期刊
JOURNAL OF CATALYSIS
卷 305, 期 -, 页码 256-263出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2013.05.026
关键词
Bimetallic; Lignin; Depolymerization; Phosphide; Lignocellulosic biomass; Biofuels; Hydrogenation
资金
- NSF [CBET-1125145]
- Center for Sustainable Energy
- Center for Environmental Science and Technology at the University of Notre Dame
- Notre Dame Integrated Imaging Facilities
- Div Of Chem, Bioeng, Env, & Transp Sys
- Directorate For Engineering [1125145] Funding Source: National Science Foundation
We report the synthesis of an industrially applicable, non-sulfided bimetallic catalyst with remarkable selectivity to the hydrodeoxygenation of aryl ethers and phenol. Bimetallic FeMo phosphide catalysts have selectivities as high as similar to 90% benzene and 10% cyclohexane at hydroprocessing temperatures (400 degrees C) and industrially low pressures (2.1 MPa H-2) at near complete conversion (>99%). Similarly, the selectivities for the hydrodeoxygenation of anisole were 90% benzene, 4% toluene, and 6% cyclohexane at 92% conversion. Furthermore, this catalyst has the ability to cleave aryl ether bonds and specifically beta-O-4 linkages with higher selectivities to aromatics compared to hydrocarbons, thus minimizing the use of expensive H-2. The selectivity to aromatics from phenol was highly dependent on H-2 pressure, where doubling the pressure to 4.2 MPa reduced the selectivity to benzene, while less substantial decreases were observed when anisole or a beta-O-4 model compound was reacted. These high selectivities were attributed to the unique FeMo phosphide material, as catalytic studies with FeP, MoP, and the combination of FeP and MoP resulted in selectivities much lower than the FeMo phosphide material. (C) 2013 Elsevier Inc. All rights reserved.
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