Influence of temperature and aging time on HA synthesized by the hydrothermal method

The influence of temperature and aging time on the morphology and mechanical properties of nano-sized hydroxyapatite (HA) synthesized by a hydrothermal method is reported here. The pre-mixed reactants were poured into a stirred autoclave and reacted at temperatures between 25–250°C for 2–10 h. HA powders thus obtained were examined using X-ray diffraction (XRD), high-resolution field emission scanning electron microscopy (FESEM) and a particle size analyzer. It was found that the aspect ratio of the particles increased with the reaction temperature. The length of the HA particles increased with the reaction temperature below 170°C, but it decreased when the temperature was raised above 170°C. The agglomerates of HA particles were formed during synthesis, and their sizes were strongly dependent on reaction temperatures. As the reaction temperature increased, the agglomerate size decreased (p = 0.008). The density of the discs pressed from these samples reached 85–90% of the theoretical density after sintering at 1200°C for 1 h. No decomposition to other calcium phosphates was detected at this sintering temperature. A correlation existed (p = 0.05) between the agglomerate sizes of HA particles synthesized at various conditions and their sintered densities. With the increase of the agglomerate size, the sintered density of the HA compact decreased. It was found that both the sintered density and flexural strength increased with increasing aging time and reaction temperature. A maximum flexural strength of 78 MPa was observed for the samples synthesized at 170°C for 5 h with the predicted average at these conditions being 65 MPa. These samples attained an average sintered density of 88%.

[1]  H. Hsiang,et al.  Effects of mechanical treatment on phase transformation and sintering of nano-sized γ-Fe2O3 powder , 2003 .

[2]  J. Viguié,et al.  Stoichiometry of hydroxyapatite: influence on the flexural strength , 1993 .

[3]  B. Biscans,et al.  Preparation of hydroxyapatite by neutralization at low temperature—influence of purity of the raw material , 1999 .

[4]  W. Weng,et al.  Alkoxide route for preparing hydroxyapatite and its coatings. , 1998, Biomaterials.

[5]  R. Legeros,et al.  Properties of osteoconductive biomaterials: calcium phosphates. , 2002, Clinical orthopaedics and related research.

[6]  T. Chin,et al.  Hydroxyapatite synthesized by a simplified hydrothermal method , 1997 .

[7]  S. Ng,et al.  Formation of Nanocrystalline Hydroxyapatite in Nonionic Surfactant Emulsions , 1999 .

[8]  F. Gnanam,et al.  The effect of powder processing on densification, microstructure and mechanical properties of hydroxyapatite , 2002 .

[9]  A. S. Posner,et al.  Crystal Structure of Hydroxyapatite , 1964, Nature.

[10]  M. Shaw,et al.  Influence of temperature and concentration on the sintering behavior and mechanical properties of hydroxyapatite , 2004 .

[11]  J. Bobick,et al.  Hydroxylapatite synthesis and characterization in dense polycrystalline form , 1976 .

[12]  M. Trunec,et al.  Injection moulded hydroxyapatite ceramics. , 1996, Biomaterials.

[13]  M. Kakihana,et al.  Hydroxyapatite/Hydroxyapatite‐Whisker Composites without Sintering Additives: Mechanical Properties and Microstructural Evolution , 1997 .

[14]  C. Rey,et al.  A resolution-enhanced Fourier Transform Infrared spectroscopic study of the environment of the CO32− ion in the mineral phase of enamel during its formation and maturation , 1991, Calcified Tissue International.

[15]  I. Manjubala,et al.  Preparation of hydroxyapatite/fluoroapatite-zirconia composites using Indian corals for biomedical applications , 2001 .

[16]  M. Ozawa,et al.  Preparation of needle-like hydroxyapatite , 1998 .

[17]  M. Boulos,et al.  Morphological study of hydroxyapatite nanocrystal suspension , 2000, Journal of materials science. Materials in medicine.

[18]  R Z LeGeros,et al.  Calcium Phosphate Materials in Restorative Dentistry: a Review , 1988, Advances in dental research.

[19]  T. Sato,et al.  Preparation of needle-like hydroxyapatite by homogeneous precipitation under hydrothermal conditions. , 2007, Journal of chemical technology and biotechnology.

[20]  L. Hermansson,et al.  Evaluation of the mechanical properties of hot isostatically pressed titania and titania-calcium phosphate composites. , 1991, Biomaterials.

[21]  W. Bonfield,et al.  Effect of powder characteristics on the sinterability of hydroxyapatite powders , 2001, Journal of materials science. Materials in medicine.

[22]  Raquel Zapanta LeGeros,et al.  Apatites in biological systems , 1981 .

[23]  John Wang,et al.  Nanosized hydroxyapatite powders from microemulsions and emulsions stabilized by a biodegradable surfactant , 1999 .

[24]  W. Weng,et al.  Sol–gel derived porous hydroxyapatite coatings , 1998, Journal of materials science. Materials in medicine.

[25]  C. Rey,et al.  Fourier transform infrared spectroscopic study of the carbonate ions in bone mineral during aging , 1991, Calcified Tissue International.

[26]  A. Ruys,et al.  Sintering effects on the strength of hydroxyapatite. , 1995, Biomaterials.

[27]  B. Milthorpe,et al.  Interdiffusion in short-fibre reinforced hydroxyapatite ceramics , 1998, Journal of materials science. Materials in medicine.

[28]  R. R. Rao,et al.  Synthesis and sintering of hydroxyapatite–zirconia composites , 2002 .

[29]  V. Castaño,et al.  Wet Chemical Synthesis of Hydroxyapatite Particles from Nonstoichiometric Solutions , 1998 .