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Synthesis of ethanol from aryl methyl ether/lignin, CO(2) and H(2)

Currently, ethanol is produced via hydration of ethene or fermentation of foods. Lignin and CO(2) are abundant, cheap and renewable feedstocks. Synthesis of ethanol using the lignin or its derivatives is of great importance, but is a great challenge and has rarely been reported. Herein, we propose a...

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Autores principales: Zhang, Jingjing, Qian, Qingli, Wang, Ying, Asare Bediako, Bernard Baffour, Yan, Jiang, Han, Buxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020791/
https://www.ncbi.nlm.nih.gov/pubmed/32110349
http://dx.doi.org/10.1039/c9sc03386f
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author Zhang, Jingjing
Qian, Qingli
Wang, Ying
Asare Bediako, Bernard Baffour
Yan, Jiang
Han, Buxing
author_facet Zhang, Jingjing
Qian, Qingli
Wang, Ying
Asare Bediako, Bernard Baffour
Yan, Jiang
Han, Buxing
author_sort Zhang, Jingjing
collection PubMed
description Currently, ethanol is produced via hydration of ethene or fermentation of foods. Lignin and CO(2) are abundant, cheap and renewable feedstocks. Synthesis of ethanol using the lignin or its derivatives is of great importance, but is a great challenge and has rarely been reported. Herein, we propose a route to synthesize ethanol from CO(2), H(2), and lignin or various aryl methyl ethers, which can be derived from lignin. The reaction could be effectively conducted using Ru–Co bimetallic catalyst and the TON of ethanol could reach 145. Interestingly, ethanol was the only liquid product when lignin was used. A series of control experiments indicate that ethanol was formed via cleavage of aryl ether bond, reverse water gas shift (RWGS) reaction, and C–C bond formation. This protocol opens a way to produce ethanol using abundant renewable resources.
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spelling pubmed-70207912020-02-27 Synthesis of ethanol from aryl methyl ether/lignin, CO(2) and H(2) Zhang, Jingjing Qian, Qingli Wang, Ying Asare Bediako, Bernard Baffour Yan, Jiang Han, Buxing Chem Sci Chemistry Currently, ethanol is produced via hydration of ethene or fermentation of foods. Lignin and CO(2) are abundant, cheap and renewable feedstocks. Synthesis of ethanol using the lignin or its derivatives is of great importance, but is a great challenge and has rarely been reported. Herein, we propose a route to synthesize ethanol from CO(2), H(2), and lignin or various aryl methyl ethers, which can be derived from lignin. The reaction could be effectively conducted using Ru–Co bimetallic catalyst and the TON of ethanol could reach 145. Interestingly, ethanol was the only liquid product when lignin was used. A series of control experiments indicate that ethanol was formed via cleavage of aryl ether bond, reverse water gas shift (RWGS) reaction, and C–C bond formation. This protocol opens a way to produce ethanol using abundant renewable resources. Royal Society of Chemistry 2019-10-02 /pmc/articles/PMC7020791/ /pubmed/32110349 http://dx.doi.org/10.1039/c9sc03386f Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Zhang, Jingjing
Qian, Qingli
Wang, Ying
Asare Bediako, Bernard Baffour
Yan, Jiang
Han, Buxing
Synthesis of ethanol from aryl methyl ether/lignin, CO(2) and H(2)
title Synthesis of ethanol from aryl methyl ether/lignin, CO(2) and H(2)
title_full Synthesis of ethanol from aryl methyl ether/lignin, CO(2) and H(2)
title_fullStr Synthesis of ethanol from aryl methyl ether/lignin, CO(2) and H(2)
title_full_unstemmed Synthesis of ethanol from aryl methyl ether/lignin, CO(2) and H(2)
title_short Synthesis of ethanol from aryl methyl ether/lignin, CO(2) and H(2)
title_sort synthesis of ethanol from aryl methyl ether/lignin, co(2) and h(2)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020791/
https://www.ncbi.nlm.nih.gov/pubmed/32110349
http://dx.doi.org/10.1039/c9sc03386f
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