Abstract

This study examined the formation mechanism of BaTiO 3 from the thermal decomposition of barium titanyl oxalate. A significant amount of O 2 evolution near 357 and 720 °C was observed by gas chromatography/mass spectroscopy, except for the previously known H 2O, CO 2, CO evolution. The metastable Ba 2Ti 2O 5CO 3(CO 2) intermediate phase seemed to be transformed mainly to Ba 2Ti 2O 5CO 3, while a certain amount of crystalline BaCO 3 and amorphous Ti-rich phase were formed simultaneously at 450–600 °C in air. A modification of the decomposition mechanism reported by Gopalakrishnamurthy et al. was proposed based on the experimental findings.

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