Sol-gel synthesis and spectrometric structural evaluation of strontium substituted hydroxyapatite

被引:25
作者
Balamurugan, A. [1 ]
Balossier, G. [2 ]
Torres, P. [1 ]
Michel, J. [2 ]
Ferreira, J. M. F. [1 ]
机构
[1] Univ Aveiro, Dept Ceram & Glass Engn, CICECO, P-3810193 Aveiro, Portugal
[2] Univ Reims, INSERM, ERM 0203, Lab Microscopie Elect Analyt, F-51685 Reims, France
来源
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS | 2009年 / 29卷 / 03期
关键词
Electronic structure; Sr-HAP; Substitution;
D O I
10.1016/j.msec.2008.09.005
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
Investigations of the electronic structures of substituted strontium apatites were carried out by using X-ray photo electron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction technique (XRD) has been used to determine the structural parameters. Electron microprobe microanalysis technique was used to estimate the elemental concentrations in each substituted apatite material. The present work aims at studying the changes in the electronic structure of Sr-s(PO4)(3)OH (Sr-HAP) upon isomorphic substitution by F and Cl at the OH site of apatite and Sr by Na at trans Sr-HAP. The ion exchange between Na+ in sodium alginate and aqueous Ca2+ was important for the preparation of calcium hydroxyapatite. In contrast, the reaction of sodium alginate with the mixture of Na4P2O7 and aqueous Sr2+ afforded strontium hydroxyapatite at the specific ratio. The structure of calcium and strontium phosphates prepared from the sol-gel process evidently depended on the amount of sodium alginate introduced into the mixture of Na4P2O7 and the corresponding divalent cations. The findings have ensured that substitution of Sr-HAP by Na enhances the binding energy of 0 and Sr core levels. It was also noticed that the same substitution decreases the binding energy of P 2s-level. These observations point out to a decrease in the electron density at P and an increase in the electron density at O in Sr atoms. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1006 / 1009
页数:4
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