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用于增强费托合成汽油馏分烃产量的钠改性Fe@C核壳催化剂

An Na-modified Fe@C core-shell catalyst for the enhanced production of gasoline-range hydrocarbons Fischer-Tropsch synthesis.

作者信息

Ma Guangyuan, Xu Yanfei, Wang Jie, Bai Jingyang, Du Yixiong, Zhang Jianli, Ding Mingyue

机构信息

School of Power and Mechanical Engineering, Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and Energy, Wuhan University Wuhan 430072 China

State Key Laboratory of High-efficiency Utilization of Coal and Green Chemical Engineering, Ningxia University Yinchuan 750021 China.

出版信息

RSC Adv. 2020 Mar 18;10(18):10723-10730. doi: 10.1039/d0ra01036g. eCollection 2020 Mar 11.

Abstract

Although numerous studies have been conducted in the field of converting syngas to value-added fuels, selectively converting syngas to gasoline-range hydrocarbons (C hydrocarbons) remains a big challenge. Alkali metal (namely, K, Na and Li)-modified Fe@C core-shell catalysts were synthesized by a one-step hydrothermal method for Fischer-Tropsch synthesis. An optimized selectivity of 56% for the C hydrocarbons with a higher CO conversion of about 95% was obtained for the FeNa@C catalyst compared to that for other alkali metal-modified Fe@C catalysts. According to the characterization results, the incorporation of alkali metals into Fe@C enhanced the conversion of FeCO to FeO, which promoted the formation of the FTS active phase iron carbides. In particular, the strongest interaction of Fe-alkali metal and the highest amount of surface carbon layers were observed after adding an Na promoter into Fe@C in contrast to that observed for K and Li promoters, which strengthened the synergistic effect of Fe-Na metals and the spatial confinement of the core-shell structure, further improving the C hydrocarbon selectivity.

摘要

尽管在合成气转化为增值燃料领域已经开展了大量研究,但将合成气选择性转化为汽油馏分烃(C烃)仍然是一个巨大挑战。采用一步水热法合成了碱金属(即K、Na和Li)改性的Fe@C核壳催化剂用于费托合成。与其他碱金属改性的Fe@C催化剂相比,FeNa@C催化剂对C烃的选择性优化至56%,同时CO转化率较高,约为95%。根据表征结果,将碱金属引入Fe@C中增强了FeCO向FeO的转化,促进了费托合成活性相碳化铁的形成。特别是,与K和Li助剂相比,在Fe@C中添加Na助剂后观察到Fe-碱金属之间的相互作用最强,表面碳层数量最多,这增强了Fe-Na金属的协同效应以及核壳结构的空间限制作用,进一步提高了C烃的选择性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ed/9050398/b8275bb8469c/d0ra01036g-f1.jpg

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