Chemical composition of the aqueous solution within crevices on two di
fferent Ni-Cr-Mo-Fe alloys immersed in natural seawater was determined
using a semiquantitative thin-layer chromatographic method. Active cr
evices were found to contain concentrated amounts of dissolved Ni2+, C
r3+, Mo3+, and Fe2+ ions. Propagation of crevice corrosion for the two
alloys was determined from anodic polarization curves in model crevic
e solutions based upon stoichiometric dissolution or selective dissolu
tion of alloy components. Both alloys 625 (UNS N06625) and C276 (UNS N
10276) underwent crevice corrosion in the model crevice electrolytes,
For the model crevice solution based upon selective dissolution of all
oy constituents, the anodic dissolution rate for alloy 625 was higher
than that for alloy C276. This trend was reversed for the model crevic
e solution based upon uniform dissolution of alloy constituents.