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Catalytic behaviors of bifunctional Fe-HZSM-5 catalyst in Fischer-Tropsch synthesis

机译:双功能Fe-HZSM-5催化剂在费托合成中的催化行为

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摘要

Fe-HZSM-5 bifunctional catalyst activity and products selectivity in Fischer-Tropsch synthesis (FTS) were investigated. HZSM-5 zeolite and iron catalyst were become near to each other step-by-step. In first step, zeolite just affected gaseous products after FTS reaction on iron catalyst. In other conditions, zeolite was incorporated in FTS process to be included in cracking and aromatization reactions. The results revealed that role of zeolite in overall reaction were increased from completely separated condition to physically mixed condition. Addition of binder in physically mixed condition was led to cover the active sites of bifunctional iron-zeolite catalyst and decrease activity of zeolite and iron catalyst. Also, decreasing amounts of Bransted acid sites after FT reaction was related to zeolite incorporation in overall reaction that was decreased by closing the zeolite to the iron catalyst. HZSM-5 addition to FT catalyst suppressed the formation of oxygenates, which are converted to hydrocarbons on the zeolite acid sites. Furthermore, zeolite increased CO2 selectivity slightly because of oxygenate decomposition into CO2 as a side reaction that showed by co-feeding of light alcohol (with ~(14)C) to FTS in previous works.
机译:研究了Fe-HZSM-5双功能催化剂在费托合成(FTS)中的活性和产物选择性。 HZSM-5沸石和铁催化剂一步一步靠近。第一步,在铁催化剂上进行FTS反应后,沸石仅影响气态产物。在其他条件下,将沸石掺入FTS工艺中,以包括在裂化和芳构化反应中。结果表明,沸石在整个反应中的作用从完全分离的状态增加到物理混合的状态。在物理混合条件下添加粘合剂导致覆盖了双功能铁沸石催化剂的活性位点并降低了沸石和铁催化剂的活性。同样,FT反应后布朗斯台德酸位点的减少与沸石在整个反应中的掺入有关,而沸石通过将沸石与铁催化剂封闭而减少。向FT催化剂中加入HZSM-5可以抑制含氧化合物的形成,这些氧化物在沸石酸性位点上转化为烃。此外,在以前的工作中,由于将轻质醇(与〜(14)C一起)供入FTS,表明副产物显示出含氧化合物分解为CO2的缘故,沸石略微提高了CO2的选择性。

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