GB1095900A - Fluorocarbon esters and polymers thereof - Google Patents

Fluorocarbon esters and polymers thereof

Info

Publication number
GB1095900A
GB1095900A GB5459765A GB5459765A GB1095900A GB 1095900 A GB1095900 A GB 1095900A GB 5459765 A GB5459765 A GB 5459765A GB 5459765 A GB5459765 A GB 5459765A GB 1095900 A GB1095900 A GB 1095900A
Authority
GB
United Kingdom
Prior art keywords
compounds
water
modification
polymers
oil
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
Application number
GB5459765A
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.)
Daikin Industries Ltd
Original Assignee
Daikin Industries Ltd
Daikin Kogyo Co Ltd
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 Daikin Industries Ltd, Daikin Kogyo Co Ltd filed Critical Daikin Industries Ltd
Publication of GB1095900A publication Critical patent/GB1095900A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F20/00Homopolymers and 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 a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/10Esters
    • C08F20/26Esters containing oxygen in addition to the carboxy oxygen
    • C08F20/28Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
    • 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
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D06M15/277Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)

Abstract

Aerosols for conferring oil- or water-repellency comprise a propellant and an organic solvent solution of a homopolymer or copolymer of a fluorinated ester of the formula <FORM:1095900/C4-C5/1> where Rf is a C3- 21 perfluoroalkyl group, R is hydrogen or a methyl group, m is 1-10, and n is 0 or 1-10. Specified propellants are dichlorodifluoromethane monofluorotrichloromethane and dichlorotetrafluoromethane. Examples 7, 8 and 10 describe the preparation of aerosol compositions.ALSO:The invention comprises homopolymers and copolymers of fluorinated esters of the formula <FORM:1095900/C3/1> where Rf is a C3- 21 perfluoroalkyl group, R is hydrogen or a methyl group, m is 1-10 and n is 0 or 1-10. The polymers are prepared by conventional techniques using heat, free-radical catalysts or U.V. or ionizing radiation to initiate polymerization. Emulsion polymerization in an aqueous medium in the presence of a surfactant and a peroxide- or azo-type free-radical catalyst is preferred. Specified comonomers are acrylic and methacrylic acids and derivatives thereof, vinyl and allyl esters of aliphatic acids, styrene and derivatives thereof, halogenated vinyl and vinylidene compounds, vinyl alkyl ketones, dienes and fluorinated unsaturated esters of the formulae Rf(CH2)qOOC.CR=CH2 and RfCH=CH(CH2)qOOC.CR=CH2, where q is 1-10. The polymers can be modified by reaction of the side-chain hydroxyl groups therein with mono- or poly-functional compounds, e.g. monoisocyanates, ureas, alkyl-pyridinium chlorides, stearic chloride or anhydride, or polyisocyanates such as toluene diisocyanate, hexamethylene diisocyanate, hexahydrobiphenyl-4,41-diisocyanate and 3,5-diisocyanates and benzotrifluorides, triazines such as cyanuric chloride, methylolmelamine or polyethylene imide derivatives. The homopolymers, copolymers and modified polymers are used in oil- and water-proofing compositions (see Divisions B2, C4 and D1). Numerous examples of polymers are provided.ALSO:The invention comprises fluorinated esters of the formula <FORM:1095900/C2/1> wherein Rf is a straight or branched chain C3- 21 perfluoroalkyl group, R is hydrogen or a methyl group, m is 1-10 and n is 0 or 1-10. The compounds are prepared by reacting a haloalkanol RfCH2CHX(CH2)mOH with a carboxylate CH2 = CR(CH2)nCOOM where X is halogen, other than fluorine, and X is an alkali metal or silver. The reaction is preferably effected at 80-200 DEG C. in the presence of an inert organic liquid in the presence of a polymerization inhibitor. Preferred compounds are those in which Rf is a straight chain radical, m is 1 and n is 0. The compounds can be polymerized to give products which are used as oiland water-proofing agents (see Divisions B2, C3, C4 and D1). Numerous compounds are specified. The haloalkanol reactants RfCH2CHX(CH2)mOH are prepared by reacting an unsaturated alcohol CH2 = CH(CH2)mOH with either a perfluoroalkylhalide RfX or a perfluorosulphonyl halide RfSO2X, preferably in the presence of a free-radical catalyst. Examples 1 and 11 describe the preparation of <FORM:1095900/C2/2> and F(CH2)8CH2CHBr(CH2)2OH.ALSO:Porous materials are treated with a composition comprising a homopolymer or copolymer of a fluorinated ester of the formula <FORM:1095900/D1-D2/1> where Rf is a C3-21 perfluoroalkyl group, R is hydrogen or a methyl group, m is 1-0 and n is 0 or 1-10, said copolymer containing at least 25% by wt. of the above fluorinated ester. The oil-repellent compositions may take the form of aqueous emulsions, organic solvent solutions or self-pressurised sprays and can be applied to the substrate by painting, dipping or spraying at room or elevated temperatures. The treated materials are dried and may be cured at elevated temperatures. During or after curing a soaping process may be applied. Water-repellent and organic-solvent-repellent compositions are obtained by modification of the fluorenated polymer by reaction of the hydroxyl groups thereof with mono- or poly-functional compounds. Modification with a hydrophobic monofunctional compound, e.g. an alkyl pyridinium salt, yields a polymer which can impart water- and oil-repellency. Modification with a polyfunctional compound, e.g. a polyisocyanate, triazine or methylolmelamine or polyethylene imide, yields a cross-linked polymer which is also insoluble in organic solvents. This modification of the polymer may be effected by treatment of the proofing composition or of the proofed substrate. Suitable substrates are woven and knitted fabrics, fibre boards, felts and papers. All the Examples describe the treatment of fabrics. Example 2 includes the treatment of paper.ALSO:Rigid and flexible substrates are rendered oil- or water-repellent by coating with a composition comprising a homopolymer or copolymer of a fluorinated ester of the formula: <FORM:1095900/B1-B2/1> where Rf is a C3-21 perfluoroalkyl group, R is hydrogen or a methyl group, m is 1-10 and n is 0 or 1-10, said copolymer containing at least 25% by wt. of said fluorinated ester. The compositions may take the form of aqueous emulsions, organic solvent solutions or aerosols and can be applied by painting, dipping or spraying. The coated materials may be dried and cured at elevated temperatures. Water-repellent compositions are obtained by modification of the polymers by reaction of the hydroxyl groups therein in with mono- and poly-functional compounds. This modification may be effected after the coating has been applied to the substrate. Specified substrates include fabrics, fibre board, felts, leather, glass and wood. Examples relate to the treatment of fabrics. Examples 6 and 7 also describe the coating glass bottles and ceilingboards with an oil-repellent composition.
GB5459765A 1964-03-30 1965-12-23 Fluorocarbon esters and polymers thereof Expired GB1095900A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP686564 1964-03-30
JP645265 1965-02-05
JP645365 1965-02-05
JP6712265 1965-11-01

Publications (1)

Publication Number Publication Date
GB1095900A true GB1095900A (en) 1967-12-20

Family

ID=27454491

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5459765A Expired GB1095900A (en) 1964-03-30 1965-12-23 Fluorocarbon esters and polymers thereof

Country Status (3)

Country Link
CH (3) CH527955A (en)
DE (1) DE1518737B2 (en)
GB (1) GB1095900A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3624139A (en) * 1969-01-02 1971-11-30 Basf Wyandotte Corp Acrylic acid esters
GB2135317A (en) * 1983-01-28 1984-08-30 Atochem Compositions and process for the oilproofing and waterproofing treatment of construction materials

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3624139A (en) * 1969-01-02 1971-11-30 Basf Wyandotte Corp Acrylic acid esters
GB2135317A (en) * 1983-01-28 1984-08-30 Atochem Compositions and process for the oilproofing and waterproofing treatment of construction materials
US4478975A (en) * 1983-01-28 1984-10-23 Atochem Compositions and process for the oilproofing and waterproofing treatment of construction materials

Also Published As

Publication number Publication date
DE1518737A1 (en) 1969-11-13
DE1518737B2 (en) 1972-01-27
CH504402A (en) 1971-03-15
CH1530066A4 (en) 1972-04-28
CH527955A (en) 1972-09-15

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