Abstract
Despite extensive research on the matter of corrosion inhibition efficiency, the interactions between the defect structure of the passive layer and the inhibitor molecules still remain poorly understood. In this study, the corrosion inhibition mechanism of ethylenediamine-tetraacetic acid as a carboxylate-based organic inhibitor on steel specimens in simulated concrete pore solution was studied. The point defect model was used to describe the response of the passive oxide film on the steel surface to the perturbation caused by the addition of the carboxylate compound. The electrochemical behavior of the steel specimens was evaluated through open circuit potential, electrochemical impedance spectroscopy and potentiodynamic analysis. The reduction in efficiency outside the optimal concentrations was discussed from an electrochemical point of view. We suggest that the performance of the inhibitor is highly dependent on the positively charged entities on the passive layer including anion vacancies and interstitial cations. To further investigate the physicochemical behavior of the organic molecules, density functional theory and adsorption isotherms were applied. The topography and morphology of the surface were analyzed through scanning electron microscopy. To confirm the inhibitive effect of EDTA, the elements and chemical bonds present on the surface were characterized via X-ray photoelectron spectroscopy. The surface analysis confirmed that the addition of EDTA formed a network of chemical bonds, which significantly hindered the corrosion phenomenon.