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Degradation behavior of protective rust layer in chloride solution

机译:氯化物溶液中保护性防锈层的降解行为

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The degradation of protective rust layer onweathering steels was investigated by electrochemical method inchloride solutions. The samples used were weathering steels whichhad been exposed in rural atmosphere for about 35 years.Electrode potential changes were measured in some chloridesolutions for the samples with protective rust layer. The restpotential shifted from original 200 to 300 mV vs. SSE to lessnoble and fairly constant values after 48 to 72 hours immersion.The constant potential gave less noble values with increasingchloride ion concentration. From the results of corrosionmonitoring and visual observation, it is concluded that thedecrease in rest potential is attributed the increased number ofactive sites for anodic dissolution. The alloying elements such asCr, P and Cu are concentrated in rust layer at correspondingportions where active dissolution occurred on metal/rust interface.It is not observed that chloride permeation under high chloride ionconcentration environments is inhibited by the presence of these elements.
机译:通过电化学方法氯化物溶液研究了耐候钢上保护性防锈层的降解。所使用的样品是耐候钢,已在农村大气中暴露了约35年。测量了带有保护性防锈层的样品在某些氯化物溶液中的电极电位变化。浸入48至72小时后,电势从最初的200到300 mV相对于SSE变为不贵且相当恒定的值。随着氯化物离子浓度的增加,恒电位给出的贵金属值降低。从腐蚀监测和视觉观察的结果可以得出结论,静息电位的降低归因于阳极溶解的活性位点数量的增加。 Cr,P和Cu等合金元素集中在相应部位的锈层中,在金属/锈界面上发生活性溶解,没有观察到这些元素的存在会抑制氯在高氯离子浓度环境下的渗透。

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