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GB1015410A - Polymerization and copolymerization of isoprene - Google Patents

Polymerization and copolymerization of isoprene

Info

Publication number
GB1015410A
GB1015410A GB3759264A GB3759264A GB1015410A GB 1015410 A GB1015410 A GB 1015410A GB 3759264 A GB3759264 A GB 3759264A GB 3759264 A GB3759264 A GB 3759264A GB 1015410 A GB1015410 A GB 1015410A
Authority
GB
United Kingdom
Prior art keywords
butadiene
isoprene
polymerization
mol
per cent
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
GB3759264A
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.)
Goodyear Tire and Rubber Co
Original Assignee
Goodyear Tire and Rubber 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 Goodyear Tire and Rubber Co filed Critical Goodyear Tire and Rubber Co
Publication of GB1015410A publication Critical patent/GB1015410A/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
    • C08F136/00Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F136/02Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F136/04Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
    • C08F136/08Isoprene
    • 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
    • C08F236/00Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F236/02Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F236/04Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
    • C08F236/08Isoprene

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

Abstract

Polyisoprene, and copolymers of isoprene with at least one other conjugated diolefin, is made by effecting the polymerization in the presence of a catalyst comprising a mixture of an organoaluminium compound containing no halogen, iodide, and a T1 tetrahalide wherein the organoaluminium compound ranges from 50 to 80 mol. per cent, the iodine from 5 to 40 mol. per cent, and the Ti halide from 10 to 45 mol. per cent of the mixture. The other diolefins may be butadiene-1,3, 2-isopropyl butadiene-1,3, 2,3-dimethyl butadiene, piperylene, or hexadiene. The organoaluminium compound may be a di- or tri-hydrocarbon aluminium compound. The polymerization may be effected in bulk or in an inert hydrocarbon diluent. The catalyst may be formed in situ or preformed. Exemplified catalysts are triisobutyl aluminium, iodine and TiCl4, in varying proportions. There are three examples of the copolymerization of isoprene and butadiene.
GB3759264A 1963-09-30 1964-09-15 Polymerization and copolymerization of isoprene Expired GB1015410A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US31235463A 1963-09-30 1963-09-30

Publications (1)

Publication Number Publication Date
GB1015410A true GB1015410A (en) 1965-12-31

Family

ID=23211077

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3759264A Expired GB1015410A (en) 1963-09-30 1964-09-15 Polymerization and copolymerization of isoprene

Country Status (2)

Country Link
GB (1) GB1015410A (en)
NL (1) NL6411391A (en)

Also Published As

Publication number Publication date
NL6411391A (en) 1965-03-31

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