Origin of the dispersion limit in the preparation of Ni(Co)Mo/Al2O3 and Ni(Co)Mo/TiO2 HDS oxidic precursors

被引:9
作者
Lamonier, Carole [1 ]
Soogund, Deana [1 ]
Mazurelle, Jean [1 ]
Blanchard, Pascal [1 ]
Guillaume, Denis
Payen, Edmond [1 ]
机构
[1] Univ Sci & Technol Lille, Unite Catalyse & Chim Solide, UMR 8181, F-59655 Villeneuve Dascq, France
来源
SCIENTIFIC BASES FOR THE PREPARATION OF HETEROGENEOUS CATALYSTS, PROCEEDINGS OF THE 9TH INTERNATIONAL SYMPOSIUM | 2006年 / 162卷
关键词
D O I
10.1016/S0167-2991(06)80972-9
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
Conventional alumina and titania oxidic precursors have been characterized by Raman spectroscopy after maturation, drying and calcination. The evolution of the impregnating solution has been followed and the nature of the precipitates has been determined. After impregnation of alumina 6molybdoaluminate entities (well dispersed or not) are characterized for both the NiMo and CoMo based solids. At high Mo loading, the formation of a CoMo oxyhydroxide that yields bulk cobalt molybdate upon calcination is also observed. In counterpart on TiO(2) surface of the NiMo precursor, the formation of 6molybdonickelate leading to bulk nickel molybdate upon calcination is observed. The formation of well defined phases i.e. CoMoO(4) and NiMoO(4) was not observed on respectively titania and alumina supports, but well dispersed polyoxomolybdate was characterized at the same Mo loading.
引用
收藏
页码:713 / 720
页数:8
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