Catalysis Meets Nonthermal Separation for the Production of (Alkyl)phenols and Hydrocarbons from Pyrolysis Oil

被引:84
作者
Cao, Zhengwen [1 ]
Engelhardt, Jan [1 ]
Dierks, Michael [1 ]
Clough, Matthew T. [1 ]
Wang, Guang-Hui [1 ]
Heracleous, Eleni [2 ,3 ]
Lappas, Angelos [2 ,3 ]
Rinaldi, Roberto [4 ]
Schueth, Ferdi [1 ]
机构
[1] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
[2] Ctr Res & Technol Hellas, Chem Proc Engn Res Inst, POB 361, Thessaloniki 57001, Greece
[3] Int Hellen Univ, Sch Sci & Technol, POB 361, Thessaloniki 57001, Greece
[4] Imperial Coll London, Dept Chem Engn, South Kensington Campus, London SW7 2AZ, England
关键词
biomass; gas chromatography; hydrocarbons; molybdenum; phenols; SUPPORTED MOLYBDENUM CARBIDE; BIO-OIL; BIOMASS; HYDRODEOXYGENATION; CONVERSION; PHENOLS; LIGNIN; PHASE; FUELS; VALORIZATION;
D O I
10.1002/anie.201610405
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A simple and efficient hydrodeoxygenation strategy is described to selectively generate and separate high-value alkylphenols from pyrolysis bio-oil, produced directly from lignocellulosic biomass. The overall process is efficient and only requires low pressures of hydrogen gas (5 bar). Initially, an investigation using model compounds indicates that MoCx/C is a promising catalyst for targeted hydrodeoxygenation, enabling selective retention of the desired Ar-OH substituents. By applying this procedure to pyrolysis bio-oil, the primary products (phenol/4-alkylphenols and hydrocarbons) are easily separable from each other by short-path column chromatography, serving as potential valuable feedstocks for industry. The strategy requires no prior fractionation of the lignocellulosic biomass, no further synthetic steps, and no input of additional (e.g., petrochemical) platform molecules.
引用
收藏
页码:2334 / 2339
页数:6
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