In this study, the electrophoretic deposition of chitosan films doped with Nd 2 Ti 2 O 7 nanoparticles was carried out as corrosion protection systems for exposed materials in aqueous environments rich in chlorides. Completely crystalline Nd 2 Ti 2 O 7 nanoparticles with an average size of 100-200 nm were obtained. Electrophoretic deposition of chitosan films with Nd 2 Ti 2 O 7 nanoparticles was possible. With a working voltage of 5 V and 20 minutes of deposition, homogenous chitosan films with a thickness of 4 microns were obtained. According to the FT-IR (Fourier transform infrared spectroscopy), Raman, and XRD (X-ray diffraction) analyses, it was observed that the presence of the nanoparticles modified the properties of the chitosan films, that is, their crystallinity was increased and their moisture absorption capacity was reduced. These modifications caused a better performance against the corrosion of chitosan films deposited on 1018 carbon steel. Its electrochemical evaluation showed that the chitosan films perform as cathodic coatings by affecting the oxygen reduction reaction. This was possible due to the barrier effect of the Nd 2 Ti 2 O 7 nanoparticles, by blocking the effective area for the diffusion of the aggressive electrolyte species.

The corrosion performance of AISI-309 exposed 5 days to molten salts 50 mol% V2O5-50 mol% Na2SO4at 700°C is reported in this paper. Such evaluation was made using three electrochemical techniques: potentiodynamic polarization curve (PC), electrochemical impedance spectroscopy (EIS), and linear polarization resistance (Rp). FromPC, the Tafel slopes,Icorr, andEcorrwere obtained. From Nyquist and Bode plots, it was possible to determine two different stages; the first one showed just one loop, which indicated the initial formation of Cr2O3layer over the metallic surface; after that, the dissolution of Cr2O3formed a porous layer, which became part of the corrosion products; at the same time a NiO layer combined with sulfur was forming, which was suggested as the second stage, represented by two capacitive loops. EIS plots were in agreement with the physical characterization made from SEM and EDS analyses. Fitting of EIS experimental data allowed us to propose two electrical circuits, being in concordance with the corrosion stages. Parameters obtained from the simulation of EIS data are also reported. From the results, it was stated that AISI-309 suffered intergranular corrosion due to the presence of sulfur, which diffused to the metallic surface through a porous Cr2O3layer.

Fe-Al intermetallic compounds have been considered excellent candidates as alternative alloys for various applications in corrosive environments compared to other Fe-based alloys. Their excellent corrosion resistance is due to the development of an Al-based passive layer. The performance of the passive layer can be improved by adding a third alloy element. Therefore, in this study the electrochemical performance of the Fe40Al intermetallic alloy modified by the addition of a third alloy element (Cr, Ti, Co, Ni) is evaluated. The corrosion resistance of intermetallic alloys has been evaluated by electrochemical tests (potentiodynamic polarization curves, and measurements of open circuit potential, linear polarization and electrochemical impedance) in artificial saliva. The performance of intermetallic alloys was compared with that of Ti. The results obtained showed that the addition of Ni and Ti substantially improves the corrosion resistance of the base intermetallic. The corrosion resistance shown is comparable or greater than that shown by Ti. However, the addition of Co reduces the corrosion resistance of the base intermetallic.

In this study, the performance evaluation of lanthanum compounds as corrosion inhibitors of vanadium salts was performed. The inhibitors tested were lanthanum acetate and La2O3. The performance of the inhibitors was tested using sodium metavanadate (NaVO3) as a corrosive medium at 700, 800, and 900 °C. The corrosion inhibitory effect was evaluated on the corrosion process of 304H stainless steel. The corrosion rate of the steel was determined by the mass loss technique after 100 h of immersion in the corrosive salt with and without the addition of the corrosion inhibitor. The results show that lanthanum compounds act as corrosion inhibitors of vanadium salts. The inhibitory effect increases by increasing the concentration and tends to decrease when increasing the test temperature. Lanthanum compounds act as excellent corrosion inhibitors due to their ability to stabilize vanadium cations. Vanadium is stabilized by forming a new compound, lanthanum vanadate (LaVO4), with a melting point much higher than the compounds formed when Mg or Ni compounds are used as corrosion inhibitors.