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A method for the preparation of polymers of hexa fluorine cyclo penta diene and / or perfluoro dicyclo penta diene

机译:一种六氟环戊二烯和/或全氟二环戊二烯的聚合物的制备方法

摘要

Octafluorocyclopentene may be hydrogenated in the presence of an alumina supported palladium catalyst at 175 DEG to 200 DEG C. to give a mixture of 1,2-dihydrooctafluorocyclopentane and a minor proportion of 1,1,2-trihydroheptafluorocyclopentane. The product may be treated with potassium hydroxide at 155 DEG to 160 DEG C. to give a mixture of hexafluorocyclopentadiene, 1-hydroheptafluorocyclopentene and 3-hydroheptafluorocyclopenteneALSO:Polymers of hexafluorocyclopentadiene may be prepared by subjecting hexafluorocyclopenta diene to polymerization conditions in the presence of a free radical forming catalyst and optionally one or more polymerizable ethylenically unsaturated compounds. Specified comonomers are ethylene, propylene, isobutylene, styrene, vinyl chloride, vinyl fluoride, vinylidene chloride, vinylidene fluoride, trifluoroethylene, tetrafluoroethylene, chlorotrifluoroethylene, hexafluoropropene, acrylic and methacrylic acids, esters and nitriles, vinyl esters, vinyl ethers and conjugated dienes. Polymerization may be effected in bulk, solution or dispersion, to give liquid polymers suitable as plasticizers and hydraulic fluids and solid polymers suitable for moulding articles and pressing into films. The polymers heat cured or vulcanized. Examples describe (1) the bulk polymerization of hexafluorocyclopentadiene in the presence of nitrogen difluoride or azobisisobutyronitrile; (2) the copolymerization of hexafluorocyclopentadiene and tetrafluoroethylene in perfluoro-(dimethylcyclobutane) in the presence of nitrogen difluoride; the bulk copolymerization of hexafluorocyclopentadiene with (3) methyl methacrylate and (4) acrylonitrile in the presence of azobisisobutyronitrile; and (5) the copolymerization of hexafluorocyclopentadiene with hexafluoropropene and vinylidene fluoride in aqueous dispersion in the presence of ammonium persulphate, ammonium perfluorooctanoate and disodium phosphate.
机译:八氟环戊烯可以在氧化铝负载的钯催化剂存在下在175℃至200℃下氢化,得到1,2-二氢八氟环戊烷和少量的1,1,2-三氢七氟环戊烷的混合物。该产物可以在155-160℃下用氢氧化钾处理,得到六氟环戊二烯,1-氢七氟环戊烯和3-氢七氟环戊烯的混合物ALSO:六氟环戊二烯的聚合物可以通过在自由存在下使六氟环戊二烯经受聚合条件来制备。自由基形成催化剂和任选的一种或多种可聚合的烯键式不饱和化合物。特定的共聚单体是乙烯,丙烯,异丁烯,苯乙烯,氯乙烯,氟乙烯,偏二氯乙烯,偏二氟乙烯,三氟乙烯,四氟乙烯,三氟氯乙烯,六氟丙烯,丙烯酸和甲基丙烯酸,酯和腈,乙烯基酯,乙烯基醚和共轭二烯。聚合可以本体,溶液或分散体的形式进行,以得到适合用作增塑剂和液压流体的液体聚合物和适合于模制品并压制成膜的固体聚合物。聚合物被热固化或硫化。实例描述(1)在二氟化氮或偶氮二异丁腈的存在下六氟环戊二烯的本体聚合; (2)在二氟化氮存在下,六氟环戊二烯与四氟乙烯在全氟-(二甲基环丁烷)中的共聚;在偶氮二异丁腈存在下,六氟环戊二烯与(3)甲基丙烯酸甲酯和(4)丙烯腈的本体共聚; (5)在过硫酸铵,全氟辛酸铵和磷酸二钠的存在下,六氟环戊二烯与六氟丙烯和偏二氟乙烯在水分散液中共聚合。

著录项

  • 公开/公告号DE1301494B

    专利类型

  • 公开/公告日1969-08-21

    原文格式PDF

  • 申请/专利权人 E. I. DU PONT DE NEMOURS AND COMPANY;

    申请/专利号DE1965P038175

  • 发明设计人 FERGUSON HARRIS JUN. JOHN;

    申请日1965-11-23

  • 分类号C08D3/14;

  • 国家 DE

  • 入库时间 2022-08-23 12:23:39

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