GB644678A - Improvements in and relating to copolymers of monovinyl-phenoxthines - Google Patents
Improvements in and relating to copolymers of monovinyl-phenoxthinesInfo
- Publication number
- GB644678A GB644678A GB13993/48A GB1399348A GB644678A GB 644678 A GB644678 A GB 644678A GB 13993/48 A GB13993/48 A GB 13993/48A GB 1399348 A GB1399348 A GB 1399348A GB 644678 A GB644678 A GB 644678A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- vinyl
- butadiene
- chlorinated
- dimethallyl
- 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
- C08F28/00—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 bond to sulfur or by a heterocyclic ring containing sulfur
- C08F28/06—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 bond to sulfur or by a heterocyclic ring containing sulfur by a heterocyclic ring containing sulfur
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)
- Laminated Bodies (AREA)
Abstract
Monovinylphenoxthines are copolymerized with a compound containing a CH2=C< group, e.g. butadiene, hexadiene-1,5, octadiene-1,4, 2-chlorobutadiene-1,3, 2,3-dimethyl-butadiene-1,3, 2-cyano-butadiene-1,3, cyclopentadiene, isoprene, piperylene; styrene, p-chlorostyrene, di- and tri-chlorostyrenes, chlorinated methyl styrene, methyl styrene, divinylbenzene, chlorinated divinylbenzenes, divinyl biphenyl, chlorinated vinyl naphthalenes, vinyl fluorenes, acenaphthylene; acrylo- and methacrylonitrile, acryl- and methacrylamide, methyl, benzyl para-chlorobenzyl, allyl, methallyl, amyl acrylates, ethylene glycol diacrylate and glyceryl triacrylate, methyl, benzyl, allyl, hexyl methacrylates, diethylene glycol dimethacrylate, methyl and propyl a -chloroacrylates and ethyl a -bromoacrylate; maleic anhydride; dimethyl and diallyl fumarates, diethyl and dimethallyl maleates; diethyl, diethylene and dimethallyl itaconates; diallyl citraconate; triallyl citrate and aconitate; methylene methyl, or ethyl malonates; vinyl methyl and ethyl ethers and divinyl ethers; dimethallyl phthalate; vinyl chloride, acetate, propionate, and butyrate; vinylidene chloride and vinyl methyl ketone, ethylene, chloro-, fluoro-, and chlorofluoroethylenes, by heating in bulk, solution, e.g. in benzene or acetone, emulsion or suspension with a catalyst, e.g. oxygen, ozone, ozonides, hydrogen peroxide, hydrochloric, hydrofluoric or sulphuric acid, boron fluoride, stannic chloride, antimony pentachloride, halogens, benzoyl, acetyl, stearyl, lauryl, sodium or barium peroxide, butyl hydroperoxide, persulphates, perchlorates or perborates, carbon black, finely divided silica, metallic powders and finely divided clays, or ultra-violet light. In an example, 3-vinylphenoxthine is heated with butadiene in aqueous emulsion with stearic acid, potassium persulphate, potassium hydroxide and dioctyl sodium sulfosuccinate. The product is dissolved in toluene and precipitated by methyl alcohol. Films may be cast from ethylene dichloride solution. Plasticizers and fillers, e.g. a -cellulose, mica dust, titanium oxide, talc, zinc oxide, magnesium oxide, asbestos, quartz, wood flour, cellulose or wool fibres may be added. The products, in combination with paper, glass fibres, cotton, silk, rayon, nylon, sheet asbestos, cellulose acetate and acetobutyrate, may be used as dielectrics, e.g. in capacitors, or as cable impregnants, or filling compounds copolymerized in situ. Specification 644,677 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US644678XA | 1947-05-29 | 1947-05-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB644678A true GB644678A (en) | 1950-10-18 |
Family
ID=22056199
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB13993/48A Expired GB644678A (en) | 1947-05-29 | 1948-05-24 | Improvements in and relating to copolymers of monovinyl-phenoxthines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB644678A (en) |
-
1948
- 1948-05-24 GB GB13993/48A patent/GB644678A/en not_active Expired
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