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Fischer-Tropsch Synthesis. Reduction Behavior and Catalytic Activity of Fe-Ce Systems

机译:Fischer-Tropsch合成。 Fe-CE系统的减少行为和催化活性

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Several Fe-Ce catalysts for FT synthesis were prepared following two different methods: coprecipitation from Fe and Ce nitrate solutions and a physical mixture of pure Fe and Ce precursors. The iron phases present in the activated catalysts were identified by XRD and M?ssbauer spectroscopy. A good correlation between both techniques was found. The results revealed that the cerium oxide in the samples prepared by coprecipitation produces two effects: (i), stabilization of metastable species (Fe1–xO), and (ii), a decrease in the crystallite size of the iron species upon increasing Ce-contents, as inferred from an increase in superparamagnetic species. The catalysts were tested in CO hydrogenation in a flow reactor. It was found that selectivity towards light olefins increases for the coprecipitated Ce-containing catalysts, whereas CO conversion followed the opposite trend. Since the Fe1–xO phase was detected in these catalysts, it is suggested that the formation of the Fe1–xO phase would be responsible for the drop in catalytic activity.
机译:通过两种不同的方法制备用于FT合成的几种Fe-Ce催化剂:来自Fe和Ce硝酸盐溶液的共沉淀和纯Fe和Ce前体的物理混合物。通过XRD和M 2 Ssbauer光谱鉴定活化催化剂中存在的铁相。发现两种技术之间的良好相关性。结果表明,通过共沉淀制备的样品中的氧化铈产生两种效果:(i),稳定性物质(Fe1-xO)和(II)的稳定,在增加Ce-时,铁物种的微晶尺寸的降低内容,从超顺磁性的增加推断。在流动反应器中以CO氢化测试催化剂。发现对光烯烃的选择性增加了含Ce含CE的催化剂,而CO转化遵循相反的趋势。由于在这些催化剂中检测到Fe1-XO相,因此建议Fe1-XO相的形成将对催化活性的下降负责。

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