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GB1029635A - Vinyl fluoride polymers - Google Patents

Vinyl fluoride polymers

Info

Publication number
GB1029635A
GB1029635A GB2793863A GB2793863A GB1029635A GB 1029635 A GB1029635 A GB 1029635A GB 2793863 A GB2793863 A GB 2793863A GB 2793863 A GB2793863 A GB 2793863A GB 1029635 A GB1029635 A GB 1029635A
Authority
GB
United Kingdom
Prior art keywords
boron
nitrogen
hydrazine
listed
exemplified
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
GB2793863A
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.)
Montedison SpA
Original Assignee
Montedison SpA
Montecatini Societa Generale per lIndustria Mineraria e Chimica SpA
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 Montedison SpA, Montecatini Societa Generale per lIndustria Mineraria e Chimica SpA filed Critical Montedison SpA
Publication of GB1029635A publication Critical patent/GB1029635A/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
    • C08F14/00Homopolymers 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 a halogen
    • C08F14/18Monomers containing fluorine
    • C08F14/20Vinyl fluoride

Landscapes

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

Abstract

Vinyl fluoride is polymerized or copolymerized using a boron compound as the catalyst of the formula <FORM:1029635/C3/1> in which R1, R11 and R111 are the same or different linear or branched-atom alkyl groups containing 1 to 6 carbon atoms, cycloalkyl, aralkyl or aryl groups and R111 may additionally be a hydrogen or halogen atom or an OR group in which R is an organic radical which may be any of the structures listed for R1 and R11, Y is a molecule of ammonia or of hydroxylamine or of a nitrogen-containing organic base or of hydrazine and n is the co-ordination number of the nitrogen atoms present in Y. The catalyst may be preformed or formed in situ by complexing boron alkyls and their derivatives with the nitrogen containing base. Specified boron alkyl derivatives are trimethyl boron, triethyl boron, tripropyl boron, triisobutyl boron, tricyclohexyl boron, triphenyl boron, tri-paratolyl boron, tribenzylboron, diphenyl borane, diethyl borane, boron dimethyl fluoride, boron di-n-butyl chloride, isobutoxy diphenyl boron and triethyl diborane. Exemplified nitrogen containing bases are: ammonia, hydrazine, hydroxylamine, pyridine, monomethylamine, piperazine, aniline, indole, urea, phenyl hydrazine, ethanolamine, morpholine, ethyleneimine, diphenylamine and benzylamine. Other bases specified are: dimethylamine, mono- and di-ethylamine, p-chloroaniline, toluidine, piperidine, quinuclidine, ethylenediamine, triethylenediamine, hexamethylenediamine, guanidine and melamine. The polymerization may be effected in bulk or in the presence of a liquid solvent or dispersing agent. A number of solvents are listed of which cyclohexane and methylene chloride are exemplified. Water may also be used, preferably together with a pH buffer and a dispersing and emulsifying agent. A number of monomers that may be copolymerized with vinyl fluoride are listed; those exemplified are ethylene, vinyl chloride, tetrafluoroethylene, perfluoropropylene and 3,3,3-trifluoropropylene. Suitable plasticizers include dibutylphthalate, tricresyl-phosphate, g - butyr - rolactone, di-methyl-sulphoxide and acetophenone. The polymers may be formed into films, fibres, laminae and shaped and extruded articles.
GB2793863A 1962-07-18 1963-07-15 Vinyl fluoride polymers Expired GB1029635A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT1444762 1962-07-18

Publications (1)

Publication Number Publication Date
GB1029635A true GB1029635A (en) 1966-05-18

Family

ID=11145066

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2793863A Expired GB1029635A (en) 1962-07-18 1963-07-15 Vinyl fluoride polymers

Country Status (4)

Country Link
AT (1) AT250005B (en)
DK (1) DK106300C (en)
ES (1) ES289945A1 (en)
GB (1) GB1029635A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1045433A1 (en) * 1997-12-27 2000-10-18 Tokyo Electron Limited Fluorocarbon film and method for forming the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1045433A1 (en) * 1997-12-27 2000-10-18 Tokyo Electron Limited Fluorocarbon film and method for forming the same
EP1045433A4 (en) * 1997-12-27 2004-08-25 Tokyo Electron Ltd FLUOROCARBON FILM AND MANUFACTURING METHOD

Also Published As

Publication number Publication date
DK106300C (en) 1967-01-16
AT250005B (en) 1966-10-25
ES289945A1 (en) 1964-04-16

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