Method for the activation of phosphomolybdic acid based catalysts
    61.
    发明授权
    Method for the activation of phosphomolybdic acid based catalysts 失效
    磷钼酸催化剂的活化方法

    公开(公告)号:US4321160A

    公开(公告)日:1982-03-23

    申请号:US107673

    申请日:1979-12-27

    CPC分类号: B01J23/94 B01J23/92 B01J27/28

    摘要: The present invention relates to a method for the activation of PMA based catalysts by treating the catalyst precursor with a nitrogen-containing compound such as an oxide of nitrogen gas or a nitrogen acid such as nitric or nitrous at a temperature of from about 125.degree. C. to about 400.degree. C. The method can be employed in a reactor by loading the catalyst precursor, adjusting the reactor temperature to one suitable for activation and optionally sweeping the reactor with an inert gas followed by the treating step. The method herein permits faster, lower temperature catalyst activation than when air activation is employed giving higher oxidative conversion yields and prolonged catalyst life.

    摘要翻译: 本发明涉及一种通过用含氮化合物如硝酸或氮酸如硝酸或亚硝酸的含氮化合物在约125℃的温度下处理催化剂前体来活化PMA基催化剂的方法 至约400℃。该方法可以通过加载催化剂前体在反应器中使用,将反应器温度调节至适合于活化的反应器温度,并任选地用惰性气体吹扫反应器,随后进行处理步骤。 与使用空气活化时相比,本文的方法允许更快,更低温度的催化剂活化,提供更高的氧化转化率和延长的催化剂寿命。

    Method for forming Pt-Si Schottky barrier contact
    63.
    发明授权
    Method for forming Pt-Si Schottky barrier contact 失效
    用于形成PT-SI肖特基屏障接触的方法

    公开(公告)号:US4135998A

    公开(公告)日:1979-01-23

    申请号:US900213

    申请日:1978-04-26

    CPC分类号: H01L21/32131 H01L21/28537

    摘要: Use of a rare gas in combination with oxygen or nitrogen to sputter etch unreacted platinum after formation of a platinum silicide contact structure for the formation of a Schottky Barrier diode in a silicon semiconductor substrate.

    摘要翻译: Pt在PtSi上的溅射蚀刻速率的差异通过在稀有气体环境中溅射蚀刻Pt而增加。 > = 1 vol。 %O2或N2,pref。 Ar contg 10卷 %O2。 该方法结合在Si衬底中形成肖特基势垒电极,特别是通过(a)在Si衬底中形成有源电路元件,(b)用绝缘层涂覆表面,该绝缘层具有暴露Si的至少一个开口( c)在绝缘体和开口中沉积铂层,(d)烧结,在开口中形成PtSi,和(e)如上所述溅射蚀刻未组合的Pt。 蚀刻速率差的增加导致Pt稀释比使用纯Ar更低。 污染较少,没有Cl和S污染。 -

    Method for reacting organic halides
    66.
    发明授权
    Method for reacting organic halides 失效
    反应有机物的方法

    公开(公告)号:US4038324A

    公开(公告)日:1977-07-26

    申请号:US569780

    申请日:1975-04-21

    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.

    Method for reacting organic halides
    67.
    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:US3933752A

    公开(公告)日:1976-01-20

    申请号:US459482

    申请日:1974-04-10

    摘要: A method for carrying out reactions of the Friedel-Crafts types, 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。