Apatite formation from simulated body fluid on various phases of TiO2 thin films prepared by filtered cathodic vacuum arc deposition

被引:17
作者
Amin, M. S. [1 ]
Randeniya, L. K. [1 ]
Bendavid, A. [1 ]
Martin, P. J. [1 ]
Preston, E. W. [1 ]
机构
[1] CSIRO Mat Sci & Engn, Lindfield, NSW 2070, Australia
关键词
Filtered cathodic vacuum arc deposition (FCVAD); Titanium oxide (TiO2); Simulated body fluid (SBF); UV treatment; Amorphous carbonated apatite; X-ray diffraction; X-ray photoelectron spectroscopy; GEL-DERIVED TITANIA; BIOMIMETIC APATITE; CHEMICAL TREATMENT; SURFACE MODIFICATION; LOW-TEMPERATURE; UV-IRRADIATION; CARBON-FILMS; OXIDE-FILM; BIOACTIVITY; SOL;
D O I
10.1016/j.tsf.2010.09.029
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Hydroxyl (OH-)-free TiO2 thin films with amorphous and crystalline phases were deposited onto (100) silicon substrates using filtered cathodic vacuum arc deposition in order to investigate the in vitro apatite formation in simulated body fluid (SBF). The surface morphology, composition and structure of the TiO2 thin films were characterized. The X-ray photoelectron spectroscopy results confirmed the presence of calcium and phosphorus on all TiO2 thin film surfaces after immersion in SBF at 37 degrees C. Fourier transform infra red results showed the presence of carbonated apatite on the surface of these films. Amorphous structured TiO2 thin film showed poor ability to form apatite on its surface in SBF. Apatite formation was more pronounced on the surfaces of the anatase films in comparison to those of rutile. The carbonated apatite deposition rate increased significantly when the TiO2 film was illuminated with UV light prior to immersing in the SBF. In particular, the UV-treated anatase and rutile films showed increased rates of carbonated apatite formation on their surfaces in comparison to samples not treated with radiation. The increase in hydrophilicity due to UV treatment appears beneficial for the apatite growth on these surfaces. Crown Copyright (C) 2010 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1300 / 1306
页数:7
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