Mh. Wahdan et Gk. Gomma, EFFECT OF COPPER CATION ON ELECTROCHEMICAL-BEHAVIOR OF STEEL IN PRESENCE OF IMIDAZOLE IN ACID-MEDIUM, Materials chemistry and physics, 47(2-3), 1997, pp. 176-183
The influence of different concentrations of imidazole in the presence
of 1 M sulphuric acid on electrochemical and corrosion behaviour of s
teel both with and without different concentrations of copper cation C
u++ was studied potentiokinetically. It was found that imidazole reduc
es the corrosion current, corrosion rate and increases the polarizatio
n resistance to a gnat extent. For each additive, the protective catio
n was incorporated into the protective layer formed on the electrode s
urface during exposure to the tested solution. It was found that at a
concentration of 10(-4) M, Cu cation strongly inhibited the corrosion
rate. The corrosion of the steel in 1 M M(2)SO(4) is appreciably reduc
ed by imidazole in combination with metallic copper cation, as a resul
t of coadsorption. At a higher concentration of the copper cation (10(
-3) M) in association with the inhibitor, the dissolution of the steel
is increased owing to the cathodic reduction of the metallic cation t
o metal The increase in the corrosion rate is a result of cationic red
uction, and the potential is shifted towards electropositive direction
, indicating a new anodic and cathodic polarization curve formation re
sulting from the deposition of the metal. In the presence of imidazole
and lower metallic copper cation concentrations (10(-5) M), the poten
tials shift in the electronegative direction, indicating suppression o
f the cathodic reaction by conjoint adsorption of the inhibitor and me
tallic cation. The corrosion potential, corrosion current, corrosion r
ate, polarization resistance, as well as activation energy and thermod
ynamic parameters were calculated at different temperatures. The tempe
rature coefficient for corrosion inhibition has a negative value which
may be explained by assuming that the corrosion reaction is no longer
the simple metal/acid reaction, but involves the adsorbed species dir
ectly.