Quantitative analysis of the polarization behavior of iron in an aerated acidic solution using SECM

被引:12
作者
Zhang, Qinhao [1 ]
Liu, Pan [1 ]
Zhu, Zejie [1 ]
Ye, Zhenni [1 ]
Zhang, Jianqing [1 ]
Cao, Fahe [1 ]
Li, Xiaogang [2 ]
机构
[1] Zhejiang Univ, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China
[2] Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing 100083, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Polarization behavior; Iron; Acidic solution; SECM; SCANNING ELECTROCHEMICAL MICROSCOPY; LOCALIZED CORROSION; IMPEDANCE SPECTROSCOPY; ELECTRODE TECHNIQUE; ANODIC-DISSOLUTION; CHLORIDE SOLUTION; NOISE-ANALYSIS; SURFACE; STEEL; PH;
D O I
10.1016/j.elecom.2018.07.007
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The apparent corrosion current of pure iron in aerated 5 mM HClO4 + 0.1 M NaClO4 solution was separated into Fe oxidation, proton reduction and oxygen reduction currents using SECM in a modified tip generation/substrate collection (TG/SC) mode. The oxidation current density of Fe was 1.11 x 10(-3) A/cm(2), equal to the sum of proton reduction and oxygen reduction current density, around 5.26 x 10(-4) and 5.84 x 10(-4) A/cm(2), respectively, implying that oxygen reduction and proton reduction are equally important at open circuit potential (OCP). Moreover, oxygen reduction was suppressed on the Fe electrode in the potential range between -0.7 and -1.1 V vs Ag/AgCl because of the inhibitory effect of the proton reduction reaction and a potential-dependent surface effect, then the suppression is weakened and oxygen reduction is enhanced. Finally, the Fe corrosion current was dominated by oxygen reduction and Fe oxidation at potentials more positive than -0.6 V.
引用
收藏
页码:143 / 147
页数:5
相关论文
共 27 条
[1]   Imaging concentration profiles of redox-active species in open-circuit corrosion processes with the scanning electrochemical microscope [J].
Bastos, AC ;
Simoes, AM ;
González, S ;
González-García, Y ;
Souto, RM .
ELECTROCHEMISTRY COMMUNICATIONS, 2004, 6 (11) :1212-1215
[2]   Detection of the Short-Lived Cation Radical Intermediate in the Electrochemical Oxidation of N,N-Dimethylaniline by Scanning Electrochemical Microscopy [J].
Cao, Fahe ;
Kim, Jiyeon ;
Bard, Allen J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (52) :18163-18169
[3]   Electrochemical noise analysis of LY12-T3 in EXCO solution by discrete wavelet transform technique [J].
Cao, FH ;
Zhang, Z ;
Su, JX ;
Shi, YY ;
Zhang, JQ .
ELECTROCHIMICA ACTA, 2006, 51 (07) :1359-1364
[4]   Fabrication of Carbon, Gold, Platinum, Silver, and Mercury Ultramicroelectrodes with Controlled Geometry [J].
Danis, Laurence ;
Polcari, David ;
Kwan, Annie ;
Gateman, Samantha Michelle ;
Mauzeroll, Janine .
ANALYTICAL CHEMISTRY, 2015, 87 (05) :2565-2569
[5]   Study of the atmospheric corrosion of galvanised steel in a micrometric electrolytic droplet [J].
Dubuisson, Emilie ;
Lavie, Philippe ;
Dalard, Francis ;
Caire, Jean-Pierre ;
Szunerits, Sabine .
ELECTROCHEMISTRY COMMUNICATIONS, 2006, 8 (06) :911-915
[6]   Evaluation of Thymus vulgaris plant extract as an eco-friendly corrosion inhibitor for stainless steel 304 in acidic solution by means of electrochemical impedance spectroscopy, electrochemical noise analysis and density functional theory [J].
Ehsani, A. ;
Mahjani, M. G. ;
Hosseini, M. ;
Safari, R. ;
Moshrefi, R. ;
Shiri, H. Mohammad .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2017, 490 :444-451
[7]   A guide to polarisation curve interpretation:: deconstruction of experimental curves typical of the Fe/H2O/H+/O2 corrosion system [J].
Flitt, HJ ;
Schweinsberg, DP .
CORROSION SCIENCE, 2005, 47 (09) :2125-2156
[8]   Microelectrode techniques for corrosion research of iron [J].
Fushimi, K. ;
Takabatake, Y. ;
Nakanishi, T. ;
Hasegawa, Y. .
ELECTROCHIMICA ACTA, 2013, 113 :741-747
[9]   An SECM observation of dissolution distribution of ferrous or ferric ion from a polycrystalline iron electrode [J].
Fushimi, K ;
Seo, M .
ELECTROCHIMICA ACTA, 2001, 47 (1-2) :121-127
[10]   A SECM assisted EQCM study of iron pitting [J].
Gabrielli, C. ;
Joiret, S. ;
Keddam, M. ;
Perrot, H. ;
Portail, N. ;
Rousseau, P. ;
Vivier, V. .
ELECTROCHIMICA ACTA, 2007, 52 (27) :7706-7714