Rapid microwave-assisted biomass delignification and lignin depolymerization in deep eutectic solvents

被引:130
|
作者
Muley, Pranjali D. [1 ,2 ]
Mobley, Justin K. [3 ]
Tong, Xinjie [4 ]
Novak, Brian [4 ]
Stevens, Joseph [5 ]
Moldovan, Dorel [4 ]
Shi, Jian [5 ]
Boldor, Dorin [1 ,2 ]
机构
[1] Louisiana State Univ, Dept Biol & Agr Engn, Baton Rouge, LA 70803 USA
[2] Agr Ctr, Baton Rouge, LA 70803 USA
[3] Univ Kentucky, Dept Chem, Lexington, KY 40546 USA
[4] Louisiana State Univ, Dept Mech & Ind Engn, Baton Rouge, LA 70803 USA
[5] Univ Kentucky, Dept Biosyst & Agr Engn, Lexington, KY 40546 USA
关键词
Deep eutectic solvents; Lignin depolymerization; Biomass deconstruction; Microwave heating; LIGNOCELLULOSIC BIOMASS; CHOLINE CHLORIDE; FORCE-FIELD; FRACTIONATION; CELLULOSE; WOOD; HEMICELLULOSE; PRETREATMENTS; EXTRACTION; GENERATION;
D O I
10.1016/j.enconman.2019.06.070
中图分类号
O414.1 [热力学];
学科分类号
摘要
Biomass deconstruction and lignin depolymerization was performed using three different deep eutectic solvents. Various temperature (110 degrees, 130 degrees, and 150 degrees C) and time (1, 5, 10, 15 min) conditions were tested in a 2450 MHz microwave reactor. Oxalic acid (130 degrees C, 15 min) and formic acid DES (150 degrees C, 15 min) gave the highest lignin yield. Microwave heating reduced the processing time significantly. NMR characterization shows that microwave heating promotes selective bond cleavage during lignin depolymerization and has a narrow molecular weight distribution compared to conventional heating techniques. Molecular dynamic simulations showed that certain lignin bonds are stretched under the electric field imparted during microwave irradiation, increasing its probability of breaking.
引用
收藏
页码:1080 / 1088
页数:9
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