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Catalytic Reduction of NO_x in Oxygen-Rich Gas Streams, Deactivation of NO_x Storage-Reduction Catalysts by Sulfur

机译:富氧气流中的NO_x催化还原,硫使NO_x储藏还原催化剂失活

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The results clearly reveal the existence of two pathways of deactivation for NO_x storage reduction catalysts. Under lean conditions (exposure to SO_2 and O_2) surface sulfates are formed on the storage component (Ba), which subsequently migrate into the bulk phase. These species are hardly reducible by C_3H_6 up to 550℃ and, thus, permanently block the Ba sites, which leads to a decrease of NO_x storage capacity during successive cyclic treatments. A second pathway of deactivation by sulfur species is proposed to occur during fuel-rich (reducing) conditions. Sulfides seem to be formed at 350 and 500℃ on platinum, which block the metal surface and, therefore, diminish the NO_x reduction function of the noble metal during the fuel rich reaction cycles.
机译:结果清楚地揭示了用于NO_x存储还原催化剂的两种失活途径的存在。在稀薄条件下(暴露于SO_2和O_2),在存储组分(Ba)上形成了表面硫酸盐,该硫酸盐随后迁移至本体相。这些物质在550℃以下几乎不能被C_3H_6还原,因此永久性地阻断了Ba的位点,从而导致在连续的循环处理过程中NO_x的储存能力降低。建议在富燃料(还原)条件下发生第二种被硫物质钝化的途径。硫化物似乎在350和500℃时在铂上形成,这会阻塞金属表面,因此会降低富燃料反应周期中贵金属的NO_x还原功能。

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