<HashMap><database>biostudies-literature</database><scores/><additional><submitter>da Cruz MGA</submitter><funding>COMET InTribology project</funding><funding>Swedish Foundation for Strategic Environmental Research</funding><funding>Carl Tryggers Stiftelse för Vetenskaplig Forskning</funding><funding>AC2T research GmbH</funding><funding>Stiftelsen för Miljöstrategisk Forskning</funding><pagination>e202200718</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9545899</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(15)</volume><pubmed_abstract>Breaking down lignin into smaller units is the key to generate high value-added products. Nevertheless, dissolving this complex plant polyphenol in an environment-friendly way is often a challenge. Levulinic acid, which is formed during the hydrothermal processing of lignocellulosic biomass, has been shown to efficiently dissolve lignin. Herein, levulinic acid was evaluated as a medium for the reductive electrochemical depolymerization of the lignin macromolecule. Copper was chosen as the electrocatalyst due to the economic feasibility and low activity towards the hydrogen evolution reaction. After depolymerization, high-resolution mass spectrometry and nuclear magnetic resonance spectroscopy revealed lignin-derived monomers and dimers. A predominance of aryl ether and phenolic groups was observed. Depolymerized lignin was further evaluated as an anti-corrosion coating, revealing enhancements on the electrochemical stability of the metal. Via a simple depolymerization process of biomass waste in a biomass-based solvent, a straightforward approach to produce high value-added compounds or tailored biobased materials was demonstrated.</pubmed_abstract><journal>ChemSusChem</journal><pubmed_title>Electrochemical Depolymerization of Lignin in a Biomass-based Solvent.</pubmed_title><pmcid>PMC9545899</pmcid><funding_grant_id>872176</funding_grant_id><funding_grant_id>2018/11</funding_grant_id><funding_grant_id>CTS 39: 194</funding_grant_id><pubmed_authors>Gueret R</pubmed_authors><pubmed_authors>Budnyk S</pubmed_authors><pubmed_authors>da Cruz MGA</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Piatek J</pubmed_authors><pubmed_authors>Frauscher M</pubmed_authors><pubmed_authors>Sipponen MH</pubmed_authors><pubmed_authors>Rodrigues BVM</pubmed_authors><pubmed_authors>Beele B</pubmed_authors><pubmed_authors>Slabon A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Electrochemical Depolymerization of Lignin in a Biomass-based Solvent.</name><description>Breaking down lignin into smaller units is the key to generate high value-added products. Nevertheless, dissolving this complex plant polyphenol in an environment-friendly way is often a challenge. Levulinic acid, which is formed during the hydrothermal processing of lignocellulosic biomass, has been shown to efficiently dissolve lignin. Herein, levulinic acid was evaluated as a medium for the reductive electrochemical depolymerization of the lignin macromolecule. Copper was chosen as the electrocatalyst due to the economic feasibility and low activity towards the hydrogen evolution reaction. After depolymerization, high-resolution mass spectrometry and nuclear magnetic resonance spectroscopy revealed lignin-derived monomers and dimers. A predominance of aryl ether and phenolic groups was observed. Depolymerized lignin was further evaluated as an anti-corrosion coating, revealing enhancements on the electrochemical stability of the metal. Via a simple depolymerization process of biomass waste in a biomass-based solvent, a straightforward approach to produce high value-added compounds or tailored biobased materials was demonstrated.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-05T20:11:16.713Z</modification><creation>2025-04-05T20:11:16.713Z</creation></dates><accession>S-EPMC9545899</accession><cross_references><pubmed>35608798</pubmed><doi>10.1002/cssc.202200718</doi></cross_references></HashMap>