EP0543911B2 - Detergent compositions - Google Patents

Detergent compositions Download PDF

Info

Publication number
EP0543911B2
EP0543911B2 EP91915442A EP91915442A EP0543911B2 EP 0543911 B2 EP0543911 B2 EP 0543911B2 EP 91915442 A EP91915442 A EP 91915442A EP 91915442 A EP91915442 A EP 91915442A EP 0543911 B2 EP0543911 B2 EP 0543911B2
Authority
EP
European Patent Office
Prior art keywords
component
composition according
detergent composition
weight
detergent
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.)
Expired - Lifetime
Application number
EP91915442A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP0543911A1 (en
EP0543911A4 (en
EP0543911B1 (en
Inventor
Alastair John Pretty
Douglas Gilbert Fraser
Paul Andrew Hardy
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10680876&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0543911(B2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Publication of EP0543911A1 publication Critical patent/EP0543911A1/en
Publication of EP0543911A4 publication Critical patent/EP0543911A4/en
Publication of EP0543911B1 publication Critical patent/EP0543911B1/en
Application granted granted Critical
Publication of EP0543911B2 publication Critical patent/EP0543911B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C11D3/39—Organic or inorganic per-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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246—Silicates, e.g. diatomaceous earth
    • C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
    • C11D3/1273—Crystalline layered silicates of type NaMeSixO2x+1YH2O
    • 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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246—Silicates, e.g. diatomaceous earth
    • C11D3/128—Aluminium silicates, e.g. zeolites
    • 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
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2075—Carboxylic acids-salts thereof
    • C11D3/2082—Polycarboxylic acids-salts thereof
    • 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
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2075—Carboxylic acids-salts thereof
    • C11D3/2086—Hydroxy carboxylic acids-salts thereof
    • 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
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3746—Macromolecular 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

Definitions

  • This invention relates to laundry detergent compositions and more especially to laundry detergent compositions that incorporate little or no phosphorus containing materials.
  • Laundry detergent compositions of this type have become widely available as a result of public concern over, and/or legislative action to control, the environmental impact of aqueous effluent from untreated or partially treated domestic sewage containing dissolved phosphates.
  • Zero phosphate compositions employ a combination of materials to replace the phosphate builder, the principal component usually being a water insoluble sodium aluminosilicate zeolite supplemented by a mixture of water soluble inorganic and polymeric organic salts.
  • EP-A-405,122 describes detergent compositions containing crystalline layered silicate and zeolite builders.
  • EP-A-337, 219 describes detergent compositions containing crystalline layered silicate and an oxygen bleaching component.
  • JP 1-153800 describes concentrated fabric softening granular detergent compositions containing bentonite, crystalline layered silicate and zeolite components.
  • a particulate detergent composition comprising an oxygen bleach and comprising
  • component (b)(iii) of the builder system is ⁇ , ⁇ , ⁇ , or ⁇ -Na 2 Si 2 O 5 and component (b)(i) is a synthetic hydrated zeolite of unit cell formula Na z [(AlO 2 ) z (SiO 2 ) y ]. xH 2 O wherein z and y are at least 6, the ratio of z to y is from 1.0 to 0.5 and x is at least 5, preferably from 7.5 to 276.
  • the monomeric or oligomeric organic carboxylate chelating agent has a first carboxyl logarithmic acidity constant (pK 1 ) of less than 9, preferably of from 2 to 8.5.
  • the present invention concerns a particulate detergent composition incorporating one or more surfactants and a detergent builder system composed of three principal components viz. a sodium aluminosilicate zeolite, a water soluble monomeric or oligomeric organic carboxylate chelating agent and a crystalline layered sodium silicate.
  • Compositions in accordance with the invention also contain an oxygen bleach and optionally other, non surfactant, non-builder detergent ingredients.
  • a wide range of surfactants can be used in the detergent compositions.
  • anionic surfactants are particularly suitable herein, especially mixtures of sulphonate and sulphate surfactants in a weight ratio of from 5:1 to 1:2, preferably from 3:1 to 2:3, more preferably from 3:1 to 1:1.
  • Preferred sulphonates include alkyl benzene sulphonates having from 9 to 15, especially 11 to 13 carbon atoms in the alkyl radical, and alpha-sulphonated methyl fatty acid esters in which the fatty acid is derived from a C 12 -C 18 fatty source, preferably from a C 16 -C 18 fatty source.
  • the cation is an alkali metal, preferably sodium.
  • Preferred sulphate surfactants are alkyl sulphates having from 12 to 22, preferably 14 to 18 carbon atoms in the alkyl radical, optionally in admixture with ethoxy sulphates having from 10 to 20, preferably 10 to 16 carbon atoms in the alkyl radical and an average degree of ethoxylation of 1 to 6.
  • the cation in each instance is again an alkali metal cation, preferably sodium.
  • One class of nonionic surfactants useful in the present invention are condensates of ethylene oxide with a hydrophobic moiety to provide a surfactant having an average hydrophilic-lipophilic balance (HLB) in the range from 8 to 17, preferably from 9.5 to 13.5, more preferably from 10 to 12.5.
  • HLB hydrophilic-lipophilic balance
  • the hydrophobic (lipophilic) moiety may be aliphatic or aromatic in nature and the length of the polyoxyethylene 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.
  • Especially preferred nonionic surfactants of this type are the C 9 -C 15 primary alcohol ethoxylates containing 3-8 moles of ethylene oxide per mole of alcohol, particularly the C 14 -C 15 primary alcohols containing 6-8 moles of ethylene oxide per mole of alcohol and the C 12 -C 14 primary alcohols containing 3-5 moles of ethylene oxide per mole of alcohol.
  • Nonionic surfactants comprises alkyl polyglucoside compounds of general formula RO (C n H 2n O) t Z x wherein Z is a moiety derived from glucose; R is a saturated hydrophobic alkyl group that contains from 12 to 18 carbon atoms; t is from 0 to 10 and n is 2 or 3; x is from 1.3 to 4, the compounds including less than 10% unreacted fatty alcohol and less than 50% short chain alkyl polyglucosides.
  • Compounds of this type and their use in detergent compositions are disclosed in EP-B 0070074, 0070077, 0075996 and 0094118.
  • a further class of surfactants are the semi-polar surfactants such as amine oxides.
  • Suitable amine oxides are selected from mono C 8 -C 20 , preferably C 10 -C 14 N-alkyl or alkenyl amine oxides and propylene-1,3-diamine dioxides wherein the remaining N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups.
  • Cationic surfactants can also be used in the detergent compositions herein and suitable quaternary ammonium surfactants are selected from mono C 8 -C 16 , preferably C 10 -C 14 N-alkyl or alkenyl ammonium surfactants wherein remaining N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups.
  • the detergent compositions can comprise from 5% to 50% by weight of surfactant but usually comprises from 5% to 30%, more preferably from 5% to 15% by weight.
  • Combinations of surfactant types are preferred, more especially anionic-nonionic and also anionic-nonionic-cationic blends. Particularly preferred combinations are described in GB-A-2040987 and EP-A-0087914.
  • the surfactants can be incorporated into the compositions as mixtures, it is preferable to control the point of addition of each surfactant in order to optimise the physical characteristics of the composition and avoid processing problems. Preferred modes and orders of surfactant addition are described hereinafter.
  • compositions in accordance with the invention is a detergent builder system comprising a mixture of sodium aluminosilicate zeolite, a water soluble monomeric or oligomeric carboxylate chelating agent and a crystalline layered sodium silicate in defined amounts.
  • preferred sodium aluminosilicate zeolites have the unit cell formula Na z [(AlO 2 ) z (SiO 2 ) y ] xH 2 O wherein z and y are at least 6; the molar ratio of z to y is from 1.0 to 0.5 and x is at least 5, preferably from 7.5 to 276, more preferably from 10 to 264.
  • the aluminosilicate materials are in hydrated form and are preferably crystalline, containing from 10% to 28%, more preferably from 18% to 22% water.
  • the above aluminosilicate ion exchange materials are further characterised by a particle size diameter of from 0.1 to 10 micrometers, preferably from 0.2 to 4 micrometers.
  • particle size diameter herein represents the average particle size diameter of a given ion exchange material as determined by conventional analytical techniques such as, for example, microscopic determination utilizing a scanning electron microscope.
  • the aluminosilicate ion exchange materials are further characterised by their calcium ion exchange capacity, which is at least 200 mg equivalent of CaCO 3 water hardness/g of aluminosilicate, calculated on an anhydrous basis, and which generally is in the range of from 300 mg eq./g to 352 mg eq./g.
  • the aluminosilicate ion exchange materials herein are still further characterised by their calcium ion exchange rate which is at least 130 mg equivalent of CaCO 3 /litre/minute/(g/litre) [2 grains Ca ++ /gallon/minute/(gram/gallon)] of aluminosilicate (anhydrous basis), and which generally lies within the range of from 130 mg equivalent of CaCO 3 /litre/minute/(gram/litre) [2 grains/gallon/minute/ (gram/gallon)] to 390 mg equivalent of CaCO 3 /litre/minute/ (gram/litre) [6 grains/gallon/minute/(gram/gallon)], based on calcium ion hardness.
  • Optimum aluminosilicates for builder purposes exhibit a calcium ion exchange rate of at least 260 mg equivalent of CaCO 3 /litre/minute/(gram/litre) [4 grains/gallon/minute/(gram/gallon)].
  • Aluminosilicate ion exchange materials useful in the practice of this invention are commercially available and can be naturally occurring materials, but are preferably synthetically derived. A method for producing aluminosilicate ion exchange materials is discussed in US Patent No. 3,985,669.
  • Preferred synthetic crystalline aluminosilicate ion exchange materials useful herein are available under the designations Zeolite A, Zeolite B, Zeolite X, Zeolite HS and mixtures thereof.
  • the crystalline aluminosilicate ion exchange material is Zeolite A and has the formula Na 12 [(AlO 2 ) 12 (SiO 2 ) 12 ]. xH 2 O wherein x is from 20 to 30, especially 27.
  • the water-soluble monomeric or oligomeric organic carboxylate chelating agent can be selected from a wide range of compounds but preferably has a first carboxyl logarithmic acidity/constant (pK 1 ) of less than 9, preferably of between 2 and 8.5, more preferably of between 4 and 7.5.
  • the logarithmic acidity constant is defined by reference to the equilibrium H + + A ⁇ H + A where A is the fully ionized carboxylate anion of the builder salt.
  • acidity constants are defined at 25°C and at zero ionic strength.
  • Literature values are taken where possible (see Stability Constants of Metal-Ion Complexes, Special Publication No. 25, The Chemical Society, London): where doubt arises they are determined by potentiometric titration using a glass electrode.
  • the polycarboxylate has a pK Ca++ in the range from about 2 to about 7 especially from about 3 to about 6.
  • the stability constant is defined at 25°C and at zero ionic strength using a glass electrode method of measurement as described in Complexation in Analytical Chemistry by Anders Ringbom (1963).
  • the carboxylate or polycarboxylate builder can be momomeric or oligomeric in type although monomeric polycarboxylates are generally preferred for reasons of cost and performance.
  • Monomeric and oligomeric builders can be selected from acyclic, alicyclic, heterocyclic and aromatic carboxylates having the general formulae wherein R 1 represents H,C 1-30 alkyl or alkenyl optionally substituted by hydroxy, carboxy, sulfo or phosphono groups or attached to a polyethylenoxy moiety containing up to 20 ethyleneoxy groups; R 2 represents H,C 1-4 alkyl, alkenyl or hydroxy alkyl, or alkaryl, sulfo, or phosphono groups;
  • Suitable carboxylates containing one carboxy group include lactic acid, glycollic acid and ether derivatives thereof as disclosed in Belgian Patent Nos. 821,368, 821, 369 and 821,370.
  • Polycarboxylates containing two carboxy groups include the water-soluble salts of succinic acid, malonic acid, (ethylenediozy) diacetic acid, maleic acid, diglycollic acid, tartaric acid, tartronic acid and fumaric acid, as well as the ether carboxylates described in German Offenlegenschrift 2,446,686, and 2,446,687 and U.S. Patent No. 3,935,257 and the sulfinyl carboxylates described in Belgian Patent No. 840,623.
  • Polycarboxylates containing three carboxy groups include, in particular, water-soluble citrates, aconitrates and citraconates as well as succinate derivatives such as the carboxymethyloxysuccinates described in British Patent No. 1,379,241, lactoxysuccinates described in British Patent No. 1,389,732, and aminosuccinates described in Netherlands Application 7205873, and the oxypolycarboxylate materials such as 2-oxa-1,1,3-propane tricarboxylates described in British Patent No. 1,387,447.
  • Polycarboxylates containing four carboxy groups include oxydisuccinates disclosed in British Patent No. 1,261,829, 1,1,2,2-ethane tetracarboxylates, 1,1,3,3-propane tetracarboxylates and 1,1,2,3-propane tetracarboxylates.
  • Polycarboxylates containing sulfo substituents include the sulfosuccinate derivatives disclosed in British Patent Nos. 1,398,421 and 1,398,422 and in U.S. Patent No. 3,936,448, and the sulfonated pyrolysed citrates described in British Patent No. 1,082,179, while polycarboxylates containing phosphone substituents are disclosed in British Patent No. 1,439,000.
  • Alicyclic and heterocyclic polycarboxylates include cyclopentane-cis,cis,cis-tetracarbozylates, cyclopentadienide pentacarbozylates, 2,3,4,5-tetrahydrofuran - cis, cis, cis-tetracarboxylates, 2,5-tetrahydrofuran -cis - dicarboxylates, 2,2,5,5-tetrahydrofuran - tetracarboxylates, 1,2,3,4,5,6-hexane -hexacarboxylates and carboxymethyl derivatives of polyhydric alcohols such as sorbitol, mannitol and xylitol.
  • Aromatic polycarboxylates include mellitic acid, pyromellitic acid and the phthalic acid derivatives disclosed in British Patent No. 1,425,343.
  • the preferred polycarboxylates are hydroxycarbozylates containing up to three carboxy groups per molecule, more particularly citrates.
  • the parent acids of the monomeric or oligomeric polycarboxylate chelating agents or mixtures thereof with their salts eg. citric acid or citrate/citric acid mixtures are also contemplated as components of builder systems useful in the present invention.
  • the third element of the builder system is a crystalline layered sodium silicate having the general formula NaMSi x O 2x+1 . yH 2 O wherein M is sodium or hydrogen, x is a number from 1.9 to 4 and y is a number from 0 to 20.
  • Crystalline layered sodium silicates of this type are disclosed in EP-A-0164514 and methods for their preparation are disclosed in DE-A-3417649 and DE-A-3742043.
  • x in the general formula above can have a value of 2, 3 or 4 and is preferably 2. More preferably M is sodium and y is 0 and preferred examples of this formula comprise the ⁇ -, ⁇ -, ⁇ - and ⁇ -forms of Na 2 Si 2 O 5 .
  • These materials are available from Hoechst AG FRG as respectively NaSKS-5, NaSKS-7, NaSKS-11 and NaSKS-6. The most preferred material is ⁇ -Na 2 Si 2 O 5 , NaSKS-6.
  • detergent builder materials can also form part of the builder system but are not essential elements thereof. Such materials can be organic or inorganic in nature.
  • Inorganic builder materials that can form optional elements of the builder system for the purposes of the invention include alkali metal carbonates, bicarbonates and silicates.
  • Suitable organic materials include the organic phosphonates and amino polyalkylene phosphonates although these materials are less preferred where the minimisation of phosphorus compounds in the compositions is desired.
  • Suitable water soluble organic salts are the homo-or co-polymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms.
  • Polymers of the latter type are disclosed in GB-A-1,596,756.
  • Examples of such salts are polyacrylates of MW 2000-5000 and their copolymers with maleic anhydride, such copolymers having a molecular weight of from 20,000 to 70,000, especially about 40,000. These materials are normally used at levels of from 0.5% to 10% by weight more preferably from 0.75% to 8%, most preferably from 1% to 6% by weight of the composition.
  • the optional builder materials if present, will total no more than 25% by weight of the composition normally less than 20% and most usually less than 15% by weight.
  • the builder system will comprise from 10% to 60% by weight of the compositions, more preferably from 20% to 60% by weight.
  • the sodium aluminosilicate zeolite will comprise from 20% to 60% by weight of the mixture
  • the monomeric or oligomeric carboxylate will comprise from 10% to 30% by weight of the mixture
  • the crystalline layered silicate will comprise from 10% to 65% by weight of the mixture.
  • the zeolite is present in an amount of from 25% to 50%
  • the monomeric or oligomeric carboxylate comprises from 15% to 25%
  • the layered silicate from 20% to 50% by weight of the builder system.
  • the builder system incorporates a combination of auxiliary inorganic and organic builders such as sodium carbonate and maleic anhydride/acrylic acid copolymers in amounts of up to 25%.
  • compositions in accordance with the invention also contain up to 40% of non-surfactant non detergent builder components including an oxygen bleach and optionally other ingredients.
  • non-surfactant non detergent builder components including an oxygen bleach and optionally other ingredients.
  • Anti-redeposition and soil-suspension agents, optical brighteners, soil release agents, dyes and pigments are examples of such optional ingredients and can be added in varying amounts as desired.
  • Anti-redeposition and soil-suspension agents suitable herein include cellulose derivatives such as methylcellulose, carboxymethylcellulose and hydroxyethylcellulose, and homo- or co-polymeric polycarboxylic acids or their salts.
  • Polymers of this type include copolymers of maleic anhydride with ethylene, methylvinyl ether, acrylic or methacrylic acid, the maleic anhydride constituting at least 20 mole percent of the copolymer. These materials are normally used at levels of from 0.5% to 10% by weight, more preferably from 0.75% to 8%, most preferably from 1% to 6% by weight of the composition.
  • polyethylene glycols particularly those of molecular weight 1000-10000, more particularly 2000 to 8000 and most preferably about 4000. These are used at levels of from 0.20% to 5% more preferably from 0.25% to 2.5% by weight. These polymers and the previously mentioned homo- or co-polymeric polycarboxylate salts are valuable for improving whiteness maintenance, fabric ash deposition, and cleaning performance on clay, proteinaceous and oxidizable soils in the presence of transition metal impurities.
  • compositions in accordance with the present invention are their ability to maintain the suspension of insoluble particulate solids (ash) with reduced levels of polymeric polycarboxylate builder/anti redeposition agents or even, in preferred compositions of the invention, with no polymeric polycarboxylate present.
  • a level of polymeric polycarboxylate of 5% in conventional products can be halved, i.e. to 2.5% with no increase in fabric ash level in compositions according to the present invention. If the polymeric polycarboxylate is removed entirely only a slight increase in fabric ash takes place in contrast to a virtual doubling of the ash level if the polymer is removed from a conventional formulation.
  • compositions in accordance with the invention also show robustness in hardness control in under built situations, i.e. where insufficient detergent builder is available to control all of the mineral hardness present. This benefit is believed to arise because of the ability of the ternary builder system components to redistribute the calcium and magnesium hardness ions amongst themselves in underbuilt situations, taking advantage of the enhanced affinity of the crystalline layered silicate component for magnesium ion.
  • compositions in accordance with the present invention are a reduction in damage to fabrics arising from the washing process. This loss is believed to arise from the interaction of heavy metal ions deposited on fabrics during the washing process with oxygen bleaches. Fabrics washed in compositions of the present invention show a level of deposition of heavy metal ions and a reduced tensile strength loss, relative to compositions in which the crystalline layered silicate component is replaced by a conventional amorphous silicate
  • Preferred optical brighteners are anionic in character, examples of which are disodium 4,4 1 -bis-(2-diethanolamino-4-anilino-s-triazin-6-ylamino)stilbene-2,2 1 -disulphonate, disodium 4, 4 1 -bis-(2-morpholino-4-anilino-s-triazin-6-ylaminostilbene-2,2 1 -disulphonate, disodium 4,4 1 -bis-(2,4-dianilino-s-triazin-6-ylamino)stilbene-2,2 1 -disulphonate, monosodium 4 1 ,4 11 -bis-(2,4-dianilino-s-triazin-6-ylamino)stilbene-2-sulphonate, disodium 4,4 1 -bis-(2-anilino-4-(N-methyl-N-2-hydroxyethylamino)-s-triazin-6-ylamino)stilbene-2,
  • Soil-release agents useful in compositions of the present invention are conventionally copolymers or terpolymers of terephthalic acid with ethylene glycol and/or propylene glycol units in various arrangements. Examples of such polymers are disclosed in the commonly assigned US Patent Nos. 4116885 and 4711730 and European Published Patent Application No. 0272033.
  • a particular preferred polymer in accordance with EP-A-0272033 has the formula (CH 3 )(PEG) 43 ) 0.75 (POH) 0.25 [T-PO) 2.8 (T-PEG) 0.4 ]T(PO- H) 0.25 ((PEG) 43 CH 3 ) 0.75 where PEG is -(OC 2 H 4 )0-, PO is (OC 3 H 6 O) and T is (pcOC 6 H 4 CO).
  • Certain polymeric materials such as polyvinyl pyrrolidones typically of MW 5000-20000, preferably 10000-15000, also form useful agents in preventing the transfer of labile dyestuffs between fabrics during the washing process.
  • Another optional but highly preferred ingredient is a particulate inorganic perhydrate bleach.
  • Any particulate inorganic perhydrate bleach can be used, in an amount of from 3% to 40% by weight, more preferably from 8% to 25% by weight and most preferably from 12% to 20% by weight of the compositions.
  • Preferred examples of such bleaches are sodium perborate monohydrate and tetrahydrate and mixtures thereof.
  • a peroxy carboxylic acid bleach precursor commonly referred to as a bleach activator
  • a bleach activator which is preferably added in a prilled or agglomerated form.
  • suitable compounds of this type are disclosed in British Patent Nos, 1586769 and 2143231 and a method for their formation into a prilled form is described in European Published Patent Application No. 0062523.
  • Preferred examples of such compounds are tetracetyi ethylene diamine and sodium 3, 5, 5 trimethyl hexanoylozybenzene sulphonate.
  • Bleach activators are normally employed at levels of from 0.5% to 10% by weight, more frequently from 1% to 8% and preferably from 2% to 6% by weight of the composition.
  • a suds suppressor exemplified by silicones, and silica-silicone mixtures.
  • Silicones can be generally represented by alkylated polysiloxane materials while silica is normally used in finely divided forms, exemplified by silica aerogels and xerogels and hydrophobic silicas of various types. These materials can be incorporated as particulates in which the suds suppressor is advantageously releasably incorporated in a water-soluble or water-dispersible, substantially non-surface-active detergent-impermable carrier. Alternatively the suds suppressor can be dissolved or dispersed in a liquid carrier and applied by spraying on to one or more of the other components.
  • useful silicone suds controlling agents can comprise a mixture of an alkylated siloxane, of the type referred to hereinbefore, and solid silica. Such mixtures are prepared by affixing the silicone to the surface of the solid silica.
  • a preferred silicone suds controlling agent is represented by a hydrophobic silanated (most preferably trimethyl-silanated) silica having a particle size in the range from 10 nanometers to 20 nanometers and a specific surface area above 50 m 2 /g, intimately admixed with dimethyl silicone fluid having a molecular weight in the range from about 500 to about 200,000 at a weight ratio of silicone to silanated silica of from about 1:1 to about 1:2.
  • a preferred silicone suds controlling agent is disclosed in Bartollota et al. U.S. Patent 3,933, 572.
  • Other particularly useful suds suppressors are the self-emulsifying silicone suds suppressors.
  • DC-544 commercially availably from Dow Corning, which is a siloxane/glycol copolymer.
  • the suds suppressors described above are normally employed at levels of from 0.001% to 0.5% by weight of the composition, preferably from 0.01% to 0.1% by weight.
  • the preferred methods of incorporation comprise either application of the suds suppressors in liquid form by spray-on to one or more of the major components of the composition or alternatively the formation of the suds suppressors into separate particulates that can then be mixed with the other solid components of the composition.
  • the incorporation of the suds modifiers as separate particulates also permits the inclusion therein of other suds controlling materials such as C 20 -C 24 fatty acids, microcrystalline waxes and high MW copolymers of ethylene oxide and propylene oxide which would otherwise adversely affect the dispersibility of the matrix. Techniques for forming such suds modifying particulates are disclosed in the previously mentioned Bartolotta et al U.S. Patent No. 3,933,672.
  • Another optional ingredient useful in the present invention is one or more enzymes.
  • Preferred enzymatic materials include the commercially availably amylases, neutral and alkaline proteases, lipases, esterases and cellulases conventionally incorporated into detergent compositions. Suitable enzymes are discussed in U.S. Patent 3,533,139.
  • Fabric softening agents can also be incorporated into detergent compositions in accordance with the present invention. These agents may be inorganic or organic in type. Inorganic softening agents are exemplified by the smectite clays disclosed in GB-A-1,400,898. Organic fabric softening agents include the water insoluble tertiary amines as disclosed in GB-A-1514276 and EP-B-0011340. Their combination with mono C 12 -C 14 quaternary ammonium salts is disclosed in EP-B-0026528. Other useful organic fabric softening agents are the dilong chain amides as disclosed in EP-B-0242919. Additional organic ingredients of fabric softening systems include high molecular weight polyethylene oxide materials as disclosed in EP-A-0299575 and 0313146.
  • Levels of smectite clay are normally in the range from 5% to 15%, more preferably from 8% to 12% by weight, with the material being added as a dry mixed component to the remainder of the formulation.
  • Organic fabric softening agents such as the water-insoluble tertiary amines or dilong chain amide materials are incorporated at levels of from 0.5% to 5% by weight, normally from 1% to 3% by weight, whilst the high molecular weight polyethylene oxide materials and the water soluble cationic materials are added at levels of from 0.1% to 2%, normally from 0.15% to 1.5% by weight.
  • these materials can be added to the aqueous slurry fed to the spray drying tower, although in some instances it may be more convenient to add them as a dry mixed particulate, or spray them as a molten liquid on to other solid components of the composition.
  • compositions of the invention can be made via a variety of methods including dry mixing, spray drying, agglomeration and granulation and preferred methods involve combinations of these techniques.
  • a preferred method of making the compositions involves a combination of spray drying, agglomeration in a high speed mixer and dry mixing.
  • Preferred detergent compositions in accordance with the invention also comprise at least two particulate multi-ingredient components.
  • the first component comprises at least 20%, conventionally from 30% to 70%, but more preferably no more than 40% by weight of the composition and the second component from 1% to 50%, more preferably 10% to 40% by weight of the composition.
  • the first component comprises a particulate incorporating an anionic surfactant in an amount of from 0.75% to 35% by weight of the powder and one or more inorganic and/or organic salts in an amount of from 99.25% to 65% by weight of the powder.
  • the particulate can have any suitable form such as granules, flakes, prills, marumes or noodles but is preferably granular.
  • the granules themselves may be agglomerates formed by pan or drum agglomeration or by in-line mixers but are preferably spray dried particles produced by atomising an aqueous slurry of the ingredients in a hot air stream which removes most of the water.
  • the spray dried granules forming the first component may themselves be subjected to densification steps, eg. by high speed cutter mixers, to increase density before being reagglomerated.
  • the first component is described hereinafter as a spray dried powder as this constitutes a preferred embodiment of the invention.
  • An important characteristic of the principal anionic surfactant in the first component is that it should have a low rate of solubility in aqueous media at the water temperatures that prevail during the fill step of the wash cycle in an automatic washing machine.
  • the water temperature during the fill step is predominantly in the range from 5°C to 20°C, more usually from 7°C to 12°C.
  • Suitable anionic surfactants for the purposes of the first component have been found to be linear alkyl sulfate salts in which the alkyl group has an average of from 16 to 22 carbon atoms, and linear alkyl carboxylate salts in which the alkyl group has an average of from 16 to 24 carbon atoms.
  • the alkyl groups for both types of surfactant are preferably derived from natural fats such as tallow. Shorter chain alkyl sulfates or carboxylates, in which the alkyl group is derived from sources comprising a mixture of alkyl moieties more than 40% of which contain 14 or less carbon atoms, are less suitable as they cause the first component to form a gel like mass during dissolution.
  • the level of anionic surfactant in the spray dried powder forming the first component is from 0.75% to 4% by weight, more usually 2.5% to 25% preferably from 3% to 20% and most preferably from 5% to 15% by weight.
  • Water-soluble surfactants such as linear alkyl benzene sulphonates can be included or alternatively may be applied subsequently to the spray dried powder by spray on.
  • the other major ingredient of the spray dried powder is one or more inorganic or organic salts that provide the crystalline structure for the granules.
  • the inorganic and/or organic salts may be water-soluble or water-insoluble, the latter type being comprised by the, or the major part of the, water-insoluble builders where these form part of the builder system.
  • Suitable water soluble inorganic salts include the alkali metal carbonates, bicarbonates, sulphates and borates.
  • Alkali metal silicates can also be present in the spray dried granule provided that aluminosilicate does not form part of the spray dried component.
  • aluminosilicate builder be incorporated into the spray dried granule and, as indicated above, where this takes place, any silicate present should not form part of the spray dried component.
  • incorporation of the silicate can be achieved in several ways, e.g. by producing a separate silicate containing spray dried particulate, by incorporating the silicate into an agglomerate of other ingredients, or more preferably by adding the silicate as a dry mixed solid ingredient.
  • any of the previously mentioned optional builder salts can also be incorporated in the spray dried powder forming the first component.
  • the spray dried powder can also include some or even all of the water soluble monomeric or oligomeric carboxylate chelating agent but this is less preferred as it tends to inhibit the rapid solution of this ingredient.
  • the organic and/or inorganic salts comprise from 60% to 90% by weight of the first component, more preferably from 70% to 90% and most preferably from 75% to 85% by weight.
  • the spray dried powder also normally contains up to 15% by weight of miscellaneous ingredients.
  • first component is a spray dried powder
  • optional ingredients included in the first component should be heat stable to the extent necessary to withstand the temperatures encountered in the spray drying process.
  • first component is a spray dried powder it will normally be dried to a moisture content of from 7% to 11% by weight, more preferably from 8% to 10% by weight of the spray dried powder.
  • Moisture contents of powders produced by other processes such as agglomeration may be lower and can be in the range 1-10% by weight.
  • the particle size of the first component is conventional and preferably not more than 5% by weight should be above 1.4 mm, while not more than 10% by weight should be less than 0.15 mm in maximum dimension.
  • Preferably at least 60% and most preferably at least 80% by weight of the powder lies between 0.7 mm and 0.25 mm in size.
  • the bulk density of the particles should lie in the range from 350 g/litre to 650g/litre but is conventionally in the range from 540 to 600 g/litre. Bulk densities in the upper part of the range from 600-650 g/litre are particularly useful where production of so called concentrated products is desired. Bulk densities above this range may be produced if the spray dried powder is subjected to further processing steps such as size reduction in a high speed cutter/mixer followed by compaction. Alternatively, processes other than spray drying may be used to form the powder.
  • a second component of a preferred composition in accordance with the invention is a particulate containing a water soluble surfactant.
  • surfactants are listed hereinbefore but preferred surfactants are linear C 11 -C 15 alkyl benzene sulfonates and fatty C 14 -C 18 methyl ester sulphonates.
  • the second component may have any suitable physical form i.e. it may take the form of flakes, prills, marumes, noodles, ribbons, or granules which may be spray-dried or non spray-dried agglomerates.
  • the second component could in theory comprise the water soluble surfactant on its own, in practice at least one organic or inorganic salt is included to facilitate processing. This provides a degree of crystallinity, and hence acceptable flow characteristics, to the particulate and may be any one or more of the organic or inorganic salts present in the first component.
  • the particle size range of the second component is not critical but should be such as to obviate segregation from the particles of the spray dried first component when blended therewith. Thus not more than 5% by weight should be above 1.4 mm while not more than 10% should be less than 0.15 mm in maximum dimension.
  • the bulk density of the second component will be a function of its mode of preparation.
  • the second component in spray dried granular form may have a density of from 350 g/litre to 650 g/litre but more preferably will be in the range from 500 g/litre to 630 g/litre.
  • the preferred form of the second component is a mechanically mixed agglomerate which may be made by adding the ingredients dry or with an agglomerating agent to a pan agglomerator, Z blade mixer or more preferably an in-line mixer such as those manufactured by Schugi (Holland) BV, 29 Chroomstraat 8211 AS, Lelystad, Netherlands and Gebruder Lodige Maschinenbau GmbH, D-4790 Paderborn 1, Elsenerstrasse 7-9, Postfach 2050 F.R.G.
  • the second component can be given a bulk density in the range from 650 g/litre to 1190 g/litre more preferably from 750 g/litre to 850 g/litre. This is particularly useful in formulating the so called 'concentrated' products.
  • compositions include a level of alkali metal carbonate in the second component corresponding to an amount of from 3% to 15% by weight of the composition, more preferably from 5% to 12% by weight. This will provide a level of carbonate in the second component of from 20% to 40% by weight.
  • a highly preferred ingredient of the second component is also a hydrated water insoluble aluminosilicate ion exchange material of the synthetic zeolite type, described hereinbefore, present at from 10% to 35% by weight of the second component.
  • the amount of water insoluble aluminosilicate material incorporated in this way is from 1% to 10% by weight of the composition, more preferably from 2% to 8% by weight.
  • the silicate may be incorporated in the first component or, if that also contains aluminosilicate, may be added as a solid, together with other dry mixed materials, to the first and second components.
  • the surfactant salt is formed in situ in an inline mixer.
  • the liquid acid form of the surfactant is added to a mixture of particulate anhydrous sodium carbonate and hydrated sodium aluminosilicate in a continuous high speed blender such as a Lodige KM mixer and neutralised to form the surfactant salt whilst maintaining the particulate nature of the mixture.
  • the resultant agglomerated mixture forms the second component which is then added to other components of the product.
  • the surfactant salt is pre-neutralised and added as a viscous paste to the mixture of the other ingredients.
  • the mixer serves merely to agglomerate the ingredients to form the second component.
  • part of the spray dried product comprising the first granular component is diverted and subjected to a low level of nonionic surfactant spray on before being reblended with the remainder.
  • the second granular component is made using the preferred process described above.
  • the first and second components together with other dry mix ingredients such as the carboxylate chelating agent, inorganic peroxygen bleach, bleach activator, soil-release polymer, silicate and enzyme are then fed to a conveyor belt, from which they are transferred to a horizontally rotating drum in which perfume and silicone suds suppressor are sprayed on to the product.
  • a further drum mixing step is employed in which a low (approx. 2% by weight) level of finely divided crystalline aluminosilicate is introduced to increase density and improve granular flow characteristics.
  • compositions in accordance with the invention can also benefit from delivery systems that provide transient localised high concentrations of product in the drum of an automatic washing machine at the start of the wash cycle, thereby also avoiding problems associated with loss of product in the pipework or sump of the machine.
  • Delivery to the drum can most easily be achieved by incorporation of the composition in a bag or container from which it is rapidly releasable at the start of the wash cycle in response to agitation, a rise in temperature or immersion in the wash water in the drum.
  • the washing machine itself may be adapted to permit direct addition of the compostion to the drum e.g. by a dispensing arrangement in the access door.
  • Products comprising a detergent composition enclosed in a bag or container are usually designed in such a way that container integrity is maintained in the dry state to prevent egress of the contents when dry, but are adapted for release of the container contents on exposure to a washing environment, normally on immersion in an aqueous solution.
  • the container will be flexible, such as a bag or pouch.
  • the bag may be of fibrous construction coated with a water impermeable protective material so as to retain the contents, such as is disclosed in European published Patent Application No. 0018678.
  • it may be formed of a water-insoluble synthetic polymeric material provided with an edge seal or closure designed to rupture in aqueous media as disclosed in European published Patent Application Nos. 0011500, 0011501, 0011502, and 0011968.
  • a convenient form of water frangible closure comprises a water soluble adhesive disposed along and sealing one edge of a pouch formed of a water impermeable polymeric film such as polyethylene or polypropylene.
  • laminated sheet products can be employed in which a central flexible layer is impregnated and/or coated with a composition and then one or more outer layers are applied to produce a fabric-like aesthetic effect.
  • the layers may be sealed together so as to remain attached during use or may separate on contact with water to facilitate the release of the coated or impregnated material.
  • An alternative laminate form comprises one layer embossed or deformed to provide a series of pouch-like containers into each of which the detergent components are deposited in measured amounts, with a second layer overlying the first layer and sealed thereto in those areas between the pouch-like containers where the two layers are in contact.
  • the components may be deposited in particulate, paste or molten form and the laminate layers should prevent egress of the contents of the pouch-like containers prior to their addition to water.
  • the layers may separate or may remain attached together on contact with water, the only requirement being that the structure should permit rapid release of the contents of the pouch-like containers into solution.
  • the number of pouch-like containers per unit area of substrate is a matter of choice but will normally vary between 500 and 25,000 per square metre.
  • Suitable materials which can be used for the flexible laminate layers in this aspect of the invention include, among others, sponges, paper and woven and non-woven fabrics.
  • the preferred means of carrying out the process of the invention is to introduce the composition into the liquid surrounding the fabrics that are in the drum via a reusable dispensing device having walls that are permeable to liquid but impermeable to the solid composition.
  • the support ring is provided with a masking arrangement to prevent egress of wetted, undissolved, product, this arrangement typically comprising radially extending walls extending from a central boss in a spoked wheel configuration, or a similar structure in which the walls have a helical form.
  • the granular detergent products were prepared having compositions as shown below in parts by weight.
  • Both products were made by a combination of spray drying, agglomeration and dry mixing techniques.
  • a spray dried powder was made incorporating all of the TAS, approximately one quarter of the LAS, all of the Maleic anhydride/acrylic acid copolymer, DETPMP, CMC and brightener and part of the carbonate and zeolite builders.
  • For Product A approximately 82% of the zeolite and 65% of the carbonate were included in the spray dried portion, while for Product B approximately 60% of the zeolite and 45% of the carbonate were added in this way.
  • the spray dried product was passed through a Lodige KM high speed mixer/cutter and the 45E7 nonionic was sprayed on to the granules.
  • the treated granules were then transferred to a conveyor belt.
  • the remainder of the LAS, carbonate and zeolite were processed in a Lodige KM high speed mixer to form agglomerated particles which were fed to the conveyor belt.
  • the other dry solid ingredients viz. the citrate, silicate, perborate and bleach activator were also added to the belt at the same time.
  • the mixed particulates were subjected to a low intensity blending step in a mix drum, during which step the perfume and suds suppressor were sprayed on to the particulates to form the finished product.
  • the test programme was designed, and contained sufficient replicates, to permit statistical treatment of the results.
  • Product A was used in an amount of 95g per load whereas Product B was used in an amount of 79g per load. The difference reflected the higher concentration of ingredients per 100 parts of Product B and thus the need to use less weight in order to provide the same levels of non builder ingredients.
  • the test programme used AEG Lavamat 980 automatic washing machines set to the No. 2 cycle. The machines were charged with water of 25° German Hardness having a 3:1 Ca:Mg ratio. Testing was carried out at three temperatures, viz.
  • Each load comprised a mixture of naturally soiled white cotton fabric articles together with swatches soiled with a variety of stains viz. greasy, clay soil, enzymatic and bleachable, to permit the assessment of whiteness and stain removal performance.
  • Each swatch comprised half of a pair, the other half being washed in the same machine using the comparison product. After washing, the fabrics were dried at ambient temperature and were then subjected to panelling by expert judges using a 1-5 Scheffe scale to characterise differences in whiteness and stain removal performance between Products A and B at the selected temperatures.
  • Each product was used to wash a load comprising 2.72 kg of new cotton terry towelling fabric and the respective washed loads were then subjected to a further 14 complete wash cycles.
  • compositions in accordance with the invention produce lower levels of inorganic salt deposition than those obtained with commercially available non-phosphate detergent products.
  • compositions identical to, Composition B of Example I were prepared in the manner of, and having compositions identical to, Composition B of Example I other than the builder system differences shown below (values are in parts by weight in the composition).
  • C D E Zeolite A 13.0 13.0 13.0 Citrate 6.0 6.0 6.0 NaSKS-6 11.0 11.0 - Silicate (2.0 Ratio) - - 13.75 MA/AA 4.25 2.0 2.0
  • the products were used to conduct full scale washing machine tests in which terry towelling cotton swatches were included with 4 kg of clean fabric ballast loads and subjected to multiple wash cycles to determine the levels of heavy metal ions (Fe and Mn) and total ash (inorganic salts) building up on the fabrics after repeated washing.
  • a heavy metal ion 'spike' of 2.5 ppm Fe as FeCl 3 and 0.2 ppm Mn as MnCl 2 was added to the water fed to the machines.
  • the wash conditions were Machine Type Miele Hydromatic W698 Machine Cycle 95°C Cotton Water Hardness Newcastle upon Tyne (UK) City Water adjusted to give 25° German Hardness with Ca:Mg ratio of 3:1. (This water source typically contains 0-3ppm Cu).
  • ppm heavy metal ion content
  • ash total inorganic salt content
  • compositions in accordance with the invention display similar ash and heavy metal ion contents.
  • Composition D contains a level of polymeric polycarboxylate auxiliary builder which is ⁇ 50% of that used conventionally, showing that the use of the ternary builder system of the invention provides enhanced robustness to detergent compositions.

Landscapes

  • 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)
  • Emergency Medicine (AREA)
  • Health & Medical Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Detergent Compositions (AREA)
  • Forging (AREA)
  • Color Television Systems (AREA)
  • Television Systems (AREA)
  • Control Of Motors That Do Not Use Commutators (AREA)
EP91915442A 1990-08-17 1991-08-05 Detergent compositions Expired - Lifetime EP0543911B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB9018157 1990-08-17
GB909018157A GB9018157D0 (en) 1990-08-17 1990-08-17 Detergent compositions
PCT/US1991/005533 WO1992003525A1 (en) 1990-08-17 1991-08-05 Detergent compositions

Publications (4)

Publication Number Publication Date
EP0543911A1 EP0543911A1 (en) 1993-06-02
EP0543911A4 EP0543911A4 (en) 1993-08-25
EP0543911B1 EP0543911B1 (en) 1997-05-02
EP0543911B2 true EP0543911B2 (en) 2000-11-08

Family

ID=10680876

Family Applications (1)

Application Number Title Priority Date Filing Date
EP91915442A Expired - Lifetime EP0543911B2 (en) 1990-08-17 1991-08-05 Detergent compositions

Country Status (27)

Country Link
EP (1) EP0543911B2 (tr)
JP (1) JP3615756B2 (tr)
CN (1) CN1059930A (tr)
AT (1) ATE152474T1 (tr)
AU (1) AU661826B2 (tr)
BR (1) BR9106749A (tr)
CA (1) CA2088275A1 (tr)
CZ (1) CZ21693A3 (tr)
DE (1) DE69125938T3 (tr)
DK (1) DK0543911T4 (tr)
EG (1) EG19654A (tr)
ES (1) ES2100957T5 (tr)
FI (1) FI930673A0 (tr)
GB (1) GB9018157D0 (tr)
GR (2) GR3023501T3 (tr)
HU (1) HUT63649A (tr)
IE (1) IE912924A1 (tr)
MA (1) MA22257A1 (tr)
MX (1) MX9100708A (tr)
NO (1) NO930528L (tr)
NZ (1) NZ239436A (tr)
PL (1) PL172300B1 (tr)
PT (1) PT98654B (tr)
SK (1) SK10093A3 (tr)
TR (1) TR26080A (tr)
TW (1) TW217420B (tr)
WO (1) WO1992003525A1 (tr)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4034131C2 (de) * 1990-10-26 1999-08-26 Henkel Kgaa Gerüststoff für Waschmittel
GB9108639D0 (en) * 1991-04-23 1991-06-12 Procter & Gamble Particulate detergent compositions
GB9216409D0 (en) * 1992-08-01 1992-09-16 Procter & Gamble Detergent compositions
DE4304474A1 (de) * 1993-02-15 1994-08-18 Henkel Kgaa Tensid- und builderhaltiges Waschmitteladditiv
US5378388A (en) * 1993-06-25 1995-01-03 The Procter & Gamble Company Granular detergent compositions containing selected builders in optimum ratios
US5961662A (en) † 1994-09-13 1999-10-05 Kao Corporation Washing method and clothes detergent composition
GB2294704A (en) * 1994-11-05 1996-05-08 Procter & Gamble Bleaching composition
DE4440328A1 (de) * 1994-11-11 1996-05-15 Huels Chemische Werke Ag Amphiphile Verbindungen mit mindestens zwei hydrophilen und mindestens zwei hydrophoben Gruppen auf der Basis von Amiden
ES2216025T3 (es) * 1995-04-20 2004-10-16 Kao Corporation Compuesto detergente blanqueante.
ID16215A (id) * 1996-03-11 1997-09-11 Kao Corp Komposisi deterjen untuk mencuci pakaian
GB9605534D0 (en) * 1996-03-15 1996-05-15 Unilever Plc Detergent compositions
WO1997034978A1 (fr) * 1996-03-19 1997-09-25 Kao Corporation Composition detergente granulaire a haute densite
CN1074457C (zh) * 1996-11-25 2001-11-07 魏忠汉 用粉煤灰制备洗用分子筛
EP0849355B1 (de) * 1996-12-21 2004-03-17 Clariant GmbH Pulverförmige Wasch- und Reinigungsmittel-Komponente
AU2284799A (en) * 1998-02-11 1999-08-30 Rhodia Chimie Detergent compositions containing an amine silicone and a polymer inhibiting colour transfer
GB2339203A (en) * 1998-07-08 2000-01-19 Procter & Gamble A method of dipensing
US6723693B1 (en) 1999-07-08 2004-04-20 The Procter & Gamble Company Method for dispensing a detergent comprising an amionic/silicate agglomerate
CN1317061C (zh) * 2005-03-30 2007-05-23 长春师范学院 螯合性表面活性剂

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3144297A1 (de) † 1981-11-07 1983-05-19 Degussa Ag, 6000 Frankfurt Phosphatsubstitut fuer waschmittel
US4664839A (en) † 1984-04-11 1987-05-12 Hoechst Aktiengesellschaft Use of crystalline layered sodium silicates for softening water and a process for softening water
EP0240356A1 (en) † 1986-04-04 1987-10-07 Unilever Plc Detergent powders and process for preparing them
EP0283885A2 (de) † 1986-07-18 1988-09-28 Henkel Kommanditgesellschaft auf Aktien Verfahren zur Herstellung von rieselfähigen alkalischen Reinigungsmitteln durch kompaktierende Granulation
EP0337219A2 (de) † 1988-04-15 1989-10-18 Hoechst Aktiengesellschaft Lagerstabilisiertes Waschmittel mit verstärkter Bleichwirkung
EP0337217A2 (de) † 1988-04-15 1989-10-18 Hoechst Aktiengesellschaft Waschmittel mit lagerstabilisiertem Bleichsystem
JPH02178397A (ja) † 1988-12-29 1990-07-11 Lion Corp 洗浄剤組成物
JPH02178399A (ja) † 1988-12-29 1990-07-11 Lion Corp 粒状洗剤組成物

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4605509A (en) * 1973-05-11 1986-08-12 The Procter & Gamble Company Detergent compositions containing sodium aluminosilicate builders
DD234878A1 (de) * 1985-03-01 1986-04-16 Genthin Waschmittelwerk Verfahren zur herstellung von waschmittelrohstoffgemischen
DE3526405A1 (de) * 1985-07-24 1987-02-05 Henkel Kgaa Schichtsilikate mit beschraenktem quellvermoegen, verfahren zu ihrer herstellung und ihre verwendung in wasch- und reinigungsmitteln
JPH01153800A (ja) * 1987-12-11 1989-06-15 Lion Corp 濃縮柔軟付与粒状洗剤組成物
DE3920704A1 (de) * 1989-06-24 1991-01-03 Hoechst Ag Builder fuer textilwaschmittel

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3144297A1 (de) † 1981-11-07 1983-05-19 Degussa Ag, 6000 Frankfurt Phosphatsubstitut fuer waschmittel
US4664839A (en) † 1984-04-11 1987-05-12 Hoechst Aktiengesellschaft Use of crystalline layered sodium silicates for softening water and a process for softening water
EP0164514B1 (de) † 1984-04-11 1989-06-14 Hoechst Aktiengesellschaft Verwendung von kristallinen schichtförmigen Natriumsilikaten zur Wasserenthärtung und Verfahren zur Wasserenthärtung
EP0240356A1 (en) † 1986-04-04 1987-10-07 Unilever Plc Detergent powders and process for preparing them
EP0283885A2 (de) † 1986-07-18 1988-09-28 Henkel Kommanditgesellschaft auf Aktien Verfahren zur Herstellung von rieselfähigen alkalischen Reinigungsmitteln durch kompaktierende Granulation
EP0337219A2 (de) † 1988-04-15 1989-10-18 Hoechst Aktiengesellschaft Lagerstabilisiertes Waschmittel mit verstärkter Bleichwirkung
EP0337217A2 (de) † 1988-04-15 1989-10-18 Hoechst Aktiengesellschaft Waschmittel mit lagerstabilisiertem Bleichsystem
JPH02178397A (ja) † 1988-12-29 1990-07-11 Lion Corp 洗浄剤組成物
JPH02178399A (ja) † 1988-12-29 1990-07-11 Lion Corp 粒状洗剤組成物

Also Published As

Publication number Publication date
JPH06500141A (ja) 1994-01-06
NO930528D0 (no) 1993-02-15
DE69125938D1 (de) 1997-06-05
DK0543911T4 (da) 2001-03-19
FI930673A (fi) 1993-02-16
DE69125938T3 (de) 2001-06-07
EP0543911A1 (en) 1993-06-02
HUT63649A (en) 1993-09-28
TR26080A (tr) 1994-12-15
PT98654B (pt) 1999-01-29
MX9100708A (es) 1992-04-01
EP0543911A4 (en) 1993-08-25
PL172300B1 (en) 1997-09-30
DK0543911T3 (da) 1997-10-13
GR3035134T3 (en) 2001-04-30
FI930673A0 (fi) 1993-02-16
EP0543911B1 (en) 1997-05-02
PT98654A (pt) 1992-06-30
CN1059930A (zh) 1992-04-01
DE69125938T2 (de) 1997-12-18
HU9300426D0 (en) 1993-05-28
ES2100957T5 (es) 2001-02-01
ATE152474T1 (de) 1997-05-15
NZ239436A (en) 1993-08-26
ES2100957T3 (es) 1997-07-01
WO1992003525A1 (en) 1992-03-05
CA2088275A1 (en) 1992-02-18
IE912924A1 (en) 1992-02-26
NO930528L (no) 1993-04-19
GB9018157D0 (en) 1990-10-03
AU8497091A (en) 1992-03-17
GR3023501T3 (en) 1997-08-29
MA22257A1 (fr) 1992-04-01
JP3615756B2 (ja) 2005-02-02
BR9106749A (pt) 1993-07-20
SK10093A3 (en) 1993-07-07
CZ21693A3 (en) 1994-04-13
AU661826B2 (en) 1995-08-10
TW217420B (tr) 1993-12-11
EG19654A (en) 1995-08-30

Similar Documents

Publication Publication Date Title
EP0591203B1 (en) Detergent compositions
EP0543911B2 (en) Detergent compositions
EP0581895B1 (en) Particulate detergent compositions
US5540855A (en) Particulate detergent compositions
US5792738A (en) Granular laundry detergent compositions containing stabilised percarbonate bleach particles
EP0634481B1 (en) Detergent compositions
US5516449A (en) Detergent compositions
EP0650518B1 (en) Process of dispensing a high bulk density percarbonate-containing laundry detergent
CA2167159C (en) Granular laundry detergent compositions containing stabilised percarbonate bleach particles
US5891837A (en) Stabilized bleaching compositions
EP0633922B1 (en) Concentrated laundry detergent containing stable amide peroxyacid bleach
EP0634483B1 (en) Stabilised bleaching compositions
EP0634480B1 (en) Detergent compositions
IE911056A1 (en) Fabric cleaning process
CA2167160C (en) Stabilised bleaching compositions

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19930201

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE

RHK1 Main classification (correction)

Ipc: C11D 3/12

A4 Supplementary search report drawn up and despatched

Effective date: 19930707

AK Designated contracting states

Kind code of ref document: A4

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE

17Q First examination report despatched

Effective date: 19950504

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE

REF Corresponds to:

Ref document number: 152474

Country of ref document: AT

Date of ref document: 19970515

Kind code of ref document: T

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: CH

Ref legal event code: NV

Representative=s name: RITSCHER & SEIFERT PATENTANWAELTE VSP

REF Corresponds to:

Ref document number: 69125938

Country of ref document: DE

Date of ref document: 19970605

ET Fr: translation filed
REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2100957

Country of ref document: ES

Kind code of ref document: T3

REG Reference to a national code

Ref country code: GR

Ref legal event code: FG4A

Free format text: 3023501

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19970805

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

26 Opposition filed

Opponent name: HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN

Effective date: 19980127

26 Opposition filed

Opponent name: CLARIANT GMBH WERK KNAPSACK

Effective date: 19980202

Opponent name: HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN

Effective date: 19980127

NLR1 Nl: opposition has been filed with the epo

Opponent name: HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN

NLR1 Nl: opposition has been filed with the epo

Opponent name: HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN

Opponent name: CLARIANT GMBH WERK KNAPSACK

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

PLAW Interlocutory decision in opposition

Free format text: ORIGINAL CODE: EPIDOS IDOP

PLAW Interlocutory decision in opposition

Free format text: ORIGINAL CODE: EPIDOS IDOP

PUAH Patent maintained in amended form

Free format text: ORIGINAL CODE: 0009272

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: PATENT MAINTAINED AS AMENDED

27A Patent maintained in amended form

Effective date: 20001108

AK Designated contracting states

Kind code of ref document: B2

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE

REG Reference to a national code

Ref country code: CH

Ref legal event code: AEN

Free format text: AUFRECHTERHALTUNG DES PATENTES IN GEAENDERTER FORM

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: THE PATENT HAS BEEN ANNULLED BY A DECISION OF A NATIONAL AUTHORITY

Effective date: 20001221

NLR2 Nl: decision of opposition
ITF It: translation for a ep patent filed
REG Reference to a national code

Ref country code: ES

Ref legal event code: DC2A

Kind code of ref document: T5

Effective date: 20001213

ET3 Fr: translation filed ** decision concerning opposition
NLR3 Nl: receipt of modified translations in the netherlands language after an opposition procedure
REG Reference to a national code

Ref country code: DK

Ref legal event code: T4

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 20080708

Year of fee payment: 18

Ref country code: DK

Payment date: 20080709

Year of fee payment: 18

Ref country code: ES

Payment date: 20080806

Year of fee payment: 18

Ref country code: NL

Payment date: 20080715

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20080816

Year of fee payment: 18

Ref country code: FR

Payment date: 20080807

Year of fee payment: 18

Ref country code: AT

Payment date: 20080708

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 20080808

Year of fee payment: 18

Ref country code: BE

Payment date: 20080828

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GR

Payment date: 20080704

Year of fee payment: 18

BERE Be: lapsed

Owner name: THE *PROCTER & GAMBLE CY

Effective date: 20090831

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

Ref country code: NL

Ref legal event code: V1

Effective date: 20100301

REG Reference to a national code

Ref country code: DK

Ref legal event code: EBP

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090831

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090831

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20100430

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090831

Ref country code: AT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090805

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20100301

Ref country code: DK

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090831

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090831

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20090806

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20100831

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20100708

Year of fee payment: 20

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090805

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090806

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 69125938

Country of ref document: DE

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 69125938

Country of ref document: DE

REG Reference to a national code

Ref country code: GB

Ref legal event code: PE20

Expiry date: 20110804

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090806

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20110804

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20110806