Characterization and hydrodesulfurization properties of catalysts derived from amorphous metal-boron materials

被引:55
作者
Parks, Greg L.
Pease, Melissa L.
Burns, Autumn W.
Layman, Kathryn A.
Bussell, Mark E.
Wang, Xianqin
Hanson, Jonathon
Rodriguez, Jose A.
机构
[1] Western Washington Univ, Dept Chem, Bellingham, WA 98225 USA
[2] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/j.jcat.2006.12.009
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
Unsupported and silica-supported amorphous metal-boron materials (Ni-B, Mo-O-B, and Ni-Mo-O-B) were prepared by NaBH4 reduction of aqueous or impregnated metal salts. The resulting materials were characterized by a range of techniques, including conventional and time-resolved X-ray diffraction. The latter technique was used to determine the onset of crystallization of the amorphous materials during annealing in He flow and to identify the phases formed. Annealing of unsupported Ni-B resulted in the crystallization of predominantly Ni3B, followed by Ni metal, whereas Ni-B/SiO2 formed Ni and then NiO. There was no evidence for crystallization of B-containing phases for Mo-O-B or Mo-O-B/SiO2 on annealing; instead, the predominant phase formed was MoO2. In general, the phases formed for Ni-Mo-O-B and Ni-Mo-O-B/SiO2 were consistent with those formed in the monometallic materials, but at higher annealing temperatures. Catalysts prepared by sulfiding Ni-B/SiO2 and Ni-MoO-B/SiO2 materials had significantly higher thiophene HDS activities than conventionally prepared sulfided Ni/SiO2 and Ni-Mo/SiO2 catalysts, whereas a sulfided Mo-O-B/SiO2 catalyst had a dramatically lower HDS activity than a sulfided MO/SiO2 catalyst. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:277 / 292
页数:16
相关论文
共 56 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]  
ANGULO M, 1987, B SOC CHIM BELG, V96, P925
[3]  
[Anonymous], 2000, JCPDS POWD DIFF FIL
[4]   Catalytic reactions of methylcyclohexane (MCH) on partially reduced MoO3 [J].
Belatel, H ;
Al-Kandari, H ;
Al-Khorafi, F ;
Katrib, A ;
Garin, F .
APPLIED CATALYSIS A-GENERAL, 2004, 275 (1-2) :141-147
[5]   STRUCTURAL SENSITIVITY OF CO ADSORPTION AND H-2/CO COADSORPTION ON NI/SIO2 CATALYSTS [J].
BLACKMOND, DG ;
KO, EI .
JOURNAL OF CATALYSIS, 1985, 96 (01) :210-221
[6]  
BRIGGS D, 1983, PRACTICAL SURFACE AN
[7]   Selective hydrogenation of citral over amorphous NiB and CoB nano-catalysts [J].
Chen, YZ ;
Liaw, BJ ;
Chiang, SJ .
APPLIED CATALYSIS A-GENERAL, 2005, 284 (1-2) :97-104
[8]  
Cheng Q. Y., 2000, J CHIN FUEL CHEM TEC, V28, P249
[9]   In situ X-ray diffraction and solid-state NMR study of the fluorination of γ-Al2O3 with HCF2Cl [J].
Chupas, PJ ;
Ciraolo, MF ;
Hanson, JC ;
Grey, CP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (08) :1694-1702
[10]  
Davydov A. A., 1990, INFRARED SPECTROSCOP