Corrosion resistance, chemistry, and mechanical aspects of Nitinol surfaces formed in hydrogen peroxide solutions

被引:13
|
作者
Shabalovskaya, Svetlana A. [1 ,2 ]
Anderegg, James W. [2 ]
Undisz, Andreas [1 ]
Rettenmayr, Markus [1 ]
Rondelli, Gianni C. [3 ]
机构
[1] Univ Jena, Inst Mat Sci & Technol, D-07743 Jena, Germany
[2] Iowa State Univ, Ames Lab DOE, Ames, IA 50011 USA
[3] CNR, Inst Energy & Interphases, I-20133 Milan, Italy
关键词
Nitinol; hydrogen peroxide surface treatment; cyclic potentiodynamic and potentiostatic polarization; localized corrosion resistance; corrosion under stress; biocompatibility; SHAPE-MEMORY ALLOY; NI-TI ALLOY; OXIDATION; ASTROCYTE; TITANIUM; NICKEL; WIRES;
D O I
10.1002/jbm.b.32717
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Ti oxides formed naturally on Nitinol surfaces are only a few nanometers thick. To increase their thickness, heat treatments are explored. The resulting surfaces exhibit poor resistance to pitting corrosion. As an alternative approach to accelerate surface oxidation and grow thicker oxides, the exposure of Nitinol to strong oxidizing H2O2 aqueous solutions (3 and 30%) for various periods of time was used. Using X-Ray Photoelectron Spectroscopy (XPS) and Auger spectroscopy, it was found that the surface layers with variable Ti (615 at %) and Ni (513 at %) contents and the thickness up to 100 nm without Ni-enriched interfaces could be formed. The response of the surface oxides to stress in superelastic regime of deformations depended on oxide thickness. In the corrosion studies performed in both strained and strain-free states using potentiodynamic and potentiostatic polarizations, the surfaces treated in H2O2 showed no pitting in corrosive solution that was assigned to higher chemical homogeneity of the surfaces free of secondary phases and inclusions that assist better biocompatibility of Nitinol medical devices. (c) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 100B: 14901499, 2012
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页码:1490 / 1499
页数:10
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