GB642050A - Improvements in or relating to isobutylene copolymers - Google Patents

Improvements in or relating to isobutylene copolymers

Info

Publication number
GB642050A
GB642050A GB8880/48A GB888048A GB642050A GB 642050 A GB642050 A GB 642050A GB 8880/48 A GB8880/48 A GB 8880/48A GB 888048 A GB888048 A GB 888048A GB 642050 A GB642050 A GB 642050A
Authority
GB
United Kingdom
Prior art keywords
divinyl
copolymers
butadiene
specified
methyl
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
GB8880/48A
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.)
Standard Oil Development Co
Original Assignee
Standard Oil Development 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 Standard Oil Development Co filed Critical Standard Oil Development Co
Publication of GB642050A publication Critical patent/GB642050A/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
    • C08F210/00Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/04Monomers containing three or four carbon atoms
    • C08F210/08Butenes
    • C08F210/10Isobutene
    • C08F210/12Isobutene with conjugated diolefins, e.g. butyl rubber

Landscapes

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

Abstract

Copolymers are made by copolymerizing a mixture of a major proportion of isobutylene, a minor proportion of a multi-olefin having from 4 to 14 carbon atoms per molecule and from 0.1 to 5 per cent by weight of the total mixture, of a divinyl aromatic compound at a temperature between - 40 DEG and - 160 DEG C. in the presence of a Friedel-Craft catalyst. Specified multi-olefins are butadiene, piperylene, dimethyl butadiene, myrcene, allo-ocymene, 2-methyl-3-butyl butadiene-1,3 and 2-methyl-4-nonyl butadiene-1,3. Specified divinyl aromatic compounds are ortho-, para- and metadivinyl benzene, divinyl-naphthyl compounds, divinyl-toluenes, divinyl-xylenes, and di-isopropenyl benzene. The Friedel-Crafts catalyst is employed as a solution in a low-freezing non-complex-forming solvent. The reduced temperature may be obtained by adding to the polymerization mixture liquid propane, ethane, ethylene, fluorochlor organic compounds or solid carbon dioxide. The polymerization may be effected in bulk or in the presence of a diluent, e.g. methyl or ethyl chloride, methylene or ethylene dichloride, chloroform, ethyl trichloride or carbon bisulphide. The diluents may be solvents for the catalyst; other specified solvents are sulphuryl chloride, heptane and hexanes. Specified catalysts are aluminium chloride or bromide, titanium tetrachloride and boron trifluoride. The copolymers may be compounded with plasticizers, e.g. hydrocarbons, dioctylphthalate; curing agents, e.g. sulphur, paraquinone dioxime, or dinitroso benzene; zinc oxide or stearic acid, carbon black, tetramethyl thiuram disulphide, 2-mercapto-benzothiazole, and copolymers of isobutylene and a multi-olefin. The copolymers may be extruded and made into inner tubes.
GB8880/48A 1947-06-06 1948-03-25 Improvements in or relating to isobutylene copolymers Expired GB642050A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US642050XA 1947-06-06 1947-06-06

Publications (1)

Publication Number Publication Date
GB642050A true GB642050A (en) 1950-08-23

Family

ID=22054273

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8880/48A Expired GB642050A (en) 1947-06-06 1948-03-25 Improvements in or relating to isobutylene copolymers

Country Status (3)

Country Link
DE (1) DE815844C (en)
GB (1) GB642050A (en)
NL (1) NL69305C (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2781334A (en) * 1952-05-01 1957-02-12 Exxon Research Engineering Co Divinyl aromatic modified isoolefinmultiolefin copolymers
US2906725A (en) * 1955-10-12 1959-09-29 Exxon Research Engineering Co Synthetic polymer compositions with improved physical properties from mixtures of rubbery polymers
EP1505083A1 (en) * 2003-08-05 2005-02-09 Bayer Inc. Method of improving reversion resistance
EP1566392A1 (en) * 2004-02-23 2005-08-24 Lanxess Inc. Butyl-type rubber with high hardness

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2781334A (en) * 1952-05-01 1957-02-12 Exxon Research Engineering Co Divinyl aromatic modified isoolefinmultiolefin copolymers
US2906725A (en) * 1955-10-12 1959-09-29 Exxon Research Engineering Co Synthetic polymer compositions with improved physical properties from mixtures of rubbery polymers
EP1505083A1 (en) * 2003-08-05 2005-02-09 Bayer Inc. Method of improving reversion resistance
EP1566392A1 (en) * 2004-02-23 2005-08-24 Lanxess Inc. Butyl-type rubber with high hardness

Also Published As

Publication number Publication date
DE815844C (en) 1951-10-04
NL69305C (en)

Similar Documents

Publication Publication Date Title
US3000866A (en) Copolymers of ethylene
US3093621A (en) Sulfur-curable elastomeric copolymers of ethylene, alpha-olefins, and 5-methylene-2-norbornene
US2476000A (en) Hydrocarbon polymers
US2521359A (en) Copolymers of cyclopentadiene
GB719098A (en) Improvements in or relating to low temperature polymerization process
GB642050A (en) Improvements in or relating to isobutylene copolymers
GB677774A (en) An improved manufacture of drying oils
US3349065A (en) Butyl rubber catalyst system utilizing air2x with an hx promoter
GB807178A (en) Improvements in the production of polymerisation products from olefinically unsaturated hydrocarbons
US3063973A (en) Ethylene sulfur-curable terpolymers of a 2-alkylnorbornadiene, ethylene and an alpha-olefin
Hopper Improved cocure of EPDM-polydiene blends by conversion of EPDM into macromolecular cure retarder
US2479450A (en) Chemical process for tripolymers
US2400129A (en) Solution polymerization process
US2577822A (en) Cyclodiene isobutylene copolymers
US2356129A (en) Olefinic polymerization process and product
GB682771A (en) Improvements in or relating to the copolymerization of aromatic divinyl compounds and isobutylene
US2477018A (en) Synthetic rubbery copolymers of normal olefins with diolefins
GB699770A (en) Improvements in or relating to the preparation of copolymers
Kelly et al. Ethylene-propylene copolymers produced with soluble catalysts
US2456354A (en) Copolymers of iso-olefins with thiophene sulfones and process for making same
US3624056A (en) Olefin interpolymers prepared with a catalyst system of a titanium compound, alkyl aryl halide and diaryl magnesium
US2525061A (en) Accelerated polymer curing method
US2694054A (en) Polymerization process using vinyl chloride as diluent
US2815335A (en) Divinyl benzene modified polymers
US2561729A (en) Polymerization of isoolefins with complex friedel-crafts metal halide catalysts