Search Results (183)

This study investigates the surface characteristics and corrosion behavior of a high-C martensitic stainless steel (AISI 440C) at different stages of its manufacturing process. As a class, these steels prioritize high mechanical properties and wear resistance over superior corrosion resistance. Hot working operations, such as rolling, create a surface oxide scale that must be removed via pickling to restore the material’s inherent corrosion resistance. This process also eliminates the underlying Cr-depleted layer, allowing for the re-establishment of a protective passive film. Using potentiodynamic polarization curves and micrographic analysis, the material’s behavior in different conditions, as-rolled, with a post-heat treatment oxide scale, and in a bare, oxide-free state, has been assessed. The results showed that the material lacks stable passive behavior under all conditions. The as-rolled and heat-treated conditions both exhibited active behavior and formed thick, non-adherent corrosion products. The oxide layer formed after heat treatment performed the worst, showing a significant increase in corrosion current density. These findings confirm the material’s susceptibility to corrosion in Cl⁻ ion-rich environments, highlighting the need for limited storage in such conditions and rapid pickling after thermal processing to mitigate surface damage. Full article

The nominal compositions of Fe₆₅Co_10−xNi_10−xCr₁₅Si_2x (x = 1, 2, and 3 at.%) medium-entropy alloys (MEAs) were designed and fabricated by vacuum arc melting. Their microstructure, hardness, and mechanical properties were systematically characterized. Corrosion behavior was evaluated in 3.5 wt.% NaCl solution by potentiodynamic polarization and electrochemical impedance spectroscopy. The investigated MEAs exhibit a dual-phase microstructure composed of face-centered cubic (FCC) and body-centered-cubic (BCC) phases. With increasing Si content, yield strength and ultimate tensile strength increase, while uniform elongation decreases. Hardness also increases with increasing Si content. For the x = 3 MEA, the yield strength, ultimate tensile strength, and hardness of are ~518 MPa, ~1053 MPa, and 262 ± 4.8 HV, respectively. The observed strengthening can be primarily attributed to solid solution strengthening effect by Si. Polarization curves indicate that the x = 3 MEA exhibits the best corrosion resistance with the lowest corrosion current density ((0.401 ± 0.19) × 10⁻⁶ A × cm⁻²) and corrosion rate ((4.65 ± 0.19) × 10^–2 μm × year⁻¹)). Equivalent electric circuit analysis suggests the formation of a stable passive oxide film on the MEAs. This conclusion is supported by the capacitive behavior, high impedance values (> 10⁴ Ω cm²) at low frequencies, and phase angles within a narrow window of 80.05°~80.64° in the medium-frequency region. The passive-film thickness was calculated and the corrosion morphology was analyzed by SEM. These results provide a reference for developing high-strength, corrosion-resistant, medium-entropy alloys. Full article

This study applies statistical approaches utilizing linear regression and artificial neural networks (ANNs) to predict the corrosion behavior of austenitic stainless steels (316L, 904L, and AL-6XN) under various environmental conditions. The environmental variables considered include temperature (30–90 °C), chloride ion concentration (20–40 g/L), and pH (2–6). Analysis of variance (ANOVA) confirmed that the input variables, including the Pitting Resistance Equivalent Number (PREN ranging from 24 to 45), significantly affect the critical pitting potential. The influence of the variables was ranked in the order: PREN, temperature, pH, and chloride ion concentration. A linear regression model was developed using significant factors and interactions identified at the 95% confidence level, achieving a predictive performance with R² = 0.789 for critical pitting potential. To predict potentiodynamic polarization curves, an ANN based on supervised learning with backpropagation was employed. The ANN model demonstrated a remarkably high predictive performance with R² = 0.972 in complex corrosion environments. The predicted polarization curves reliably estimated electrochemical characteristics such as corrosion current, corrosion potential, and pitting potential. These results provide a valuable tool for predicting and understanding the corrosion behavior of stainless steels, which can aid in corrosion prevention strategies and material selection decisions. Full article

Biocompatible coatings are widely employed in dental applications to enhance the biofunctionality of metallic implants exposed to the aggressive oral environment. Among them, hydroxyapatite (HAp)-based and carbide-reinforced coatings have been explored due to their favorable mechanical and biological performance. In this study, Cr₃C_-20(Ni20Cr)-20HAp-XSi coatings were deposited using the high-velocity oxy-fuel (HVOF) technique. The coatings were applied onto commercially pure titanium substrates, with the silicon content varied between X = 0, 5, 10, and 20 wt%. To evaluate the coatings’ corrosion resistance, electrochemical techniques such as potentiodynamic polarization curves, linear polarization resistance (LPR), electrochemical impedance spectroscopy (EIS), and open circuit potential (OCP) were employed. Artificial saliva was used as the corrosive medium at 37 °C for 168 h. The feasibility of producing carbide-HAp-Si coatings with excellent corrosion resistance and cytocompatibility via HVOF was demonstrated here, although some of the tested coatings (20 wt% Si) showed reduced electrochemical stability, attributed to faster dissolution processes and associated with a thinner coating layer, as confirmed by SEM analyses. X-ray diffraction (XRD) analyses revealed the formation of new phases in the coatings during thermal spraying, including Cr₂O₃ and Cr₇C₃. Additionally, MTT assays using 3T3-L1 fibroblasts showed no significant cytotoxic effects after 24 and 72 h of exposure to some of the coatings, confirming their biocompatibility for potential dental applications. Full article

In this research work, the electrochemical evaluation of a non-ionic gemini surfactant as a green corrosion inhibitor for X100 pipeline steel in CO₂-saturated brine solution was carried out by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization curves (PPC). The corrosion inhibition performance of the gemini surfactant was studied in static and hydrodynamic conditions at room temperature and 60 °C. Electrochemical measurements showed that the inhibitor’s performance was enhanced with increasing inhibitor concentration and with increasing exposure time at room temperature, reaching the highest inhibition efficiency (η) at 100 ppm. With increasing temperature, the inhibitor efficiency decreased, with similar behavior at all concentrations. The analysis of the cathodic polarization curves at different rotation speeds showed the strong influence of mass transport on the cathodic process in the absence and the presence of the inhibitor. Under hydrodynamic conditions, PPC and EIS results indicated that the best inhibitor performance was with a concentration of 50 ppm, achieving a maximum inhibition efficiency of 91%. The adsorption of the inhibitor molecules on the surface obeyed the Langmuir isotherm, and the type of adsorption was mixed in all the study conditions. Surface characterization by scanning electron microscopy (SEM) revealed the formation of a protective corrosion inhibitor film. Full article

UNS S41003 is a low-cost, low-carbon ferritic stainless steel that exhibits moderate corrosion resistance but limited mechanical performance. This study evaluates the electrochemical behavior of untreated and thermomechanically treated UNS S41003 samples. Corrosion tests were conducted in acidic electrolytes with varying pH to simulate aggressive environments relevant to industrial and structural applications where exposure to acidic media and corrosive pollutants occurs. Potentiodynamic polarization curves for all samples displayed passive regions typically associated with protective oxide film formation; however, localized pitting corrosion was detected post-test. Electrochemical impedance spectroscopy indicated a marked decrease in corrosion resistance as pH decreased. The corrosion resistance of the treated alloy remained comparable to that of the untreated condition, indicating that thermomechanical processing did not detrimentally affect passivity or corrosion performance under the tested conditions. The literature suggests that the applied treatment enhances mechanical properties, supporting the potential use of this alloy in structural components subjected to acidic environments requiring a balance of mechanical strength and corrosion resistance. Full article

Titanium alloys are frequently subjected to surface treatments to enhance their biocompatibility and corrosion resistance in biological environments. Plasma electrolytic oxidation (PEO) is an environmentally friendly electrochemical technique capable of forming oxide layers characterized by high corrosion resistance, biocompatibility, and strong adhesion to the substrate. In this study, the PEO process was performed using a low-melting-point ternary eutectic electrolyte composed of Ca(NO₃)₂–NaNO₃–KNO₃ (41–17–42 wt.%) with the addition of ammonium dihydrogen phosphate (ADP). The use of this electrolyte system enables a reduction in the operating temperature from 280 to 160 °C. The effects of applied voltage from 200 to 400V, current frequency from 50 to 1000 Hz, and ADP concentrations of 0.1, 0.5, 1, 2, and 5 wt.% on the growth of titanium oxide composite coatings on a Ti-6Al-4V substrate were investigated. The incorporation of Ca and P was confirmed by phase and chemical composition analysis, while scanning electron microscopy (SEM) revealed a porous surface morphology typical of PEO coatings. Corrosion resistance in Hank’s solution, evaluated via Tafel plot fitting of potentiodynamic polarization curves, demonstrated a substantial improvement in electrochemical performance of the PEO-treated samples. The corrosion current decreased from 552 to 219 nA/cm², and the corrosion potential shifted from −102 to 793 mV vs. the Reference Hydrogen Electrode (RHE) compared to the uncoated alloy. These findings indicate optimal PEO processing parameters for producing composite oxide coatings on Ti-6Al-4V alloy surfaces with enhanced corrosion resistance and potential bioactivity, which are attributed to the incorporation of Ca and P into the coating structure. Full article

In this study, the corrosion inhibition of a Phalaris canariensis extract on brass in a CO₂-saturated 3.5% NaCl solution is evaluated with the aid of potentiodynamic polarization curves and electrochemical impedance spectroscopy tests. The results indicate that the Phalaris canariensis extract is an excellent CO₂ corrosion inhibitor with an efficiency that increases with its concentration, reaching its maximum value of 99% with an inhibitor concentration of 100 ppm, decreasing the corrosion current density by more than two orders of magnitude. The addition of the Phalaris canariensis extract increased the pitting potential, decreased the passive current density values, and affected cathodic reactions, behaving as a mixed type of inhibitor. The corrosion process was under charge transfer control, and it was neither affected by the addition of the inhibitor nor by the elapsing time. The main compounds found in the Phalaris canariensis extract included antioxidants such as palmitic and oleic acids. Full article

Plasma electrolytic oxidation (PEO) is an advanced electrochemical surface treatment technology. It can effectively improve the corrosion resistance of magnesium and its alloys. This paper aims to form protective PEO coatings on an AZ31 substrate with different electrolytes, while monitoring the micro-discharge evolution by noise intensity and morphology analysis. By setting the PEO parameters and monitoring process characteristics, such as current density, spark appearance, and noise intensity, it was deduced that the PEO process consists of the following three stages: anodic oxidation, spark discharge, and micro-arc discharge. The PEO oxide coating formed on the AZ31 alloy exhibits various irregular volcano-like structures. Oxygen species are uniformly distributed along the coating cross-section. Phosphorus species tend to be enriched inwards to the coating/magnesium substrate interface, while aluminum piles up towards the surface region. Surface roughness of the PEO coating formed in the silicate-based electrolyte was the lowest in an arithmetic average height (Sa) of 0.76 μm. Electrochemical analysis indicated that the corrosion current density of the PEO coating decreased by about two orders of magnitude compared to that of untreated blank AZ31 substrate, while, at the same time, the open-circuit potential shifted significantly to the positive direction. The corrosion current density of the 10 min/400 V coating was 1.415 × 10⁻⁶ A/cm², approximately 17% lower than that of the 2 min/400 V coating (1.738 × 10⁻⁶ A/cm²). For a fixed 10 min treatment, the longer the PEO duration time, the lower the corrosion current density. Finally, the tested potentiodynamic polarization curve reveals the impact of different types of PEO electrolytes and different durations of PEO treatment on the corrosion resistance of the oxide coating surface. Full article

To enhance interaction with the host tissue and protect the metal surface, various surface treatments can be applied to dental implants. This study aimed to produce layer-by-layer (LbL) films by alternated immersion of the titanium sample into polyacrylic acid (PAA) and chitosan solutions, obtaining a PAA/chitosan bilayer architecture, seeking to improve the corrosion resistance. For this purpose, 03 experimental groups (n = 05) were performed: Ti-Cp (as control), Ti-Cp+8 bilayers PAA/chitosan, and Ti-Cp+12 bilayers PAA/chitosan. The corrosion behavior was assessed by using open-circuit potential (OCP), potentiodynamic polarization curves (PPcs) and electrochemical impedance spectroscopy (EIS) techniques, conducted in 0.9 wt% NaCl solution at a controlled temperature of 25 ± 1 °C. The samples were characterized morphologically and structurally by atomic force microscope (AFM), scanning electron microscopy/energy-dispersive X-ray (SEM/EDX), and X-ray diffraction (XRD) techniques before and after the corrosion tests. The electrochemical results significantly highlight the beneficial influence of coatings based on PAA/chitosan in enhancing the corrosion resistance of titanium. These findings not only corroborate the feasibility of using alternative materials for the protection of titanium but also open new possibilities for the development of innovative coatings that can be applied within the biomedical sector, serving as mediators for medicinal purposes, particularly in osteoconductive interventions. Full article

This study provides a systematic comparison of three types of phosphate coatings, applied by identical immersion phosphating processes and tested under two different environmental conditions representative of real industrial scenarios. The focus of this study is the investigation of the corrosion behaviour of zinc, magnesium, and manganese phosphate coatings on reinforcing steel in two different corrosion environments: river water and seawater. The phosphate coatings were obtained via the immersion phosphating technique. Various techniques, including scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), potentiodynamic polarization curve (PDP) testing, and electrochemical impedance spectroscopy (EIS), were used to evaluate the morphology and corrosion resistance of the coatings. The overall corrosion protection performance of the coatings followed the order of Zn phosphate > Mn phosphate > Mg phosphate. The results indicate that the samples with the Zn-phosphated coating showing the highest improvement. This coating showed no major morphological changes and achieved significantly reduced corrosion rates—0.258 µm/year in river water and 3.060 µm/year in seawater—compared to the typical corrosion rate of uncoated steel, which is about 45 µm/year. These findings emphasize the effectiveness of Zn phosphate coatings in mitigating corrosion in both river water and marine conditions. Full article

Portland cement is one of the most widely used construction materials employed in both large-scale structures and everyday applications. Although various materials are often added during production to enhance their performance, NaCl can be introduced in the process for various reasons. Despite this issue, existing studies lack sufficient quantitative data on the effects of NaCl on cement properties. Therefore, this study aims to investigate the physical and chemical degradation mechanisms in cement containing NaCl. Cement specimens were prepared by mixing cement, water, and NaCl, followed by stirring at 60 rpm and curing at room temperature for seven days. Microstructural changes as a function of the NaCl concentration were analyzed using scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Electrochemical properties were evaluated via open-circuit potential (OCP) measurements, electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization tests. The results indicate that increasing the NaCl concentration leads to the formation of fine precipitates, the degradation of the cement matrix, and the reduced stability of major hydration products. Furthermore, the electrochemical analysis revealed that higher NaCl concentrations weaken the passive layer on the cement surface, resulting in an increased corrosion rate from 1 × 10⁻⁷ to 4 × 10⁻⁷ on the active polarization of the potentiodynamic polarization curve. Additionally, the pitting potential (E_pit) decreased from 0.73 V to 0.61 V with an increasing NaCl concentration up to 3 wt.%. This study quantitatively evaluates the impact of NaCl on the durability of Portland cement and provides fundamental data to ensure the long-term stability of cement structures in chloride-rich environments. Full article

This study investigates the tribocorrosion behavior of 304 stainless steel (304SS), S31254 super austenitic stainless steel (S31254 SASS), and a medium-entropy austenitic stainless steel (MEASS) in 3.5 wt.% NaCl solution under sliding conditions. The objective is to clarify the performance differences among these alloys when exposed to simultaneous mechanical wear and corrosion. Electrochemical techniques, including potentiodynamic polarization and potentiostatic sliding tests, were used to evaluate corrosion resistance and repassivation behavior. Quantitative analysis based on ASTM G119 revealed that MEASS showed a 68% lower total material loss compared to 304SS and a 55% lower loss compared to S31254. MEASS also exhibited the lowest corrosion current density (1.46 μA/cm²) under tribocorrosion conditions, representing an 83% reduction compared to 304SS. These improvements are attributed to the higher chromium and nickel contents of MEASS, which enhance passive film stability and reduce susceptibility to localized corrosion. The results demonstrate that MEASS offers superior resistance to combined mechanical and corrosive degradation in chloride-containing environments. Full article

Sealing treatment is widely used as a simple and low-cost process to improve the long-term corrosion resistance of Fe-based amorphous coatings. In this study, an eco-friendly graphene modified waterborne acrylic sealant(WFS) with strong permeability was prepared by emulsion polymerization and GO@SiO₂ was introduced as a reinforcing material to increase the withstand resistance of the hybrid sealant to Cl⁻. A combination of ultrasonic excitation and vacuum sealing effectively promotes the penetration of the waterborne hybrid sealant into the pores of the coating. A 3D X-ray scan confirmed the sealant penetration depth of 160 μm. The natural properties of the emulsion were characterized by a particle size analyzer, FTIR, TGA-DSC and TEM. Potentiodynamic polarization curves and AC impedance spectroscopy analysis showed that GO@SiO₂ has a strong blocking ability to Cl⁻, which greatly promotes the integrity of the passive film. It is anticipated that the novel eco-friendly waterborne hybrid sealants with strong permeability will find applications in a variety of porous hard coatings. Full article

In the present work, the effect of quenching and partitioning cycles on the microstructure, hardness, and corrosion behavior of SAE 9254 spring steel was investigated. Initially, the critical phase transformation temperatures were analyzed by dilatometry. The samples were then treated by four routes of quenching and partitioning in a dilatometer with quenching stop temperatures of 250 and 220 °C. The partitioning temperatures were 300 and 400 °C. The partitioning time was 480 s. Quantitative characterization of austenite and martensite volume fractions was carried out by X-ray diffraction. Qualitative characterization was carried out by optical microscopy and scanning electron microscopy in addition to quantitative assessments of the chemical composition of segregations by EDS. The formation of martensite, retained austenite, and bainite was observed. The dilatometric curves displayed the occurrence of volumetric expansion in the partitioning step, indicating the formation of secondary martensite (fresh martensite) during the final cooling process (final quenching). The mechanical properties were evaluated by Vickers microhardness and nanoindentation tests. There was heterogeneity of hardness inside and outside the banding regions. The electrochemical properties were evaluated by electrochemical impedance spectroscopy and potentiodynamic polarization tests in a 0.1 M H₂SO₄ solution. The best corrosion resistance was achieved for samples quenched at 250 °C and partitioned at 400 °C due to the higher volume fraction of retained austenite when compared to the other heat treatment conditions. Full article