Highly Selective CO2 Conversion to Methanol in a Bifunctional Zeolite Catalytic Membrane Reactor

被引:69
作者
Yue, Wenzhe [1 ]
Li, Yanhong [1 ]
Wei, Wan [2 ]
Jiang, Jianwen [2 ]
Caro, Jurgen [3 ]
Huang, Aisheng [1 ]
机构
[1] East China Normal Univ, Shanghai Key Lab Green Chem & Chem Proc, Dept Chem, 500 Dongchuan Rd, Shanghai 200241, Peoples R China
[2] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 117576, Singapore
[3] Leibniz Univ Hannover, Inst Phys Chem & Electrochem, Callinstr 3A, D-30167 Hannover, Germany
基金
中国国家自然科学基金;
关键词
catalytic membrane reactor; CO2-to-methanol; reaction-separation integration; zeolites; HYDROTALCITE-LIKE PRECURSORS; DIMETHYL ETHER; HYDROGENATION; TEMPERATURE; DEACTIVATION; PERFORMANCE; STABILITY; ZR;
D O I
10.1002/anie.202106277
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The hydrogenation of sequestrated CO2 to methanol can reduce CO2 emission and establish a sustainable carbon circuit. However, the transformation of CO2 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 CO2 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-Al2O3-ZrO2 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 CO2 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.
引用
收藏
页码:18289 / 18294
页数:6
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