首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >New Insights into the Active Surface Species of Silver Alumina Catalysts in the Selective Catalytic Reduction of NO
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New Insights into the Active Surface Species of Silver Alumina Catalysts in the Selective Catalytic Reduction of NO

机译:银氧化铝选择性催化还原NO活性表面物种的新见解

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The performance of silver alumina catalysts and silver aluminate was studied in the selective catalytic reduction (SCR) of NO by propene. The use of boehmite during the impregnation step ensured a strong interaction between the silver species and the alumina surface in the final calcined catalyst. Thus, higher silver loadings (5-7 wt % silver) could be used without significant loss in selectivity to N2 during SCR. The nature of the silver species and the formation of adsorbed surface species during SCR and hydrogen-assisted SCR (H2-SCR) was studied by activity measurements and by combined in situ IR and X-absorption spectroscopic measurements. The combination of these techniques in the same reaction cell allowed simultaneous monitoring of the state of silver and the formation of surface species under realistic reaction conditions. The active silver species on alumina support were concluded to be 2-dimensional oxidic Ag_n~(δ+) species. Silver aluminate was ruled out as a possibility for an active phase for the SCR reaction. The oxidic Ag_n~(δ+)species were present under both SCR and H2-SCR reaction conditions and even on a prereduced catalyst under the SCR reaction conditions. Hydrogen is proposed to enhance the formation of adsorbed surface species, especially nitrites, but not to change the nature of the active silver sites.
机译:在丙烯选择性催化还原NO的过程中,研究了氧化铝银催化剂和铝酸银的性能。在浸渍步骤中使用勃姆石可确保最终煅烧催化剂中银与氧化铝表面之间的牢固相互作用。因此,可以使用较高的银载量(5-7重量%的银),而在SCR期间对N 2的选择性没有显着损失。通过活性测量以及原位红外和X吸收光谱测量研究了SCR和氢辅助SCR(H2-SCR)期间银物质的性质和吸附表面物质的形成。在同一个反应池中结合使用这些技术,可以在实际反应条件下同时监测银的状态和表面物质的形成。氧化铝载体上的活性银物质被认为是二维氧化性Ag_n〜(δ+)物质。排除了铝酸银作为SCR反应活性相的可能性。在SCR和H2-SCR反应条件下,甚至在SCR反应条件下,在预还原的催化剂上都存在Ag_n〜(δ+)氧化物。提出氢可增强吸附的表面物质(尤其是亚硝酸盐)的形成,但不改变活性银位点的性质。

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