Hydrothermal synthesis of fine bismuth titanate powders

Bismuth titanate (Bi4Ti3O12) fine powders were synthesized from a low temperature hydrothermal method. Bismuth nitrate and titanium isopropoxide were used as the starting materials with the mole ratio of Bi:Ti = 4:3. Sodium hydroxide was added to adjust the pH of the mixed final solution at 13. The...

Full description

Saved in:
Bibliographic Details
Main Authors: Pookmanee P., Uriwilast P., Phanichpant S.
Other Authors: Zhu W.Yao X.Kimura T.Bhalla A.
Format: Conference or Workshop Item
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-4344667474&partnerID=40&md5=185fa47c71f192d279bfa8ab805d0713
http://cmuir.cmu.ac.th/handle/6653943832/6714
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
Language: English
id th-cmuir.6653943832-6714
record_format dspace
spelling th-cmuir.6653943832-67142014-08-30T03:51:08Z Hydrothermal synthesis of fine bismuth titanate powders Pookmanee P. Uriwilast P. Phanichpant S. Zhu W.Yao X.Kimura T.Bhalla A. Bismuth titanate (Bi4Ti3O12) fine powders were synthesized from a low temperature hydrothermal method. Bismuth nitrate and titanium isopropoxide were used as the starting materials with the mole ratio of Bi:Ti = 4:3. Sodium hydroxide was added to adjust the pH of the mixed final solution at 13. The temperature of reaction in the hydrothermal Teflon-lined vessel was 150°C. The effect of reaction time at 5, 10, and 15h was investigated. The phase structure was identified by X-ray diffraction (XRD) technique. Orthorhombic structure of Bi4Ti3O12 fine powders was obtained without calcination step. The morphology and microstructure were investigated by scanning electron microscopic (SEM) technique. The powders were generally sphered in shapes and the average sizes were 0.50-1.20 μm. © 2004 Elsevier Ltd and Techna Group S.r.l. All rights reserved. 2014-08-30T03:51:08Z 2014-08-30T03:51:08Z 2004 Conference Paper 02728842 10.1016/j.ceramint.2003.12.043 63470 CINND http://www.scopus.com/inward/record.url?eid=2-s2.0-4344667474&partnerID=40&md5=185fa47c71f192d279bfa8ab805d0713 http://cmuir.cmu.ac.th/handle/6653943832/6714 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Bismuth titanate (Bi4Ti3O12) fine powders were synthesized from a low temperature hydrothermal method. Bismuth nitrate and titanium isopropoxide were used as the starting materials with the mole ratio of Bi:Ti = 4:3. Sodium hydroxide was added to adjust the pH of the mixed final solution at 13. The temperature of reaction in the hydrothermal Teflon-lined vessel was 150°C. The effect of reaction time at 5, 10, and 15h was investigated. The phase structure was identified by X-ray diffraction (XRD) technique. Orthorhombic structure of Bi4Ti3O12 fine powders was obtained without calcination step. The morphology and microstructure were investigated by scanning electron microscopic (SEM) technique. The powders were generally sphered in shapes and the average sizes were 0.50-1.20 μm. © 2004 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
author2 Zhu W.Yao X.Kimura T.Bhalla A.
author_facet Zhu W.Yao X.Kimura T.Bhalla A.
Pookmanee P.
Uriwilast P.
Phanichpant S.
format Conference or Workshop Item
author Pookmanee P.
Uriwilast P.
Phanichpant S.
spellingShingle Pookmanee P.
Uriwilast P.
Phanichpant S.
Hydrothermal synthesis of fine bismuth titanate powders
author_sort Pookmanee P.
title Hydrothermal synthesis of fine bismuth titanate powders
title_short Hydrothermal synthesis of fine bismuth titanate powders
title_full Hydrothermal synthesis of fine bismuth titanate powders
title_fullStr Hydrothermal synthesis of fine bismuth titanate powders
title_full_unstemmed Hydrothermal synthesis of fine bismuth titanate powders
title_sort hydrothermal synthesis of fine bismuth titanate powders
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-4344667474&partnerID=40&md5=185fa47c71f192d279bfa8ab805d0713
http://cmuir.cmu.ac.th/handle/6653943832/6714
_version_ 1681420665442271232