Enhanced HDO activity of Ni2P promoted with noble metals

被引:33
作者
Cecilia, J. A. [1 ]
Infantes-Molina, A. [1 ]
Sanmartin-Donoso, J. [1 ]
Rodriguez-Aguado, E. [1 ]
Ballesteros-Plata, Daniel [1 ]
Rodriguez-Castellon, E. [1 ]
机构
[1] Univ Malaga, Fac Ciencias, Dept Quim Inorgan Cristalog & Mineral, Campus Teatinos, E-29071 Malaga, Spain
关键词
NICKEL PHOSPHIDE CATALYSTS; MOLYBDENUM NITRIDE CATALYSTS; MODEL-COMPOUND; BIO-OIL; HYDROPROCESSING CATALYSTS; OXYGEN-REMOVAL; HYDRODEOXYGENATION; DIBENZOFURAN; GUAIACOL; SILICA;
D O I
10.1039/c6cy00639f
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
A series of bimetallic Ni2P-noble metal (Pt, Rh, Ir or Ru) catalysts supported on commercial silica were prepared in order to evaluate the promoter effect of noble metals on the activity and stability of these catalysts in the hydrodeoxygenation (HDO) of dibenzofuran (DBF), as a model oxygenated compound, at P = 3.0 MPa and 175-300 degrees C. Ni2P and Ni1.8M0.2P catalysts were characterized by X-ray diffraction (XRD), N-2 adsorption-desorption at -196 degrees C, X-ray photoelectron spectroscopy (XPS), CO chemisorption and H-2-thermoprogrammed desorption. Bimetallic catalysts containing Rh, Ru and Ir showed excellent catalytic behavior in the HDO reaction of DBF, greater than their corresponding monometallic counterparts. The results suggest that there is a synergic effect between both phases mainly at low temperatures. The addition of Pt worsened the catalytic activity of the monometallic phases. The enhanced activity of the catalysts containing Rh, Ru and Ir was ascribed to the presence of greater amounts of H-active species on the surface as well as an increase in Ni surface exposure during the catalytic test. The poor catalytic activity of the Pt-containing catalyst could be due to the possible formation of a solid solution as observed from XPS and CO-chemisorption data, which seems to be detrimental to the catalytic response of these systems.
引用
收藏
页码:7323 / 7333
页数:11
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