GB783790A - - Google Patents

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Publication number
GB783790A
GB783790A GB783790DA GB783790A GB 783790 A GB783790 A GB 783790A GB 783790D A GB783790D A GB 783790DA GB 783790 A GB783790 A GB 783790A
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GB
United Kingdom
Prior art keywords
polythene
free radical
polymerization
monomers
radical generating
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
Publication date
Publication of GB783790A publication Critical patent/GB783790A/en
Expired legal-status Critical Current

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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
    • C08F255/00Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
    • C08F255/02Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Graft Or Block Polymers (AREA)

Abstract

783,790. Ethylene graft polymers. BRITISH CELLOPHANE, Ltd. Dec. 5, 1955 [Dec. 9, 1954], No. 35735/54. Class 2 (6). Ethylene graft polymers are prepared by polymerizing one or more monomers of the formula where R 1 and R 2 are hydrogen or halogen atoms or alkyl, cycloaliphatic, aromatic, nitrile, ester, amide, ketone or ether radicals, with polythene in solution or dispersion and which has previously been activated by treatment with one or more free radical generating substances. The monomers may be vinyl acetate, methyl vinyl ketone, styrene, methyl, ethyl, butyl or isobutyl acrylate or methacrylate, acrylonitrile, methacrylonitrile, vinyl chloride or vinylidene chloride. The free radical generating substances may be benzoyl, lauroyl or phthaloyl peroxide, cumene or tertiary butyl hydroperoxide, azo-diisobutyronitrile or a water-soluble persulphate. The polythene may be prepared by polymerization of gaseous ethylene and should preferably have an average molecular weight of at least 20,000. Activation and polymerization may be carried out in solution in organic solvents, e.g. toluene, petroleum ether, trichloroethylene and benzene, and the product recovered by precipitation, e.g. with methanol or ethanol, or in dispersion in a non-solvent, e.g. aqueous media containing salts of long-chain alkyl sulphates such as sodium dodecyl sulphate, and the product recovered by coagulation, e.g. with aluminium sulphate solution. Preferably polythene solutions are heated with free radical generating substances for 5 minutes to 1 hour and, after cooling, if necessary, the monomers added and the polymerization effected, optionally under pressure. Films may be produced by extrusion or casting from hot solutions and may be heat sealed to plain and moisture-proof regenerated cellulose films. Specifications 679,562, 694,408, 718,515, 764,297 and Canadian Specification 494,421 are referred to.
GB783790D Expired GB783790A (en)

Publications (1)

Publication Number Publication Date
GB783790A true GB783790A (en) 1900-01-01

Family

ID=1752007

Family Applications (1)

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GB783790D Expired GB783790A (en)

Country Status (1)

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GB (1) GB783790A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3102050A (en) * 1960-04-21 1963-08-27 Phillips Petroleum Co Method of coating particulated resinous material by polymerization technique
US3222423A (en) * 1961-11-15 1965-12-07 Monsanto Chemicals Method of increasing grafting efficiency in graft copolymerization
US3342900A (en) * 1964-05-05 1967-09-19 Grace W R & Co Process of grafting acrylonitrile onto peroxidized polyethylene
US3347956A (en) * 1964-08-27 1967-10-17 Monsanto Co Graft blends and method of preparing same
US3356762A (en) * 1965-11-15 1967-12-05 Dow Chemical Co Vulcanizable ethylene copolymer rubbers
US3509236A (en) * 1966-02-19 1970-04-28 Dynamit Nobel Ag Molding compositions comprising vinylidene chloride
FR2179780A1 (en) * 1972-03-30 1973-11-23 Bayer Ag
US4578428A (en) * 1983-12-16 1986-03-25 Montedison S.P.A. Modified olefine polymers and process for their manufacture

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3102050A (en) * 1960-04-21 1963-08-27 Phillips Petroleum Co Method of coating particulated resinous material by polymerization technique
US3222423A (en) * 1961-11-15 1965-12-07 Monsanto Chemicals Method of increasing grafting efficiency in graft copolymerization
US3342900A (en) * 1964-05-05 1967-09-19 Grace W R & Co Process of grafting acrylonitrile onto peroxidized polyethylene
US3347956A (en) * 1964-08-27 1967-10-17 Monsanto Co Graft blends and method of preparing same
US3356762A (en) * 1965-11-15 1967-12-05 Dow Chemical Co Vulcanizable ethylene copolymer rubbers
US3509236A (en) * 1966-02-19 1970-04-28 Dynamit Nobel Ag Molding compositions comprising vinylidene chloride
FR2179780A1 (en) * 1972-03-30 1973-11-23 Bayer Ag
US4578428A (en) * 1983-12-16 1986-03-25 Montedison S.P.A. Modified olefine polymers and process for their manufacture

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