0000000000776678
AUTHOR
M. L. Varsanyi
A Mössbauer study of the crystalline structure of the passive film formed on iron in aqueous sulfate solution containing sulfite in low concentration
Electrochemically induced passivation of evaporated, enriched 57Fe in 0.5 mol dm−3 Na2SO4 + 0.001 mol dm−3 NaHSO3 aqueous solution (pH 6.5) was followed by conversion electron Mossbauer spectroscopy. The transformation of amorphous iron oxide or hydroxide into crystalline γ-FeOOH could be observed with the increase of the polarization time. The comparison of the original quantity of evaporated, enriched 57Fe layer on the surface of the samples with the dissolved iron, measured in the solutions after the polarization, proved the existence of pitting corrosion at this pH.
Influence of sulphite on the passivation of iron
Abstract Mossbauer spectroscopy and electrochemical measurements were used to study the passivation of iron and steels in a sulphite containing solution. The potentiodynamic curves show that passivation occurs at −140 mV potential vs saturated calomel electrode ( sce ). The main phase of the passive layer was found to be γ-FeOOH, while FeSO 4 ·H 2 O on the surface and FeSO 3 ·3H 2 O inside the layer were identified as minor phases in the case of polarization in a solution of pH 3.37. Only γ-FeOOH was observed on the surface of samples polarized at pH 6.6.