Preparation and characterisation of bioactive hydroxyapatite–silica composite nanopowders via sol–gel method for medical applications

Abstract

This study focuses on preparation and characterisation of hydroxyapatite–silica composite nanopowders with different contents of silica. Hydroxyapatite–silica composite nanopowders with 10, 20, 30 and 40 wt‐% silica were prepared using a sol–gel method at 600°C with phosphoric pentoxide and calcium nitrate tetrahydrate as the source of hydroxyapatite, also tetraethylorthosilicate and methyltriethoxisilane as the source of silica. XRD, FTIR, SEM, EDAX and TEM techniques were used for characterisation and evaluation of the phase composition, crystallinity, crystallite size, functional groups, morphology and composition of the products. Dissolution behaviour of the products was evaluated at predetermined time periods by an atomic absorption spectrometer and a pH meter. Results indicated the presence of nanocrystalline hydroxyapatite phase and amorphous silica nanoparticles in composite nanopowders. Also, by increasing the content of silica in composite nanopowders, the crystallite size and crystallinity of hydroxyapatite phase decreased and the Ca ion release rate changed.