Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids
Abstract 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, electroche...
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2017-07-01
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doaj-c02d82018e7640c897f568a29c1157d42020-12-08T03:10:05ZengNature Publishing GroupScientific Reports2045-23222017-07-017111210.1038/s41598-017-05316-xSustainable Electrochemical Depolymerization of Lignin in Reusable Ionic LiquidsTobias K. F. Dier0Daniel Rauber1Dan Durneata2Rolf Hempelmann3Dietrich A. Volmer4Institute of Bioanalytical Chemistry, Saarland University, Campus B2.2Institute of Physical Chemistry, Saarland University, Campus B2.2Institute of Physical Chemistry, Saarland University, Campus B2.2Institute of Physical Chemistry, Saarland University, Campus B2.2Institute of Bioanalytical Chemistry, Saarland University, Campus B2.2Abstract 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.https://doi.org/10.1038/s41598-017-05316-x |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tobias K. F. Dier Daniel Rauber Dan Durneata Rolf Hempelmann Dietrich A. Volmer |
spellingShingle |
Tobias K. F. Dier Daniel Rauber Dan Durneata Rolf Hempelmann Dietrich A. Volmer Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids Scientific Reports |
author_facet |
Tobias K. F. Dier Daniel Rauber Dan Durneata Rolf Hempelmann Dietrich A. Volmer |
author_sort |
Tobias K. F. Dier |
title |
Sustainable Electrochemical Depolymerization of Lignin in Reusable Ionic Liquids |
title_short |
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_sort |
sustainable electrochemical depolymerization of lignin in reusable ionic liquids |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2017-07-01 |
description |
Abstract 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. |
url |
https://doi.org/10.1038/s41598-017-05316-x |
work_keys_str_mv |
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