Effect of metal triflates on the microwave-assisted catalytic hydrogenolysis of birch wood lignin to monophenolic compounds

被引:9
作者
Liu, Xudong [1 ,2 ]
Bouxin, Florent P. [2 ]
Fan, Jiajun [2 ]
Gammons, Richard [2 ]
Budarin, Vitaliy L. [2 ]
Hu, Changwei [1 ]
Clark, James H. [2 ]
机构
[1] Sichuan Univ, Coll Chem, Key Lab Green Chem & Technol, Minist Educ, Chengdu 610064, Peoples R China
[2] Univ York, Dept Chem, Green Chem Ctr Excellence, York YO10 5DD, N Yorkshire, England
基金
英国工程与自然科学研究理事会; “创新英国”项目; 中国国家自然科学基金; 英国生物技术与生命科学研究理事会;
关键词
Lignin; Birch; Microwave; Metal triflates; Monophenolic compounds; PHENOLIC MONOMERS; LIGNOCELLULOSE FRACTIONATION; DEPOLYMERIZATION; ACID; CONVERSION; BIOMASS; WATER; CHEMICALS; VALORIZATION; CLEAVAGE;
D O I
10.1016/j.indcrop.2021.113515
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
The lignin-first biorefinery strategy could produce bio-based phenols from the extraction and depolymerization of native lignin in lignocellulosic biomass. Herein, we report an effective Lewis acid-promoted delignification and production of monophenolic compounds in birch sawdust assisted by microwave heating without external hydrogen for the first time. The screening of different metal triflates revealed that Fe(OTf)(3) was best for the delignification and depolymerization of birch sawdust. Without the addition of a Lewis acid, the yield of monophenolic compounds was 10.5 wt% (based on the lignin content in birch sawdust), while it increased significantly to 32.9 wt% with the addition of Fe(OTf)(3) (0.0276 g) under the identical conditions (190 degrees C, 1 h), which demonstrated the catalytic C-O-C bond scission promoted by Fe(OTf)(3). Simultaneously, the delignification degree also rose sharply from 32.6 wt% to 47.5 wt%. This work demonstrated the efficient Fe(OTf)(3)-induced delignification and depolymerization of lignin in birch sawdust to obtain a high yield of monophenolic compounds without external hydrogen assisted by microwave heating, representing a novel advance in the "lignin-first" biorefinery field.
引用
收藏
页数:8
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