首页> 外文会议>China-Japan Symposium on Coal and C1 Chemistry; 20061022-28; Chengdu(CN) >Removal of residual CO from CO_2-rich hydrogenous gas via thermally differential methanation: principle and entailed challenge
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Removal of residual CO from CO_2-rich hydrogenous gas via thermally differential methanation: principle and entailed challenge

机译:通过热差式甲烷化从富CO_2的氢气中去除残留CO:原理和面临的挑战

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摘要

Fischer-Tropsch synthesis (FTS) is a promising way to convert coal and natural gas to clean fuels and chemicals via syngas. Cobalt-based catalysts attract most of current attention in FTS because of their high activity, high selectivity for long chain paraffins, and low water gas shift activity. For cobalt based catalysts, the chemical and texture properties of the support influence the catalytic activity and product selectivity, via their modifications on the reducibility and dispersion of cobalt or the formation of well-fined phases. Synthesis of highly dispersed Co catalysts requires strong interaction between the support and the Co precursor, but in turn such strong interactions generally lower the reducibility of such precursors. To solve this problem, introduction of metal oxide to modify cobalt-support interaction of cobalt-based catalyst was studied. ZrO_2 addition to cobalt/silica was found to enhance the FTS activity significantly [1, 2]. Here we report that Al_2O_3 as well as TiO_2 also improved cobalt/silica FTS catalyst remarkably, acting as promoters.
机译:费-托合成(FTS)是一种有前途的方法,可以通过合成气将煤和天然气转化为清洁燃料和化学物质。钴基催化剂因其高活性,对长链烷烃的高选择性以及低水煤气变换活性而吸引了FTS当前的大多数关注。对于钴基催化剂,载体的化学和织构性质通过对钴的还原性和分散性或精细相的形成进行修饰,从而影响催化活性和产物选择性。高度分散的Co催化剂的合成需要载体与Co前驱体之间有很强的相互作用,但是这种强相互作用通常会降低此类前驱体的还原性。为了解决该问题,研究了引入金属氧化物以改变钴基催化剂的钴-载体相互作用。发现在钴/二氧化硅中添加ZrO_2可以显着增强FTS活性[1、2]。在这里,我们报道Al_2O_3和TiO_2还显着改善了钴/二氧化硅FTS催化剂,起到了促进剂的作用。

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