Localized corrosion of Al90Fe5Gd5 and Al87Ni8.7Y4.3 alloys in the amorphous, nanocrystalline and crystalline states:: resistance to micrometer-scale pit formation

被引:68
作者
Sweitzer, JE [1 ]
Shiflet, GJ [1 ]
Scully, JR [1 ]
机构
[1] Univ Virginia, Dept Mat Sci & Engn, Charlottesville, VA 22904 USA
基金
美国国家科学基金会;
关键词
amorphous; alloy; devitrification; metallic coatings; nanocrystalline; pitting corrosion;
D O I
10.1016/S0013-4686(02)00830-7
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The role of isothermal aging on the localized corrosion behavior of Al90Fe5Gd5 and Al87Ni8.7Y4.3 alloys was characterized in 0.6 M NaCl solution. The pitting (E-pit) and repassivation (E-rp) potentials were both increased similar to 400 mV by the presence of transition and rare earth metal additions in supersaturated solid solution and amorphous structure. A statistical distribution in:Epit observed on small electrodes was due, in part, to the sensitivity of this critical potential to the presence of a population of critical surface flaws that serve as pit initiation sites. Mechanistic insight on the spacing of critical flaws was enabled by varying the tested electrode surface area. E-rp was not dependent on electrode surface area due to the similarity of pit depths in all electrode sizes. The critical potentials were also characterized after heat treating the amorphous ribbons isothermally at 150 degreesC for 25 h and 550 degreesC for 1 h. The former produced Al-rich nanocrystals embedded in the remaining amorphous matrix while the latter produced a fully crystalline condition containing intermetallic phases. Notably, the improved resistance to the formation of micrometer-scale pits was not lost compared with the fully amorphous condition when small Al-rich nanocrystals were present in an amorphous matrix: However, improvement in pitting corrosion resistance was completely lost in the fully crystallized condition as indicated by values for E-pit and E-rp that were similar to those of high purity, polycrystalline aluminum. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1223 / 1234
页数:12
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