GB1095900A - Fluorocarbon esters and polymers thereof - Google Patents
Fluorocarbon esters and polymers thereofInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers 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
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F20/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
-
- 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
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.
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)
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 |
-
1965
- 1965-12-23 GB GB5459765A patent/GB1095900A/en not_active Expired
- 1965-12-29 DE DE19651518737 patent/DE1518737B2/en not_active Withdrawn
- 1965-12-30 CH CH1530066A patent/CH527955A/en not_active IP Right Cessation
- 1965-12-30 CH CH1806865A patent/CH504402A/en not_active IP Right Cessation
- 1965-12-30 CH CH1530066D patent/CH1530066A4/xx unknown
Cited By (3)
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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