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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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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2011
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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. |
format | Text |
id | pubmed-3092508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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