首页> 外文会议>International conference on environmental degradation of materials in nuclear power systems-water reactors >THE CORROSION BEHAVIOR OF NICKEL-BASED ALLOYS 182 AND 52 AND 316 STAINLESS STEEL IN CYCLIC HYDROGENATED AND OXYGENATED WATER CHEMISTRY IN HIGH TEMPERATURE AQUEOUS ENVIRONMENT
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THE CORROSION BEHAVIOR OF NICKEL-BASED ALLOYS 182 AND 52 AND 316 STAINLESS STEEL IN CYCLIC HYDROGENATED AND OXYGENATED WATER CHEMISTRY IN HIGH TEMPERATURE AQUEOUS ENVIRONMENT

机译:镍基合金182和52和316不锈钢在高温水环境中的循环加氢和加氧水化学中的腐蚀行为

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In the present work, Ni based Alloys 52 and 182 and solution-annealed 316 stainless steel (SS) were exposed to a cyclic hydrogenated and oxygenated water chemistry in the high temperature aqueous environment. The corresponding corrosion behavior was examined by in situ technologies of contact electric resistance (CER) and electrochemical impedance spectroscopy (EIS) and ex situ surface analysis methods including scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. It was found that the film resistance in DO periods is much higher than that in DH periods for all the materials. The difference of electrochemical corrosion potential (E_(corr)) in DO and DH periods is also huge (about 0.7 V) for all the materials. The evolution of the oxide film (morphology and composition etc.) with cyclic changing environment seems to be varied with material. For 316 SS and Alloy 52 the oxide film seems not changeable while for Alloy 182 some cyclic changes can be found with cyclic changing environment.
机译:在当前的工作中,Ni基合金52和182以及固溶退火的316不锈钢(SS)在高温水环境中暴露于循环氢化和氧化水化学作用。通过接触电阻(CER)和电化学阻抗谱(EIS)的原位技术以及包括扫描电子显微镜(SEM),X射线光电子能谱(XPS)和拉曼光谱的非原位表面分析方法来检查相应的腐蚀行为。发现所有材料在溶解氧(DO)期间的膜电阻都比溶解氧(DH)期间的膜电阻高得多。对于所有材料,DO和DH期间的电化学腐蚀电位(E_(corr))的差异也很大(约0.7 V)。氧化膜的演化(形态和组成等)随着环境的周期性变化似乎随材料而变化。对于316 SS和52合金,氧化膜似乎不可改变,而对于182 SS,随着环境的变化,可以发现一些循环变化。

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