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:高温含水环境中环氢化和含氧水化学中镍基合金182和52和316不锈钢的腐蚀行为

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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:在本作工作中,将基于Ni的合金52和182和溶液退火316不锈钢(SS)暴露于高温含水环境中的环状氢化和氧化水化学。通过接触电阻(CER)和电化学阻抗光谱(EIS)和EX原位表面分析方法的原位技术研究了相应的腐蚀行为,包括扫描电子显微镜(SEM),X射线光电子能谱(XPS)和拉曼光谱。发现在所有材料的DH期间膜抗性远高得多。对于所有材料,电化学腐蚀电位(E_(COR))的差异和DH周期也是巨大的(约0.7V)。氧化膜(形态学和组成等)与循环变化环境的演变似乎与材料变化。对于316 S和合金52,氧化物薄膜似乎不可变化,而对于合金182,可以发现一些循环变化,循环变化环境。

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