Titanium and its alloys have superior electrochemical properties compared to other alloy systems due to the formation of a protective TiO₂ film on metal surfaces. The ability to generate the protective oxide layer will depend upon the type of alloy to be used. The aim of this work was to characterize the electrochemical corrosion behavior of titanium Ti-CP2 and alloys Ti-6Al-2Sn-4Zr-2Mo, Ti-6Al-4V, and Ti Beta-C. Samples were anodized in 1 M H₂SO₄ and H₃PO₄ solutions with a current density of 0.025 A/cm². Electrochemical tests on anodized alloys were carried out using a three-electrode cell and exposed in two electrolytes, i.e., 3.5 wt % NaCl and 3.5 wt % H₂SO₄ solutions at room temperature. Scanning electron microscopy (SEM) was used to observe the morphology of anodized surfaces. The electrochemical techniques used were cyclic potentiodynamic polarization (CPP) and electrochemical noise (EN), based on the ASTM-G61 and G199 standards. Regarding EN, two methods of data analysis were used: the frequency domain (power spectral density, PSD) and time-frequency domain (discrete wavelet transform). For non-anodized alloys, the results by CCP and EN indicate icorr values of ×10⁻⁶ A/cm². However, under anodizing conditions, the icorr values vary from ×10⁻⁷ to ×10⁻⁹ A/cm². The PSD Ψ⁰ values are higher for non-anodized alloys, while in anodized conditions, the values range from −138/−122 dBi (A²·Hz⁻¹)^1/2 to −131/−180 dBi (A²·Hz⁻¹)^1/2. Furthermore, the results indicated that the alloys anodized in the H₃PO₄ bath showed an electrochemical behavior that can be associated with a more homogeneous passive layer when exposed to the 3.5 wt % NaCl electrolyte. Alloys containing more beta-phase stabilizers formed a less homogeneous anodized layer. These alloys are widely used in aeronautical applications; thus, it is essential that these alloys have excellent corrosion performance in chloride and acid rain environments.

Titanium alloys have been used in aerospace, aeronautic, automotive, biomedical, structural, and other applications because titanium alloys have less density than materials like steel and support higher stress than Al-alloys. However, components made of titanium alloys are exposed to corrosive environments, the most common being industrial and marine atmospheres. This research shows the corrosion behavior of three titanium alloys, specifically Ti-CP2, Ti-6Al-2Sn-4Zr-2Mo, and Ti-6Al-4V with α, near α, and α + β alloys phases. Alloys were exposed in two electrolytes to a 3.5 wt. % H₂SO₄ and NaCl solution at room temperature, and their electrochemical behavior was studied by electrochemical noise technique (EN) according to ASTM ASTM-G199 standard. EN signal was filtered by three different methods, and the polynomial method was employed to obtain R_n, kurtosis, skew, and the potential spectral density analysis (PSD). The wavelets method was used, from which energy dispersion plots were obtained. The last method was Hilbert–Huang Transform (HHT), where Hilbert Spectra were analyzed. Results indicated that R_n compared with PSD showed that Ti-6Al-2Sn-4Zr-2Mo presented less dissolution in both electrolytes. Statistical methods showed that the passive layer created on Ti alloys’ surfaces is unstable; this condition is notable for Ti-6Al-2Sn-4Zr-2Mo in NaCl solution.

Precipitation-hardening (PH) stainless steels (SS) are widely used in various aerospace applications. These steels exhibit good mechanical and corrosion resistance. The electrochemical behavior of 15-5PH, 17-4PH, Custom450 and AM 350 stainless steels passivated with citric and nitric acid baths for 60 and 90 min at 25 and 49 °C were evaluated in 5 wt.% sodium chloride (NaCl) and 1 wt.% sulfuric acid (H₂SO₄) solutions. The electrochemical behavior was studied with potentiodynamic polarization curves (PPC) according to the ASTM G5-13 standard. The results indicated that there are two characteristic mechanisms that are present in the potentiodynamic polarization curves. When the PHSS is immersed in an H₂SO₄ solution, there is a secondary passivation, and in the NaCl solution, there is a pseudo-passivation (not stable passivation film). The current densities in the NaCl solution were between 10⁻⁴ and 10⁻⁵ mA/cm², while those of H₂SO₄ were recorded around 10⁻² and 10⁻³ mA/cm². Citric acid does work as a passivating solution, and in some cases, the corrosion resistance of the stainless steel was comparable to that of nitric acid.

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 (E_corr), 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.

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.