催化作用
甲醇
沸石
双功能
化学
膜
选择性
化学工程
材料科学
无机化学
膜反应器
有机化学
生物化学
工程类
作者
Wenzhe Yue,Yanhong Li,Wei Wan,Jianwen Jiang,Jürgen Caro,Aisheng Huang
标识
DOI:10.1002/anie.202106277
摘要
Abstract The hydrogenation of sequestrated CO 2 to methanol can reduce CO 2 emission and establish a sustainable carbon circuit. However, the transformation of CO 2 into methanol is challenging because of the thermodynamic equilibrium limitation and the deactivation of catalysts by water. In the present work, different reactor types have been evaluated for CO 2 catalytic hydrogenation to methanol. Best results have been obtained in a bifunctional catalytic membrane reactor (CMR) based on a zeolite LTA membrane and a catalytic Cu‐ZnO‐Al 2 O 3 ‐ZrO 2 layer on top. Due to the in situ and rapid removal of the produced water from the catalytic layer through the hydrophilic zeolite LTA membrane, it is effective to break the thermodynamic equilibrium limitation, thus significantly increasing the CO 2 conversion (36.1 %) and methanol selectivity (100 %). Further, the catalyst deactivation by the produced water can be effectively inhibited, thus maintaining a high long‐term activity of the CMR.
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