishwashing compositions containing sodium polyacrylate
DE2403894A1 (de) * 1973-01-31 1974-08-01 Unilever Nv Textilwaschmittelpulver
US4019998A (en) * 1974-09-27 1977-04-26 The Procter & Gamble Company Process for preparing a pyrophosphate-silicate detergent product
DE2744569A1 (de) * 1976-10-04 1978-04-06 Lion Fat Oil Co Ltd Koerniges wasch- und reinigungsmittel hervorragender pulvereigenschaften und verfahren zur herstellung desselben

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3579455A (en) * 1968-08-02 1971-05-18 Grace W R & Co Machine dishwashing compositions containing sodium polyacrylate
DE2403894A1 (de) * 1973-01-31 1974-08-01 Unilever Nv Textilwaschmittelpulver
US4019998A (en) * 1974-09-27 1977-04-26 The Procter & Gamble Company Process for preparing a pyrophosphate-silicate detergent product
DE2744569A1 (de) * 1976-10-04 1978-04-06 Lion Fat Oil Co Ltd Koerniges wasch- und reinigungsmittel hervorragender pulvereigenschaften und verfahren zur herstellung desselben

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0130639B1 (fr) * 1983-06-30 1987-09-23 THE PROCTER & GAMBLE COMPANY Compositions détergentes contenant du polyéthylène glycol et du polyacrylate
EP0179533A2 (fr) * 1984-10-26 1986-04-30 The Procter & Gamble Company Compositions détergentes granulaires séchées par pulvérisation et leur procédé de préparation
EP0179533A3 (fr) * 1984-10-26 1987-06-16 The Procter & Gamble Company Compositions détergentes granulaires séchées par pulvérisation et leur procédé de préparation
EP0208534A2 (fr) * 1985-07-09 1987-01-14 The Procter & Gamble Company Procédé de préparation de compositions détergentes granulaires séchées par atomisation
EP0208534A3 (fr) * 1985-07-09 1989-07-05 The Procter & Gamble Company Procédé de préparation de compositions détergentes granulaires séchées par atomisation
EP0221776A3 (en) * 1985-11-01 1988-09-21 Unilever Plc Detergent compositions, components therefor, and processes for their preparation
EP0221776A2 (fr) 1985-11-01 1987-05-13 Unilever Plc Compositions détergentes, parties constituantes et leurs procédés de préparation
US4900466A (en) * 1985-11-01 1990-02-13 Lever Brothers Company Process for preparing needle-shaped crystal growth modified burkeite detergent additive
EP0282863A2 (fr) * 1987-03-14 1988-09-21 Henkel Kommanditgesellschaft auf Aktien Concentrés de nettoyage liquides alcalins
EP0282863A3 (fr) * 1987-03-14 1990-06-13 Henkel Kommanditgesellschaft auf Aktien Concentrés de nettoyage liquides alcalins
EP0289768A2 (fr) * 1987-05-06 1988-11-09 Degussa Aktiengesellschaft Agent de renforcement pour détergents sans phosphate
EP0289768A3 (fr) * 1987-05-06 1989-09-06 Degussa Aktiengesellschaft Agent de renforcement pour détergents sans phosphate
US5076957A (en) * 1987-05-06 1991-12-31 Degussa Aktiengesellschaft Phosphate-free detergent builders
EP0323659A2 (fr) * 1987-12-11 1989-07-12 Unilever N.V. Procédé de préparation d'un produit détergent granulaire
EP0323659A3 (en) * 1987-12-11 1990-10-24 Unilever Nv Method for preparing a granular detergent material and granular detergent material thereby obtained

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MA19894A1 (fr) 1984-04-01

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