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Influence of oxygen redox property and anchoring behavior on co supported catalyst during toluene steam reforming reaction

机译:氧氧化铈性能及锚定行为对甲苯蒸汽重整反应过程中CO负载催化剂的影响

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Catalytic steam reforming is a practical way for producing hydrogen and carbon monoxide from biomass tar or brown coal which includes plenty amount of aromatic hydrocarbons. These aromatic hydrocarbons are comparatively less-reactive and liable to form coke on catalytic surface during this reaction [1], Therefore, suppressing coke formation is especially significant in steam reforming of toluene as a model compound of aromatic hydrocarbons. Many contributions were dedicated for this topic. Trimm reported secondary metal addition to Ni catalyst decreased coke formation rate on methane steam reforming [2]. Also, Rostrup-Nielsen described partial sulfur poisoning of Ni deters coke formation on Ni catalyst [3]. However, these blockages of active metal might bring on lowering catalytic activity during the reforming reaction. Coking suppression without deactivation of catalyst was desired in steam reforming of aromatic hydrocarbon.
机译:催化蒸汽重整是从生物质焦油或棕色煤制造氢和一氧化碳的实用方法,其包括大量的芳烃。 这些芳烃在该反应期间对催化表面进行相对较低的反应性和易于在催化表面上形成焦炭[1],因此抑制焦炭形成在甲苯的蒸汽重整中是芳烃化合物的蒸汽重整。 许多贡献是专门为此主题。 TriMM报道Ni催化剂的二次金属加入下降甲烷蒸汽重整对焦炭形成速率[2]。 此外,ROSTRUP-NIELSEN描述了NI抗钙蛋白酶的部分硫中毒在Ni催化剂上的焦炭中毒[3]。 然而,这些活性金属的堵塞可能在重整反应过程中引起降低催化活性。 在芳烃烃的蒸汽重整中需要焦化而不停用催化剂。

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