GB896981A - Method for manufacturing polyvinyl ethers - Google Patents

Method for manufacturing polyvinyl ethers

Info

Publication number
GB896981A
GB896981A GB4478860A GB4478860A GB896981A GB 896981 A GB896981 A GB 896981A GB 4478860 A GB4478860 A GB 4478860A GB 4478860 A GB4478860 A GB 4478860A GB 896981 A GB896981 A GB 896981A
Authority
GB
United Kingdom
Prior art keywords
aluminium
diethyl
ethyl
magnesium
chloride
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
GB4478860A
Inventor
Senji Nakano
Koichiro Iwasaki
Hideo Fukutani
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.)
Mitsubishi Kasei Corp
Original Assignee
Mitsubishi Kasei Corp
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 Mitsubishi Kasei Corp filed Critical Mitsubishi Kasei Corp
Priority to GB4478860A priority Critical patent/GB896981A/en
Publication of GB896981A publication Critical patent/GB896981A/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
    • C08F16/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
    • C08F16/12Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical

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

Crystalline polyvinyl ethers are prepared by a method which comprises polymerizing vinyl ethers at a temperature not below -30 DEG C. in the presence of a catalyst composition comprising (A) boron trifluoride or a complex thereof with water, an alcohol, ether, aldehyde or carboxylic acid and (B) an organometallic compound of a metal of Group I, II or III of the Periodic Table. The ether may be methyl, ethyl, propyl, n-butyl, isobutyl, amyl, octyl, 2-ethylhexyl, lauryl, stearyl, benzyl or cyclohexyl vinyl ether. Specified organometallic compounds are trimethyl aluminium, triethyl aluminium, tributyl aluminium, triisobutyl aluminium, trioctyl aluminium, dimethyl magnesium, diethyl magnesium, diethyl zinc, butyl magnesium chloride, hexyl magnesium chloride, phenyl magnesium bromide, dimethyl aluminium chloride, diethyl aluminium bromide, diethyl aluminium chloride, ethyl aluminium dichloride, diisobutyl aluminium chloride, diisobutyl aluminium fluoride, ethyl magnesium methoxide, ethyl aluminium dimethoxide, diethyl aluminium hydride, diisobutyl aluminium hydride, butyl lithium, phenyl sodium, and complex salts of ethyl sodium with aluminium triethyl and diethyl aluminium chloride and lithium octyl with aluminium trioctyl. Polymerization may be effected in an inert diluent such as petroleum ether, n-hexane, n-heptane, benzene, toluene and ethyl ether. Amorphous polymer may be removed from the product by extraction with a selective solvent, e.g. water, methanol or methyl ethyl ketone. The products may be used in adhesives and coatings, and made into filaments, films and sheets. Examples described the polymerization of isobutyl vinyl ether in the presence of boron trifluoride etherate and (1) triethyl aluminium and (4) diethyl magnesium; and of methyl vinyl ether in the presence of (2) boron trifluoride etherate and triethyl aluminium, and boron trifluoride and (3) triethyl aluminium and (5) triisobutyl aluminium.
GB4478860A 1960-12-30 1960-12-30 Method for manufacturing polyvinyl ethers Expired GB896981A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4478860A GB896981A (en) 1960-12-30 1960-12-30 Method for manufacturing polyvinyl ethers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4478860A GB896981A (en) 1960-12-30 1960-12-30 Method for manufacturing polyvinyl ethers

Publications (1)

Publication Number Publication Date
GB896981A true GB896981A (en) 1962-05-23

Family

ID=10434742

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4478860A Expired GB896981A (en) 1960-12-30 1960-12-30 Method for manufacturing polyvinyl ethers

Country Status (1)

Country Link
GB (1) GB896981A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5393856A (en) * 1993-08-11 1995-02-28 Amoco Corporation Liquid phase and aqueous solutions of poly(vinyl methyl ether) from highly purified vinyl methyl ether monomer

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5393856A (en) * 1993-08-11 1995-02-28 Amoco Corporation Liquid phase and aqueous solutions of poly(vinyl methyl ether) from highly purified vinyl methyl ether monomer

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