The dissolution kinetics of amalgamated zinc has been studied by imped
ance spectroscopy. A single relaxation is observed in the complex impe
dance diagram. Two plausible mechanisms are considered, the one-step t
wo-electron transfer and the two-step consecutive mechanism with one a
dsorbed intermediate. The impedance behaviour of these mechanisms was
simulated and compared to the experimental results. For the two-electr
on transfer mechanism a good agreement between experimental and theore
tical data is observed at anodic potentials. However, in the cathodic
region a disagreement occurs, and the reason for this is discussed. Fo
r the two-step mechanism, with the first step in equilibrium, it was s
hown that, if this mechanism prevails, the single relaxation observed
descends from the intermediate adsorbed on the surface. This is due to
the fact that the charge-transfer resistance becomes negligible compa
red to the polarisation resistance when the first step is in pseudo eq
uilibrium. The potential dependencies of the time constants involved a
re discussed.