稀土氧化物和钍在沉淀铁基费托合成催化剂中的促进剂作用

Ding-zhu Wang, Xiao-ping Cheng, Zhi-er Huang, Xiu-zhi Wang, Shao-yi Peng
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引用次数: 19

摘要

Fischer-Tropsch合成的催化结果表明,在沉淀的铁基催化剂中加入La、Ce、Nd、Eu和Th氧化物,增加了合成气向烃类产物的转化,并将选择性转移到汽油和中间馏分,同时显著抑制了甲烷和蜡的形成。稀土氧化物比钍更有效,其中Eu2O3表现出独特的促进作用。通过x射线衍射(XRD)、x射线光电子能谱(XPS)、程序升温还原(TPR)、一氧化碳程序升温解吸(TPD)、二氧化碳TPD和程序升温表面反应(TPSR)测试对催化剂的表征结果表明,这些促进剂的存在极大地改变了铁催化剂的体结构和表面状态,特别是当铕促进时。发现它们增加了铁颗粒的分散,由于形成了混合的Fe-RE(Th)氧化物界面,抑制了铁颗粒的生长和进一步还原,促进了一氧化碳的吸附和解离,并且由于它们的碱度带来的电子捐赠性质,降低了表面碳种对氢的反应性。这些结果解释了观察到的催化性能的变化。由于其优越的结构和化学效应,Eu2O3对催化活性和选择性具有独特的促进作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of rare-earth oxides and thoria as promoters in precipitated iron-based catalysts for Fischer-Tropsch synthesis

The catalytic results in Fischer-Tropsch synthesis indicate that the addition of La, Ce, Nd, Eu and Th oxides to a precipitated iron-based catalyst increases the syngas conversion to hydrocarbon products and shifts the selectivity to the gasoline and middle fractions with significant suppression of both methane and wax formation. Rare-earth (RE) oxides are more effective than thoria, of which Eu2O3 shows a unique promoting effect. The results of catalyst characterization obtained from the X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), temperature-programmed reduction (TPR),carbon monoxide temperature-programmed desorption (TPD), carbon dioxide TPD and temperature-programmed surface reaction (TPSR) measurements demonstrate that the presence of these promoters greatly changes both the bulk structure and surface states of the iron catalyst, especially when promoted with europium. It is found that they increase the dispersion of the iron particles, inhibiting their growth and further reduction due to the formation of a mixed Fe-RE(Th) oxide interface, encourage the adsorption and dissociation of carbon monoxide and decrease the reactivity of the surface carbon species towards hydrogen due to the electronic donation properties brought about by their basicities. These results explain the observed variation in the catalytic performances. Eu2O3 exhibits a unique promoting effect on the catalytic activity and selectivity due to its superior structural and chemical effects.

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