有机溶剂
木质素
化学
酶水解
木质纤维素生物量
纤维素
纤维素酶
蔗渣
水解
有机化学
半纤维素
甘油
PEG比率
生物炼制
制浆造纸工业
原材料
财务
经济
工程类
作者
Guojie Song,Meysam Madadi,Xianzhi Meng,Chihe Sun,Mortaza Aghbashlo,Fubao Sun,Arthur J. Ragauskas,Meisam Tabatabaei,Alireza Ashori
标识
DOI:10.1016/j.cej.2024.148713
摘要
Organosolv pretreatment effectively fractionates lignocellulosic biomass for efficient enzymatic hydrolysis, yielding fermentable sugars. However, substantial lignin redeposition on the substrate surface and residual lignin content exacerbate lignin's inhibitory effects on subsequent enzymatic hydrolysis. An in-situ lignin modification is proposed to address this challenge by incorporating polyethylene glycol (PEG) series into glycerol organosolv (GO) pretreatment. According to the results obtained, PEG-assisted GO pretreated substrate exhibited significantly increased sugar yield during enzymatic hydrolysis, particularly with PEG 4000, showing 35.4% higher glucose yield over 72 h. The improved glucose yield with PEG could be attributed to changes in the physicochemical structure and properties of residual lignin, mitigating its non-productive interaction with cellulase enzymes. PEG's presence in GO pretreatment also increased β-O-4 linkages preservation by 55% and reduced phenolic hydroxyl groups by 28% in lignin fragments versus no surfactants. This outcome resulted from introducing glycerol and PEG hydroxyl tails into the lignin structure, forming α-etherified lignin and rendering it more hydrophilic. Simulations confirmed strong Van Der Waals and hydrogen bonding interactions between lignin units and PEG, hindering lignin fragments repolymerization. Incorporating PEG in the organosolv pretreatment proves highly beneficial for cellulase-mediated lignocellulosic biorefinery, resembling a lignin-first strategy. The optimized process enables efficient biomass utilization for sustainable fuels and chemicals production.
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