Electrochemical Study of β-Titanium Alloy in High-Temperature and -Pressure Water Environment

The in situ electrochemical behaviors of Ti-39Nb-6Zr alloy were investigated in 2.3 ppm Li+ and 1500 ppm B3+ solution at 300 °C and 14 MPa. The activation energy is 12.84 kJ/mol, and the oxidation of titanium is controlled by oxygen ions diffusion in the liquid phases. The morphology, phase structure, and composition of the oxide film after 700 h exposure time in 300 °C and 14 MPa solution were characterized. The oxide film mainly included anatase TiO2 phases, ZrO2, Nb2O5, and a slight B2O3. The morphology of the film is shown by many nanocrystalline grains and the thickness is about 5 μm. The passivation film on the alloy substrate transforms from a single-layer film structure to a double-layer film structure. The impedance of the passivation decreases with the increase in temperature, which is related to the enhanced ion conductivity of the passivation film at high temperatures. The impedance of the dense layer inside the passivation film is much greater than that of the loose layer outside, and the dense layer inside plays a crucial role in the corrosion resistance of the Ti-39Nb-6Zr alloy. During the insulation process, the impedance of the dense layer inside the passivation film first increases and then slowly decreases, and the corrosion resistance of the passivation film first increases and decreases.