By means of the potentiodynamic method, the anodic behavior of copper is st
udied in perchlorate solutions in a wide range of pH and ClO4- ion concentr
ations. The activating action of CLO4- ions in the anodic process is associ
ated with their weak ability to form hydrates, which facilitates their inco
rporation into the electrical layer and displacement of OH- ions from the s
urface complexes. The schemes of mechanisms proposed for the copper anodic
dissolution imply the possibility of the formation of intermediate adsorpti
on complexes with participation of CLO4- ions. By the technique of nonlinea
r regression analysis, the constants in the kinetic equations are calculate
d for the proposed schemes.