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Kinetics of the NO+H-2 reaction over supported noble metal based catalysts: Support effect on their adsorption properties

机译:负载型贵金属基催化剂上NO + H-2反应的动力学:载体对其吸附性能的影响

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摘要

This paper reports a kinetic investigation of the global reduction of NO by H-2 which has been considered as a probe reaction for characterising the adsorption properties of supported palladium based catalysts. A particular attention has been paid towards the influence of the support on the catalytic properties of Pd, particularly towards the production of undesirable by-products such as nitrous oxide (N2O) and ammonia (NH3). It has been found that the kinetics of the overall NO + H-2 reaction on Pd/Al2O3 can be correctly depicted according to a Langmuir-Hinshelwood mechanism involving the dissociation of nitrosyl species assisted by chernisorbed hydrogen atoms. On the other hand, Pd/LaCoO3 exhibits a different kinetic behaviour towards the adsorption of hydrogen depending on the pre-activation thermal treatment. In that case, different mechanisms may occur. (c) 2006 Elsevier B.V. All rights reserved.
机译:本文报道了H-2整体还原NO的动力学研究,H-2被认为是表征负载型钯基催化剂吸附性能的探针反应。特别注意了载体对Pd催化性能的影响,特别是对产生不良副产物(如一氧化二氮(N2O)和氨(NH3))的影响。已经发现,可以根据朗缪尔-欣谢尔伍德(Langmuir-Hinshelwood)机理正确地描述在Pd / Al 2 O 3上的整个NO + H-2反应的动力学,该机理涉及通过吸附的氢原子辅助的亚硝酰基物质的解离。另一方面,取决于预活化热处理,Pd / LaCoO3对氢的吸附表现出不同的动力学行为。在这种情况下,可能会发生不同的机制。 (c)2006 Elsevier B.V.保留所有权利。

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