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 |
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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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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.</abstract><pub>ROYAL SOC CHEMISTRY</pub></addata></record> |
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title | Direct conversion of syngas into aromatics over a bifunctional catalyst: inhibiting net CO2 release |
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