摘要
The corrosion behavior of tantalum in tetraethyl ammonium chloride （TEA） ethanol solutions was investigated using potentiodynamic polarization, cyclic voltammetry, and impedance techniques along with scanning electron microscopy （SEM）. At the early stage of scanning, the current density in the cyclic voltammetry curves very slowly increased because of the presence of a thin oxide film on the electrode surface. Pitting corrosion then occurred as a result of the passivity breakdown caused by the aggressive attack of the Cl^- anions. SEM images showed the growth process of the pits on the electrode surface. The pitting potential decreased with the increase in TEA concentration but increased with the increase in water concentration. The apparent activation energy of the electrochemical reaction was 36 kJ/mol. The impedance spectra exhibited two time constants for all the potentials. Both the passive layer resistance and the charge transfer resistance decreased with the increase in the potential.
