4.7 Article

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

期刊

RENEWABLE ENERGY
卷 160, 期 -, 页码 612-622

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.renene.2020.07.002

关键词

Hydrothermal liquefaction; Herbaceous biomass; Fractionation; Biocrude; Solid residue

资金

  1. International Research & Development Program of the National Research Foundation of Korea (NRF) - Ministry of Science and ICT, Republic of Korea [2019K1A3A1A73070631]
  2. National Research Foundation of Korea [2019K1A3A1A73070631] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

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.

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