Improved electrochemical performance of trivalent-chrome coating on Al 6063 alloy via urea and thiourea addition

This project aims at improving the electrochemical performance of trivalent-chrome coating through urea and thiourea addition. The electrochemical behaviors of coatings formed with different concentrations of urea and thiourea were investigated in 3.5 wt.% NaCl solution at 25 °C, using potentiodynamic polarization curves and EIS. The corrosion resistance of coatings is improved greatly by adding a small amount of inhibitors, whereas the excessive addition deteriorates the corrosion resistance. Thiourea addition presents better effect than urea. To explain the EIS results of the coatings, a simple equivalent circuit was designed. The EIS parameters were obtained by fitting the EIS plots. The results of the polarization curves and EIS show that the inhibitor-containing coatings present better corrosion resistance than the coating without inhibitor. The morphology and composition and valence state of the conversion coatings were examined by SEM and EDS and XPS, respectively. The results indicated that the trivalent chromium coating was developed on Al 6063 alloy, urea and thiourea inhibitors were also deposited on the substrates, respectively. A noticeable chemical shift was also observed.     

Thermomechanical and corrosion inhibition properties of graphene/epoxy ester–siloxane–urea hybrid polymer nanocomposites

The effect of graphene on the corrosion inhibition properties of a hybrid epoxy–ester–siloxane–urea polymer was investigated. The weight fraction of graphene was varied from 1 to 2 wt%. Direct current polarization (DCP) and electrochemical impedance spectroscopic (EIS) techniques were used to measure the polarization and coating resistance of the coated aluminum alloy substrate. The grapheme/hybrid polymer composite coatings showed much higher corrosion inhibition property when compared to the neat hybrid polymer coating. An increase in glass transition temperature and rubbery region modulus was also observed for composites containing 1–2 wt.% of graphene. A direct correlation between the rubbery plateau modulus of free standing composite thin films and corrosion resistance of the composite coatings was made, indicating that the corrosion protection mechanism is due to restriction of the polymer chain motion by graphene which causes a decrease in coating permeability.     

Preparation and properties of thermosetting powder/graphene oxide coatings for anticorrosion application

The goal of this research was to simplify the preparation process of graphene-contained powder coatings for metal anticorrosion. To do this, thermosetting powder/graphene oxide (TP@GO) composites were prepared via a facile planetary ball-milling technique and were painted onto tinplates by electrostatic spraying. After immersion in a 3.5 wt % NaCl solution for 9 days, potentiodynamic polarization curves revealed superior anticorrosion performance for the 1.5 wt % graphene oxide coating (TP@GO₁₅), providing 74.1% decreased corrosion current and 34.2% increased corrosion potential compared to pure thermosetting powder coating. After 48 days of immersion, the electrochemical impedance spectroscopy analysis of the prepared materials revealed that the anticorrosion properties were in the sequence TP < TP@GO₁₀ < TP@GO₂₀ < TP@GO₁₅. The results indicated that addition of moderate amount of graphene oxide to prepare TP@GO coatings can significantly promote the anticorrosion performance of metals. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48264.     

Comparison of electrochemical behavior of CrN single-layer coating and Cr/CrN nanolayered coating produced by cathodic arc evaporation physical vapor deposition

The aim of the present work is to study the CrN single-layer coating and the Cr/CrN nanolayered coating by cathodic arc evaporation physical vapor deposition (CAE-PVD) on AISI 304 stainless steel and to assess the electrochemical behavior of the coatings. Field emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD) were utilized to study the morphology and microstructure of the coatings. The mechanical behavior of the coatings was studied by the nanoindentation technique. The electrochemical behavior of the formed coatings in 3.5 wt.% NaCl solution was investigated via electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization (PDP) tests. Based on the microscopic images, it was realized that both CrN and Cr/CrN coatings were formed having a dense structure on the substrate. The results of EIS measurements showed gradual changes in the polarization resistance of the Cr/CrN nanolayered coating during the immersion time. However, significant changes in the polarization resistance of the CrN single-layer coating were seen by increasing immersion time comparing with the Cr/CrN coating. The higher polarization resistance of the Cr/CrN coating can be attributed to the effects of the interface between the layers in comparison to the CrN coating.     

Anticorrosion and electromagnetic interference shielding behavior of candle soot-based epoxy coating

This article presents candle soot (CS) as anticorrosion coating material for mild steel (MS) in 3.5 wt % of NaCl solution using potentiodynamic polarization and electrochemical impedance spectroscopy. CS is easily available, low-cost material, and characterized by using X-Ray diffraction (XRD), Raman spectroscopy, UV–vis spectroscopy, Fourier-transform infrared (FTIR), and scanning electron microscopy (SEM). CS is superhydrobhobic in nature that helps to prevent corrosion by repelling water molecules from MS surface. The electrochemical results confirmed the prevention in corrosion process for MS using candle soot-epoxy (CS-EP) based anticorrosion coatings. The CS-based coatings displayed outstanding barrier properties in 3.5 wt % of NaCl solution in comparison to the neat EP coating. Different candle CS-EP coating combinations were tested that exhibited excellent corrosion inhibition performance with highest protection increased up to 98.45% at 0.2 wt % of CS. The surface morphological studies were used to analyze the MS surface conditions in absence and presence of CS-EP coating in 3.5 wt % of NaCl solution. CS-EP admixtures were also tested for their shielding effectiveness in the frequency range of 8.2–12.4 GHz and it has been found that on incorporation of 0.2 wt % of CS in EP resin total shielding effectiveness (SE_T) increased to −5.3 dB as compared to −0.33 dB for neat EP. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 137, 48675.     

Investigation on corrosion and wear resistance of MgO-Al2O3 composite coating prepared by plasma electrolytic oxidation

Ceramic coatings were prepared on 6061 Al alloy in a mixed electrolyte with/without MgO powders at different treatment durations. The results of energy dispersive spectroscopy (EDS) and X-ray diffraction (XRD) showed that MgO powder was incorporated into the coatings, and Mg species gradually aggregated into coating inside as prolonging the oxidation time. Scanning electron microscopy (SEM) showed that MgO additive had a certain effect on the microstructures and coating thickness. The corrosion behavior tests evaluated by potentiodynamic polarization tests and electrochemical impedance spectroscopy (EIS) in 3.5 wt% NaCl solution suggested that at the same treatment time, the addition of MgO powders can improve the corrosion resistance of the coating, and the Mg-rich layer can affect the corrosion resistance of the coating. The tests of mechanical properties showed that the addition of MgO powders improved the stability and hardness of the coating.     

Preparation and corrosion resistance studies of nanometric sol-gel-based CeO2 film with a chromium-free pretreatment on AZ91D magnesium alloy

Magnesium alloy, although valuable, is reactive and requires protection before it can be applied in many fields. In this study, a novel protective environmental-friendly gradient coating was performed on AZ91D magnesium alloy by non-chromate surface treatments, which consisted of phytic acid chemical conversion coating and the sol-gel-based CeO₂ thin film. The surface morphologies, microstructure and composition of the coatings were investigated by scanning electron microscopy (SEM), energy disperse spectroscopy (EDS) and X-ray diffraction (XRD), respectively. The corrosion resistance of the coatings was evaluated by potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) in 3.5 wt.% NaCl solution. The effects of the concentration, layers, temperature of heat treatment of CeO₂ sol on the anti-corrosion properties of the gradient coating for magnesium were also investigated. The results showed that the gradient coating was mainly composed of crystalline CeO₂. According to the results of electrochemical tests, the corrosion resistance of AZ91D magnesium alloy was found to be greatly improved by means of this new environmental-friendly surface treatment.     

Electrochemical corrosion behaviour of plasma electrolytic oxidation coatings on AM50 magnesium alloy formed in silicate and phosphate based electrolytes

PEO coatings were produced on AM50 magnesium alloy by plasma electrolytic oxidation process in silicate and phosphate based electrolytes using a pulsed DC power source. The microstructure and composition of the PEO coatings were analyzed by scanning electron microscopy (SEM) and X-ray Diffraction (XRD). The corrosion resistance of the PEO coatings was evaluated using open circuit potential (OCP) measurements, potentiodynamic polarisation tests and electrochemical impedance spectroscopy (EIS) in 0.1 M NaCl solution. It was found that the electrolyte composition has a significant effect on the coating evolution and on the resulting coating characteristics, such as microstructure, composition, coating thickness, roughness and thus on the corrosion behaviour. The corrosion resistance of the PEO coating formed in silicate electrolyte was found to be superior to that formed in phosphate electrolyte in both the short-term and long-term electrochemical corrosion tests.     

Corrosion Behaviour of Niobium in Sodium Hydroxide Solutions

The electrochemical behaviour of niobium was investigated in sodium hydroxide solutions at different temperatures, using open-circuit potential (OCP) measurements, potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). OCP and polarization measurements show that Nb is spontaneously active in 10, 15 and 30 wt % NaOH at 25, 50 and 75 °C. The anodic polarization curves in all cases show a dissolution/passivation peak followed by a current plateau, corresponding to Nb₂O₅ formation. The spontaneous active corrosion of Nb leads to the formation of soluble niobates that precipitate to sodium niobates. The evaluation of the corrosion current densities obtained from Tafel extrapolation of polarization curves and the polarization resistance values determined from EIS measurements indicates that the corrosion rates of niobium increase with increasing NaOH concentration and temperature.     

Studying the corrosion protection properties of an epoxy coating containing different mixtures of strontium aluminum polyphosphate (SAPP) and zinc aluminum phosphate (ZPA) pigments

Epoxy/polyamide coatings were loaded with different mixtures of strontium aluminum polyphosphate (SAPP) and zinc aluminum phosphate (ZPA) pigments. Moreover, a coating containing zinc phosphate (ZP) was prepared as a reference sample. The coatings were applied on St-37 steel substrates and then were exposed to 3.5 wt% NaCl solution up to 35 days. The corrosion inhibition properties of the pigments extracts were studied on bare steel samples by a potentiodynamic polarization technique after 24 h immersion. The morphological properties and corrosion resistance of the coatings were investigated by scanning electron microscope (SEM), optical microscope, electrochemical impedance spectroscopy (EIS) and salt spray tests.     

Inhibition of steel corrosion by electrosynthesized poly(o-anisidine)-dodecylbenzenesulfonate coatings

Poly(o-anisidine)-dodecylbenzenesulfonate (POA-DBSA) coatings were synthesized on stainless steel from aqueous solution containing o-anisidine and dodecylbenzene sulfonic acid by using cyclic voltammetry. These coatings were characterized by Fourier transform infrared spectroscopy (FTIR), UV-vis absorption spectroscopy, scanning electron microscopy (SEM) and cyclic voltammetry (CV). Corrosion tests of these coatings were carried out in aqueous 3% NaCl solution by using open circuit potential (OCP) measurements, potentiodynamic polarization technique, cyclic potentiodynamic polarization measurements and electrochemical impedance spectroscopy (EIS). The results reveal that POA-DBSA acts as a corrosion protective coating on steel and reduces the corrosion rate (CR) of steel almost by a factor of 14.5.     

Improved corrosion resistance of AZ91D magnesium alloy coated by novel cold-sprayed Zn-HA/Zn double-layer coatings

In order to improve the corrosion resistance and bioactivity of biodegradable Mg alloy substrate, novel Zn-HA/Zn double-layer coatings with different HA/Zn ratios in weight were deposited on AZ91D substrates by cold spraying. Phase compositions and microstructures of as-sprayed coatings and coatings after corrosion tests were analyzed by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). Electrochemical corrosion behaviors of both Zn-HA/Zn double-layer coatings were investigated in Hanks’ simulated body fluid using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). Results showed that both the pure Zn coating and HA/Zn composite coatings presented the similar phase compositions with their primary powders in addition to Zn oxidizations. Zn powders were plastically deformed and partially oxidized due to its low melting point, while HA powders were mainly crashed into fragments and hill-like splats. Both Zn under layer and HA/Zn upper layer were well bonded and presented dense structures, differences in HA/Zn upper layers were related to the HA/Zn ratios. Potentiodynamic polarization and EIS measurements illustrated that the cold-sprayed Zn-HA/Zn double-layer coatings not only improve the corrosion resistance of Mg alloy substrates, but also enhance its bioactivity due to the HA existed in composite upper layer.     

Effect of cerium concentration on microstructure,morphology and corrosion resistance of cerium–silica hybrid coatings on magnesium alloy AZ91D

The aim of this work was to investigate the effect of cerium concentration on microstructure, morphology and anticorrosion performance of cerium–silica hybrid coatings on magnesium alloy AZ91D. Vinyltriethoxysilane (VETO) and γ-glycidoxypropyltrimethoxysilane (GPTMS) were employed as precursors to prepare sol–gel based silica coating. Cerium nitrate hexahydrate as dopant in five different concentrations was added into the silica coatings. Fourier transform infrared (FT-IR) spectrum analysis, viscosity measurements and scanning electron microscopy (SEM) were employed to characterize the microstructure and morphology of these coatings. It was found that with the increase of cerium concentration, the degree of decomposition of silane chains in the coating network increased. The corrosion resistance of the cerium–silica hybrid coatings was estimated by electrochemical impedance spectroscopy (EIS) measurements and potentiodynamic polarization tests. The results demonstrated that corrosion resistance of coatings initially increases and then decreases as cerium concentration goes up. When the cerium concentration is 0.01 M, corrosion resistance reaches its maximum.     

Corrosion protective poly(o-ethoxyaniline) coatings on copper

Poly(o-ethoxyaniline) (POEA) coatings were synthesized on copper (Cu) by electrochemical polymerization of o-ethoxyaniline in aqueous salicylate solution by using cyclic voltammetry. These coatings were characterized by cyclic voltammetry, UV-vis absorption spectroscopy, Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM). The performance of POEA as protective coating against corrosion of Cu in aqueous 3% NaCl was assessed by the potentiodynamic polarization technique and electrochemical impedance spectroscopy (EIS). The results of the potentiodynamic polarization and EIS studies demonstrate that the POEA coating has ability to protect the Cu against corrosion. The corrosion potential was about 0.330 V versus SCE more positive in aqueous 3% NaCl for the POEA coated Cu than that of uncoated Cu and reduces the corrosion rate of Cu almost by a factor of 140.     

Synthesis and Characterization of Water-Based Epoxy-Acrylate/Graphene Oxide Decorated with Fe3O4 Nanoparticles Coatings and Its Enhanced Anticorrosion Properties

ABSTRACT

In this article, water-based epoxy–acrylate (EP/AC) emulsion coatings and its nanocomposites with Fe₃O₄ nanoparticles, graphene oxide nanosheets and graphene oxide which was decorated with Fe₃O₄ nanoparticles were synthesized. This was executed by means of a pre-emulsion seeded semi-batch emulsion polymerization handle with a blend of conventional anionic surfactant (Polyalkylene glycol ether sulfate, ammonium salt-EXOSEL 20 S) and typical nonionic type emulsifier (Octylphenol polyoxyethylene ether OP-10) for emulsion polymerization (schematic 1). Prepared nanoparticles were investigated with different analyzing methods like FT-IR, XRD, SEM-EDAX and TGA. The impact of the distinctive nanostructures in an (EP/AC) resin, on coated steel panels with the features of corrosion conservation, was investigated by the test of electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization. Morphology of surface and thermal behavior of nanocomposite tests were executed using surface filtering electron microscopy (FE-SEM) and thermal gravimetric analysis (TGA). Different analyses resulted from nanostructures and nanocomposites approved very good dispersion of fillers in nanocomposite beads. Besides, they indicate the effective role of nanoparticles especially graphene oxide which was decorated with Fe₃O₄ nanoparticles in corrosion resistance of water-based EP/AC coatings and other properties of coated instances.     

Mica/polypyrrole (doped) composite containing coatings for the corrosion protection of cold rolled steel

Micas/polypyrroles (PPys) doped with molybdate, p-toluene sulfonate, dodecyl benzene sulfonate, and 2-naphthalene sulfonate composite pigments were synthesized by chemical oxidative polymerization and characterized in coatings for corrosion protection on cold rolled steel substrate by various electrochemical techniques. Synthesized composite pigments were characterized for morphology by scanning electron microscopy, which indicated physical formation of PPy on the surface of mica. Chemical composition of the composite pigments was analyzed by X-ray photoelectron spectroscopy which chemically confirmed doped PPy formation on the mica surface. Coatings were formulated at 20% pigment volume concentration (composite pigments or as-received mica pigment) and were applied on cold rolled steel substrate. Coatings were exposed to salt spray test conditions (ASTM B117) for 30 days and were periodically assessed for corrosion with electrochemical impedance spectroscopy (EIS), open circuit potential (OCP), and potentiodynamic polarization. EIS and circuit modeling results demonstrated higher coating resistance (R _c) for mica/PPy (doped) composite coatings as compared to as-received mica pigment containing coating after 30 days of salt spray exposure. Lower current density and more positive corrosion potential values were observed for mica/PPy (doped) composite coatings as compared to mica pigment-based coating in potentiodynamic polarization measurements, indicating improved corrosion protection for cold rolled steel substrate. OCP measurements revealed more positive values for mica/PPy (doped) composite coatings as compared to mica pigment-based coating suggesting superior corrosion protection for mica/PPy (doped) composites.     

Preparation of transparent nanocomposites from UV‐ and thermo‐curable epoxyacrylate and graphene oxide for the application of corrosion protection coatings

In this study, we report UV‐ and thermo‐curable epoxyacrylate/graphene oxide (EA/GO) nanocomposites that present good transparency, excellent pencil hardness and promising improvement in corrosion protection. A dual‐curable EA oligomer with one terminal epoxide and one double bond at the other end was synthesized by reaction of diglycidyl ether of bisphenol‐A and acrylic acid. After mixing EA and GO with the curing agents and reactive diluent followed by UV cure and thermo‐cure, the resulting EA/GO films on a glass slide with GO loading up to 3 phr exhibited over 86% light transmittance. Furthermore, the pencil hardness was enhanced from 3H for EA to 6H for the EA/GO composite at 2 phr GO loading. The corrosion protection of the EA/GO coatings was evaluated by a potentiodynamic polarization technique and electrochemical impedance spectra. The corrosion potential (E_corr) of the EA/GO‐coated steel increased with increasing GO loading. Meanwhile, Nyquist and Bode plots indicated that the higher the GO content in the EA/GO coating was, the higher was the coating resistance and also the charge transfer resistance after immersion in salt solution. All these results proved that the GO had positive effects on enhancement of the corrosion resistance. The improved corrosion protection by the EA/GO coatings was mainly due to the enhanced hydrophobicity, the deviation of electron transfer and the increased tortuosity of the diffusion path. The improved corrosion protection and hardness together with the useful dual‐curability make the EA/GO nanocomposite a competitive candidate for corrosion protection coatings. © 2019 Society of Chemical Industry     

3种溶液体系中镁合金微弧氧化研究第一部分——氧化膜的相组成及其耐蚀性

利用直流脉冲方法在3种溶液体系中于AZ91D镁合金表面制得了微弧氧化陶瓷膜,分析了各膜层的厚度、显微硬度、相组成和耐蚀性能。结果表明,不同体系中的膜层增厚速率不同,形成膜层的相关成分也不同。通过比较微弧氧化前后镁合金的动电位极化曲线和交流阻抗发现,处理后的AZ91D镁合金的耐蚀性得到了明显改善。     

稀土盐对水性锌铝合金涂层的微观结构与耐蚀性能的影响

研究了稀土盐对水性锌铝合金涂层的组织结构和耐蚀性能的影响.扫描电镜、能谱和X射线衍射分析表明,合金涂层由片层状的锌和铝紧密构成,在片层间存在致密的稀土转化膜;中性盐雾试验、电化学阻抗谱(EIS)和极化曲线测试表明,当Ce(NO3)3的含量为5 g/L时,涂层耐盐雾腐蚀时间达到600h,是没有加入稀土的涂层的2倍.含稀土盐的涂层的高耐蚀性与其中形成的硅烷-稀土协同钝化作用有关.     

Performance of EP/PpPDA and EP/PpPDA/SiO2 nanocomposite on corrosion inhibition of steel in hydrochloric acid solution

Epoxy-poly p-phenylendiamine (EP/PpPDA) and its nanocomposite with SiO₂ nanoparticles (EP/PpPDA/SiO₂) were synthesized and tested as potential corrosion inhibitors of steel in 1 M HCl solution. Performance of EP/PpPDA/SiO₂ and EP/PpPDA coatings on protection of steel against corrosion was investigated using potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), and Atomic force microscopy (AFM) and at various temperatures between 298 and 328 K. Changes in the coating resistance and charge-transfer resistance with temperature were analyzed to determine the activation energies of the processes involved. The determined values of activation energy showed that the EP/PpPDA/SiO₂ coating has better anti-corrosion effect than EP/PpPDA. The thermodynamic functions of dissolution processes were also calculated and discussed. The results from AFM observations indicated that the presence of SiO₂ nanoparticles increased the roughness of Epoxy-poly p-phenylendiamine/SiO₂ nanocomposite (EP/PpPDA/SiO₂). It was finally concluded that the presence of silica nanoparticles enhance the protection properties of EP/PpPDA coating as a novel potential corrosion inhibitor for steel.