Degradation of Ti-6A1-4V alloy under cyclic loading in a simulated body environment with cell culturing

被引:6
|
作者
Doi, Kotaro [1 ,2 ]
Miyabe, Sayaka [1 ]
Tsuchiya, Hiroaki [1 ]
Fujimoto, Shinji [1 ]
机构
[1] Osaka Univ, Grad Sch Engn, Div Mat & Mfg Sci, 2-1 Yamada Oka, Suita, Osaka 5650871, Japan
[2] Natl Inst Mat Sci, Environm & Energy Mat Div, Environm Durabil Grp, Mat Reliabil Unit, 1-2-1 Sengen, Tsukuba, Ibaraki 3050047, Japan
基金
日本学术振兴会;
关键词
Ti-6A1-4V alloy; Corrosion fatigue; Passivity breakdown; Dissolution; Repassivation; Simulated body environment; 316L STAINLESS-STEEL; IN-VIVO MEASUREMENT; CORROSION BEHAVIOR; TITANIUM; IMPLANT; FATIGUE; VITRO; REPASSIVATION; DEFORMATION; BREAKDOWN;
D O I
10.1016/j.jmbbm.2015.10.032
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The present study reports the corrosion fatigue of the Ti-6A1-4V alloy using cyclic deformation test in a simulated body fluid under cell culturing for the first time. Cyclic deformation tests were carried out using three types of specimens to reveal the effects of proteins and cells on the corrosion fatigue of the alloy. For the 1-day-immersed and 1 week-immersed specimens, tensile specimens were soaked in a simulated body fluid for 1 day and 1 week, respectively, before cyclic deformation test, whereas for the cell-cultured specimen, MC3T3-E1 osteoblast-like cells were seeded and then cultured on tensile specimens for 1 week. The incubation period for crack initiation was longer for the cell cultured and 1-week-immersed specimens compared to that for the 1-day-immersed specimen. On the other hand, crack propagation period for the cell-cultured and 1-week immersed specimens was shorter than that for the 1-day-immersed specimen. These results indicate that proteins and cells adhered on the alloy surface inhibit metal dissolution at newly created surface emerged by cyclic deformation to suppress crack initiation, whereas they accelerate crack propagation because dissolution at crack tip is accelerated in the occluded space formed under proteins and cells. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6 / 13
页数:8
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