木质素
深共晶溶剂
共晶体系
解聚
氯化胆碱
溶剂
化学
单体
化学工程
材料科学
有机化学
聚合物
工程类
合金
作者
Haichao Li,Deqiang Li,Yuan He,Chaobing Luo,Wu Lan,Arthur J. Ragauskas,Tingting You,Feng Xu
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-07-04
卷期号:11 (27)
标识
DOI:10.1126/sciadv.adv7299
摘要
Highly efficient conversion of lignin into value-added chemicals and materials is trapped in the inevitable cleavage of β-O-4 linkages and formation of highly condensed structures with deep colors during lignin isolation. Here, we develop a trifunctional choline chloride/glyoxylic acid (ChCl/GA) binary deep eutectic solvent with a π-π conjugate structure and moderate acidity for the fast isolation of light-colored lignin with near proto-structures (exceeding 88% of delignification ratio for 1 hour). The synergetic interaction of GA and ChCl substantially reduced Gibbs free energy of acetal reaction and thoroughly captured reactive intermediates, precisely activating the following key functions: stabilizing β-O-4 linkages, inhibiting condensation reaction, and shielding –OH groups. These enabled efficient isolation of uncondensed, abundant β-O-4 linkage (45.80/100 C9; 79% retention) and light-colored lignin. A near-theoretical yield of aromatic monomers upon depolymerization and high performances as adhesives for lignocellulosic bioplastics were achieved. This work unleashes the valorization potential of lignin by a relatively green and fast strategy for sustainable biorefineries.
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