A novel approach to on-line measurement of gas evolution kinetics: Application to the negative difference effect of Mg in chloride solution

被引:103
作者
Lebouil, S. [1 ]
Duboin, A. [2 ]
Monti, F. [2 ]
Tabeling, P. [2 ]
Volovitch, P. [1 ]
Ogle, K. [1 ]
机构
[1] Chim Paristech, F-75005 Paris, France
[2] ESPCI PSL, Lab Microfluid MEMS & Nanostruct, F-75005 Paris, France
关键词
Anodic dissolution; Magnesium; Negative difference effect; Kinetics; Gas volume; ANODIC-DISSOLUTION; PURE MAGNESIUM; CORROSION; MECHANISM; OXIDATION; HYDROGEN; ALLOY; AL;
D O I
10.1016/j.electacta.2013.07.131
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
Gas evolution at the surface of a dissolving material plays an important role in the overall dissolution process. In order to measure the kinetics of the gas evolution as a function of time (time resolved volumetry, TRV), a microfluidic system was constructed combined with high speed camera and a dedicated image analysis algorithm to measure the volume of gas as a function of time. This instrumental set up was added to an existing coupling between an electrochemical cell and a time resolved atomic emission spectroscopic detection. This article presents the instrumental development and first results concerning the spontaneous dissolution of zinc in a dilute HCl solution, the spontaneous dissolution of Mg in 0.01 M NaCl at open circuit potential and under an applied anodic potential. For Zn dissolution, an excellent correlation was obtained between the quantity of hydrogen measured and the quantity of zinc dissolved, with average accuracy of 5%. For Mg however, the anomalous production of hydrogen was observed attributed to the negative difference effect. A steady Mg dissolution was observed correlating with the electrochemical current for an n = 2 dissolution mechanism with superimposed bursts of Mg dissolution and hydrogen release corresponding to the anomalous dissolution mechanism. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:176 / 182
页数:7
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