Highly selective hydrodeoxygenation of wood pallet sawdust pyrolysis oil to methyl phenol derivatives using cobalt and iron on activated carbon supported catalysts

•Effect of Co, Fe, and Co-Fe on AC support was investigated for WPS bio-oil upgrading.•20 wt% 4Co-1Fe/AC catalyst was optimal with HHV (34.16 MJ/kg) and liquid yield (68.85%) at 350 °C and 60 bar.•Methyl Phenol derivates was the main component in upgraded bio-oil.•The deactivation was occurred by ex...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Energy conversion and management. X 2022-05, Vol.14, p.100184, Article 100184
Hauptverfasser: Khanh Tran, Quoc, Vu Ly, Hoang, Anh Vo, Thuan, Tae Hwang, Hyun, Kim, Jinsoo, Kim, Seung-Soo
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•Effect of Co, Fe, and Co-Fe on AC support was investigated for WPS bio-oil upgrading.•20 wt% 4Co-1Fe/AC catalyst was optimal with HHV (34.16 MJ/kg) and liquid yield (68.85%) at 350 °C and 60 bar.•Methyl Phenol derivates was the main component in upgraded bio-oil.•The deactivation was occurred by external coke formation and oxidation of metals. The catalytic hydrodeoxygenation (HDO) processes for upgrading pyrolysis bio-oils from wood pallet sawdust (WPS) were studied using activated carbon (AC) as a support of mono- (Co/AC and Fe/AC) and bi-metallic (Co-Fe/AC) catalysts. The effects of the reaction temperature and hydrogen pressure on products and high heating value (HHV) were systematically investigated. At 350 °C and 60 bar, 20 wt% Co/AC showed the highest liquid yield (70.46 wt%) along with HHV of 34.22 MJ/Kg. Among the tested bimetallic catalysts, comparable liquid yield (68.85 wt%) and HHV (34.16 MJ/kg) were achieved with 20 wt% 4Co-1Fe/AC catalyst. Methyl phenol derivatives were found to be the main component in upgraded bio-oil. The carbon number of the upgraded bio-oil was mainly distributed in C5–C11 fraction, especially with the C8 component (20.40 wt%). The catalysts were deactivated by the formation of carbonaceous compounds on the external surface, oxidation of metal species, and blocking of active sites on catalysts.
ISSN:2590-1745
2590-1745
DOI:10.1016/j.ecmx.2022.100184