The oxidation and reduction of Pd/ceria and Pd/zirconia catalysts were inve
stigated using pulse-reactor studies in which products were monitored follo
wing step changes in the reactant composition. The results demonstrate that
both ceria and zirconia can be partially reduced by CO and partially reoxi
dized by CO2. Steady-state rates for methane reforming by CO2 were also mea
sured on Pd/ceria, Pd/zirconia, and Pd/silica. The Pd/ceria catalyst was sl
ightly more active than Pd/zirconia and similar to 10(4) times as active as
Pd/silica. The high activities of Pd/ceria and Pd/zirconia are explained a
s resulting from oxidation and reduction of the supports. (C) 2000 Academic
Press.