Synthesis and biodegradation evaluation of nano-Si and nano-Si/TiO2 coatings on biodegradable Mg–Ca alloy in simulated body fluid
In the present study, nano-Si and nano-Si/TiO2 composite coatings have been successfully synthesized on the surface of Mg–1wt%Ca alloy by the physical vapor deposition (PVD) method. The surface morphology and compositions of the coated specimens were characterized by X-ray diffraction (XRD), Fourier...
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Veröffentlicht in: | Ceramics international 2014-11, Vol.40 (9), p.14009-14018 |
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Sprache: | eng |
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Zusammenfassung: | In the present study, nano-Si and nano-Si/TiO2 composite coatings have been successfully synthesized on the surface of Mg–1wt%Ca alloy by the physical vapor deposition (PVD) method. The surface morphology and compositions of the coated specimens were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The results show the formation of thin and compact coating layers which homogeneously cover the surface of Mg alloy. Some micro-pores and micro-cracks were observed in the Si and Si/TiO2 films. It was also found that the Si and TiO2 nanoparticle had a spherical morphology with an average particle size of 30–40nm and 70–80nm, respectively. Electrochemical studies revealed that nano-Si/TiO2 coating offers a significant reduction in the corrosion rate (0.57mm/year) compared to the Si coated (0.91mm/year) and the uncoated alloys (6.21mm/year) in simulated body fluid (SBF). Hydrogen evolution studies showed a lower degradation rate of nano-Si/TiO2 (1.57ml/cm2/day) than that of nano-Si coated alloy (2.22ml/cm2/day). Immersion test showed that the nano-Si/TiO2 coating presented a greater nucleation site of hydroxyapatite (HA) than the uncoated sample. Thus nano-Si/TiO2 composite coating prepared by PVD on the Mg–Ca alloy is more appropriate for biomedical applications. |
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ISSN: | 0272-8842 1873-3956 |
DOI: | 10.1016/j.ceramint.2014.05.126 |