Anodic polarization behavior of annealed, high purity Fe and five binary Fe-Si alloys in hydrogen saturated, 1, 5, and 10N sulfuric acid solutions was investigated at 22 ± 1 C (72 F) using a potentiostatic technique. All specimens exhibited active, passive, and transpassive behavior in all acid environments. Additions of 12 arid 15 wt % Si eliminated the critical current density plateau, significantly decreased the value of critical current density, and increased the width of the passive region. Corrosion potentials, Ecorr, for pure Fe and the Fe-Si alloys were linear functions of pH over the pH range −1.07 to +1.09. Slope dependency of the corrosion potential with pH (dEcorr/dpH) varied from −0.046 to −0.068, independent of composition. Critical potentials, Ecr, for the 88Fe-12Si and 85Fe-15Si alloys shifted linearly in the noble potential direction with decreasing pH; slope dependency (dEcr/dpH) for these alloys was −0.053 and −0.066, respectively. As the Si content was increased from 0 to 9 wt %, the passive current density, ip, increased. Maximum ip occurred with the addition of 6 wt % Si. Addition of 12 wt % Si markedly decreased the value of ip. All specimens exhibited transpassive Tafel behavior. Visible oxygen evolution was not observed for the 88Fe-12Si and 85Fe-15Si alloys.

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