Abstract
CeO 2 powders have been prepared by aging a cerium(III) nitrate solution in the presence of hexamethylenetetramine. Oxidation of Ce 3+ occurs in the precipitate and the wet precipitate is identified as crystallized CeO 2 before any heat treatment. The cold‐pressed powders can be sintered to full density at temperatures as low as 1250°C in just 6 min. Moreover, the sinterability of the powders is insensitive to the calcination temperatures, particle size, or green density. The powders calcined at 850°C with a crystallite size of 600 Å have a sinterability as good as the powders calcined at 450°C with a crystallite size of 145 Å. The mechanisms for direct CeO 2 precipitation and its relation to the excellent sinterability are discussed.

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