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Novel organo siloxy-aluminium oxide polymers and method for their preparation

机译:新型有机甲硅烷氧基-氧化铝聚合物及其制备方法

摘要

An organosiloxy-aluminium oxide polymer is made by reacting a triorganosiloxy hydrocarbonoxy aluminium with water, a carboxylic acid anhydride or a triorganosiloxy acyloxy aluminium. Reactants (other than water) specified are R3SiOAl(OR1)2, (R11CO)2O and R1113SiOAl(OOCR11)2, wherein R, R1, R11 and R111 are each an alkyl, aryl, aralkyl or alkaryl radical. If desired the chain-stopper (R3SiO)2AlOR1 and cross-linking reactant Al(OR1)3 can be added. The siloxy-aluminium reactants can be made by reacting a triorganoacyloxy silane with an alkoxy-aluminium. In typical examples (2) triisopropoxy aluminium and triphenylacetoxy silane were heated at 80 DEG C. in dry cumene to yield, after removal of solvent and isopropyl acetate formed during the reaction, triphenylsiloxy diisopropoxy aluminium; (3) trimethylsiloxy diisopropoxy aluminium in toluene and isopropanol were reacted with water to yield a polymer. Uses: The polymers alone or in admixture with other resins, pigments, fillers, &c., can be used as varnishes, lacquers and paints; as moulding and laminating resins; as finishing agents for glass fibres; as hydraulic, heatexchange and lubricating liquids; as modifiers for silicone, alkyd, epoxy and phenolic resins; and for making block and graft polymers.
机译:通过使三有机甲硅烷氧基烃氧基铝与水,羧酸酐或三有机甲硅烷氧基酰氧基铝反应来制备有机甲硅烷氧基-氧化铝聚合物。指定的反应物(水除外)为R3SiOAl(OR1)2,(R11CO)2O和R1113SiOAl(OOCR11)2,其中R,R1,R11和R111分别为烷基,芳基,芳烷基或烷芳基。如果需要,可以添加链终止剂(R3SiO)2AlOR1和交联反应物Al(OR1)3。可以通过使三有机酰氧基硅烷与烷氧基铝反应来制备甲硅烷氧基铝反应物。在典型的实施例中,(2)将三异丙氧基铝和三苯基乙酰氧基硅烷在无水异丙苯中于80℃加热,除去反应过程中形成的溶剂和乙酸异丙酯后,得到三苯基甲硅烷氧基二异丙氧基铝。 (3)使在甲苯中的三甲基甲硅烷氧基二异丙氧基铝和异丙醇与水反应,得到聚合物。用途:单独或与其他树脂,颜料,填料等混合使用的聚合物,可用作清漆,清漆和油漆;作为模塑和层压树脂;作为玻璃纤维的整理剂;用作液压,热交换和润滑液体;作为有机硅,醇酸,环氧和酚醛树脂的改性剂;用于制造嵌段和接枝聚合物。

著录项

  • 公开/公告号GB915714A

    专利类型

  • 公开/公告日1963-01-16

    原文格式PDF

  • 申请/专利权人 HUGHES AIRCRAFT COMPANY;

    申请/专利号GB19610007391

  • 发明设计人

    申请日1961-02-28

  • 分类号C07F7/08;C08G79/10;

  • 国家 GB

  • 入库时间 2022-08-23 17:01:03

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