Hydrothermal Synthesis of Barium Titanate: Effect of Titania Precursor and Calcination Temperature on Phase Transition
Nanosized barium titanate powders were synthesized by a hydrothermal method. The effect of titania precursors on the phase transition of BaTiO3 with respect to Ba/Ti ratio, reaction temperature, reaction time, and calcination temperature was investigated. The synthesized materials were characterized...
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Published in | Industrial & engineering chemistry research Vol. 47; no. 6; pp. 1868 - 1875 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Chemical Society
19.03.2008
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Subjects | |
Online Access | Get full text |
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Summary: | Nanosized barium titanate powders were synthesized by a hydrothermal method. The effect of titania precursors on the phase transition of BaTiO3 with respect to Ba/Ti ratio, reaction temperature, reaction time, and calcination temperature was investigated. The synthesized materials were characterized by X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. BaTiO3 in pure cubic phase with spherical morphology was observed with a lower calcination temperature, Ba/Ti ratio, reaction temperature, and time. Increase in the tetragonal phase was ascertained in treatments at higher reaction temperature with a longer reaction time. The lattice hydroxyl release is believed to be the reason for tetragonality at high reaction and calcination temperatures. To prepare tetragonal BaTiO3 using HClO4-TiO2, the optimum synthesis conditions viz., Ba/Ti ratio, reaction temperature, and reaction time, are 1.2, 160 °C, and 3 h, respectively, at a calcination temperature of 1150 °C. The reaction time and reaction temperature for the cubic−tetragonal phase transformation of BaTiO3 shifted toward shorter reaction time and lower reaction temperature when TiO2 was synthesized by hydrolysis using HClO4 as the acid catalyst. |
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Bibliography: | istex:E47A1F31A034E9EF624B4B7261D6F9ABDEBB271F ark:/67375/TPS-Q1TCHDQK-P |
ISSN: | 0888-5885 1520-5045 |
DOI: | 10.1021/ie070986m |