## Abstract The passivating oxide layer on iron grows by transfer of oxygen ions from the solution into the oxide. As expected theoretically, the dissolution rate of iron ions increases with the growth rate of the layer. In neutral solution the current efficiency for oxide growth is larger than in
Film growth and proton sorption-desorption on passive iron in neutral solution
โ Scribed by Norio Sato
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- English
- Weight
- 845 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0013-4686
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โฆ Synopsis
Abrtraet-Iron in the passive state in neutral boric-acid-borate solution was anodically oxidixed or cathodicagy reduced in the potential regions of passivity and oxygen evolution. It is shown that the potential of passivated iron is not a single-valued function of the surface tilm thickness but is controlled by only a small amount of charge, equivalent to less than 1 r cent of the Slm thickness, which can be associated with protons sorbed in the outermost layer oft e oxide. llY The rate of proton sorption at constant potential decreases with increasing the amount of proton sorbed, according to is = A. exp (-AQ43.1, which is of the same form as the equation for the steady growth of the surface oxide on iron. Constant B. depends on the tilm thickness Qr, and a kinetic parameter ba = d&/dQr is a function of the potential at which proton is sorbed. The parameter b. decreases with potential, extrapolating to zero at the oxygenevolution potential, suggesting a correlation between the sorption-desorption kinetics of proton in the outermost layer of the surface oxide and the onset of oxygen evolmion.
R&mrn&L'on a proc&ie a l'oxydation anodique et B la reduction catbodique du fer a p&at passif dans une solution neutre d'acide bori ue-borate, d'evolution d'oxyglne. On montre
๐ SIMILAR VOLUMES
The formation and reduction of the passive film on iron was investigated in a phosphate-borate buffer solution. The passive film produced in the present solution was approximately 12% thicker than that produced in the borate-boric acid solution (pH 8.4). The formation ofthe passive film obeyed the m
The rate of dissolution of Armco Fe has been measured as a function of time for deaerated solutions of constant ionic strengtb (HCl + NaCl). For pH < 1.5, no appreciable change of the measured polarisation resistance was observed. For 1.5 -=I pH < 3 the polarisation resistance gave straight lines w