EP1724333A1 - Procédé de traitement de matériaux fibreux textiles - Google Patents

Procédé de traitement de matériaux fibreux textiles Download PDF

Info

Publication number
EP1724333A1
EP1724333A1 EP06118810A EP06118810A EP1724333A1 EP 1724333 A1 EP1724333 A1 EP 1724333A1 EP 06118810 A EP06118810 A EP 06118810A EP 06118810 A EP06118810 A EP 06118810A EP 1724333 A1 EP1724333 A1 EP 1724333A1
Authority
EP
European Patent Office
Prior art keywords
peroxide
detergent
weight
compound
activator
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Withdrawn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
EP06118810A
Other languages
German (de)
English (en)
Inventor
Jürgen Kaschig
Robert Hochberg
Oliver Becherer
Georges Metzger
Claude Eckhardt
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.)
BASF Schweiz AG
Original Assignee
Ciba Spezialitaetenchemie Holding AG
Ciba SC Holding AG
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
Application filed by Ciba Spezialitaetenchemie Holding AG, Ciba SC Holding AG filed Critical Ciba Spezialitaetenchemie Holding AG
Priority to EP06118810A priority Critical patent/EP1724333A1/fr
Publication of EP1724333A1 publication Critical patent/EP1724333A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments
    • C11D3/42Brightening agents ; Blueing agents
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3902Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905Bleach activators or bleach catalysts
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3902Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905Bleach activators or bleach catalysts
    • C11D3/3907Organic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3902Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905Bleach activators or bleach catalysts
    • C11D3/3932Inorganic compounds or complexes

Definitions

  • the present invention is directed to detergent formulations containing certain fluorescent whitening agents and a peroxide, a peroxide activator and/or a bleaching catalyst.
  • the present invention provides, as a first aspect, a detergent composition comprising at least one compound of formula or wherein M is hydrogen or cation, and wherein the detergent contains a peroxide, a peroxide activator and/or a bleaching catalyst.
  • the cation M is preferably an alkali metal atom, an alkaline earth metal atom, ammonium or a cation formed from an amine.
  • Preferred are Na, K, Ca, Mg, ammonium, mono-, di-, tri- or tetra-C 1 -C 4 alkylammonium, mono-, di- or tri-C 2 -C 4 -hydroxyalkylammonium or ammonium that is di- or tri-substituted with a mixture of C 1 -C 4 -alkyl and C 2 -C 4 -hydroxyalkyl groups.
  • Highly preferred is sodium.
  • Compounds of formulae (1), (2), (3) and (4) can for example be prepared by first reacting cyanuric chloride with methanol, reacting the product obtained with 4,4'-diaminostilbene-2,2'-disulfonic acid and then reacting the intermediate with the corresponding amines.
  • the detergent compositions used preferably comprise
  • detergent compositions used comprise
  • an amount of compounds of formulae (1), (2), (3) or (4) of 0.001-5%, especially an amount of 0.01-5% is used. Highly preferred is an amount of 0.05-5%, especially 0.05 to 2%.
  • amounts given in percent are to be understood as being percent by weight, based on the total weight, unless otherwise stated.
  • the detergent may be formulated as a solid, as an aqueous liquid comprising, e.g., 5-50, preferably 10-35% water or as a non-aqueous liquid detergent, containing not more than 5, preferably 0-1 wt.% of water, and based on a suspension of a builder in a non-ionic surfactant, as described, e.g., in GB-A-2158454 .
  • the anionic surfactant component may be, e.g., an alkylbenzenesulfonate, an alkylsulfate, an alkylethersulfate, an olefinsulfonate, an alkanesulfonate, a fatty acid salt, an alkyl or alkenyl ether carboxylate or an ⁇ -sulfofatty acid salt or an ester thereof.
  • alkylbenzenesulfonates having 10 to 20 carbon atoms in the alkyl group
  • alkylsulfates having 8 to 18 carbon atoms
  • alkylethersulfates having 8 to 18 carbon atoms
  • fatty acid salts being derived from palm oil or tallow and having 8 to 18 carbon atoms.
  • the average molar number of ethylene oxide added in the alkylethersulfate is preferably 1 to 20, preferably 1 to 10.
  • the salts are preferably derived from an alkaline metal like sodium and potassium, especially sodium.
  • alkali metal sarcosinates of formula R-CO(R 1 )CH 2 COOM 1 in which R is alkyl or alkenyl having 9-17 carbon atoms in the alkyl or alkenyl radical, R 1 is C 1 -C 4 alkyl and M 1 is alkali metal, especially sodium.
  • the nonionic surfactant component may be, e.g., primary and secondary alcohol ethoxylates, especially the C 8 -C 20 aliphatic alcohols ethoxylated with an average of from 1 to 20 moles of ethylene oxide per mole of alcohol, and more especially the C 10 -C 15 primary and secondary aliphatic alcohols ethoxylated with an average of from 1 to 10 moles of ethylene oxide per mole of alcohol.
  • Non-ethoxylated nonionic surfactants include alkylpolyglycosides, glycerol monoethers, and polyhydroxyamides (glucamide).
  • the total amount of anionic surfactant and nonionic surfactant is preferably 5-50% by weight, preferably 5-40% by weight and more preferably 5-30% by weight. As to these surfactants it is preferred that the lower limit is 10% by weight.
  • the builder component may be an alkali metal phosphate, especially a tripolyphosphate; a carbonate or bicarbonate, especially the sodium salts thereof; a silicate or disilicate; an aluminosilicate; a polycarboxylate; a polycarboxylic acid; an organic phosphonate; or an aminoalkylene poly (alkylene phosphonate); or a mixture of these.
  • Preferred silicates are crystalline layered sodium silicates of the formula NaHSi m O 2m+1 .pH 2 O or Na 2 Si m O 2m+1 .pH 2 O in which m is a number from 1.9 to 4 and p is 0 to 20.
  • Preferred aluminosilicates are the commercially-available synthetic materials designated as Zeolites A, B, X, and HS, or mixtures of these. Zeolite A is preferred.
  • Preferred polycarboxylates include hydroxypolycarboxylates, in particular citrates, polyacrylates and their copolymers with maleic anhydride.
  • Preferred polycarboxylic acids include nitrilotriacetic acid and ethylene diamine tetra-acetic acid.
  • Preferred organic phosphonates or aminoalkylene poly (alkylene phosphonates) are alkali metal ethane 1-hydroxy diphosphonates, nitrilo trimethylene phosphonates, ethylene diamine tetra methylene phosphonates and diethylene triamine penta methylene phosphonates.
  • the amount of builders is preferably 5-70% by weight, preferably 5-60% by weight and more preferably 10-60% by weight. As to the builders it is preferred that the lower limit is 15% by weight, especially 20% by weight.
  • Suitable peroxide components include, for example, the organic and inorganic peroxides (like sodium peroxides) known in the literature and available commercially that bleach textile materials at conventional washing temperatures, for example at from 5 to 95°C.
  • the organic peroxides are, for example, monoperoxides or polyperoxides having alkyl chains of at least 3, preferably 6 to 20, carbon atoms; in particular diperoxydicarboxylates having 6 to 12 C atoms, such as diperoxyperazelates, diperoxypersebacates, diperoxyphthalates and/or diperoxydodecanedioates, especially their corresponding free acids, are of interest.
  • very active inorganic peroxides such as persulphate, perborate and/or percarbonate. It is, of course, also possible to employ mixtures of organic and/or inorganic peroxides.
  • the amount of peroxide is preferably 0.5-30% by weight, preferably 1-20% by weight and more preferably 1-15% by weight.
  • the lower limit is preferably 2% by weight, especially 5% by weight.
  • the peroxides are preferably activated by the inclusion of a bleach activator.
  • a bleach activator Preferred are such compounds that, under perhydrolysis conditions, yield unsubstituted or substituted perbenzo- and/or peroxo-carboxylic acids having from 1 to 10 carbon atoms, especially from 2 to 4 carbon atoms.
  • Suitable compounds include those that carry O- and/or N-acyl groups having the said number of carbon atoms and/or unsubstituted or substituted benzoyl groups.
  • polyacylated alkylenediamines especially tetraacetylethylenediamine (TAED), acylated glycolurils, especially tetraacetylglycoluril (TAGU), N,N-diacetyl-N,N-dimethyl-urea (DDU), acylated triazine derivatives, especially 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), compounds of formula wherein R is a sulfonate group, a carboxylic acid group or a carboxylate group, and wherein R' is linear or branched (C 7 -C 15 )alkyl; also activators that are known under the names SNOBS, SLOBS, NOBS and DOBA, acylated polyhydric alcohols, especially triacetin, ethylene glycol diacetate and 2,5-diacetoxy-2,5-dihydrofuran
  • the amount of bleach activator is preferably 0-10% by weight, preferably 0-8% by weight.
  • the lower limit is preferably 0.5% by weight, especially 1% by weight.
  • Bleaching catalysts which may be added, include, e.g., enzymatic peroxide precursors and/or metal complexes.
  • Preferred metal complexes are manganese, cobalt or iron complexes such as manganese or iron phthalocyanines or the complexes described in EP-A-0509787 .
  • the amount is preferably 0.005 to 2% by weight, more preferably 0.01 to 2% by weight, especially 0.05 to 2% by weight. Highly preferred is an amount of 0.1-2% by weight.
  • bleaching catalysts As examples for bleaching catalysts the following are mentioned:
  • the detergent can optionally contain enzymes. Enzymes can be added to detergents for stain removal.
  • the enzymes usually improve the performance on stains that are either protein- or starch-based, such as those caused by blood, milk, grass or fruit juices.
  • Preferred enzymes are cellulases, proteases, amylases and lipases.
  • Preferred enzymes are cellulases and proteases, especially proteases.
  • Cellulases are enzymes which act on cellulose and its derivatives and hydrolyze them into glucose, cellobiose, cellooligosaccharide. Cellulases remove dirt and have the effect of mitigating the roughness to the touch. Examples of enzymes to be used include, but are by no means limited to, the following:
  • the enzymes can optionally be present in the detergent.
  • the enzymes are usually present in an amount of 0.01-5% by weight, preferably 0.05-5% and more preferably 0.1-4% by weight, based on the total weight of the detergent.
  • Further preferred additives for the detergents according to the invention are polymers that, during the washing of textiles, inhibit staining caused by dyes in the washing liquor that have been released from the textiles under the washing conditions (dye fixing agents, dye transfer inhibitors).
  • Such polymers are preferably polyvinylpyrrolidones, polyvinylimidazoles or polyvinylpyridine N-oxides which may have been modified by the incorporation of anionic or cationic substituents, especially those having a molecular weight in the range from 5000 to 60 000, more especially from 10 000 to 50 000.
  • Such polymers are usually used in an amount of from 0.01 to 5 %, preferably 0.05 to 5 % by weight, especially 0.1 to 2 % by weight, based on the total weight of the detergent.
  • Preferred polymers are those given in WO-A-02/02865 (see especially page 1, last paragraph and page 2, first paragraph).
  • the detergents used will usually contain one or more auxiliaries such as soil suspending agents, for example sodium carboxymethylcellulose; salts for adjusting the pH, for example alkali or alkaline earth metal silicates; foam regulators, for example soap; salts for adjusting the spray drying and granulating properties, for example sodium sulphate; perfumes; and also, if appropriate, antistatic and softening agents; such as smectite clays; photobleaching agents; pigments; and/or shading agents.
  • auxiliaries can be present in an amount of, for example, 0.1 to 20% by weight, preferably 0.5 to 10 % by weight, especially 0.5 to 5 % by weight, based on the total weight of the detergent.
  • the detergent compositions can take a variety of physical forms including powder, granular, tablet and liquid forms. Examples thereof are conventional powder heavy-duty detergents, compact and supercompact heavy-duty detergents and tablets, like heavy-duty detergent tablets.
  • One important physical form is the so-called concentrated granular form adapted to be added to a washing machine.
  • compact detergents Of importance are also the so-called compact (or supercompact) detergents.
  • compact detergents In the field of detergent manufacture, a trend has developed recently towards the production of compact detergents which contain increased amounts of active substance. In order to minimize energy expenditure during the washing process, the compact detergents are required to operate efficiently at temperatures as low as 40°C, or even at room temperatures, e.g. at 25°C.
  • Such detergents usually contain only low amounts of fillers or processing aids, like sodium sulfate or sodium chloride.
  • the amount of such fillers is usually 0-10% by weight, preferably 0-5 % by weight, especially 0-1 % by weight, based on the total weight of the detergent.
  • Such detergents usually have a bulk density of 650-1000 g/I, preferably 700-1000 g/I and especially 750-1000 g/I.
  • the detergents can also be present in the form of tablets. Relevant characteristics of tablets are ease of dispensing and convenience in handling. Tablets are the most compact delivery of solid detergents and have a bulk density of, for example, 0.9 to 1.3 kg/litre. To enable fast disintegration laundry detergent tablets generally contain special disintegrants:
  • the detergent may also be formulated as a an aqueous liquid comprising 5-50, preferably 10-35% water or as a non-aqueous liquid detergent, containing not more than 5, preferably 0-1 wt.% of water.
  • Non-aqueous liiquid detergent compositions can contain other solvents as carriers.
  • Low molecular weight primary or secondary alcohols exemplified by methanol, ethanol, propanol, and isopropanol are suitable.
  • Monohydric alcohols are preferred for solubilizing surfactant, but polyols such as those containing from 2 to about 6 carbon atoms and from 2 to about 6 hydroxy groups (e.g., 1,3-propanediol, ethylene glycol, glycerine, and 1,2-propanediol) can also be used.
  • the compositions may contain from 5% to 90%, typically 10% to 50% of such carriers.
  • the detergents can also be present as the so-called "unit liquid dose" form.
  • This detergent treatment of textiles can be conducted as a domestic treatment in normal washing machines.
  • the textile fibres treated may be natural or synthetic fibres or mixtures thereof.
  • natural fibres include vegetable fibres such as cotton, viscose, flax, rayon or linen, preferably cotton and animal fibres such as wool, mohair, cashmere, angora and silk, preferably wool.
  • Synthetic fibres include polyester, polyamide and polyacrylonitrile fibres.
  • Preferred textile fibres are cotton, polyamide and wool fibres, especially cotton fibres.
  • textile fibres treated according to the method of the present invention have a density of less than 200 g/m 2 .
  • the process is usually conducted in the temperature range of from 5 to 100°C, especially 5 to 60°C.
  • Preferred is a temperature range of 5 to 40°C, especially 5 to 35°C and more preferably 5 to 30°C.
  • the detergent compositions herein will preferably be formulated such that, during use in aqueous cleaning operations, the wash water will have a pH of between about 6.5 and about 11, preferably between about 7.5 and 11. Laundry products are typically at pH 9-11. Techniques for controlling pH at recommended usage levels include the use of buffers, alkalis, acids, etc., and are well known to those skilled in the art.
  • Machine laundry methods herein typically comprise treating soiled laundry with an aqueous wash solution in a washing machine having dissolved or dispensed therein an effective amount of a machine laundry detergent composition in accordance with the invention.
  • an effective amount of the detergent composition it is meant, e.g., from 20 g to 300 g of product dissolved or dispersed in a wash solution of volume from 5 to 85 litres, as are typical product dosages and wash solution volumes commonly employed in conventional machine laundry methods. Examples are
  • the liquor ratio is preferably 1:4 to 1:40, especially 1:4 to 1:15. Highly preferred is a liquor ratio of 1:4 to 1:10, especially 1:5 to 1:9.
  • a further object of the present invention is to provide a process for the domestic washing treatment of a textile fibre material wherein the textile fibre material is contacted with an aqueous solution of a detergent comprising a compound of formula (1) as defined above, and wherein the detergent contains a peroxide, a peroxide activator and/or a bleaching catalyst, and wherein the temperature of the solution is between 5°C and 40°C, preferably between 5°C and 30°C, throughout the process.
  • the compounds used according to the present invention are particularly advantageous in that they exhibit not only extremely high whitening ability, but, in addition, in many cases highly desirable water solubilities and also possess excellent white aspects in the solid state.
  • a further advantage of the present invention is that the detergent composition delivers improved whiteness performance and fabric feel. Furthermore the compounds show very good results with respect to exhaustion properties.
  • the compounds have the advantage that they are also effective in the presence of active chlorine donors, such as, for example, hypochlorite and can be used without substantial loss of the effects in washing baths with non-ionic washing agents, for example alkylphenol polyglycol ethers.
  • active chlorine donors such as, for example, hypochlorite
  • non-ionic washing agents for example alkylphenol polyglycol ethers.
  • perborate or peracids and activators for example tetraacetylglycoluril or ethylenediamine-tetraacetic acid are the compounds stable both in pulverulent washing agent and in washing baths. In addition, they impart a brilliant appearance in daylight.
  • a wash liquor is prepared by dissolving 0.8 g of a washing powder in 200 ml of tap water. 10 g of bleached cotton fabric is added to the bath and washed at 40°C over 15 minutes and then rinsed, spin-dried and ironed at 160°C.
  • washing powders A and B are used (amounts given in the following Tables 3a and 3b are in g): Table 3a (Ingredients of washing powders A and B) A B Sodium laurylbenzene-sulfonate (LAS) 10g 10g Sodium lauryl ether sulfate (AES) 3g 3g Dobanol 23-6.5 (nonionic alcoholethoxylate) 4g 4g Sodium tripolyphosphate 30g ----- Zeolite A ----- 20g Sodium carbonate 15g 15g Sodium silicate 5g 5g Sodium sulfate 11g 17g Sodium perborate monohydrate 10g 10g TAED 3g 3g Polycarboxylate (co-builder) ----- 4g Carboxymethylcellulose 2g 2g Perfume 0.1g 0.1g Water 5g 5g Fluorescent whitener used Xg Xg Table 3b (Washing powders used) Amount of fluorescent whitener used Washing powder Compound of Prep.
  • a wash liquor is prepared by dissolving 0.8 g of a washing powder in 200 ml of tap water. 10 g of bleached cotton fabric is added to the bath and washed at 30°C over 15 minutes and then rinsed, spin-dried and ironed at 160°C.
  • washing powders are used (amounts given in the following Tables 4a and 4b are percent by weight, based on the total weight of the detergent): Table 4a (Ingredients of washing powders C and D) C D Sodium laurylbenzene-sulfonate (LAS) 8% 8% Sodium lauryl ether sulfate (AES) 3% 3% Dobanol 23-6.5 ( on-ionic alcoholethoxylate) 5% 5% 5% Zeolite A 20% 20% Polycarboxylate (co-builder) 5% 5% Soda ash 18% 18% Sodium silicate 4% 4% Sodium sulfate 5% 5% Hydroxyethanediphosphonic acid (complexing agent) 0.5% 0.5% Cellulase 1.5% ----- Protease ----- 1.5% Carboxymethylcellulose 1% 1% Sodium perborate monohydrate 15% 15% TAED 5% 5% Soap 2% 2% Fluorescent whitener used X% X%

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)
  • Detergent Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Cleaning By Liquid Or Steam (AREA)
EP06118810A 2002-02-25 2003-02-18 Procédé de traitement de matériaux fibreux textiles Withdrawn EP1724333A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP06118810A EP1724333A1 (fr) 2002-02-25 2003-02-18 Procédé de traitement de matériaux fibreux textiles

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP02405136 2002-02-25
EP02405876 2002-10-11
EP06118810A EP1724333A1 (fr) 2002-02-25 2003-02-18 Procédé de traitement de matériaux fibreux textiles
EP03706527A EP1478724B1 (fr) 2002-02-25 2003-02-18 Procede de traitement de materiaux fibreux textiles

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
EP03706527A Division EP1478724B1 (fr) 2002-02-25 2003-02-18 Procede de traitement de materiaux fibreux textiles

Publications (1)

Publication Number Publication Date
EP1724333A1 true EP1724333A1 (fr) 2006-11-22

Family

ID=27758773

Family Applications (4)

Application Number Title Priority Date Filing Date
EP06118792.8A Expired - Lifetime EP1715029B1 (fr) 2002-02-25 2003-02-18 Procédé de traitement de materiaux fibreux textiles
EP03706527A Expired - Lifetime EP1478724B1 (fr) 2002-02-25 2003-02-18 Procede de traitement de materiaux fibreux textiles
EP06118810A Withdrawn EP1724333A1 (fr) 2002-02-25 2003-02-18 Procédé de traitement de matériaux fibreux textiles
EP03702652A Expired - Lifetime EP1485460B1 (fr) 2002-02-25 2003-02-18 Procede de traitement de materiaux fibreux textiles

Family Applications Before (2)

Application Number Title Priority Date Filing Date
EP06118792.8A Expired - Lifetime EP1715029B1 (fr) 2002-02-25 2003-02-18 Procédé de traitement de materiaux fibreux textiles
EP03706527A Expired - Lifetime EP1478724B1 (fr) 2002-02-25 2003-02-18 Procede de traitement de materiaux fibreux textiles

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP03702652A Expired - Lifetime EP1485460B1 (fr) 2002-02-25 2003-02-18 Procede de traitement de materiaux fibreux textiles

Country Status (12)

Country Link
EP (4) EP1715029B1 (fr)
JP (2) JP4567975B2 (fr)
CN (2) CN1294247C (fr)
AR (3) AR038582A1 (fr)
AT (2) ATE340847T1 (fr)
AU (2) AU2003208870B2 (fr)
BR (3) BRPI0306187B1 (fr)
DE (2) DE60308485T2 (fr)
ES (3) ES2271529T3 (fr)
TW (2) TWI332045B (fr)
WO (2) WO2003070870A1 (fr)
ZA (2) ZA200402942B (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2271529T3 (es) * 2002-02-25 2007-04-16 Ciba Specialty Chemicals Holding Inc. Procedimiento para el tratamiento de materiales de fibra textil.
AU2004224146B2 (en) * 2003-03-24 2010-03-04 Basf Se Detergent compositions
ATE395404T1 (de) 2004-01-20 2008-05-15 Ciba Holding Inc Triazinylaminostilbendisulfonsäuremischungen
BRPI0510089A (pt) * 2004-04-20 2007-10-16 Ciba Sc Holding Ag agentes de branqueamento anfótericos fluorescentes em formulações de detergente
JP5236289B2 (ja) * 2004-08-30 2013-07-17 チバ ホールディング インコーポレーテッド シェーディング方法
JP2009537680A (ja) * 2006-05-23 2009-10-29 チバ ホールディング インコーポレーテッド 紡織繊維材料用洗剤組成物
CN109158366B (zh) * 2014-01-26 2021-08-24 艺康美国股份有限公司 原位清洗工艺和原位清洗系统
PE20211337A1 (es) 2014-01-31 2021-07-26 Goldcorp Inc Proceso para la separacion y recuperacion de sulfuros de metales de una mena o concentrado de sulfuros mixtos
CN105001671A (zh) * 2015-06-29 2015-10-28 纳爱斯丽水日化有限公司 一种复合型增白剂及含所述增白剂的洗涤剂组合物
CN107857738A (zh) * 2017-11-28 2018-03-30 贺州学院 十六烷基氨基三嗪衍生物的合成与应用

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1107667B (de) * 1959-07-30 1961-05-31 Wolfen Filmfab Veb Verfahren zur Herstellung von optischen Aufhellungsmitteln
GB2026054A (en) * 1978-07-17 1980-01-30 Ciba Geigy Ag Concentrated aqueous solution of sulfo groupcontaining fluorescent brighteners which are stable on storage
GB2158454A (en) 1984-04-06 1985-11-13 Colgate Palmolive Co Liquid laundry detergent composition
EP0509787A2 (fr) 1991-04-17 1992-10-21 Unilever Plc Compositions détergentes concentrées en poudre
WO1995013354A1 (fr) * 1993-11-10 1995-05-18 The Procter & Gamble Company Compositions detersives inhibant le transfert de colorants
EP0682145A2 (fr) * 1994-05-12 1995-11-15 Ciba-Geigy Ag Traitement textile
WO1995030681A1 (fr) 1994-05-10 1995-11-16 Basf Aktiengesellschaft Complexes metalliferes a un ou a plusieurs noyaux et leur utilisation comme catalyseurs de blanchiment et d'oxydation
DE4443177A1 (de) 1994-12-05 1996-06-13 Henkel Kgaa Aktivatormischungen für anorganische Perverbindungen
EP0728749A2 (fr) * 1995-02-22 1996-08-28 Ciba-Geigy Ag Dérivés de triazine, leur préparation et leur application
EP0808837A1 (fr) * 1996-05-23 1997-11-26 Ciba SC Holding AG Composés stilbéniques comme azurants optiques, comme absorbants d'UV et leur utilisation dans l'augmentation du facteur de protection solaire de matériaux textiles
WO2001005925A1 (fr) 1999-07-14 2001-01-25 Ciba Specialty Chemicals Holding Inc. Complexes metalliques a ligands tripodaux
WO2001009276A1 (fr) 1999-07-28 2001-02-08 Ciba Specialty Chemicals Holding Inc. Complexes de manganese de type salen sous forme de granules hydrosolubles
US6242405B1 (en) 1995-12-29 2001-06-05 Novo Nordisk A/S Enzyme-containing particles and liquid detergent concentrate
WO2002002865A2 (fr) 2000-07-04 2002-01-10 Ciba Specialty Chemicals Holding Inc. Procede pour le traitement de materiaux en fibre textile ou du cuir
WO2002088289A2 (fr) 2001-04-30 2002-11-07 Ciba Specialty Chemicals Holding Inc. Utilisation de composes complexes metalliques en tant que catalyseurs d'oxydation

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS515308A (ja) * 1974-07-03 1976-01-17 Kao Corp Hakushokugoseisenzaisoseibutsu
EP0003568B1 (fr) * 1978-02-14 1982-06-02 Bayer Ag Préparation à base d'agents d'éclaircissement optique et son utilisation pour le blanchiment des compositions de couchage pour papier
JPS5817199A (ja) * 1981-07-23 1983-02-01 花王株式会社 洗浄剤組成物
US4460485A (en) * 1983-07-15 1984-07-17 Lever Brothers Company Polyester fabric conditioning and whitening composition
GB9409465D0 (en) * 1994-05-12 1994-06-29 Ciba Geigy Ag Protective use
JPH09241693A (ja) * 1996-03-05 1997-09-16 Lion Corp 高嵩密度粒状洗剤組成物の製造方法
ZA974226B (en) * 1996-05-17 1998-12-28 Procter & Gamble Detergent composition
GB2318360A (en) * 1996-10-15 1998-04-22 Ciba Geigy Ag Fluorescent whitening agent formulation
GB9626851D0 (en) * 1996-12-24 1997-02-12 Ciba Geigy Ag Compounds
US6294047B1 (en) * 1999-07-30 2001-09-25 Institute Of Paper Methods for reducing fluorescence in paper-containing samples
JP2001342495A (ja) * 2000-06-05 2001-12-14 Kao Corp 洗剤組成物
ES2271529T3 (es) * 2002-02-25 2007-04-16 Ciba Specialty Chemicals Holding Inc. Procedimiento para el tratamiento de materiales de fibra textil.

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1107667B (de) * 1959-07-30 1961-05-31 Wolfen Filmfab Veb Verfahren zur Herstellung von optischen Aufhellungsmitteln
GB2026054A (en) * 1978-07-17 1980-01-30 Ciba Geigy Ag Concentrated aqueous solution of sulfo groupcontaining fluorescent brighteners which are stable on storage
GB2158454A (en) 1984-04-06 1985-11-13 Colgate Palmolive Co Liquid laundry detergent composition
EP0509787A2 (fr) 1991-04-17 1992-10-21 Unilever Plc Compositions détergentes concentrées en poudre
WO1995013354A1 (fr) * 1993-11-10 1995-05-18 The Procter & Gamble Company Compositions detersives inhibant le transfert de colorants
WO1995030681A1 (fr) 1994-05-10 1995-11-16 Basf Aktiengesellschaft Complexes metalliferes a un ou a plusieurs noyaux et leur utilisation comme catalyseurs de blanchiment et d'oxydation
EP0682145A2 (fr) * 1994-05-12 1995-11-15 Ciba-Geigy Ag Traitement textile
DE4443177A1 (de) 1994-12-05 1996-06-13 Henkel Kgaa Aktivatormischungen für anorganische Perverbindungen
EP0728749A2 (fr) * 1995-02-22 1996-08-28 Ciba-Geigy Ag Dérivés de triazine, leur préparation et leur application
US6015504A (en) * 1995-02-22 2000-01-18 Ciba Specialty Chemicals Corporation Method for increasing the SPF rating of textile fibers by treatment with triazinyldiamino stilbene compounds
US6242405B1 (en) 1995-12-29 2001-06-05 Novo Nordisk A/S Enzyme-containing particles and liquid detergent concentrate
EP0808837A1 (fr) * 1996-05-23 1997-11-26 Ciba SC Holding AG Composés stilbéniques comme azurants optiques, comme absorbants d'UV et leur utilisation dans l'augmentation du facteur de protection solaire de matériaux textiles
WO2001005925A1 (fr) 1999-07-14 2001-01-25 Ciba Specialty Chemicals Holding Inc. Complexes metalliques a ligands tripodaux
WO2001009276A1 (fr) 1999-07-28 2001-02-08 Ciba Specialty Chemicals Holding Inc. Complexes de manganese de type salen sous forme de granules hydrosolubles
WO2002002865A2 (fr) 2000-07-04 2002-01-10 Ciba Specialty Chemicals Holding Inc. Procede pour le traitement de materiaux en fibre textile ou du cuir
WO2002088289A2 (fr) 2001-04-30 2002-11-07 Ciba Specialty Chemicals Holding Inc. Utilisation de composes complexes metalliques en tant que catalyseurs d'oxydation

Also Published As

Publication number Publication date
ES2556971T3 (es) 2016-01-21
BR0306187A (pt) 2004-10-19
DE60308485T2 (de) 2007-09-06
ES2271529T3 (es) 2007-04-16
WO2003070870A1 (fr) 2003-08-28
ZA200402942B (en) 2005-02-23
AU2003208870B2 (en) 2008-05-15
JP4567975B2 (ja) 2010-10-27
AR038582A1 (es) 2005-01-19
JP2005517801A (ja) 2005-06-16
TW200303358A (en) 2003-09-01
AR038583A1 (es) 2005-01-19
JP2005517800A (ja) 2005-06-16
EP1478724A1 (fr) 2004-11-24
DE60308661T2 (de) 2007-08-09
EP1715029B1 (fr) 2015-09-23
EP1715029A2 (fr) 2006-10-25
ATE340847T1 (de) 2006-10-15
AU2003205777B2 (en) 2008-01-31
BR0306184A (pt) 2004-10-19
EP1478724B1 (fr) 2006-09-20
ES2271534T3 (es) 2007-04-16
DE60308485D1 (de) 2006-11-02
BR0306184B1 (pt) 2013-08-27
TWI324177B (en) 2010-05-01
EP1485460A1 (fr) 2004-12-15
CN1596299A (zh) 2005-03-16
CN1294248C (zh) 2007-01-10
AU2003208870A1 (en) 2003-09-09
TW200303386A (en) 2003-09-01
DE60308661D1 (de) 2006-11-09
CN1294247C (zh) 2007-01-10
AR067835A2 (es) 2009-10-28
WO2003070869A1 (fr) 2003-08-28
AU2003205777A1 (en) 2003-09-09
ZA200402941B (en) 2005-02-23
EP1715029A3 (fr) 2009-04-01
TWI332045B (en) 2010-10-21
JP4567976B2 (ja) 2010-10-27
EP1485460B1 (fr) 2006-09-27
BRPI0306187B1 (pt) 2021-01-12
ATE340242T1 (de) 2006-10-15
CN1596300A (zh) 2005-03-16

Similar Documents

Publication Publication Date Title
EP1606380B1 (fr) Compositions détergentes
EP1715029B1 (fr) Procédé de traitement de materiaux fibreux textiles
EP1592675B1 (fr) Modification cristallines des triazinylaminostilbenes
EP2024480B1 (fr) Composition detergente pour des matieres textiles

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: 20060811

AC Divisional application: reference to earlier application

Ref document number: 1478724

Country of ref document: EP

Kind code of ref document: P

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PT SE SI SK TR

17Q First examination report despatched

Effective date: 20070612

AKX Designation fees paid

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PT SE SI SK TR

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

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: CIBA HOLDING INC.

18D Application deemed to be withdrawn

Effective date: 20071228