Anodic Polarization Research Articles

Predicting the Rate of Degradation Related to Oxygen Electrode Delamination in Solid Oxide-Ion Electrolyzers

One of the leading causes for the performance degradation in H2-producing solid oxide electrolytic cells (SOECs) is the gradual delamination of oxygen electrode (OE) from the electrolyte under a strong anodic polarization. Identification of the key factor that controls the rate of OE delamination is of paramount importance to achieve long-term stable operation of SOECs. Here we show from thousands of hours of testing data that the exchange current density (i°) of OE can be leveraged as a predictor for the rate of delamination. To obtain i°, we apply DC-biased electrochemical impedance spectroscopy on a three-electrode symmetrical cell to measure polarization resistance (Rp) of OE as a function of current density (i) and time (t). The collected Rp-i-t raw data are then converted to overpotential (η)-i-t, from which i° is extracted from the “low-field” approximation. An analytical relationship between i° and time-to-delamination (TTD) is further established from the established i°-i-t relationship. We show that under a constant anodic polarization current density i, the greater the ratio i/i°, the faster the delamination. Therefore, we conclude that the exchange current density of an OE, i°, can be used to predict the rate of OE degradation in solid oxide-ion electrolyzers.

Embeddable Chloride Sensor for Monitoring Chloride Penetration into Cement Mortar.

A composite solid chloride sensor consisting of two single sensors, i.e., Ag/AgCl working electrode and Mn/MnO2 reference electrode, was developed. The Ag/AgCl electrode was prepared by the anodic polarization method, while the Mn/MnO2 reference electrode was prepared using the powder compaction technique. Then, the electrochemical performances such as stability, reproducibility, and sensitivity of the composite and single sensors were investigated in a saturated Ca(OH)2 solution and mortar specimen. A current density of 0.5 mA/cm2 and polarization time of 2.5 h were the optimal preparation parameters of the Ag/AgCl selective electrode. The Ag/AgCl selective electrode showed a linear potential response with the logarithm of chloride ion content in solution and had good stability, reproducibility, and anti-polarization performances. In addition, the Mn/MnO2 electrode exhibited potential stability after being activated in an alkaline solution for 60 days. The composite sensor demonstrated exceptional sensitivity to the Cl- content, boasting a slope of approximately 51.1 mV/decade, and showcased excellent stability in both solution and mortar specimens. In every measurement, the time needed for the potential of a composite sensor to become stable was less than 30 s. The sensor enables non-destructive in situ monitoring of the chloride ion content in cement mortar, thus realizing early warning of deterioration of reinforcement and guaranteeing long service life of the structure.

CORROSION EVALUATION OF LPBF-MANUFACTURED DUPLEX STAINLESS STEEL

In this study, the effect of as built and heat-treated additively manufactured 2507 super duplex stainless steel (SDSS) on electrochemical corrosion performance was examined. The corrosion was studied by Tafel polarization and electrochemical impedance spectroscopy (EIS) methods in a 3.5% NaCl solution. For this purpose, the as-built and heat-treated printed samples (solution annealed and stress-relieved) were examined by LOM/SEM and X-ray diffraction to evaluate the phase changes of steel at different processing stages. The correlation between corrosion resistance, structure, and heat treatment was assessed. As a result of the very fast cooling rate of the LPBF process, SDSS reveals ferrite as the major phase in the printed samples. To enhance the corrosion resistance of LPBF-produced duplex stainless steel, it's crucial to balance its two-phase structure and minimize residual stresses. The ferrite grains are elongated in the build direction, with some austenite precipitation along the grain boundaries or as Widmanstatten laths. The stress-relieved and as-printed SDSS exhibits reduced corrosion characteristics by around 20% compared to the solution-annealed SDSS, according to anodic polarization curves. Based on EIS results, the solution-annealed SDSS revealed an almost double increase in corrosion resistance (based on charge transfer resistance values) compared to the as-printed and stress-relieved conditions.

Three-Layer Electrorefining of Molten Zinc Held on Porous Carbon or Silica Sheets in Molten LiCl–KCl–ZnCl2

We investigated a three-layer electrolysis process utilizing porous holding materials with poor wettability to molten metal, which enables to establish a three-layer configuration of metal(l)/electrolyte(l)/metal(l) by holding metals above the electrolyte regardless of their densities. In this study, porous carbon or silica sheets were used as the holding materials for electrorefining experiments of Zn metal in molten LiCl–KCl–ZnCl2 at 723 K. Three types of experiments were carried out focusing on anodic polarization, electrorefining with cathodic carbon, and three-layer electrolysis using liquid Zn as cathode. The concentration of impurity elements in the Zn was reduced by a factor of 8 to 200 in this experimental condition, highlighting the purification effectiveness of the method. From the results obtained, we have identified certain challenges associated with the three-layer electrolysis process. Furthermore, we discuss potential prospects for industrialization.

Simultaneous Realization of Multilayer Interphases on a Ni-Rich NCM Cathode and a SiOx Anode by the Combination of Vinylene Carbonate with Lithium Difluoro(oxalato)borate.

Ni-rich NCM and SiOx electrode materials have garnered the most attention for advanced lithium-ion batteries (LIBs); however, severe parasitic reactions occurring at their interfaces are critical bottlenecks in their widespread application. In this study, an effective additive combination (VL) composed of vinylene carbonate (VC) and lithium difluoro(oxalato)borate (LiDFOB) is proposed for both Ni-rich NCM and SiOx electrode materials. The LiDFOB additive individually delivers inorganic-rich cathode-electrolyte interphase (CEI) and solid-electrolyte interphase (SEI) layers in anodic and cathodic polarizations before the VC additive. Subsequently, the VC additive is capable of the formation of additional CEI and SEI layers composed of relatively organic-rich components through an electrochemical reaction; thus, inorganic-organic hybridized CEI and SEI layers are simultaneously formed at the Ni-rich NCM and SiOx electrodes. Accordingly, the VL-assisted electrolyte exhibits remarkably prolonged cycling retention for the Ni-rich NCM cathode (86.5%) and SiOx anode (72.7%), whereas the standard electrolyte shows a substantial decrease in cycling retention for the Ni-rich NCM cathode (59.2%) and SiOx anode (18.1%). Further systematic analyses prove that VL-assisted electrolytes form effective interphases for Ni-rich NCM and SiOx electrodes simultaneously, thereby leading to stable and prolonged cycling behaviors of LIBs that offer high energy densities.

Corrosion behavior of high- and low-chromium steel grinding balls in chloride solution

The corrosion behaviour of three types of alloys (two low-alloy carbon steel and one stainless iron with ~15 wt.% Cr), in a solution which simulates seawater (3% NaCl solution, pH 8.1) was tested. Tested samples are used to make steel (iron) balls applied in mils for grinding copper and other ore. The corrosion tests were performed using three electrochemical methods, at room temperature in the presence of atmospheric oxygen. The linear polarization resistance (LPR) method, electrochemical impedance spectroscopy (EIS) method, and linear sweep voltammetry (LSV) method were applied. Based on measurements by LPR and EIS methods (as non-destructive methods), the value of polarization resistance (Rp) was determined and the general corrosion rate (vcorr) of the examined samples was calculated. The obtained values of the general corrosion rate can be used to calculate the service life of steel (iron) balls under exploitation conditions (seawater). The appearance of the surface after linear sweep voltammetry (LSV) measurement showed the presence of localized corrosion (pits were formed) of the tested samples, especially stainless iron, and the LSV method is not suitable for the determination of the general corrosion rate of tested samples in seawater. This form of corrosion occurs at high anodic polarizations, during performing LSV measurements.

Experiments on shear behavior of reinforced concrete continuous beams strengthened by C‐FRCM

AbstractThe dual‐function retrofitting system that uses the carbon‐fabric reinforced cementitious matrix (C‐FRCM) as both the anode of impressed current cathodic protection (ICCP) system and the structural strengthening (SS) material, that is, an ICCP‐SS system, is investigated. The experimental program mainly focused on the shear behavior of C‐FRCM strengthened reinforced concrete (RC) continuous beam under the dual‐function retrofitting system. The influence of anode polarization on the shear strengthening of RC continuous beams is analyzed. Shear tests were conducted on a total of 14 corroded RC continuous beams to investigate the influence of key parameters, including anode polarization degree of prefabricated C‐FRCM plate, layer of carbon fiber mesh and side‐wrapping. The failure modes, shear capacities, and load‐deflection curves of the shear‐strengthened RC continuous beams are reported. Based on the test results, the applicability of relevant design codes was evaluated and found to provide rather conservative predictions for the shear capacity of the examined C‐FRCM strengthened RC continuous beams.

Interfacial bonding and corrosion inhibition of 2-mercaptobenzimidazole organic films formed on copper surfaces under electrochemical control in acidic chloride solution

The interfacial bonding and the layered structure of 2-mercaptobenzimidazole (2-MBI) organic films adsorbed on electrochemically controlled copper surfaces and their corrosion inhibition effects in acidic chloride aqueous solution were investigated using an integrated approach of electrochemical methods and advanced surface analyses by X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry. It is shown that organic films formed on the copper surfaces are bi-layered with a chemisorbed inner layer and a physisorbed outer layer. In the chemisorbed inner layer, 2-MBI is bonded primarily by its nitrogen atoms with metallic and oxidized copper surfaces. Sulphur atoms are also involved in the bonding mechanism when metallic copper is directly accessible to the 2-MBI molecules. The initial presence of native copper oxides at the interface promotes the formation of Cu(I)-2-MBI metal-organic complexes in the chemisorbed inner layer using cathodic reduction to dissociate the oxide. Metal-organic complexes also form upon anodic polarisation due to Cu(I) ions generated by oxidation of the copper metal. 2-MBI effectively inhibits copper anodic dissolution in varying degrees, between 84% and 93%, depending on the pre-treatment used for the formation of the organic bi-layers. An enhanced protection of the substrate is obtained by adsorbing the 2-MBI inhibitor on an initially oxide-free surface, which is achieved by cathodic pre-treatment in absence of the inhibitor followed by 1 hour exposure to the inhibitor.

Effects of volume-confinement on lithium-ion battery with silicon-based anode

The heightened resistivity and volumetric expansion stemming from alloy formation between silicon and lithium pose significant obstacles to the widespread adoption of silicon-based anodes. We demonstrate that internal pressure induced by volume confinement of a lithium ion battery with silicon-based anode helps retain anode density and form uniform and dense solid electrolyte interphase (SEI). Anode polarization and uneven lithium deposition are minimized, and thereby the consumption of electrolyte and lithium sources is reduced. Experimental data reveals that the interfacial resistance is reduced while specific capacity, coulombic efficiency and cycle stability of a battery improve due to the restriction against the expansion of the volume of half-cells and full-cells of lithium ion battery. The approach holds promise for advanced packaging technology to apply effective means of restricting the volume of lithium ion batteries from increase further during long-term cycling.

Unveiling the potent corrosion-inhibiting power of Ammophila arenaria aqueous extract for mild steel in acidic environments: An integrated experimental and computational study

Plant extracts have emerged as potent inhibiting compounds for metallic corrosion, offering numerous advantages including simple accessibility, low toxicity, eco-friendliness, biocompatibility, effectiveness, and renewability. In this study, the potential of Ammophila arenaria extract as a green corrosion inhibitor for mild steel in 1.0 M HCl over the concentration range of 25–700 ppm was evaluated, using various electrochemical analyses such as Open circuit potential (OCP), potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS). Results revealed a notable reduction in the corrosion rate of steel, particularly at 700 ppm, where Ammophila arenaria extract demonstrated its highest inhibition efficiency, reaching 83.67% for polarization and 84.32% for EIS. The cathodic and anodic polarization curves indicated that the aqueous extract of Ammophila arenaria functions as a mixed-type inhibitor. The thermodynamic analysis revealed a negative Gibbs free energy value (∆Gads°), suggesting spontaneous physisorption as the predominant adsorption mechanism. To delve into the inhibition mechanism at the molecular level, the surface morphology of mild steel exposed to 1.0 M HCl solutions, both in the absence and presence of Ammophila arenaria aqueous extract, was scrutinized through Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM). Theoretical techniques, including Quantum Calculation Theory, Non-Covalent Interaction (NCI), and Atom In Molecule (QTAIM), were concurrently employed, providing valuable insights into molecular-level interactions. Remarkably, the computational studies complemented and corroborated the experimental data. These comprehensive results significantly contribute to the understanding of Ammophila arenaria extract's corrosion inhibiting properties, endorsing its potential as a sustainable and environmentally friendly corrosion inhibitor suitable for diverse industrial applications. The synergistic integration of experimental and computational approaches establishes a robust foundation for future endeavors in the field of green corrosion inhibitors.

Inhibition Localized Corrosion of N80 Petroleum Pipeline Steel in NaCl-Na2S Solution Using an Imidazoline Quaternary Ammonium Salt

In this paper, the local corrosion inhibition effect of imidazoline on N80 oil pipeline steel in a NaCl-Na2S solution was studied by the simulated blocking tank cell method, and the corrosion processes of the cathode and anode in the blocking zone were simulated. The blocking corrosion behavior of the pipeline tubing steel N80 in simulated corrosion solutions without and with different concentrations of an imidazoline corrosion inhibitor was studied by chemical analysis and electrochemical analysis. The results show that in the three solution systems, after the anode polarization of the occluded cell, the solution in the occluded region is acidified, the pH value decreases sharply, the migration of Cl− and S2− increases, and the concentration is increased in the blocked area. After adding the imidazoline corrosion inhibitor, the imidazoline inhibitor can reduce the migration of small-radius anions (Cl− and S2−) to the occluded area, inhibit the acidification of the solution in the occluded area, and prevent the dissolution of metals in the occluded area. As a result, the corrosion of the occluded area is slowed down due to the change in the chemical and electrochemical state of the occluded area. In the three corrosion solution systems of 2% Na2S + 5% NaCl, 2% Na2S + 8% NaCl, and 2% Na2S + 10% NaCl, the imidazoline corrosion inhibitor can form an adsorption film on the metal surface, thereby increasing the polarization resistance and decreasing the corrosion rate. The addition of an imidazoline corrosion inhibitor can significantly increase the kinetic constant of anode polarization, which can effectively inhibit the local corrosion of N80 steel in these corrosion systems.

Mechanistic insights into the corrosion inhibition of mild steel by eco-benign Asphodelus Tenuifolius aerial extract in acidic environment: Electrochemical and computational analysis

This study explores the novel application of Asphodelus Tenuifolius aerial extract (ATAE) as a corrosion inhibitor for mild steel in a 0.5 M HCl acidic environment. By utilizing techniques such as electrochemical measurements, gravimetric analysis, SEM, and CA assessments, the inhibitory potential of ATAE has been comprehensively evaluated. The results revealed a concentration-dependent enhancement in corrosion resistance, classifying ATAE as a mixed-type inhibitor by measuring the anodic (βa) and cathodic (βc) polarization slope values of 108.89 and −129.33 mV/dec. The peak inhibition efficiency was observed at 250 ppm, reaching an impressive IE% of 94.40 % at 298 K (Kelvin). The electrochemical analysis demonstrated a significant increase in charge transfer resistance (Rct) and polarization resistance (Rp) values, coupled with a decrease in Constant Phase Element (CPE.Yo) value to 162.94 μF, indicating heightened corrosion inhibition potential. Additionally, Theoretical calculations emphasized a strong interaction between ATAE and mild steel surface, characterized by a low energy gap (ΔE), indicating excellent anti-corrosion abilities at the micro-level. This study positions ATAE as a promising corrosion inhibitor, offering insights for further research in corrosion prevention strategies using a sustainable corrosion inhibitor.

Corrosion fatigue performance of modified 17-4PH in simulated geothermal environment

Corrosion fatigue behavior of a new candidate material for geothermal turbine blade, modified 17-4PH, was investigated in detail. The environmental acceleration of crack growth rate was discussed in terms of ∆K. Fracture surface and side surface were observed by SEM. The crack path on side surface was also analyzed by EBSD. Then, the corrosion mechanism was discussed. Striation width on the fracture surface was compared to the crack growth per cycle. Since pitting occurred during the corrosion fatigue test, anodic polarization test was exercised to measure the pitting potential, and the cause for the pitting was also discussed. The hardness was also characterized by micro-hardness test and auger electron mapping.

Study on deterioration of mechanical properties and voltage-strength theoretical model of CFRP/ conductive ECC composites under coupling effect of anode polarization, load and erosion environment

This study aims to systematically investigate the deterioration of tensile properties, voltage variation, and voltage-strength theoretical model of CFRP/ conductive ECC composites under coupling effect of anode polarization, load and erosion environment. The effects of testing parameters including conductive ECC mixture type, electric current density, polarization time, tensile stress value, sulfate soak time, and sulfate attack-wet and dry cycle time were synthetically investigated. The experimental results indicated that the voltage increases approximately linearly with the increase of degradation time in the voltage-deterioration time curves. The stress-strain curve can be divided into three stages: the stress-strain linear increase stage, the strain hardening characteristic stage, and the decline stage during failure. The conductive ECC mixture type, polarization time, current density, tensile stress value, sulfate soak time, and sulfate attack-wet and dry cycle time all have significant effects the deterioration of tensile strength and the voltage change ratio of CFRP/ conductive ECC composite. More importantly, an innovative voltage-strength theoretical model was proposed, which can predict the relationship between voltage and material deterioration strength. The theoretical model is in good agreement not only with the experimental results of this study, but also with the results of other studies. The model proposed can be used to predict deterioration degree of materials in real time, which has very important guiding significance for impressed current cathodic protection-structural strengthening technology (ICCP-SS) technology. This study is expected to promote a more comprehensive understanding of the deterioration of mechanical properties and voltage-strength theoretical model of CFRP/conductive ECC composites for ICCP-SS technology.

Corrosion Behavior of Aluminum Alloys in Different Alkaline Environments: Effect of Alloying Elements and Anodization Treatments

Aluminum alloys are extensively used to manufacture mechanical components. However, when exposed to alkaline environments, like lubricants, refrigerants, or detergents, they can be corroded, reducing their durability. For this reason, the aim of this study is to investigate the influence of aggressive alkaline solutions (i.e., pH and presence of chlorides) on the corrosion resistance of three aluminum alloys (AA 5083-H111, AA 6082-T6, and AA 7075-T6) with and without anodizing treatments. Open circuit potential (EOCP) and anodic polarization measurements were carried out and typical corrosion parameters such as corrosion current density (icor) and corrosion rate (CR) were determined. Morphology of the corrosion attack and samples microstructure were investigated by scanning electron microscope. Results show that corrosion behavior of the three investigated alloys is influenced by (i) the aggressiveness of the testing environments; (ii) the thickness of the anodizing treatment; (iii) the alloy chemical composition; (iv) the distribution of intermetallic phases in the aluminum matrix. Moreover, three galvanic series have been built also testing other metallic alloys commonly used in mechanical applications, i.e., carbon steel (C40), stainless-steel (AISI 304), and Cu-based alloys (Cu-Ni alloy and CW 617 N, respectively). Results clearly indicate that galvanic series play a fundamental role when it is necessary to select an alloy for a specific environment, highlighting the thermodynamic conditions for corrosion occurrence. On the other hand, kinetic measurements and microstructural studies carried out on the three aluminum alloys stress the importance of the surface treatments and relevant thickness as well as the effect of metal exposure. Future work will involve the study of other surface treatments on aluminum alloys and the evaluation of their corrosion behavior in acidic environments.

Effect of red clover (Trifolium pratense L.) aqueous extract as an additive on nickel electrodeposition: Experimental and theoretical study

Enhancements in nickel electrodeposition have been achieved using organic additives, some of which are not environmentally friendly and may produce undesirable deposits. Red clover leaf extract (RCLE) containing isoflavones was extracted aqueously from the Trifolium pratense L. plant. It was used as a green additive for nickel electrodeposition on a copper substrate in an acid-sulfate bath. The mechanism of Ni2+ electrodeposition was examined by anodic linear stripping voltammetry, cyclic voltammetry, and cathodic polarization. The surface morphology of the Ni2+ coatings were examined using SEM, EDX, XRD, and AFM. The adsorption of RCLE on the Cu substrate inhibited Ni2+ deposition and resulted in finer-grained, smoother, more uniform, and stronger hardness deposits. The corrosion protection of nickel coatings in a marine environment containing a 3.5 % NaCl solution was also investigated. The findings demonstrated that the addition of RCLE enhanced the corrosion resistance of Ni2+ deposition. The optimal structures of RCLE molecules and their active sites were examined using DFT computations. The results provide concise explanations of the precise atoms and functional groups responsible for the donation and acceptance of electrons. Thus, RCLE showed significant improvements in the process of nickel electrodeposition on a copper substrate in an acid sulfate solution.

Electrochemical Promotion of Bimetallic Palladium‐Cobalt Nano‐Catalysts for Complete Methane Oxidation

AbstractThe catalytic activity and electrochemical promotion of catalysis (EPOC) of the bimetallic Pd−Co nanoparticles (10 nm) deposited on yttria‐stabilized zirconia were investigated for complete methane oxidation. The reaction was conducted under open‐circuit and under polarization in a temperature range of 320–400 °C in reducing, stoichiometric, and oxidizing conditions. The catalytic activity of the catalyst nanoparticles increased to 40 % upon positive polarization in all gaseous compositions. A comparison of three reaction conditions revealed that the highest reaction rate increase (enhancement ratio, ρ=1.4) occurs under reducing conditions. The reaction rate increased upon anodic polarization, resulting in non‐Faradaic electrochemical modification of catalytic activity (Λ≫1) in reducing and oxidizing conditions and Faradaic or electrochemical enhancement (Λ<1) in stoichiometric reaction condition. This work demonstrates that the formation of different Pd and Co oxide phases can be accurately controlled by electrochemical stimuli and, in reducing conditions, result in pseudo‐capacitor behaviour.

High temperature electrochemical reaction parameters affecting electrochemical corrosion potential of nickel-base Alloy 82 weld metal

ABSTRACT The electrochemical corrosion potential (ECP) data of nickel-base alloy 82 weld metal (Alloy 82) in both O2 and H2O2 environments were measured. Although Alloy 82 is used at various welds in boiling water reactors (BWRs), the ECP data of Alloy 82 under BWR conditions are limited. The ECP data measured in this study revealed that Alloy 82 had higher ECPs than 304 and 316 L stainless steels and nickel-base alloy 182 weld metal (Alloy182) at low oxidant concentrations in both O2 and H2O2 environments. The ECPs of Alloy 82 calculated with an analytical ECP model that was developed in this study agreed with measured values in the cases that it was acceptable for the model to have an error range of ± 0.1 V in the tested range of O2 and H2O2 concentrations. The possible reason for the ECPs of Alloy 82 to be higher than those other materials at low oxidant concentrations is given as follows: the anodic polarization curve of Alloy 82 exhibits a lower current density at low potentials because of its higher Ni and Cr contents. The developed ECP model validated by the ECP data will contribute to evaluations of the effectiveness of mitigation technologies for stress corrosion cracking environments.

Anodic surface treatment of nickel in eutectic ionic liquids based on choline chloride for electrochemical polishing and enhancement of electrocatalytic activity in hydrogen evolution reaction

The paper reports the impact of anodic potentiostatic treatment of nickel in two representatives of a new type of eutectic ionic liquids (deep eutectic solvents), ethaline and reline, which are eutectic mixtures of choline chloride with ethylene glycol and urea, respectively. The influence of anodic treatment on surface morphology, roughness coefficients, and electrocatalytic activity towards the hydrogen evolution reaction is characterized. It is demonstrated that the current densities of nickel anodic dissolution in reline are approximately an order of magnitude lower than in ethaline under all other identical conditions. Significant differences in the kinetics of nickel anodic dissolution and passivation during anodic polarization in ethaline and reline have been established, which may be attributed to both a substantial difference in the viscosity of these solvents and differences in the chemical nature and composition of the ions present in them. It is found that anodic treatment in ethaline, at certain potentials, results in electrochemical polishing of the surface, confirmed by a decrease in measured roughness coefficients, while anodic treatment in reline does not allow effective electropolishing and only surface etching (increase in roughness coefficients) is observed. Anodic potentiostatic treatment of nickel in both investigated deep eutectic solvents at specific electrode potential values significantly enhances the electrocatalytic activity of the surface towards the hydrogen evolution reaction in an alkaline environment. This finding can be utilized in the development of electrocatalytic materials for the electrolytic synthesis of green hydrogen.

Corrosion Investigation by Scanning Electrochemical Microscopy of AISI 446 and Ti-Coated AISI 446 Ferritic Stainless Steel as Potential Material for Bipolar Plate in PEMWE

AbstractThe components of proton exchange membrane water electrolysers frequently experience corrosion issues, especially at high anodic polarization, that restrict the use of more affordable alternatives to titanium. Here, we investigate localized corrosion processes of bare and Ti-coated AISI 446 ferritic stainless steel under anodic polarization by scanning electrochemical microscopy (SECM) in sodium sulphate and potassium chloride solutions. SECM approach curves and area scans measured at open-circuit potential (OCP) of the samples in the feedback mode using a redox mediator evidence a negative feedback effect caused by the surface passive film. For the anodic polarization of the sample, the substrate generation-tip collection mode enables to observe local generation of iron (II) ions, as well as formation of molecular oxygen. For the uncoated AISI 446 sample, localized corrosion is detected in sodium sulphate solution simultaneously with oxygen formation at anodic potentials of 1.0 V vs. Ag/AgCl, whereas significant pitting corrosion is observed even at 0.2 V vs. Ag/AgCl in potassium chloride solution. The Ti-coated AISI 446 sample reveals enhanced corrosion resistance in both test solutions, without any evidence of iron (II) ions generation at anodic potentials of 1.2 V vs. Ag/AgCl, where only oxygen formation is observed.