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Direct conversion of syngas into aromatics over a bifunctional catalyst: inhibiting net CO2 release
Wei Zhou1, Cheng Zhou1, Haoren Yin1
1State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethersand Esters, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, P. R. China. zhangqh@xmu.edu.cn wangye@xmu.edu.cn.
Abstract:
Tandem catalysis via methanol intermediate is a promising route for the direct conversion of syngas into aromatics. However, the simultaneous formation of CO2 is a serious problem. Here, we demonstrate that CO2 was formed by the water-gas shift (WGS) reaction (CO + H2O → CO2 + H2) over a ZnO-ZrO2/H-ZSM-5 catalyst, and the net CO2 formation could be inhibited without affecting the formation of aromatics by co-feeding CO2.
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