4.7 Article

Efficient upgrading of pyrolysis bio-oil over Ni-based catalysts in supercritical ethanol

Journal

FUEL
Volume 241, Issue -, Pages 207-217

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2018.12.025

Keywords

Bio-oil; Upgrading; Supercritical ethanol; Ni-based catalysts; Reaction parameters

Funding

  1. National Research Council of Science & Technology grant (NST) by the Korea government (MSIP) [CAP-16-05-KIMM]
  2. Waste-to-Energy Technology Development Program of Korea Environment Industry & Technology Institute
  3. Ministry of Environment, Republic of Korea [2018001580001]
  4. Korea Environmental Industry & Technology Institute (KEITI) [ARQ201807018002] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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An efficient method to upgrade bio-oil derived from fast pyrolysis of woody biomass was investigated in supercritical ethanol without external hydrogen supply. A set of Ni-based catalysts (Ni, Ni-Mo, and Mg-Ni-Mo) supported on activated charcoal (AC) was tested to understand their catalytic effect on the yield and the quality of upgraded liquid fuel in supercritical ethanol. Mg-Ni-Mo/AC was found to be the most effective catalyst among the tested Ni-based catalysts; the liquid product obtained at 350 degrees C showed the highest yield (70.5 wt%) and the lowest oxygen-to-carbon (O/C) molar ratio (0.19). The catalyst also formed the lowest amount of solid product (9.8 wt%) at 350 degrees C by suppressing coke formation. At 350 degrees C, a higher quality liquid product with a total acid number (TAN) value of 6.2 mgKOHg(-1) and a higher heating value (HHV) of 33.4 MJkg(-1) was obtained compared with bio-oil feed (TAN: 48.0 mgKOHg(-1) and HHV: 19.5 MJkg(-1)). A gas chromatography-mass spectrometer (GC-MS) analysis of the liquid product demonstrated that major oxygenated components in the bio-oil feed such as acids, aldehydes, and levoglucosan were effectively destroyed through hydrogenation, esterification, and deoxygenation reactions in the catalytic upgrading process.

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