Carbon-supported bimetallic Pd-Fe catalysts for vapor-phase hydrodeoxygenation of guaiacol

被引:371
|
作者
Sun, Junming [1 ]
Karim, Ayman M. [1 ]
Zhang, He [2 ]
Kovarik, Libor [1 ]
Li, Xiaohong Shari [1 ]
Hensley, Alyssa J. [2 ]
McEwen, Jean-Sabin [2 ]
Wang, Yong [1 ,2 ]
机构
[1] Pacific NW Natl Lab, Inst Integrated Catalysis, Richland, WA 99352 USA
[2] Washington State Univ, Gene & Linda Voiland Sch Chem Engn & Bioengn, Pullman, WA 99164 USA
关键词
Pd-Fe; Hydrodeoxygenation; Bimetallic catalysis; Bio-oil upgrading; Alloy catalyst; EXAFS; Carbon support; RAY-ABSORPTION SPECTROSCOPY; PYROLYSIS OIL; TRANSPORTATION FUELS; BIO-OIL; REFINERY UNITS; BIOMASS; CONVERSION; HYDROGEN; PLATINUM; HYDROTREATMENT;
D O I
10.1016/j.jcat.2013.05.020
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
Carbon-supported metal catalysts (Cu/C, Fe/C, Pd/C, Pt/C, PdFe/C, and Ru/C) were characterized and evaluated for vapor-phase hydrodeoxygenation (HDO) of guaiacol (GUA), aiming at the identification/elucidation of active catalysts for high-yield production of completely hydrodeoxygenated products (e.g., benzene). Phenol was found to be the major intermediate on all catalysts. Saturation of the aromatic ring is the major pathway over the precious metal catalysts, forming cyclohexanone and cyclohexanol, followed by ring opening to form gaseous products. Base metal catalysts exhibit lower activity than the precious metal catalysts, but selectively form benzene along with small amounts of toluene, trimethylbenzene (TMB), and cresol without forming ring-saturated or ring-opening products. Compared with Fe/C and Pd/C, PdFe/C catalysts exhibit a substantially enhanced activity while maintaining the high selectivity to HDO products without ring saturation or ring opening. The enhanced activity of PdFe/C is attributed to the modification of Fe nanoparticles by Pd as evidenced by STEM, EDS, EXAFS, TPR, and theoretical calculations. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:47 / 57
页数:11
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