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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Wang, Xueying
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Publications (6/6 displayed)
- 2024Hydroxyl transport mechanisms upon passivation of Cr-Fe-Co-Ni-Mo multi-principal element alloy surfaces investigated by isotopic labellingcitations
- 2023Effects of Chloride Ions on Passive Oxide Films Formed on Cr-Fe-Co-Ni(-Mo) Multi-Principal Element Alloy Surfacescitations
- 2023XPS study of the thermal stability of passivated NiCrFeCoMo multi‐principal element alloy surfacescitations
- 2023XPS study of the thermal stability of passivated NiCrFeCoMo multi‐principal element alloy surfacescitations
- 2023Origin of enhanced passivity of Cr–Fe–Co–Ni–Mo multi-principal element alloy surfacescitations
- 2022Enhanced passivity of Cr-Fe-Co-Ni-Mo multi-component single-phase face-centred cubic alloys: design, production and corrosion behaviourcitations
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article
Effects of Chloride Ions on Passive Oxide Films Formed on Cr-Fe-Co-Ni(-Mo) Multi-Principal Element Alloy Surfaces
Abstract
International audience ; The composition and stratification of the passive oxide films formed on three Cr-Fe-Co-Ni(-Mo) multi-principal element alloys by electrochemical anodic passivation in sulfuric acid electrolyte containing 0.2 and 4.7 M NaCl were investigated, combining X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry surface analysis. The passive films show a bilayer structure similar to that formed in Cl −-free electrolyte with an inner layer mostly consisting of Cr oxide and an outer layer containing of Cr hydroxide, Ni hydroxide, Mo oxides, and Fe (hydr)oxide. The Mo-free alloy exhibits a thickening of the inner Cr oxide layer and the thinning of the outer layer in 0.2 M Cl − , whereas the two Mo-containing alloys do not show significant alteration even in 4.7 M Cl − evidencing their higher stability in Cl −-containing solutions. The chloride penetration is limited to the external part of the outer oxide layer, except in the most severe tested conditions where traces reach the inner barrier layer, and the chloride entry into the layer is strongly reduced after pre-passivation in Cl −-free solution. The results allow us to discuss the beneficial effects of pre-passivation in Cl −-free conditions and Mo addition providing these alloys enhanced resistance to passivity breakdown.