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Constructing carbon supported copper-based catalysts for efficient CO(2) hydrogenation to methanol

An activated carbon-supported Cu/ZnO catalyst (CCZ-AE-ox) was successfully obtained by the ammonia evaporation method for the hydrogenation of carbon dioxide to methanol, and the surface properties of the catalyst post-calcination and reduction were investigated. Activated carbon facilitated the inc...

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Autores principales: Xie, Zhong, Hei, Jinpei, Li, Chuan, Yin, Xiaojie, Wu, Fengyi, Cheng, Lei, Meng, Sugang
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/PMC10177214/
https://www.ncbi.nlm.nih.gov/pubmed/37188247
http://dx.doi.org/10.1039/d3ra01502e
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author Xie, Zhong
Hei, Jinpei
Li, Chuan
Yin, Xiaojie
Wu, Fengyi
Cheng, Lei
Meng, Sugang
author_facet Xie, Zhong
Hei, Jinpei
Li, Chuan
Yin, Xiaojie
Wu, Fengyi
Cheng, Lei
Meng, Sugang
author_sort Xie, Zhong
collection PubMed
description An activated carbon-supported Cu/ZnO catalyst (CCZ-AE-ox) was successfully obtained by the ammonia evaporation method for the hydrogenation of carbon dioxide to methanol, and the surface properties of the catalyst post-calcination and reduction were investigated. Activated carbon facilitated the increased dispersion of the loaded metals, which promote the CO(2) space-time yield (STY) of methanol and turnover frequency (TOF) on the active sites. Furthermore, the factors affecting the catalyst in the hydrogenation of CO(2) to methanol were in-depth investigated. The larger surface area and higher CO(2) adsorption capacity are found to make possible the main attributions of the superior activity of the CCZ-AE-ox catalyst.
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spelling pubmed-101772142023-05-13 Constructing carbon supported copper-based catalysts for efficient CO(2) hydrogenation to methanol Xie, Zhong Hei, Jinpei Li, Chuan Yin, Xiaojie Wu, Fengyi Cheng, Lei Meng, Sugang RSC Adv Chemistry An activated carbon-supported Cu/ZnO catalyst (CCZ-AE-ox) was successfully obtained by the ammonia evaporation method for the hydrogenation of carbon dioxide to methanol, and the surface properties of the catalyst post-calcination and reduction were investigated. Activated carbon facilitated the increased dispersion of the loaded metals, which promote the CO(2) space-time yield (STY) of methanol and turnover frequency (TOF) on the active sites. Furthermore, the factors affecting the catalyst in the hydrogenation of CO(2) to methanol were in-depth investigated. The larger surface area and higher CO(2) adsorption capacity are found to make possible the main attributions of the superior activity of the CCZ-AE-ox catalyst. The Royal Society of Chemistry 2023-05-12 /pmc/articles/PMC10177214/ /pubmed/37188247 http://dx.doi.org/10.1039/d3ra01502e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Xie, Zhong
Hei, Jinpei
Li, Chuan
Yin, Xiaojie
Wu, Fengyi
Cheng, Lei
Meng, Sugang
Constructing carbon supported copper-based catalysts for efficient CO(2) hydrogenation to methanol
title Constructing carbon supported copper-based catalysts for efficient CO(2) hydrogenation to methanol
title_full Constructing carbon supported copper-based catalysts for efficient CO(2) hydrogenation to methanol
title_fullStr Constructing carbon supported copper-based catalysts for efficient CO(2) hydrogenation to methanol
title_full_unstemmed Constructing carbon supported copper-based catalysts for efficient CO(2) hydrogenation to methanol
title_short Constructing carbon supported copper-based catalysts for efficient CO(2) hydrogenation to methanol
title_sort constructing carbon supported copper-based catalysts for efficient co(2) hydrogenation to methanol
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177214/
https://www.ncbi.nlm.nih.gov/pubmed/37188247
http://dx.doi.org/10.1039/d3ra01502e
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