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This paper presents corrosion resistance results of a 12Cr ferritic ODS steel (Fe-12Cr-2W-0.5Zr-0.3Y2O3) fabricated via a powder metallurgy route as a prospective applicant for fuel cladding materials. In a spent nuclear fuel reprocessing facility, nitric acid serves as the primary solvent in the PUREX method. Therefore, fundamental immersion and electrochemical tests were conducted in various nitric acid solutions to evaluate corrosion degradation behavior. Additionally, polarization tests were also performed in 0.61 M of sodium chloride solutions (seawater-like atmosphere) as a more general, all-purpose procedure that produces valid comparisons for most metal alloys. For comparison, martensitic X46Cr13 steel was also examined under the same conditions. In general, the corrosion resistance of the 12Cr ODS steel was better than its martensitic counterpart despite a lower nominal chromium content. Potentiodynamic polarization plots exhibited a lower corrosion current and higher breakdown potentials in chloride solution in the case of the ODS steel. It was found that the corrosion rate during immersion tests was exceptionally high in diluted (0.1–3 M) boiling nitric acid media, followed by its sharp decrease in more concentrated solutions (>4 M). The results of the polarization plots also exhibited a shift toward more noble corrosion potential as the concentrations increased from 1 M to 4 M of HNO3. The results on corrosion resistance were supported by LSCM and SEM observations of surface topology and corrosion products. [ABSTRACT FROM AUTHOR]

Magnesium (Mg) and its alloys offer promise for aerospace, railway, and 3D technology applications, yet their inherent limitations, including inadequate strength, pose challenges. Magnesium matrix composites, particularly with metallic reinforcements like titanium (Ti) and its alloys, present a viable solution. Therefore, this study investigates the impact of Ti6Al4V reinforcement on AZ31 magnesium alloy composites produced using pulse plasma sintering (PPS). Results show enhanced microhardness of the materials due to improved densification and microstructural refinement. However, Ti6Al4V addition decreased corrosion resistance, leading to strong microgalvanic corrosion and substrate dissolution. Understanding these effects is crucial for designing Mg-based materials for industries like petrochemicals, where degradation-resistant materials are vital for high-pressure environments. This research provides valuable insights into developing Mg-Ti6Al4V composites with tailored properties for diverse industrial applications, highlighting the importance of considering corrosion behavior in material design. Further investigation is warranted to establish predictive correlations between Ti6Al4V content and corrosion rate for optimizing composite performance. [ABSTRACT FROM AUTHOR]

High temperature corrosion of thermoelectric materials is one of the most important issues linked with their application for power generation, especially in terrestrial conditions. The high chemical affinity of elements composing thermoelectric material to oxygen results in continuous degradation at high temperatures of most state-of-the-art materials. This issue is also well recognized in the case of antimonide skutterudites. The simplest way to protect against this process is the use of coatings. Complicated geometry of thermoelectric module favors coatings that can be deposited in a simple way on an assembled module. Such an opportunity, besides good thermal stability and appropriate thermal and electrical properties, is provided by amorphous silicon oxycarbide Si-O-C coatings. In this work, the results on Si-O-C coatings deposited on In0.4Co4Sb12 skutterudite are presented. The influence of heat treatment temperature and substrate roughness on the deposited layer is shown. Protective properties of the Si-O-C layer are presented by comparison of electrical conductivity and Seebeck coefficient of coated and uncoated samples, before and after isothermal oxidation in air at 430 °C for 24 h. In such conditions, the uncoated samples are distinctly oxidized (weight gain of 2.4%) with strongly affected electrical properties, while the coated samples show a slight weight gain of 0.1% and almost unchanged electrical properties. [ABSTRACT FROM AUTHOR]