Preparation of PrOy (Pr6O11) or single-phase fluorite-structured PrOy-ZrO2
mixed oxide, supported on high-surface-area gamma-alumina, was achieved for
the first time by impregnation of gamma-alumina powder with Pr((OC3H7)-C-1
)(3) or a mixture of Pr((OC3H7)-C-1)(3)and Zr((OC3H7)-C-1)(4)(C3H7OH)-C-.1
and calcination 600 degrees C. Subsequent calculation at 900 degrees C caus
ed partial transformation of Pr6O11 to PrAlO3 but only improved the crystal
linity of the mixed oxide. Further calcination at 1200 degrees C led to com
plete transformation df Pr6O11 but only partial disproportionation of PrOy-
ZrO2 to PrAlO3 and ZrO2, transformation of gamma- to alpha-alumina was also
inhibited in the case of the mixed oxide. In contrast, there was no eviden
ce of any crystalline phase containing praseodymium upon calcination of gam
ma-alumina powder impregnated with a mixture of praseodymium nitrate and zi
rconium chloride in a 1 :0 or 1 : 1 molar ratio. These results show that pr
aseodymium oxide can be supported on alumina and stabilized against reactio
n with the alumina by the incorporation of zirconium in the form of the mix
ed oxide, PrOy,ZrO2, provided it is deposited using alkoxide precursors. Th
is stabilization should allow praseodymia to undergo redox processes and th
us provide oxygen storage capacity when supported on alumina in a catalyst
washcoat.