GB1057894A - Crystalline block copolymers - Google Patents

Crystalline block copolymers

Info

Publication number
GB1057894A
GB1057894A GB5098864A GB5098864A GB1057894A GB 1057894 A GB1057894 A GB 1057894A GB 5098864 A GB5098864 A GB 5098864A GB 5098864 A GB5098864 A GB 5098864A GB 1057894 A GB1057894 A GB 1057894A
Authority
GB
United Kingdom
Prior art keywords
polymerization
branched chain
methylpentene
molecular weight
control agent
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
GB5098864A
Inventor
James Keith Hambling
Geoffrey Winton Alderson
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.)
BP PLC
Original Assignee
BP PLC
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 BP PLC filed Critical BP PLC
Priority to GB5098864A priority Critical patent/GB1057894A/en
Priority to FR41603A priority patent/FR1457931A/en
Priority to NL6516232A priority patent/NL6516232A/xx
Priority to BE673795D priority patent/BE673795A/xx
Publication of GB1057894A publication Critical patent/GB1057894A/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
    • C08F297/00Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
    • C08F297/06Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
    • C08F297/08Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (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

Crystalline block copolymers of normal alpha-olefins and branched chain olefins of the formula CH2=CHR in which R is a C3-C10 branched chain alkyl group are made by polymerizing a normal alpha-olefin in the absence of a molecular weight control agent to form a first living polymer and polymerizing the branched chain olefin in the presence of the first living polymer, a molecular weight control agent being admitted to the polymerization zone some time after the start of the polymerization of the branched chain olefin, both stages of polymerization being effected in the presence of a catalyst obtained from (a) a solid crystalline compound of a metal from Groups IV, V, VI, VII and VIII of the Periodic Table, the metal being in a valency state lower than its maximum, and (b) an organometallic compound or hydride of a metal of Groups I, II or III, or an organometallic compound of tin. Normal and branched chain olefins specified are ethylene, propylene, pentene-1, heptene-1, 3-methylbutene-1, 3-methylpentene - 1, 4 - methylpentene - 1, 3-ethylpentene-1 and 4,6-dimethylheptene-1. The preferred molecular weight control agent is hydrogen. The resulting copolymers are insoluble in hot acetone and are capable of forming transparent mouldings. The example describes polymerizing decene-1 in heptane in the presence of a titanium trichloride/aluminium diethylchloride catalyst, continuing polymerization with 4-methylpentene-1, and admitting hydrogen to the polymerization after the start of the polymerization of the 4-methylpente-1.
GB5098864A 1964-12-15 1964-12-15 Crystalline block copolymers Expired GB1057894A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
GB5098864A GB1057894A (en) 1964-12-15 1964-12-15 Crystalline block copolymers
FR41603A FR1457931A (en) 1964-12-15 1965-12-09 Process for producing a substantially crystalline block copolymer of a branched chain alpha-ethylenic hydrocarbon and copolymer obtained
NL6516232A NL6516232A (en) 1964-12-15 1965-12-14
BE673795D BE673795A (en) 1964-12-15 1965-12-15

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB5098864A GB1057894A (en) 1964-12-15 1964-12-15 Crystalline block copolymers

Publications (1)

Publication Number Publication Date
GB1057894A true GB1057894A (en) 1967-02-08

Family

ID=10458203

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5098864A Expired GB1057894A (en) 1964-12-15 1964-12-15 Crystalline block copolymers

Country Status (4)

Country Link
BE (1) BE673795A (en)
FR (1) FR1457931A (en)
GB (1) GB1057894A (en)
NL (1) NL6516232A (en)

Also Published As

Publication number Publication date
NL6516232A (en) 1966-06-16
FR1457931A (en) 1966-01-24
BE673795A (en) 1966-06-15

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