Organosolv and ionosolv processes for autohydrolyzed poplar fractionation: Lignin recovery and characterization

被引:14
|
作者
Ovejero-Perez, Antonio [1 ]
Rigual, Victoria [1 ]
Oliet, Mercedes [1 ]
Rodriguez, Francisco [1 ]
Dominguez, Juan Carlos [1 ]
Alonso, M. Virginia [1 ]
机构
[1] Univ Complutense Madrid, Dept Chem Engn & Mat, Av Complutense s-n, Madrid 28040, Spain
关键词
Wood fractionation; Lignin recovery; Lignin characterization; ACIDIC IONIC LIQUID; MOLECULAR-WEIGHT; UNIVERSAL CALIBRATION; SIDE-STREAMS; PRETREATMENT; WOOD; CELLULOSE; DEPOLYMERIZATION; BIOMASS; DELIGNIFICATION;
D O I
10.1016/j.ijbiomac.2021.12.079
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Biomass fractionation plays a major role in the search for competitive biorefineries, where the isolation and recovery of the three woody fractions is key. In this sense, we have used autohydrolyzed hemicellulose-free poplar as feedstock to compare two fractionation processes, organosolv and ionosolv, oriented to lignin recov-ery. The recovered lignins were then characterize by different techniques (NMR, GPC, TGA). Both treatments were tested at different temperatures to analyze temperature influence on lignin recovery and properties. The highest lignin recovery was obtained with the ionosolv process at 135 ?, reaching a solid yield of 70%. Lignin characterization showed differences between both treatments. Lignins enriched in C-O linkages and G units were recovered with the organosolv process, where increasing temperature led to highly depolymerized lignins. However, lignins with higher C-C linkages and S units contents were obtained with the ionosolv process, pro-ducing more thermically stable lignins. In addition, increasing temperature caused lignin repolymerization when employing ionic liquids as solvents. Therefore, this work outlines the most important differences between ionosolv and organosolv processes for biomass fractionation, focusing on lignin recovery and its properties, which is the first step in order to valorize all biomass fractions.
引用
收藏
页码:131 / 140
页数:10
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