Lee T M, Chang E, Yang C Y
Department of Materials Science and Engineering, National Cheng Kung University, Tainan, Taiwan.
J Mater Sci Mater Med. 1999 Sep;10(9):541-8. doi: 10.1023/a:1008916314329.
This work aims to investigate the effects of three factors, namely: (1) two differently prepared materials (as-polished Ti6A14V and 2 h brazed Ti6A14V); (2) three different surface passivation treatments (34% nitric acid passivation, 400 degrees C heated in air, and aged in 100 degrees C de-ionized water); and (3) periods of immersion time (up to 32 days), on trace element release in Hank's ethylene diamine tetra-acetic acid (EDTA) solution. After passivation and autoclaving treatment, the specimens were immersed in 8.0 mM EDTA in Hank's solution and maintained at 37 degrees C for periods of time up to 32 days. The 400 degrees C -treated specimens exhibit a substantial reduction in constituent release, which may be attributed to the higher thickness and rutile structure of the surface oxides. For acid-passivated and water-aged treatments, a highly significant decrease in the trace levels of Ti, A1, and V is detected from the brazed Ti6A14V compared to those obtained from the Ti6A14V specimens. It is hypothesized that an anatase-rutile transformation of surface TiO_2 is likely to occur, accelerated by the elements of copper and nickel in the brazed specimens. In addition, a significant time-related decrease in constituent release rate is observed for all kinds of specimens throughout the 0-8 day experimental period. The implication of the results is discussed.
本研究旨在探究三个因素的影响,即:(1)两种不同制备的材料(研磨态Ti6A14V和钎焊2小时的Ti6A14V);(2)三种不同的表面钝化处理(34%硝酸钝化、在空气中400℃加热以及在100℃去离子水中时效处理);(3)浸泡时间(长达32天),对汉克斯乙二胺四乙酸(EDTA)溶液中微量元素释放的影响。经过钝化和高压灭菌处理后,将试样浸泡在汉克斯溶液中的8.0 mM EDTA中,并在37℃下保持长达32天。400℃处理的试样成分释放大幅减少,这可能归因于表面氧化物的更高厚度和金红石结构。对于酸钝化和水时效处理,与Ti6A14V试样相比,钎焊Ti6A14V中Ti、Al和V的痕量水平显著降低。据推测,钎焊试样中的铜和镍元素会加速表面TiO₂的锐钛矿-金红石转变。此外,在整个0-8天的实验期内,所有试样的成分释放速率均随时间显著降低。对结果的意义进行了讨论。