Although their exceptional re-passivation ability, Al-alloys are susceptible to corrosion due to the amphoteric nature of the alumina passivation films. This issue is exacerbated by the disruption of these films by intermetallics on the surfaces of highly doped ones, like AA2024-T3 aircraft alloy. The combination of anodized aluminium oxide (AAO) and cerium conversion coatings (CeCC) shows promise as a coating primer. However, the defective structures of CeO2 and Al2O3 require additional sealing. This research proposes sealing the CeCC/AAO layer by boiling it for 10 minutes in two relatively neutral Lourier buffers, adjusted to pH 7.75, and in a mixture of them. The samples underwent a series of analyses to compare the impact of the sealing procedure on surface topology, properties (e.g., colour and wettability on two samples from each set), and corrosion protective ability. It was assessed after 24 hours of exposure to 3.5 % NaCl model corrosive medium on six samples from each set. The assessments included electrochemical impedance spectroscopy (EIS) and potentiodynamic scanning (PDS) techniques. The results indicate that the borate buffer improves the corrosion protection of the coating primers more effectively than the phosphate and mixed ones.

The dependence of the reaction rate on the solution layer thickness discovered in a previous work could be a powerful tool for investigating photocatalytic reactions. A reduction of the apparent rate constant with the growth of the dye concentration was found using this dependence. This decrement follows a hyperbolic law. This dependence is explained based on the observed increment of the solution conductivity. In addition, it is confirmed experimentally that the reaction rate decreases with the solution depth growth. The possibility of independent determination of the reaction rate constant and the adsorption equilibrium constant has been discussed. Additionally, it is demonstrated that the vessel’s reflective bottom could increase the chemical reaction rate. The reason why other authors have not yet reported this effect is also discussed.

The model for photodegradation with a modified rate constant that was developed and presented in previous study, was generalized for the application of ZnO-based photocatalyst in both thin film and powder form. The applicability of the model was proved on methylene blue discoloration on both types of photocatalysts. The photocatalytic reaction rate was found to be dependent on the depth of the solution in case of small depths for this photocatalyst. This correlataion was valid in both high and low transparency. In addition, the impact of the solution pH on the model pollutant decomposition rate was defined.

The influence of suspension depth and pollutant concentration on the rate and efficiency of photocatalytic degradation was investigated in aqueous TiO₂ suspensions using methyl orange (MO) as a model pollutant. Both the reaction rate and the efficiency increased by more than one order of magnitude upon a relatively small decrease in suspension layer thickness. The reaction rate exhibited a complex N-shaped dependence on dye concentration, deviating from the monotonic behavior predicted by the Eley–Rideal and Langmuir–Hinshelwood mechanisms, as well as from the relationship derived in our previous study. To elucidate the origin of this behavior, nanoparticle aggregation was examined by sedimentation kinetics, low-acceleration centrifugation, and scanning electron microscopy (SEM). The results suggest that the interplay between enhanced dye adsorption and the reduction in the available photocatalyst surface area due to aggregation leads to the appearance of a maximum in the concentration dependence of the reaction rate. The relationship between reaction rate and photocatalytic efficiency was also analyzed. Although both parameters are correlated, efficiency values strongly depend on the selected reaction time interval, which complicates direct comparison between studies employing different experimental protocols. Consequently, the reaction rate appears to be a more reliable parameter for describing photocatalytic kinetics.

The anodic behavior of zinc electrodes is important for energy storage, corrosion protection, electrochemical processing, and other practical applications. This study investigates the anodic galvanostatic polarization of zinc foil and bulk electrodes in aqueous oxalic acid solutions, revealing significant differences in their electrochemical behavior, particularly in induction period durations. The induction period’s duration depended on electrolyte concentration, current density, and temperature. Notably, the temperature dependence of the kinetics exhibited contrasting trends: the induction period for foil electrodes increased with temperature, while that of bulk electrodes decreased. Chemical analysis and polishing treatment comparisons showed no significant differences between the foil and bulk electrodes. However, Scanning Electron Microscopy (SEM) observations of samples anodized at different temperatures, combined with Inductively Coupled Plasma–Optical Emission Spectroscopy (ICP-OES) analysis of dissolved electrode material, provided insights into the distinct anodic behaviors. X-ray Diffraction (XRD) studies further confirmed these findings, revealing a crystallographic orientation dependence of the anodic behavior. These results provide detailed information about the electrochemical properties of zinc electrodes, with implications for optimizing their performance in various applications.