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The oxidation behavior of 316L in simulated pressurized water reactor environments with cyclically changing concentrations of dissolved oxygen and hydrogen

机译:用溶解氧和氢气循环变化浓度的模拟加压水反应器环境中316L的氧化行为

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摘要

The oxidation behavior of 316L stainless steel in the simulated pressurized water reactor primary water with cyclic exposure to hydrogenated and oxygenated water conditions was investigated by contact electric resistance, electrochemical impedance spectroscopy, scanning electron microscopy, Raman spectroscopy and X-ray photoelectron spectroscopy techniques. The electrochemical resistance of the oxide film exhibits significant changes as the environment is shifted from hydrogenated water chemistry to oxygenated water chemistry and vice versa. However, in different hydrogenated periods (or oxygenated periods) with the same water chemistry, the electrochemical resistance of the oxide film is very similar. On the contrary, the oxide morphology and composition do not show obvious changes, and the oxide film thickness has a generally increasing trend. The reason for this phenomenon was also discussed. (C) 2018 Elsevier B.V. All rights reserved.
机译:通过接触电阻,电化学阻抗光谱,扫描电子显微镜,拉曼光谱和X射线光电子体光谱技术,研究了用循环暴露于氢化和含氧水条件的循环暴露和含氧水条件的模拟加压水反应器初级水中的氧化行为。 氧化膜的电化学抗性表现出显着的变化,因为环境从氢化水化学转移到氧化水化学,反之亦然。 然而,在具有相同水化学的不同氢化时期(或含氧时段)中,氧化物膜的电化学抗性非常相似。 相反,氧化物形态和组合物不显示明显的变化,氧化物膜厚度具有普遍越来越大的趋势。 还讨论了这种现象的原因。 (c)2018年elestvier b.v.保留所有权利。

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