Facile fractionation of lignocellulosic biomass: a review on promising green technology of deep eutectic solvent for bioethanol production

被引:4
作者
Parveen, Fouziya [1 ]
Saxena, Ayush [1 ]
Hussain, Akhtar [1 ]
Giri, Balendu Shekher [2 ]
Ashfaque, Mohammad [1 ]
机构
[1] Integral Univ, Dept Biosci, Lignocellulose & Biofuel Lab, Lucknow 226026, India
[2] Univ Petr & Energy Studies UPES, Fac Sustainabil Cluster, Sch Engn, Bhidholi Campus, Dehra Dun 248007, India
关键词
Lignocellulosic biomass; Pretreatment; Green solvent; Delignification; Deep eutectic solvent (DES); Bioethanol; CATALYTIC FAST PYROLYSIS; HOT-WATER PRETREATMENT; ENZYMATIC-HYDROLYSIS; WHEAT-STRAW; CORN STOVER; BIOLOGICAL PRETREATMENT; METHANE PRODUCTION; ETHANOL-PRODUCTION; FUNCTIONAL-GROUPS; SODIUM-HYDROXIDE;
D O I
10.1007/s13399-024-06146-4
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Sustainable bioethanol production from lignocellulosic biomass to meet the energy demand and generate wealth from waste is the need of the hour. A surplus amount of lignocellulosic biomass is produced worldwide as organic waste which can be utilized for bioethanol production. Pretreatment is a crucial step in biorefinery application, the selection of the best pretreatment technology will reduce the intensive energy requirements, and the operational costs make biofuel production economically feasible and sustainable. Every pretreatment technology has its own drawbacks which needs to be addressed. Among these technologies, deep eutectic solvent (DES) is being investigated as an ideal solvent for the pretreatment of lignocellulosic biomass to improve the enzymatic digestibility, surface area solubility, and lowering lignin content and cellulose crystallinity. DES offers a green way of deconstructing lignocellulosic biomass with minimum environmental hazard. DES is an inexpensive and environment-friendly solvent effective in biomass valorization. This review focuses on the current status and advancements in pretreatment technologies using DES and its future prospects.
引用
收藏
页码:13303 / 13322
页数:20
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