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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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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Casati, R. |
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Kočí, Jan | Prague |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Ali, M. A. |
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Rančić, M. |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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- 2024Effect of Molten Salts Composition on the Corrosion Behavior of Additively Manufactured 316L Stainless Steel for Concentrating Solar Powercitations
- 2023Microstructure and Wear Behavior of Heat-Treated Mg-1Zn-1Ca Alloy for Biomedical Applicationscitations
- 2023Effect of Heat Treatment on the Dry Sliding Wear Behavior of the Mg-3Zn-0.4Ca Alloy for Biodegradable Implantscitations
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article
Effect of Molten Salts Composition on the Corrosion Behavior of Additively Manufactured 316L Stainless Steel for Concentrating Solar Power
Abstract
<jats:p>The effects of different molten salts on the corrosion resistance of laser powder bed fusion (L-PBF) 316L stainless steel was evaluated at 650 and 700 °C. The samples were characterized via XRD and SEM/EDX after high-temperature corrosion tests to evaluate the corrosion damage to the L-PBF 316L stainless steel caused by the molten salts. The presence of the salts accelerated the corrosion process, the chloride-based salts being the most aggressive ones, followed by the carbonate-based and the nitrate/nitrite-based salts, respectively. The L-PBF 316L did not react strongly with the nitrate/nitrite-based salts, but some corrosion products not found in the samples tested in the absence of salts, such as NaFeO2, were formed. LiFeO2 and LiCrO2 were identified as the main corrosion products in the samples exposed to the carbonate-based molten salts, due to the high activity of Li ions. Their growth produced the depletion of Fe and Cr elements and the formation of vacancies that acted as diffusion paths on the surface of the steel. In the samples exposed to chloride-based molten salts, the attacked area was much deeper, and the corrosion process followed an active oxidation mechanism in which a chlorine cycle is assumed to have been involved.</jats:p>