The objective of this study was to examine the effects of high levels of S in the nearsurface region on the passivity of Alloy 22, a corrosion resistant Ni-Cr-Mo alloy, in deaerated 1 M NaCl solution. Near-surface concentrations of S up to 2 at.% were achieved in Alloy 22 test specimens by implanting them with S. The S-implanted samples were then evaluated in short-term electrochemical tests in the salt solution and subsequently analyzed with X-ray Photoelectron Spectroscopy (XPS) for film thickness and composition. Specimens tested included non-implanted and annealed Alloy 22 samples, samples implanted with S, and "blanks" implanted with Ar as an ion that would simulate the "damage" of S implantation without the chemical effect. A sample of Simplanted Alloy 22 was also exposed to solution for 29 days and analyzed for evidence of S accumulation at the surface over longer times.Three primary findings resulted from this work: (1) There was very little, if any, reproducible influence from the S on the corrosion current in the short term when present in the surface layers of the alloy at concentrations up to 2 at.%. One experiment on a sample containing S exhibited a minor irregular current excursion in the polarization that suggested a localized corrosion process, but the event could not be corroborated using other methods. (2) The presence of S caused a significant and reproducible negative potential offset to the alloy (separate from the effects of ion implantation) and the effect appears to be related to the amount of S present. (3) There is strong evidence that S can enrich on the surface of Alloy 22 during corrosion under normally passive conditions in deaerated solutions. The above results suggest that, although the short-term effects of S at 2 at.% or lower are minimal for Alloy 22 corrosion in deaerated 1 M NaCI, long-term exposure (I00 years) of the alloy with bulk impurity concentrations as low as 10 ppm has the potential of raising surface-S concentrations higher than tested in this work and thereby influencing the corrosion process. This conclusion is based upon our observations that S appears to accumulate on the surface under all the conditions tested in this work and that there is a systematic shift in the open-circuit potential that depends on the amount of S. Studies on the impact of this buildup will require samples with even higher levels of surface-S than were tested in this work and should be the subject of additional study. It should also be noted that the role of dissolved oxygen on surface-S buildup needs to be studied in future work as well. In aerated environments, it is possible that the S may be significantly oxidized and removed (by dissolution) from the surface, thus ameliorating the long-term effects of the S-sulfur on corrosion.iii Acknowledgment