Mechanism for Converting Al₂O₃-containing Borate Glass to Hydroxyapatite in Aqueous Phosphate Solution
The effect of replacing varying amounts (0-2.5 mol.%) of B2O3 with Al2O3 in a borate glass on (1) the conversion of the glass to HA in an aqueous phosphate solution and (2) the compressive strength of the as-formed HA product was investigated. Samples of each glass (10 × 10 × 8 mm) were placed in 0.25 M K2HPO4 solution at 60 °C, and the conversion kinetics to HA were determined from the weight loss of the glass and the pH of the solution. The structure and composition of the solid reaction products were characterized using X-ray diffraction, Fourier transform infrared spectroscopy and scanning electron microscopy. While the conversion rate of the glass to HA decreased considerably with increasing Al2O3 content, the microstructure of the HA product became denser and the compressive strength of the HA product increased. The addition of SiO2 to the Al2O3-containing borate glass reversed the deterioration of the conversion rate, and produced a further improvement in the strength of the HA product. The compressive strength of the HA formed from the borate glass with 2.5 mol.% Al2O3 and 5 mol.% SiO2 was 11.1 ± 0.2 MPa, which is equal to the highest strengths reported for trabecular bone. The results indicated that simultaneous additions of Al2O3 and SiO2 could be used to control the bioactivity of the borate glass and to enhance the mechanical strength of the HA product. Furthermore, the HA product formed from the glass containing both SiO2 and Al2O3 could be applied to bone repair.
D. Zhao et al., "Mechanism for Converting Al₂O₃-containing Borate Glass to Hydroxyapatite in Aqueous Phosphate Solution," Acta Biomaterialia, vol. 5, no. 4, pp. 1265 - 1273, Elsevier, May 2009.
The definitive version is available at https://doi.org/10.1016/j.actbio.2008.11.021
Materials Science and Engineering
Keywords and Phrases
Bioactivity; Borate Glass; Mechanical Strength; Porous Structure; Hydroxyapatite
International Standard Serial Number (ISSN)
Article - Journal
© 2009 Elsevier, All rights reserved.
01 May 2009