GB825882A - Process for producing modified polymers - Google Patents

Process for producing modified polymers

Info

Publication number
GB825882A
GB825882A GB2422/57A GB242257A GB825882A GB 825882 A GB825882 A GB 825882A GB 2422/57 A GB2422/57 A GB 2422/57A GB 242257 A GB242257 A GB 242257A GB 825882 A GB825882 A GB 825882A
Authority
GB
United Kingdom
Prior art keywords
methyl
vinyl
metal
butadiene
dimethyl
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
GB2422/57A
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.)
Phillips Petroleum Co
Original Assignee
Phillips Petroleum Co
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 Phillips Petroleum Co filed Critical Phillips Petroleum Co
Publication of GB825882A publication Critical patent/GB825882A/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
    • C08F279/00Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
    • C08F279/02Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes

Abstract

An olefinically unsaturated hydrocarbon is polymerized in the presence of a conjugated diene polymer and a catalyst selected from (A) a metal halide selected from halides of titanium, zirconium, hafnium, or germanium, and (B) at least one component selected from (a) a compound of the formula M1R1x where M1 is a metal selected from sodium, potassium, lithium, rubidium, cesium, beryllium, magnesium, zinc, cadmium, mercury, aluminium, gallium, indium, or thallium and R1 is hydrogen, an alkyl radical, a cycloalkyl radical or an aryl radical, and x is equal to the valency of the metal; (b) an organometal halide of the formula RmMXn where R is an alkyl, cycloalkyl, or aryl radical, M is a metal selected from aluminium, gallium, indium, thallium, or beryllium, X is a halogen, and m and n are integers whose sum is that of the valency of the metal; and (c) a mixture of an organic halide and at least one metal selected from sodium, potassium, lithium, rubidium, cesium, beryllium, magnesium, zinc, cadmium, mercury, aluminium, gallium, indium, and thallium. The polymerization is preferably effected in the presence of an inert diluent. Specified catalyst mixtures are triethylalumium and/or titanium tri- or tetrachloride, and triethylaluminium and zirconium tetrachloride. The hydrocarbon monomer may be ethylene, propylene, 1-butene, 1-hexene, 1-octene, styrene, alpha-methylstyrene, alkyl-substituted styrenes, 1,3-butadiene, isoprene, piperylene, or 2-methylpentadiene. The diene polymer may be a homopolymer of 1,3-butadiene, isoprene, piperylene, 2-methylpentadiene, 2,3 - dimethyl - 1,3 - butadiene, 1,3-hexadiene, 2,4-hexadiene, 2,4-heptadiene, 2,4-dimethyl - 1,3 - hexadiene, 2,4 - dimethyl - 1,3-octadiene, 2,3 - dimethyl - 4 - phenyl - 1,3-butadiene, or chloroprene, or a copolymer of one or more of the above monomers with one or more of the following monomers, e.g. isoprene, styrene, alpha - methylstyrene, vinyl naphthalene, acrylic acid, methacrylic acid, methyl or ethyl acrylate, methyl or ethyl methacrylate, methyl alpha-chloroacrylate, acrylonitrile, 2-vinyl pyridine, 2 - methyl - 5 - vinylpyridine, methyl isopropenyl ketone, methyl vinyl ketone, methyl vinyl ether, vinyl acetate, vinyl chloride, vinylidene chloride, vinyl furane, or vinylcarbazole. The diluents may be pentane, isooctane, cyclohexane, methylcyclohexane, benzene, toluene, xylene, diethyl ether, or mixtures. The products of the process may be used for making gaskets, tubing, and automobile tyres.
GB2422/57A 1956-01-30 1957-01-23 Process for producing modified polymers Expired GB825882A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US56202556A 1956-01-30 1956-01-30

Publications (1)

Publication Number Publication Date
GB825882A true GB825882A (en) 1959-12-23

Family

ID=22172116

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2422/57A Expired GB825882A (en) 1956-01-30 1957-01-23 Process for producing modified polymers

Country Status (4)

Country Link
CH (1) CH370922A (en)
DE (1) DE1106079B (en)
FR (1) FR1172129A (en)
GB (1) GB825882A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1111831B (en) * 1959-05-29 1961-07-27 Exxon Research Engineering Co Process for the manufacture of hardened resins from liquid polydiolefins
US3458599A (en) * 1965-10-23 1969-07-29 Basf Ag Production of unsaturated graft copolymers from isobutylene polymers

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2917403A1 (en) * 1979-04-28 1980-11-06 Bayer Ag POLYBUTADIEN / ALPHA -OLEFIN-COPOLYMERE
DE3428496A1 (en) * 1984-08-02 1986-02-13 Bayer Ag, 5090 Leverkusen MODIFIED EPDM RUBBER, THEIR PRODUCTION AND THEIR USE FOR THE PRODUCTION OF IMPACT RESISTANT VINYL POLYMERS AND THE VINYL POLYMERS THEREFORE OBTAINED

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE973626C (en) * 1953-11-17 1960-04-14 Karl Dr Dr E H Ziegler Process for the production of high molecular weight polyethylenes
DE1012460B (en) * 1953-11-17 1957-07-18 Dr Dr E H Karl Ziegler Process for the production of high molecular weight polyethylenes
DE1016022B (en) * 1954-01-19 1957-09-19 Dr Dr E H Karl Ziegler Process for the production of high molecular weight polyethylenes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1111831B (en) * 1959-05-29 1961-07-27 Exxon Research Engineering Co Process for the manufacture of hardened resins from liquid polydiolefins
US3458599A (en) * 1965-10-23 1969-07-29 Basf Ag Production of unsaturated graft copolymers from isobutylene polymers

Also Published As

Publication number Publication date
FR1172129A (en) 1959-02-05
CH370922A (en) 1963-07-31
DE1106079B (en) 1961-05-04

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