<p> An investigation is reported of oxygen diffusion in monoclinic zirconia at elevated temperatures. </p> <p> A method was developed for production of solid zirconia spheres of a quality suitable for diffusion measurements. The spheres, 60μ and 90μ diameter were subsequently used for the determination of the coefficient of self-diffusion of oxygen in stoichiometric zirconia at 800°C, 850°C, 900°C, 950°C and 1000°C. Oxygen O18 isotope exchange using mass spectrometry for the gas analysis was employed for this investigation. </p> <p> The oxygen self-diffusion coefficent was found to conform to the Arrhenius equation (see online text for equation) Theoretical considerations indicate that this diffusivity represents virtually the lattice diffusion of oxygen in zirconia. </p> <p> Diffusivities of oxygen in zirconia scale calculated from zirconium oxidation studies are 104 times higher and are believed to be due to short-circuit diffusion through line defects. To substantiate this hypothesis, "slabs" of stoichiometric zirconia scale and irregular, but equiaxed particles of the same material were used for oxygen diffusion experiments employing the same method. The diffusivities for the slabs were 10^3 times higher than those for spheres, supporting the validity of the short-circuit diffusion theory for zirconia scale. </p> <p> Oxygen concentration drop across zirconia scale on metal, during its formation by parabolic kinetics was calculated for 600°C and 850°C, and was found to be 0.04 g/cm3 approximately, while the concentration drop across the interface between the oxide and the oxygen-saturated metal was about 1.07 g/cm3. </p> / Thesis / Doctor of Philosophy (PhD)