Kinetics and mechanisms of hydrothermal synthesis of barium titanate
Journal Article
·
· Journal of the American Ceramic Society
- Rutgers Univ., Piscataway, NJ (United States). Dept. of Ceramics
Reaction mechanisms for the hydrothermal synthesis of barium titanate are evaluated. Feedstocks of barium hydroxide octahydrate and anatase titania are reacted for varying durations (1--72 h) to provide intermediate-stage samples for characterization by transmission electron microscopy/energy-dispersive spectroscopy (TEM/EDS), X-ray diffractometry (XRD), and inductively coupled plasma spectroscopy (ICP) and XRD methods permits the analysis of data with the Johnson-Mehl-Avrami equation. This analysis reveals two reaction-rate regimes. Kinetic analysis, based on reaction progress, yields insight into the first reaction-rate regime but is inconclusive in the analysis of the second reaction-rate regime. In the first regime, at the early stage of barium titanate formation, a dissolution-precipitation mechanism dominates. In contrast, in the second regime, at longer reaction times, an in-situ transformation mechanism is probably dominant. However, multiple reaction mechanisms (e.g., in-situ transformation and dissolution-precipitation) may be competing for rate control. Alternatively, dissolution-precipitation may be the dominant mechanism throughout the barium titanate synthesis, with nucleation and growth controlling the first regime and dissolution rate controlling the second regime.
- Sponsoring Organization:
- National Science Foundation, Washington, DC (United States)
- OSTI ID:
- 417779
- Journal Information:
- Journal of the American Ceramic Society, Journal Name: Journal of the American Ceramic Society Journal Issue: 11 Vol. 79; ISSN 0002-7820; ISSN JACTAW
- Country of Publication:
- United States
- Language:
- English
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