加氢脱氧
热解
催化作用
热解油
浸出(土壤学)
化学
化学工程
间歇式反应器
碳纤维
有机化学
残留物(化学)
废物管理
材料科学
加氢脱硫
氧气
油砂
制浆造纸工业
生物量(生态学)
协同处理
开裂
化石燃料
石油
二氧化碳
催化重整
无机化学
作者
Amalie
Paarup Krebs (21989466),Hannah Abildgaard Sløk (21989469),Martin Høj (1863478),Magnus Zingler Stummann (11872856),Lived Yegres Lemus-Olsen (21989472),Michael Brorson (1743859),Anker Degn Jensen (1288884)
出处
期刊:
[Figshare (United Kingdom)]
日期:2025-08-05
标识
DOI:10.1021/acs.energyfuels.5c02630.s001
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/Al2O3 and sulfided NiMo/Al2O3) were used in this study to stabilize wood fast pyrolysis bio-oil in a batch reactor for 2 h at 90 bar initial H2 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/Al2O3 catalyst at 15 wt % catalyst to oil ratio. However, leaching of Ni was observed for all experiments with the Ni/Al2O3 catalyst, which may prove to be a significant issue for continuous operation. The sulfided NiMo/Al2O3 catalyst only reduced the carbonyl number marginally, and increasing the reaction time did not improve this.
科研通智能强力驱动
Strongly Powered by AbleSci AI