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用于在高空速下将CO直接转化为轻质烃的串联Pt/TiO和FeC催化剂。

Tandem Pt/TiO and FeC catalysts for direct transformation of CO to light hydrocarbons under high space velocity.

作者信息

Kang Xin, Liu Jiancong, Wang Dongxu, Tian Chungui, Fu Honggang

机构信息

Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People's Republic of China, Heilongjiang University. Harbin 150080, China.

Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People's Republic of China, Heilongjiang University. Harbin 150080, China.

出版信息

J Colloid Interface Sci. 2025 Jan 15;678(Pt A):1165-1175. doi: 10.1016/j.jcis.2024.09.053. Epub 2024 Sep 7.

Abstract

CO hydrogenation to hydrocarbons under high space velocity is crucial for industrial applications, but traditional Fe-based catalysts often suffer from the low activity and poor stability. Herein, we report a new tandem catalyst system combining Pt/TiO catalysts with FeC catalysts for the direct conversion of CO into C-C hydrocarbons under high space velocity. The Pt/TiO component promotes *CO intermediate production with an enhanced Reverse Water-Gas Shift (RWGS) reaction efficiency, providing a highly reactive species for the FeC catalyst to achieve Fischer-Tropsch synthesis (FTS). By maximizing the contact interface between the Pt/TiO and Fe-based components through a granule mixing configuration, we achieve significant enhancements in both CO conversion rate (24.0 %) and C-C hydrocarbons selectivity (51.1 %) under the gaseous hourly space velocity (GHSV) of 100000 mL gh. Besides, excellent stability is achieved by the tandem catalysts with continuous catalysis for up to 80 h without significant decrease in activity. Through modulation of the reduction states of iron oxide, we effectively tune the composition of Fe-based catalyst, thereby tailoring the product distribution. Through this work, we not only offer a promising avenue for reducing CO for efficient CO utilization but also highlight the importance of catalyst design in advancing sustainable chemical synthesis.

摘要

在高空速下将CO加氢转化为碳氢化合物对工业应用至关重要,但传统的铁基催化剂往往活性低且稳定性差。在此,我们报道了一种新的串联催化剂体系,该体系将Pt/TiO催化剂与FeC催化剂相结合,用于在高空速下将CO直接转化为C-C碳氢化合物。Pt/TiO组分通过提高逆水煤气变换(RWGS)反应效率促进*CO中间体的生成,为FeC催化剂实现费托合成(FTS)提供高活性物种。通过颗粒混合构型最大化Pt/TiO与铁基组分之间的接触界面,在100000 mL g h的气体时空速(GHSV)下,我们实现了CO转化率(24.0%)和C-C碳氢化合物选择性(51.1%)的显著提高。此外,串联催化剂具有出色的稳定性,可连续催化长达80小时而活性无明显下降。通过调节氧化铁的还原态,我们有效地调整了铁基催化剂的组成,从而定制产物分布。通过这项工作,我们不仅为减少CO以实现高效CO利用提供了一条有前景的途径,还突出了催化剂设计在推进可持续化学合成中的重要性。

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