Abstract

Because of the significant effect of the sol–gel method on the glass morphology at the relatively low processing temperature, in the present work, phosphate glass and glass-ceramic nanopowders with the general formula of (P2O5)55–CaO)25–(Na2O)20−x–(TiO2)x, (x = 5, 10, and 15 mol%) have been synthesized via a facile sol–gel method. For this purpose, acetone and dimethylformamide (DMF) have been used as a polar and non-protic solvent. The proportion of triethylphosphate to acetone or DMF has been selected 1:3 that they have been synthesized at 25 °C and pH = 5–6. The glass powders have been dried at 315 °C. Then, the powders synthesized by acetone have been calcined at 500 and 750 °C, and the powders synthesized by DMF have been calcined at 550, 650, and 750 °C. The glass and glass-ceramic nanopowders have been analyzed by several techniques, X-ray powder diffraction (XRD), Differential thermal analysis (STA), Fourier transform infrared spectroscopy (FT-IR), Brunauer–Emmett–Teller and Barrett–Joyner–Halenda (BET–BJH), and Scanning electron microscopy (SEM-EDS). The XRD results have been confirmed the amorphous nature of all glass samples, while after calcination, the samples have been shown the peaks assigned to β-TCP and hydroxyapatite. The SEM images have shown that the synthesized glass and glass-ceramic powders by both acetone and DMF solvents have a particle size below 50 nm and spherical morphology. Also, the glass and glass-ceramic powders, after soaking in the simulated body fluid (SBF) for 7 days, depicted the formation of hydroxyapatite and carbonated-hydroxyapatite layer on the surface of the glass and glass-ceramic powders, respectively.

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