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Abstract:
The optimizing utilization of carbon resources has drawn wide attention all over the world, while exploiting the high-efficiency catalytic routes remains a challenge. Here, a direct methanol synthesis route is realized from pure CO and H2O over 10%Cu/t-ZrO2 catalyst, where the time yield of methanol is 144.43 mmol molCu1 h-1 and the methanol selectivity in hydrocarbons is 100%. The Cu species highly dispersed in the t-ZrO2 support lead parts of them in the cationic state. The Cu+ sites contribute to the dissociation of H2O, providing the H* source for methanol synthesis, while the formed Cu0 sites promote the absorption and transfer of H* during the reaction. Moreover, the H2O is even a better H resource than H2 due to its better dissociation effectivity in this catalytic system. The present work offers a new approach for methanol synthesis from CO and new insight into the process of supplying H donor. (c) 2024 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
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JOURNAL OF ENERGY CHEMISTRY
ISSN: 2095-4956
CN: 10-1287/O6
Year: 2024
Volume: 93
Page: 126-134
1 4 . 0 0 0
JCR@2023
Cited Count:
WoS CC Cited Count: 25
SCOPUS Cited Count: 25
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 3
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