GB1000804A - Diolefine polymerisation - Google Patents

Diolefine polymerisation

Info

Publication number
GB1000804A
GB1000804A GB13905/63A GB1390563A GB1000804A GB 1000804 A GB1000804 A GB 1000804A GB 13905/63 A GB13905/63 A GB 13905/63A GB 1390563 A GB1390563 A GB 1390563A GB 1000804 A GB1000804 A GB 1000804A
Authority
GB
United Kingdom
Prior art keywords
component
formula
compound
iodine
compounds
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
GB13905/63A
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.)
Bayer AG
Original Assignee
Bayer AG
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 Bayer AG filed Critical Bayer AG
Publication of GB1000804A publication Critical patent/GB1000804A/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
    • C08F136/06Butadiene
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/06Aluminium compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/003Compounds containing elements of Groups 4 or 14 of the Periodic Table without C-Metal linkages

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

A polymerization catalyst for 1,3-butadiene is made by reacting (a) an alkyl aluminium compound of the formula AlR1R11R111, in which R1, R11 and R111 may be a C1-C12 aliphatic or cycloaliphatic hydrocarbon radical, and R1 and R11 may also be hydrogen, (b) one or more compounds selected from iodine monochloride, iodine monobromide, or an organic iodine compound, and (c) a titanium compound of the formula T1(R)nX4-n in which n is 1 to 4, X is Cl or Br, and R is an organic carboxylic acid group having 2-20 C-atoms, or an acid group of the formula <FORM:1000804/C3/1> in which R1 represents an alkyl, aryl, or alkoxy radical. In the catalyst 1 mol. of titanium compound (c) is used for 0.5 to 10 mols. of component (b) and 1-20 mols. of component (a) and the molar ratio of component (b) to component (a) is 1 : 1 to 1 : 3. The polymerization is effected by conventional techniques in an inert organic solvent, and small amounts of water may be present. The Specification includes lists of suitable mono- and dibasic acids and also compounds of the given formula, as well as titanium compounds. The organic iodine compound may be methyl, ethyl, n-octyl, isopropyl, tert-butyl, cyclohexyl, or benzyl iodide, iodoform, 1-chloro-4-iodobutane, or 4-iodo-n-butylphenyl ether. The polybutadiene is recovered from the polymerizate by known techniques, e.g. addition of methanol, and vulcanized by conventional methods.
GB13905/63A 1962-04-07 1963-04-08 Diolefine polymerisation Expired GB1000804A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEF36497A DE1165863B (en) 1962-04-07 1962-04-07 Process for the production of polybutadiene
DEF36670A DE1158716B (en) 1962-04-07 1962-04-28 Process for the production of polybutadiene

Publications (1)

Publication Number Publication Date
GB1000804A true GB1000804A (en) 1965-08-11

Family

ID=25975289

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13905/63A Expired GB1000804A (en) 1962-04-07 1963-04-08 Diolefine polymerisation

Country Status (4)

Country Link
BE (1) BE630580A (en)
DE (2) DE1165863B (en)
GB (1) GB1000804A (en)
NL (1) NL291138A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL252800A (en) * 1959-06-19

Also Published As

Publication number Publication date
NL291138A (en) 1900-01-01
DE1165863B (en) 1964-03-19
DE1158716B (en) 1963-12-05
BE630580A (en) 1900-01-01

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