EP0869168A2 - Composition pour rendre les textiles hydrophiles - Google Patents

Composition pour rendre les textiles hydrophiles Download PDF

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Publication number
EP0869168A2
EP0869168A2 EP98105575A EP98105575A EP0869168A2 EP 0869168 A2 EP0869168 A2 EP 0869168A2 EP 98105575 A EP98105575 A EP 98105575A EP 98105575 A EP98105575 A EP 98105575A EP 0869168 A2 EP0869168 A2 EP 0869168A2
Authority
EP
European Patent Office
Prior art keywords
alkyl
carbon atoms
contain
alcohol
numbers
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Withdrawn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
EP98105575A
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German (de)
English (en)
Other versions
EP0869168A3 (fr
Inventor
Rafael Dr. Pi Subirana
Teresa Copete
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 Personal Care and Nutrition GmbH
Original Assignee
Henkel AG and Co KGaA
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP0869168A2 publication Critical patent/EP0869168A2/fr
Publication of EP0869168A3 publication Critical patent/EP0869168A3/fr
Withdrawn legal-status Critical Current

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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
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C11D3/3734Cyclic silicones
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/835Mixtures of non-ionic with cationic 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
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • 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
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C11D3/3742Nitrogen containing silicones
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/165Ethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/165Ethers
    • D06M13/17Polyoxyalkyleneglycol ethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • D06M13/463Compounds containing quaternary nitrogen atoms derived from monoamines
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/53Polyethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/662Carbohydrates or derivatives
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • finishing agents with improved rewettability which are a mixture of ester quats and silicone compounds, optionally in combination with other nonionic surfactants contain as well as the use of these mixtures for the production of finishing agents.
  • Textiles are usually treated with cationic surfactants to give them a pleasant soft feel. Less well known is that cationic surfactants also have an impact on the rewettability of textiles.
  • cationic surfactants also have an impact on the rewettability of textiles.
  • dish towels treated with an anti-aging agent are very soft, but may not absorb water, which makes them completely unsuitable for use.
  • the reason for this is usually the use of fabric softener with good softening properties, but which also make the textiles water-repellent, i.e. hydrophobic. As already explained, however, this effect is far from desirable for certain applications.
  • German patent DE-C1 4243550 Heenkel
  • finishing agents based on esterquats and polyolefin waxes which may also contain silicone compounds as further additives.
  • the object of the present invention was to provide new finishing agents To provide the textiles not only a pleasant soft feel and the electrostatic Reduce charge between the fibers, but especially the tissues good rewettability, i.e. Impart hydrophilicity so that after washing in are able to absorb water easily.
  • Esterquats are generally understood to be quaternized fatty acid triethanolamine ester salts . These are known substances which can be obtained by the relevant methods of preparative organic chemistry.
  • WO 91/01295 Hexkel
  • Triethanolamine in the presence of hypophosphorous acid is partially esterified with fatty acids, air is passed through and then quaternized with dimethyl sulfate or ethylene oxide
  • German patent step DE 4308794 C1 (Henkel)
  • a process for the production of solid ester quats is also known, in which the quaternization of triethanolamine esters in the presence of suitable dispersants, preferably fatty alcohols, and reviews on this topic are given, for example, by R.Puchta et al.
  • the quaternized fatty acid triethanolamine ester salts follow the formula (I) in which R 1 CO stands for an acyl radical with 6 to 22 carbon atoms, R 2 and R 3 independently of one another for hydrogen or R 1 CO, R 4 for an alkyl radical with 1 to 4 carbon atoms or a (CH 2 CH 2 O) q H- Group, m, n and p in total stands for 0 or numbers from 1 to 12, q for numbers from 1 to 12 and X for halide, alkyl sulfate or alkyl phosphate.
  • R 1 CO stands for an acyl radical with 6 to 22 carbon atoms
  • R 2 and R 3 independently of one another for hydrogen or R 1 CO
  • R 4 for an alkyl radical with 1 to 4 carbon atoms or a (CH 2 CH 2 O) q H- Group
  • m, n and p in total stands for 0 or numbers from 1 to 12
  • X for halide, alky
  • ester quats which can be used in the context of the invention are products based on caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, isostearic acid, stearic acid, oleic acid, elaidic acid, arachic acid, behenic acid and erucic acid and their technical mixtures, such as they occur, for example, in the pressure splitting of natural fats and oils.
  • Technical C 12/18 coconut fatty acids and in particular partially hardened C 16/18 tallow or palm fatty acids as well as high elaidic acid C 16/18 fatty acid cuts are preferably used.
  • the fatty acids and the triethanolamine can be used in a molar ratio of 1.1: 1 to 3: 1 to produce the quaternized esters.
  • an application ratio of 1.2: 1 to 2.2: 1, preferably 1.5: 1 to 1.9: 1 has proven to be particularly advantageous.
  • the preferred esterquats are technical mixtures of mono-, di- and triesters with an average degree of esterification of 1.5 to 1.9 and are derived from technical C 16/18 - tallow or palm fatty acid (iodine number 0 to 40).
  • quaternized fatty acid triethanolamine ester salts of the formula (I) have proven to be particularly advantageous in which R 1 CO for an acyl radical having 16 to 18 carbon atoms, R 2 for R 1 CO, R 3 for hydrogen, R 4 for a methyl group, m , n and p is 0 and X is methyl sulfate.
  • quaternized ester salts of fatty acids with diethanolalkylamines of the formula (II) are also suitable as esterquats, in which R 1 CO for an acyl radical with 6 to 22 carbon atoms, R 2 for hydrogen or R 1 CO, R 4 and R 5 independently of one another for alkyl radicals with 1 to 4 carbon atoms, m and n in total for 0 or numbers from 1 to 12 and X represents halide, alkyl sulfate or alkyl phosphate.
  • ester quats in which R 1 CO for an acyl radical with 6 to 22 carbon atoms, R 2 for hydrogen or R 1 CO, R 4 , R 6 and R 7 independently of one another for alkyl radicals with 1 to 4 carbon atoms, m and n in total for 0 or numbers from 1 to 12 and X represents halide, alkyl sulfate or alkyl phosphate.
  • esterquats of the formulas (II) and (III) .
  • the esterquats usually come on the market in the form of 50 to 90% strength by weight alcoholic solutions, which can be diluted with water if required.
  • Suitable silicone compounds are, for example, silicone oils of the dimethylpolysiloxane type, Methylphenylpolysiloxanes, cyclic silicones as well as amino, fatty acid, alcohol, polyether, epoxy, fluorine and / or alkyl modified silicone compounds that are both liquid at room temperature can be resinous.
  • the hydrophilicity of the finishing agents according to the invention can be further improved by adding further anionic, cationic, amphoteric, zwitterionic, but preferably nonionic, surfactants.
  • suitable nonionic surfactants are fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, fatty acid polyglycol esters, fatty acid amide polyglycol ethers, fatty amine polyglycol ethers, alkoxylated triglycerides, mixed ethers or mixed formals, alk (en) yl oligoglycosides, fatty acid-N-alkyl glucosate ester, especially vegetable hydrolysis fatty acid, vegetable oil polyglycol ester, sugar-based polyglycol ester, vegetable oil-based polyglycol ester, Sorbitan esters, polysorbates and amine oxides.
  • nonionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution.
  • the agents according to the invention preferably contain fatty alcohol polyglycol ethers of the formula (IV), in which R 8 is a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms and n is a number from 1 to 50.
  • Typical examples of this are addition products of 1 to 50, preferably 5 to 30 and in particular 10 to 15 moles of ethylene oxide onto primary alcohols having 6 to 22, preferably 12 to 18 carbon atoms, such as the ethoxylates of capron alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, Isododecyl alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, linolyl alcohol, linolenyl alcohol, deryl alcohol alcohol, methylene alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, blends, aryl alcohol alcohol, benzyl alcohol, benzyl alcohol, B based on fats and oils or aldehydes from Roelen's
  • the agents according to the invention are characterized in that they contain both preliminary products such as yarns, Fabrics and other textile fabrics as well as the end products made from them, i.e. the textiles, a pleasant soft feel, easy rewettability, i.e. Hydrophilicity lend and at the same time reduce the electrostatic charge, which leads to improved wrinkle resistance and ironability leads.
  • Another object of the invention therefore relates to the use of mixtures containing esterquats and silicone compounds for the production of hydrophilic Finishing agents that are free of polyolefin waxes and that are particularly suitable for aftertreatment of towels and underwear.
  • Soft grip and rewettability Composition / performance 1 2nd 3rd 4th V1 V2 V3 V4 Ditallow fatty acid triethanolamine ester, methyl quaternized, methyl sulfate salt 95 - 90 80 95 - - - Ditallow fatty acid methyl diethanolamine ester, methyl quaternized, methyl sulfate salt - 90 - - - 95 - - Dimethyldisteaylammonium chloride - - - - - - 95 90 modified dimethylpolysiloxane 5 7 5 12th - - 5 4th Isododecanol + 6EO - 3rd 5 - 5 - - 6
  • Coconut alkyl polyglucoside - - - 8th - 5 - - Soft grip 1.0 1.0 1.0 1.5 2.0 2.0 3.0 2.5 Rewettability [mm] 11 12th 12th 15 10th 9 8th 8th 8th

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Textile Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
EP98105575A 1997-04-05 1998-03-27 Composition pour rendre les textiles hydrophiles Withdrawn EP0869168A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19714044 1997-04-05
DE1997114044 DE19714044C1 (de) 1997-04-05 1997-04-05 Hydrophile Avivagemittel sowie Verwendung von Mischungen, enthaltend Esterquats und Siliconverbindungen zur Herstellung derselben

Publications (2)

Publication Number Publication Date
EP0869168A2 true EP0869168A2 (fr) 1998-10-07
EP0869168A3 EP0869168A3 (fr) 1999-01-20

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EP98105575A Withdrawn EP0869168A3 (fr) 1997-04-05 1998-03-27 Composition pour rendre les textiles hydrophiles

Country Status (2)

Country Link
EP (1) EP0869168A3 (fr)
DE (1) DE19714044C1 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001036575A1 (fr) * 1999-11-15 2001-05-25 The Procter & Gamble Company Traitement renforçateur de tissus
US6358913B1 (en) 1997-05-01 2002-03-19 Ciba Specialty Chemicals Corporation Use of selected polydiorganosiloxanes in fabric softener compositions
DE102010063696A1 (de) 2010-12-21 2012-06-21 Wacker Chemie Ag Zusammensetzungen enthaltend Quatverbindungen und Organopolysiloxane
WO2016102470A1 (fr) * 2014-12-22 2016-06-30 Schill + Seilacher Gmbh Composition d'apprêt destinée à conférer des propriétés hydrophiles permanentes à des fibres textiles et des produits textiles

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102019219905A1 (de) 2019-12-17 2021-06-17 Henkel Ag & Co. Kgaa Textilbehandlungsmittel
DE102020202017A1 (de) 2020-02-18 2021-08-19 Henkel Ag & Co. Kgaa Textilbehandlungsmittel

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0075770A2 (fr) * 1981-09-25 1983-04-06 Bayer Ag Composition de traitement pour textile et son utilisation pour le finissage de matériaux textiles
EP0442098A2 (fr) * 1990-02-16 1991-08-21 Wacker-Chemie Gmbh Procédé de préparation d'emulsions d'organopolysiloxanes à particules fines
EP0503221A1 (fr) * 1991-03-08 1992-09-16 The Procter & Gamble Company Compositions concentrées d'adoucissants textiles
WO1992015745A1 (fr) * 1991-03-08 1992-09-17 The Procter & Gamble Company Assouplisseurs textiles concentres
US5258129A (en) * 1987-12-02 1993-11-02 Takemoto Yushi Kabushiki Kaisha Fluid-permeable agent for non-woven sheets of polyolefin fibers and method of application thereof
DE4243550C1 (de) * 1992-12-22 1994-06-01 Henkel Kgaa Faserhilfsmittel und deren Verwendung
WO1994016677A1 (fr) * 1993-01-23 1994-08-04 Henkel Kommanditgesellschaft Auf Aktien Melanges detergents possedant de meilleures proprietes d'avivage
WO1995019465A1 (fr) * 1994-01-14 1995-07-20 Danaklon A/S Fibres de polyolefines hydrophobes, cardables, contenant des apprets de filage cationiques

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0075770A2 (fr) * 1981-09-25 1983-04-06 Bayer Ag Composition de traitement pour textile et son utilisation pour le finissage de matériaux textiles
US5258129A (en) * 1987-12-02 1993-11-02 Takemoto Yushi Kabushiki Kaisha Fluid-permeable agent for non-woven sheets of polyolefin fibers and method of application thereof
EP0442098A2 (fr) * 1990-02-16 1991-08-21 Wacker-Chemie Gmbh Procédé de préparation d'emulsions d'organopolysiloxanes à particules fines
EP0503221A1 (fr) * 1991-03-08 1992-09-16 The Procter & Gamble Company Compositions concentrées d'adoucissants textiles
WO1992015745A1 (fr) * 1991-03-08 1992-09-17 The Procter & Gamble Company Assouplisseurs textiles concentres
DE4243550C1 (de) * 1992-12-22 1994-06-01 Henkel Kgaa Faserhilfsmittel und deren Verwendung
WO1994016677A1 (fr) * 1993-01-23 1994-08-04 Henkel Kommanditgesellschaft Auf Aktien Melanges detergents possedant de meilleures proprietes d'avivage
WO1995019465A1 (fr) * 1994-01-14 1995-07-20 Danaklon A/S Fibres de polyolefines hydrophobes, cardables, contenant des apprets de filage cationiques

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6358913B1 (en) 1997-05-01 2002-03-19 Ciba Specialty Chemicals Corporation Use of selected polydiorganosiloxanes in fabric softener compositions
WO2001036575A1 (fr) * 1999-11-15 2001-05-25 The Procter & Gamble Company Traitement renforçateur de tissus
DE102010063696A1 (de) 2010-12-21 2012-06-21 Wacker Chemie Ag Zusammensetzungen enthaltend Quatverbindungen und Organopolysiloxane
WO2012084830A1 (fr) 2010-12-21 2012-06-28 Wacker Chemie Ag Compositions contenant des composés quaternaires et des organosiloxanes
US8722612B2 (en) 2010-12-21 2014-05-13 Wacker Chemie Ag Compositions comprising quat compounds and organopolysiloxanes
WO2016102470A1 (fr) * 2014-12-22 2016-06-30 Schill + Seilacher Gmbh Composition d'apprêt destinée à conférer des propriétés hydrophiles permanentes à des fibres textiles et des produits textiles
CN107109774A (zh) * 2014-12-22 2017-08-29 希尔和塞拉彻有限公司 用于永久亲水性整理纺织纤维和纺织制品的组合物
US10233589B2 (en) 2014-12-22 2019-03-19 Schill + Seilacher Gmbh Composition for the permanent hydrophilic finishing of textile fibers and textile products
CN107109774B (zh) * 2014-12-22 2020-05-19 希尔和塞拉彻有限公司 用于永久亲水性整理纺织纤维和纺织制品的组合物

Also Published As

Publication number Publication date
EP0869168A3 (fr) 1999-01-20
DE19714044C1 (de) 1998-04-16

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