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Effect of Dissolved Hydrogen on Corrosion Behavior of Ni-base Alloy in High-Temperature Water

机译:溶解氢对高温水中镍基合金腐蚀行为的影响

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The corrosion behavior of Alloy 690 (UNS N06690) was investigated in a 500 h immersion test conducted in varying hydrogenated Li/B solutions at 330°C. The corrosion rates were determined by the chemical descaling of the oxides; rates were found to decrease as the hydrogen concentration increased from 35 to 100 cc/kg. Scanning electron microscopy and X-ray diffraction were used to characterize the morphology of the oxide layers. Two oxide layers were identified: an inner layer composed of very small grains of a few nm in diameter and; an outer layer composed of some plate-like crystals clustered together. The sizes of the crystals built up on the outer layer decreased with increasing of the hydrogen content. The difference in crystal size may be due to changes in the crystal growth environment. The composition of the oxide film built up on the specimen surfaces depended on the hydrogen concentration in the test environments, as determined by XPS depth analyses. The chromium and iron contents of the oxide films increased with increasing hydrogen levels from 35 to 65 cc/kg, whereas the nickel content increased with decreasing hydrogen concentration. Under a 35 cc/kg hydrogen level, related to the corrosion potential of the Ni/NiO equilibrium, a rapid change of nickel into nickel oxides containing chromium and iron occurs. Under high hydrogen level of 65 cc/kg, the nickel oxides reduced to metallic nickel, which was confirmed by XPS results of the nickel 2p spectrum. At lower potential with 65 cc/kg hydrogen content, there was a potential zone in which the chromium and iron oxides were stable at testing temperature and pH. As a result of this, it is thought that increasing the hydrogen content of the environment is likely to increase the amount of the chromium and iron oxides.
机译:合金690(UNS N06690)的腐蚀行为在在330℃下氢化不同而不同锂/ B溶液进行了500ħ浸渍试验进行了研究。腐蚀速率是由氧化物的化学除锈确定;发现率降低为氢浓度从35提高到100毫升/千克。扫描电子显微镜和X射线衍射进行了表征氧化层的形态。两个氧化物层被确定:在直径和几nm的非常小的晶粒组成的内层;一些组成的外层板状晶体聚集在一起。建立了在外层上的晶体的大小与氢含量的增加而降低。在晶体尺寸的差异可能是由于在晶体生长环境的变化。该氧化膜的组成堆积在试样表面取决于在测试环境中的氢浓度,通过XPS深度分析来确定。氧化膜中的铬和铁的含量随着氢水平为35〜65立方厘米/ kg的增加,而镍的含量随氢浓度增加。下一个35毫升/千克氢水平,涉及到的镍/氧化镍平衡的腐蚀电位,发生镍的含铬和铁的快速变化成氧化镍。下65毫升/公斤的高的氢水平,镍氧化物还原为金属镍,这是由镍的2p光谱的XPS结果证实。在用65毫升/千克氢含量较低的电势,存在其中铬和铁的氧化物分别稳定在测试温度和pH的电势区域。作为其结果,据认为增加了环境中的氢含量可能增加的铬和铁的氧化物的量。

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