The rate law for the oxidation of zirconium was found to be initially intermediate to linear and parabolic, then parabolic, and then nearly cubic over the first 10-rain interval at both 400 ~ and 500~ At 400~ the oxidation rate became parabolic for an oxide thickness of about 300A. At 500~ the oxidation rate became nearly cubic at about 3300A, the transition from one rate to another being gradual rather than sharp. The activation energy for the parabolic region was 29.3 kcal/mole and for the nearly cubic region approximately 42 kcal/mole. The results obtained were independent of the shape of the specimen and its surface preparation. An analysis shows that the high solubility of oxygen in zirconium is not a sufficient condition to account for a cubic rate law of oxidation for a concentration-independent diffusion constant.