在合成气合成烯烃过程中增强传热和传质的泡沫结构铁催化剂

Zhiqiang Zhang, Yu Le, Lei Jing, Gongxun Huang, Jincan Kang, Qinghong Zhang, Ye Wang
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引用次数: 0

摘要

费托合成(FT)具有高放热和高通量的特点,传统上会产生 C 类烃类和 C1 类副产品的混合物,从而对碳的利用效率产生不利影响。在此,我们设计了一种铁泡沫结构催化剂,用于在傅立叶变换工艺中选择性地生产高价值烯烃。Na-Zn-Fe/Fe-foam 催化剂是通过水热合成法制备的,其中 FeCO 前驱体由 Fe-foam 生成,然后加入钠和锌改性剂。在一氧化碳转化率为 98% 的条件下,这些催化剂的烯烃选择性高达 ∼80 %,时空产率达∼0.70 g g h,而且具有出色的稳定性。这种结构催化剂空隙体积大,网络结构完全开放,具有优异的传质和传热能力,能有效减少 CO 和 CH 的生成,在 FT 合成中具有显著优势。这项工作为开发高放热催化反应中的高效催化剂提供了一种新策略。
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Foam-structured Fe catalysts for enhanced heat and mass transfer in synthesis of olefins from syngas
The Fischer-Tropsch (FT) synthesis, characterized by its highly exothermic and high-throughput nature, traditionally yields a mix of C hydrocarbons and C1 by-products, which adversely affect carbon utilization efficiency. Herein, we design a Fe-foam structured catalyst to selectively produce high-value olefins in FT process. The Na-Zn-Fe/Fe-foam catalysts are prepared through a hydrothermal synthesis method, where the FeCO precursor is formed from Fe-foam, followed by addition of sodium and zinc modifiers. These catalysts achieve a remarkable olefin selectivity of ∼80 % and a space-time yield of ∼0.70 g g h at a CO conversion of 98 %, and further demonstrate outstanding stability. The structured catalysts, with expansive void volume and fully open network architecture, provide superior mass and heat transfer capabilities, and effectively mitigate the generation of CO and CH, offering a significant advantage in FT synthesis. This work presents a new strategy for the development of efficient catalysts in high exothermic catalytic reactions.
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