Vanadium oxide-zirconia catalysts were prepared by dry impregnation of
powdered Zr(OH)(4) with an aqueous solution of NH4VO3. The surface ch
aracterization of prepared catalysts was performed using FTIR, DSC, V-
51 solid state NMR, and XRD, and by the measurement of surface area. T
he addition of vanadium oxide up to 9 mol% to zirconia shifted the pha
se transitions of ZrO2 from amorphous to tetragonal toward higher temp
eratures due to the interaction between vanadium oxide and zirconia. O
n the basis of results of IR, XRD, and DSC, it is concluded that the c
ontent of V2O5 monolayer covering most of the available zirconia is 9
mol%, giving 2.3 V2O5 molecules/nm(2). Since the ZyO(2) dispersed vana
dium oxide, the crystalline V2O5 was observed only with the samples co
ntaining V2O5 content exceeding the formation of complete monolayer (9
mol%) on the surface of ZrO2. For the samples calcined at 673 K the a
cidity and surface area increase abruptly upon the addition of 0.2 mol
% V2O5 to ZrO2, and then both of them increase with increasing V2O5 co
ntent up to 5 mol%, showing the presence of Bronsted and Lewis acid si
tes on the V2O5/ZrO2 catalyst. (C) 1996 Academic Press, Inc.