The reduction of N2O to N-2 on iron oxide under transient conditions w
as studied in the temperature range of 270-340 degrees C. Six differen
t models were used to simulate the experimental data. The conventional
second-order reaction between gas phase N2O and surface oxygen vacanc
ies failed to describe the dynamic experiments. Upon introducing linea
r or exponential distributions of the second-order surface reaction ra
te constant in function of the degree of reduction of the surface, sat
isfactory fittings to the experiment could not be achieved either. It
was necessary to take into account subsurface oxygen diffusion to desc
ribe the low rates of reaction measured at low degrees of reduction of
the catalyst. The combination of subsurface oxygen diffusion with a l
inear activity distribution for the surface reaction provided a good d
escription of the transient N2O reduction. Finally, the surface reacti
on rate constant as well as the diffusion coefficient of oxygen in iro
n oxide could be fitted with the Arrhenius law.