In this research, the Pistia stratiotes leaf (PSL) extract was evaluated as a green corrosion inhibitor for the corrosion of mild steel in 1 M HCl using electrochemical measurements and surface characterization. Electrochemical impedance spectroscopy (EIS) spectra showed that the inhibitory activity of the phytochemical compounds enhanced with increasing concentration up to 400 ppm, which was reflected in the increase in the charge transfer resistance and double-layer capacitance. Regarding the effect of immersion time, EIS results indicated that the persistence of the PSL extract was between 4 h and 8 h of exposure time. From polarization curve (PCC) results, the best performance of the corrosion inhibitor was achieved at 400 ppm with an inhibition efficiency of 93.7%. The PSL extract acted as a mixed-type corrosion inhibitor. The adsorption of the phytomolecules on the metal surface obeyed the Langmuir isotherm through a mixed mechanism (physical and chemical interactions) dominated by physisorption. Scanning electron microscopy (SEM) examinations and energy-dispersive X-ray spectroscopy (EDS) elemental analysis of the corroded samples confirmed the anticorrosive protection of the PSL extract. Chemical characterization of the PSL extract by GC-MS revealed the presence of phytol, steroids, and aromatic and long-chain unsaturated fatty acid esters, in order of abundance. Chemical quantum calculations by DFT allowed for determining that the phthalic acid, di(2-propylpentyl) ester compound has the most significant potential to act as the main active component in corrosion inhibition activity.

One of the alternative materials used for conducting conservation treatment of iron artifacts is the rust converter, since it generates barrier properties and more stable oxides. The protective properties and surface modifications from using Mimosa tenuiflora extract as a green rust converter on a gray iron oxide layer were studied. The surface characterization was carried out using a Scanning Electron Microscope coupled to an energy-dispersive X-ray spectrometer (SEM-EDS), along with infrared spectroscopy (IR), Raman spectroscopy, X-ray Diffraction (XRD), and Water Contact Angle (WCA). Electrochemical characterization was performed with an Electrochemical Impedance Spectroscope (EIS) using 3.5 wt.% NaCl as the electrolyte. According to the results of the Raman spectroscopy and XRD, the layer of corrosion products formed after 90 days in the atmosphere was composed of goethite, lepidocrocite, maghemite, hematite, and magnetite. The surface of the corrosion products was transformed with the rust converter into an amorphous and microcracked layer. By IR, the Fe-O and C-O-Fe bonds associated with the iron chelate were found with absorption bands at 1540 and 1567 cm⁻¹, respectively. By XRD, a modification of the magnetite crystallinity was observed. Finally, the Water Contact Angle and the protective capacity of the corrosion products were improved by the presence of the rust converter.

The effect of concentration of an organic imidazoline as inhibitor on internal stress corrosion cracking (SCC) behavior of an API X70 pipeline steel exposed to a brine solution was studied. The SCC process using simultaneously the slow strain rate stress test (SSRT) and electrochemical measurements was performed. Fracture surface analysis and secondary cracking were observed through a scanning electron microscopy (SEM). According to SEM fractography and SSRT results, the steel showed high SCC susceptibility with a brittle fracture and several secondary cracks without addition of inhibitor, whereas the addition of inhibitor to brine solution was effective to increase the SCC resistance of steel at concentrations of inhibitor of 50 and 100 ppm. A further addition of concentration of inhibitor had a negative effect on the mechanical properties of the steel. Electrochemical measurements results are in accordance with the SCC susceptibility, indicating that corrosion inhibitor film suppressed the anodic and cathodic reactions increasing the resistance to SCC until concentration of 100 ppm. Further addition of inhibitor aggravated the localized corrosion due to local desorption of inhibitor molecules. The Hilbert–Huang transform (HHT) analysis revealed the contribution of different corrosion process contained in the electrochemical current noise (ECN) signals at several inhibitor concentrations.

An electrochemical study of stress corrosion cracking (SCC) of API X70 steel in a simulated soil solution at different pH values (3, 8 and 10) was carried out. The stress conditions were implemented by slow strain rate stress test (SSRT) and the SCC process was simultaneously monitored by electrochemical impedance spectroscopy (EIS). Fracture surface analysis and corrosion product analysis were performed by scanning electron microscopy (SEM) and X-ray diffraction (XRD), respectively. The results show that the susceptibility to SCC was higher as the pH decreases. In the acid solution, hydrogen evolution can occur by H⁺ and H₂CO₃ reduction, and more atomic hydrogen can diffuse into the steel, producing embrittlement. EIS results indicated that the anodic dissolution contributed to SCC process by reducing the charge transfer resistances during the SSRT test. While SEM micrographs shown a general corrosion morphology on the longitudinal surface of samples. At higher pH (pH 8 and pH 10), the SCC susceptibility was lower, which it is attributed to the presence of corrosion products film, which could have limited the process. Using the angle phase (φ) value it was determined that the cracking process started at a point close to the yield strength (YS).

In this work, electrochemical monitoring of stress corrosion cracking (SCC) behavior of a X70 steel in acidic synthetic soil solution during the slow strain rate test (SSRT) was performed by electrochemical noise (EN) using the conventional arrangement of symmetrical electrodes and electrochemical emission spectroscopy (EES) using the asymmetrical arrangement replacing the second working electrode for a platinum micro-cathode. The statistical method, fast Fourier transform, and discrete wavelet transform were used for analyzing the potential and current signals recorded by both arrangements. The results showed that EN arrangement was more effective to detect the crack initiation at a point close to yield strength despite stress-induced asymmetry in one of the electrodes. For the EES arrangement, the micro-cathode had a strong influence on the electrochemical noise of the current and potential under stress conditions. From the transient features, statistical parameters, and wavelet analysis, a discontinuous transgranular SCC mechanism was found. The resistance values obtained by EN measurements had better correlation with the electrochemical impedance spectroscopy results (EIS) than EES measurements.

In this research work, the electrochemical evaluation of a non-ionic gemini surfactant as a green corrosion inhibitor for X100 pipeline steel in CO₂-saturated brine solution was carried out by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization curves (PPC). The corrosion inhibition performance of the gemini surfactant was studied in static and hydrodynamic conditions at room temperature and 60 °C. Electrochemical measurements showed that the inhibitor’s performance was enhanced with increasing inhibitor concentration and with increasing exposure time at room temperature, reaching the highest inhibition efficiency (η) at 100 ppm. With increasing temperature, the inhibitor efficiency decreased, with similar behavior at all concentrations. The analysis of the cathodic polarization curves at different rotation speeds showed the strong influence of mass transport on the cathodic process in the absence and the presence of the inhibitor. Under hydrodynamic conditions, PPC and EIS results indicated that the best inhibitor performance was with a concentration of 50 ppm, achieving a maximum inhibition efficiency of 91%. The adsorption of the inhibitor molecules on the surface obeyed the Langmuir isotherm, and the type of adsorption was mixed in all the study conditions. Surface characterization by scanning electron microscopy (SEM) revealed the formation of a protective corrosion inhibitor film.