SURFACE MODIFICATION OF SUPPORTED Ru : Mn/SiO2 FISCHER-TROPSCH SYNTHESIS CATALYSTS

S. Hussain, F. Larachi
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引用次数: 1

Abstract

ABSTRACT Co-impregnated ruthenium–manganese bimetallic catalysts supported on high-surface area silica support were exposed to high-temperature reduction–oxidation–reduction (R/O/R) treatment to generate catalytic surfaces having specific geometry. The impact of R/O/R modifications was probed via a model Fischer-Tropsch synthesis (FTS) reaction aided by various characterisation techniques (TEM, XPS, s-SIMS, selective chemisorption). The characterisation results indicated that alternating reduction and oxidation of the catalyst was propitious to the formation of a specific surface landscape enriched in Ru : Mn bimetallic sites as well as in ruthenium and manganese oxides. The increase in metal dispersion and BET surface area following R/O/R exposures of the catalysts was due to re-dispersion of particles in the range of 2–10 nm, to surface modification, and to changes in active sites. The presence of ruthenium oxide, manganese oxide and Ru : Mn was likely to be at the origin of the enhancement in the production of unsaturated hydrocarbons in the FTS reaction.
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负载Ru: Mn/SiO2费托合成催化剂的表面改性
摘要采用高温还原-氧化-还原(R/O/R)处理,在高表面积二氧化硅载体上负载共浸渍钌锰双金属催化剂,生成具有特定几何形状的催化表面。通过各种表征技术(TEM, XPS, s-SIMS,选择性化学吸附)辅助的模型费托合成(FTS)反应,探讨了R/O/R修饰的影响。表征结果表明,催化剂的交替还原和氧化有利于形成富含Ru: Mn双金属位以及钌和锰氧化物的特定表面景观。在R/O/R暴露后,金属分散和BET表面积的增加是由于颗粒在2-10 nm范围内的再分散、表面修饰和活性位点的变化。氧化钌、氧化锰和Ru: Mn的存在可能是FTS反应中不饱和烃产量增加的原因。
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