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Selective CO oxidation over CuO-CeO2 catalysts doped with transition metal oxides

机译:过渡金属氧化物掺杂的CuO-CeO2催化剂上的选择性CO氧化

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摘要

CuO-CeO2 catalysts doped with transition metal oxides (ZnO, MnO2 and Fe2O3) were prepared by co-precipitation method for the selective CO oxidation. The effect of different metal oxides on the catalyst performance was examined by H2-TPR, in situ DRIFTS and XPS techniques. The results showed that CO adsorption mainly occurred on the Cu~+ site. The catalytic activity at lower temperatures was related to the amounts of lattice oxygen and CO desorption. The doping of ZnO remarkably improved the catalytic activity, while Fe2O3 or MnO2 deteriorated the catalytic properties. Addition of ZnO to CuO-CeO2 catalyst stabilized the reduced Cu~+ species and increased the amounts of CO adsorption and lattice oxygen. For Cu1Fe1Ce9O_δ, CO was mainly desorbed from the catalyst surface in the reversible form, which was not beneficial to the selective CO oxidation. Strong adsorption of CO on the Cu~+ site at lower temperatures and the poor redox performance led to the poor catalytic property for Cu1Mn1Ce9O_δ catalyst
机译:采用共沉淀法制备了过渡金属氧化物(ZnO,MnO2和Fe2O3)掺杂的CuO-CeO2催化剂,用于选择性CO氧化。通过H2-TPR,原位DRIFTS和XPS技术检查了不同金属氧化物对催化剂性能的影响。结果表明,CO吸附主要发生在Cu〜+位点。较低温度下的催化活性与晶格氧和一氧化碳解吸量有关。 ZnO的掺杂显着提高了催化活性,而Fe2O3或MnO2则降低了催化性能。在CuO-CeO2催化剂中添加ZnO可稳定还原的Cu〜+种类,并增加CO的吸附量和晶格氧。对于Cu1Fe1Ce9O_δ,CO主要以可逆的形式从催化剂表面脱附,这不利于选择性CO的氧化。较低温度下,CO强烈吸附在Cu〜+位上,氧化还原性能差,导致Cu1Mn1Ce9O_δ催化剂的催化性能差。

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