Abstract
The inhibitory effect of thiourea-based compounds was evaluated using carbon steel body specimens in hydrochloric acid media. Thiourea derivatives, N-(pyrimidin-2-ylcarbamothioyl)benzamide and N-(6-methylpyridin-2-ylcarbamothioyl)benzamide, were synthesized using a simple route with good yields of approximately 70%. The inhibitory efficiencies were obtained by means of weight-loss experiments and electrochemical techniques (e.g., polarization curves and electrochemical impedance spectroscopy). The presence of a methyl functional group showed a better inhibitory efficiency compared with the derivate inhibitor without such modification. Analyzing Langmuir isotherms, ΔG0ads values indicate the chemical adsorption of thiourea-based compounds. The ECorr values obtained for the thiourea derivative with the methyl functionality was cathodically shifted by approximately −0.08 V, with an inhibition efficiency of 81%.