Transformation of levoglucosan into liquid fuel via catalytic upgrading over Ni-CeO2 catalysts

被引:7
|
作者
Hamid, Ala -H. [1 ]
Ali, Labeeb [1 ]
Shittu, Toyin [1 ]
Kuttiyathil, Mohamed Shafi [1 ]
Ismail, Ola [1 ]
Khaleel, Abbas [2 ]
Altarawneh, Mohammednoor [1 ]
机构
[1] United Arab Emirates Univ, Dept Chem & Petr Engn, Sheikh Khalifa bin Zayed St, Al Ain 15551, U Arab Emirates
[2] United Arab Emirates Univ, Dept Chem, Sheikh Khalifa bin Zayed St, Al Ain 15551, U Arab Emirates
来源
MOLECULAR CATALYSIS | 2023年 / 547卷
关键词
Levoglucosan; Hydrodeoxygenation; Catalysis; Reaction pathways; Fuel; FAST PYROLYSIS; CELLULOSE; HYDRODEOXYGENATION;
D O I
10.1016/j.mcat.2023.113382
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This contribution presents a viable gaseous hydrodeoxygenation (HDO) route for Levoglucosan (LG) that leads to the formation of non-oxygenated hydrocarbon cuts that make commercial transportation fuels, namely gasoline, diesel, and jet fuels. The outlined process encompasses HDO of an evaporated stream of dissolved LG over 5% NiCeO2 catalysts between 100 degrees C-500 degrees C. It is found that the load of the aliphatic compounds attains values between 68.1% and 75.3% across the investigated temperature window. Similarly, fractions of aromatic compounds remain within 8.1%-13.9%. Major observed aliphatic compounds include tetradecane, dodecane, octane, and decane. Alkylated benzenes appear in appreciable quantities. Governing HDO's mechanisms were mapped out by density functional theory (DFT) calculations. Utilizing a 10% load of Ni has slightly reduced the relative area of aliphatic compounds. The combined area of the oxygenated compounds remains less than 10% at all temperatures. This finding entails a profound HDO's capacity of the deployed catalyst and opens a direct venue for the effective utilization of LG in fuel production.
引用
收藏
页数:12
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