根据铜电路板缝腐蚀特征,研制了阵列式Ag/AgCl、IrO2电极,设计缝隙腐蚀模拟装置,在0.5mol.L-1的NaCl溶液中分别同时原位检测电子线路板缝隙腐蚀过程,缝隙内的氯离子浓度分布、pH分布及其随时间的变化.研究表明,在电子线路板发生缝隙腐蚀的过程中,缝隙内部不同深度的Cl-及H+浓度逐渐增大,且随着与缝口距离的增大而增大,从而导致缝隙腐蚀不断向纵深方向发展.
Although the crevice corrosion of metals had been extensively studied in the past years,it remained lack of direct experimental information of the micro chemical environments and electrochemical conditions inside the corroding crevice.The distribution of chloride concentration and local pH in the occluded area are the most crucial factors in development of crevice corrosion.The array probes in one dimension of Ag/AgCl and IrO2 array were developed in this work to in situ follow the distribution of chloride concentration and local pH in the occluded area during the crevice corrosion propagation.Based on a designed simulated crevice corrosion system in 0.5mol/L NaCl solution,the distribution of chloride concentration and local pH for the electronic circuit board inside corroding crevice were imaged correlated with corrosion potential in the crevice.It is found that the chloride concentration increases and the local pH decreases inside the corroding crevice with the immersion time.And the Cl-concentration and local pH at the deeper location inside the crevice are always higher and lower,respectively,than that near the mouth of crevice,due to the mass transfer difficulty by geometrical limitation of crevice.That is the reason why the crevice corrosion always develops in depth direction.All obtained experimental results provide a further understanding to the mechanism of crevice corrosion of electronic materials in the given environments.
[1]Cho K H,Abdulsalam M I,Pickering H W.The effectof electrolyte properties on the mechanism of crevice cor-rosion in pure iron[J].Electrochemical Society,1998,145(6):1862.
[2]Buchheit R G,Moran J P,Stoner G E.Localized corro-sion behavior of alloy 2090-the role of microstructuralheterogeneity[J].Corrosion,1990,46(8):610.
[3]Kelly R G,Yuan J,Weyant C M,et al.Applications ofcapillary electrophoresis in corrosion science and engi-neering[J].Chromatography A,1999,834(1~2):433.
[4]Mankowski J,Szklarska-Smialowska Z.Studies on accu-mulation of chloride ions in pits growing during anodicpolarization[J].Corrosion Science,1975,15(8):493.
[5]Ryan C Wolfe,Konrad G Weil,Howard W Pickering.Electrochemical probes for metal/electrolyte systemcharacterization during crevice corrosion[J].PhysicalChemistry B,2004,108(38):14298.
[6]El Warraky A,El Shayeb HA,Sherif E M.Pitting cor-rosion of copper in chloride solutions[J].Anti-Corro-sion Methods And Materials,2004,51(1):52.
[7]Zhong Qing-dong(钟庆东).Study on crevice corrosionof copper using wire beam electrode[J].Journal of Chi-nese Society for Corrosion and Protection,1999,19(3):189.
[8]Wharton J A,Mellor B G,Wood R J K,et al.Crevicecorrosion studies using electrochemical noise measure-ments and a scanning electrode technique[J].Journalof the Electrochemical Society,2000,147(9):3294.
[9]Wolfe Ryan C,Weil Konrad G,Shaw Barbara A.Measurement of pHgradients in the crevice corrosion ofiron using a palladium hydride microelectrode[J].Jour-nal of the Electrochemical Society,2005,152(2):B82.
[10]Wolfe Ryan C,Pickiering Howard W,Shaw BarbaraA.Microprobe study of pHduring the induction periodpreceding crevice corrosion[J].Journal of the Elec-trochemical Society,2006,153(2):B25.
[11]Sagara M,Noda K,Katada Y,et al.Measurement forsurface pH distribution in crevice corrosion process ofstainless steel[J].Journal of the Japan Institute ofMetals,2002,66(9):925.