Abstract

Many attempts have been focused on preparing of synthetic hydroxyapatite (HA), which closely resembles bone apatite and exhibits excellent osteoconductivity. Low temperature formation and fusion of the apatite crystals have been the main contributions of the sol–gel process in comparison with conventional methods for HA powder synthesis. This paper describes the synthesis of nano-HA particles via a sol–gel method. Nanocrystalline powder of hydroxyapatite (HA) was prepared using Ca(NO 3) 2·4H 2O and P 2O 5 by a simple sol–gel approach. X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used for characterization and evaluation of the phase composition, morphology and particle size of products. The presence of amorphous and crystalline phases in the as-dried gel precursor was confirmed by the evaluating technique. Single phase of HA was also identified in the heat treated powder by XRD patterns. SEM and TEM evaluations showed that the obtained powder after heat treatment at 600 °C was agglomerated and composed of nanocrystalline (25–28 nm) HA particles. Increasing the sintering temperature and time could cause decomposition of HA into β-tricalcium phosphate and calcium oxide. The prepared nanocrystalline HA is able to improve the contact reaction and the stability at the artificial/natural bone interface for medical applications.

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