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Alumina supported molybdenum-nickel carbides as catalysts for the dry reforming of methane

机译:氧化铝支持钼 - 碳化镍作为甲烷干燥重整的催化剂

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Bimetallic molybdenum-nickel catalysts supported on alumina have been studied in the carbon dioxide reforming of methane. Two different temperature-programmed reduction (TPR) pretreatments have been followed for their synthesis: using hydrogen to obtain metallic molybdenum and using a CH_4/H_2 reactant mixture to obtain molybdenum carbides, which have shown better performance in the reaction. Although in nickel catalysts the surface mobility of carbon species generated from methane decomposition leads to the accumulation of great amounts of carbon deposits in the support surface, the presence of molybdenum has been observed to avoid these migration processes. The synergic effect found between both metals in Ni-Mo bimetallic samples reduces the temperature of carburization of molybdenum, improves its catalytic activity and its selectivity to hydrogen in the CH_4+CO_2 reaction at the same time that avoids the formation of undesired carbon structures caused by methane decomposition.
机译:已经研究了氧化铝中负载的双金属钼 - 镍催化剂在二氧化碳重整甲烷中。两种不同的温度编程的减少(TPR)预处理已遵循它们的合成:使用氢气获得金属钼并使用CH_4 / H_2反应物混合物获得钼碳化物,这在反应中表现出更好的性能。尽管在镍催化剂中,由甲烷分解产生的碳物质的表面迁移率导致支撑表面中大量碳沉积物的积累,但已经观察到钼的存在以避免这些迁移过程。在Ni-Mo双金属样品中的两个金属之间发现的协同作用降低了钼的渗碳温度,同时改善其在CH_4 + CO_2反应中的催化活性及其对氢的选择性,避免形成不需要的碳结构甲烷分解。

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