In this study, the corrosion properties of Ti-6Mo-6V-5Cr-3Sn-2.5Zr alloy were investigated as a function of the cold rolling ratio and annealing temperature. The annealing treatment was carried out at temperature of 680°C, 730°C, and 780°C. The highest corrosion potential observed in the specimen with a 10% rolling ratio was 179 mV, which was more positive than that of the non-rolled specimen (–0.214 Vssc). The lowest corrosion current density (1.30×10–8 A/cm2) was observed in the non-rolled specimen which suggested that the integrity of its passive oxide layer was superior to that of the cold-rolled specimens. Time-dependent EIS evaluation revealed that the consistency of the passive oxide layer was highly affected by the subjected rolling ratio over time.
Al2Cu phase has been obtained by melting pure metals in the electric arc furnace. It has been found that the intermetallic phase undergoes selective corrosion in the H3PO4 aqueous solutions. Aluminium is dissolved, the surface becomes porous and enriched with copper. The corrosion rate equals to 371 ± 17 g·m–2·day–1 (aerated solution) and 284 ± 9 g·m–2·day–1 (deaerated solution). The surface of Al2Cu phase after selective corrosion was characterised by using electrochemical impedance spectroscopy. It was found that the surface area of the specimens increases with temperature due to higher corrosion rate and is between 2137 and 3896 cm2.
Sodium orthovanadate was tested as a corrosion inhibitor of intermetallic Al2Cu in 1 M H3PO4. The Al2Cu – H3PO4 – Na3VO4 system was studied using the following methods: inductively coupled plasma optical emission spectrometry, scanning electron microscopy with energy dispersive x-ray spectroscopy, x-ray diffraction, electrochemical impedance spectroscopy, polarisation and open circuit potential. It was found that the corrosion rate decreased as the inhibitor concentration increased. The highest inhibition efficiency 99% was obtained when sodium orthovanadate initial concentration was equal to 100 mM, pH = 1.11, due to precipitation of a protective layer of insoluble salt, containing vanadium, phosphorus, sodium and oxygen, on the surface. At pH = 0.76 the protective layer was not formed and inhibition efficiency decreased to 76%. Selective corrosion of the intermetallic phase caused a significant increase of an electric double layer capacitance and decrease of a charge transfer resistance.
In this work, we developed the lanthanum strontium cobalt ferrite and it’s composite with yttrium iron cobaltite (mass ratio of 1:1) cathodes as a thin layer on Ce0.8Sm0.2O1.9 electrolyte. Two kinds of electrode pastes were prepared, with and without 6 mm polystyrene beads as an additional pore former. The performance of cathode materials was investigated by electrochemical impedance spectroscopy as a function of electrode morphology, oxygen partial pressure, potential, and temperature. The polarization resistance of the more porous electrodes was lower than those electrodes prepared without additional pore former in the whole potential range at 800°C, slightly lower at 700°C and 600°C. The addition of yttrium iron cobaltite decreased the performance of both types of cathodes. The lower polarization resistance of porous cathodes is due to the facilitated gas diffusion through their structure.