4.8 Article

Exploration of in-situ formed MoSx catalyst for co-hydrodeoxygenation of sawdust and vacuum gas oil in pilot-scale plant

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 297, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2021.120499

Keywords

MoSx catalyst; co-HDO; Bio-fuels; Oxygen content; Active hydrogen

Funding

  1. National key R & D program of China [2018YFC1801901]
  2. Natural Science Foundation of Shandong Province [ZR2019BB050]
  3. Fundamental Research Funds for the Central Universities of China [18CX02144A, 18CX05024A]
  4. Benefiting People Special Fund for Qingdao Science and Technology Project [20-3-4-27-nsh]
  5. Opening Fund of State Key Laboratory of Heavy Oil Processing [SKLOP202003003]
  6. Special Funds of Taishan Scholars Project of Shandong Province [ts20190919]
  7. University of Calgary's Canada First Research Excellence Fund, the Global Research Initiative (GRI) for Sustainable Low Carbon Unconventional Resources

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The use of MoSx catalyst can effectively enhance the co-HDO reaction by promoting oxygen transfer, leading to bio-fuels with reduced oxygen content and high combustion heat.
Obtaining bio-fuels (including gas and bio-oil) with high energy density remains a huge challenge due to their high oxygen content. Here we report a novel MoSx catalyst in-situ formed in a pilot-scale plant can effectively promote the co-hydrodeoxygenation (co-HDO) reaction of poplar wood sawdust and vacuum gas oil with H-2. Because of the sulfur vacancies on MoSx the co-HDO reaction is facilitated along with a significant accumulation of oxygen (over 50.0 wt.%) into an oil-insoluble polar-liquid, leading to a high combustion heat of similar to 47 MJ kg(-1) of the bio-fuels. Besides, the presence of MoSx also affords a lowered molecular weight of the deoxidized biofuels. Based on the underlying conversion mechanisms, the co-HDO reaction can be enhanced in the presence of MoSx catalyst by promoting oxygen transfer towards the polar-liquid during the co-HDO process.

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