EP0763594A1 - Process for making granular detergents - Google Patents

Process for making granular detergents Download PDF

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Publication number
EP0763594A1
EP0763594A1 EP19950306547 EP95306547A EP0763594A1 EP 0763594 A1 EP0763594 A1 EP 0763594A1 EP 19950306547 EP19950306547 EP 19950306547 EP 95306547 A EP95306547 A EP 95306547A EP 0763594 A1 EP0763594 A1 EP 0763594A1
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EP
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Prior art keywords
weight
aqueous slurry
inorganic salt
sodium
process according
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EP19950306547
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German (de)
French (fr)
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EP0763594B1 (en
Inventor
Andrew Dorset
Kay Emma Fitzgibbon
Zayeed Alam
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Procter and Gamble Co
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Procter and Gamble Co
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Priority to EP19950306547 priority Critical patent/EP0763594B1/en
Priority claimed from US09/043,183 external-priority patent/US5998356A/en
Publication of EP0763594A1 publication Critical patent/EP0763594A1/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz, glass beads
    • C11D3/1246Silicates, e.g. diatomaceous earth
    • C11D3/128Aluminium silicates, e.g. zeolites
    • 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
    • C11D11/00Special methods for preparing compositions containing mixtures of detergents ; Methods for using cleaning compositions
    • C11D11/02Preparation in the form of powder by spray drying
    • 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

Abstract

The invention provides an aqueous slurry which comprises anionic surfactant and aluminosilicate, and at the same time has a low viscosity suitable for spray-drying to form crisp, free-flowing powder. The aqueous slurry further comprises less than 5% by weight of silicate and at least 1% by weight of an inorganic salt, or a mixture of inorganic salts, whereby the addition of the inorganic salt increases the ionic conductivity of the aqueous slurry. The slurry is subsequently dried to form a particulate detergent composition.

Description

  • The present invention relates to a process for preparing a particulate detergent composition, in particular by spray drying an aqueous slurry. Particulate detergent compositions are also disclosed.
  • Many granular detergents which are sold commercially comprise sodium aluminosilicate as the sole builder, or as a component of a builder system. It is known, for example from JP204098/1983, laid open on November 28th 1983, that heated aqueous slurries, such as those used in conventional spray-drying processes, which comprise both sodium aluminosilicate and water-soluble silicate, cause insoluble complexes to form. These insoluble complexes are undesirable in laundry detergents because they can result in residues on washed fabrics. Furthermore, without the silicate to act as a powder structurant, the particle size distribution of the spray-dried powder may be unacceptably broad.
  • In the absence of water-soluble silicate in the aqueous slurry, various other components have been proposed as powder structurants, useful to achieve a crisp, free-flowing spray-dried powder. Included amongst the powder structurants that have been suggested are film-forming polymer: polycarboxylates (for example, US-A-4 379 080); polyacrylates (for example, JP204098/1983); sucrose and derivatives (for example, EP-A-0 215 637) ; sodium sesquicarbonate (for example, EP-A-0 242 138).
  • However, unless the powder structurants are required by the formulator as active ingredients, then they are an expensive processing aid.
  • An aqueous slurry which does not comprise either water-soluble silicate, or one of the alternative powder structurants is difficult to spray dry. In particular high water concentrations are generally needed in order to maintain the viscosity of the slurry low enough to provide crisp, free-flowing particles of the desired particle size when spray-dried. The disadvantage of high water concentrations is that the excess water must be removed during the drying step and a lot of energy is needed to do this.
  • WO90/04630, published on 3rd May 1990, describes a process for preparing a carbonate containing detergent slurry comprising an alkylpolyglycoside and an alkali metal chloride. Zeolite A is suggested as one possible builder albeit in the presence of silicate (at 7% by weight in Table VI).
  • The object of the present invention is to avoid residue problems by substantially omitting silicate from an aqueous slurry which comprises anionic surfactant and aluminosilicate, and at the same time to provide a low viscosity slurry suitable for spray-drying to form crisp, free-flowing powder.
  • Summary of the Invention
  • According to the invention this object is achieved by forming an aqueous slurry which further comprises less than 5% by weight of silicate and at least 1% by weight of an inorganic salt, or a mixture of inorganic salts, and whereby the addition of the inorganic salt increases the ionic conductivity of the aqueous slurry, and subsequently drying the aqueous slurry to form the particulate detergent composition.
  • Preferably the inorganic salt is an alkali metal or alkaline earth metal salt, or mixtures thereof of halide, nitrate or citrate, most preferably sodium chloride.
  • In a more preferred embodiment of the invention the step of adding the inorganic salt raises the ionic conductivity of the aqueous slurry by at least 3 milliSiemens, and preferably by at least 5 milliSiemens.
  • A further aspect of the invention concerns spray-dried detergent powder compositions. Preferred compositions comprise:
    • at least one surfactant, and preferably at least 5% by weight of surfactant;
    • from 2 to 80%, and preferably from 10% to 50% by weight of aluminosilicate
    • from 1% to 20% by weight of an inorganic salt selected from the group consisting of alkali metal halides, nitrates, citrates or mixtures thereof, and preferably from 2% to 10% by weight of an alkali metal, preferably sodium, chloride, and
    • less than 5%, preferably less than 2% by weight of silicate.
    Detailed Description of the Invention
  • Essential components of the compositions of the present invention are aluminosilicate builders such as those having the empirical formula:

            Mz (zAlO2)y ] · x H2O

    wherein z and y are integers of at least 6, the molar ratio of z to y is in the range from 1.0 to about 0.5, and x is an integer from about 15 to about 264.
    Useful aluminosilicate ion exchange materials are commercially available. These aluminosilicates can be crystalline or amorphous in structure and can be naturally-occurring aluminosilicates or synthetically derived. A method for producing aluminosilicate ion exchange materials is disclosed in US Patent 3,985,669, Krummel et al, issued October 12, 1976. Preferred synthetic crystalline aluminosilicate ion exchange materials useful herein are available under the designations zeolite A, zeolite P(B), zeolite MAP, zeolite X and zeolite Y. In an especially preferred embodiment, the crystalline aluminosilicate ion exchange material has the formula :

            Na12 [(AlO2)12 (SiO2)12 ] · x H2O

    wherein x is from about 20 to about 30, especially about 27. This material is known as zeolite A. Dehydrated zeolites (x=0-10), and "overdried" zeolites (x=10-20) may also be used herein. The "overdried" zeolites are particularly useful when a low moisture environment is required, for example to improve stability of detergent bleaches such as perborate and percarbonate. Preferably, the aluminosilicate has a particle size of about 0.1-10 micrometers in diameter. Preferred ion exchange materials have a particle size diameter of from about 0.2 micrometers to about 4 micrometers. The term "particle size diameter" herein represents the average particle size diameter by weight of a given ion exchange material as determined by conventional analytical techniques such as, for example, microscopic determination utilizing a scanning electron microscope. The crystalline zeolite A materials herein are usually further characterized by their calcium ion exchange capacity, which is at least about 200 mg equivalent of CaCO3 water hardness/g of aluminosilicate, calculated on an anhydrous basis, and which generally is in the range of from about 300 mg eq./g to about 352 mg eq./g. The zeolite A materials herein are still further characterized by their calcium ion exchange rate which is at least about 2 grains Ca++/gallon/minute/gram/gallon (0.13g Ca++/litre/minute/gram/litre) of aluminosilicate (anhydrous basis), and generally lies within the range of from about 2 grains/gallon/minute/gram/gallon(0.13g Ca++/litre/minute/gram/litre) to about 6 grains/gallon/minute/gram/gallon (0.39g Ca++/litre/minute/gram/litre), based on calcium ion hardness. Optimum aluminosilicate for builder purposes exhibit a calcium ion exchange rate of at least about 4 grains/gallon/minute/gram/gallon (0.26g Ca++/litre/minute/gram/litre).
  • The granular agglomerates of the present invention also comprise other detergent ingredients.
  • Water-soluble salts of the higher fatty acids, i.e., "soaps", are useful anionic surfactants in the compositions herein. This includes alkali metal soaps such as the sodium, potassium, ammonium, and alkylammonium salts of higher fatty acids containing from about 8 to about 24 carbon atoms, and preferably from about 12 to about 18 carbon atoms. 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 alkylolammonium salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from about 10 to about 20 carbon atoms and a sulfonic acid or sulfuric acid ester group. (Included in the term "alkyl" is the alkyl portion of acyl groups.) Examples of this group of synthetic surfactants are the sodium and potassium 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 sodium and potassium alkyl benzene sulfonates in which the alkyl group contains from about 9 to about 15 carbon atoms, in straight or branched chain configuration, e.g., those of the type described in U.S. Pat. Nos. 2,220,099 and 2,477,383; and methyl ester sulphonates. Especially valuable are linear straight chain alkyl benzene sulfonates in which the average number of carbon atoms in the alkyl group is from about 11 to 13, abbreviated as C11-C13 LAS.
  • Other 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 wherein the alkyl groups contain from about 8 to about 12 carbon atoms; and sodium or potassium salts of alkyl ethylene oxide ether sulfates containing from about 1 to about 10 units of ethylene oxide per molecule and wherein the alkyl group contains from about 10 to about 20 carbon atoms.
  • Other useful anionic surfactants herein 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; watersoluble 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 about 20 carbon atoms in the alkane moiety.
  • Water-soluble nonionic surfactants are also useful as surfactants in the compositions of the invention. Indeed, preferred processes use anionic/nonionic blends. 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 16 carbon atoms, in either a straight chain or branched chain configuration, with from about 4 to 25 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 1 to 25 moles of ethylene oxide per mole of alcohol, especially 2 to 7 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; and condensation products of propylene glycol with ethylene oxide.
  • Other preferred nonionics are polyhydroxy fatty acid amides which may be prepared by reacting a fatty acid ester and an N-alkyl polyhydroxy amine. The preferred amine for use in the present invention is N-(R1)-CH2(CH2OH)4-CH2-OH and the preferred ester is a C12-C20 fatty acid methyl ester. Most preferred is the reaction product of N-methyl glucamine (which may be derived from glucose) with C12-C20 fatty acid methyl ester.
  • Methods of manufacturing polyhydroxy fatty acid amides have been described in WO 9206073, published on 16th April, 1992. This application describes the preparation of polyhydroxy fatty acid amides in the presence of solvents. In a highly preferred embodiment of the invention N-methyl glucamine is reacted with a C12-C20 methyl ester. It also says that the formulator of granular detergent compositions may find it convenient to run the amidation reaction in the presence of solvents which comprise alkoxylated, especially ethoxylated (EO 3-8) C12-C14 alcohols (page 15, lines 22-27). This directly yields nonionic surfactant systems which are suitable for use in the present invention, such as those comprising N-methyl glucamide and C12-C14 alcohols with an average of 3 ethoxylate groups per molecule.
  • Semi-polar nonionic surfactants include water-soluble amine oxides containing one alkyl moiety of from about 10 to 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from 1 to about 3 carbon atoms; water-soluble phosphine oxides containing one alkyl moiety of about 10 to 18 carbon atoms and 2 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 either straight or branched chain 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.
  • Useful cationic surfactants include water-soluble quaternary ammonium compounds of the form R4R5R6R7N+X-, wherein R4 is alkyl having from 10 to 20, preferably from 12-18 carbon atoms, and R5, R6 and R7 are each C1 to C7 alkyl preferably methyl; X- is an anion, e.g. chloride. Examples of such trimethyl ammonium compounds include C12-14 alkyl trimethyl ammonium chloride and cocalkyl trimethyl ammonium methosulfate.
  • The granular detergents of the present invention can contain neutral or alkaline salts which have a pH in solution of seven or greater, and can be either organic or inorganic in nature. The builder salt assists in providing the desired density and bulk to the detergent granules herein. While some of the salts are inert, many of them also function as detergency builder materials in the laundering solution.
  • Useful water-soluble salts include the compounds commonly known as detergent builder materials. Builders are generally selected from the various water-soluble, alkali metal, ammonium or substituted ammonium phosphates, polyphosphates, phosphonates, polyphosphonates, carbonates, silicates, borates, and polyhyroxysulfonates. Preferred are the alkali metal, especially sodium, salts of the above.
  • Specific examples of inorganic phosphate builders are sodium and potassium tripolyphosphate, pyrophosphate, polymeric metaphosphate having a degree of polymerization of from about 6 to 21, and orthophosphate. Examples of polyphosphonate builders are the sodium and potassium salts of ethylene diphosphonic acid, the sodium and potassium salts of ethane 1-hydroxy-1,1-diphosphonic acid and the sodium and potassium salts of ethane, 1,1,2-triphosphonic acid. Other phosphorus builder compounds are disclosed in U.S. Pat. Nos. 3,159,581; 3,213,030; 3,422,021; 3,422,137; 3,400,176 and 3,400,148, incorporated herein by reference.
  • Examples of nonphosphorus, inorganic builders are sodium and potassium carbonate, bicarbonate, sesquicarbonate, tetraborate decahydrate, and silicate having a molar ratio of SiO2 to alkali metal oxide of from about 0.5 to about 4.0, preferably from about 1.0 to about 2.4.
  • Polymers
  • Also useful are various organic polymers, some of which also may function as builders to improve detergency. Included among such polymers may be mentioned sodium carboxy-lower alkyl celluloses, sodium lower alkyl celluloses and sodium hydroxy-lower alkyl celluloses, such as sodium carboxymethyl cellulose, sodium methyl cellulose and sodium hydroxypropyl cellulose, homo & co polymers of amino acids (particularly homo and co polymers of aspartic acid glutamic acid), polyvinyl alcohols (which often also include some polyvinyl acetate), polyacrylamides, polyacrylates and various copolymers, such as those of maleic and acrylic acids, in particular maleic/acrylic/vinyl alcohol terpolymers. Molecular weights for such polymers vary widely but most are within the range of 2,000 to 100,000. Other suitable polymers are polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinylpyrrolidone polymers, polyvinyloxazolidones and polyvinylimidazoles or mixtures thereof.
  • Polymeric polycarboxyate builders are set forth in U.S. Patent 3,308,067, Diehl, issued March 7, 1967. Such materials include the water-soluble salts of homo-and copolymers of aliphatic carboxylic acids such as maleic acid, itaconic acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid, methylenemalonic acid, methyl acrylic and PEG. In the present invention it is preferred that polymeric polycarboxylates are substantially omitted from the aqueous slurry. By substantially omitted, less than 5% by weight of the aqueous slurry is preferred, and less than 2% by weight is more preferred.
  • Inorganic salts
  • Whilst the skilled person has a wide range of inorganic salts from which to choose, it is an essential feature of the present invention that the inorganic salt should result in an increased ionic conductivity of the aqueous slurry. The ionic conductivity of the aqueous slurry depends not only on the inorganic salt used, but also on the amount of inorganic salt used, and also on the composition of the aqueous slurry. Halides, especially chlorides, nitrates and citrates have been found to be particularly effective inorganic salts which when used at the preferred levels, have the effect of increasing the ionic conductivity of the aqueous slurry. Carbonates and sulphates are less effective, and may well cause a decrease in the ionic conductivity of the slurry. Without wishing to be bound by theory, it is believed that the higher ionic conductivity of the aqueous slurry suppresses the formation of highly viscous surfactant phases which are subsequently difficult to dry. By promoting less viscous surfactant phases the aqueous slurry is more readily formed into free-flowing, crisp particles having a good particle size distribution.
  • Silicone Oils
  • Particulate suds suppressors may also be incorporated into the finished composition by dry adding. Preferably the suds suppressing activity of these particles is based on fatty acids or silicones.
  • Optionals
  • Other ingredients commonly used in detergent compositions can be included in the compositions of the present invention. These include flow aids, color speckles, bleaching agents and bleach activators, suds boosters or suds suppressors, antitarnish and anticorrosion agents, soil suspending agents, anionic and nonionic soil release agents, dyes, clays, flocculating agents, STS, fillers, optical brighteners, germicides, pH adjusting agents, nonbuilder alkalinity sources, hydrotropes, enzymes, enzyme-stabilizing agents, chelating agents, (including EDDS) and perfumes.
  • These optional ingredients, especially optical brighteners, may be incorporated either directly in the agglomerates herein or may be components of separate particles suitable for dry adding to the agglomerates of the present invention.
  • Processing
  • The aqueous slurry may be prepared by a batch or continuous process. Most conveniently a batch mixer, or "crutcher" is used in which the various detergent components or dissolved in, or slurried with, water. Typically the aqueous slurry contains from about 20% to about 60% by weight of water, in particular from about 30% to about 40% by weight of water. This is referred to as the crutcher mix moisture. In the process of the present invention, the order of addition of the inorganic salt and the other components of the aqueous slurry (or "crutcher mix") is not considered to be critical. It is an essential feature of the present invention that the ionic conductivity of the aqueous slurry which comprises the inorganic salt must be greater than the ionic conductivity of the aqueous slurry in the absence of the inorganic salt. It is preferred that the addition of the inorganic salt results in an aqueous slurry having an ionic conductivity which is at least 3 milliSiemens higher than a corresponding aqueous slurry from which the inorganic salt has been omitted.
  • The drying of the aqueous slurry may be achieved by any one of several processes known to the skilled man, but it is preferably prepared by spray drying. Following the spray drying route, an aqueous slurry is prepared comprising the solids. The slurry is then pumped at high pressure through atomising nozzles into a drying tower where excess water is driven off, producing a flowable powder. The resulting powder may then be oversprayed with liquid ingredients, especially nonionic surfactants for which the powder has a high adsorption capacity before it loses its good flow characteristics. Other powdered components of the finished laundry detergent may be dry mixed with the flowable powder produced by the above process.
  • TEST METHOD Procedure for the Conductivity Test
    • 1. Prepare a 15kg sample of aqueous slurry ready for spray drying.
    • 2. Place the sample in a large bucket 400mm diameter and 500mm in height.
    • 3. Let the mix cool to 30°C.
    • 4. Using a Jenwat 4020 Conductivity Meter, measure the conductivity of the aqueous slurry.
    EXAMPLES
  • Aqueous Slurry Composition (% by weight)
    Reference Ex. 1 Ex. 2 Ex. 3 Ex.4
    LAS 11.2 11.2 11.7 11.2 11.2
    Zeolite A 26.2 26.2 30.0 26.2 26.2
    Water 33.0 33.0 34.5 33.0 33.0
    Chelant 0.3 0.3 0.3 0.3 0.3
    Brightener 0.1 0.1 0.1 0.1 0.1
    Magnesium Sulphate 0.3 0.3 0.3 0.3 0.3
    Carboxy Methyl Cellulose 0.3 0.3 0.3 0.3 0.3
    HEDP 0.3 0.3 0.3 0.3 0.3
    Copolymer of acrylic & maleic acid 0.4 0.4 0.4 0.4 0.4
    Miscellaneous 2.2 2.2 2.3 2.2 2.2
    Sodium Sulphate 25.7 21.4 21.4 24.3 18.5
    Sodium Chloride 0 4.3 1.4 7.2 0
    Sodium Citrate 0 0 0 0 4.3
    Conductivity (milliSiemens) 10 19 17 21 13
    Aqueous Slurry Composition (% by weight)
    Ex. 5 Ex. 6 Ex. 7 Ex. 8 Ex. 9
    LAS 11.2 11.2 11.7 11.2 11.2
    Zeolite A 26.2 26.2 30.0 26.2 26.2
    Water 33.0 33.0 34.5 33.0 33.0
    Chelant 0.3 0.3 0.3 0.3 0.3
    Brightener 0.1 0.1 0.1 0.1 0.1
    Magnesium Sulphate 0.3 0.3 0.3 0.3 0.3
    Carboxy Methyl Cellulose 0.3 0.3 0.3 0.3 0.3
    HEDP 0.3 0.3 0.3 0.3 0.3
    Copolymer of acrylic & maleic acid 0.4 0.4 0.4 0.4 0.4
    Miscellaneous 2.2 2.2 2.3 2.2 2.2
    Sodium Sulphate 21.4 21.4 21.4 21.4 21.4
    Potassium Chloride 4.3 0 0 0 0
    Potassium Nitrate 0 4.3 0 0 0
    Potassium Citrate 0 0 4.3 0 0
    Calcium Chloride 0 0 0 4.3 0
    Calcium Nitrate 0 0 0 0 4.3
    Conductivity (milliSiemens) 19 17 13 16 14
  • The aqueous slurry is heated to 70°C and is fed through to a series of pressure pumps. This increases the pressure of the mix up to 80 bar. Air is then injected into the mix at a pressure of 100 bar. The high pressure mix is then directed to the top of the spray drying tower. Here it is blown through a set of nozzles, which range in aperture diameter up to 1mm. These atomise the slurry into droplets. The moisture is driven off these particles as they fall through the tower with a residence time of up to 180 seconds by contact with hot air at 275°C. At the bottom of the tower a blown powder is collected with a density in the range of 300 - 550g/l. The resulting blown powder has a moisture in the range of 5 -_15% with the majority of the particles having a size in the range of 150 - 1200 micrometers.

Claims (10)

  1. A process for preparing a particulate detergent composition which comprises:
    (a) forming an aqueous slurry comprising water, anionic surfactant and at least 0.5% of sodium aluminosilicate,
    (b) adding an inorganic salt, or mixture of inorganic salts, to the aqueous slurry,
    (c) drying the slurry
    characterised in that the aqueous slurry comprises at least 1% by weight of the inorganic salt, and whereby the addition of the inorganic salt increases the ionic conductivity of the aqueous slurry, and wherein the aqueous slurry comprises less than 5% by weight of silicate.
  2. A process according to claim 1 wherein the inorganic salt is selected from the group consisting of alkali metal salts of halides, nitrates, citrates or mixtures thereof.
  3. A process according to claim 1 wherein the inorganic salt is selected from the group consisting of alkaline earth metal salts of halides, nitrates, citrates or mixtures thereof.
  4. A process according to claim 2 wherein the inorganic salt is sodium chloride.
  5. A process according to any of the previous claims wherein the step of adding the inorganic salt raises the ionic conductivity of the aqueous slurry by at least 3 milliSiemens.
  6. A process according to claim 1 wherein the range of anionic surfactant is 1% to 50 %, more preferably from 5% to 20 % by weight.
  7. A process according to claim 1 wherein the range of sodium aluminosilicate is 1% to 50 %, more preferably from 5% to 30 % by weight.
  8. A process according to claim 1 wherein the range of inorganic salt is 1% to 50 %, more preferably from 1% to 10% by weight.
  9. A spray-dried powder comprising :
    (a) at least one surfactant,
    (b) from 2% to 80% by weight of aluminosilicate
    (c) from 1% to 20% by weight of an inorganic salt selected from the group consisting of alkali metal, alkaline earth metal salts, or mixtures thereof of halides, nitrates, citrates or mixtures thereof, and
    (d) less than 5% by weight of silicate.
  10. A spray-dried powder according to claim 9 comprising :
    (a) at least 5% by weight of surfactant ;
    (b) from 10% to 50% by weight of aluminosilicate,
    (c) from 2% to 10% by weight of an alkali metal, preferably sodium, chloride, and
    (d) less than 2% by weight of silicate.
EP19950306547 1995-09-18 1995-09-18 Process for making granular detergents Expired - Lifetime EP0763594B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP19950306547 EP0763594B1 (en) 1995-09-18 1995-09-18 Process for making granular detergents

Applications Claiming Priority (17)

Application Number Priority Date Filing Date Title
ES95306547T ES2202343T3 (en) 1995-09-18 1995-09-18 Process for preparing detergent granules.
DE1995631207 DE69531207D1 (en) 1995-09-18 1995-09-18 A process for the preparation of granular detergents
AT95306547T AT244294T (en) 1995-09-18 1995-09-18 A process for the preparation of granular detergent:
DE69531207T DE69531207T2 (en) 1995-09-18 1995-09-18 A process for the preparation of granular detergents
EP19950306547 EP0763594B1 (en) 1995-09-18 1995-09-18 Process for making granular detergents
ZA9607561A ZA9607561B (en) 1995-09-18 1996-09-06 Process for making granular detergents
PCT/US1996/014864 WO1997011149A1 (en) 1995-09-18 1996-09-13 Process for making granular detergents
HU9901581A HU9901581A3 (en) 1995-09-18 1996-09-13 Process for making granular detergents
TR1998/00489T TR199800489T1 (en) 1995-09-18 1996-09-13 Process for its granular detergents.
US09/043,183 US5998356A (en) 1995-09-18 1996-09-13 Process for making granular detergents
BR9610630A BR9610630A (en) 1995-09-18 1996-09-13 Process for the manufacture of granular detergent
IL12365196A IL123651D0 (en) 1995-09-18 1996-09-13 Process for making granular detergents
CNB96198239XA CN1168814C (en) 1995-09-18 1996-09-13 Process for making granular detergents
CA 2231577 CA2231577C (en) 1995-09-18 1996-09-13 Process for making granular detergents
CZ98708A CZ70898A3 (en) 1995-09-18 1996-09-13 Process for preparing granulated detergents
ARP960104387A AR003608A1 (en) 1995-09-18 1996-09-18 Process for manufacturing a particulate detergent composition and spray dried powder obtained by the same.
MX9802108A MX9802108A (en) 1995-09-18 1998-03-17 Process for making granular detergents.

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EP0763594A1 true EP0763594A1 (en) 1997-03-19
EP0763594B1 EP0763594B1 (en) 2003-07-02

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CN (1) CN1168814C (en)
AR (1) AR003608A1 (en)
AT (1) AT244294T (en)
BR (1) BR9610630A (en)
CA (1) CA2231577C (en)
CZ (1) CZ70898A3 (en)
DE (2) DE69531207T2 (en)
ES (1) ES2202343T3 (en)
HU (1) HU9901581A3 (en)
IL (1) IL123651D0 (en)
MX (1) MX9802108A (en)
TR (1) TR199800489T1 (en)
WO (1) WO1997011149A1 (en)
ZA (1) ZA9607561B (en)

Cited By (4)

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DE19936614B4 (en) * 1999-08-04 2008-12-24 Henkel Ag & Co. Kgaa A process for the production of a detergent
DE19936613B4 (en) * 1999-08-04 2010-09-02 Henkel Ag & Co. Kgaa A process for the production of a detergent builder system with soluble
EP2669001A1 (en) * 2012-06-01 2013-12-04 The Procter and Gamble Company Spray-drying process
WO2016041778A1 (en) * 2014-09-18 2016-03-24 Henkel Ag & Co. Kgaa Method for producing spray-dried detergent powders

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CN1109579C (en) * 1999-08-17 2003-05-28 中国石油化工集团公司 Process for preparation of molecular sieve slurry for catalyst
CN1164611C (en) 2002-06-17 2004-09-01 厦门大学 Synthesizing method for propyl-glutdipeptide
CN103937620A (en) * 2014-04-04 2014-07-23 广州立白企业集团有限公司 Neutral detergent powder compound and preparation method thereof

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WO1990004630A1 (en) 1988-10-21 1990-05-03 Henkel Corporation A process for preparing a detergent slurry and particulate detergent composition
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US3159581A (en) 1962-04-13 1964-12-01 Procter & Gamble Detergency composition
US3213030A (en) 1963-03-18 1965-10-19 Procter & Gamble Cleansing and laundering compositions
US3422021A (en) 1963-03-18 1969-01-14 Procter & Gamble Detergent composition
US3308067A (en) 1963-04-01 1967-03-07 Procter & Gamble Polyelectrolyte builders and detergent compositions
US3400148A (en) 1965-09-23 1968-09-03 Procter & Gamble Phosphonate compounds
US3400176A (en) 1965-11-15 1968-09-03 Procter & Gamble Propanepolyphosphonate compounds
US3422137A (en) 1965-12-28 1969-01-14 Procter & Gamble Methanehydroxydiphosphonic acids and salts useful in detergent compositions
US3985669A (en) 1974-06-17 1976-10-12 The Procter & Gamble Company Detergent compositions
US4379080A (en) 1981-04-22 1983-04-05 The Procter & Gamble Company Granular detergent compositions containing film-forming polymers
JPS58204098A (en) 1982-05-25 1983-11-28 Kao Corp Detergent composition
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EP0215637A2 (en) 1985-09-12 1987-03-25 Unilever N.V. Process for manufacture of detergent powder
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EP0257514A2 (en) * 1986-08-22 1988-03-02 Dow Corning Corporation Zeolite built detergent compositions
EP0326208A2 (en) * 1988-01-26 1989-08-02 THE PROCTER & GAMBLE COMPANY Pouched granular detergent compositions containing hygroscopic builders
WO1990004630A1 (en) 1988-10-21 1990-05-03 Henkel Corporation A process for preparing a detergent slurry and particulate detergent composition
WO1992006151A1 (en) * 1990-09-28 1992-04-16 The Procter & Gamble Company Polyhydroxy fatty acid amides in zeolite/layered silicate built detergents
WO1992006073A1 (en) 1990-09-28 1992-04-16 The Procter & Gamble Company Preparation of polyhydroxy fatty acid amides in the presence of solvents
EP0520582A1 (en) * 1991-06-28 1992-12-30 Colgate-Palmolive Company Zeolite based spray-dried detergent compositions and process for preparing same

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19936614B4 (en) * 1999-08-04 2008-12-24 Henkel Ag & Co. Kgaa A process for the production of a detergent
DE19936613B4 (en) * 1999-08-04 2010-09-02 Henkel Ag & Co. Kgaa A process for the production of a detergent builder system with soluble
EP2669001A1 (en) * 2012-06-01 2013-12-04 The Procter and Gamble Company Spray-drying process
WO2013181205A1 (en) * 2012-06-01 2013-12-05 The Procter & Gamble Company Spray-drying process
WO2016041778A1 (en) * 2014-09-18 2016-03-24 Henkel Ag & Co. Kgaa Method for producing spray-dried detergent powders

Also Published As

Publication number Publication date
TR199800489T1 (en) 1998-06-22
CN1168814C (en) 2004-09-29
MX9802108A (en) 1998-08-30
HU9901581A2 (en) 1999-08-30
AT244294T (en) 2003-07-15
HU9901581A3 (en) 2000-10-30
CA2231577C (en) 2002-11-19
IL123651D0 (en) 1998-10-30
DE69531207T2 (en) 2004-04-22
ZA9607561B (en) 1997-06-10
EP0763594B1 (en) 2003-07-02
CZ70898A3 (en) 1998-10-14
BR9610630A (en) 1999-03-16
DE69531207D1 (en) 2003-08-07
WO1997011149A1 (en) 1997-03-27
CA2231577A1 (en) 1997-03-27
CN1202195A (en) 1998-12-16
ES2202343T3 (en) 2004-04-01
AR003608A1 (en) 1998-08-05

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