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Morphology and hydrodesulfurization activity of CoMo sulfide supported on amorphous ZrO2 nanoparticles combined with Al2O3
被引:46
作者:
Li, GR
[1
]
Li, W
[1
]
Zhang, MH
[1
]
Tao, KY
[1
]
机构:
[1] Nankai Univ, Inst New Catalyt Mat Sci, Coll Chem, Tianjin 300071, Peoples R China
基金:
中国国家自然科学基金;
关键词:
ZrO2;
nanoparticles;
mixed supports;
hydrodesulfurization (HDS);
morphology;
D O I:
10.1016/j.apcata.2004.06.038
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 ZrO2-Al2O3(designated as ZA) mixed supports with different ZrO2 contents were prepared by a simple complexing-deposition method using ZrOCl2.8H(2)O and Al2O3 as starting materials. These samples were characterized by inductively coupled plasma-atomic emission spectroscopy (ICP-AES), X-ray diffraction (XRD), N-2 adsorption analysis, X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). The results demonstrated that zirconia nanoparticles with a size of about 5 nm in amorphous phase were well dispersed on alumina. The sulfided CoMo catalysts supported on the mixed supports showed a higher dibenzothiophene (DBT) hydrodesulfurization (HDS) activity than those supported on alumina and a commercial HDS catalyst KF757. The NO adsorption analysis revealed that the CoMo/ZA catalysts provided more active sites when the support contained a suitable ZrO2 content. Further, it was found, by high-resolution transmission electron microscopy (HRTEM), that the addition of ZrO2 had an obvious effect on the sulfide component's morphology: a multi-layered structure of CoMoS was formed on ZA supports while a mono-layered structure was formed on Al2O3. The multi-layered CoMoS on the mixed supports provided more active sites and higher activity for HDS of DBT due to a less steric hindrance. (C) 2004 Elsevier B.V. All rights reserved.
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页码:233 / 238
页数:6
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