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聚γ-甲硒基丙基硅氧烷铂配合物的合成与催化硅氢化性能 被引量:6
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作者 赵红 陈健 蔡明中 《江西师范大学学报(自然科学版)》 CAS 2000年第4期333-336,共4页
γ-氯丙基三乙氧基硅烷依次与气相法二氧化硅、甲硒基钠、氯亚铂酸钾作用,合成了聚γ-甲硒基丙基硅氧烷铂配合物,研究了该配合物对烯烃与三乙氧基硅烷硅氢加成反应的催化特性.
关键词 负载型催化剂 硅氢加成催化剂 硒铂配合物
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制备铂有机硅氧烷络合物的方法
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《齐鲁石油化工》 2020年第2期119-119,共1页
铂有机硅氧烷络合物通过以下方法制备,所述方法包括:将卤化亚铂和酮混合,然后添加聚有机硅氧烷,其每分子具有2~4个硅键合的具有2~6个碳原子的末端不饱和烃基团。通过该方法制备的铂有机硅氧烷络合物可用作硅氢加成催化剂。
关键词 有机氧烷 硅氢加成催化剂 不饱和烃 碳原子 络合物 卤化
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Effect of Aminoaromatic Acids as Additives on the Activity and Selectivity of the Platinum-catalyzed Hydrosilylation of Alkenes 被引量:1
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作者 白赢 彭家建 +3 位作者 胡应乾 厉嘉云 邱化玉 来国桥 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2009年第6期1038-1042,共5页
A series of aromatic acids has been tested as additives for the platinum-catalyzed hydrosilylation of styrene with triethoxysilane. Both excellent conversion of styrene and selectivity in favor of the ,β-adduct were ... A series of aromatic acids has been tested as additives for the platinum-catalyzed hydrosilylation of styrene with triethoxysilane. Both excellent conversion of styrene and selectivity in favor of the ,β-adduct were achieved using aminobenzoic acids as additive. Moreover, the use of 4-aminobenzoic acid led to significantly superior enhancement in both catalytic activity and selectivity among the tested aminobenzoic acids. Indeed, 100% conversion of styrene and 98.4% selectivity in favor of the β-adduct were obtained. Additionally, hydrosilylations of various alkenes with a variety of platinum catalysts have also been tested, and in each case the conversion of substrate and the selectivity of the β-adduct were promoted by using 4-aminobenzoic acid as additive. 展开更多
关键词 HYDROSILYLATION platinum catalyst aminoaromatic acid additive
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Al-modified mesocellular silica foam as a superior catalyst support for dibenzothiophene hydrodesulfurization 被引量:2
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作者 Shaotong Song Xu Yang +7 位作者 Bo Wang Xiaofeng Zhou Aijun Duan Kebin Chi Zhen Zhao Chunming Xu Zhentao Chen Jianmei Li 《Chinese Journal of Catalysis》 CSCD 北大核心 2017年第8期1347-1359,共13页
A series of Al‐containing mesostructured cellular silica foams(Al‐MCFs)with different Si/Al molar ratios(x;x=10,20,30,40,or50)were prepared by a post synthetic method using aluminum isopropoxide as an alumina source... A series of Al‐containing mesostructured cellular silica foams(Al‐MCFs)with different Si/Al molar ratios(x;x=10,20,30,40,or50)were prepared by a post synthetic method using aluminum isopropoxide as an alumina source.The corresponding NiMo catalysts supported on Al‐MCFs were prepared and evaluated using dibenzothiophene(DBT)as the probe reactant.All the synthesized samples were characterized by small‐angle X‐ray scattering,scanning electron microscopy,nitrogen adsorption‐desorption,UV‐Vis diffuse reflectance spectroscopy,H2temperature‐programmed reduction,27Al MAS NMR,temperature‐programmed desorption of ammonia,pyridine‐FTIR,Raman spectroscopy,HRTEM,and X‐ray photoelectron spectroscopy to analyze their physicochemical properties and to gain a deeper insight of the interrelationship between the structures and the catalytic performance.The synthesis mechanism was proposed to involve the formation of Br?nsted acid and Lewis acid sites through the replacement of Si4+with Al3+.Aluminum introduced into MCFs by the post synthetic method has a negligible influence on the mesostructure of the parent MCFs but can form silicoaluminate materials with moderate Br?nsted acidity.For Al‐MCFs(x)materials,the detection of tetrahedrally coordinated Al3+cations demonstrated that the Al species had been successfully incorporated into the silicon frameworks.Furthermore,the DBT hydrodesulfurization(HDS)catalytic activity of the NiMo/Al‐MCFs(x)catalysts increased with increasing Si/Al molar ratio,and reached a maximum at a Si/Al molar ratio of20.The interaction of Ni and Mo species with the support became stronger when Al was incorporated into the MCFs supports.The high activities of the NiMo/Al‐MCFs catalysts for the DBT HDS were attributed to the suitable acidity properties and good dispersions of the Ni and Mo active phases. 展开更多
关键词 Al‐MCFs Si/Al ratio Post‐synthesis Hydrodesulfurization catalyst DIBENZOTHIOPHENE
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