首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Deactivation of a Fe-ZSM-5 catalyst during the selective catalytic reduction of NO by n-decane: An operando DRIFT study
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Deactivation of a Fe-ZSM-5 catalyst during the selective catalytic reduction of NO by n-decane: An operando DRIFT study

机译:正癸烷选择性催化还原NO过程中Fe-ZSM-5催化剂的失活:操作DRIFT研究

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摘要

The selective catalytic reduction (SCR) of NO by n-decane was investigated on a Fe-ZSM-5 prepared by the FeCl3 sublimation method. NO conversion profiles versus temperature were followed in both temperature programmed surface reaction (TPSR, 10 degrees C min(-1)) and steady state experiments. A higher NO conversion with a maximum of ca. 80% at 400 degrees C is observed in the course of the TPSR tests. This phenomenon has been attributed to strong adsorption of n-decane which protects the active sites against the poisoning. Indeed, in steady state experiments at 390 degrees C the strong decrease of activity as a function of time on stream is due to the polymerisation of conjugated nitriles. This study indicates that long chain alkanes are not the most adequate reductants of NO for high temperature SCR applications. Moreover, due to an easier polymerization of conjugated nitriles on iron zeolites (stronger Fe Lewis sites), this type of catalyst seems less attractive than Cu-zeolite catalysts for the SCR of NO by hydrocarbons in this respect. (c) 2006 Elsevier B.V. All rights reserved.
机译:在用FeCl3升华法制备的Fe-ZSM-5上,研究了正癸烷对NO的选择性催化还原(SCR)。在程序升温的表面反应(TPSR,10摄氏度min(-1))和稳态实验中均跟踪了NO转化曲线与温度的关系。 NO转化率更高,最大值约为。在TPSR测试过程中,观察到在400摄氏度时80%。该现象归因于正癸烷的强吸附,保护了活性位点免受中毒。确实,在390摄氏度的稳态实验中,活性随时间推移的强烈下降是由于共轭腈的聚合所致。这项研究表明,对于高温SCR应用,长链烷烃不是最合适的NO还原剂。此外,由于共轭腈在铁沸石上的聚合更容易(Fe Lewis位点更强),在这方面,这类催化剂似乎不如Cu沸石催化剂对烃的NO SCR有吸引力。 (c)2006 Elsevier B.V.保留所有权利。

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