Coatings with a thickness from ~40 to ~50 µm on Ti6Al4V titanium alloy were formed by micro-arc oxidation in a silicate-hypophosphite electrolyte with additions of graphene oxide. Micro-arc oxidation treatment was carried out in the anode–cathode mode (50 Hz) with a ratio of anode to cathode currents of 1:1, a total density of 20 A/dm², and a treatment duration of 30 min. The effect of the graphene oxide concentration in electrolytes on the thickness, roughness, hardness, surface morphology, structure, composition of micro-arc oxidation coatings, and its electrochemical corrosion behavior in 3.5% NaCl solution was studied. The input of graphene oxide additives into the base silicate hypophosphite electrolyte led to an increase in the hardness of micro-arc oxidation coatings. Electrochemical polarization studies and impedance data showed that the best characteristics in terms of corrosion-protective ability among coatings formed in electrolytes with graphene oxide additives were those formed in the electrolyte with a graphene oxide concentration of 0.1 g·L^−l. A further increase in the graphene oxide concentration in the electrolyte did not improve the protective properties of micro-arc oxidation coatings.

Using a membrane electrode, atomic hydrogen is shown to decelerate the dissolution of iron in sulfate and sulfate-citrate electrolytes (pH 5.5) in a potential range of the active metal dissolution...

Reducing the risks caused by losses due to the atmospheric corrosion of metal structures has been relevant for many years and is an important scientific and technical task. Previously, for this purpose, the preliminary modification of the surface of structural metals with solutions of compositions, based on both individual organosilanes and their mixtures with amine-containing corrosion inhibitors, was proposed. Such treatment leads to the formation of self-assembled siloxane polymeric/oligomeric nanoscale layers on the metal surface, which are capable of changing the physicochemical properties of the metal surface (namely, by reducing the tendency of the metal to corrosive destruction). In this work, annual atmospheric corrosion tests of samples of steel, copper, zinc, and aluminum without protection, and samples modified with compositions based on organosilanes in an urban atmosphere, were carried out. It was established (by the gravimetric method) that the corrosion rate of unmodified (without protection) metals is as follows: steel—0.0022 mm/year; aluminum—0.0015 mm/year; copper—0.00018 mm/year; and zinc—0.00023 mm/year. Using gravimetry and optical microscopy, it was shown that the preliminary modification of metal surfaces with compositions based on organosilanes led to the inhibition of both uniform and local corrosion of metals. The corrosion rates of samples that were modified with one-component compositions decreased by almost two times. The maximum inhibitory effect for the studied systems was demonstrated by mixed binary modifying compositions: mixtures of vinyl- and aminosilane, vinylsilane, and benzotriazole. The corrosion rate decreased for all the studied metals. The minimum effect was observed on zinc (2.5 times) and the maximum inhibition of the corrosion rate was obtained on copper (5.1 times). The mechanism of corrosion inhibition by layers formed as a result of surface modification with two-component mixtures was considered.

The effect of sign-alternating cycling polarisation (SACP) on the localised corrosion of X70pipeline steel in solutions of various compositions was studied. Localised corrosion of steel at anodic potentials was accelerated with an increase in the duration of the cathodic half-cycle, in the presence of a promoter of hydrogen absorption in aqueous electrolyte, and with an increase in the concentrations of chloride and bicarbonate ions. It was pointed out that the corrosion rate is determined by the amount of hydrogen absorbed by the steel. A quantitative indicator to determine the intensity of localised corrosion under SACP was suggested.

The mechanism of anodic dissolution of hydrogenated iron in sulfate electrolyte (pH 5.5) is studied with the use of electrochemical impedance spectroscopy in combination with bipolar membrane...

The process of metal dissolution under a delaminated insulating polymer coating (underfilm dissolution) has been studied. For this purpose, we used an experimental setup that simulates the process of corrosion of underground metal structures in the presence of through defects in the polymer coating and/or extended areas of peeling of the polymer coating from the metal (loss of adhesion)—subfilm cavities partially or completely filled with electrolyte. In particular, the distribution of the protective current under a peeled polymer coating was studied, and a sharp decrease in the value of the protective current was shown at a distance of 1–3 cm from the edge of the defect with a gap between the metal and the coating of 1–6 mm. The localized nature of metal corrosion under the exfoliated polymeric coating has been demonstrated. The ratio of the areas with accelerated corrosion to the total area of the metal can be 1 to 100. It has been established that there are areas of anodic dissolution of the metal during cathodic polarization of the entire sample with a peeled coating. The activating effect of carbon dioxide and hydrogen sulfide on the corrosion and anodic dissolution of steel under the coating was shown. So, it has been established that the dissolution current flowing from the anodic sections on a surface can increase approximately 10 times in the presence of carbon dioxide and hydrogen sulfide. A synergistic effect of these compounds on the process of localized underfilm corrosion of steel was detected. It has been developed a mechanism for the formation of localized corrosion damage to steel under a delaminated polymeric coating, which can be the nuclei of corrosion cracks upon reaching a certain level of mechanical loads, i.e., stress corrosion cracking (SCC) of carbon steel. Possible manners of inhibiting underfilm dissolution of metals are considered, and a method for pre-treatment of the surface with solutions of organosilanes, which ensures the formation of surface self-assembled polymeric siloxane nanolayers responsible for inhibiting underfilm corrosion of steel, is proposed.