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Sintering Behavior of Magnesium-Substituted Fluorapatite Powders Prepared by Hydrothermal Method

Magnesium-substituted fluorapatite powders were synthesized by hydrothermal method, and their sintering behavior was investigated by dilatometry in the temperature range 25–1100°C. Analysis of the obtained powders by X-ray diffraction and (31)P NMR spectroscopy showed that the powders consisted of a...

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Detalles Bibliográficos
Autores principales: Nasr, S., Bouzouita, K.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3092508/
https://www.ncbi.nlm.nih.gov/pubmed/21577315
http://dx.doi.org/10.1155/2011/453759
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author Nasr, S.
Bouzouita, K.
author_facet Nasr, S.
Bouzouita, K.
author_sort Nasr, S.
collection PubMed
description Magnesium-substituted fluorapatite powders were synthesized by hydrothermal method, and their sintering behavior was investigated by dilatometry in the temperature range 25–1100°C. Analysis of the obtained powders by X-ray diffraction and (31)P NMR spectroscopy showed that the powders consisted of a single apatite phase and no amorphous phase has been formed. Compared to pure fluorapatite, the shrinkage of the substituted samples occurred in two steps and the temperature at which the sintering rate was maximum is lower. In addition, the shrinkage was interrupted by an expansion of the samples due to the formation of a liquid phase. The latter phase led to the crystallization of needle-crystals by a dissolution-diffusion-reprecipitation process.
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spelling pubmed-30925082011-05-16 Sintering Behavior of Magnesium-Substituted Fluorapatite Powders Prepared by Hydrothermal Method Nasr, S. Bouzouita, K. Bioinorg Chem Appl Research Article Magnesium-substituted fluorapatite powders were synthesized by hydrothermal method, and their sintering behavior was investigated by dilatometry in the temperature range 25–1100°C. Analysis of the obtained powders by X-ray diffraction and (31)P NMR spectroscopy showed that the powders consisted of a single apatite phase and no amorphous phase has been formed. Compared to pure fluorapatite, the shrinkage of the substituted samples occurred in two steps and the temperature at which the sintering rate was maximum is lower. In addition, the shrinkage was interrupted by an expansion of the samples due to the formation of a liquid phase. The latter phase led to the crystallization of needle-crystals by a dissolution-diffusion-reprecipitation process. Hindawi Publishing Corporation 2011 2011-03-15 /pmc/articles/PMC3092508/ /pubmed/21577315 http://dx.doi.org/10.1155/2011/453759 Text en Copyright © 2011 S. Nasr and K. Bouzouita. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nasr, S.
Bouzouita, K.
Sintering Behavior of Magnesium-Substituted Fluorapatite Powders Prepared by Hydrothermal Method
title Sintering Behavior of Magnesium-Substituted Fluorapatite Powders Prepared by Hydrothermal Method
title_full Sintering Behavior of Magnesium-Substituted Fluorapatite Powders Prepared by Hydrothermal Method
title_fullStr Sintering Behavior of Magnesium-Substituted Fluorapatite Powders Prepared by Hydrothermal Method
title_full_unstemmed Sintering Behavior of Magnesium-Substituted Fluorapatite Powders Prepared by Hydrothermal Method
title_short Sintering Behavior of Magnesium-Substituted Fluorapatite Powders Prepared by Hydrothermal Method
title_sort sintering behavior of magnesium-substituted fluorapatite powders prepared by hydrothermal method
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3092508/
https://www.ncbi.nlm.nih.gov/pubmed/21577315
http://dx.doi.org/10.1155/2011/453759
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