Characterization of alumina, silica, and titania supported cobalt catalysts

被引:151
作者
Voss, A [1 ]
Borgmann, D [1 ]
Wedler, G [1 ]
机构
[1] Univ Erlangen Nurnberg, Inst Phys & Theoret Chem, D-91058 Erlangen, Germany
关键词
cobalt; manganese; alumina; silica; titania; supported catalysts; electron microscopy; X-ray diffraction; photoelectron spectroscopy; temperature-programmed reduction and oxidation; dynamic and static adsorption studies;
D O I
10.1006/jcat.2002.3739
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 multiple technique approach was used to characterize the structural, chemical, and electronic properties of Co catalysts supported on Al2O3, SiO2, and TiO2 as well as Co/Mn catalysts on TiO2. The morphology of the catalysts was studied by transmission electron microscopy followed by X-ray diffraction to determine the phase composition and the distribution of the crystallite size. The electronic properties of the calcined catalysts were investigated by X-ray photoelectron spectroscopy. Comparison with reference data allows identification of the cobalt-containing species in the surface. In agreement with adsorption experiments, the signal intensities yield the dispersion of the applied catalysts in the sequence Co/Al2O3 > Co/TiO2 > Co/SiO2. Temperature-programmed reduction and oxidation reveal the formation of various oxides in dependence on temperature as well as, in case of the alumina- and titania-supported cobalt catalysts, the formation of high-temperature compounds CoAl2O4 and CoTiO3, respectively. Dynamic and static adsorption studies and BET measurements complete the characterization of the supported catalysts. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:10 / 21
页数:12
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