REFeO(3) (RE = La, Pr, Nd, Sm, Eu, Gd, Tb and Dy) were prepared by the
complex method with citric acid. The perovskite structure for REFeO(3
) was determined with XRD. The Redox mechanism for oxidation of CO was
proven by the pulse method of reduction with CO and reoxidation with
O-2 over REFeO(3) catalyst. The steady-state kinetics of oxidation for
CO has been investigated with external circulation flow reactor. The
parameters of kinetic equation were estimated by the method of orthogo
nal design. The rate constants of reduction for catalysts with CO, k(1
), were more than the rate contants of reoxidation for reduced catalys
ts with O-2, k(2). The ratios of k(1) to k(2) varied within the range
of 4.24-133, which showed that the control step for oxidation of CO ov
er REFeO(3) was the reoxidation step of reduced catalyst. The conversi
ons of CO, X(CO), were more than the conversions of O-2, X(O2), with p
ulse method. These pulse data proved the conclusion of control step fo
r the steady-state kinetics. The Redox equation (9) can be simplified
to the equation of control step (11). The linear relationship between
the rate constants of reduction for catalysts and the reaction rate at
the constsnts of partial pressures P-CO and P-O2 over REFeO(3) cataly
sts was approximately. The oxidation of CO over REFeO(3) has compensat
ion effect.