EP0548019B1 - Dispersion d'agent de blanchiment stable au stockage - Google Patents

Dispersion d'agent de blanchiment stable au stockage Download PDF

Info

Publication number
EP0548019B1
EP0548019B1 EP92810974A EP92810974A EP0548019B1 EP 0548019 B1 EP0548019 B1 EP 0548019B1 EP 92810974 A EP92810974 A EP 92810974A EP 92810974 A EP92810974 A EP 92810974A EP 0548019 B1 EP0548019 B1 EP 0548019B1
Authority
EP
European Patent Office
Prior art keywords
weight
shelf life
long shelf
life according
dispersion
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP92810974A
Other languages
German (de)
English (en)
Other versions
EP0548019A3 (en
EP0548019A2 (fr
Inventor
Claude Dr. 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 Geigy AG
Ciba Spezialitaetenchemie 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 Geigy AG, Ciba Spezialitaetenchemie Holding AG filed Critical Ciba Geigy AG
Publication of EP0548019A2 publication Critical patent/EP0548019A2/fr
Publication of EP0548019A3 publication Critical patent/EP0548019A3/de
Application granted granted Critical
Publication of EP0548019B1 publication Critical patent/EP0548019B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06LDRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
    • D06L4/00Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
    • 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
    • C11D3/3947Liquid compositions
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06LDRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
    • D06L4/00Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
    • D06L4/10Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
    • D06L4/15Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen using organic agents
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06LDRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
    • D06L4/00Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
    • D06L4/60Optical bleaching or brightening
    • D06L4/614Optical bleaching or brightening in aqueous solvents
    • D06L4/636Optical bleaching or brightening in aqueous solvents with disperse brighteners

Definitions

  • the invention relates to a storage-stable bleach dispersion, which in addition to at least a peracid, a peracid-forming system or its salts, one or more optical brighteners of the bis-benzofuranyl type contains, as well as the production and use of these Bleach dispersion for simultaneous bleaching and lightening of fabrics in the Household and in industry, at temperatures from + 10 ° C or higher.
  • the invention thus relates to an aqueous storage-stable bleaching agent dispersion containing 2 to 70% by weight, based on the total weight of the formulation, one or more peracids, peracid-forming systems or their salts, and 0.01 to 1% by weight of an optical brightener or a mixture of optical brighteners, characterized in that the optical brighteners are bis-benzofuranyl brighteners of the formula (1) are in which R 1 and R 2 are independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, halogen, benzyloxy or phenoxy, R 3 C 1 -C 4 alkyl, halogen or phenyl, M hydrogen or an equivalent of a non-chromophoric cation and n is 1 to 4; that hydrogen peroxide, diperoxyalkyl dicarboxylic acids, phthaloamino peracids or sulfonyl pers acids are used as peracids; and that as peracid-
  • C 1 -C 4 alkyl and C 1 -C 4 alkoxy are methyl, ethyl, butyl and tert-butyl as well as methoxy, ethoxy and butoxy.
  • sodium and potassium are preferred for the alkali metal ions.
  • R 1 is hydrogen, methyl or methoxy and R 3 is methyl, ethyl or phenyl, the optical brighteners of the formulas (3), (4) and (5) is of particular importance.
  • the optical brightener content is 0.01 to 1% by weight, preferably 0.05 to 0.25 % By weight, based on the total weight of the formulation.
  • optical brighteners of formulas (1) to (5) are known and can e.g. according to EP-A-395 588.
  • the peracids present in the bleach dispersions, peracid-generating systems or their salts are in an amount of 2 to 70 wt.% And preferably in an amount of 5 to 40% by weight, based on the total weight of the Formulation, added.
  • Hydrogen peroxide comes into question as inorganic peracids.
  • Hydrogen peroxide and diperoxyalkyldicarboxylic acids such as that are preferred Diperoxydodecanedicarboxylic acid, or a mixture thereof.
  • Tetraacetylethylenediarnin TAED
  • NOBS Nonoyloxybenzenesulfonate
  • i-NOBS iso-nonoyloxybenzenesulfonate
  • Sulfonate phenyl benzoates can be used.
  • a catalyst or one Catalyst mixture can be added.
  • Suitable catalysts are, for example, transition metal compounds such as copper, cobalt and manganese compounds. Examples include CuSO 4 , cobalt-amine complexes or manganese complexes with multidentate ligands.
  • Suitable sulfonates are, for example, water-soluble salts of alkylphenyl sulfonates, paraffin sulfonates, ⁇ -olefin sulfonates, fatty acid monoglycerol sulfonates, 2-acyloxy-alkane-1-sulfonates and ⁇ -alkyloxy-alkane sulfonates, as mentioned in GB-A-2 141 754.
  • Examples include sodium pentadecyl sulfonate or dioctyl sulfosuccinate, and especially the C 9 -C 15 alkylphenyl sulfonates.
  • nonionic surfactants are compounds which are characterized by the Condensation of ethylene oxide, propylene oxide or a mixture of both with one Hydrocarbon bearing an active hydrogen atom is formed.
  • alkyl or alkylene, mono- or polyglucosides are suitable. These preferably have alkyl or alkylene groups with 9 to 15 carbon atoms and 1-10 glucoside units. Examples include nonyldiglucoside and allyl (C 12 -C 15 ) poly (1-10) glucoside. Sorbitan esters such as polyoxyethylene sorbitan monopalmitate, fatty acid ethanolamides such as coconut fatty acid diethanolamide and fatty acid ethanolamine oxides such as tetradecylamine oxide can also be used.
  • Saturated and unsaturated carboxylic acids such as e.g. Oil, caprine, Lauric, myristic, coconut, palm kernel acid or salts thereof, e.g. the sodium, Potassium or ammonium salts are used, the coconut fatty acid derivatives are particularly preferred.
  • Examples of the group of phosphonates and polyphosphonates are e.g. Aminotrimethylphosphonic acid, Aminotriethylphosphonic acid, ethylenediaminetetramethylphosphonic acid and diethylenediaminetetramethylphosphonic acid and compounds such as they are described in US-A4 321 165.
  • additives such as further surfactants, Emulsifiers, thickeners, foam regulators, stabilizers, odor improvers, Sequestering agents, salts or dyes.
  • the bleach dispersion is produced by using the optical brightener (s) as a moist press cake or dry powder with one or more peracids or peracid-forming systems together with water and possibly other additives mixed and homogenized.
  • the bleach dispersion thus obtained is for months stable and does not sediment.
  • the optical brightener can be incorporated without visible sedimentation and its After neutralizing the oxidizing agent with hydrosulfite, the amount is determined spectroscopically to 100% of the amount used. The dispersion obtained is stable.
  • the bleach dispersions according to Examples 1 and 2 are at 14 days stored at a temperature of 20 ° C in the dark. When determining the Optical brightener content in both cases results in a content of 100% of the Baseline.
  • the optical brightener content is 85% after 3 days at 26 ° C Output quantity.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (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)
  • Detergent Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Claims (18)

  1. Dispersion d'agents de blanchiment stable au stockage contenant de 2 à 70 % en poids, rapporté au poids total de la formulation, d'un ou de plusieurs peroxyacides ou systèmes formateurs de peroxyacides ou leurs sels, ainsi que de 0,01 à 1 % en poids d'un azurant optique ou d'un mélange d'azurants optiques, caractérisée en ce que les azurants optiques sont des azurants de type bis-benzofuranyle de formule (1)
    Figure 00180001
    dans laquelle R1 et R2 représentent, indépendamment l'un de l'autre, un atome d'hydrogène, un groupe alkyle en C1-4, alcoxy en C1-4, halogéno, benzyloxy ou phénoxy, R3 représente un groupe alkyle en C1-4, un atome d'halogène ou un groupe phényle, M représente un proton ou un équivalent d'un cation non chromophore et n vaut de 1 à 4, en ce que l'on utilise comme peroxyacides, du peroxyde d'hydrogène, des acides diperoxyalcanedicarboxyliques, des acides peroxyaminophtaliques ou des acides peroxysulfoniques, et en ce que l'on utilise, comme systèmes formateurs de peroxyacides ou comme sels de ceux-ci, la tétraacétyléthylènediamine, des sels de type nonoyloxybenzènesulfonate, iso-nonoyloxybenzènesulfonate ou benzoate de phénylsulfonate.
  2. Dispersion d'agents de blanchiment stable au stockage selon la revendication 1, caractérisée en ce qu'elle contient un azurant optique de formule (2)
    Figure 00180002
    dans laquelle R1 représente un atome d'hydrogène, un groupe alkyle en C1-4, alcoxy en C1-4, halogéno, benzyloxy ou phénoxy et R3 représente un groupe alkyle en C1-4 halogéno ou phényle et M représente un atome d'hydrogène, un ion d'un métal alcalin ou un ion d'ammonium.
  3. Dispersion d'agents de blanchiment stable au stockage selon la revendication 2, caractérisée en ce qu'elle contient un azurant optique de formule (2)
    Figure 00190001
    dans laquelle R1 représente un atome d'hydrogène ou un groupe méthyle ou méthoxy, et R3 représente un groupe méthyle, éthyle ou phényle, et M représente un atome d'hydrogène ou un ion alcalin.
  4. Dispersion d'agents de blanchiment stable au stockage selon la revendication 3, caractérisée en ce qu'elle contient un azurant optique de formule (3)
    Figure 00190002
  5. Dispersion d'agents de blanchiment stable au stockage selon la revendication 3, caractérisée en ce qu'elle contient un azurant optique de formule (4)
    Figure 00190003
  6. Dispersion d'agents de blanchiment stable au stockage selon la revendication 3, caractérisée en ce qu'elle contient un azurant optique de formule (5)
    Figure 00190004
  7. Dispersion d'agents de blanchiment stable au stockage selon la revendication 1, caractérisée en ce que la teneur en azurant optique est de 0,05 à 0,25 % en poids rapporté au poids total de la formulation.
  8. Dispersion d'agents de blanchiment stable au stockage selon la revendication 1, caractérisée en ce que la teneur en peroxyacides, en systèmes formant des peroxyacides ou en sels de tels composés est de 5 à 40 % en poids rapporté au poids total de la composition.
  9. Dispersion d'agents de blanchiment stable au stockage selon la revendication 1, caractérisée en ce que l'on utilise comme peroxyacides du peroxyde d'hydrogène, de l'acide diperoxydodécanedicarboxylique ou un mélange de ces deux acides.
  10. Dispersion d'agents de blanchiment stable au stockage selon la revendication 1, caractérisée en ce qu'elle contient de 0,01 à 5 % en poids, rapporté au poids total de la formulation, d'un catalyseur ou d'un mélange de catalyseurs.
  11. Dispersion d'agents de blanchiment stable au stockage selon la revendication 10, caractérisée en ce qu'elle contient de 0,05 à 2 % en poids, rapporté au poids total de la formulation, d'un catalyseur ou d'un mélange de catalyseurs.
  12. Dispersion d'agents de blanchiment stable au stockage selon la revendication 10, caractérisée en ce que le catalyseur est un catalyseur qui fait partie du groupe des métaux de transition.
  13. Dispersion d'agents de blanchiment stable au stockage selon la revendication 12, caractérisée en ce que le catalyseur est un composé de cuivre, de cobalt ou de manganèse.
  14. Dispersion d'agents de blanchiment stable au stockage selon la revendication 13, caractérisée en ce qu'elle contient
    a) de 0 à 10 % en poids d'un ou de plusieurs sulfonates,
    b) de 0 à 10 % en poids d'un ou de plusieurs agents tensioactifs non ioniques,
    c) de 0 à 5 % en poids d'un ou de plusieurs acides gras, et
    d) de 0 à 1 % en poids d'un ou de plusieurs phosphonates toutes ces quantités étant rapportées au poids total de la formulation.
  15. Dispersion d'agents de blanchiment stable au stockage selon la revendication 1, caractérisée en ce qu'elle contient
    a) de 5 à 10 % en poids de peroxyde d'hydrogène,
    b) de 3 à 7 % en poids d'acide diperoxydodécanedicarboxylique,
    c) de 0,05 à 0,25 % en poids d'un azurant optique de formule (3), (4) ou (5)
    Figure 00210001
    Figure 00210002
    Figure 00210003
    d) de 0 à 7 % en poids d'un alkylsulfonate secondaire,
    e) de 1 à 8 % d'un alcool éthoxylé non ionogène,
    f) de 0 à 3 % en poids d'un dérivé d'acide gras de coco,
    g) de 0 à 0,5 % en poids d'un phosphonate,
    toutes ces quantités étant rapportées au poids total de la formulation.
  16. Dispersion d'agents de blanchiment stable au stockage selon la revendication 1, caractérisée en ce qu'elle contient d'autres additifs tels que des agents tensioactifs, des agents émulsionnants, des épaississants, des agents régulateurs de mousse, des stabilisants, des agents améliorant l'odeur, des agents séquestrants, des sels ou des colorants.
  17. Procédé de préparation de la dispersion d'agents de blanchiment conforme à la revendication 1, caractérisé en ce que l'on mélange le ou les azurant(s) optique(s) sous forme de gâteau de filtration ou sous forme de poudre sèche avec un ou plusieurs peroxyacides ou avec les systèmes formateurs de peroxyacides, avec de l'eau et, éventuellement, avec d'autres additifs, et en ce que l'on homogénéise ce mélange.
  18. Utilisation de la dispersion d'agents de blanchiment conforme à la revendication 1 pour le blanchiment de matières textiles à des températures supérieures ou égales à 10 °C.
EP92810974A 1991-12-19 1992-12-10 Dispersion d'agent de blanchiment stable au stockage Expired - Lifetime EP0548019B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH377791 1991-12-19
CH3777/91 1991-12-19

Publications (3)

Publication Number Publication Date
EP0548019A2 EP0548019A2 (fr) 1993-06-23
EP0548019A3 EP0548019A3 (en) 1995-06-14
EP0548019B1 true EP0548019B1 (fr) 1998-06-24

Family

ID=4263268

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92810974A Expired - Lifetime EP0548019B1 (fr) 1991-12-19 1992-12-10 Dispersion d'agent de blanchiment stable au stockage

Country Status (12)

Country Link
US (1) US5449477A (fr)
EP (1) EP0548019B1 (fr)
JP (1) JPH05271691A (fr)
KR (1) KR930013349A (fr)
AT (1) ATE167699T1 (fr)
AU (1) AU660747B2 (fr)
BR (1) BR9205072A (fr)
DE (1) DE59209385D1 (fr)
ES (1) ES2118804T3 (fr)
MX (1) MX9207050A (fr)
NZ (1) NZ245506A (fr)
ZA (1) ZA929832B (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH684485A5 (de) * 1992-11-17 1994-09-30 Ciba Geigy Ag Flüssigwaschmittel.
GB9224052D0 (en) * 1992-11-17 1993-01-06 Unilever Plc Non aqueous liquid detergent compositions
US5968881A (en) * 1995-02-02 1999-10-19 The Procter & Gamble Company Phosphate built automatic dishwashing compositions comprising catalysts
TR199701626T1 (xx) * 1995-06-16 1998-04-21 The Procter & Gamble Company Kobalt kataliz�r i�eren a�art�c� bile�imler.
EP0832176B1 (fr) * 1995-06-16 2001-07-11 The Procter & Gamble Company Compositions detergentes pour lave-vaisselle automatiques, contenant des catalyseurs au cobalt
US5703034A (en) * 1995-10-30 1997-12-30 The Procter & Gamble Company Bleach catalyst particles
GB9611063D0 (en) * 1996-05-28 1996-07-31 Warwick Int Group Concentrated alkaline isotropic detergent liquid with bleach
DE19700799C2 (de) * 1997-01-13 1999-02-04 Henkel Kgaa Wäßrige Textilbleichmittel
US6584988B1 (en) * 1998-10-30 2003-07-01 Cognis Corp. Process for removing contaminants from water
TWI400330B (zh) 2005-12-28 2013-07-01 Kao Corp Liquid detergent
JP5197949B2 (ja) * 2006-12-21 2013-05-15 ライオン株式会社 漂白剤物品
JP5342757B2 (ja) * 2007-07-26 2013-11-13 ライオン株式会社 液体漂白剤組成物

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0293040A1 (fr) * 1987-05-27 1988-11-30 The Procter & Gamble Company Composition détergente liquide contenant un agent de blanchiment peroxydant

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1286459A (en) * 1968-12-12 1972-08-23 Unilever Ltd Detergent compositions
US4002423A (en) * 1971-08-13 1977-01-11 Hoechst Aktiengesellschaft Benzofuran derivatives process for their preparation and their use as optical brighteners
BE787576A (fr) * 1971-08-13 1973-02-14 Hoechst Ag Derives de benzofuranne et leur utilisation comme azureurs optiques
US3994879A (en) * 1972-12-18 1976-11-30 Hoechst Aktiengesellschaft Process for the preparation of benzofuran compounds
US4028263A (en) * 1973-08-24 1977-06-07 Colgate-Palmolive Company Bleaching and brightening detergent composition
NL7815014A (nl) * 1977-06-29 1979-10-31 Procter & Gamble Vloeibaar wasmiddel ter betere verwijdering van vet vuil.
GB8316760D0 (en) * 1983-06-20 1983-07-20 Unilever Plc Detergent bleach compositions
GB2141755B (en) * 1983-06-20 1987-01-07 Unilever Plc Detergent bleach compositions
GB8332682D0 (en) * 1983-12-07 1984-01-11 Procter & Gamble Laundry additive products
US4659519A (en) * 1984-07-02 1987-04-21 The Clorox Company Process for synthesizing alkyl monoperoxysuccinic acid bleaching compositions
GB8603961D0 (en) * 1986-02-18 1986-03-26 Interox Chemicals Ltd Concentrated liquid composition
US4735740A (en) * 1986-10-03 1988-04-05 The Clorox Company Diperoxyacid precursors and method
US5004558A (en) * 1986-11-03 1991-04-02 Monsanto Company Sulfone peroxycarboxylic acids
US4778618A (en) * 1986-11-06 1988-10-18 The Clorox Company Glycolate ester peracid precursors
DE3868462D1 (de) * 1987-08-26 1992-03-26 Ciba Geigy Ag Dispersionsaufheller-praeparate.
US5230820A (en) * 1987-11-23 1993-07-27 Ciba-Geigy Corporation Storage-stable bleaching detergents containing bis-benzofuranyl fluoescent whitening agents
DE3852379D1 (de) * 1987-11-26 1995-01-19 Ciba Geigy Ag Stabile, optische Aufheller enthaltende Waschmittel.
EP0321715B1 (fr) * 1987-12-23 1994-06-15 Ciba-Geigy Ag Détergents stables contenant des azurants optiques
IT1233846B (it) * 1988-01-20 1992-04-21 Ausimont Spa Perossiacidi immido aromatici
EP0333248A3 (fr) * 1988-03-17 1990-08-29 Unilever N.V. Précurseurs de blanchiment et leur utilisation dans des compositions de blonchiment et/ou de détergents
US4822510A (en) * 1988-03-25 1989-04-18 Lever Brothers Company Stably suspended 4,4'-sulfonylbisperoxybenzoic acid bleach in an aqueous liquid
US5030244A (en) * 1988-06-08 1991-07-09 Ciba-Geigy Corporation Preparation of granules of dyes, optical whiteners or photoactivators from an aqueous suspension of naphthalene sulfonic acid-formaldehyde condensate dispersant
JPH0259406A (ja) * 1988-08-25 1990-02-28 Sankyo Kasei Kk 無水硫化ナトリウム結晶の製造法
GB8824108D0 (en) * 1988-10-14 1988-11-23 Unilever Plc Bleaching & detergent compositions
US5279772A (en) * 1989-04-28 1994-01-18 Ciba-Geigy Corporation Liquid detergents containing specifically disulfonated dibenzofuranyl-biphenyls as flourescent whitening agents
US5326491A (en) * 1989-04-28 1994-07-05 Ciba-Geigy Corporation Detergents containing certain sulfonated dibenzofuranylbiphenyls
DE59010228D1 (de) * 1989-04-28 1996-05-02 Ciba Geigy Ag Flüssigwaschmittel
ES2055399T3 (es) * 1989-04-28 1994-08-16 Ciba Geigy Ag Dibenzofuranilbifenilos.
US5078907A (en) * 1989-11-01 1992-01-07 Lever Brothers Company, Division Of Conopco, Inc. Unsymmetrical dicarboxylic esters as bleach precursors
US5055218A (en) * 1990-04-13 1991-10-08 The Procter & Gamble Company Bleach granules containing an amidoperoxyacid

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0293040A1 (fr) * 1987-05-27 1988-11-30 The Procter & Gamble Company Composition détergente liquide contenant un agent de blanchiment peroxydant

Also Published As

Publication number Publication date
ATE167699T1 (de) 1998-07-15
EP0548019A3 (en) 1995-06-14
BR9205072A (pt) 1993-06-22
US5449477A (en) 1995-09-12
MX9207050A (es) 1993-06-01
AU3028392A (en) 1993-06-24
KR930013349A (ko) 1993-07-21
DE59209385D1 (de) 1998-07-30
ZA929832B (en) 1993-06-21
ES2118804T3 (es) 1998-10-01
AU660747B2 (en) 1995-07-06
NZ245506A (en) 1994-12-22
JPH05271691A (ja) 1993-10-19
EP0548019A2 (fr) 1993-06-23

Similar Documents

Publication Publication Date Title
DE69434227T3 (de) Durchsichtige, isotrope, wässrige Bleichmittelzusammensetzung
DE68922237T2 (de) Wässrige Bleichmittelzusammensetzung.
DE4493996B4 (de) Neue Sulfonate, Verfahren zu deren Herstellung und deren Verwendung in einer Bleichmittelzusammensetzung
EP0548019A2 (fr) Dispersion d'agent de blanchiment stable au stockage
DE2422691A1 (de) Stabile bleichmittel
EP0210952A1 (fr) Composition aqueuse, alcaline contenant des silicates pour le blanchiment de matières fibreuses cellulosiques en présence de composés "per"
EP0024340A1 (fr) Procédé de lavage
EP0011166B1 (fr) Détergent de lavage concentré, liquide et stable au froid et son utilisation
DE2365172A1 (de) Bleichmittel fuer wasch- und reinigungsmittel
CH642677A5 (de) Bleich- und reinigungsmittel.
EP0172534A2 (fr) Agent de nettoyage liquide
CH650764A5 (de) Alkyl-polyoxyalkylen-carboxylate.
EP0601967B1 (fr) Composition détergente liquide
EP0210132B1 (fr) Composition aqueuse alcaline contenant des silicates pour le blanchiment de matières fibreuses cellulosiques en présence de composés "per"
EP0011715B1 (fr) Détergent de lavage à deux composants, liquide et stable au froid et procédé de lavage
EP0112801B1 (fr) Complexes de magnésium d'acides phosphoniques oligomères, leur procédé de préparation et leur utilisation comme stabilisants dans des bains de blanchiment contenant des péroxydes alcalins
EP0409846A1 (fr) Activateurs de percomposes anorganiques
DE2539349C2 (de) Wäschenachbehandlungsmittel
DE69025728T2 (de) Verfahren zum Erhöhen des Bleicheffektes beim Waschen und Verwendung bestimmter amphoterer Verbindungen in einer Waschmittelzusammensetzung zum Erhöhen des Bleicheffektes
DE1289815B (de) Stabile waessrige Bleichmittelloesung
US2119523A (en) Pyrophosphate ester bleaching agent
DE4015859A1 (de) Aktivatoren fuer anorganische perverbindungen
EP0116887A2 (fr) Composés cyanamides organiques comme activeurs pour composés péroxidés
DE60133821T2 (de) Verfahren zum optischen aufhellen von baumwolle
DE1094696B (de) Verfahren zum optischen Aufhellen von Materialien aus Polyestern

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

AK Designated contracting states

Kind code of ref document: A2

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

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

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

17P Request for examination filed

Effective date: 19951110

17Q First examination report despatched

Effective date: 19960924

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

Owner name: CIBA SC HOLDING AG

RAP3 Party data changed (applicant data changed or rights of an application transferred)

Owner name: CIBA SPECIALTY CHEMICALS HOLDING INC.

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

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

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

Ref country code: GR

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

Effective date: 19980624

REF Corresponds to:

Ref document number: 167699

Country of ref document: AT

Date of ref document: 19980715

Kind code of ref document: T

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

ET Fr: translation filed
REF Corresponds to:

Ref document number: 59209385

Country of ref document: DE

Date of ref document: 19980730

GBT Gb: translation of ep patent filed (gb section 77(6)(a)/1977)

Effective date: 19980713

ITF It: translation for a ep patent filed
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19980924

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19980924

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2118804

Country of ref document: ES

Kind code of ref document: T3

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

Ref country code: LU

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

Effective date: 19981210

Ref country code: GB

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

Effective date: 19981210

Ref country code: AT

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

Effective date: 19981210

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

Ref country code: LI

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

Effective date: 19981231

Ref country code: CH

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

Effective date: 19981231

Ref country code: BE

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

Effective date: 19981231

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

26N No opposition filed
BERE Be: lapsed

Owner name: CIBA SPECIALTY CHEMICALS HOLDING INC.

Effective date: 19981231

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

Ref country code: NL

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

Effective date: 19990701

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19981210

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

Ref country code: FR

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

Effective date: 19990831

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 19990701

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

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

Ref country code: DE

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

Effective date: 19991001

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

Ref country code: ES

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

Effective date: 19991211

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20000114

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

Ref country code: IT

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

Effective date: 20051210