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Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids
Lignin’s aromatic building blocks provide a chemical resource that is, in theory, ideal for substitution of aromatic petrochemicals. Moreover, degradation and valorization of lignin has the potential to generate many high-value chemicals for technical applications. In this study, electrochemical deg...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5505966/ https://www.ncbi.nlm.nih.gov/pubmed/28698638 http://dx.doi.org/10.1038/s41598-017-05316-x |
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author | Dier, Tobias K. F. Rauber, Daniel Durneata, Dan Hempelmann, Rolf Volmer, Dietrich A. |
author_facet | Dier, Tobias K. F. Rauber, Daniel Durneata, Dan Hempelmann, Rolf Volmer, Dietrich A. |
author_sort | Dier, Tobias K. F. |
collection | PubMed |
description | Lignin’s aromatic building blocks provide a chemical resource that is, in theory, ideal for substitution of aromatic petrochemicals. Moreover, degradation and valorization of lignin has the potential to generate many high-value chemicals for technical applications. In this study, electrochemical degradation of alkali and Organosolv lignin was performed using the ionic liquids 1-ethyl-3-methylimidazolium trifluoromethanesulfonate and triethylammonium methanesulfonate. The extensive degradation of the investigated lignins with simultaneous almost full recovery of the electrolyte materials provided a sustainable alternative to more common lignin degradation processes. We demonstrate here that both the presence (and the absence) of water during electrolysis and proton transport reactions had significant impact on the degradation efficiency. Hydrogen peroxide radical formation promoted certain electrochemical mechanisms in electrolyte systems “contaminated” with water and increased yields of low molecular weight products significantly. The proposed mechanisms were tentatively confirmed by determining product distributions using a combination of liquid chromatography-mass spectrometry and gas-chromatography-mass spectrometry, allowing measurement of both polar versus non-polar as well as volatile versus non-volatile components in the mixtures. |
format | Online Article Text |
id | pubmed-5505966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55059662017-07-13 Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids Dier, Tobias K. F. Rauber, Daniel Durneata, Dan Hempelmann, Rolf Volmer, Dietrich A. Sci Rep Article Lignin’s aromatic building blocks provide a chemical resource that is, in theory, ideal for substitution of aromatic petrochemicals. Moreover, degradation and valorization of lignin has the potential to generate many high-value chemicals for technical applications. In this study, electrochemical degradation of alkali and Organosolv lignin was performed using the ionic liquids 1-ethyl-3-methylimidazolium trifluoromethanesulfonate and triethylammonium methanesulfonate. The extensive degradation of the investigated lignins with simultaneous almost full recovery of the electrolyte materials provided a sustainable alternative to more common lignin degradation processes. We demonstrate here that both the presence (and the absence) of water during electrolysis and proton transport reactions had significant impact on the degradation efficiency. Hydrogen peroxide radical formation promoted certain electrochemical mechanisms in electrolyte systems “contaminated” with water and increased yields of low molecular weight products significantly. The proposed mechanisms were tentatively confirmed by determining product distributions using a combination of liquid chromatography-mass spectrometry and gas-chromatography-mass spectrometry, allowing measurement of both polar versus non-polar as well as volatile versus non-volatile components in the mixtures. Nature Publishing Group UK 2017-07-11 /pmc/articles/PMC5505966/ /pubmed/28698638 http://dx.doi.org/10.1038/s41598-017-05316-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dier, Tobias K. F. Rauber, Daniel Durneata, Dan Hempelmann, Rolf Volmer, Dietrich A. Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids |
title | Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids |
title_full | Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids |
title_fullStr | Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids |
title_full_unstemmed | Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids |
title_short | Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids |
title_sort | sustainable electrochemical depolymerization of lignin in reusable ionic liquids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5505966/ https://www.ncbi.nlm.nih.gov/pubmed/28698638 http://dx.doi.org/10.1038/s41598-017-05316-x |
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