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Pyrophoricity and stability of copper and platinum based water-gas shift catalysts during oxidative shut-down/start-up operation

机译:氧化关闭/启动操作过程中铜和铂基水煤气变换催化剂的发火性和稳定性

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The pyrophoricity of Cu/ZnO-based and Pt-based catalysts was studied during oxidative shut-down/start-up of the low-temperature water-gas shift (LT-WGS) reaction to assess whether these catalysts are suitable for fuel cell application. The Cu/ZnO-based catalysts were observed to display high levels of pyrophoricity manifested as a sharp temperature rise of the catalyst bed upon air introduction. This promoted severe sintering of the bulk and metallic phases of the catalyst facilitating catalyst deactivation. No pyrophoricity was observed for any of the Pt-based catalysts; however, sintering of the metallic phase in Pt/TiO_2 and Pt/ZrO_2 persisted, leading to a decrease in activity. It was likely that the sintering of Pt occurred during LT-WGS operation itself. In contrast, Pt/CeO_2 was the only catalyst which retained its activity, displaying no loss in specific surface area or metal dispersion throughout the entire process making it the most suitable candidate of the materials investigated for fuel cell systems. Temperature-programmed oxidation studies indicated deactivation by the oxidative shut-down/start-up operation did not result from the build-up of carbonaceous species.
机译:在低温水煤气变换(LT-WGS)反应的氧化关闭/启动过程中研究了Cu / ZnO基和Pt基催化剂的自燃性,以评估这些催化剂是否适合燃料电池应用。观察到基于Cu / ZnO的催化剂显示出高水平的自燃性,这表现为在引入空气时催化剂床的温度急剧升高。这促进了催化剂的本体相和金属相的严重烧结,从而促进了催化剂的失活。对于任何基于Pt的催化剂均未观察到自燃性。但是,Pt / TiO_2和Pt / ZrO_2中的金属相持续烧结,导致活性降低。 Pt的烧结很可能是在LT-WGS操作本身期间发生的。相反,Pt / CeO_2是唯一保持其活性的催化剂,在整个过程中没有显示出比表面积或金属分散度的损失,使其成为燃料电池系统研究材料的最合适的候选者。程序升温的氧化研究表明,氧化关闭/启动操作引起的失活并非碳质物质的积累引起的。

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