4.6 Article

Electrochemical and Computational Insights on the Application of Expired Metformin Drug as a Novel Inhibitor for the Sweet Corrosion of C1018 Steel

Journal

ACS OMEGA
Volume 6, Issue 1, Pages 65-76

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.0c03364

Keywords

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Funding

  1. King Fahd University of Petroleum and Minerals, Deanship of Scientific Research (DSR) [DF191051]

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The study shows that the expired metformin drug MET exhibits high corrosion inhibition efficiency in a CO2-saturated NaCl and acetic acid solution, with an inhibition efficiency of up to 90%. The adsorption of the drug follows the Langmuir isotherm, indicating a mixed type of physical and chemical adsorption.
An expired metformin drug (MET) was used as a corrosion inhibitor for C1018 carbon steel in a CO2-saturated 3.5 wt % NaCl + 340 ppm acetic acid solution under static conditions. The inhibitor was evaluated using electrochemical methods complemented with surface analytical measurements and computational modeling. The drug displayed a high inhibition efficiency of similar to 90% at 200 ppm. Impedance analyses revealed a rise in the charge transfer resistance at the steel-solution interface upon the addition of the inhibitor. Polarization measurements suggested that MET acted more like a cathodic-type corrosion inhibitor and significantly reduced the corrosion current density. The adsorption of MET on the steel substrate followed the Langmuir isotherm, showing a mixed type of physical and chemical modes of adsorption. The thermodynamic parameters revealed strong and spontaneous adsorption on the steel surface. The surface analysis using SEM supported the inhibitor adsorption on the steel substrate. Based on the DFT simulation, inhibition by MET is mainly achieved by its protonated form, which leads to the formation of a thin film on the steel surface rather than the modification of the work function of the steel surface. The experimental and theoretical estimations of pKa complemented the DFT results, both agreeing that the monoprotonated form of MET is the dominant form in which the inhibitor adsorbs on the steel surface to form a thin film rather than modify the work function of the steel surface.

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