The interaction of CO at room temperature with a ceria supported rhodi
um catalyst was investigated using TPD-MS and a magnetic balance. The
results have shown important differences in comparison with the H-2-Rh
/CeO2 system. In the presence of rhodium, the treatment with CO result
ed in a much smaller degree of reduction of CeO2 than with hydrogen. W
hen, after CO adsorption at 294 K, the catalyst was heated at 773 K un
der vacuum, the reduction extent increased. In the case of hydrogen, t
he thermodesorption at 773 K almost completely reoxidized the ceria su
rface.