The oxidation kinetics of 304L particles dispersed into a zirconia matrix at 800 °C showed a short initial acceleration followed by a much slower period.

Inward growth of Cr₂O₃ nodules was observed first along zirconia/metal interfaces whereas an iron-rich (Fe, Cr) mixed oxide scale developed outwards around the metal particles.

The jumps method was used to prove that the oxidation kinetics in the second period of time was controlled by a rate-determining step and enhanced by an increase in the oxygen partial pressure.

Mechanisms decomposed into elementary steps were proposed to describe the inward and outward growths. The oxidation kinetics in the second period of time, related to the outward growth of the Fe–Cr mixed oxide layer, was found to be controlled by cations vacancy diffusion and to obey a $P_{{\mathrm{o}}_2}^{3/16}$ law.