Polymerization of olefins
    31.
    发明授权
    Polymerization of olefins 失效
    烯烃聚合

    公开(公告)号:US6048817A

    公开(公告)日:2000-04-11

    申请号:US65464

    申请日:1998-04-24

    摘要: A particulate phyllosilicate mixture comprising a mixture containing a phyllosilicte belonging to the smectite group and a phyllosilicate belogning to the mica group, the phyllosilicate particle having a content of the phyllosilicate belonging to the smectite group of 0.1 to 50% by weight and optionally satisfying the following requirements (a) to (c):(a): the average particle diameter is 20 to 1000 .mu.m with not more than 20% of the total number of particles being accounted for by particles having a particle diameter of not more than 10 .mu.m;(b): the crushing strength of the particle is not less than 0.5 MPa as measured with a microcompression tester and(c): the bulk density of the particle of not less than 0.6 g/cm.sup.3.Polymerization of olefins with catalyst comprising the particulate phyllosilicate mixture as a carrier or support for the catalysts is also disclosed.

    摘要翻译: 一种颗粒状页硅酸盐混合物,其包含含有属于蒙脱石组的页硅酸盐的混合物和与云母基团相连的页硅酸盐,具有属于蒙皂石组的页硅酸盐含量为0.1至50重量%的页硅酸盐颗粒,并且任选地满足以下 要求(a)至(c):(a):平均粒径为20〜1000μm,粒径不大于10μm的粒子占总粒数的20%以下 m; (b):使用微压缩试验机测定,颗粒的抗碎强度不小于0.5MPa,(c)颗粒的堆积密度不小于0.6g / cm3。 还公开了含有颗粒状页硅酸盐混合物的催化剂的烯烃与催化剂的载体或载体的聚合。

    Method for reacting organic halides
    39.
    发明授权
    Method for reacting organic halides 失效
    使有机卤化物反应的方法

    公开(公告)号:US3984483A

    公开(公告)日:1976-10-05

    申请号:US459483

    申请日:1974-04-10

    摘要: A method for carrying out reactions of the Friedel-Crafts type, such as alkylation, acylation, polymerization, sulfonylation and dehydrohalogenation. The reactions are catalyzed by arene-metal tricarbonyl complexes and when the reaction vessel contains aromatic substrates the catalyst may be generated in situ from a metallic hexacarbonyl. The arene-metal tricarbonyl catalyst is more selective than conventionally employed Friedel-Craft catalysts in that it yields generally para isomers with little of the ortho variety and very little if any of the meta variety when the aromatic substrate is reacted with organic halide. It is also possible to form the arene-metal tricarbonyl catalyst outside of the reaction vessel and then proceed by adding it to the vessel containing the substrate and the organic halide as is the case with dehydrohalogenation reactions wherein there are no aromatic rings available, the substrate in that instance being aliphatic.

    摘要翻译: 用于进行Friedel-Crafts类型的反应的方法,例如烷基化,酰化,聚合,磺酰化和脱卤化氢。 反应由芳族金属三羰基络合物催化,并且当反应容器含有芳族基底时,可以从金属六羰基原位产生催化剂。 芳族金属三羰基催化剂比常规使用的Friedel-Craft催化剂更具选择性,因为当芳族底物与有机卤化物反应时,它产生通常具有少量邻位变化的非对位异构体,并且如果有任何间位异构体则极少。 也可以在反应容器的外部形成芳族金属三羰基催化剂,然后通过将其加入到含有底物和有机卤化物的容器中进行,如脱卤化氢反应的情况,其中不存在芳环,基材 在这种情况下是脂肪族的。