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Enhanced ORR performance to electrochemical lignin valorization in a mixture of ionic liquid/organic solvent binary electrolytes.

Authors :
Jiang, Haomin
Li, Ang
Sun, Yanzhi
Wang, Lei
Chen, Yongmei
Source :
New Journal of Chemistry; 10/28/2023, Vol. 47 Issue 40, p18682-18689, 8p
Publication Year :
2023

Abstract

Lignin is the largest renewable source of aromatic compounds, creating an opportunity for the chemical industry as a feedstock provided that the deconstruction and upgrading methods become economically feasible. Lignin valorization is performed using superoxide radicals (˙O<subscript>2</subscript><superscript>−</superscript>) as an oxidizing reagent, which are electro-generated in situ through the oxygen reduction reaction (ORR) in an aprotic ionic liquid [BMIM]BF<subscript>4</subscript>. In this study, both the current efficiency and the percent conversion of lignin valorization are improved by simply reducing the viscosity of the electrolyte. The electrochemical analysis and molecular dynamics (MD) simulation results indicate that the presence of non-proton organic solvent CH<subscript>3</subscript>CN in [BMIM]BF<subscript>4</subscript> can significantly improve the mass transfer process of O<subscript>2</subscript>, thereby accelerating the generation rate of ˙O<subscript>2</subscript><superscript>−</superscript>. It is verified using p-benzylethoxyphenol (PBP) as a lignin model compound with a higher Faraday efficiency of 35.3% in [BMIM]BF<subscript>4</subscript>/CH<subscript>3</subscript>CN (7 : 3 v/v) than that of 15.5% in pure [BMIM]BF<subscript>4</subscript>. Finally, an actual lignin sample in [BMIM]BF<subscript>4</subscript>/CH<subscript>3</subscript>CN exhibited a percent conversion of 50.3% to selectively obtain only 4 kinds of the main small molecule aromatic compounds. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
11440546
Volume :
47
Issue :
40
Database :
Complementary Index
Journal :
New Journal of Chemistry
Publication Type :
Academic Journal
Accession number :
173011301
Full Text :
https://doi.org/10.1039/d3nj03967f