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Identification of the active species in the working alumina-supported cobalt catalyst under various conditions of Fischer-Tropsch synthesis

机译:费-托合成条件下工作氧化铝负载钴催化剂中活性物质的鉴定

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摘要

An in situ time-resolved XRD/XANES/EXAFS investigation combined with on-line evaluation of catalytic performance indicates considerable structural transformations of the conventional Pt-promoted alumina supported cobalt catalyst under the realistic conditions of Fischer-Tropsch synthesis. Cobalt and platinum are reduced into metallic states after pre-treatment in hydrogen at 623 K and form Co-Pt bimetallic nanoparticles. Depending on catalyst and reaction conditions, the metallic nanoparticles can undergo sintering, carbidisation, and fcc-hcp phase transformations. The observed changes in the catalyst structure significantly affect the performance in the Fischer-Tropsch reaction. Cobalt hcp phase seems more active in Fischer-Tropsch synthesis than cobalt fcc metal phase.
机译:现场时间分辨的XRD / XANES / EXAFS研究与在线催化性能评估相结合,表明在费托合成的实际条件下,传统的Pt促进的氧化铝负载的钴催化剂有相当大的结构转化。在623 K的氢气中进行预处理后,钴和铂还原为金属态,并形成Co-Pt双金属纳米粒子。取决于催化剂和反应条件,金属纳米粒子可能会经历烧结,碳化和fcc-hcp相变。观察到的催化剂结构变化显着影响了费-托反应的性能。钴hcp相在费托合成中似乎比钴fcc金属相更具活性。

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