Increasingly stringent environmental regulations in different sectors of industry, especially the aeronautical sector, suggest the need for more investigations regarding the effect of environmentally friendly corrosion protective processes. Passivation is a finishing process that makes stainless steels more rust resistant, removing free iron from the steel surface resulting from machining operations. This results in the formation of a protective oxide layer that is less likely to react with the environment and cause corrosion. The most commonly used passivating agent is nitric acid. However, it is know that high levels of toxicity can be generated by using this agent. In this work, a study has been carried out into the electrochemical behavior of 15-5PH (precipitation hardening) and 17-4PH stainless steels passivated with (a) citric and (b) nitric acid solutions for 60 and 90 min at 49 °C, and subsequently exposed to an environment with chlorides. Two electrochemical techniques were used: electrochemical noise (EN) and potentiodynamic polarization curves (PPC) according to ASTM G199-09 and ASTM G5-13, respectively. The results obtained indicated that, for both types of steel, the passive layer formed in citric acid as passivating solution had very similar characteristics to that formed with nitric acid. Furthermore, after exposure to the chloride-containing solution and according with the localization index (LI) values obtained, the stainless steels passivated in citric acid showed a mixed type of corrosion, whereas the steels passivated in nitric acid showed localized corrosion. Overall, the results of the R n values derived show very low and similar corrosion rates for the stainless steels passivated with both citric and nitric acid solutions.

AlCrN/TiSi, AlCrN/TiCrSiN and AlCrN/AlCrN + CrN coatings were deposited on Inconel 718 alloy by physical vapour deposition (PVD). The corrosion behaviour of uncoated and coated specimens was evaluated using electrochemical impedance spectroscopy (EIS) at open circuit potential in a 3.5 wt.% NaCl and 2 wt.% H2SO4 solutions. The EIS data acquired were curve fitted and analysed by equivalent circuit models to calculate the pore resistance, the charge transfer resistance and the capacitance. The Nyquist diagrams of all systems showed one part of the semicircle which could relate that reaction is a one step process, except for the AlCrN/TiCrSiN and AlCrN/AlCrN + CrN coatings in H2SO4 solution, for which two semicircles related to active corrosion in substrate alloy were found. However, from the Bode plots, it was possible to identify two the time constants for all systems exposed to NaCl and H2SO4 solutions. According to electrochemical results, the corrosion resistance of the AlCrN/TiSiN coating was better in the NaCl solution, whereas the AlCrN/AlCrN + CrN coating show better performance in the Sulphuric Acid solutions.

The thermal spraying process is a surface treatment which does not adversely affect the base metal on which it is performed. The coatings obtained by HVOF thermal spray are employed in aeronautics, aerospace, and power generation industries. Alloys and coatings designed to resist oxidizing environments at high temperatures should be able to develop a surface oxide layer, which is thermodynamically stable, slowly growing, and adherent. MCrAlY type (M = Co, Ni or combination of both) coatings are used in wear and corrosion applications but also provide protection against high temperature oxidation and corrosion attack in molten salts. In this investigation, CoNiCrAlY coatings were produced employing a HVOF DJH 2700 gun. The work presented here focuses on the influences of process parameters of a gas-drive HVOF system on the microstructure, adherence, wear, and oxygen content of CoNiCrAlY. The results showed that spray distance significantly affects the properties of CoNiCrAlY coatings.

Aluminum is a material widely used in aeronautical and transport industries due to its excellent mechanical and corrosion resistance properties. Unfortunately, aluminum alloys are susceptible to corrosion, which limits their use in some corrosive environments. The aim of this work is to characterize hard coat film fabricated by anodizing in a citric–sulfuric acid system using electrochemical techniques. The anodization process was carried out using an aluminum alloy AA 6061 anodization bath: a mix of citric and sulfuric acid solutions were used. For the anodizing process, two current densities were used, 1 and 7.2 A·cm−2. Anodized specimens obtained under different conditions were exposed to a 3.5 wt.% NaCl solution, and their electrochemical behavior was studied by electrochemical impedance spectroscopy (EIS) and cyclic potentiodynamic polarization (CPP) according to ASTM G106-15 and ASTM G5-13, respectively. Scanning electron microscopy (SEM) was employed to determinate the morphology and thickness of coatings. The results showed improved corrosion resistance in 6061 aluminum anodized in citric–sulfuric acid electrolyte compared to those anodized in sulfuric acid solution.

Titanium alloys are used in different industries like biomedical, aerospace, aeronautic, chemical, and naval. Those industries have high requirements with few damage tolerances. Therefore, they are necessary to use materials that present fatigue, mechanical, and corrosion resistance. Although Ti-alloys are material with high performance, they are exposed to corrosion in marine and industrial environments. This research shows the corrosion behavior of three titanium alloys, specifically Ti CP2, Ti-6Al-2Sn-4Zr-2Mo, and Ti-6Al-4V. Alloys were exposed on two electrolytes to a 3.5 wt % H2SO4 and NaCl solutions at room temperature using cyclic potentiodynamic polarization (CPP) and electrochemical noise (EN) according to ASTM G61 and ASTM G199 standards. CPP technique was employed to obtain electrochemical parameters as the passivation range (PR), corrosion type, passive layer persistence, corrosion potential (Ecorr), and corrosion rate. EN was analyzed by power spectral density (PSD) in voltage. Results obtained revealed pseudopassivation in CPP and PSD exposed on NaCl for Ti-6Al-2Sn-4Zr-2Mo, indicating instability and corrosion rate lower. However, Ti-6Al-4V presented the highest corrosion rate in both electrolytes. Ti-6Al-2Sn-4Zr-2Mo revealed pseudopassivation in CPP and PSD in NaCl, indicating a passive layer unstable. However, the corrosion rate was lower in both solutions.

The titanium alloy, Ti6Al4V, is used in dentistry for dental implants because of its excellent resistance to corrosion and its high biocompatibility. However, periimplantitis is considered the main reason for treatment failure. The Ti6Al4V alloy was used to study the corrosion behavior for dental implant applications, using an experimental arrangement of three electrodes with the bacteria Streptococcus gordonii and Fusobacterium nucleatum, in addition to Ringer’s lactate as electrolytes, at 37 °C and a pH of 5.6. Their electrochemical behavior was studied by open circuit potential (OCP) and cyclic potentiodynamic polarization (CPP) according to ASTM G3-14 and ASTM G61-11, respectively. Scanning electron microscopy (SEM) was employed to determine the morphology of the alloy studied. An experimental model, in situ, was established with the bacteria present in an oral environment to understand the electrochemical behavior of the alloy used in dental implants. The greatest corrosion in Ti6Al4V alloy was produced by the medium that contained the bacterium Streptococcus gordonii, which is considered a primary colonizer. In addition, the Ti6Al4V alloy presented uniform corrosion in the three solutions at the different exposure times showing a negative hysteresis in CPP.

Nickel or Cobalt-based superalloys represent an important class of engineering materials, finding widespread application in critical components within the gas turbine engines used for jet propulsion and electricity generation. This research aimed at the frequency analysis of transients in electrochemical noise of Waspaloy and Ultimet superalloys, immersed in 3.5 wt.% in H2SO4 and NaCl solutions at two different temperatures, 25 and 60 °C. Localized corrosion behavior of superalloys was assessed using the electrochemical noise technique (EN) according to ASTM-G199 standard. Three different statistical methods filtered the EN signal, and the polynomial method was employed to obtain the noise resistance (Rn), the localization index (LI), skew and kurtosis, and the power spectral density analysis (PSD). Results indicate that the current and potential noise transients have a better behavior with better clarity when a polynomial is used to show a localized corrosion kurtosis for both superalloys.

Selective laser melting (SLM) technology is ushering in a new era of advanced industrial production of metal components. It is of great importance to understand the relationship between the surface features and electrochemical properties of manufactured parts. This work studied the influence of surface orientation on the corrosion resistance of 316L stainless-steel (SS) components manufactured with SLM. The corrosion resistance of the samples was measured using linear polarization resistance (LPR) and electromechanical noise (EN) techniques under three different environments, H2O, 3.5 wt.% NaCl, and 20% H2OSO4,, analyzing the horizontal (XY) and vertical (XZ) planes. The microstructure and morphology of the samples were obtained by optical (OM) and scanning electron microscopy (SEM). The obtained microstructure showed the grains growing up from the fusion line to the melt pool center and, via SEM-EDS, the presence of irregular and spherical pores was observed. The highest corrosion rate was identified in the H2SO4 solution in the XZ plane with 2.4 × 10−2 mm/year and the XY plane with 1.31 × 10−3 mm/year. The EN technique along with the skewness factor were used to determine the type of corrosion that the material developed. Localized corrosion was observed in the electrolyte, for the XY and XZ planes (−1.65 and −0.012 skewness factors, respectively), attacking mainly the subgrains of the microstructure and, in some cases, the pores, caused by Cl ions. and solutions presented a uniform corrosion mechanism for the two observed orientations. The morphology identified by SEM was correlated with the results obtained from the electrochemical techniques.