摘要
Anodic dissolution behaviour of Ni in mono-, di- and trichloroacetic acids has been investigated by measuring current densities of Ni electrode (versus SCE) at different potentials. Effects of acid concentration, pH, scan rate and additive inhibitor on the potential were studied and they revealed that there is a considerable shift of potential. Potentiodynamic polarization measurements show that the corrosion rate of Ni in chloroacetic acid solutions increases by increasing the previous factors. However, by adding inhibitor, it decreases.
Anodic dissolution behaviour of Ni in mono-, di- and trichloroacetic acids has been investigated by measuring current densities of Ni electrode (versus SCE) at different potentials. Effects of acid concentration, pH, scan rate and additive inhibitor on the potential were studied and they revealed that there is a considerable shift of potential. Potentiodynamic polarization measurements show that the corrosion rate of Ni in chloroacetic acid solutions increases by increasing the previous factors. However, by adding inhibitor, it decreases.
