Dibenzothiophene hydrodesulfurization activity and surface sites of silica-supported MoP, Ni2P, and Ni-Mo-P catalysts

被引:167
作者
Sun, FX [1 ]
Wu, WC [1 ]
Wu, ZL [1 ]
Guo, J [1 ]
Wei, ZB [1 ]
Yang, YX [1 ]
Jiang, ZX [1 ]
Tian, FP [1 ]
Li, C [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
hydrodesulfurization; transition metal phosphides; MoP; Ni2P; NiMoP; dibenzothiophene; IR spectroscopy; CO adsorption;
D O I
10.1016/j.jcat.2004.09.002
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
Silica-supported binary and ternary phosphides, MoP/SiO2, Ni2P/SiO2, and Ni-Mo-P/SiO2 have been prepared and characterized by X-ray diffraction (XRD), BET surface area, CO chemisorption, transmission electron microscopy (TEM), and infrared spectroscopy (IR). The hydrodesulfurization (HDS) activities of dibenzothiophene (DBT) were measured and compared at 593 K and 3.0 MPa for MoP/SiO2, Ni2P/SiO2, and Ni-Mo-P/SiO2 catalysts with different Mo and Ni loadings. The activities of the phosphides follow the order Ni2P/SiO2 > Ni-Mo-P/SiO2 > MOP/SiO2. The Ni sites in the Ni-MO-P/SiO2 catalysts play a major role in the conversion of DBT, and the activity of the catalysts increases with increasing Ni content. This is different from sulfides, nitrides, and carbides, as no synergetic effect is observed between the phosphided Ni and the Mo atoms. The surface of these phosphide catalysts is partially sulfided forming a surface phosphosulfide phase, while the bulk structure of the phosphides is maintained in the HDS reactions. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:298 / 310
页数:13
相关论文
共 43 条
[1]   Thiophene hydrodesulfurization over alumina-supported molybdenum carbide and nitride catalysts: Adsorption sites, catalytic activities, and nature of the active surface [J].
Aegerter, PA ;
Quigley, WWC ;
Simpson, GJ ;
Ziegler, DD ;
Logan, JW ;
McCrea, KR ;
Glazier, S ;
Bussell, ME .
JOURNAL OF CATALYSIS, 1996, 164 (01) :109-121
[2]   INFRARED STUDIES OF NITRIC-OXIDE ADSORPTION ON REDUCED AND SULFIDED P-NI-MO/AL2O3 CATALYSTS [J].
ATANASOVA, P ;
AGUDO, AL .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1995, 5 (04) :329-341
[3]   NiMoNx/γ-Al2O3 catalyst for HDN of pyridine [J].
Chu, YJ ;
Wei, ZB ;
Yang, SW ;
Li, C ;
Xin, Q ;
Min, EZ .
APPLIED CATALYSIS A-GENERAL, 1999, 176 (01) :17-26
[4]   Synthesis and activity of a new catalyst for hydroprocessing: Tungsten phosphide [J].
Clark, P ;
Li, W ;
Oyama, ST .
JOURNAL OF CATALYSIS, 2001, 200 (01) :140-147
[5]   Characterization of silica-supported molybdenum and tungsten phosphide hydroprocessing catalysts by 31P nuclear magnetic resonance spectroscopy [J].
Clark, P ;
Wang, X ;
Oyama, ST .
JOURNAL OF CATALYSIS, 2002, 207 (02) :256-265
[6]   THE ADSORPTION AND DISSOCIATION OF CARBON-MONOXIDE ON CLEAN AND OXYGEN-MODIFIED MO(110) SURFACES [J].
COLAIANNI, ML ;
CHEN, JG ;
WEINBERG, WH ;
YATES, JT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (10) :3735-3743
[7]   Competitive hydrodesulfurization of 4,6-dimethyldibenzothiophene, hydrodenitrogenation of 2-methylpyridine, and hydrogenation of naphthalene over sulfided NiMo/γ-Al2O3 [J].
Egorova, M ;
Prins, R .
JOURNAL OF CATALYSIS, 2004, 224 (02) :278-287
[8]   ROLE OF MOS2 AND WS2 IN HYDRODESULFURIZATION [J].
FURIMSKY, E .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1980, 22 (03) :371-400
[9]   CATALYTIC HYDRODESULFURIZATION [J].
GRANGE, P .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1980, 21 (01) :135-181
[10]   In situ X-ray absorption fine structure studies on the structure of nickel phosphide catalyst supported on K-USY [J].
Kawai, T ;
Sato, S ;
Suzuki, S ;
Chun, WJ ;
Asakura, K ;
Bando, KK ;
Matsui, T ;
Yoshimura, Y ;
Kubota, T ;
Okamoto, Y ;
Lee, YK ;
Oyama, ST .
CHEMISTRY LETTERS, 2003, 32 (10) :956-957