GB766534A - New copolymers of acrylonitrile and process of preparing them - Google Patents
New copolymers of acrylonitrile and process of preparing themInfo
- Publication number
- GB766534A GB766534A GB27225/52A GB2722552A GB766534A GB 766534 A GB766534 A GB 766534A GB 27225/52 A GB27225/52 A GB 27225/52A GB 2722552 A GB2722552 A GB 2722552A GB 766534 A GB766534 A GB 766534A
- Authority
- GB
- United Kingdom
- Prior art keywords
- beta
- quaternized
- vinyl
- bis
- acrylate
- 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
- C08F20/62—Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
-
- 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
- C08F220/00—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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
- C08F220/44—Acrylonitrile
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Artificial Filaments (AREA)
Abstract
Acrylonitrile and alpha-substituted acrylonitriles are copolymerized, if desired, in the presence of another copolymerizable compound, with a derivative of an alpha, beta-unsaturated carboxylic acid which contains as a substituent in the carboxyl group a group containing quaternary nitrogen, such as quaternary esters, amides and imides of acrylic, methacrylic, chloroacrylic, phenylacrylic, beta-cyanacrylic, itaconic, fumaric and maleic acids of which many are specified, the preferred being the quaternization products of beta-dimethylaminoethyl acrylate and methacrylate, beta-diethylaminoethyl acrylate and acrylamide, betabromethylacrylamide, 1 : 3 - bis - (diethylamino) - 2 - propyl acrylate, bis - (beta - pyrrolidinoethyl) fumarate, bis - (beta - dimethylaminoethyl) itaconate, and beta-N-pyrollidinoethyl acrylamide. Optional copolymerizable monomers specified are N-vinyl imidazole, N- or C-vinyl benzimidazole, vinyl pyrrolidone, vinyl - beta - dimethylaminoethyl ether, vinyl - beta - morpholinoethyl ether, vinyl butyl ether, vinyl pyridine and its quaternary derivatives, acrylic acid, acrylamide, N-methyl and N - beta - hydroxyethyl acrylamides, dimethyl methacrylamide, itaconic diamide, maleic acid monomethylamide, bisdimethyl itaconamide, bis-di-gamma-hydroxypropylitaconamide, vinyl formate, acetate and chloracetate, methyl vinylsulphone, N-vinylbenzenesulphonamide, vinyl chloride and styrene. Polymerization may be carried out in solution in a solvent such as dioxane or isopropanol, or in aqueous emulsion in the presence or absence of an emulsifier such as sodium cetyl sulphate, sodium isododecyl benzenesulphonate, sodium octadecyl sulphate and alkali metal or ammonium salts of condensation products of naphthalene sulphonic acids with formaldehyde. Specified polymerization catalysts are azodiisobutyronitrile, hydrogen peroxide and alkali metal persulphates or perborates. The oxidizing catalysts may be activated by reducing agents such as sulphites, hyposulphites, pyrosulphites and mercaptans, e.g. dodecyl mercaptan, which latter also function as chain terminators. The pH of the aqueous polymerization media is preferably kept within the weakly acid to weakly alkaline range. During the course of polymerization further quantities of monomer and catalyst may be added gradually to the reaction mixture. The copolymers produced are soluble in dimethyl formamide, a mixture of dimethyl formamide and cyclohexanone, cyclotetramethylene sulphone, butyrolactone, ethylene cyanhydrin, ethylene carbonate, alpha-chlorobeta-hydroxypropyl cyanide, and, in the case of copolymers containing lesser amounts of acrylonitrile, acetone and cyclohexanone; from solutions thus formed may be produced films and fibres which may be stretched and dyed. In an Example (6) a dimethylformamide solution of a copolymer of acrylonitrile and betadimethylaminoethyl acrylate methosulphate is wet spun into a coagulating bath consisting of fatty acids containing 7 to 11 carbon atoms. In addition, copolymers derived from quaternary monomers containing more than one ethylenic linkage, e.g. the reaction product of methyl bromide with di-N-methyl-bis-betahydroxy ethylamine acrylate, may be used as anion-exchangers.ALSO:Derivatives of alpha, beta-unsaturated carboxylic acids which contain as a substituent in the carboxyl group a group containing quaternary nitrogen are prepared either by treating with an alkylating agent a derivative of the acid having an ester or amide group containing a tertiary amino group, or by treating with a tertiary amine a derivative of the acid containing a halogen atom in an alkyl radical of the ester or amide group. In examples: (1) betadiethylaminoethyl acrylate is quaternized with dimethyl sulphate; (2) beta-dimethylaminoethyl methacrylate is quaternized with methyl bromide; (3) beta-diethylaminoethyl acrylamide is quaternized with dimethyl sulphate; (4) trimethylamine is quaternized with betabromethyl acrylamide; (5) 1 : 3 - bis - (diethylamino)-2-propyl acrylate is quaternized with dimethyl sulphate; (6) beta-dimethylaminoethyl acrylate is quaternized with dimethyl sulphate; (7) beta-dimethylaminoethyl acrylate is quaternized with ethyl monochloracetate; (9) bis - (beta - dimethylaminoethyl) itaconate is quaternized with dimethyl sulphate; (10) bis-(beta-pyrollidinoethyl) fumarate is quaternized with dimethyl sulphate; and (12) beta-N-pyrrolidinoethyl acrylamide is quaternized with dimethyl sulphate. Other quaternizing agents and derivatives of unsaturated acids are listed.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE318830X | 1951-10-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB766534A true GB766534A (en) | 1957-01-23 |
Family
ID=6151189
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB27225/52A Expired GB766534A (en) | 1951-10-29 | 1952-10-29 | New copolymers of acrylonitrile and process of preparing them |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE515194A (en) |
CH (1) | CH318830A (en) |
FR (1) | FR1065145A (en) |
GB (1) | GB766534A (en) |
NL (1) | NL84188C (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1213996B (en) * | 1962-04-25 | 1966-04-07 | Basf Ag | Process for the production of high polymer quaternary ammonium compounds |
DE1227241B (en) * | 1964-07-16 | 1966-10-20 | Bayer Ag | Process for the production of acrylonitrile copolymers |
DE2240291A1 (en) * | 1971-08-16 | 1973-03-15 | Mitsubishi Rayon Co | ACRYLIC NITRILE CO-POLYMERS, FIBERS MANUFACTURED FROM THEM AND THE PROCESS FOR THE PRODUCTION THEREOF |
CN105452213A (en) * | 2013-03-14 | 2016-03-30 | 阿尔克梅斯制药爱尔兰有限公司 | Prodrugs of fumarates and their use in treating various deseases |
CN106566492A (en) * | 2016-11-07 | 2017-04-19 | 天津博科瑞精细化学有限公司 | Gel sealing agent for well drilling fluid and preparation method of gel sealing agent |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3095390A (en) * | 1953-10-30 | 1963-06-25 | Ciba Ltd | Copolymerisation products of amides of copolymerisable carboxylic acids containing quaternary ammonium groups bound to amide nitrogen |
US3287305A (en) * | 1953-10-30 | 1966-11-22 | Ciba Ltd | Cationactive dispersions of finely divided water-insoluble cationactive polymers containing quaternary ammonium groups |
US2980657A (en) * | 1954-07-06 | 1961-04-18 | Rohm & Haas | Quaternary ammonium compounds of polymers of acrylamido type and methods for making them |
BE634566A (en) * | 1957-10-21 | |||
US3170901A (en) * | 1960-12-27 | 1965-02-23 | Rohm & Hans Company | Novel quaternary ammonium compounds and polymers thereof |
US3166540A (en) * | 1960-12-27 | 1965-01-19 | Rohm & Haas | Novel polymeric quaternary ammonium compounds |
CN113663597A (en) * | 2021-08-23 | 2021-11-19 | 濮阳市盛源能源科技股份有限公司 | Gemini surfactant with antibacterial function and preparation method thereof |
-
0
- NL NL84188D patent/NL84188C/xx active
- BE BE515194D patent/BE515194A/xx unknown
-
1952
- 1952-10-22 CH CH318830D patent/CH318830A/en unknown
- 1952-10-29 GB GB27225/52A patent/GB766534A/en not_active Expired
- 1952-10-29 FR FR1065145D patent/FR1065145A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1213996B (en) * | 1962-04-25 | 1966-04-07 | Basf Ag | Process for the production of high polymer quaternary ammonium compounds |
DE1227241B (en) * | 1964-07-16 | 1966-10-20 | Bayer Ag | Process for the production of acrylonitrile copolymers |
DE2240291A1 (en) * | 1971-08-16 | 1973-03-15 | Mitsubishi Rayon Co | ACRYLIC NITRILE CO-POLYMERS, FIBERS MANUFACTURED FROM THEM AND THE PROCESS FOR THE PRODUCTION THEREOF |
CN105452213A (en) * | 2013-03-14 | 2016-03-30 | 阿尔克梅斯制药爱尔兰有限公司 | Prodrugs of fumarates and their use in treating various deseases |
CN105452213B (en) * | 2013-03-14 | 2017-09-22 | 阿尔克梅斯制药爱尔兰有限公司 | Fumarate prodrugs and their application in the treatment of various diseases |
CN106566492A (en) * | 2016-11-07 | 2017-04-19 | 天津博科瑞精细化学有限公司 | Gel sealing agent for well drilling fluid and preparation method of gel sealing agent |
CN106566492B (en) * | 2016-11-07 | 2019-11-15 | 天津天诚拓源科技发展有限公司 | Drilling fluid GEL USED FOR PLUGGING WELL LOST CIRCULATION and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
FR1065145A (en) | 1954-05-20 |
CH318830A (en) | 1957-01-31 |
BE515194A (en) | |
NL84188C (en) |
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