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Direct oxidation of methane to methanol using CuMoO(4)

Upgrading methane into methanol or other high value-added chemicals is not only beneficial to mitigate the greenhouse effect, but also provides basic raw materials for industrial production. Nowadays, most research is limited to zeolite systems, and it is a considerable challenge to extend the suppo...

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Autores principales: Wu, Wenjian, Li, Wenzhi, Wu, Mingwei, Zhang, Hao, Zhu, Chen, Jiang, Yihang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923457/
https://www.ncbi.nlm.nih.gov/pubmed/36793293
http://dx.doi.org/10.1039/d3ra00058c
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author Wu, Wenjian
Li, Wenzhi
Wu, Mingwei
Zhang, Hao
Zhu, Chen
Jiang, Yihang
author_facet Wu, Wenjian
Li, Wenzhi
Wu, Mingwei
Zhang, Hao
Zhu, Chen
Jiang, Yihang
author_sort Wu, Wenjian
collection PubMed
description Upgrading methane into methanol or other high value-added chemicals is not only beneficial to mitigate the greenhouse effect, but also provides basic raw materials for industrial production. Nowadays, most research is limited to zeolite systems, and it is a considerable challenge to extend the support to metal oxides while achieving a high yield of methanol. In this paper, we take advantage of impregnation methods to synthesise a novel Cu/MoO(3) catalyst, which can convert methane to methanol in the gaseous phase. At 600 °C, the Cu(2)/MoO(3) catalyst can achieve a maximum STY(CH(3)OH) of 47.2 μmol (g(−1) h(−1)) with a molar ratio CH(4) : O(2) : H(2)O = 5 : 1.4 : 10. Consequences of SEM, TEM, HRTEM and XRD substantiate that Cu is incorporated into the lattice of MoO(3) to form CuMoO(4). And transmission infrared spectroscopy, Raman spectroscopy together with XPS characterization techniques confirm the generation of CuMoO(4), which is the main active site provider. This work provides a new support platform for Cu-based catalyst research in the methane-to-methanol system.
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spelling pubmed-99234572023-02-14 Direct oxidation of methane to methanol using CuMoO(4) Wu, Wenjian Li, Wenzhi Wu, Mingwei Zhang, Hao Zhu, Chen Jiang, Yihang RSC Adv Chemistry Upgrading methane into methanol or other high value-added chemicals is not only beneficial to mitigate the greenhouse effect, but also provides basic raw materials for industrial production. Nowadays, most research is limited to zeolite systems, and it is a considerable challenge to extend the support to metal oxides while achieving a high yield of methanol. In this paper, we take advantage of impregnation methods to synthesise a novel Cu/MoO(3) catalyst, which can convert methane to methanol in the gaseous phase. At 600 °C, the Cu(2)/MoO(3) catalyst can achieve a maximum STY(CH(3)OH) of 47.2 μmol (g(−1) h(−1)) with a molar ratio CH(4) : O(2) : H(2)O = 5 : 1.4 : 10. Consequences of SEM, TEM, HRTEM and XRD substantiate that Cu is incorporated into the lattice of MoO(3) to form CuMoO(4). And transmission infrared spectroscopy, Raman spectroscopy together with XPS characterization techniques confirm the generation of CuMoO(4), which is the main active site provider. This work provides a new support platform for Cu-based catalyst research in the methane-to-methanol system. The Royal Society of Chemistry 2023-02-13 /pmc/articles/PMC9923457/ /pubmed/36793293 http://dx.doi.org/10.1039/d3ra00058c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wu, Wenjian
Li, Wenzhi
Wu, Mingwei
Zhang, Hao
Zhu, Chen
Jiang, Yihang
Direct oxidation of methane to methanol using CuMoO(4)
title Direct oxidation of methane to methanol using CuMoO(4)
title_full Direct oxidation of methane to methanol using CuMoO(4)
title_fullStr Direct oxidation of methane to methanol using CuMoO(4)
title_full_unstemmed Direct oxidation of methane to methanol using CuMoO(4)
title_short Direct oxidation of methane to methanol using CuMoO(4)
title_sort direct oxidation of methane to methanol using cumoo(4)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923457/
https://www.ncbi.nlm.nih.gov/pubmed/36793293
http://dx.doi.org/10.1039/d3ra00058c
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