Hydrothermal synthesis and formation mechanism of tetragonal barium titanate in a highly concentrated alkaline solution

被引:42
作者
Ozen, Murat [1 ]
Mertens, Myrjam [2 ]
Snijkers, Frans [2 ]
Cool, Pegie [1 ]
机构
[1] Univ Antwerp, Dept Chem, Lab Adsorpt & Catalysis, Univ Pl 1, B-2610 Antwerp, Belgium
[2] Flemish Inst Technol Res VITO Nv, Boeretang 200, B-2400 Mol, Belgium
关键词
Powders: Chemical preparation; Spectroscopy; BaTiO3 and titanates; DISSOLUTION-PRECIPITATION MECHANISM; BATIO3; POWDERS; FACILE SYNTHESIS; GRAIN-GROWTH; KINETICS; CRYSTALLIZATION; PARTICLES; TRANSITION; MORPHOLOGY; CHEMISTRY;
D O I
10.1016/j.ceramint.2016.03.234
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Tetragonal cube-shaped barium titanate (BaTiO3) was produced by the hydrothermal treatment of a peroxo-hydroxide precursor, a single-source amorphous barium titanate precursor, in a highly concentrated sodium hydroxide solution. Phase pure barium titanate with cube-shaped morphology and particle-sizes in the 0.2-0.5 mu m range were formed at temperatures above 80 degrees C. Also, the cube-shaped morphology of the BaTiO3 product was preceded by spherical- and plate-like morphologies with, respectively, a Ti-excess and Ba-excess. Coinciding with these morphological observations, changes in the reaction product were also observed. The formation of crystalline BaTiO3 proceeded alongside secondary BaTi2O5 and Ba2TiO4 phases. These secondary phases disappeared as the reaction time was increased leaving only BaTiO3 as the sole reaction product. Kinetic analysis of the formation of hydrothermal BaTiO3 crystallization by the Johnson-Mehl-Avrami method showed that BaTiO3 crystallization is a homogeneous dissolution-precipitation reaction. The mechanism is governed by nucleation and growth in the beginning of the reaction and dissolution-precipitation dominating throughout the hydrothermal reaction process. (C) 2016 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:10967 / 10975
页数:9
相关论文
共 59 条
[1]   The role of material chemistry in processing BaTiO3 in aqueous suspensions [J].
Adair, J. H. ;
Crampo, J. ;
Mandanas, M. M. ;
Suvaci, E. .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2006, 89 (06) :1853-1860
[2]   Hydroxyl Content of BaTiO3 Nanoparticles with Varied Size [J].
Adam, Jens ;
Klein, Gabi ;
Lehnert, Tobias .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2013, 96 (09) :2987-2993
[3]   Granulation, Phase Change, and Microstructure - Kinetics of Phase Change. III [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1941, 9 (02) :177-184
[4]  
Burfoot J., 1967, FERROELECTRICS INTRO
[5]  
Byrappa K., 2012, HDB HHYDROTHERMAL TE
[6]  
Carlos J., 2012, CRYSTALLIZATION SCI
[7]   Ferroelectric ceramics by sol-gel methods and applications: a review [J].
Chilibon, Irinela ;
Marat-Mendes, Jose N. .
JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY, 2012, 64 (03) :571-611
[8]   Formation of tubular BaTiO3 nanoparticle assembly through the Kirkendall effect using Na2Ti3O7 nanowires as template [J].
Ding, S. ;
Xu, C. Y. ;
Wang, W. S. ;
Huang, Y. D. ;
Zhen, L. .
MATERIALS RESEARCH BULLETIN, 2013, 48 (11) :4565-4569
[9]   Kinetics and mechanisms of hydrothermal synthesis of barium titanate [J].
Eckert, JO ;
HungHouston, CC ;
Gersten, BL ;
Lencka, MM ;
Riman, RE .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1996, 79 (11) :2929-2939
[10]   The Effect of Stoichiometry to the Phase Formation of Barium Titanate [J].
Faris, M. A. ;
Yeoh, C. K. ;
Arif, W. M. ;
Teh, P. L. ;
Abdullah, Nadia .
ADVANCED X-RAY CHARACTERIZATION TECHNIQUES, 2013, 620 :198-202