EP0287514A1 - Détergent pour le postlavage de teintures réactives, son procédé de préparation et son emploi - Google Patents

Détergent pour le postlavage de teintures réactives, son procédé de préparation et son emploi Download PDF

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Publication number
EP0287514A1
EP0287514A1 EP88810227A EP88810227A EP0287514A1 EP 0287514 A1 EP0287514 A1 EP 0287514A1 EP 88810227 A EP88810227 A EP 88810227A EP 88810227 A EP88810227 A EP 88810227A EP 0287514 A1 EP0287514 A1 EP 0287514A1
Authority
EP
European Patent Office
Prior art keywords
adduct
component
acid
moles
ethylene oxide
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.)
Withdrawn
Application number
EP88810227A
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German (de)
English (en)
Inventor
Heinz Abel
Hans-Ulrich Berendt
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.)
Novartis AG
Original Assignee
Ciba Geigy AG
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Filing date
Publication date
Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of EP0287514A1 publication Critical patent/EP0287514A1/fr
Withdrawn legal-status Critical Current

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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
    • C11D3/02—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
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/83—Mixtures of non-ionic with anionic 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
    • C11D3/2003—Alcohols; Phenols
    • C11D3/2065—Polyhydric alcohols
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/02—After-treatment
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29—Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/34—Derivatives of acids of phosphorus
    • C11D1/345—Phosphates or phosphites
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/72—Ethers of polyoxyalkylene glycols

Definitions

  • the present invention relates to an aqueous detergent which can be used in the washing of prints or dyeings with reactive dyes on cellulose-containing textile materials, a process for its preparation and its use for the washing of said textile materials both on an industrial scale and on a household scale.
  • the detergent according to the invention is particularly suitable for washing with "hard” water, such as tap water.
  • detergents are used for washing color materials in the form of piece goods. However, they are not suitable for washing dyeing material in the form of packages or loose material. These detergents are also less stable in storage.
  • the detergent according to the invention can additionally contain an anionic surfactant as component (C) and a nonionic surfactant as component (D).
  • the detergent according to the invention can contain further auxiliaries and additives customary in detergents.
  • the detergent according to the invention can also contain polymers or copolymers of an acrylamide.
  • component (A) which is the actual active substance of the new post-washing agent
  • p is a number from 0.7 to 1.5
  • q is a number from 0.8 to 6, preferably 1.3 to 4, into consideration.
  • the alkali aluminum silicates used as component (A) can be prepared synthetically in a simple manner, for example by reaction of water-soluble silicates with water-soluble aluminates in the presence of water. For this purpose, aqueous solutions of the starting materials are mixed with one another or a component present in the solid state is reacted with the other component present as an aqueous solution. Mixing the two components in the solid state also gives the desired aluminum silicates in the presence of water.
  • Alkali aluminum silicates can also be prepared from Al (OH) 3, Al2O3 or SiO2 by reaction with alkali silicate or aluminate solutions. Finally, such substances can also form from the melt.
  • the alkali aluminum silicates prepared by precipitation or converted into aqueous suspension in a finely divided state by other processes can be converted from the amorphous to the aged or to the crystalline state by heating to temperatures of 50 to 200 ° C.
  • the amorphous or crystalline alkali aluminum silicate present in aqueous suspension can be separated from the remaining aqueous solution by filtration and, if desired, at temperatures of e.g. Dry 50 to 800 ° C.
  • alkali aluminum silicates which are suitable as component (A), including their preparation and preparation, are described in DE-OS 27 14 954.
  • the alkali aluminum silicates produced by this process have a particle size of 1 to 12 ⁇ .
  • Detergents containing alkali aluminum silicates of such particle size are well suited for washing coloring materials which are in the form of pieces, such as fabrics. Just like the detergents of the above-mentioned US Pat. No. 4,545,919, they are also unsuitable for washing the coloring materials in the form of wound packages, such as cross-wound bobbins, since the calcium silicate complexes formed are too large to penetrate the large-volume dye material in the washing process.
  • the grinding process takes place at temperatures between 18 and 30 ° C (room temperature) and extends over several hours, preferably 4 to 7, particularly 4.5 to 5.5 hours.
  • the grinding (stirring) speed is 200-700, preferably 200-400 revolutions per minute.
  • the glass beads used should be so large that they can achieve a particle size of the alkali aluminum silicate of 0.01 to 2 ⁇ .
  • the average of the glass beads is 1.5 - 3, preferably 2 mm.
  • Component (A) can also be ground in the absence of components (C) and (D).
  • the glass beads are separated from the regrind by methods known per se, e.g. carried out by centrifugation.
  • component (B) come e.g. Glycerin, trimethylolpropane, 1,2,4-butanetriol, erythritol, mannitol, pentaerythritol, 1,2,6-hexanetriol, tetramethylolethylene diamine and especially sorbitol.
  • the anionic surfactants of component (C) are preferably acidic derivatives of nonionic or cationic alkylene oxide adducts, such as, for example, acidic ether groups or preferably addition products of 2 to 100 mol of alkylene oxides, especially ethylene oxide, containing ester groups of inorganic or organic acids and / or propylene oxide or styrene oxide onto aliphatic hydrocarbon radicals with a total of at least 4, preferably 12, carbon atoms, organic hydroxyl, carboxyl, amino and / or amido compounds or mixtures of these substances.
  • acidic ethers or esters can be present as free acids or as salts, for example alkali metal, alkaline earth metal, ammonium or amine salts.
  • anionic surfactants are prepared by known methods, e.g. at least 2 moles, preferably more than 2 moles, e.g. Adds 10 to 100 mol, ethylene oxide or propylene oxide or alternating ethylene oxide or propylene oxide in any order and then etherifies or esterifies the adducts and, if appropriate, converts the ethers or esters into their salts.
  • Higher fatty alcohols i.e.
  • Alkanols or alkenols each having 8 to 22 carbon atoms, di- to hexavalent aliphatic alcohols having 2 to 9 carbon atoms, alicyclic alcohols, phenylphenols, benzylphenols, alkylphenols with one or more alkyl substituents which, or which together have at least 4 carbon atoms, fatty acids with 8 up to 22 carbon atoms, amines which have aliphatic and / or cycloaliphatic hydrocarbon radicals of at least 8 carbon atoms, in particular fatty amines containing such radicals, hydroxyalkylamines, hydroxyalkylamides and aminoalkyl esters of fatty acids or dicarboxylic acids and higher alkylated aryloxycarboxylic acids.
  • Highly suitable anionic polyalkylene oxide adducts are acidic esters or their salts of a polyadduct of 2 to 100 mol, preferably up to 50 mol, of ethylene oxide with 1 mol of fatty alcohol having 8 to 22 carbon atoms or with 1 mol of a phenol which has at least one benzyl group, one phenyl group or preferably one Has alkyl group with at least 4 carbon atoms, such as benzylphenol, dibenzylphenol, dibenzyl (nonyl) phenol, o-phenylphenol, butylphenol, tributylphenol, octylphenol, nonylphenol, dodecylphenol or pentadecylphenol, these acidic esters can be used individually or as a mixture.
  • Preferred anionic polyalkylene oxide adducts correspond to the formula (2) YO- (CH2CH2O) X, wherein Y is alkyl or alkenyl each with 8 to 22 carbon atoms, alkylphenyl with 4 to 16 carbon atoms in the alkyl part or o-phenylphenyl, X is the acid residue of an inorganic, oxygen-containing acid, such as sulfuric acid or phosphoric acid or else the rest of an inorganic acid and m 2 to 40, preferably 2 to 15.
  • the alkyl radical in the alkylphenyl is preferably in the para position.
  • the alkyl radicals in the alkylphenyl can be butyl, hexyl, n-octyl, iso-octyl, p-tert-octyl, n-nonyl, iso-nonyl, decyl or dodecyl.
  • the alkyl radicals having 8 to 12 carbon atoms are preferred, in particular the octyl or nonyl radicals.
  • the fatty alcohols for the preparation of the anionic surfactants of formula (2) are e.g. those with 8 to 22, in particular 8 to 18, carbon atoms, such as octyl, decyl, lauryl, tridecyl, myristyl, cetyl, stearyl, oleyl, arachidyl or behenyl alcohol.
  • the acid residue X is derived, for example, from low molecular weight dicarboxylic acids, such as of maleic acid, succinic acid or sulfosuccinic acid, and is connected to the ethyleneoxy part of the molecule via an ester bridge.
  • X is derived from inorganic polybasic acids, such as sulfuric acid or orthophosphoric acid.
  • the acid residue X can be in the form of a free acid or in salt form, i.e. e.g. as an alkali metal, ammonium or amine salt.
  • alkali metal, ammonium or amine salt examples of such salts are lithium, sodium, potassium, ammonium, trimethylamine, ethanolamine, diethanolamine or triethanolamine salts.
  • Anionic surfactants of the formula are particularly preferred wherein Y ⁇ is octyl or nonyl, m1 is 2 to 15 and X ⁇ is an acid residue which is derived from sulfuric acid or from o-phosphoric acid, and the surfactants are present as free acids, sodium or ammonium salts.
  • Y ⁇ is octyl or nonyl
  • m1 is 2 to 15
  • X ⁇ is an acid residue which is derived from sulfuric acid or from o-phosphoric acid
  • the surfactants are present as free acids, sodium or ammonium salts.
  • the acidic sulfuric acid ester of the adduct of 2 to 12 moles of ethylene oxide with 1 mole of p-nonylphenol.
  • the anionic alkylene oxide adducts can be used individually or as mixtures with one another to produce the new post-washing agent.
  • component (D) e.g. Alkylene oxide adducts from natural alcohols such as e.g. Amyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol or oleyl alcohol or synthetic alcohols, e.g. Oxo-alcohols such as in particular 2-ethylbutanol, 2-ethylhexanol, isooctyl alcohol, trimethylhexanol, trimethylnonyl alcohol, hexadecyl alcohol or the fatty alcohols commercially available under the ®Alfol brand.
  • natural alcohols such as e.g. Amyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol or oleyl alcohol or synthetic alcohols, e.g. Oxo-alcohols such as in particular 2-ethylbutanol, 2-ethylhexanol, isooctyl alcohol, trimethyl
  • alkylene oxide addition products from the water-insoluble monoalcohols mentioned such as, for example, 1,2-propylene oxide addition products, for example those which contain 1 to 15 mol of propylene oxide, but preferably the ethylene oxide addition products of these alcohols can also be used as component (D).
  • Preferred ethylene oxide addition products are exemplified by the following formula (4) RO- (CH2CH2O) H represented in which R is a saturated or unsaturated aliphatic radical, preferably alkyl or alkenyl each having 8 to 18 carbon atoms and s 1 to 10, preferably 1 to 3.
  • component (D) are fatty acid-alkanolamine reaction products which are advantageously derived from fatty acids with 8 to 22 carbon atoms and from alkanolamines with 2 or 3 carbon atoms per alkanol radical.
  • the reaction products of fatty acids having 12 to 18 carbon atoms are preferred.
  • alkanolamine one can e.g. Use ethanolamine, diethanolamine, propanolamine, isopropanolamine or di-isopropanolamine.
  • Dialkanolamines, especially diethanolamine, are preferred.
  • the molar ratio between fatty acid and dialkanolamine can be 1: 1 to 1: 2.
  • Examples of fatty acids are: decene, lauric, coconut fat, myristic, palmitic, tallow, oil, ricinol, linole, linolen -, stearic, arachic or behenic acid.
  • alkylene oxide in particular ethylene oxide, adducts from the above-mentioned fatty acid-alkanolamine reaction products, it being possible for individual ethylene oxide units to be replaced by substituted epoxides, such as propylene oxide.
  • the number of alkylene oxide groups in these glycol ethers can be 1 to 8 and preferably 1 to 4. Addition products of 1 to 4 moles of ethylene oxide with 1 mole of reaction product of 1 mole of coconut fatty acid, stearic acid and / or palmitic acid with 1 mole of diethanolamine are preferred.
  • reaction products which are suitable as component (D) are addition products of preferably 2 to 15 mol of alkylene oxide, e.g. Ethylene oxide and / or propylene oxide, on optionally substituted phenols, trihydric to hexavalent aliphatic alcohols of 3 to 9 carbon atoms or on the aforementioned fatty acids.
  • alkylene oxide e.g. Ethylene oxide and / or propylene oxide
  • Suitable optionally substituted phenols are, for example, phenol, benzylphenol, o-phenylphenol or alkylphenols, the alkyl radical of which is advantageously a total of 4 to 16, preferably 4 to Has 12 carbon atoms.
  • alkylphenols are butylphenol, tributylphenol, octylphenol and especially nonylphenol.
  • the trihydric to hexavalent alcohols preferably contain 3 to 6 carbon atoms and are in particular glycerol, trimethylolpropane, 1,2,4-butanetriol, erythritol, mannitol, pentaerythritol, 1,2,6-hexanetriol, tetramethylolethylenediamine or sorbitol.
  • the three to hexavalent alcohols are preferably reacted with ethylene oxide or preferably with propylene oxide or mixtures of these alkylene oxides.
  • the fatty acids preferably have 8 to 22 carbon atoms and can be saturated or unsaturated, e.g. capric, lauric, myristic, palmitic or stearic acid or decenic, dodecenic, tetradecenic, hexadecenic, oleic, linoleic, linolenic or preferably ricinoleic acid.
  • component (D) is present alone or as a mixture of two, three or more components in the detergent range from 0 to 10 percent by weight, preferably 0.1 to 2 percent by weight, based on the detergent as a whole.
  • Detergents according to the invention can also contain, as component (E), an aliphatic monoalcohol having at least 5, preferably 8 to 18, carbon atoms.
  • component (E) an aliphatic monoalcohol having at least 5, preferably 8 to 18, carbon atoms.
  • These alcohols can be saturated or unsaturated and branched or straight-chain and can be used alone or in a mixture. the natural or synthetic alcohols mentioned above.
  • Detergents according to the invention preferably contain, based in each case on the mixture, 10 - 50% by weight of component (A), 15-65% by weight of component (B), 0-10% by weight of component (C), 0-5% by weight of component (D) and at least 10% by weight of water.
  • AA a sodium aluminum silicate
  • BB a hexavalent alcohol
  • CC an aqueous solution of the ammonium salt of the acid sulfuric acid ester of the adduct from 1 mol of p-tert-nonylphenol and 2 mol of ethylene oxide
  • DD an adduct of 1 mol of p-tert-nonylphenol and 10 mol of ethylene oxide and a graft polymer made from acrylamide and the adduct of propylene oxide with glycerin.
  • mixtures of this type can additionally contain silicone oils.
  • the detergents according to the invention are used in particular when washing dyeings or prints on cellulose fibers or blended fabrics made of cellulose and synthetic organic material, e.g. linear polyesters or modified cellulose (cellulose esters) are used, the cellulose material being that of natural or regenerated cellulose, such as Hemp, linen, jute, viscose silk, cellulose or in particular cotton and any polyester content, if necessary, is dyed before or after the cellulose.
  • Cellulose dyeings or cellulose prints are understood here to mean the dyeings or prints produced by any process with reactive dyes, the detergents according to the invention being used as aftertreatment.
  • the dyeing material can be in any processing stages, for example as a loose material (flake), as a doubled, pre-stretched staple fiber tape or in the form of threads, yarns, fabrics, knitted fabrics, but especially wound packages.
  • Reactive dyes are understood to be the customary anionic dyes which form a chemical bond with the cellulose, for example the "Reactive Dyes” listed on pages 3391-3562 in the Color Index, 3rd Edition (1971) Vol. 3.
  • the detergent according to the invention makes it possible to carry out the usual washing operations of the abovementioned prints or dyeings produced with reactive dyes with hard water (process water), as is directly available from the water pipe, with good success.
  • process water hard water
  • the water hardness is reduced without the usual addition of electrolytes, ion exchangers and / or complexing agents and, above all, without the use of phosphorus-containing compounds, e.g. Phosphonic acids or inorganic phosphates eliminated, which have recently been increasingly restricted by the ecological and legislative requirements for phosphorus-free products.
  • the invention thus further relates to a method for washing prints or dyeings produced with reactive dyes on cellulose-containing textile materials using the detergents according to the invention.
  • This process consists in treating the printed or dyed textiles at a temperature of 60 to 100 ° C. in an aqueous washing liquor which contains the detergent according to the invention, preferably in amounts of 1-10 g / l.
  • the textiles are then removed from the wash liquor and rinsed with fresh water until the wash liquor components have been completely removed. This gives printing dyeings whose white base is not stained, and dyeings from the exhaust process which have the desired wet fastness properties, especially wash fastness properties.
  • the following products are examples of the anionic surfactants or alkylene oxide adducts used as components (C) and (D).
  • Dispersions which are similarly pourable are obtained if, instead of sorbitol, the same number of proportions of glycerol, an ethoxylated pentaerythritol (mol. Wt. 500-700) or an ethoxylated tetramethylolethylenediamine (mol. Wt. 400-600) is used.
  • washing liquors 2 and 3 With washing liquors 2 and 3, a product is obtained which has no staining on unprinted parts. In contrast, the white portion of the print treated with wash liquor 1 is strongly stained.
  • the individual wash samples are then rinsed together in cold permutite water for 10 minutes.
  • the treated dyed samples are spun onto 100% water absorption and tested for wet ironing in accordance with SNV standard 19832.
  • a white section of cotton is wetted in distilled water and spun to 100% water absorption.
  • the wet dyed yarn is placed on a dry white cotton strand and covered with the wet white section.
  • the wash samples are then pressed together for 2 minutes in an ironing press set at 180 °.
  • the white, pre-wetted accompanying fabric is then assessed for fastness to ironing.
  • the dyed sections obtained according to washing tests 2 and 3 do not stain the white section when testing the fastness to ironing, while the white cotton is strongly stained by the section obtained according to washing test 1.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Textile Engineering (AREA)
  • Detergent Compositions (AREA)
EP88810227A 1987-04-15 1988-04-06 Détergent pour le postlavage de teintures réactives, son procédé de préparation et son emploi Withdrawn EP0287514A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH149487 1987-04-15
CH1494/87 1987-04-15

Publications (1)

Publication Number Publication Date
EP0287514A1 true EP0287514A1 (fr) 1988-10-19

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Application Number Title Priority Date Filing Date
EP88810227A Withdrawn EP0287514A1 (fr) 1987-04-15 1988-04-06 Détergent pour le postlavage de teintures réactives, son procédé de préparation et son emploi

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US (1) US4902439A (fr)
EP (1) EP0287514A1 (fr)

Cited By (2)

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NL1006703C2 (nl) * 1997-07-31 1999-02-02 Sybron Chemie Nederland B V Werkwijze voor het nawassen van gekleurd textiel.
WO2010018073A1 (fr) 2008-08-11 2010-02-18 Basf Se Procédé de post-traitement ménagé de textiles teints

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US5403509A (en) * 1992-07-20 1995-04-04 Kao Corporation, S.A. Detergent composition comprising a mono-, di- and tri-ester mixture and method of manufacturing same
US5372611A (en) * 1992-09-30 1994-12-13 Apollo Chemical Corporation Liquid alkali for reactive dyeing of textiles
US5378242A (en) * 1992-12-22 1995-01-03 Apollo Chemical Company Liquid alkali for soaping off reactive dyes
US6730650B1 (en) 2002-07-09 2004-05-04 The Dial Corporation Heavy-duty liquid detergent composition comprising anionic surfactants
CN103409254A (zh) * 2013-08-20 2013-11-27 南通市通州区益君劳务有限公司 一种汽车玻璃洗涤剂

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EP0008060A1 (fr) * 1978-08-03 1980-02-20 BASF Aktiengesellschaft Utilisation d'alcools polyvalents, d'acides (hydroxy)carboxyliques et/ou de leurs esters avec des alcools polyvalents comme régulateurs de viscosité
EP0102923A1 (fr) * 1982-08-31 1984-03-14 Ciba-Geigy Ag Détergent approprié pour le post-lavage de teintures réactives et procédé de lavage correspondant

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EP0894890A1 (fr) * 1997-07-31 1999-02-03 Sybron Chemie Nederland B.V. Procédé de lavage de textiles teints
WO2010018073A1 (fr) 2008-08-11 2010-02-18 Basf Se Procédé de post-traitement ménagé de textiles teints
US8475538B2 (en) 2008-08-11 2013-07-02 Basf Se Method for gently aftertreating dyed textiles
CN102177291B (zh) * 2008-08-11 2013-07-17 巴斯夫欧洲公司 对已染色的织物进行温和后处理的方法

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