A study on corrosion mechanism of 15CrMo in saline (Na2SO4) steam at high temperature

B. Bai, L. Deng, D. Che
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引用次数: 1

Abstract

To clarify the corrosion mechanism of 15CrMo in saline (Na2SO4) steam, the experiments were conducted on a novel setup. The samples were analyzed by scanning electron microscope and X‐ray photoelectron spectroscopy. The results indicate that insoluble sulfide, FexSy, would form on the gas‐phase corroded surface while it would not occur on the liquid‐phase corroded surface. The salinity of water/steam has a destructive effect on hydrogen bonds. Compared with deionized steam/water, salinity accelerates the corrosion of steel in two ways electric current intensification in primary cell and energy promotion of the solution system. FeOOH does not change obviously with the increase of salt concentration. The relative variation values of FeOOH content with salt concentration are only 2.43% (gas) and 3.40% (liquid), respectively. Besides, the FeOOH content on the liquid‐phase corroded surface is much greater than that on the gas‐phase corroded surface regardless of the salt concentration. The content of Fe3O4 in the gas/liquid phase decreases from 17.01%/24.58% to 6.02%/18.30%. The Fe2O3 content in the gas/liquid phase increases from 40.12%/9.85% to 73.62%/17.05%.
15CrMo在盐水(Na2SO4)蒸汽中的高温腐蚀机理研究
为了弄清15CrMo在盐水(Na2SO4)蒸汽中的腐蚀机理,在一种新型装置上进行了实验。用扫描电镜和X射线光电子能谱对样品进行了分析。结果表明,气相腐蚀表面会形成不溶性硫化物,而液相腐蚀表面不会形成不溶性硫化物。水/蒸汽的盐度对氢键有破坏作用。与去离子化蒸汽/水相比,盐度从两个方面加速了钢的腐蚀:一次槽内的电流增强和溶液体系的能量提升。FeOOH随盐浓度的增加变化不明显。FeOOH含量随盐浓度的相对变化值仅为2.43%(气体)和3.40%(液体)。此外,无论盐浓度如何,液相腐蚀表面的FeOOH含量都远大于气相腐蚀表面。气液相中Fe3O4的含量由17.01%/24.58%降至6.02%/18.30%。气液相中Fe2O3含量由40.12%/9.85%增加到73.62%/17.05%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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