Stability of an acid activated carbon based bifunctional catalyst for the raw bio-oil hydrodeoxygenation

Tomás Cordero-Lanzac, Roberto Palos, José M. Arandes, Pedro Castaño*, José Rodríguez-Mirasol, Tomás Cordero, Javier Bilbao

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

117 Scopus citations

Abstract

The performance (activity, selectivity and stability) of a Pt-Pd catalyst supported on a phosphorus-containing activated carbon (ACP) has been studied in the hydrodeoxygenation (HDO) of raw bio-oil, and compared with another bifunctional catalyst prepared with a FCC (Fluid Catalytic Cracking) catalyst as acid support. Experiments have been carried out in a fixed bed reactor under the following conditions: 400–450 °C; 65 bar; space time, 0.18 gcat h g−1 bio-oil; H2:bio-oil ratio, 20 cm3 H2 (STP) cm−3 bio-oil; time on stream, 0–10 h. The catalyst reaches a pseudo-steady state at 450 °C after 6 h of time on stream, preserving a constant activity as a consequence of the simultaneous formation and hydrocracking of the deposited coke. In these conditions, the yield of C5+ hydrocarbons is 20 wt%. This organic liquid fraction mainly contains aromatics, and thus, it may require an additional mild hydrocracking treatment for its valorization as fuel. On the other hand, the gas fraction obtained can be used directly as fuel, and the aqueous liquid fraction (with a high concentration of methanol, 58 wt%) is interesting as co-feedstock with methanol in a methanol to olefins (MTO) unit.

Original languageEnglish (US)
Pages (from-to)389-399
Number of pages11
JournalApplied Catalysis B: Environmental
Volume203
DOIs
StatePublished - Apr 1 2017
Externally publishedYes

Keywords

  • Activated carbon
  • Bio-Oil upgrading
  • Biofuels
  • Coke deactivation
  • Pt-Pd bifunctional catalyst

ASJC Scopus subject areas

  • Catalysis
  • General Environmental Science
  • Process Chemistry and Technology

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