Progress in the solvent depolymerization of lignin

被引:0
|
作者
Patil, Vivek [1 ]
Adhikari, Sushil [1 ,2 ]
Cross, Phillip [1 ]
Jahromi, Hossein [1 ,2 ]
机构
[1] Auburn Univ, Dept Biosyst Engn, 350 Mell St, Auburn, AL 36849 USA
[2] Auburn Univ, Ctr Bioenergy & Bioprod, 350 Mell St, Auburn, AL 36849 USA
来源
基金
美国食品与农业研究所;
关键词
Lignin depolymerization; Solvent liquefaction; Sustainability; Reaction conditions; QUANTITATIVE P-31 NMR; C BOND-CLEAVAGE; KRAFT LIGNIN; CATALYTIC DEPOLYMERIZATION; ORGANOSOLV LIGNIN; ALKALI LIGNIN; FORMIC-ACID; LIGNOCELLULOSE FRACTIONATION; HYDROTHERMAL CONVERSION; OXIDATIVE CLEAVAGE;
D O I
10.1016/j.rscr.2020.110359
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Solvent liquefaction of lignin is a simultaneous depolymerization and hydrodeoxygenation process used to generate monomer products for fuel and specialty chemical applications. Lignin source, its isolation technique, and the process conditions play essential roles in overall lignin conversion and product distribution. This paper reviews major structural changes that occur during Kraft, organosolv, soda, and other novel lignin extraction processes and how these structural changes affect the solvent liquefaction performances. Reaction conditions, including temperature, residence time, solvent characteristics, and catalyst, are reviewed. Finally, pathways for getting commercially valuable chemicals from lignin is explored. The role of non-water solvents in achieving high-value products from lignin depolymerization is also discussed. The structure of lignin was found to be more critical than reaction conditions in determining the product yields, and future research should have more emphasis on this aspect. Overall, high temperature and longer residence time were found to be useful for depolymerization under certain conditions, such as the presence of homogeneous catalysts, condensed lignin structure, and water as a solvent.
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页数:20
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