X-ray photoelectron spectroscopy (XPS) technique was employed to characteri
ze Al2O3 TiO2 support and MoO3/Al2O3-TiO2 catalyst calcined at different te
mperatures from 773 to 1073 K, The Al2O3-TiO2 (1:1.3 mole ratio) binary oxi
de support was obtained by a coprecipitation procedure with in situ generat
ed ammonium hydroxide. A nominal 12 wt.% MoO3 was impregnated over the calc
ined (773 K) support by a wet impregnation method, The initial characteriza
tion by X-ray powder diffraction, Fourier transform-infrared (FT-IR), and O
-2 chemisorption techniques revealed that the impregnated MoO3 is in a high
ly-dispersed state on the surface of the support. XPS electron binding ener
gy (Eb) values indicate that the MoO3/Al2O3-TiO2 catalyst contains the mixe
d-oxide elements in the highest oxidation states, Ti(IV), AI(III), and Mo(V
I), respectively. However, the core level Eb Of Al 2p slightly increased wi
th increase of calcination temperature, and this effect was more prominent
in the case of molybdena-doped samples. A better resolved Mo 3d doublet was
observed at all calcination temperatures. This was explained as due the co
verage of alumina surface by titania, thereby lowering the interaction betw
een molybdena and alumina, The XPS atomic ratios indicate that the Ti/Al ra
tio is sensitive to the calcination temperature. The Mo/Al ratio was found
to be more than that of Mo/Ti ratio and decreased with increasing calcinati
on temperature. A clear difference between the Al2O3 and the TiO2 surfaces,
in terms of surface free energy, isoelectric point, and surface hydroxyl d
istribution was considered to be responsible for different distributions of
molybdena over these supports. (C) 2001 Elsevier Science B.V, All rights r
eserved.