In this work, the high temperature oxidation behavior of Al₇₁Co₂₉ and Al₇₆Co₂₄ alloys (concentration in at.%) is presented. The alloys were prepared by controlled arc-melting of Co and Al granules in high purity argon. The as-solidified alloys were found to consist of several different phases, including structurally complex m-Al₁₃Co₄ and Z-Al₃Co phases. The high temperature oxidation behavior of the alloys was studied by simultaneous thermal analysis in flowing synthetic air at 773–1173 K. A protective Al₂O₃ scale was formed on the sample surface. A parabolic rate law was observed. The rate constants of the alloys have been found between 1.63 × 10⁻¹⁴ and 8.83 × 10⁻¹² g cm⁻⁴ s⁻¹. The experimental activation energies of oxidation are 90 and 123 kJ mol⁻¹ for the Al₇₁Co₂₉ and Al₇₆Co₂₄ alloys, respectively. The oxidation mechanism of the Al-Co alloys is discussed and implications towards practical applications of these alloys at high temperatures are provided.

The present work investigates the influence of isothermal annealing on the microstructure and oxidation behavior of nanocomposite coatings. AlTiSiN/TiSiN coatings with TiSiN adhesive layer were deposited onto a high-speed steel substrate via physical vapor deposition. The coatings were investigated in the as-deposited state as well as after annealing in air at 700, 800, 900 and 1000 °C, respectively. The microstructure and morphology of the coatings were observed using scanning electron microscopy and transmission electron microscopy. The chemical composition and presence of oxidation products were studied by energy-dispersive X-ray spectroscopy. The phase identification was performed by means of X-ray diffraction. In the microstructure of the as-deposited coating, the (Ti_1−xAl_x)N particles were embedded in an amorphous Si₃N₄ matrix. TiO₂ and SiO₂ were found at all annealing temperatures, and Al₂O₃ was additionally identified at 1000 °C. It was found that, with increasing annealing temperature, the thickness of the oxide layer increased, and its morphology and chemical composition changed. At 700 and 800 °C, a Ti-Si-rich surface oxide layer was formed. At 900 and 1000 °C, an oxidized part of the coating was observed in addition to the surface oxide layer. Compared to the as-deposited sample, the oxidized samples exhibited considerably worse mechanical properties.

Corrosion is the degradation of materials in oxidizing environments. In aqueous solutions, it is initiated by the surface reaction of the metallic material with the surrounding electrolyte. The corrosion rate of metals can be significantly reduced by the presence of organic compounds. Crude glycerol is an organic by-product of biodiesel, soap, and fatty acid production. It is produced in substantial amounts through transesterification. Crude glycerol contains several impurities and has low economic value. Its disposal in the environment is unwanted and potential applications need to be explored. In the present short communication, steel corrosion in crude glycerol has been investigated for the first time. The corrosion behavior of low-alloy structural steel S355MC in non-purified crude glycerol was studied by electrochemical methods. The results were compared with the use of tap water. The open-circuit potential (OCP) of S355MC in crude glycerol was more negative compared with that of tap water. The OCP was stable over time, indicating the rapid passivation of the steel substrate. The corrosion resistance was further studied by electrode polarization. On the polarization curve of S355MC in crude glycerol, a wide passivation region was found. Furthermore, the corrosion rate was 2.2 times smaller compared with that of tap water. The surface exposed to tap water was significantly degraded by red rust. The surface of S355MC after exposure to crude glycerol, on the other hand, was less affected by corrosion and covered with a protective layer. The results demonstrate a significant corrosion-inhibiting activity of crude glycerol that could be utilized in various technologies.