The corrosion behavior of mild steel was investigated in artificial sea water containing hydrogen sulfide, the concentration of which was controlled during an experimental period. The pH of this testing solution was controlled at 7.0. Instantaneous corrosion rate was measured by the linear polarization method. Relationship between the corrosion rate and the concentration of hydrogen sulfide was as follows. Before the surface of mild steel was not covered by sulfide film, the corrsoion rate was proportional to the concentration of hydrogen sulfide. But the corrosion rate in the higher concentration range showed larger dependance on the concentration than that in the lower or middle concentration range did. When a steady state was reached, the corrosion rate in the lower concentration range (<0.3μg-atom S/m
l) was proportional to the concentration of hydrogen sulfide and no film formed. In the middle concentration range, (0.3-1.5μg-atom S/m
l), the corrosion rate showed a constant small value because sulfide film covered the surface of the steel, and the corrosion rate did not change regardless of great increase or decrease in concentration. In the higher concentration range (>1.5μg-atom S/m
l), the corrosion rate increased with a rise in concentration. The surface of the steel was also covered with sulfide film, but the corrosion resistance of this film was poor. After hydrogen sulfide was expelled from test solutions, these films decayed gradually with galvanic corrosion. These corrosion behaviors were almost the same as those observed in a culture of sulfate-reducing bacteria. That is, the corrosion of the steel seems to be caused by biogenetic hydrogen sulfide, not by the bacteria themselves.
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