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Degradation Behavior of Protective Rust Layer in Chloride Solution

机译:氯化物溶液中保护性锈层的降解行为

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摘要

The degradation of a protective rust layer on weathering steels was investigated using an electrochemical method in chloride solutions. The samples used were weathering steels which had been exposed in a rural atmosphere for about 35 years. Electrode potential changes were measured in some chloride solutions for the samples with a protective rust layer. The rest potential shifted from original 200 to 300 mV vs. SSE to less noble and fairly constant values after 48 to 72 hours immersion. The constant potential gave less noble values with increasing chloride ion concentration. From the results of corrosion monitoring and visual observation, it was concluded that the decrease in rest potential is attributed the increased number of active sites for anodic dissolution. The alloying elements such as Cr, P and Cu are concentrated in the rust layer at corresponding portions where active dissolution occurred on metal/rust interface. It was not observed that chloride permeation under high chloride ion concentration environments is inhibited by the presence of these elements.
机译:使用电化学方法在氯化物溶液中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,它们已在农村大气中暴露了约35年。对于带有保护性防锈层的样品,在某些氯化物溶液中测量了电极电位的变化。浸泡48到72小时后,剩余电位从相对于SSE的原始200 mV变为300 mV,变为较低的贵重且相当恒定的值。随着氯离子浓度的增加,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,静息电位的下降归因于阳极溶解活性位点的增加。诸如Cr,P和Cu之类的合金元素集中在锈层的相应部位,在该部位上,金属/锈界面发生了活性溶解。没有观察到在这些元素的存在下在高氯离子浓度环境下氯离子的渗透受到抑制。

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