GB678943A - Method of polymerisation and products produced thereby - Google Patents
Method of polymerisation and products produced therebyInfo
- Publication number
- GB678943A GB678943A GB2988849A GB2988849A GB678943A GB 678943 A GB678943 A GB 678943A GB 2988849 A GB2988849 A GB 2988849A GB 2988849 A GB2988849 A GB 2988849A GB 678943 A GB678943 A GB 678943A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alpha
- butyl
- methyl
- methallyl
- ethyl
- 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
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
-
- 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
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
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)
Abstract
Polymers of at least one compound containing in the molecule the grouping <FORM:0678943/IV (a)/1> where Z is a halogen atom or an alkyl radical, are made by polymerizing, e.g. in solution or aqueous emulsion, by heating for between 4 and 10 minutes to a temperature of at least 90 DEG C. but below the decomposition temperature of the compound, then cooling within ten minutes to a temperature between -10 DEG C. and 25 DEG C. and completing the polymerization, preferably in the dark, at this lower temperature. The polymerizable mixture may contain initially another polymerizable unsaturated compound, or the compound may be added at any later stage, e.g. when the polymerization of the compounds originally present is substantially complete. Plasticizers, e.g. dioctyl phthalate, emulsion stabilizers, dyes, lubricants and pigments may also be added before or during the polymerization. The polymerization may be effected in batch, continuously or semi-continuously, in the presence of catalysts, and preferably in the absence of light and molecular oxygen, e.g. the oxygen in the reaction vessel being replaced by nitrogen, methane or carbon dioxide. Specified compounds containing the above grouping are methacrylonitrile, methyl methacrylate, 4-ethyl - 4 - pentoate, amyl - 4 - butyl - 4 - pento-ate, 4 - butyl - 4 - pentenenitrile, 5 - isopropyl-5 - hexenenitrile, 4 - isobutyl - 4 - pentenamide, 4 - amyl - 4 - pentenamide, 3 - methyl - 3-butene - 2 - one, 4 - isopropyl - 4 - pentene - 3-one, 2 - chloropropene - 1, 2 - methylbutene - 1, 2 - ethylbutene - 1, alpha - chlorostyrene, methallyl chloride, methallyl acetate, ethallyl benzoate, alpha - chloroallylcaproate, dimethallyl phthalate, 3 - methallyl - cyclohexanone, alpha - chloro - 4 - ethylstyrene, alpha - chloroacrylonitrile, butyl - 4 - chloro - 4 - pentenoate, ethyl alpha - bromoacrylate, alpha - methyl - 4-methoxystyrene, butyl alpha-chloroacrylate, 2-bromo - 1 - heptene - 3 - one, 4 - methallylbenzonitrile, 4 - chloro - 4 - pentenamide, 4-butyl - 4 - pentene - 2 - one, 4 - iodo - 4 - pentenamide, 3 - fluoro - 3 - butenenitrile, 3 - chloro-3 - butenenitrile, 5 - isopropyl - 5 - hexenenitrile, 3 - alpha - chlorovinyl - 1 - carbethoxycyclohexane, 4 - methallyl - 1 - acetoxy - benzene, 4 - carbamyl - 2 - butyl - 1 - butene, alphamethyl - vinylcyclopentane, beta - chloroallylbenzene, 4 - carboxy - 2 - chloro - 1 - pentene, 4 - methallyl - benzamide, 3 - alpha - methyl vinylcyclohexanamide, 2 - methallyl - cyclohexanecarboxamide, 7 - ethallyl - 2 - naphthamide, 7 - ethallyl - 2 - naphthonitrile, 2-alpha - ethylvinylcyclohexanenitrile, 4 - ethallyl - 2 - cyclopentanenitrile, 3 - methallylcyclopentanone, 3 - ethallyl - 1 - acetylbenzene, butyl - 2 - methyl - 2, propenoate, ethyl - 3-methyl - 3, butenoate, isobutyl - 4 - ethyl pentenoate, 2 - methyl - 2 - propenenitrile, 3-ethyl - 3 - butenenitrile, 2 - methallyl - 1-carboethoxybenzene, 3 - ethallyl - 2 - naphthamide, 5 - isopropyl - 5 - hexenenitrile, 2-methyl - 2 - propenamide, 3 - ethyl - 3 - butenamide, 3 - butyl - 3 - butenamide, 2 - methallylbenzonitrile, 3 - ethyl - butene - 2 - one, 2-methallylcyclohexanone - 5 - amyl - 5 - pentene-2 - one, 5 - ethyl - 5 - pentene - 4 - one, and mixtures. The other polymerizable compound may be styrene, alpha methyl styrene, dichlorostyrene, vinyl naphthalene, vinyl phenol, acrylic acid, alpha-substituted acrylic acids, acrylonitrile, methacrylonitrile, methyl and propyl acrylate, methyl and butyl methacrylate, vinylidene chloride and bromide, vinyl chloride, bromide or fluoride, vinyl acetate, chloroacetate, benzoate and valerate, divinyl adipate, divinyl succinate, vinyl allyl phthalate, vinyl methallyl pimelate, diallyl phthalate, allyl acetate and diallyl succinate. In solution the solvents may be water, cyclohexanone, cyclohexane, butane and hexane. In aqueous emulsion the emulsifying agent may be ammonium, sodium and potassium myristates, laurates, palmitates, oleates, stearates, rosinates, and hydrobietates, sodium lauryl and potassium stearyl sulphates, sodium lauryl and potassium stearyl sulphonates, sodium cetyl sulphonate, sulphonated mineral oils, lauryl amine hydrochloride and stearyl amine hydrobromide. Specified catalysts are benzoyl or acetyl or hydrogen or t-butyl or sodium or succinyl peroxide, persulphuric acid, peracetic acid, perphthalic acid, potassium persulphate, t-butyl perbutyrate, and di-t-butyl dipermalonate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1000243XA | 1948-11-22 | 1948-11-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB678943A true GB678943A (en) | 1952-09-10 |
Family
ID=26748379
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2988849A Expired GB678943A (en) | 1948-11-22 | 1949-11-22 | Method of polymerisation and products produced thereby |
Country Status (4)
Country | Link |
---|---|
DE (1) | DE829222C (en) |
FR (1) | FR1000243A (en) |
GB (1) | GB678943A (en) |
NL (1) | NL73429C (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2840447A (en) * | 1954-04-28 | 1958-06-24 | Du Pont | Process for preparing filaments from dispersions containing graft polymers obtained from ethylenically unsaturated monomers |
-
0
- NL NL73429D patent/NL73429C/xx active
-
1949
- 1949-11-22 GB GB2988849A patent/GB678943A/en not_active Expired
- 1949-11-22 DE DE1949N0000186 patent/DE829222C/en not_active Expired
- 1949-11-22 FR FR1000243D patent/FR1000243A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2840447A (en) * | 1954-04-28 | 1958-06-24 | Du Pont | Process for preparing filaments from dispersions containing graft polymers obtained from ethylenically unsaturated monomers |
Also Published As
Publication number | Publication date |
---|---|
DE829222C (en) | 1952-01-24 |
FR1000243A (en) | 1952-02-11 |
NL73429C (en) |
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