GB764296A - Improvements in the polymerisation of acrylonitrile - Google Patents
Improvements in the polymerisation of acrylonitrileInfo
- Publication number
- GB764296A GB764296A GB2742652A GB2742652A GB764296A GB 764296 A GB764296 A GB 764296A GB 2742652 A GB2742652 A GB 2742652A GB 2742652 A GB2742652 A GB 2742652A GB 764296 A GB764296 A GB 764296A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dimethyl
- vinyl
- alkali metal
- ethyl
- methyl
- 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
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/10—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of amides or imides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Graft polymers are prepared by polymerizing in the presence of a polymerization catalyst a solution or dispersion of 60 to 90 per cent by weight of acrylonitrile and 10 to 40 per cent by weight of an isolated homopolymer or interpolymer of an amide of an alkenyl carboxylic acid which contains from 3 to 5 carbon atoms in the acid radical such as those derived from acrylamide, the N-monoalkyl and N:N-dialkyl substitution products of acrylamide and methacrylamide, itaconamide and its N-monoalkyl and N:N1-dialkyl substitution products in which the alkyl groups contain from 1 to 4 carbon atoms, citraconamide and its N-methyl and N-ethyl substitution products, alphachloracrylamide, alpha - chloro - N - methylacrylamide, and methyl and ethyl acetaminoacrylates. The amide interpolymers used are those obtained by polymerizing the above amides with one another or with monomers such as alkyl acrylates and methacrylates containing 1 to 4 carbon atoms in the alkyl group, vinyl acetate and propionate, styrene, alpha-methyl styrene, p-acetaminostyrene, alpha-acetoxystyrene, vinyl chloride, vinyl fluoride, vinyldene chloride, perfluoroethylene, ethyl vinyl and isopropyl vinyl ethers, vinyl methyl, vinyl ethyl, isopropenyl methyl and isopropenyl ethyl ketones, dimethyl, diethyl and diisopropyl maleates and fumarates, acrylic and methacrylic acids, acrylonitrile, methacrylonitrile, fumaronitrile, N-vinylphthalimide, ethylene, butadiene, and vinyl pyridines. Polymerization catalysts specified are peroxides such as benzoyl, acetyl, acetyl benzoyl, lauryl, oleoyl, triacetone and urea peroxides, tert.-butyl hydroperoxide, alkyl percarbonates, hydrogen peroxide, alkali metal perborates, alkali metal and ammonium persulphates which may be used in conjunction with an alkali metal bisulphite, and ketazines and azines. Polymerization may be carried out in an aqueous medium or in solution in a solvent such as acetonitrile or a mixture of water with acetone or acetonitrile. Aqueous polymerization media may contain emulsifiers such as sodium lauryl sulphate, sodium isobutylnaphthalenesulphonate, sodium 7 - ethyl - 2 - methylundecan - 4 - sulphonate, sulphonated ethers, alkali metal or amine addition salts of sulphosuccinic acid esters, alkali metal salts of fatty acids containing from 12 to 20 carbon atoms, sulphonated fatty acid amides and alkali metal salts of alkane sulphonic acids. Also present in the reaction mixture may be chain regulators such as hexyl, octyl, lauryl, dodecyl and myristyl mercaptans. The resulting graft polymers may be formed into dyeable films and fibres from solution in solvents such as dimethyl formamide, dimethyl acetamide, dimethyl cyanamide, dimethyl cyanoacetamide, dimethyl - beta - cyanopropionamide, dimethyl methoxyacetamide, ethylene carbonate, ethylene carbamate, gamma-butyrolactone, N-methyl-2-pyrrolidone, glycolonitrile, malononitrile, ethylene cyanhydrin, dimethyl sulphone, dimethyl sulphoxide, tetramethylene sulphone, tetramethylene sulphoxide, N-formylpyrrolidine, N-formylmorpholine and N:N1-tetramethylmethane-phosphonamide. Specifications 358,534, [Group IV], 715,194, 764,297 and 764,298 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2742652A GB764296A (en) | 1952-10-31 | 1952-10-31 | Improvements in the polymerisation of acrylonitrile |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2742652A GB764296A (en) | 1952-10-31 | 1952-10-31 | Improvements in the polymerisation of acrylonitrile |
Publications (1)
Publication Number | Publication Date |
---|---|
GB764296A true GB764296A (en) | 1956-12-28 |
Family
ID=10259392
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2742652A Expired GB764296A (en) | 1952-10-31 | 1952-10-31 | Improvements in the polymerisation of acrylonitrile |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB764296A (en) |
-
1952
- 1952-10-31 GB GB2742652A patent/GB764296A/en not_active Expired
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