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Hydrogen permeation behavior and corrosion monitoring of steel in cyclic wet - dry atmospheric environment

机译:循环干湿气氛下钢的氢渗透行为与腐蚀监测。

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摘要

Hydrogen permeation of 16Mn steel under a cyclic wet-dry condition was investigated by Devanathan-Stachurski's electrolytic cell with a membrane covered on the exit side by a nickel layer and the weight loss was measured for each wet-dry cycle. The results show that hydrogen permeation current change with different atmospheric environment: distilled water, seawater, and seawater containing 100 ppm H{sub}2S. The results show that seawater can induce an increase in the hydrogen permeation current due to the hydrolyzation reaction. And after the increase, equilibrium is reached due to the equilibrium of hydrolyzation reaction effect and the block of the rust layer. On the other hand, H{sub}2S contamination also can induce an increase in the maximum hydrogen permeation current due to the hydrolyzation reaction. And H{sub}2S contamination delays the time that hydrogen permeation is detected because of the formation of the FeS{sub}(1-x) film. The FeS{sub}(1-x) film can block the absorption of hydrogen onto the specimen surface. The surface potential change and the pH change of the metal surface control the hydrogen permeation current. And a clear linear correlation exists between the quantities of hydrogen permeated through the 16Mn steel and the weight loss. Based on the linear correlation, we monitored the corrosion rate by monitoring the hydrogen permeation current by a sensor outside. Good coherences were shown between results in laboratory and outside.
机译:用Devanathan-Stachurski's电解池研究了16Mn钢在循环干湿条件下的氢渗透,其电解池的出口侧被镍层覆盖,并测量了每个湿干循环的重量损失。结果表明,氢渗透电流随不同的大气环境而变化:蒸馏水,海水和含100 ppm H {sub} 2S的海水。结果表明,由于水解反应,海水可以引起氢渗透电流的增加。并且在增加之后,由于水解反应效果的平衡和锈层的阻塞而达到平衡。另一方面,由于水解反应,H {sub} 2S污染也可引起最大氢渗透电流的增加。由于FeS {sub}(1-x)膜的形成,H {sub} 2S污染会延迟检测到氢渗透的时间。 FeS {sub}(1-x)膜可以阻止氢吸收到样品表面。金属表面的表面电势变化和pH值变化控制氢渗透电流。并且,透过16Mn钢的氢气量与重量损失之间存在明显的线性关系。基于线性关系,我们通过外部传感器监测氢渗透电流来监测腐蚀速率。在实验室和外部结果之间显示出良好的一致性。

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