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A.C. Impedance Properties of HA/Ti Compound Layer coated Ti-30Ta-(3~15)Nb Alloys
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A.C. Impedance Properties of HA/Ti Compound Layer coated Ti-30Ta-(3~15)Nb Alloys
Jeong, Y.H.; Lee, H.J.; Moong, Y.P; Park, G.H.; Jang, S.H.; Son, M.K.; Choe, H.C.;
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A.C. impedance properties of HA/Ti compound layer coated Ti-30Ta-()Nb alloys have been studied by electrochemical method. Ti-30Ta binary alloys contained 3, 7, 10 and 15 wt% Nb were manufactured by the vacuum furnace system. And then specimen was homogenized at for 24 hrs. The sample was cut and polished for corrosion test and coating. It was coated with HA/Ti compound layer by magnetron sputter. The non-coated and coated morphology of Ti alloy were analyzed by X-ray diffractometer (XRD), energy X-ray dispersive spectroscopy (EDX) and filed emission scanning electron microscope (FE-SEM). The corrosion behaviors were investigated using A.C. impedance test (PARSTAT 2273, USA) in 0.9% NaCl solution at . Ti-30Ta-()Nb alloys showed the phase, and phase peak was predominantly appeared in the case of increasingly Nb contents. The microstructures of Ti alloy were transformed from needle-like structure to equiaxed structure as Nb content increased. From the analysis of coating surface, HA/Ti composite surface uniformed coating layer with 750 nm thickness. The growth directions of film were (211), (112), (300) and (202) for HA/Ti composite coating on the surface after heat treatment at , whereas, the growth direction of film was (110) for Ti coating. The polarization resistance () of HA/Ti composite coated Ti-alloys were higher than those of the Ti and HA coated samples in 0.9% NaCl solution at . Especially, corrosion resistance of Ti-Ta-Nb system increased as Nb content increased.
Electrochemical Properties;Ti-30Ta-(315)Nb alloy;Hydoxyapatite;Magnetron sputter;
 Cited by
J. Breme, E. Einsenbarth, H. Hilerbrand, Titanium '95, Science and Technology (1995) 1792

G. C. McKay, R. Macnair, C. McDonald, M.H. Grant, J. Biomater. 17 (1996) 1339-1344 crossref(new window)

M. Niinomi, J. Mater. Sci. Eng. A 243 (1998) 231- 236 crossref(new window)

M. F. Semlitsch, H. Weber, R.M. Streicher, R. Schon, J. Biomater. 13 (1992) 781-786 crossref(new window)

Y. Okazaki, S. Rao, S. Asao, T. Tateishi, S. Katsuda, Y. Furuki, J. Japan Inst. Metals 9 (1996) 890-895

J. A. Davidson, P. Kovacks, U.S. Patent no. 5 (1992) 169, 597

E. W. Collings, ASM (1986) 329-334

J. A. Helsen, H. J. Breme, Metals as Biomaterials, Jhon Wiley & Sons (1998) 138

V. Nelea, C. Morosanu, M. Iliescu, I.N, Surf. and Coat. Tech. 173 (2003) 315-322 crossref(new window)

H. C. Choe, W. Brantley, Adv. Mater. Res. 26-28 (2007) 825-828 crossref(new window)

S. J. Ding, Biomater. 24 (2003) 4233-4238 crossref(new window)

Y. H. Jeong, H. C. Choe, Y. M. Ko, J. Kor. Inst. Surf. Eng. 41 (2008) 1-6 crossref(new window)

A. R. Boyd, H. Duffy, R. McCann, B. J, Meenan, Mat Sci and Eng. (2007)

N. bris, J. C. M. Rosca, J Electro. Chem. 526 (2002) 53-62 crossref(new window)

J. E. G. Gonzalez, J. C. Mirza-Rosca, J. Electroanalytical Chem. 471 (1999) 109-115 crossref(new window)