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Oxidic precursors of molybdena supported on nickel and magnesium aluminate hydrotreating catalysts
Authors:S Houssenbay  E Payen  S Kasztelan and J Grimblot
Affiliation:

a Laboratoire de Catalyse Hétérogène, U.R.A. C.N.R.S. No 402, Université des Sciences et Techniques de Lille Flandres-Artois, Bâtiment C3, F - 59655 Villeneuve d'Ascq Cédex, France.

b L.A.S.I.R., U.P.R. C.N.R.S. No 2631, Université des Sciences et Techniques de Lille Flandres-Artois, Bâtiment C5, F - 59655 Villeneuve d'Ascq, Cédex, France.

c Institut Français du Pétrole, 1 et 4 Avenue de Bois Préau, B.P. 311, F -92506 Rueil-Malmaison Cédex, France.

Abstract:The oxidic precursors of molybdena-based hydrotreating catalysts have been prepared using nickel and magnesium aluminates and characterized by laser Raman spectroscopy (LRS) and X-ray photoelectron spectroscopy (XPS). Three series of supports (not, vert, similar80, 120 and 140 m2.g?1) have been investigated. Their aluminate spinel structure was confirmed both by X-ray diffraction (XRD) and LRS. Nickel oxide and magnesia have also been detected on the low surface area systems. In both series, a surface deficit of the foreign cation has been observed relative to the Al3+ of the aluminate phase. This deficit was more pronounced for Ni2+. Deposition of molybdate species does not modify the surface composition of these supports and a monolayer-like coverage up to 4.5 to 5 Mo at.nm?2 was obtained. Nickel added by impregnation was shown to interact with the supported oxomolybdate species, whereas the nickel of the support does not. These investigated supports closely resemble γ --- Al2O3 in the preparation of hydrotreating catalysts.
Keywords:
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