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The effect of Opuntia ficus-indica (Nopal) as green corrosion inhibitor for carbon steel in 1 M HCl solution has been investigated by using weight loss tests, potentiodynamic polarization curves, and electrochemical impedance spectroscopy measurements. Also, scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR) analysis were performed. The inhibitor concentrations used ranged from 0 to 300 ppm at 25, 40, and 60 ∘ C. Results indicated the inhibition efficiency increases with increasing extract concentration and decreases with the temperature, and the inhibitor acted as a cathodic-type inhibitor which is physically absorbed onto the steel surface. In fact, the adsorption of the inhibitor on the steel surface follows the Langmuir adsorption isotherm, indicating monolayer adsorption. The presence of heteroatoms such as C, N, and O and OH groups were responsible for the corrosion inhibition.

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A study of H 2 S corrosion inhibition of pipeline steel by hydroxyethyl imidazoline has been carried out by using electrochemical techniques. Inhibitor concentration included 5, 10, 25, 50, and 100 ppm in a H 2 S-containing 3% NaCl solution at 50°C. Techniques included linear polarization resistance (LPR), electrochemical impedance spectroscopy (EIS), and electrochemical noise (EN) measurements. In addition to the traditional noise in voltage and current, noise resistance (R n ) measurements were used. All techniques showed that the most efficient inhibitor concentration was between 5 and 10 ppm, but inhibitor efficiency decreased after 8 h of testing. Furthermore, EN measurements showed that steel was highly susceptible to localized corrosion at inhibitor doses lower than 10 ppm due to the establishment of a porous inhibitor film. However, with 50 or 100 ppm of inhibitor, the steel was susceptible to a mixture of uniform and localized corrosion. Hurst exponent was higher in presence of inhibitor for times shorter than 8 h, indicating a short residence time of the inhibitor. The data could not be fitted to any adsorption isotherm model, indicating a lack of strong adsorption of the inhibitor to the metal surface.