GB1069364A - Improvements in or relating to polyvinyl halide resins - Google Patents
Improvements in or relating to polyvinyl halide resinsInfo
- Publication number
- GB1069364A GB1069364A GB3805564A GB3805564A GB1069364A GB 1069364 A GB1069364 A GB 1069364A GB 3805564 A GB3805564 A GB 3805564A GB 3805564 A GB3805564 A GB 3805564A GB 1069364 A GB1069364 A GB 1069364A
- Authority
- GB
- United Kingdom
- Prior art keywords
- resin
- washed
- methanol
- vinyl
- solvent
- 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
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
- C08J3/11—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids from solid polymers
-
- 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
- C08F14/00—Homopolymers and 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 a halogen
-
- 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
- C08F14/00—Homopolymers and 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 a halogen
- C08F14/18—Monomers containing fluorine
- C08F14/20—Vinyl fluoride
-
- 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
- C08F6/00—Post-polymerisation treatments
- C08F6/14—Treatment of polymer emulsions
-
- 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
- C08F6/00—Post-polymerisation treatments
- C08F6/26—Treatment of polymers prepared in bulk also solid polymers or polymer melts
- C08F6/28—Purification
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of 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 a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use of 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use of 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2327/14—Homopolymers or copolymers of vinyl fluoride
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
Polyvinyl halide dispersions are prepared by a process which comprises polymerizing a vinyl halide in an aqueous medium in the presence of a polymerization initiator and a surface-active agent, separating the vinyl halide polymer resin from the reaction mixture, washing the resin with a wash solvent to remove the surface-active agent therefrom and blending the solvent-containing resin with a latent solvent effective for coalescing the resin when heated. The vinyl halide may be vinyl fluoride. Polymerization may be effected in suspension in the presence of conventional monomer-soluble initiators and suspending agents, or in emulsion in the presence of water-soluble initiators and emulsifying agents, many suitable initiators and surface-active agents being listed. Many suitable wash solvents are listed, including water, alcohol, esters, ketones, aliphatic and aromatic hydrocarbons and halogen-substituted hydrocarbons, ethers and aqueous solutions of acids and bases. Many suitable latent solvents are listed, including sulphones, sulphoxides, nitriles, carbonates, amides, amines, heterocyclic compounds, lactones, nitro compounds, ketones and esters, particularly dimethyl acetamide, dimethyl formamide, dimethyl sulphoxide and N-methyl-2-pyrrolidone. The dispersions may be used to coat leather, textiles, resins, wood, stone, cement, concrete and metals. In examples, vinyl fluoride is polymerized in aqueous media in the presence of methyl cellulose, lauroyl peroxide and (A) stearyl dimethyl benzyl ammonium chloride and isopropanol, (B) alkaryl polyether alcohol and isopropanol, (C) alkaryl polyether alcohol and titanium dioxide, and (D) magnesium lauroyl sulphonate and isopropanol; and (1) resin (A) is washed with methanol, (2) resin (B) is washed with methanol, (3) resin (C) is washed with methanol and (4) resin (D) is washed with water, acetone or methanol, the washed resins being blended with dimethyl acetamide.ALSO:Substrates may be coated by applying thereto dispersions prepared by polymerising a vinyl halide in an aqueous medium in the presence of a polymerisation initiator and a surface active agent, separating the vinyl halide resin from the reaction mixture, washing the resin with a wash solvent to remove surface active agent therefrom and blending the solvent-containing resin with a latent solvent effecting for coalescing the resin when heated, and heating the coating to effect coalesce of the resin. Specified substrates are leather, cloth, resins, wood, stone, concrete, cement, glass and metals, e.g. steel, aluminium, iron, p magnesium, nickel and alloys thereof; and the coatings may be applied by spraying, dipping or roller- or knife-coating. The preferred vinyl halide is vinyl fluoride, which may be copolymerised with vinylidene fluoride, vinyl chloroacetate, chlorostyrene or chlorobutadiene. Many suitable wash solvents are listed including water, alcohols, esters, ketones, aliphatic and aromatic hydrocarbons and halogen-substituted hydrocarbons, ethers, and aqueous solutions of acids and bases. Many suitable latent solvents are listed, including sulphones, sulphoxides, nitriles, carbonates, amides, amines, heterocyclic compounds, lactones, nitro compounds, ketones and esters; particularly dimethyl acetamide, dimethyl formamide, dimethyl sulphoxide and N-methyl-2-pyrrolidone. The coatings may also comprise conventional plasticisers, pigments, fillers, stabilisers and fungicides; and may be post-cured at a temperature higher than that used in the coalescence. In examples polyvinyl fluorides prepared in the presence of methyl cellulose and (A) stearyl dimethyl benzyl ammonium chloride and (B) alkaryl polyether alcohol together with (C) titanium dioxide are washed with methanol; and polyvinyl fluoride prepared in the presence of methyl cellulose and (D) magnesium lauroyl sulphonate is washed with water, acetone or methanol; and the washed resins blended with dimethyl acetamide and coated on (A to C) glass and (D) glass or aluminium.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31015763A | 1963-09-19 | 1963-09-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1069364A true GB1069364A (en) | 1967-05-17 |
Family
ID=23201240
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3805564A Expired GB1069364A (en) | 1963-09-19 | 1964-09-17 | Improvements in or relating to polyvinyl halide resins |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE653231A (en) |
GB (1) | GB1069364A (en) |
NL (1) | NL6410926A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0019404A1 (en) * | 1979-05-02 | 1980-11-26 | Nippon Zeon Co., Ltd. | Process for producing a blending vinyl chloride resin, paste dispersion comprising such blending vinyl chloride resin, and molded articles prepared from such paste dispersion |
EP0718364A1 (en) * | 1994-07-11 | 1996-06-26 | Du Pont-Mitsui Fluorochemicals Co., Ltd | Aqueous fluoropolymer emulsion and process for producing the same |
EP0718363A1 (en) * | 1994-07-11 | 1996-06-26 | Du Pont-Mitsui Fluorochemicals Co., Ltd | Aqueous fluoropolymer emulsion |
EP0774498A1 (en) * | 1994-08-04 | 1997-05-21 | Daikin Industries, Limited | Aqueous fluoropolymer dispersion |
EP1963380A1 (en) * | 2005-12-23 | 2008-09-03 | 3M Innovative Properties Company | Fluoropolymer dispersion and method for making the same |
US20080287599A1 (en) * | 2001-09-05 | 2008-11-20 | 3M Innovative Properties Company | Fluoropolymer dispersion containing no or little low molecular weight fluorinated surfactant |
US8119750B2 (en) | 2006-07-13 | 2012-02-21 | 3M Innovative Properties Company | Explosion taming surfactants for the production of perfluoropolymers |
US20120116016A1 (en) * | 2010-11-09 | 2012-05-10 | E. I. Du Pont De Nemours And Company | Vinyl fluoride polymerization and aqueous dispersion of vinyl fluoride polymer |
US8404790B2 (en) | 2005-07-15 | 2013-03-26 | 3M Innovative Properties Company | Aqueous emulsion polymerization process for producing fluoropolymers |
US9567413B2 (en) | 2010-09-30 | 2017-02-14 | Daikin Industries, Ltd. | Method for producing fluorine-containing polymer |
-
1964
- 1964-09-17 GB GB3805564A patent/GB1069364A/en not_active Expired
- 1964-09-18 BE BE653231D patent/BE653231A/xx unknown
- 1964-09-18 NL NL6410926A patent/NL6410926A/xx unknown
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0019404A1 (en) * | 1979-05-02 | 1980-11-26 | Nippon Zeon Co., Ltd. | Process for producing a blending vinyl chloride resin, paste dispersion comprising such blending vinyl chloride resin, and molded articles prepared from such paste dispersion |
EP0718364A1 (en) * | 1994-07-11 | 1996-06-26 | Du Pont-Mitsui Fluorochemicals Co., Ltd | Aqueous fluoropolymer emulsion and process for producing the same |
EP0718363A1 (en) * | 1994-07-11 | 1996-06-26 | Du Pont-Mitsui Fluorochemicals Co., Ltd | Aqueous fluoropolymer emulsion |
EP0718363A4 (en) * | 1994-07-11 | 1997-02-05 | Mitsui Du Pont Fluorchemical | Aqueous fluoropolymer emulsion |
EP0718364A4 (en) * | 1994-07-11 | 1997-02-19 | Mitsui Du Pont Fluorchemical | Aqueous fluoropolymer emulsion and process for producing the same |
US5985966A (en) * | 1994-07-11 | 1999-11-16 | Du Pont - Mitsui Fluorochemicals Co., Ltd. | Aqueous emulsion of fluorine-containing polymer |
EP0774498A1 (en) * | 1994-08-04 | 1997-05-21 | Daikin Industries, Limited | Aqueous fluoropolymer dispersion |
EP0774498A4 (en) * | 1994-08-04 | 1998-10-14 | Daikin Ind Ltd | Aqueous fluoropolymer dispersion |
US20080287599A1 (en) * | 2001-09-05 | 2008-11-20 | 3M Innovative Properties Company | Fluoropolymer dispersion containing no or little low molecular weight fluorinated surfactant |
US8598267B2 (en) * | 2001-09-05 | 2013-12-03 | 3M Innovative Properties Company | Fluoropolymer dispersion containing no or little low molecular weight fluorinated surfactant |
US8404790B2 (en) | 2005-07-15 | 2013-03-26 | 3M Innovative Properties Company | Aqueous emulsion polymerization process for producing fluoropolymers |
EP1963380A1 (en) * | 2005-12-23 | 2008-09-03 | 3M Innovative Properties Company | Fluoropolymer dispersion and method for making the same |
EP1963380A4 (en) * | 2005-12-23 | 2011-07-13 | 3M Innovative Properties Co | Fluoropolymer dispersion and method for making the same |
US8119750B2 (en) | 2006-07-13 | 2012-02-21 | 3M Innovative Properties Company | Explosion taming surfactants for the production of perfluoropolymers |
US9567413B2 (en) | 2010-09-30 | 2017-02-14 | Daikin Industries, Ltd. | Method for producing fluorine-containing polymer |
US20120116016A1 (en) * | 2010-11-09 | 2012-05-10 | E. I. Du Pont De Nemours And Company | Vinyl fluoride polymerization and aqueous dispersion of vinyl fluoride polymer |
JP2014501803A (en) * | 2010-11-09 | 2014-01-23 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Vinyl fluoride polymerization and aqueous dispersion of vinyl fluoride polymer |
US8735520B2 (en) | 2010-11-09 | 2014-05-27 | E.I. Du Pont De Nemours And Company | Vinyl fluoride polymerization and aqueous dispersion of vinyl fluoride polymer |
Also Published As
Publication number | Publication date |
---|---|
BE653231A (en) | 1965-03-18 |
NL6410926A (en) | 1965-03-22 |
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