The corrosion rate monitoring of SUS 304 and Fe in deaerated autoclave water of 250°C and 50kg/cm
2 was attempted through overvoltage measurements by using the galvanostatic linear polarization method. It was found that the overvoltage due to solution resistance could be separated from the total overvoltage without using a compensation circuit for solution resistance and 10min as the polarization time was adequate enough to estimate the corrosion rate. The large corrosion rate of Fe in initial period decreased with time up to about 50h to attain an apparent steady value, while the transient period for SUS 304 was remarkably short. The electron diffraction and IMA analyses of corrosion products on SUS 304 gave spinel-type oxides corresponding to NiO·Fe
2O
3 at the outer layer and NiO·(Fe, Cr)
2O
3 at the inner layer as main products, and corrundum (Fe, Cr)
2O
3 as minor one. Further, it was found that the spinel consisted of outer iron rich layers and inner chromium rich ones.
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