Effect of Doping Simultaneously with Iron and Titanium on the Diffusional Creep of Polycrystalline A12O3

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Abstract
The effect of doping simultaneously with iron and titanium was studied in dense, polycrystalline alumina over a range of grain sizes (10 to 100 μm) and temperatures (1250° to 1550°C). In the double‐doped system, the titanium concentration was varied between 0.05 and 0.15 cation %, whereas the iron‐dopant level was varied between 0.05 and 6 cation %. For iron concentrations below about 2 to 3%, the aluminum vacancy concentration was dominated by the presence of quadrivalent titanium in substitutional solid solution and Nabarro‐Herring diffusional creep at 1450°C was rate‐limited by aluminum lattice diffusion. As the iron‐dopant level was increased, the concentration of divalent iron became comparable to that of quadrivalent titanium, leading to a suppression in the cation lattice diffusivity at an iron‐to‐titanium ratio of ∼60. These results suggested that, at the dopant levels and temperatures studied, more than 98% of the iron was in the trivalent state. The diffusional creep of polycrystalline alumina doped with a single iron impurity (0.2 to 2%) was reinterpreted in terms of simultaneous contributions of aluminum lattice and grain‐boundary diffusion, consistent with a grain‐size dependence corresponding to a mixture of Nabarro‐Herring and Coble creep. Aluminum grain‐boundary diffusion was found to be significantly enhanced by the presence of iron in solid solution. Evidence is presented to suggest that the diffusional creep of polycrystalline Al2O3 doped with a single titanium dopant is interface‐controlled. Interfacial kinetics can be promoted by several factors, including (1) a small grain size, (2) a high cation lattice diffusivity, (3) slow cation grain‐boundary diffusion, and (4) the presence of a grain‐boundary second phase.
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