EP0113978B1 - Procédé pour le lavage de tissu - Google Patents

Procédé pour le lavage de tissu Download PDF

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Publication number
EP0113978B1
EP0113978B1 EP83307640A EP83307640A EP0113978B1 EP 0113978 B1 EP0113978 B1 EP 0113978B1 EP 83307640 A EP83307640 A EP 83307640A EP 83307640 A EP83307640 A EP 83307640A EP 0113978 B1 EP0113978 B1 EP 0113978B1
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EP
European Patent Office
Prior art keywords
water
builder
fatty acid
particles
sodium
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EP83307640A
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German (de)
English (en)
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EP0113978A1 (fr
Inventor
James Francis Davies
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Unilever PLC
Unilever NV
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Unilever PLC
Unilever NV
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Priority to AT83307640T priority Critical patent/ATE29151T1/de
Publication of EP0113978A1 publication Critical patent/EP0113978A1/fr
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    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • 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
    • C11D3/2079—Monocarboxylic acids-salts thereof

Definitions

  • This invention relates to a method of washing fabrics.
  • detergency builders used in the past have been of three main types, namely water-soluble sequestering builders, water-insoluble ion exchange builders and water-soluble precipitating builders.
  • Atypical precipitating builder is an alkali metal carbonate, especially sodium carbonate.
  • Other water-soluble precipitating builders include sodium silicate (particularly effective against magnesium hardness), sodium orthophosphate and water-soluble alkali metal soaps. While from a cost point of view sodium carbonate is an attractive builder, it has at least two significant disadvantages. Firstly, sodium carbonate alone is not usually capable of reducing the calcium ion concentration in calcium hard water to sufficiently low levels to achieve good detergency under practical washing conditions.
  • the calcium ion concentration in a wash liquor can be reduced to sufficiently low levels by the use of, for example, a sequestering builder material such as sodium tripolyphosphate, and considerable commercial success has been achieved with phosphate-built formulations.
  • a sequestering builder material such as sodium tripolyphosphate
  • DE-A-3004140 discloses compositions containing alkyl benzene sulphonate mixed in an unspecified fashion with smaller quantities of sodium palmitate or sodium stearate.
  • GB-A-2047264 discloses a detergent composition containing sodium citrate and a sodium soap which is predominantly of 16 and 18 carbon atoms. These are said to act as builders if, and only if, both are present together. High wash temperature is recommended. Sodium alkylbenzene sulphonate is also present. US-A-4196095 discloses dry blended compositions containing alkyl benzene sulphonate with magnesium stearate, which is insoluble in hot water as well as cold.
  • a method of washing fabrics in water containing calcium hardness ions by contacting the fabrics at a temperature below 50°C with a wash liquor obtained by adding to water a particulate solid detergent composition
  • a particulate solid detergent composition comprising: builder particles, the majority of which have a particle size of between 100 micrometres and 1500 micrometres and comprising an alkyl benzene sulphonate as a dispersant in solid solution with a builder material selected from salts of fatty acids, at least 30% of which are saturated fatty acids, and which contain at least 16 carbon atoms, said salts being the salts of said fatty acids with alkali metals or organic nitrogen containing cations, optionally together with a non-soap detergent active material separate from the builder particles.
  • the builder particles essentially consist of an alkyl benzene sulphonate (ABS) and a fatty acid salt. It is essential that the ABS is soluble in the fatty acid salt.
  • ABS alkyl benzene sulphonate
  • the alkyl benzene sulphonate may be selected from sodium and potassium alkyl (C 9 -C 2o ) benzene sulphonates, particularly sodium linear secondary alkyl (C,,7--C,,) benzene sulphonates.
  • the alkali metal alkyl benzene sulphonates the corresponding ammonium salts or the complexes of alkyl benzene sulphonic acids with organic nitrogen containing basic materials may be used.
  • one or more further dispersant materials may be present in the particles.
  • Examples of further dispersants which may be used to form builder particles include organic long chain (>C 4 ) compounds with a straight or branched chain, an optional aromatic ring or cycloaliphatic group and one or more hydrophilic groups, e.g. hydroxyl, amino, amine oxide, sulphate, sulphonate, phosphate, phosphonate, carboxy or sulphobetaine groups. These compounds may be soluble or insoluble in water. Examples of such compounds are other surfactants (anionic, nonionic, amine oxide, carboxy or sulphobetaine), alkanols, alkanediols, alkanedioic acids, alkanoic acid mono- or diethanolamides, and alkyl amines.
  • organic long chain (>C 4 ) compounds with a straight or branched chain, an optional aromatic ring or cycloaliphatic group and one or more hydrophilic groups, e.g. hydroxyl, amino, amine oxide, sulph
  • An optional feature of the builder particles of the present invention is the presence of a carrier material in which the fatty acid salt is insoluble, to effectively increase and maintain the surface area of the fatty acid salt in the composition.
  • carrier materials which may be used include: inorganic water-soluble salts such as sodium perborate (monohydrate, correctly designated anhydrate and tetrahydrate, correctly designated hexahydrate), mono-, di- and trivalent metal sulphates, especially alkali metal sulphates and more especially the alums, alkali metal phosphates, especially sodium tripolyphosphate, pyrophosphate and orthophosphate, alkali metal carbonates, especially sodium carbonate, sodium hydrogen carbonate and sodium sesquicarbonate, and their mixed carbonates, and also mixtures of any of these inorganic water soluble salts; inorganic water insoluble materials such as naturally occurring silicas, precipitated silicas and silica gels, alumina and aluminosilicate minerals including zeolites and clays; water-soluble organic materials such as carbohydrates, especially crystalline sugars such as sucrose, solid, preferably crystalline, polyhydric alcohols, such as pentaerythritol, sorbitol and mannito
  • the builder particles may further contain a material for improving the structure thereof.
  • a material for improving the structure thereof may be water-soluble inorganic salts such as sodium silicate.
  • the preferred level of fatty acid salt in the builder particles depends inter alia on the nature of the dispersant and the carrier material, if any, and on whether the composition contains further builder materials. Thus, where the dispersant and the carrier material, if any, serve little or no purpose in the composition other than to disperse and carry the fatty acid salt it is clearly desirable that the level of dispersant and carrier material, if any, should be as low as possible. In this case, the level of fatty acid salt may be up to 95% by weight. However, where the dispersant and the carrier material, if any, serve some other useful purpose in the composition, the level of fatty acid salt in the builder particles can be less, say up to 80% by weight.
  • a further consideration is that the efficiency of building, all other factors remaining the same, depends on size of fatty acid salt particles which are released into the wash liquor, smaller sizes resulting in faster building.
  • the builder particles include a carrier material
  • a lower level of fatty acid salt in the builder particles may lead to smaller particles of fatty acid salt being released into the wash liquor, which in turn leads to more efficient building.
  • the level of fatty acid salt in the builder particles is between 20% and 95% by weight.
  • the ratio by weight of the fatty acid salt to the dispersant in the builder particles is from 0.5:1 to 5:1, most preferably from 0.8:1 to 3:1.
  • the builder particle may be made by a variety of techniques.
  • the fatty acid salt/ABS builder particles described herein may be processed by conventional spray-drying, by spray-cooling or granulation techniques.
  • fatty acid salt and/or the alkyl benzene sulphonate are salts with organic N-containing cations and are meltable at convenient temperatures
  • a molten mixture of ABS and the fatty acid salt may be transformed into builder particles by spray-cooling.
  • the particles may also be processed by melting the solid solution which is then sprayed as fine droplets by means of suitable atomising equipment on a moving bed of carrier material, or mixture of carrier materials, by any convenient granulation technique, e.g. rotating drum, inclined pan granulator, fluidised bed and solid mixer.
  • Any convenient granulation technique e.g. rotating drum, inclined pan granulator, fluidised bed and solid mixer.
  • An even distribution of solidified fatty acid salt/ABS solution through the carrier material can thus be obtained.
  • the carrier material can be milled to smaller particle sizes (e.g. using a swing-hammer mill) before the fatty acid salt/ABS solution is applied so as to increase the weight of fatty acid salt/ABS that can be carried by a given weight of said carrier material.
  • the particle size of the builder particles is such that the majority of the particles have a size between 100 micrometers and 1500 micrometers, preferably between 200 micrometers and 1200 micrometers.
  • the fatty acid salt which can be used in the present invention should be saturated and contains at least 16 carbon atoms, preferably not more than 18 carbon atoms.
  • Fatty acid salts containing less than 16 carbon atoms are unsuitable for present purposes, their corresponding calcium salts having a solubility product which is not sufficiently low for acceptable building to be possible.
  • Salts of fatty acids derived from natural sources will normally contain a mixture of alkyl chain lengths, and may often contain unsaturated and/or hydroxy-substituted alkyl chains. In such circumstances it is essential that at least 30%, preferably at least 40% of the fatty acid consists of acids which are saturated and contain at least 16 carbon atoms, preferably from 16 to 18 carbon atoms.
  • Suitable fatty acid salts for use in the present invention include the salts of palmitic acid, stearic acid and fatty acid derived from tallow fat or palm oil.
  • the fatty acid salts as with the ABS referred to above, which can be used in the present invention include not only the alkali metal salts of the above fatty acids but also the organic salts which can be formed by complexing fatty acids with organic nitrogen containing materials such as amines and derivatives thereof.
  • Suitable fatty acid salts include sodium stearate, sodium palmitate, and complexes between stearic and/or palmitic fatty acid with water-soluble alkanolamides such as ethanolamine, di- or tri- ethanolamine, N-methylethanolamine, N-ethylethanolamine, 2-methylethanolamine and 2,2-dimethyl ethanolamine and N-containing ring compounds such as morpholine, 2'-pyrrolidone and their methyl derivatives.
  • Mixtures of fatty acid salts, and mixtures of fatty acids with fatty acid salt may also be used.
  • the level of builder particles in the detergent composition should be such that the composition contains the equivalent of more than 10% up to 70% by weight, preferably up to 50%, most preferably up to 40% by weight of fatty acid or up to 15% by weight sodium carbonate is present as a further builder material. These levels render the compositions capable of softening water of typical calcium hardness under typical dosage conditions.
  • a desired feature of the compositions used in the present invention is the presence of an alkaline material.
  • compositions of the invention are required to be alkaline, but not too strongly alkaline as this could result in fabric damage and also be hazardous for domestic usage.
  • the compositions should give a pH of more than 8.0, preferably from 9.5 to 11 in use in aqueous wash solution.
  • the pH measured at the lowest normal usage concentration of 0.1% w/v of the product in water of 12° FH (Ca) (French permanent hardness, calcium only) at 25°C so that a satisfactory degree of alkalinity can be assured in use at all normal product concentrations.
  • the alkaline material may be selected from alkali metal and ammonium salts of weak acids such as alkali metal and ammonium carbonates including sodium carbonate and sodium sesquicarbonate, alkali metal and ammonium silicates including sodium alkaline silicate, alkali metal and ammonium phosphates including sodium orthophosphate, alkali metal hydroxides including sodium hydroxides, alkali metal borates and the alkali metal and ammonium water-soluble salts of weak organic acids including sodium citrate, sodium acetate, and the cold water soluble soaps such as sodium oleate, and mixtures of such materials.
  • weak acids such as alkali metal and ammonium carbonates including sodium carbonate and sodium sesquicarbonate
  • alkali metal and ammonium silicates including sodium alkaline silicate
  • alkali metal and ammonium phosphates including sodium orthophosphate
  • alkali metal hydroxides including sodium hydroxides
  • alkali metal borates and the alkali metal and ammonium water-
  • the alkaline material will itself also act as a builder.
  • sodium carbonate will contribute to building by precipitation of calcium carbonate while sodium citrate will contribute to building by sequestering calcium ions.
  • a material which is relatively calcium insensitive such as sodium silicate
  • the other ingredients in the alkaline detergent compositions of the invention should of course be chosen for alkaline stability, especially the pH sensitive materials such as enzymes.
  • the detergent compositions are particularly suitable for washing fabrics at low temperatures, i.e., below 50°C, even below 35°C. Successful results can also be achieved at temperatures above 50°C.
  • the wash liquor according to the invention necessarily includes a synthetic detergent active material otherwise referred to herein simply as a detergent compound.
  • the detergent compounds may be selected from anionic, nonionic, zwitterionic and amphoteric synthetic detergent active materials. Many suitable detergent compounds are commercially available and are fully described in the literature, for example in "Surface Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch.
  • ABS is itself a detergent active material, this may constitute the whole of the detergent active material in the composition, but more usually further detergent active material may be included as a further dispersant in the builder particles and/or separate from the builder particles.
  • the preferred detergent compounds which can be used are synthetic anionic and nonionic compounds.
  • the former are usually water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from 8 to 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals.
  • suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher (C S- C 18 ) alcohols produced for example from tallow or coconut oil, sodium and potassium alkyl (C 9 C zo ) benzene sulphonates, particularly sodium linear secondary alkyl (C 10 ⁇ C 15 ) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (C 8 ⁇ C 18 ) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esterified with isethionic acid and neutralised with sodium hydroxide; sodium and potassium salts of fatty acid amides of methyl taurate
  • Suitable nonionic detergent compounds which may be used include in particular the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
  • Specific nonionic detergent compounds are alkyl (Cs-C22) phenols-ethylene oxide condensates, generally 5 to 25 EO, i.e. 5 to 25 units of ethylene oxide per molecule, the condensation products of aliphatic (C 8 ⁇ C 18 ) primary or secondary linear or branched alcohols with ethylene oxide, generally 5 to 40 EO, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine.
  • Other so-called nonionic detergent compounds include long chain tertiary amine oxides, long chain tertiary phosphine oxides and dialkyl sulphoxides.
  • detergent compounds for example mixed anionic or mixed anionic and nonionic compounds may be used in the detergent compositions, particularly in the latter case to provide controlled low sudsing properties. This is beneficial for compositions intended for use in suds- intolerant automatic washing machines.
  • Amounts of amphoteric or zwitterionic detergent compounds can also be used in the compositions of the invention but this is not normally desired due to their relative high cost. If any amphoteric or zwitterionic detergent compounds are used it is generally in small amounts in compositions based on the much more commonly used synthetic anionic and/or nonionic detergent compounds.
  • mixtures of amine oxides and ethoxylated nonionic detergent compounds can be used.
  • Cold-water soluble soaps may also be present in the detergent compositions of the invention.
  • the soaps are particularly useful at low levels in binary and ternary mixtures, together with nonionic or mixed synthetic anionic and nonionic detergent compounds, which have low sudsing properties.
  • the soaps which are used are the water-soluble salts of unsaturated fatty acids in particular with inorganic cations such as sodium and potassium.
  • the amount of such soaps can be between 2% and 20%, especially between 5% and 15% by weight, can advantageously be used to give a beneficial effect on detergency.
  • compositions of the invention may contain a further builder material other than the fatty acid salt.
  • the further builder material is other than sodium or potassium carbonate this may be present at levels less than the level of the fatty acid salt.
  • the composition contains sodium or potassium carbonate as the alkaline material and as a further builder, this may be present at a level more than the level of the fatty acid salt.
  • any such further builder material may be selected from other precipitating builder materials, optionally together with a precipitation seed material, or from sequestering builder materials and ion-exchange builder materials and materials capable of forming such builder materials in situ.
  • the further builder material is a water-soluble precipitating material
  • it may be selected from soaps, alkyl malonates, alkyl or alkenyl succinates, sodium fatty acid sulphonates, orthophosphates of sodium, potassium and ammonium, or in their water-soluble partially or fully acidified forms.
  • the silicates of sodium and potassium may be included in the compositions.
  • the further builder may also be constituted by a sequestering builder material, particularly those selected from water-soluble pyrophosphates, polyphosphates, phosphonates, polyhydroxysulfonates, polyacetates, carboxylates, polycarboxylates, and succinates.
  • a sequestering builder material particularly those selected from water-soluble pyrophosphates, polyphosphates, phosphonates, polyhydroxysulfonates, polyacetates, carboxylates, polycarboxylates, and succinates.
  • inorganic phosphate sequestering builders include sodium and potassium tripolyphosphates, pyrophosphates, and polymerphosphates such as hexametaphosphate or glassy phosphates.
  • the polyphos- phonates specifically include, for example, 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.
  • compositions will not contain more than about 5% by weight phosphate builder materials or phosphorus containing materials of any kind.
  • Water-soluble, organic sequestering builders are also useful herein as further builder materials.
  • the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates, polyacetylcarboxylates and polyhydroxysulfonates are useful sequestering builders in the present compositions.
  • Specific examples of the polyacetate and polycarboxylate builder salts include sodium, potassium, ammonium and substituted ammonium salts of ethylene diamine tetraacetic acid, nitriloacetic acid, dipicolinic acid, oxydisuccinic acid, benzene polycarboxylic acids, e.g. mellitic acid, citric acid and the polyacetalcarboxylates disclosed in US-A-4. 144 226 and 4 146 495. The acid forms of these materials may also be used.
  • Highly preferred organic sequestering builder materials herein include sodium citrate, sodium oxydisuccinate, sodium mellitate, sodium nitrilotriacetates, and sodium ethylene diamine tetraacetate and mixtures thereof.
  • sequestering builders are the polycarboxylate builders.
  • examples of such materials include the water-soluble salts of the homo- and copolymers of aliphatic carboxylic acids such as maleic acid, itaconic acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid, methylenemalonic acid, 1,1,2,2-ethane tetracarboxylic acid, dihydroxy tartaric acid, and keto- malonic acid.
  • Additional preferred sequestering builders herein include the water-soluble salts, especially the sodium and potassium salts of carboxy methyloxymalonate, carboxy methyloxy- succinate, cis-cyclohexanehexacarboxylate, cis- cyclopentanetetracarboxylate, and phloroglucinol trisulfonate.
  • the further builder material may also be constituted by an ion-exchange material.
  • Suitable ion-exchange materials include the amorphous or crystalline aluminosilicates such as disclosed in GB-A-1 473 201/2 (HENKEL).
  • the further builder material is an ion-exchange material
  • it may be present at a level which is more than the level of the fatty acid salt.
  • a preferred composition used in the method of this invention comprises
  • the non-soap detergent active material and the alkaline material can be incorporated in the builder and/or can be separate therefrom.
  • the precipitation of calcium carbonate by reaction between the calcium hardness and the sodium carbonate takes place via a series of steps which are transient in the absence of crystal growth poisons, but can be isolated in their presence. If the builder particles are added after the system has reached a particular state referred to herein as the "critical state", the free calcium ion concentration in the wash liquor is reduced to about 10- 5 molar or lower. If, on the other hand, the builder particles are added prior to the system reaching the critical state, this reduction in free calcium ion concentration may not be achieved at all or not within a reasonable time.
  • the time period required for a system to reach the critical state after the addition of sodium carbonate to the hard water is thought to depend on a number of factors among which are the initial water hardness, the quantity of sodium carbonate added, the quantity of crystal growth poisons present either from the wash load, from the added composition or in the liquor itself, the pH of the liquor, the temperature or temperature profile of the liquor and the nature of other materials which may be present.
  • a method of washing fabrics in water containing calcium hardness comprising contacting the fabrics with a wash liquor to which has been added at least a synthetic detergent active material and an alkali metal carbonate and bringing into effective contact with the wash liquor the fatty acid builder particles, the latter being brought into effective contact with the wash liquor at or after the wash liquor has reached the critical state as hereinbefore defined, and being added in such an amount as to reduce the free calcium ion concentration in the wash liquor to 10- 5 or less within at most 60 minutes preferably within 30 minutes from the addition of the alkali metal carbonate to the hard water.
  • the time at which the critical state is reached for a given composition and wash condition may be determined by a series of experiments as follows. A substantially similar load of fabrics is washed in an identical wash liquor under identical conditions and the builder particles are added at various times between 1 minute and 30 minutes from the addition of the alkali metal carbonate to the liquor. After 60 minutes the free calcium ion concentration is measured. The critical state has been achieved when this final free calcium ion concentration is not more than 10- 5 molar. Alternatively, or where a similar load of soiled fabrics is not available, this series of experiments may be carried out with a clean load of similar fabrics while an appropriate level of crystal growth poison is included in the hard water.
  • the form of the calcium carbonate precipitate changes from an X-ray amorphous form to an X-ray crystalline form.
  • the calcium carbonate precipitate is colloidally suspended.
  • the critical state the precipitate settles rapidly.
  • Alternative calcium carbonate growth poison suppressing agents include the soluble salts of lanthanum ion, cobalt, manganese and copper.
  • this material is preferably calcite having a surface area of from 2 to 80 m 2 /g.
  • Suitable materials are Calofort U, available from Sturge Chemicals having a surface area of about 16 m 2 /g and calcite having a larger surface area (such as for example 80 m 2 fg) as available from Solvay. In the latter case less of the material would be necessary.
  • a level of up to 15% by weight of calcite in the composition is suitable. "Calofort" is a Registered Trade Mark.
  • the builder particles are added to the wash liquor or the fatty acid content thereof is released into the wash liquor between about one and about ten minutes after the addition of the sodium carbonate.
  • compositions according to the invention contain, based on the weight of the total composition:
  • the balance of the composition, if any, will be water and other conventional additives as referred to below.
  • the fabric washing composition contains sodium carbonate as a further builder material and in which effective contact between the wash liquor and the fatty acid salt is delayed until the system reaches the critical state, it may also be beneficial to arrange that the fatty acid salt comes into effective contact with the wash liquor relatively rapidly, and the reaction between the sodium carbonate and the free calcium ions in the wash liquor is retarded by including in the composition a calcium-carbonate crystal growth inhibitor, such as a phosphate material.
  • a calcium-carbonate crystal growth inhibitor such as a phosphate material.
  • the detergent compositions used in the process of the invention can contain any of the conventional additives in the amounts in which such materials are normally employed in fabric washing detergent compositions.
  • these additives include lather boosters such as alkanolamines, particularly the monoethanolamides derived from palm kernel fatty acids and coconut fatty acids, lather depressants such as alkyl phosphate, long-chain fatty acids or soaps thereof, waxes and silicones, antiredeposition agents such as sodium carboxymethylcellulose and cellulose ethers, oxygen- releasing bleaching agents such as sodium perborate and sodium percarbonate, peracid bleach precursors, chlorine-releasing bleaching agents such as trichloroisocyanuric acid, fabric softening agents, inorganic salts, such as sodium sulphate, and magnesium silicate, and usually present in very minor amounts, fluorescent agents, perfumes, enzymes such as proteases and amylases, germicides and colourants.
  • lather boosters such as alkanolamines, particularly the monoethanolamide
  • an amount of sodium perborate or percarbonate preferably between 10% and 40%, for example 15% to 30% by weight.
  • antideposition agents are anionic polyelectrolytes, especially polymeric aliphatic carboxylates.
  • the amount of any such antideposition agent can be from 0.01% to 5% by weight, preferably from 0.2% to 2% by weight of the compositions.
  • Specific preferred antideposition agents are the alkali metal or ammonium, preferably the sodium, salts or homo-and copolymers of acrylic acid or substituted acrylic acids, such as sodium polyacrylate, the sodium salt of copolymethacryl- amide/acrylic acid and sodium polyalphahydroxy- acrylate, salts of copolymers of maleic anhydride with ethylene, acrylic acids, vinylmethylether allyl acetate or styrene, especially 1:1 1 copolymers, and optionally with partial esterification of the carboxyl groups.
  • Such copolymers preferably have relatively low molecular weights, e.g. in the range of 1,000 to 50,000.
  • antideposition agents include the sodium salts of polyitaconic acid and polyaspartic acid, phosphate esters of ethoxy- lat6d aliphatic alcohols, polyetheylene glycol phosphate esters, and certain phosphonates such as sodium ethane-1-hydroxy-1,1-diphosphonate, sodium ethylenediamine tetramethylene phosphonate, and sodium 2-phosphonobutane tricarboxylate. Mixtures of organic phosphonic acids or substituted acids or their salts with protective colloids such as gelatin may also be used.
  • the most preferred antideposition agent is sodium polyacrylate having a MW of 10,000 to 50,000, for example 20,000 to 30,000. Where the antideposition agent is itself a calcium carbonate crystal growth poison, or in any case, and the composition contains sodium carbonate as a further builder material, it may be desirable to delay contact between this agent and the wash liquor until after the critical state is reached.
  • the alkaline material other than an alkali metal silicate is included in the composition, it is generally also desirable to include an amount of an alkali metal silicate, to decrease the corrosion of metal parts in washing machines and provides processing benefits and generally improved powder properties.
  • the more highly alkaline ortho- and meta- silicates would normally only be used at lower amounts within this range, in admixture with the neutral or alkaline silicates.
  • the washing process of the invention can be accomplished manually, if desired, but is normally accomplished in a domestic or commercial laundry washing machine.
  • the latter permits the use of higher alkalinity, and more effective agitation, all of which contribute generally to better detergency.
  • the type of washing and machine used, if any, is not significant.
  • the detergent compositions of the invention should be solid particulate compositions. Dry- mixing and granulation of all components may be used or alternatively the fatty acid salt containing particles may be post-dosed to a spraydried base powder.
  • the following particles were added at room temperature (about 20°C) to hard water, having a hardness of 20° FH (Ca).
  • the particles consisted of 2 parts of the sodium salt of mixture of C 16 and C 18 saturated fatty acids to 1 part of DOBS 055, an anionic detergent active material which approximates to sodium dodeconyl benzene sulphonate acting as both dispersant for the soap and detergent active material.
  • the particles had sizes between 355 and 1000 micrometers.
  • the particles were added at 3.0 g/I.
  • DOBS 055 by DOBANOL 45 11 EO, which is an ethoxylated linear primary alcohol (ex SHELL), a nonionic surface active material
  • DOBANOL 45 11 EO which is an ethoxylated linear primary alcohol (ex SHELL)
  • ex SHELL ethoxylated linear primary alcohol
  • the soap control containing no dispersant showed very little calcium ion lowering. A final free calcium concentration of 15° FH was achieved.
  • the following particles were added at room temperature (about 20°C) to hard water, having a hardness of 20° FH (Ca).
  • the particles consisted of 2 parts by weight sodium oleate, 1 part by weight sodium stearate, 1 part by weight sodium palmitate, 2 parts by weight DOBS 055 (as in Example 1) and 1 part by weight sodium silicate (as a structurant).
  • the particles were dosed at the level of 1.3 g/I to the water together with 0.5 g/I calcite, 1.5 g/I sodium carbonate (measured as anhydrous) and 10 ppm sodium tripolyphosphate as a crystal growth poison.

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  • Treatment Of Fiber Materials (AREA)

Claims (11)

1. Procédé de lavage des tissus dans de l'eau contenant des ions de dureté de calcium, en mettant en contact les tissus à une température inférieure à 50°C avec une liqueur de lavage qu'on obtient en ajoutant à l'eau une composition détergente solide particulaire, caractérisé en ce que la composition comprend des particules adjuvantes qui sont une matière dispersant soluble dans l'eau ou dispersable dans l'eau en solution solide avec la matière adjuvante choisie parmi les sels d'acides gras, dont plus de 30% sont des acides gras saturés et qui contiennent au moins 16 atomes de carbone, lesdits sels étant les sels desdits acides gras avec des métaux alcalins ou des cations organiques renfermant de l'azote, le dispersant étant constitué d'un alkylbenzène- sulfonate et la majeure partie des particules ayant une granulométrie de 100 à 1500 (lm.
2. Procédé selon la revendication 1, dans lequel la composition contient également une matière étergente active non savonneuse séparée des particules adjuvantes et/ou incorporée dans lesdites particules adjuvantes à titre d'une autre matière dispersante qui est différente dudit alkyl- benzène-sulfonate.
3. Procédé selon la revendication 1 ou 2, dans lequel la composition comprend une matière alcaline capable de donner à la composition un pH de plus de 8,0 quand on l'ajoute à l'eau d'une dureté French de plus de 12° (Ca) à 25°C et à une concentration de 1,0 g/I.
4. Procédé selon la revendication 3, dans lequel ladite matière alcaline est choisie parmi les carbonates de métaux alcalins, les silicates de métaux alcalins et leurs mélanges.
5. Procédé selon l'une quelconque des revendications 1 à 4, dans lequel la matière dispersante est choisie parmi les s-alkyl (C1o-,s)benzène- sulfonates linéaires de sodium.
6. Procédé selon l'une quelconque des revendications précédentes, dans lequel lesdites particules adjuvantes comprennent une matière de support dans laquelle le sel d'acide gras est insoluble.
7. Procédé selon la revendication 6, dans lequel ledit support est choisi parmi les sels minéraux hydrosolubles, les matières minérales insolubles dans l'eau, les matières organiques solubles dans l'eau, les matières filmogènes hydrosolubles, les polymères synthétiques et les protéines.
8. Procédé selon l'une quelconque des revendications précédentes, dans lequel l'adjuvant est choisi parmi les sels d'acide palmitique, d'acide stéarique, d'acide gras de suif et d'acide gras d'huile de palmier.
9. Procédé selon l'une quelconque des revendications précédentes, dans lequel la composition comprend:
(i) 2 à 30% en poids d'au moins un détergent actif non savonneux;
(ii) au moins 3% en poids d'une matière alcaline; et
(iii) lesdites particules adjuvantes étant en une proportion équivalente à au moins 15% en poids d'un sel d'acide gras.
10. Procédé selon l'une quelconque des revendications précédentes, dans lequel la composition comprend:
(i) de 5 à 30% en poids d'un détergent actif choisi parmi les détergents actifs synthétiques anioniques, les détergents actifs non ioniques et leurs mélanges;
(ii) de 10 à 80% en poids de carbonate de sodium;
(iii) jusqu'à 15% en poids de calcite; et
(iv) de 10 à 20% en poids d'un sel d'acide gras sous forme de particules adjuvantes comprenant, par rapport au poids des particules, de 5 à 80% dudit dispersant et de 20 à 95% dudit sel d'acide gras.
11. Procédé selon l'une quelconque des revendications précédentes, dans lequel les particules adjuvantes contiennent lesdits sels d'acides gras en une proportion plus élevée qu'un sel d'adjuvant séquestrant quelconque.
EP83307640A 1982-12-17 1983-12-15 Procédé pour le lavage de tissu Expired EP0113978B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT83307640T ATE29151T1 (de) 1982-12-17 1983-12-15 Waschverfahren fuer gewebe.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8236003 1982-12-17
GB8236003 1982-12-17

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EP0113978A1 EP0113978A1 (fr) 1984-07-25
EP0113978B1 true EP0113978B1 (fr) 1987-08-26

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EP83307640A Expired EP0113978B1 (fr) 1982-12-17 1983-12-15 Procédé pour le lavage de tissu

Country Status (7)

Country Link
EP (1) EP0113978B1 (fr)
AT (1) ATE29151T1 (fr)
AU (1) AU551234B2 (fr)
DE (1) DE3373195D1 (fr)
NO (1) NO834649L (fr)
PH (1) PH19239A (fr)
ZA (1) ZA839296B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8415302D0 (en) * 1984-06-15 1984-07-18 Unilever Plc Fabric washing process
US6133217A (en) * 1998-08-28 2000-10-17 Huntsman Petrochemical Corporation Solubilization of low 2-phenyl alkylbenzene sulfonates
US6083897A (en) * 1998-08-28 2000-07-04 Huntsman Petrochemical Corporation Solubilization of low 2-phenyl alkylbenzene sulfonates
US6617303B1 (en) 1999-01-11 2003-09-09 Huntsman Petrochemical Corporation Surfactant compositions containing alkoxylated amines

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4196095A (en) * 1978-07-11 1980-04-01 Church & Dwight Co. Inc. Dry blending using magnesium stearate
JPS55104400A (en) * 1979-02-06 1980-08-09 Kureha Chemical Ind Co Ltd Detergent composition
IT1124027B (it) * 1979-03-23 1986-05-07 Mira Lanza Spa Composizione detersiva a basso o nullo tenore di fosforo

Also Published As

Publication number Publication date
PH19239A (en) 1986-02-14
ATE29151T1 (de) 1987-09-15
AU2236483A (en) 1984-06-21
DE3373195D1 (en) 1987-10-01
AU551234B2 (en) 1986-04-24
ZA839296B (en) 1985-07-31
EP0113978A1 (fr) 1984-07-25
NO834649L (no) 1984-06-18

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