In situ measurement of corrosion of type 316L stainless steel in 553 K pure water via the electrical resistance of a thin wire

Abstract

A system for the in situ monitoring of corrosion depth via electrical resistance measurements was applied to study the corrosion rate of type 316L stainless steel at 553 K in pure water. Corrosion depth was measured using a 50 μm diameter wire probe mounted axially in the tube. Measurements were in good agreement with literature data for both the hydrogen water chemistry (HWC) condition and the normal water chemistry (NWC) condition. Oxide film analyses by scanning electron microscopy and laser Raman spectroscopy on the wire probe and the tube showed no effects from shape of the test specimens or the application of electric current. Corrosion kinetics was evaluated by fitting equations to the measurements. Data for the HWC condition could be fitted by a two-step logarithmic–parabolic law. A single-step logarithmic law fitted data for the NWC condition. Changes in corrosion rate by the water chemistry changes were readily detected with the technique. Corrosion depth change could be observed for the water chemistry change from the NWC condition to the HWC condition with electrochemical corrosion potential (ECP) of −0.56 V vs. standard hydrogen electrode, which is lower than the ECP that the phase of iron oxide changes from α-Fe2O3 to Fe3O4.