Assessing the corrosion protection property of coatings loaded with corrosion inhibitors using the real-time atmospheric corrosion monitoring technique

The atmospheric corrosion monitoring(ACM)technique has been widely employed to track the real-time corrosion behavior of metal materials.However,limited studies have applied ACM to the corrosion protection properties of organic coatings.This study compared a bare epoxy coating with one containing zinc phosphate corrosion inhibitors,both applied on ACM sensors,to observe their corrosion protection properties over time.Coatings with artificial damage via scratches were exposed to immersion and alternating dry and wet environments,which allowed for monitoring galvanic corrosion currents in real-time.Throughout the corrosion tests,the ACM currents of the zinc phosphate/epoxy coating were considerably lower than those of the blank epoxy coating.The trend in ACM current variations closely matched the results obtained from regular electrochemical tests and surface analysis.This alignment highlights the potential of the ACM technique in evaluating the corrosion protection capabilities of organic coatings.Compared with the blank epoxy coating,the zinc phosphate/epoxy coating showed much-decreased ACM current values that confirmed the effective inhibition of zinc phosphate against steel corrosion beneath the damaged coating.

Prediction model for corrosion rate of low-alloy steels under atmospheric conditions using machine learning algorithms

This work constructed a machine learning(ML)model to predict the atmospheric corrosion rate of low-alloy steels(LAS).The material properties of LAS,environmental factors,and exposure time were used as the input,while the corrosion rate as the output.6 dif-ferent ML algorithms were used to construct the proposed model.Through optimization and filtering,the eXtreme gradient boosting(XG-Boost)model exhibited good corrosion rate prediction accuracy.The features of material properties were then transformed into atomic and physical features using the proposed property transformation approach,and the dominant descriptors that affected the corrosion rate were filtered using the recursive feature elimination(RFE)as well as XGBoost methods.The established ML models exhibited better predic-tion performance and generalization ability via property transformation descriptors.In addition,the SHapley additive exPlanations(SHAP)method was applied to analyze the relationship between the descriptors and corrosion rate.The results showed that the property transformation model could effectively help with analyzing the corrosion behavior,thereby significantly improving the generalization ability of corrosion rate prediction models.

In-situ investigation of atmospheric corrosion behavior of bronze under thin electrolyte layers using electrochemical technique

The atmospheric corrosion behavior of bronze under thin electrolyte layer （TEL） with different thicknesses was monitored using cathodic polarization curves, open circuit potential （OCP） and electrochemical impedance spectroscopy （EIS）. Cathodic polarization result indicates that the cathodic limiting current density increases with decreasing the TEL thickness. EIS result shows that the corrosion rate increases with decreasing the TEL thickness at the initial stage because the corrosion is dominated by the cathodic process, whereas after long immersion time, the corrosion degree with the TEL thickness is in the sequence of 150 μm 〉 310 μm〉 10μm ≈ bulk solution 〉 57 μm. The measurements of OCP and EIS present in-situ electrochemical corrosion information and their results are in good agreement with that of physical characterizations.

Effects of magnesium chloride-based multicomponent salts on atmospheric corrosion of aluminum alloy 2024

Atmospheric corrosion of aluminum alloy 2024 （AA2024） with salt lake water was simulated through a laboratory- accelerated test of cyclic wet-dry and electrochemical techniques. Effects of the soluble magnesium salt contained in the salt water were investigated by scanning electron microscope （SEM）, transmission electron microscope （TEM）, energy dispersive spectrometer （EDS）, electron probe micro analyzer （EPMA）, X-ray diffraction （XRD）, infrared transmission spectroscope （IR）, and atmospheric corrosion monitor （ACM）. The results showed that, with the deposition, atmospheric corrosion of AA2024 could occur when the relative humidity （RH） was lower than 30%. A main crystalline component of corrosion products, layered double hydroxides （LDH）, [Mg1-xAlx（OH）2]^x＋ Clx-·mH2O （LDH-C1）, was determined, which meant that magnesium ion played an important role in the corrosion process. It not only facilitated the corrosion as a result of deliquescence, but also was involved in the corrosion process as a reactant.

Copper corrosion in hot and dry atmosphere environment in Turpan, China

The atmospheric corrosion behavior of pure copper exposed for three years in Turpan, China, which is a typical hot and dry atmosphere environment, was investigated using mass-loss tests, morphology observations, composition analyses, and electrochemical techniques. The results indicated that the annual corrosion rate of pure copper was approximately 2.90 μm/a. An uneven distribution of corrosion products was observed by scanning electron microscopy; this uneven distribution was attributed to the dehydration process during wet–dry and cold–hot cycles, and the compositions mainly consisted of cuprite （Cu2O） and atacamite （Cu2Cl（OH）3）. Electrochemical measurements showed that deposits on copper improved its resistance to corrosion and the protectiveness decreased with increasing temperature. On the other hand, results obtained using the scanning vibrating electrode technique showed that the porous and uneven structure of the deposit layer generated a spatial separation of cathodic and anodic reaction sites, which accelerated the corrosion process in wet and rainy weather.

Corrosion behavior and corrosion products of a low-alloy weathering steel in Qingdao and Wanning

A newly developed low-alloy weathering steel has been exposed in two coastal sites （Qingdao in the north, Wanning in the south） in China for one year. The samples in Wanning corroded far more seriously than those in Qingdao. The rust layer formed on the steel was analyzed by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, N2 adsorption approach, polarization curves, and electrochemical impedance spectroscopy （EIS）. The rust formed in Qingdao contains more X-ray amorphous compounds and is more compact than that formed in Wanning. Cr and Cu are enriched in the rust layer near the steel matrix, and the phenomenon is more obvious in Qingdao than in Wanning. The rust layer formed in Qingdao suppresses the anodic and cathodic reaction more remarkably than that formed in Wanning does. The rust layer formed in Qingdao possesses a higher ability to block the permeation of chloride ions than that formed in Wanning does.

INFLUENCE OF NaCl DEPOSITION ON ATMOSPHERIC CORROSION OF A3 STEEL IN THE PRESENCE OF SO_2

The regularities of atmospheric corrosion of A3 steel deposited with different amount of NaCl exposed to the air containing 1ppm SO2 at 80%RH and 25℃ were studied in laboratory. NaCl can accelerate the corrosion of A3 steel obviously under such condition. The relationship between the weight loss of A3 steel and the amount of NaCl deposition can be well described by using a quadratic function. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Scanning electron microscopy and electron dispersion X-ray analysis (SEM/EDAX) were used to characterize the corrosion products. In the absence of NaCl, FeSO4 · xH2O is the dominant corrosion products, while Fe3O4, FeSO4·H2O, β-FeOOH and γ-FeOOH dominate in the presence of NaCl.

Corrosion behavior of copper in extremely harsh marine atmosphere in Nansha Islands,China

The corrosion behavior of pure copper exposed to the atmosphere of Nansha Islands for 21 months was studied by mass loss method,composition analysis,morphology observation and electrochemical measurements.The results showed that the average corrosion rate of copper exposed for one year was approximately 7.85μm/a,implying that Nansha Islands was classified as a corrosion category of CX.The structure and properties of the corrosion product layer generated on the front and back sides of the exposed sample differed significantly.The inner corrosion product layer(Cu2O)on the front side was relatively thick and dense,whereas the outer product layer(Cu2Cl(OH)3)was extremely thin.However,the outer product layer on the back side was thicker than the inner layer.Electrochemical measurements indicated that the protection afforded by the corrosion product layer on the front side was improved gradually,while that on the back side was deteriorated.

Comparison of the corrosion behavior of AM60 Mg alloy with and without self-healing coating in atmospheric environment

Coatings on the surface of Mg alloys are inevitably damaged during their practical applications,and corrosion can easily initiate from the damaged areas to accelerate the failure of Mg parts.A dual self-healing coating has already been developed to solve this problem in our previous work.Considering the practical application of this coating,it is necessary to investigate its service behavior in atmospheric environment.Thus,the corrosion behavior of AM60 Mg substrate with and without the self-healing coating was compared in Shenyang industrial atmospheric environment.The results show that the enrichment of sediments and rainwater on the scratch areas can accelerate the corrosion of the exposed Mg substrate.The inhibitors can be released from the damaged coating to inhibit corrosion.The dual self-healing coating shows better inhibition ability to narrow scratches due to the higher inhibitor concentration and less resumption.Also,the coating with wide scratches displays enough inhibition ability as well.The dual self-healing coating is a good alternative for Mg alloy parts in the practical applications.

Role of CO_2 in the initial stage of atmospheric corrosion of AZ91 magne-sium alloy in the presence of NaCl

The effect of CO2 and NaCl on the initial stage of atmospheric corrosion of AZ91 magnesium alloy was studied. The observation of surface morphology by optical microscopy （OM）, scanning electron microscopy （SEM） and the analysis of corrosion products by X-ray diffraction （XRD） were integrated to investigate corrosion evolution. The results showed that NaCl stimulated the corrosion by promoting the formation of thin electrolyte film, increasing the conductivity and breaking the protective film in the absence of CO2. The morphology of the corroded samples with deposited NaCl was more homogenous in the presence of CO2. It was suggested that NaCl-induced corrosion was inhibited in the presence of CO2 by the formation of slightly soluble corrosion products containing hydroxy carbonates and hydroxy chlorides that provided a partly protective layer on the surface of the magnesium alloy.

Corrosion and pitting behavior of pure aluminum 1060 exposed to Nansha Islands tropical marine atmosphere

The corrosion and pitting behavior of pure aluminum 1060 exposed to Nansha Islands marine atmosphere for 34 months was investigated based on mass loss measurement,scanning electron microscopy(SEM),energy dispersive spectroscopy(EDS),X-ray photoelectron spectroscopy(XPS),and electrochemical impedance spectroscopy(EIS).The results indicated that serious pitting corrosion occurred on the surfaces of pure aluminum.The corrosion rate after exposure for 13 months was approximately 1.28 g/(m^(2)·a).The XPS results showed that the corrosion products were Al_(2)O_(3),Al(OH)_(3),and AlCl_(3).Moreover,the corrosion product layer was more protective than the native oxide film,and the protectiveness first increased and then decreased.Finally,the shape of the pits was evaluated using statistical analysis.

Comparative investigation on copper atmospheric corrosion by electrochemical impedance and electrical resistance sensors

Electrochemical impedance(EIS)and thin electrical resistance(ER)sensors were invented for atmospheric corrosion measurement of copper(Cu)during cyclic wetting−drying/high−low temperature tests and field exposure tests.Three-month field exposure results showed that average corrosion rate of Cu measured by ER sensor was well in accordance with that by weight loss method.During cyclic wetting−drying test,EIS was proven to reflect sensitively time of wetting and drying on the surface of sensor.Although corrosion rate obtained from EIS had a similar tendency to that obtained from ER sensors,the former was more dependent on environmental humidity than the latter.When relative humidity was low than 60%,corrosion rate of Cu measured by EIS was much lower than that by weight loss method,mainly attributing to the fact that impedance sensor failed to detect corrosion current of interlaced Cu electrodes due to the breakdown of conductive passage composed of absorbed thin liquid film under low humidity condition.Promisingly,ER sensor was proven to be more suitable for atmospheric corrosion monitoring than electrochemical techniques because it could sensitively monitor thickness loss of Cu foil according to the Ohmic law,no matter how dry or wet the sensor surface is.

Kinetics of Atmospheric Corrosion of Mild Steel in Marine and Rural Environments

In continuation of the extensive studies carried out to update the corrosion map of India, in this study, the degradation of mild steel by air pollutants was studied at 16 different locations from Nagore to Ammanichatram along the east coast of Tamilnadu, India over a period of two years. The weight loss study showed that the mild steel corrosion was more at Nagapattinam site, when compared to Ammanichatram and Maravakadu sites. A linear regression analysis of the experimental data was attempted to predict the mechanism of the corrosion. The composition of the corrosion products formed on the mild steel surfaces was identified by XRD technique. The corrosion rate values obtained are discussed in the light of the weathering parameters, atmospheric pollutants such as salt content ＆ SO2 levels in the atmosphere, corrosion products formed on the mild steel surfaces.

GALVANIC CORROSION AND PROTECTION OF GECM/LY12CZ COUPLES UNDER DIFFERENT ATMOSPHERIC EXPOSURE CONDITIONS

Galvanic, compatibility between graphite epoxy composite materials (GECM) and LY12CZ aluminum alloy was evaluated in different atmospheric corrosion environments and by laboratory electrochemical measurements. Open circuit potential electrochemical measurements showed a relatively large potential difference about 1 volt between the GECM and LY12CZ aluminum alloy, and this difference provided the driving force for galvanic corrosion of the LY12CZ aluminum alloy as an anode. Having been exposed for 1, 3 or 5 years in Beijing, Tuandao and Wanning station, GECM/LY12CZ couples showed significant losses of strength and elongation. Protective coatings and non-conductive barriers breaking the galvanic corrosion circuit were evaluated under the same atmospheric corrosive conditions. Epoxy primer paint, glass cloth barriers and LY12CZ anodizing were effective in galvanic corrosion control for GECM/LY12CZ couples.

Atmospheric corrosion behavior of Nb-and Sb-added weathering steels exposed to the South China Sea

The atmospheric corrosion behavior of new-type weathering steels(WSs)was comparatively studied,and the effects of Nb and Sb during corrosion were clarified in detail through field exposure and characterization.The results showed that the addition of Nb and Sb played positive roles in corrosion resistance,but there was a clear difference between these two elements.Nb addition slightly improved the rust property of conventional WS but could not inhibit the electrochemical process.In contrast,Sb addition significantly improved the corrosion resistance from the aspects of electrochemistry and rust layer.Compared with only 0.06wt%Nb,the combination of 0.05wt%Sb and 0.06wt%Nb could better optimize the rust structure,accelerate the formation of a high proportion of dense and protectiveα-FeOOH,repel the invasion of Cl^(−),and retard the localized acidification at the bottom of the pit.

Influence of NaCl Deposition on Atmospheric Corrosion of A3 Steel

Regularity of the initial atmospheric corrosion of A3 steel in the presence of NaCI was investigated. The results showed that NaCI can accelerate the corrosion of A3 steel. Dry mass gain of A3 steel in the presence of NaCI deposition increases with the exposure time, which can be correlated by using exponential decay function. The relationship between dry mass gain and amount of NaCI deposition at a certain exposure time follows a quadratic function. More amount of NaCI deposition will slow down the corrosion rate to some extent after exposure for a certain time. SEM/EDAX was used to characterize the corrosion surface and products. The surfaces of the NaCI treated A3 steel were obviously uneven, and some tiny crevices appear in the corrosion products that could help O2 transmit to the inner layer. The amount of oxygen in atomic percentage in the corrosion products increases with the amount of NaCI deposition.

ATMOSPHERIC CORROSION OF 304AND 316 STAINLESS STEELS

Atmospheric corrosion of 304 and 316 stainless steels was studied by field exposure test, in which rain water was collected and analyzed by atomic absorption spectroscope (AAS). Emphasis was put on the dissolution of chromium and nickel from the stainless steels by atmospheric corrosion and rain runoff. AAS analyses shows that the amounts of yearly chromium and nickel dissolution were less than 150ng/cm 2 and 50ng/cm 2 respectively for both 304 and 316 stainless steels. XPS analysis reveals the marked Cr enrichment on the 316 stainless steel after one year field exposure. SEM shows the morphology of corrosion pits on the steel surfaces.

Atmospheric Corrosion of Steel A3 Deposited with Ammonium Sulfate and in the Presence of Sulfur Dioxide

A laboratory study of the atmospheric corrosion of carbon steel deposited with (NH4)2SO4 in the presence of SO2 is reported. The different levels of (NH4)2SO4 (0, 15, 30, 45, 60 μg·cm-2) were added on the surface of the samples before the exposure. The corrosion was investigated by a combination of gravimetry, Fourier transform infrared spectroscope and scanning electron microscopy. A detailed knowledge about the corrosion products was acquired, both quantitatively and qualitatively. The results show that the metal loss increased and the increasing tendency of corrosion rates slowed down with the increasing exposure time. The phase constituents of the corrosion products are mainly α-FeO(OH), γ-FeO(OH), and δ-FeO(OH).

Effect of CO_2 on Atmospheric Corrosion of UNS G10190 Steel under Thin Electrolyte Film

The atmospheric corrosion of UNS G10190 steel under a thin electrolyte film in the atmosphere polluted by CO_2, has been studied in the lab using an atmospheric corrosion monitor (ACM) in combination with XRD and SEM observations of the surface of steel. The ACM study indicated that the corrosion rate of the steel increased with increasing carbon dioxide concentration. The XRD and SEM observations showed that no carbonate was found in the corrosion product on the steel surface. The corrosion product consisted of two layers, i. e., inner and outer layer. From the experimental results, it was concluded that CO_2 played an enhancing role in the atmospheric corrosion of UNS G10190 steel. The film of the corrosion product showed slight protection.

Corrosion behavior of 907 steel under thin electrolyte layers of artificial seawater

The corrosion behavior of 907 steel under thin electrolyte layer(TEL) has been investigated by means of cathodic polarization curve measurement, electrochemical impedance spectroscopy(EIS) and scanning electron microscopy(SEM). The results show that the cathodic diffusion current density presents the variation trend of initial increase and subsequent decrease with the decrease of TEL thickness, and the maximum deposits at 58 μm. The cotangent-hyperbolic impedance(O) is rationally first introduced to study the diffusion process of the reactants through the corrosion products layer with many permeable holes. The initial corrosion rate of 907 steel under different TEL thickness increases with the decrease of TEL thickness except that of 104 μm,whereas the corrosion rate after long time corrosion can be ranked as 104 μm﹥402 μm﹥198 μm﹥301 μm﹥bulk solution.