Local flux of hydrogen from magnesium alloy corrosion investigated by scanning electrochemical microscopy

被引:57
作者
Tefashe, Ushula Mengesha [1 ]
Snowden, Michael Edward [1 ]
Ducharme, Philippe Dauphin [1 ]
Danaie, Mohsen [2 ,3 ]
Botton, Gianluigi A. [2 ,3 ]
Mauzeroll, Janine [1 ]
机构
[1] McGill Univ, Lab Electrochem React Imaging & Detect Biol Syst, Montreal, PQ H3A 0B8, Canada
[2] McMaster Univ, Brockhouse Inst Mat Res, Dept Mat Sci & Engn, Hamilton, ON L8S 4M1, Canada
[3] McMaster Univ, Canadian Ctr Electron Microscopy, Hamilton, ON L8S 4M1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Magnesium alloy; Corrosion; Scanning electrochemical microscopy; Substrate-generation/tip-collection; Hydrogen detection; LINEAR SWEEP VOLTAMMETRY; IN-SITU; MICRODISK ELECTRODES; MICROSTRUCTURE; MECHANISM; BEHAVIOR; EVOLUTION; SURFACES; INSIGHTS; SINGLE;
D O I
10.1016/j.jelechem.2014.03.002
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein, we report the successful electrochemical detection and quantification of H-2 fluxes produced from a corroding magnesium alloy using the substrate-generation/tip-collection mode of scanning electrochemical microscopy (SECM). Using a platinum microelectrode, the variation in H-2 fluxes was imaged revealing the time-dependent corrosion reaction. Our results demonstrate that through careful control of the corroding media and immersion time, quantitative SECM approach curves, devoid of convective effects, were acquired. Comparison to an idealized numerical model enabled the quantification of the local H-2 flux for a given corroding area. These data demonstrated that the active site size increases throughout the reaction, whereas the flux of H-2 generated at an active site increased for the first hour of immersion followed by decrease in the flux of H-2 for times greater than 1 h. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:121 / 127
页数:7
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