首页> 外文会议>Third Tokyo Conference on Advanced Catalytic Science and Technology,Tokyo July 19-24,1998 >Kinetic and in situ DRIFT spectroscopy studies of NO oxidation,and reduction by C_3H_6 in excess O_2 over gamma -Al_2O_3 and Au/ gamma -Al_2O_3
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Kinetic and in situ DRIFT spectroscopy studies of NO oxidation,and reduction by C_3H_6 in excess O_2 over gamma -Al_2O_3 and Au/ gamma -Al_2O_3

机译:动力学和原位DRIFT光谱研究了NO的氧化以及在过量O_2上被C_3H_6还原的程度高于γ-Al_2O_3和Au /γ-Al_2O_3

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摘要

The in situ DRIFT spectroscopy studies of NO and NO_2 SCR were performed on gamma -Al_2O_3 and Au/ gamma -Al_2O-3.The obtained results indicate that the initiation of No SCR on Au/ gamma -Al_2O_3 involves the oxidation of NO to NO_2 at active centers at the interface between Au and Al_2O-3 followed by coupling of the NO-2 or its adspecies.NO-_x,with activated C_3H_6 on active sites on Al_2O_3 to form C_nH_mN_xO_y species,which are responsible for the propagation step.Its subsequent internal rearrangement and decomposition leadsto the formation of N_2 and other other products.Taken together,the obtained results suggest that the No_2 intermediacy benefits the NO SCR over gold catalysts as a reaction initiator or oxygen transfer agent.
机译:对γ-Al_2O_3和Au /γ-Al_2O-3进行了NO和NO_2 SCR的原位DRIFT光谱研究。结果表明,在Au /γ-Al_2O_3上NO SCR的引发涉及NO在NO氧化为NO_2活性中心位于Au和Al_2O-3之间的界面上,然后将NO-2或它的种类NO-_x与Al_2O_3上活性位点上的活化C_3H_6偶联形成C_nH_mN_xO_y物种,这些物种负责传播步骤。内部的重排和分解导致N_2和其他产物的形成。综上所述,所获得的结果表明,与作为反应引发剂或氧转移剂的金催化剂相比,No_2中间物比NO SCR更有利于NO SCR。

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