过渡金属催化剂上一氧化碳和氢气合成气态烃的研究(一)

E. Kikuchi, T. Inō, N. Ito, Y. Morita
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引用次数: 6

摘要

所有这些催化剂上的反应产物。然而,有些催化剂在生成C2或更高的气态烃方面表现出相当高的选择性。对C2烃的选择性顺序如下:Fe>Pd>Rh>Ru>Pt>Co>Ni。在测试的催化剂中,石墨负载的Rh催化剂生成C2烃的速率最高。在整个转化过程中,石墨负载的Rh催化剂比氧化铝负载或木炭负载的催化剂更有选择性地生成C2烃。这种差异被认为是由于石墨负载催化剂中强烈的金属支撑相互作用,涉及铑和石墨之间的电子转移。在使用不同气体进行的预处理中,空气预处理对石墨负载Rh催化剂活性的增强作用最大。
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Synthesis of Gaseous Hydrocarbons from Carbon Monoxide and Hydrogen over Transition Metal Catalysts (Part 1)
reaction product on all these catalysts. Some of the catalysts, however, exhibited considerably high selectivity for production of C2 or higher gaseous hydrocarbons. The following sequence of selectivity for C2 hydrocarbons was obtained: Fe>Pd>Rh>Ru>Pt>Co>Ni. Among the catalysts tested, the graphite-supported Rh catalyst showed the highest rate of production of C2 hydrocarbons. In the whole range of conversions, the graphite-supported Rh catalyst produced C2 hydrocarbons more selectively than the alumina-supported or charcoal-supported catalysts. This difference was considered due to the strong metal-support interaction in the graphite-supported catalyst that involved electron transfer between rhodium and graphite. Among the various pretreatments rendered using different gases, pretreatment in air enhanced most the activity of the graphite-supported Rh catalyst.
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