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Corrosion Behaviour of Fe-Cr-(Mn, Si) Ferritic Alloys in Wet and Dry CO2-SO2 Atmospheres at 650 A degrees C

机译:在650℃下湿湿的Fe-Cr-(Mn,Si)铁素体合金的腐蚀行为及干燥CO2-SO2大气压

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Model alloys of Fe-9Cr, Fe-20Cr and their ternaries containing 2Mn or 0.5Si (wt%) were exposed to Ar-20%CO2 and Ar-20%CO2-0.5%SO2 at 650 A degrees C, and the results were compared with those in wet CO2, with and without SO2. In S-free, dry CO2, all 9Cr alloys went into breakaway, and the 20Cr alloys formed regions of protective Cr2O3, but also fast-growing Fe-rich nodules. Addition of SO2 to dry CO2 led to little change for 9Cr alloys and less protective scaling of 20Cr alloys, but decreased the extent of internal carburisation. Addition of H2O to CO2 caused breakaway for all alloys. Simultaneous addition of both H2O and SO2 to CO2, however, achieved the best results: passivation of 20Cr alloys, and partial protection of 9Cr alloys. The detection by XPS of sulphide species within the chromia scale allows a discussion of competitive adsorption of S-, C- and H-bearing species on oxide grain boundaries.
机译:Fe-9cr,Fe-20cr及其含有2ml或0.5si(wt%)的含有2ml或0.5si(wt%)的二元的模型合金在650℃下暴露于Ar-20%CO 2和Ar-20%CO 2 -0.5%SO 2,结果是 与湿二氧化碳的那些相比,有和没有SO2。 在S无S干二氧化碳中,所有9CR合金都进入分离,20Cr合金形成保护Cr2O3的区域,也是快速生长的Fe富含的结节。 加入SO2至干CO2导致9Cr合金的变化几乎没有变化,较少的20cr合金的保护性缩放,但降低了内部碳碳化的程度。 添加H2O至CO2导致所有合金的分离。 然而,同时添加H2O和SO2至CO2,实现了最佳结果:20Cr合金的钝化和9Cr合金的部分保护。 在染色率范围内XPS的硫化物物种检测允许讨论氧化物晶界对S-,C-和H-轴承物种的竞争吸附。

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