Insight into lignin oxidative depolymerization in ionic liquids and deep eutectic solvents

解聚 木质素 离子液体 化学 有机化学 电化学 生物高聚物 化学工程 材料科学 聚合物 催化作用 电极 工程类 物理化学
作者
Chandrakant Mukesh,Huang Guo,Hongling Qin,Yanrong Liu,Xiaoyan Ji
出处
期刊:Biomass & Bioenergy [Elsevier BV]
卷期号:188: 107305-107305 被引量:8
标识
DOI:10.1016/j.biombioe.2024.107305
摘要

Lignin is a biopolymer generated from the pulp and paper industry as a natural resource. Lignin valorization is advantageous for biorefineries to produce aromatic compounds, fragrance, biofuel, material, and commodity chemicals, which could be an alternative of crude oil-derived products. However, several barriers are involved in natural lignin extraction and depolymerization, which need to be solved for its full utilization. The electrochemical oxidative upgrading of lignin into the oxygenated molecule is a promising method, which cleaves the C–O and C–C bond by direct oxidative or indirect oxidative method. As promising solvents, electrolytes, as well as catalysts in organic synthesis and electrochemical processes, ionic liquids (ILs) and deep eutectic solvents (DESs) have gained significant attention as dissolution media and catalysts for lignin depolymerization. In this work, aromatic carbon-rich lignin macromolecule depolymerization in ILs/DESs was reviewed to gain a better understanding of barriers, covering the interaction of ILs/DESs with lignin structure, degradation mechanism, thermochemical and electrochemical transformations, as well as COSMO-RS theoretical modeling and screening. In-situ generation of free radicals as catalysts (reactive oxygen species or H2O2) for lignin degradation into value-added products was also discussed. All these studies give importance to ILs/DESs for thermochemical, electrochemical lignin cleavage and upgrading to value-added products for achieving sustainable future goals.
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