Effect of thermochemically fractionation before hydrothermal liquefaction of herbaceous biomass on biocrude characteristics

被引:22
|
作者
Kim, Seong Ju [1 ,2 ]
Um, Byung Hwan [2 ,3 ]
机构
[1] Hankyong Natl Univ, Dept Biomol & Chem Engn, Anseong 17579, Gyeonggi Do, South Korea
[2] Hankyong Natl Univ, Interagcy Convergence Energy New Biomass Ind, Anseong 17579, Gyeonggi Do, South Korea
[3] Hankyong Natl Univ, Sch Food Biotechnol & Chem Engn, Anseong 17579, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
Hydrothermal liquefaction; Herbaceous biomass; Fractionation; Biocrude; Solid residue; BIO-OIL; PRETREATMENT; TEMPERATURE; CONVERSION; ETHANOL; OPTIMIZATION; MULBERRY; ROLES; ALGAE; YIELD;
D O I
10.1016/j.renene.2020.07.002
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Hydrothermal liquefaction (HTL) of fractionated two types herbaceous biomass (kenaf and miscanthus) by dilute acid, organosolv, alkaline, or demineralization process was carried out under ethanol water co-solvent at 350 degrees C for 30 min to examine the biocrude yield and characteristics. The biocrude properties were comprehensively characterized by HPLC, elemental, GC-MS, and TGA analysis. Fractionation technologies before HTL effectively increased biocrude yield up to 38% compared to that of untreated herbaceous biomass (31%), except for organosolv fractionation of miscanthus, especially, HTL after alkaline fractionation showed high yield and energy recovery ratio up to 70%. Elemental analysis showed that HHV of biocrude was negatively affected by hydrolysis reaction of high lignin content after dilute acid fractionation. The GC-MS analysis revealed that carbohydrates-derived compound significantly increased in the biocrude obtained after organosolv and alkaline fractionation due to holocellulose increases through fractionation process. Additionally, TGA results indicated that the ratio of high-boiling-point compounds in biocrude obtained after demineralization was expanded compared with untreated due to ash removal, which could act as a catalyst. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:612 / 622
页数:11
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