The effects of doping of CuO/Al2O3 solids with CeO2 on their surface and ca
talytic properties were investigated using nitrogen adsorption measurements
at - 196 degreesC and oxidation of CO by O-2 at 100-175 degreesC. The dopa
nt concentrations were varied between on 0.75-4.5 mol% CeO2 and the amount
of copper was fixed at 16.7 mol% CuO. Pure and variously doped solids were
prepared by wet impregnation method using finely-powdered Al(OH)(3) and sol
utions containing different amounts of cerium nitrate. The impregnated soli
d samples were dried at 100 degreesC and calcined at 400 degreesC. The obta
ined solids were treated with solutions containing fixed amounts of copper
nitrate, drying then calcination at 300, 500 and 700 degreesC. The results
showed that the doping process resulted in a measurable increase in the BET
-surface area of the treated solids. The maximum increase in the S-BET atta
ined 51, 22.5 and 5% for the solids precalcined at 300, 500 and 700 degrees
C, respectively. The doping process brought about a considerable increase i
n the catalytic activity of the treated catalysts. Furthermore, the catalyt
ic activity of pure solids decreased considerably (about 60%) by increasing
the precalcination temperature from 300 to 700 degreesC. On the other hand
, the catalytic activity of doped samples remained almost unchanged or incr
eased slightly (about 22%) upon increasing the temperature of heat treatmen
t from 300 to 700 degreesC. The maximum increase in the catalytic activity,
expressed as reaction rate constant per unit surface area measured at 125
degreesC attained 27, 150 and 422% for the catalysts doped with 3 mol% CeO2
and precalcined at 300, 500, and 700 degreesC, respectively. The doping pr
ocess did not modify the activation energy of the catalyzed reaction i.e. d
oping of CuO/Al2O3, solids with CeO2 followed by heating at 300-700 degrees
C did not alter the mechanism of the catalytic reaction but increased the c
oncentration of catalytically active constituents taking part in the cataly
tic process without changing their energetic nature. (C) 2001 Elsevier Scie
nce B.V. All rights reserved.