Surface neutralization and H(2)S oxidation at early stages of sewer corrosion: influence of temperature, relative humidity and H(2)S concentration.

While the involvement of a range of environmental factors in sewer corrosion is known, a comprehensive understanding of the processes involved and the exact role of individual environmental factors in sewer corrosion is still lacking. The corrosion of concrete in sewer systems is reported to be initiated through chemical reactions (involving H(2)S and CO(2)) that lower the surface pH to a level then conducive for biological activity. However, the specific influence of environmental variables, such as H(2)S level, temperature, and relative humidity etc. remains unclear; although, they are expected to control these initial surface reactions of the concrete sewer pipe. We examined changes in the surface chemistry of concrete during the early stages of corrosion by exposing concrete coupons to thirty-six independent conditions in well-controlled laboratory chambers that simulated conditions typically found in various sewer environments across Australia. The conditions employed were combinations of six H(2)S levels, three gas-phase temperatures and two relative humidity levels. Our results indicate that the role of CO(2) on initial surface pH reduction is insignificant when compared to the influence of H(2)S. Within the first 12 months, a decrease in surface pH by 4.8 units was observed for coupons exposed to 30 °C and 50 ppm H(2)S, while significantly lower pH reductions of 3.5 and 1.8 units were detected for coupons exposed to 25 °C and 18 °C respectively, and 50 ppm H(2)S. Elemental sulphur was found to be the major oxidation product of H(2)S and elevated concentrations were detected at the higher levels of H(2)S, temperature and relative humidity. More significantly, the data obtained from the controlled chamber experiments correlated with those obtained from the field-exposed coupons. Hence, these findings can be extended to real sewer corrosion processes.