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Effect of the activation atmosphere on the activity of Fe catalysts supported on SBA-15 in the Fischer-Tropsch Synthesis

机译:活化气氛对费-托合成中SBA-15负载的Fe催化剂活性的影响

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摘要

An iron catalyst supported on SBA-15 was prepared and activated in H _2 stream and in synthesis gas (H_2:CO = 2:1) stream, in order to be used in the Fischer-Tropsch Synthesis. The different activation treatments led to different Fe species in fresh catalysts: α-Fe, Fe _3O_4 and Fe~(2+) diffused into the SBA-15 walls in H2-Fe/SBA-15 and χ-Fe_5C_2, Fe_3O_4 and Fe~(2+) in H2:CO-Fe/SBA-15. These initial differences in the "bulk" structure of the solids disappear when both catalysts are "working". However, a higher production of total hydrocarbons, higher CO conversion and more CH_4 and light gases were obtained for H2-Fe/SBA-15 over 6 days. Besides, a higher selectivity toward light olefins was obtained with H2-Fe/SBA-15 during the first 24 h on reaction stream, but this selectivity decreases with the reaction time. These results are explained considering that the iron carbides produced from α-Fe are more active and/or have smaller sizes than that obtained from α-Fe_2O _3.
机译:制备了负载在SBA-15上的铁催化剂,并在H _2物流和合成气(H_2:CO = 2:1)物流中活化,以便用于费-托合成。不同的活化处理导致新鲜催化剂中的铁种类不同:α-Fe,Fe _3O_4和Fe〜(2+)扩散到H2-Fe / SBA-15中的SBA-15壁和χ-Fe_5C_2,Fe_3O_4和Fe〜 (2+)在H2:CO-Fe / SBA-15中。当两种催化剂都“起作用”时,固体的“本体”结构中的这些初始差异消失了。但是,在6天内,H2-Fe / SBA-15的总烃产量更高,CO转化率更高,CH_4和轻质气体更多。此外,在反应流的最初24小时内,使用H2-Fe / SBA-15获得了对轻质烯烃的更高选择性,但该选择性随反应时间而降低。考虑到从α-Fe生成的碳化铁比从α-Fe_2O_3生成的碳化铁更具活性和/或具有较小的尺寸,解释了这些结果。

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