Sintering Kinetics of Hydroxyapatite Prepared by Chemical Coprecipitation Method

Article Preview

Abstract:

With chemical coprecipitation method, high purity hydroxyapatite was successfully prepared in this paper. The microstructure and components of HA were characterized by XRD, SEM, FTIR, atomic emission spectrum and particle size analyzer. The results demonstrate that synthesized HA is very pure and is harmless to human body. Average particle size of HA powder is about 10.4μm. Crystallization degree of hydroxyapatite increases with the increase of sintering temperature and the optimal preparing technique is sintering at 750 for 2h with temperature-rising rate of 5°C·min-1. Grain growing activation energy of HA can be calculated as 24.8 kJ·mol-1 according to the relationship between grain size and sintering temperature. HA’s grain growth mechanism is interfacial diffusion controlling mechanism.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 233-235)

Pages:

1511-1515

Citation:

Online since:

May 2011

Authors:

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2011 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] Liu DM, Troczynski T, Tseng WJ. Water-based sol-gel synthesis of hydroxyapatite: process development [J]. Biomaterials, 2001, 22:1721-1730

DOI: 10.1016/s0142-9612(00)00332-x

Google Scholar

[2] Layrolle P, Ito A, Tateishi T. Sol-gel synthesis of amorphous calcium phosphate and sintering into microporous hydroxyapatite bioceramics[J]. J. Am. Ceram. Soc., 1998, 81(6):1421-1428

DOI: 10.1111/j.1151-2916.1998.tb02499.x

Google Scholar

[3] Bezzi G, Celotti G, Landi E, et al. A novel sol-gel technique for hydroxyapatite preparation[J]. Materials Chemistry and Physics, 2003, 78:816-824

DOI: 10.1016/s0254-0584(02)00392-9

Google Scholar

[4] Li SP. Introduction for Biomedical Materials[M]. Wuhan: Press of Wuhan university of Science and Technology, (2001)

Google Scholar

[5] Hayakawa S, Osaka A. Biomimetic deposition of calcium phosphate on oxides soaked in a simulated body fluid[J]. Journal of Non-crystal Solids, 2000, 264&264: 409-415

DOI: 10.1016/s0022-3093(99)00649-3

Google Scholar

[6] Tang XL, Xiao XF, Liu RF. Hydrothermal synthesis and characterization of silicon-substituted hydroxyapatite[J]. Chinese Journal of Inorganic Chemistry, 2005, 21(10):1501-1505

Google Scholar

[7] Hu JS, Agrawal DK, fang Y, et al. Preparation of hydroxyapatite ceramics by supersonic[J]. Journal of Materials Science, 1993, 28: 5297-5300

Google Scholar

[8] Ruan JM, Zou JP, Huang BY. Biomaterials Science[M]. Beijing: Science Press, (2004)

Google Scholar

[9] Lim GK, Wang J, Ng SC, et al. Processing of hydroxyapatite via microemulsion and emulsion route[J]. Biomaterials, 1997, 18(21): 1433-1439

DOI: 10.1016/s0142-9612(97)00081-1

Google Scholar

[10] Hu H L. X-ray diffractive technique[M]. Beijing: Textile Industry Press, 1988, 202-211

Google Scholar

[11] Qian Y T. Crystallization chemistry [M]. Beijing: Press of University of Science and Technology of China, 1988, 140

Google Scholar

[12] Tang A D, Huang K L. Mn3O4:Solvo-thermal Synthesis and Crystallization Kinetics, Chinese Journal of Inorganic Chemistry, 2005, 21(6): 929-933

Google Scholar