A metal-depassivation model involving the migration of L(-n) anions th
rough an oxide-hydroxide film (the ion-exchange mechanism of adsorptio
n and migration through an ion-exchange layer to Al-Al2O3 phase bounda
ry) is considered. Negative (iminodiacetate- and sulfosilanes) and pos
itive (ammonium- and amine-containing silanes) adsorption monolayers a
re synthesized on an aluminum surface. Electrochemical and corrosion t
ests of the layers in Cl- containing electrolytes show that negative r
adicals stimulate inhibition, while positive radicals lead to depassiv
ation. The surface charge and potential psi1 affect the pitting-corros
ion potential and depassivation susceptibility of aluminum in chloride
-containing electrolytes.