Abstract

Phosphate-based glasses have been investigated for tissue engineering applications. This study details the properties and structural characterization of titanium ultra-phosphate glasses in the 55(P2O5)–30(CaO)–(25−x)(Na2O)–x(TiO2) (0⩽x⩽5) system, which have been prepared via melt-quenching techniques. Structural characterization was achieved by a combination of X-ray diffraction (XRD), and solid-state nuclear magnetic resonance, Raman and Fourier transform infrared spectroscopies. Physical properties were also investigated using density, degradation and ion release studies; additionally, differential thermal analysis was used for thermal analysis of these glasses. The results show that with the addition of TiO2 the density and glass transition temperature increased whereas the degradation and ion release properties are decreased. From XRD data, TiP2O7 and CaP2O6 were detected in 3 and 5mol.% TiO2-containing glasses. Magic angle spinning nuclear magnetic resonance results confirmed that as TiO2 is incorporated into the glass; the amount of Q3 increases as the amount of Q2 consequently decreases, indicating increasing polymerization of the phosphate network. Spectroscopy results also showed that the local structure of glasses changes with increasing TiO2 content. As TiO2 is incorporated into the glass, the phosphate connectivity increases, indicating that the addition of TiO2 content correlates unequivocally with an increase in glass stability.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.