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在核壳 FeO@MnO 催化剂上将合成气直接转化为直链 α-烯烃。

Directly Converting Syngas to Linear α-Olefins over Core-Shell FeO@MnO Catalysts.

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.

Synfuels China Co. Ltd. , Beijing 101407 , China.

出版信息

ACS Appl Mater Interfaces. 2018 Dec 19;10(50):43578-43587. doi: 10.1021/acsami.8b11820. Epub 2018 Dec 6.

Abstract

Converting syngas to value-added chemicals via Fischer-Tropsch synthesis has attracted much attention, whereas the direct hydrogenation of CO to heavy olefins, especially linear α-olefins (LAOs), remains a challenge. In this study, we designed a core-shell FeO@MnO catalyst to realize the direct conversion of syngas to LAOs with high efficiency. This catalyst exhibited a high selectivity of 79.60% for total alkenes and 64.95% for C alkenes, 91% of which are LAOs, at a CO conversion of approximately 75%. Promotion of the electron transfer from MnO to FeO inside the core-shell FeO@MnO catalyst facilitated the dissociative adsorption of CO molecules on FeO and the spillover of H atoms onto the MnO, which enhanced C-C coupling, weakened the hydrogenation activity of the catalyst, and improved the production of LAOs. A superior stability over 100 h was observed, demonstrating the promising potential of this catalyst for industrial applications.

摘要

通过费托合成将合成气转化为高附加值化学品引起了广泛关注,然而,将 CO 直接加氢转化为重烯烃,特别是线性 α-烯烃(LAOs),仍然是一个挑战。在本研究中,我们设计了一种核壳结构的 FeO@MnO 催化剂,以实现高效地将合成气直接转化为 LAOs。该催化剂在 CO 转化率约为 75%时,表现出总烯烃 79.60%和 C 烯烃 64.95%的高选择性,其中 91%为 LAOs。核壳结构的 FeO@MnO 催化剂中 MnO 向 FeO 的电子转移促进了 CO 分子在 FeO 上的解离吸附以及 H 原子在 MnO 上的溢流,从而增强了 C-C 偶联,削弱了催化剂的加氢活性,提高了 LAOs 的生成。该催化剂经过 100 小时以上的稳定性测试,显示出在工业应用中的巨大潜力。

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