Stabilization of Pyrolysis Oil from Woody Biomass Using Ni/Al2O3 and Sulfided NiMo/Al2O3 Catalysts

催化作用 热解 生物量(生态学) 材料科学 冶金 矿物学 化学工程 化学 有机化学 地质学 工程类 海洋学
作者
Amalie Paarup Krebs,Hannah Abildgaard Sløk,Martin Høj,Magnus Zingler Stummann,Lived Yegres Lemus-Olsen,Michael Brorson,Anker Degn Jensen
出处
期刊:Energy & Fuels [American Chemical Society]
被引量:7
标识
DOI:10.1021/acs.energyfuels.5c02630
摘要

In the action against climate change, it is vital to find alternatives to conventional fossil fuels. One such alternative is biomass-derived pyrolysis oils. However, these pyrolysis oils contain high levels of oxygen and water and therefore need to be upgraded to be suitable for further processing in a refinery. It has been proposed to upgrade pyrolysis oils in two steps to minimize operational issues, particularly coking and reactor plugging: a stabilization step at lower temperatures followed by hydrodeoxygenation at elevated temperatures. Two different catalysts (metallic Ni/Al 2 O 3 and sulfided NiMo/Al 2 O 3 ) were used in this study to stabilize wood fast pyrolysis bio-oil in a batch reactor for 2 h at 90 bar initial H 2 pressure and 120, 180, and 220 °C. The impact of the catalyst to oil ratio as well as reaction time were also investigated. The stabilized pyrolysis oil was characterized for elemental composition, carbonyl number, and micro carbon residue (MCR). The best results toward stabilizing the pyrolysis oil, in terms of lowering the carbonyl number and MCR, were achieved with the Ni/Al 2 O 3 catalyst at 15 wt % catalyst to oil ratio. However, leaching of Ni was observed for all experiments with the Ni/Al 2 O 3 catalyst, which may prove to be a significant issue for continuous operation. The sulfided NiMo/Al 2 O 3 catalyst only reduced the carbonyl number marginally, and increasing the reaction time did not improve this.
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