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首页> 外文期刊>Journal of Catalysis >Supported metal catalysts; Preparation, characterisation, and function - Part VI. Hydrogenolysis of ethane, propane, n-butane and iso-butane over supported platinum catalysts
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Supported metal catalysts; Preparation, characterisation, and function - Part VI. Hydrogenolysis of ethane, propane, n-butane and iso-butane over supported platinum catalysts

机译:负载型金属催化剂;准备,表征和功能-第六部分。负载铂催化剂上乙烷,丙烷,正丁烷和异丁烷的氢解

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摘要

The catalytic properties of three supported platinum catalysts, 0.75 wt% Pt/SiO2, 0.89 wt% Pt/Al2O3, and 0.48 wt% Pt/MoO3, are reported for the hydrogenolysis of ethane, propane, n-butane, and iso-butane. The reactions were carried out in a flow reactor at atmospheric pressure. The apparent activation energies, E-app, for the hydrogenolysis reactions and the isomerisation reactions of n-butane and iso-butane, all show a compensation effect with the corresponding values of In A(app). This compensation effect can be accounted for by the dehydrogenative chemisorption of the alkanes as the first step in the reaction mechanisms to both hydrogenolysis and isomerisation. No apparent structure sensitivity was demonstrated by the three catalysts for the hydrogenolysis of ethane. The Pt/Al2O3 catalyst showed the highest activity of the three catalysts for the hydrogenolysis of propane. This high activity can be related to the strong adsorption of alkane fragments on platinum sites on the Pt/Al2O3 catalyst which exhibit delta+ polarisation. Over the Pt/SiO2 and Pt/Al2O3 catalysts the isomerisation of n-butane and iso-butane can be explained by a metal-only catalysed isomerisation route, Very high levels of isomerisation over the Pt/MoO3 catalyst agree with a bifunctional mechanism involving acid sites on the MoO3 support. (C) 1998 Academic Press. [References: 43]
机译:据报道,对于乙烷,丙烷,正丁烷和异丁烷的氢解反应,三种负载型铂催化剂的催化性能分别为0.75 wt%Pt / SiO2、0.89 wt%Pt / Al2O3和0.48 wt%Pt / MoO3。反应在大气压下在流动反应器中进行。正丁烷和异丁烷的氢解反应和异构化反应的表观活化能E-app均显示出相应的In A(app)值的补偿作用。这种补偿作用可以通过烷烃的脱氢化学吸附作为氢解和异构化反应机理的第一步来解释。三种用于乙烷氢解的催化剂均未显示出明显的结构敏感性。 Pt / Al2O3催化剂对丙烷的氢解反应表现出三种催化剂中最高的活性。这种高活性可能与烷烃碎片在Pt / Al2O3催化剂上铂位上的强吸附有关,该位点表现出δ+极化。在Pt / SiO2和Pt / Al2O3催化剂上,正丁烷和异丁烷的异构化可以通过仅金属催化的异构化途径来解释。在Pt / MoO3催化剂上很高的异构化水平与涉及酸的双功能机理相符。 MoO3支持的网站。 (C)1998年学术出版社。 [参考:43]

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