Direct conversion of syngas into aromatics over a bifunctional catalyst: inhibiting net CO2 release

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-...

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Veröffentlicht in:CHEMICAL COMMUNICATIONS 2020-05, Vol.56 (39), p.5239-5242
Hauptverfasser: Zhou, Wei, Zhou, Cheng, Yin, Haoren, Shi, Jiaqing, Zhang, Guoquan, Zheng, Xinlei, Min, Xiaojian, Zhang, Zhiqiang, Cheng, Kang, Kang, Jincan, Zhang, Qinghong, Wang, Ye
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container_issue 39
container_start_page 5239
container_title CHEMICAL COMMUNICATIONS
container_volume 56
creator Zhou, Wei
Zhou, Cheng
Yin, Haoren
Shi, Jiaqing
Zhang, Guoquan
Zheng, Xinlei
Min, Xiaojian
Zhang, Zhiqiang
Cheng, Kang
Kang, Jincan
Zhang, Qinghong
Wang, Ye
description 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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title Direct conversion of syngas into aromatics over a bifunctional catalyst: inhibiting net CO2 release
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