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US20050257325A1 - Aqueous dispersions for hydrophobically finishing fibres and flat textile materials - Google Patents

Aqueous dispersions for hydrophobically finishing fibres and flat textile materials Download PDF

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Publication number
US20050257325A1
US20050257325A1 US10/527,244 US52724405A US2005257325A1 US 20050257325 A1 US20050257325 A1 US 20050257325A1 US 52724405 A US52724405 A US 52724405A US 2005257325 A1 US2005257325 A1 US 2005257325A1
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Prior art keywords
weight
aqueous dispersion
formula
copolymers
monomers
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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.)
Abandoned
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US10/527,244
Inventor
Ludwig Schieferstein
Ludwig Bonniger
Joachim Conradi
Manfred Gorzinski
Bernd Wahle
Tunte Clemens
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Cognis IP Management GmbH
Original Assignee
Cognis Deutschland GmbH and Co KG
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Assigned to COGNIS DEUTSCHLAND GMBH & CO. KG reassignment COGNIS DEUTSCHLAND GMBH & CO. KG ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SCHIEFERSTEIN, LUDWIG, GORZINSKI, MANFRED, TUENTE, CLEMENS, WAHLE, BERND, BOENNIGER, LUDWIG, CONRADI, JOACHIM
Publication of US20050257325A1 publication Critical patent/US20050257325A1/en
Assigned to COGNIS IP MANAGEMENT GMBH reassignment COGNIS IP MANAGEMENT GMBH PATENT AND TRADEMARK TRANSFER AGREEMENT Assignors: COGNIS DEUTSCHLAND GMBH & CO. KG
Abandoned legal-status Critical Current

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Classifications

    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04—Homopolymers or copolymers of esters
    • C08L33/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur, or oxygen atoms in addition to the carboxy oxygen
    • C08L33/16—Homopolymers or copolymers of esters containing halogen atoms
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04—Homopolymers or copolymers of esters
    • C09D133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
    • C09D133/16—Homopolymers or copolymers of esters containing halogen atoms
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D06M15/277—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04—Homopolymers or copolymers of esters
    • C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/10—Repellency against liquids
    • D06M2200/12—Hydrophobic properties

Definitions

  • This invention relates to aqueous dispersions containing fluorinated and non-fluorinated poly(meth)acrylates and to the use of such dispersions for the hydrophobic finishing of fibers and flat textiles.
  • Perfluoroacrylates provide textile materials with both strongly hydrophobic and strongly oleophobic properties. Perfluoroacrylates such as these are described, for example, in DE 1 247 659.
  • EP 1 146 103 A1 also describes aqueous dispersions containing polyfluorinated polymers which are used for finishing textiles.
  • the present invention relates to aqueous dispersions containing at least:
  • Both the compounds of formula (I) and (Ia) and the compounds of formula (II) are known per se. They are derivatives, more particularly esters, of acrylic acid or methacrylic acid.
  • the perfluorinated compounds corresponding to formula (II) are generally prepared from tetrafluoroethane which is polymerized and iodized and converted into a perfluorinated alcohol in a Grignard reaction with ethylene oxide. In a final reaction step, the perfluorinated alcohol is reacted with acrylic acid or methacrylic acid to form the required perfluorinated acrylates or methacrylate esters.
  • the index n is a number of 6 to 10.
  • the compounds of formula (I) are also known esters of acrylic or methacrylic acid with fatty alcohols, the fatty alcohols having to contain 8 to 22 carbon atoms.
  • the monomers of formulae (I) and (II) independently of one another are reacted with the acrylates or methacrylates of formula (Ia), generally by emulsion polymerization in aqueous medium, to form copolymers using emulsifiers c), after which the two components a) and b), which already contain the emulsifiers from the production process, are mixed to form the dispersions according to the invention.
  • the emulsion polymerization is a special polymerization process in which water-insoluble monomers are emulsified in water with the aid of emulsifiers and polymerized using water-soluble initiators (for example potassium persulfate; redox initiators).
  • water-soluble initiators for example potassium persulfate; redox initiators.
  • Particularly preferred monomers of formula (Ia) are selected from the group consisting of methyl, ethyl, n-propyl, i-propyl and/or butyl esters of acrylic or methacrylic acid.
  • the compounds of formula (Ia) independently of one another may be used for the preparation of polymer dispersions a) and b).
  • the percentage of monomers corresponding to formula (I) and (I)) is at least 50% by weight and preferably at least 70% by weight, based on the comonomers (Ia). It is also possible to polymerize only monomers of formulae (I) and (II). However, the percentage of comonomers of formula (Ia) in the polymerization is preferably at least 5% by weight.
  • the ratio by weight between components a) and b) must be between 10:1 and 1:10 and preferably between 5:1 and 1:3.
  • the range from 3:1 to 1:1 is particularly preferred.
  • the dispersions according to the invention must contain emulsifiers c) for stabilization.
  • the emulsifiers are preferably selected from nonionic and/or cationic emulsifiers.
  • the emulsifiers are cationic emulsifiers, i.e. compounds containing a positive charge in the form of a quaternized ammonium group or an amine group with a neutral charge which change into the ionically protonated form on acidification of the system as a whole. Examples of such cationic compounds can be found in WO 88/00991, pages 2 and 3.
  • esterquats i.e. quaternized alkyl ammonium compounds containing at least one ester group in the alkyl group, are also suitable for stabilizing the dispersions according to the invention.
  • the aqueous dispersions according to the invention contain components a) and b) in total quantities of 0.1 to 50% by weight and preferably in total quantities of 1 to 35% by weight, based on the total weight of the aqueous dispersion.
  • the emulsifiers c) are present in quantities of 0.1 to 10% by weight and preferably in quantities of 0.5 to 5% by weight, based on the total weight of the dispersion. It can be of advantage to use water-miscible organic solvents besides components a) and b) and the emulsifiers c).
  • Preferred water-miscible organic solvents are polyols containing 2 to 6 carbon atoms and 2 to 6 hydroxyl groups, alkyl ethers or partial alkyl ethers of these polyols or the completely or partly alkoxylated derivatives of the polyols or acetone.
  • the dispersions according to the invention are prepared by first mixing an aqueous cationically or nonionically stabilized dispersion a) with an aqueous cationically or nonionically stabilized dispersion b).
  • the mixture thus obtained may be applied to textiles and fibers by suitable methods known per se. Suitable textile materials are both cotton and polyester or polyamide fibers and blends.
  • the aqueous dispersions according to the invention are applied to the fibers or to the textile material by conventional techniques, for example using a padding roller.
  • the concentration of active substance is preferably between 1 and 5 g per liter, based on the liquor.
  • the present invention also relates to the use of the aqueous dispersions described in the foregoing for the hydrophobic finishing of fibers and flat textile materials.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Textile Engineering (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Colloid Chemistry (AREA)

Abstract

Aqueous dispersions containing at least: a) a copolymer of compounds corresponding to formula (I):
R1—O—CO—CR2═CH2  (I),
    •  in which R1 is a branched or unbranched alkyl group containing 8 to 22 carbon atoms and R2 is a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms, with monomers selected from compounds corresponding to formula (Ia):
      R3—O—CO—CR4═CH2  (Ia),
    •  in which R3 is a branched or unbranched alkyl group containing 1 to 6 carbon atoms and R4 is a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms, and b) a copolymer of compounds corresponding to formula (II):
      CnF2n—CH2—CH2—O—CO—CR5═CH2  (II),
    •  in which R5 is a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms and n is a number of 4 to 12, with monomers selected from compounds corresponding to formula (Ia), and c) emulsifiers, with the proviso that the ratio by weight between the copolymers a) and the copolymers b) is 10:1 to 1:10.

Description

  • This invention relates to aqueous dispersions containing fluorinated and non-fluorinated poly(meth)acrylates and to the use of such dispersions for the hydrophobic finishing of fibers and flat textiles.
  • It is known and common practice in the textile industry to treat fibers and flat textiles with aqueous dispersions containing fluorine-containing copolymers based on perfluoroacrylates. Perfluoroacrylates provide textile materials with both strongly hydrophobic and strongly oleophobic properties. Perfluoroacrylates such as these are described, for example, in DE 1 247 659. EP 1 146 103 A1 also describes aqueous dispersions containing polyfluorinated polymers which are used for finishing textiles.
  • Although the finishing of textiles with perfluoroacrylates or other suitable polyfluorinated compounds does lead to the desired properties of the textile materials, the fluorinated compounds are still very expensive. Accordingly, there is a need to make the hydrophobic finishing of textiles less expensive without losing the effectiveness of the finish.
  • It has now been found that, by combining polymeric perfluoroacrylates known per se with non-fluorinated polymeric acrylates, the proportion of the expensive fluorinated products can be reduced without diminishing the effectiveness of the hydrophobic finish.
  • Accordingly, the present invention relates to aqueous dispersions containing at least:
      • a) a copolymer of compounds corresponding to formula (I): R1——O—CO—CR 2═CH2 (I), in which R1 is a branched or unbranched alkyl group containing 8 to 22 carbon atoms and R2 is a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms, with monomers selected from compounds corresponding to formula (Ia): R3—O—CO—CR4═CH2 (Ia), in which R3 is a branched or unbranched alkyl group containing 1 to 6 carbon atoms and R4 is a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms, and
      • b) a copolymer of compounds corresponding to formula (II): CnF2n—CH2—CH2—O—CO—CR5═CH2 (II), in which R5 is a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms and n is a number of 4 to 12, with monomers selected from compounds corresponding to formula (Ia), and
      • c) emulsifiers, with the proviso that the ratio by weight between the copolymers a) and the copolymers b) is 10:1 to 1:10.
  • Both the compounds of formula (I) and (Ia) and the compounds of formula (II) are known per se. They are derivatives, more particularly esters, of acrylic acid or methacrylic acid.
  • The perfluorinated compounds corresponding to formula (II) are generally prepared from tetrafluoroethane which is polymerized and iodized and converted into a perfluorinated alcohol in a Grignard reaction with ethylene oxide. In a final reaction step, the perfluorinated alcohol is reacted with acrylic acid or methacrylic acid to form the required perfluorinated acrylates or methacrylate esters. When it comes to selecting the compounds corresponding to formula (II), it is of advantage to use perfluorinated compounds of formula (II) where the index n is a number of 6 to 10.
  • The compounds of formula (I) are also known esters of acrylic or methacrylic acid with fatty alcohols, the fatty alcohols having to contain 8 to 22 carbon atoms.
  • The monomers of formulae (I) and (II) independently of one another are reacted with the acrylates or methacrylates of formula (Ia), generally by emulsion polymerization in aqueous medium, to form copolymers using emulsifiers c), after which the two components a) and b), which already contain the emulsifiers from the production process, are mixed to form the dispersions according to the invention.
  • The emulsion polymerization is a special polymerization process in which water-insoluble monomers are emulsified in water with the aid of emulsifiers and polymerized using water-soluble initiators (for example potassium persulfate; redox initiators). Particularly preferred monomers of formula (Ia) are selected from the group consisting of methyl, ethyl, n-propyl, i-propyl and/or butyl esters of acrylic or methacrylic acid. The compounds of formula (Ia) independently of one another may be used for the preparation of polymer dispersions a) and b). In the polymerization reaction to form components a) and b), it is of advantage for the percentage of monomers corresponding to formula (I) and (I)) to be at least 50% by weight and preferably at least 70% by weight, based on the comonomers (Ia). It is also possible to polymerize only monomers of formulae (I) and (II). However, the percentage of comonomers of formula (Ia) in the polymerization is preferably at least 5% by weight.
  • According to the invention, the ratio by weight between components a) and b) must be between 10:1 and 1:10 and preferably between 5:1 and 1:3. The range from 3:1 to 1:1 is particularly preferred.
  • The dispersions according to the invention must contain emulsifiers c) for stabilization. The emulsifiers are preferably selected from nonionic and/or cationic emulsifiers. In a particularly preferred embodiment, the emulsifiers are cationic emulsifiers, i.e. compounds containing a positive charge in the form of a quaternized ammonium group or an amine group with a neutral charge which change into the ionically protonated form on acidification of the system as a whole. Examples of such cationic compounds can be found in WO 88/00991, pages 2 and 3. However, other quaternized compounds known to the expert, more particularly so-called esterquats, i.e. quaternized alkyl ammonium compounds containing at least one ester group in the alkyl group, are also suitable for stabilizing the dispersions according to the invention.
  • The aqueous dispersions according to the invention contain components a) and b) in total quantities of 0.1 to 50% by weight and preferably in total quantities of 1 to 35% by weight, based on the total weight of the aqueous dispersion. The emulsifiers c) are present in quantities of 0.1 to 10% by weight and preferably in quantities of 0.5 to 5% by weight, based on the total weight of the dispersion. It can be of advantage to use water-miscible organic solvents besides components a) and b) and the emulsifiers c). Preferred water-miscible organic solvents are polyols containing 2 to 6 carbon atoms and 2 to 6 hydroxyl groups, alkyl ethers or partial alkyl ethers of these polyols or the completely or partly alkoxylated derivatives of the polyols or acetone.
  • The dispersions according to the invention are prepared by first mixing an aqueous cationically or nonionically stabilized dispersion a) with an aqueous cationically or nonionically stabilized dispersion b). The mixture thus obtained may be applied to textiles and fibers by suitable methods known per se. Suitable textile materials are both cotton and polyester or polyamide fibers and blends. The aqueous dispersions according to the invention are applied to the fibers or to the textile material by conventional techniques, for example using a padding roller. The concentration of active substance is preferably between 1 and 5 g per liter, based on the liquor.
  • The present invention also relates to the use of the aqueous dispersions described in the foregoing for the hydrophobic finishing of fibers and flat textile materials.

Claims (21)

1-13. (canceled)
14. An aqueous dispersion comprising:
a) a copolymer comprising constituent units provided by monomers of the formula:

R1-0-CO—CR2═CH2  (I),
in which R1 is a branched or unbranched alkyl group containing 8 to 22 carbon atoms and R2 is a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms, and constituent units provided by monomers of the formula:

R3—O—CO—CR4═CH2  (Ia),
in which R3 is a branched or unbranched alkyl group containing 1 to 6 carbon atoms and R4 is a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms; and
b) a copolymer comprising constituent units provided by monomers of the formula

CnF2n+1—CH2—CH2—O—CO—CR5═CH2  (II),
in which R5 is a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms and n is a number of 4 to 12, and constituent units provided by monomers of the formula (Ia); and
c) an emulsifier, wherein, the ratio by weight of the copolymer a) and the copolymer b) is 10:1 to 1:10.
15. The aqueous dispersions as claimed in claim 14, wherein, the copolymers a) contain constituent units provided by monomers of the formula (I) where R1 is a linear alkyl group containing 12 to 18 carbon atoms.
16. The aqueous dispersion as claimed in claim 14, wherein, the copolymer b) contains constituent units provided by monomers of formula (II) where n is a number of 6 to 10.
17. The aqueous dispersion as claimed in claim 14, wherein, the ratio by weight of copolymers a) to copolymers b) is 5:1 to 1:3.
18. The aqueous dispersion as claimed in claim 14, wherein, the ratio by weight of copolymers a) to copolymers b) is 3:1 to 1:1.
19. The aqueous dispersion as claimed in claim 14, wherein, at least 50% by weight of the constituent units in the copolymer a) is provided by monomers of the formula (I).
20. The aqueous dispersion as claimed in claim 14, wherein, at least 70% by weight of the constituent units in the copolymer a) is provided by
21. The aqueous dispersion as claimed in claim 14, wherein, at least 50% by weight of the constituent units in the copolymer b) is provided by monomers of the formula (II).
22. The aqueous dispersion as claimed in claim 14, wherein, the monomers of formula (Ia) independently of one another comprise at least one member selected from the group consisting of methyl, ethyl, n-propyl, i-propyl and butyl esters of acrylic or methacrylic acid.
23. The aqueous dispersion as claimed in claim 14, wherein, the emulsifier comprises at least one member selected from the group consisting of nonionic and cationic emulsifiers.
24. The aqueous dispersion as claimed in claim 14, wherein, a sum of the weight of copolymers a) and b) comprises from 0.1% to 50% by weight of the dispersion, based on a total weight of the dispersion.
25. The aqueous dispersion as claimed in claim 14, wherein, a sum of the weight of copolymers a) and b) comprises from 1% to 35% by weight of the dispersion, based on a total weight of the dispersion.
26. The aqueous dispersion as claimed in claim 14 which contains emulsifiers in a quantity of 0.1 to 10% by weight, based on the total weight of the dispersion.
27. The aqueous dispersion as claimed in claim 14, which further comprises a water-miscible organic solvent.
28. The aqueous dispersion as claimed in claim 27, wherein, the solvent comprises at least one member selected from the group consisting of polyols containing 2 to 6 carbon atoms and 2 to 6 hydroxyl groups, alkyl ethers or partial alkyl ethers of these polyols, partly or completely alkoxylated derivatives of these polyols, and acetone.
29. A fiber or a flat textile comprising a hydrophobic finish comprising a dried polymer dispersion of claim 14.
30. The aqueous dispersion as claimed in claim 14 which contains emulsifiers in a quantity of 0.5% to 5% by weight, based on the total weight of the dispersion.
31. The aqueous dispersion as claimed in claim 15, wherein, the copolymer b) contains constituent units provided by monomers of formula (II) where n is a number of 6 to 10.
32. The aqueous dispersion as claimed in claim 15, wherein, the ratio by weight of copolymers a) to copolymers b) is 5:1 to 1:3.
33. The aqueous dispersion as claimed in claim 16, wherein, the ratio by weight of copolymers a) to copolymers b) is 5:1 to 1:3.
US10/527,244 2002-09-14 2003-09-05 Aqueous dispersions for hydrophobically finishing fibres and flat textile materials Abandoned US20050257325A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10242762.3 2002-09-14
DE10242762A DE10242762A1 (en) 2002-09-14 2002-09-14 Aqueous dispersion of copolymerisates and emulsifiers which when combined with fluorinated compounds enable the proportion of these to be decreased without impairing hydrophobization efficiency of fibers and textiles
PCT/EP2003/009854 WO2004026959A1 (en) 2002-09-14 2003-09-05 Aqueous dispersions for hydrophobically finishing fibres and flat textile materials

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Publication Number Publication Date
US20050257325A1 true US20050257325A1 (en) 2005-11-24

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US10/527,244 Abandoned US20050257325A1 (en) 2002-09-14 2003-09-05 Aqueous dispersions for hydrophobically finishing fibres and flat textile materials

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US (1) US20050257325A1 (en)
EP (1) EP1537176A1 (en)
CN (1) CN1289598C (en)
DE (1) DE10242762A1 (en)
TW (1) TW200407338A (en)
WO (1) WO2004026959A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9967397B2 (en) 2007-12-28 2018-05-08 Genesys Telecommunications Laboratories, Inc. System for facilitating loosely configured service worker groups in a dynamic call center environment
EP3778824A4 (en) * 2018-03-26 2021-12-15 Agc Inc. Oil-repellent and water-repellent agent composition, article, and method for producing article

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2804391A (en) * 1954-06-15 1957-08-27 Atlantic Refining Co Mothproofing and waterproofing composition
US3256230A (en) * 1961-05-03 1966-06-14 Du Pont Polymeric water and oil repellents
US3536779A (en) * 1967-05-16 1970-10-27 Louise C Decnyf Method for imparting a durable water resistant coating to a substrate
US4966725A (en) * 1986-08-01 1990-10-30 Ciba-Geigy Corporation Aqueous dispersions for simultaneously providing fibrous materials with a softening and hydrophilic finish, a process for their production and their use
US5387640A (en) * 1992-01-22 1995-02-07 Bayer Aktiengesellschaft Fluorine-containing copolymers and aqueous dispersions prepared therefrom

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4201603A1 (en) * 1992-01-22 1993-07-29 Bayer Ag MIXTURES OF FLUORINE COPOLYMERISATE

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2804391A (en) * 1954-06-15 1957-08-27 Atlantic Refining Co Mothproofing and waterproofing composition
US3256230A (en) * 1961-05-03 1966-06-14 Du Pont Polymeric water and oil repellents
US3536779A (en) * 1967-05-16 1970-10-27 Louise C Decnyf Method for imparting a durable water resistant coating to a substrate
US4966725A (en) * 1986-08-01 1990-10-30 Ciba-Geigy Corporation Aqueous dispersions for simultaneously providing fibrous materials with a softening and hydrophilic finish, a process for their production and their use
US5387640A (en) * 1992-01-22 1995-02-07 Bayer Aktiengesellschaft Fluorine-containing copolymers and aqueous dispersions prepared therefrom

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9967397B2 (en) 2007-12-28 2018-05-08 Genesys Telecommunications Laboratories, Inc. System for facilitating loosely configured service worker groups in a dynamic call center environment
US10264123B2 (en) 2007-12-28 2019-04-16 Genesys Telecommunications Laboratories, Inc. System for facilitating loosely configured service worker groups in a dynamic call center environment
EP3778824A4 (en) * 2018-03-26 2021-12-15 Agc Inc. Oil-repellent and water-repellent agent composition, article, and method for producing article

Also Published As

Publication number Publication date
CN1289598C (en) 2006-12-13
EP1537176A1 (en) 2005-06-08
WO2004026959A1 (en) 2004-04-01
TW200407338A (en) 2004-05-16
DE10242762A1 (en) 2004-03-18
CN1681882A (en) 2005-10-12

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