Deep Eutectic Solvent Aqueous Solutions as Efficient Media for the Solubilization of Hardwood Xylans

被引:82
|
作者
Morais, Eduarda S. [1 ]
Mendonca, Patrcia V. [2 ]
Coelho, Jorge F. J. [2 ]
Freire, Mara G. [1 ]
Freire, Carmen S. R. [1 ]
Coutinho, Joao P. [1 ]
Silvestre, Armando J. D. [1 ]
机构
[1] Univ Aveiro, Dept Chem, CICECO Aveiro Inst Mat, P-3810193 Aveiro, Portugal
[2] Univ Coimbra, Dept Chem Engn, CEMMPRE, P-3030790 Coimbra, Portugal
基金
欧洲研究理事会;
关键词
biorefinery; deep eutectic solvents; extraction; green solvents; xylans; LIGNOCELLULOSIC BIOMASS; IONIC LIQUIDS; KRAFT PULP; EXTRACTION; WOOD; OIL; HEMICELLULOSES; VALORIZATION; CHEMICALS; CHLORIDE;
D O I
10.1002/cssc.201702007
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work contributes to the development of integrated lignocellulosic-based biorefineries by the pioneering exploitation of hardwood xylans by solubilization and extraction in deep eutectic solvents (DES). DES formed by choline chloride and urea or acetic acid were initially evaluated as solvents for commercial xylan as a model compound. The effects of temperature, molar ratio, and concentration of the DES aqueous solutions were evaluated and optimized by using a response surface methodology. The results obtained demonstrated the potential of these solvents, with 328.23g L-1 of xylan solubilization using 66.7 wt% DES in water at 80 degrees C. Furthermore, xylans could be recovered by precipitation from the DES aqueous media in yields above 90%. The detailed characterization of the xylans recovered after solubilization in aqueous DES demonstrated that 4-O-methyl groups were eliminated from the 4-O-methylglucuronic acids moieties and uronic acids (15%) were cleaved from the xylan backbone during this process. The similar M-w values of both pristine and recovered xylans confirmed the success of the reported procedure. DES recovery in four additional extraction cycles was also demonstrated. Finally, the successful extraction of xylans from Eucalyptus globulus wood by using aqueous solutions of DES was demonstrated.
引用
收藏
页码:753 / 762
页数:10
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