Synthesis of anodic titania nanotubes in Na2SO4/NaF electrolyte: A comparison between anodization time and specimens with biomaterial based approaches

被引:24
作者
Balakrishnan, M. [1 ,2 ]
Narayanan, R. [3 ]
机构
[1] PSG Coll Technol, Dept Met Engn, Coimbatore 641004, Tamil Nadu, India
[2] Indian Inst Technol Madras, Dept Met & Mat Engn, Chennai 600036, Tamil Nadu, India
[3] Saveetha Sch Engn, Dept Mech Engn, Chennai 602105, Tamil Nadu, India
关键词
Titanium; Anodization; Nanotubes; Hydroxyapatite; Polarization; CORROSION-RESISTANCE; OXIDE-FILMS; OXIDATION; ALLOY; HYDROXYAPATITE; FABRICATION; TIO2;
D O I
10.1016/j.tsf.2013.05.122
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Surface modification of commercially pure titanium (cp-Ti) has been carried out by electrochemical anodic oxidation at constant voltage for different time periods (0.5, 1, 2 and 4.5 h). Currents developed during the anodization indicate that the nanotubes are formed due to the competition of titania formation and dissolution under the assistance of electric field. Topologies of the anodized titanium change remarkably with time of oxidation. The morphology of the as-prepared nanotubes was characterized by scanning electron microscopy and atomic force microscopy while the chemistry and crystallinity were characterized by energy-dispersive X-ray spectroscopy and X-ray diffraction respectively. The as-anodized oxide was of amorphous but transformed to anatase and/or rutile crystal structure upon annealing for 3 h at 600 degrees C. The anatase structure showed excellent apatite-forming ability and produced a compact apatite layer covering the surface completely upon treatment in simulated body fluid (SBF) solution for 30 h. Corrosion of anodized titanium samples was studied in a SBF solution using open circuit potential, polarization and electrochemical impedance measurements and compared with that of non-oxidized titanium. Among these samples, titanium anodized for 4.5 h exhibited superior corrosion properties. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:23 / 30
页数:8
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