GB644678A - Improvements in and relating to copolymers of monovinyl-phenoxthines - Google Patents

Improvements in and relating to copolymers of monovinyl-phenoxthines

Info

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
Application number
GB13993/48A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
British Thomson Houston Co Ltd
Original Assignee
British Thomson Houston Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by British Thomson Houston Co Ltd filed Critical British Thomson Houston Co Ltd
Publication of GB644678A publication Critical patent/GB644678A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F28/00Homopolymers 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
    • C08F28/06Homopolymers 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.
GB13993/48A 1947-05-29 1948-05-24 Improvements in and relating to copolymers of monovinyl-phenoxthines Expired GB644678A (en)

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)

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