tudied in short term tests. Mill Annealed (MA) and thermally aged PCA (Prism Crevice
Assembly) specimens were used. Thermally aged specimens were obtained by aging at
760 ºC for 10 hours. Precipitation of secondary phases (TCP: Topologically Close Packed
phases) at grain boundaries occurred. Electrochemical tests performed included open circuit
potential monitoring for up to 48 hours, electrochemical impedance spectroscopy (EIS) and
galvanic coupling with an MA Alloy 22 foil. Crevice corrosion propagation started in Alloy 22
after a few hours of immersion in pH 2, NaCl at 90 ºC. Steady state open circuit potential was
higher for thermally aged specimens than for MA specimens. Galvanic coupling was performed
in order to asses the effect of an increasing cathodic area. Galvanic current and potential
were recorded with time. A potential maximum was correlated with a current minimum,
indicating the onset of crevice corrosion propagation. Crevice corrosion kinetics was limited by
oxygen reduction on passive Alloy 22 surface areas. Crevice corrosion attacked area and
propagation potential (ECORR) were set to balance oxygen reduction rate. Oxygen reduction on
passive Alloy 22 was inhibited. Low crevice corrosion propagation rates can be expected for
crevice corrosion provided that oxygen is the only oxidant and the ratio of creviced area / passive
area is large.
Keywords: N06022, chloride, crevice corrosion, thermal aging, galvanic coupling