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A method for the production of composite materials with improved strength on the basis of silicate materials and polyolefin resins

机译:一种基于硅酸盐材料和聚烯烃树脂生产强度提高的复合材料的方法

摘要

1278808 Coating DOW CORNING CORP 4 Dec 1969 [3 Jan 1969] 59191/69 Heading B2E [Also in Divisions B5 C1 and C3] Composites of (a) solid siliceous materials and (b) polymers and copolymers of ethylene and propylene are produced by (1) applying to the surface of a silane X a R 3-a SiRSP1/SP (c) and partial condensates thereof (in which X is the hydroxyl group or a hydrolysable radical; R is a 1-6 C alkyl; RSP1/SP is an organo-functional radical selected from amino, mercapto, aryl, alkaryl and aralkyl of no more than 14C, monovalent linear aliphatic hydrocarbon containing a tertiary hydrogen atom and having no more than 18C and monovalent hydrocarbon containing a vinyl linkage and having no more than 18 C; and a has a value of 2 or 3), (2) applying to the surface of at least one of the silane treated (a) or (b) a chlorinated organic compound (d) selected from octachloro cyclopentene, chlorinated xylene, perchlorinated xylene, perchloro-4, 4-dimethylbiphenyl, chlorendic acid, chlorendic anhydride, octochloropropane, hexachloroethane and trichloromelamine; (3) contacting (a) and (b) with the treated surface or surfaces between them, and (4) applying energy, e.g. heat to the composite of (a), (c), (d) and (b) until a bond is formed between them. The chlorinated organic compound (d) may be applied to (a) or to the surface of (b). The siliceous material may be glass fibres and cloth, asbestos, mica, silica in the form of sand and glass panels. The glass fibres may be in the form of rovings, yarn, chopped fibres, strand and bundles. The silane coating can be applied from aqueous solution and the chlorinated organic compound from, e.g. toluene or acetone, by dipping, brushing or spraying. In a modification the silane and chlorinated material can be dissolved in a mutual solvent and applied from a single bath. The treated siliceous material and the resins may be bonded by contacting the material with molten resin; heating and pressing laminates of treated glass cloth and polymer film; blending the chopped coated glass fibres with resin pellets or powder to form a moulding compound which is injection moulded. Ultraviolet light or gamma radiation can also be applied to the composite. Alternatively, the silane coated siliceous material may be bonded with the chlorinated organic compound coated resins, e.g. by thermo-forming or injection moulding. Further, a blend of the resin particles and a particulate inert carrier, e.g. talc, silicas and clays which has been impregnated or coated with the chlorinated organic compound may be heated to the softening point of the polymer and bonded to the silanetreated siliceous material. In the Examples (3) chopped glass fibres which had been treated with a 2-4% by weight solution of N-(2- aminoethyl)-3-aminopropyl trimethoxy silane and then immersed in a 1.5% by weight solution of octachloro cyclopentene and polypropylene powder were blended using glass fibre loadings of 15, 25, 35 and 45% by weight and injection moulded; (4) polypropylene was blended with 35% chopped glass roving which had been treated by dipping in a toluene bath containing 2% by weight chlorinated xylene and a silane coupling agent. The silanes used were a) mercaptopropyl trimethoxy silane (0.5%), b) as (a) (1%), (c) isobutyl trimethoxy silane (1%), d) vinyltrimethoxy silane (0.8%), phenyltrimethoxy silane (1%), e) gammamethyl-4-dimethylpentyltrichlorosilane (1.2%) and injection moulded; (6) talc was impregnated with various amounts of chlorinated organic material ((a) 20% octochloro cyclopentene, (b) 10% (a), (c) 20% chlorinated xylene, (d) 20% chlorendic anhydride) and added to a blend of 65% by weight polypropylene powder and 35% by weight chopped glass fibre. The glass had been treated with 1.5% by weight solution of: The blends were injection moulded; (7) ground quartz (particle size 5 microns) was ballmilled with 10% by weight octachloro cyclopentene and the treated carrier added to the polypropylene-glass fibre blends described in 6).
机译:1278808 Coating DOW CORNING CORP涂料1969年12月4日[1969年1月3日] 59191/69标题B2E [也在B5 C1和C3部门中]由(a)固体硅质材料和(b)乙烯与丙烯的聚合物及共聚物制成的复合物,其制备方法如下: 1)在硅烷X的表面上施加R 3-a SiR 1 (c)及其部分缩合物(其中X为羟基或可水解基团; R为1-6 C烷基; R 1 是选自氨基,巯基,芳基,烷芳基和芳烷基的不超过14C的有机官能团,是含叔氢原子且不超过18C的单价线性脂肪烃含有乙烯基键且不超过18 C的一价烃;且a的值为2或3),(2)将氯代氯化物涂在至少一种经硅烷处理的(a)或(b)的表面上选自八氯环戊烯,氯化二甲苯,高氯二甲苯,全氯4、4-二甲基联苯,氯苯二酸,氯的有机化合物(d)酸酐,八氯丙烷,六氯乙烷和三氯三聚氰胺; (3)使(a)和(b)与已处理表面或它们之间的表面接触,以及(4)施加能量,例如加热至(a),(c),(d)和(b)的复合材料,直到它们之间形成键。氯化有机化合物(d)可以施用于(a)或(b)的表面。硅质材料可以是玻璃纤维和布,石棉,云母,沙子和玻璃板形式的二氧化硅。玻璃纤维可以是粗纱,纱线,短切纤维,线和束的形式。硅烷涂层可以从水溶液中施加,而氯化有机化合物可以从例如水中施加。甲苯,丙酮,浸涂,刷涂或喷涂。在一种改型中,可以将硅烷和氯化材料溶解在互溶剂中并从单个浴中施加。处理过的硅质材料和树脂可以通过使材料与熔融树脂接触而粘结;例如,加热和压制处理过的玻璃布和聚合物薄膜的层压板;将切碎的涂层玻璃纤维与树脂粒料或粉末共混以形成模塑料,然后将其注塑成型。紫外线或伽马射线也可以施加到复合材料上。可选择地,硅烷涂覆的硅质材料可以与氯化有机化合物涂覆的树脂例如树脂结合。通过热成型或注塑成型。此外,树脂颗粒和颗粒状惰性载体的共混物如可以将已经用氯化有机化合物浸渍或涂覆的滑石,二氧化硅和粘土加热到聚合物的软化点,并结合到硅烷处理的硅质材料上。在实施例(3)中,将短切玻璃纤维用2-4重量%的N-(2-氨基乙基)-3-氨丙基三甲氧基硅烷溶液处理,然后浸入1.5重量%的八氯环戊烯溶液中。用15、25、35和45%(重量)的玻璃纤维混合聚丙烯粉末并注塑。 (4)将聚丙烯与35%的切碎的玻璃粗纱混合,该粗纱通过浸入含有2%(重量)的氯化二甲苯和硅烷偶联剂的甲苯浴中进行处理。使用的硅烷为a)巯基丙基三甲氧基硅烷(0.5%),b)(a)(1%),(c)异丁基三甲氧基硅烷(1%),d)乙烯基三甲氧基硅烷(0.8%),苯基三甲氧基硅烷(1%) ),e)γ-甲基-4-二甲基戊基三氯硅烷(1.2%)并注塑成型; (6)将滑石粉浸入各种量的氯化有机物质中((a)20%的八氯环戊烯,(b)10%的(a),(c)20%的氯化二甲苯,(d)20%的氯丁酸酐)并添加到65%(重量)的聚丙烯粉末和35%(重量)的短切玻璃纤维的混合物。玻璃已经用1.5重量%的以下溶液处理:将共混物注塑成型; (7)将磨碎的石英(粒度为5微米)与10重量%的八氯环戊烯进行球磨并将处理过的载体加入到6)中所述的聚丙烯-玻璃纤维共混物中。

著录项

  • 公开/公告号DE1964538A1

    专利类型

  • 公开/公告日1970-06-25

    原文格式PDF

  • 申请/专利权人 DOW CORNING CORP.;

    申请/专利号DE19691964538

  • 发明设计人 CHARLES HARTLEINROBERT;

    申请日1969-12-23

  • 分类号C08K1/20;

  • 国家 DE

  • 入库时间 2022-08-23 10:47:13

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