Abstract

Aqueous mixtures of zirconium acetate and aluminum nitrate were pyrolyzed and crystallized to form a metastable solid solution, Zr1‐xAlxO2−x/2 (x < 0.57). The initial, metastable phase partitions at higher temperatures to form two metastable phases, viz., t−ZrO2+γ‐Al2O3 with a nano‐scale microstructure. The microstructural observations associated with the γ‐ →α‐Al2O3 phase transformation in the t‐ZrO2 matrix are reported for compositions containing 10, 20, and 40 mol% A12O3. During this phase transformation, the α‐Al2O3 grains take the form of a colony of irregular, platelike grains, all with a common crystallographic orientation. The plates contain ZrO2 inclusions and are separated by ZrO2 grains. The volume fraction of A12O3 and the heat treatment conditions influence the final microstructure. At lower volume fractions of A12O3, the colonies coarsen to single, irregular plates, surrounded by polycrystalline ZrO2. Interpenetrating microstructures produced at high volume fractions of A12O3 exhibit very little grain growth for periods up to 24 h at 1400°C.

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