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    • 14. 发明授权
    • Olefin disproportionation catalyst and process
    • 烯烃歧化催化剂和工艺
    • US5098876A
    • 1992-03-24
    • US572736
    • 1990-08-27
    • Jiang-Jen LinRandall T. DePueHoward L. Fong
    • Jiang-Jen LinRandall T. DePueHoward L. Fong
    • B01J23/28B01J31/14B01J31/34C07C6/04C07C6/06
    • B01J31/146B01J23/28C07C6/04C07C6/06B01J2231/543
    • This present invention relates to a disproportionation catalyst and to a process for preparing a disproportionation catalyst comprising forming a calcined composite comprising at least one of molybdenum and rhenium supported on an inorganic oxide support and contacting the calcined composite with an organoborane compound. The invention further relates to a process for the disproportionation of olefinic hydrocarbons comprising contacting at least one olefinic hydrocarbon with a catalyst comprising at least one of molybdenum and rhenium supported on an inorganic oxide support promoted with an organoborane compound. More specifically, the invention relates to the uses of an organoborane compound promoted molybdenum and rhenium supported on an inorganic oxide support for the production of linear alpha olefins from a mixture of internal olefins and ethylene. The invention also relates to the application of the described promoted catalyst for the production of 1,6-heptadiene and 1,6-octadiene from the reaction of cyclopentene with ethylene and propylene, respectively, and the fact that the presence of organoborane in the catalyst allows the reaction to be carried out at very mild temperature while obtaining high product selectivity.
    • 本发明涉及歧化催化剂和制备歧化催化剂的方法,包括形成包含负载在无机氧化物载体上的钼和铼中的至少一种的煅烧复合物,并将煅烧的复合材料与有机硼烷化合物接触。 本发明还涉及一种用于歧化烯烃的方法,包括使至少一种烯烃与包含负载在有机硼烷化合物促进的无机氧化物载体上的钼和铼中的至少一种的催化剂接触。 更具体地,本发明涉及有机硼烷化合物促进负载在无机氧化物载体上的钼和铼用于从内烯烃和乙烯的混合物生产线性α-烯烃的用途。 本发明还涉及分别由环戊烯与乙烯和丙烯反应生成1,6-庚二烯和1,6-辛二烯的所述促进催化剂的应用,以及有机硼烷在催化剂中的存在 允许反应在非常温和的温度下进行,同时获得高的产物选择性。
    • 18. 发明授权
    • Liquid amine terminated derivatives of diglycidyl ethers
    • 液体胺封端的二缩水甘油醚衍生物
    • US5025100A
    • 1991-06-18
    • US475516
    • 1990-02-06
    • Jiang-Jen LinGeorge P. Speranza
    • Jiang-Jen LinGeorge P. Speranza
    • C07D303/24C08G59/10C08G59/18C08G59/32C08L63/00
    • C08G59/3227C07D303/24C08G59/10C08G59/184C08L63/00
    • Tetrafunctional amine derivatives of digyclidyl ethers of Bisphenol A that are liquid at ambient temperatures and that are useful as curing agents for epoxy resins are disclosed together with the method by which they are prepared which comprises the steps of:dissolving the diglycidyl ether in a solvent (acetone or methyl ethyl ketone) and adding a polyoxyalkylene diamine in the mole ratio of about 4 to about 5 moles of the diglycidyl ether per mole of said polyoxyalkylene diamine to provide an initial reaction mixture,heating the initial reaction mixture with agitation at a temperature of about 80.degree. to about 160.degree. C. for about 1 to about 4 hours sufficient to permit the diglycidyl ether to quantitatively react with the polyoxyalkylene diamine and to substantially completely volatilize the solvent to thereby form an intermediate reaction product,adding to the intermediate reaction product about 4 moles or more of a polyoxyethylene diamine per mol of initially used polyoxyalkylene diamine and heating the thus-formed second reaction mixture at a temperature of about 100.degree. to about 150.degree. C. for about 0.5 to about 5 hours, to form the tetrafunctional amine derivative.
    • 公开了在环境温度下为液态并可用作环氧树脂固化剂的双酚A的二环氧基醚的四官能胺衍生物及其制备方法,其包括以下步骤:将二缩水甘油醚溶解在溶剂( 丙酮或甲基乙基酮),并且每摩尔所述聚氧亚烷基二胺以约4至约5摩尔的二缩水甘油醚的摩尔比加入聚氧亚烷基二胺以提供初始反应混合物,在初始反应混合物的搅拌下,在 约80至约160℃约1至约4小时足以使二缩水甘油醚与聚氧亚烷基二胺定量反应并基本上完全挥发溶剂,从而形成中间反应产物,向中间反应产物 每摩尔最初使用的聚氧化烯约4摩尔以上的聚氧乙烯二胺 二胺,并将由此形成的第二反应混合物在约100至约150℃的温度下加热约0.5至约5小时,以形成四官能胺衍生物。