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This research aimed to create a substrate-coating system based on zinc and an epoxy resin incorporating modified graphene oxide, which possesses two key characteristics: effective resistance against corrosion and the ability to harness photocatalytic properties. Furthermore, correlations between the anti-corrosion properties and the photocatalytic behaviour of the coatings were made. Thin epoxy (EP) layers embedding 0.1 wt% graphene oxide (GO), reduced graphene oxide (rGO), and modified graphene oxide with (3-aminopropyl)-triethoxysilane (APTES) or poly(amidoamine) (PAMAM) dendrimer were applied on a zinc (Zn) substrate using the dip-coating method. Anti-corrosion properties of coated Zn samples were investigated through electrochemical impedance spectroscopy (EIS) measurements. They showed that the corrosion protection effect is more prominent for EP containing functionalized GO, the highest in the case of GO-PAMAM. The results of the EIS measurements indicated also that the corrosion protection provided by EP-rGO is smaller than that of EP. The photocatalytic properties of the coatings were studied by exposure of the samples to Methylene Blue (MB) solution followed by monitoring the model dye degradation through UV-Vis measurements. To determine the changes in the anti-corrosion properties due to photocatalysis, the coated Zn samples were put through additional EIS measurements. The same coatings applied to a glass substrate lacked photocatalytic properties, indicating that the Zn substrate is accountable for the degradation of MB. Furthermore, the incorporation of GO or functionalized GO into the coating amplifies this effect. From EIS spectra, it was determined that the protective properties loss observed after 3 days is due to coating delamination during exposure to MB solution, the EP-GO-APTES retaining the best adhesion of the coating, 98% remaining on Zn after a cross-hatch test. The corrosion measurements were complemented by examining the morphology and structure of the coatings and the modified GO particles. All things considered, the Zn/EP-GO-APTES system shows the best ability to break down organic pollutants, keeping a good anti-corrosive property and adhesion.
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Nanocomposites are high-performance materials with exceptional characteristics that possess properties that their individual constituents, by themselves, cannot provide. They have useful applications in many fields, ranging from membrane processes to fuel cells, biomedical devices, and anti-corrosion protection. Well-tailored nanocomposites are promising materials for anti-corrosion coatings on metals and alloys, exhibiting simple barrier protection or even smart auto-responsive and self-healing functionalities. Nanocomposite coatings can be prepared by using a large variety of matrices and reinforcement materials, often acting in synergy. In this context, recent advances in the preparation and characterization of corrosion-resistant nanocomposite coatings based on metallic, polymeric, and ceramic matrices, as well as the incorporation of various reinforcement materials, are reviewed. The review presents the most important materials used as matrices for nanocomposites (metals, polymers, and ceramics), the most popular fillers (nanoparticles, nanotubes, nanowires, nanorods, nanoplatelets, nanosheets, nanofilms, or nanocapsules), and their combinations. Some of the most important characteristics and applications of nanocomposite coatings, as well as the challenges for future research, are briefly discussed.
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In practice, metal structures are frequently transported or stored before being used. Even in such circumstances, the corrosion process caused by environmental factors (moisture, salty air, etc.) can occur quite easily. To avoid this, metal surfaces can be protected with temporary coatings. The objective of this research was to develop coatings that exhibit effective protective characteristics while also allowing for easy removal, if required. Novel, chitosan/epoxy double layers were prepared on zinc by dip-coating to obtain temporary tailor-made and peelable-on-demand, anti-corrosive coatings. Chitosan hydrogel fulfills the role of a primer that acts as an intermediary between the zinc substrate and the epoxy film to obtain better adhesion and specialization. The resulting coatings were characterized using electrochemical impedance spectroscopy, contact angle measurements, Raman spectroscopy, and scanning electron microscopy. The impedance of the bare zinc was increased by three orders of magnitude when the protective coatings were applied, proving efficient anti-corrosive protection. The chitosan sublayer improved the adhesion of the protective epoxy coating. The structural integrity and absolute impedance of the protective layers were conserved in both basic and neutral environments. However, after fulfilling its lifespan, the chitosan/epoxy double-layered coating could be removed after treatment with a mild acid without damaging the substrate. This was because of the hydrophilic properties of the epoxy layer, as well as the tendency of chitosan to swell in acidic conditions.
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The dissolution of the main metals (Cu, Zn, Sn, Pb and Fe) found in waste printed circuit boards (WPCBs) was investigated by electrochemical corrosion measurements (potentiodynamic polarization and electrochemical impedance spectroscopy (EIS)) in different bromide-based systems that could be used as lixiviants in hydrometallurgical route of metals recovery. The analysis of the corrosion products was carried out by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) measurements. All measurements showed that the addition of bromine in the electrolyte favors to great extents the dissolution process of all studied metals as compared to bromine-free electrolytes. In the investigated experimental conditions, the highest dissolution rates of the metals were obtained in acidic KBr solution containing 0.01 mol/L bromine and they decreased in the following order: Zn >> Sn > Pb > Fe > Cu. The XRD and XPS chemical assessment allowed the identification of the dissolution products formed on the metallic surfaces after exposure to the electrolytes. They consisted mainly of oxides in the case of Cu, Zn, Sn and Fe, while the presence of PbBr2 was also noticed on the lead surface. Based on the results of EIS and surface investigations, several models explaining the corrosion behavior of the metals were proposed and discussed. The obtained results demonstrate that all studied metals could be successfully leached using brominated solutions, providing a viable alternative for the selective and efficient recovery of the base metals from WPCBs through a multi-step hydrometallurgical processing route.
RESUMEN
Chitosan (Chit) coatings were applied on zinc substrates by the dip-coating method. Subsequently, the coatings were impregnated with a corrosion inhibitor, 2-Acetylamino-5-mercapto-1,3,4-thiadiazole (AcAMT) to obtain an increased anticorrosive effect. The coating thickness and the AcAMT accumulation were determined using UV-Vis spectroscopy on glass and quartz substrates, respectively. The surface morphology and coverage were investigated with atomic force microscopy. Electrochemical impedance spectroscopy and potentiodynamic polarization techniques were used to investigate the protective properties of the impregnated coatings. The chitosan coatings facilitated the accumulation of the corrosion inhibitor inside the polymeric matrix (a multiplication of 380 times compared to the impregnating solution concentration was calculated), channeling high amounts of AcAMT to the Zn surface, which resulted in an inhibition efficiency of >90%. This effect demonstrates the applicability of chitosan coatings as carriers for corrosion inhibitors, significantly reducing the amount of inhibitor needed to achieve good anticorrosive effects.
Asunto(s)
Quitosano/química , Materiales Biocompatibles Revestidos/química , Corrosión , Tiadiazoles/química , Zinc/química , Espectroscopía Dieléctrica , Ensayo de Materiales , Microscopía de Fuerza Atómica , Estructura Molecular , Análisis Espectral , Propiedades de SuperficieRESUMEN
Four different samples of ordered mesoporous silica powders (MCM-41 and SBA-15) and amino-functionalized mesoporous silica (MCM-41-NH2 and SBA-15-NH2) were used to prepare modified glassy carbon electrodes coated with ion-exchange polymer Nafion to be used for the electrochemical detection of Cd(II). The mesoporous silica samples were characterized through transmission electron microscopy, small-angle X-ray scattering, and N2-adsorption/desorption isotherms. The electrodes were characterized by using square wave anodic stripping voltammetry. The effect of pH and of the silica type on the electrodes' response was investigated. The influence of amino functional groups grafted on the silica surface toward Cd(II) ion detection was also examined. The detection limits determined with the new silica-modified electrodes [between 0.36 and 1.68 µM Cd(II)] are slightly higher than those reported in the literature, but they are lower than those stipulated in the European legislation [45 µM Cd(II)] and, consequently, the electrodes could be successfully used to detect Cd(II) in aqueous solutions.
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Chitosan (Chit) coatings were prepared on zinc and glass substrates by dip-coating method. The coatings were impregnated with a non-toxic compound, indigo carmine (IC). The novel, eco-friendly, IC-loaded chitosan coatings were characterized morpho-structurally, and their corrosion protection behavior was investigated using potentiodynamic polarization and electrochemical impedance spectroscopy techniques. The surface properties of the coated samples were evaluated by wettability measurements. The thickness of the native chitosan layers and the stability of the impregnated layers in terms of dye release on glass substrates were studied by UV-vis spectrophotometry. The good corrosion inhibiting efficiency of the coatings (>90%) was attributed to the ionic crosslinking of the positively charged Chit with negatively charged IC. The Chit-IC coatings can be successfully used as model systems for chitosan-based coatings incorporating ionic inhibitors and in less demanding applications, such as temporary protective coatings for metals, removable on demand by scrubbing with mild acidic solutions.
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A new carbon paste electrode (CPE) incorporating Ru - nanoparticles (RuNP) stabilized on graphite powder was developed for H(2)O(2) amperometric detection. Cyclic voltammetric measurements, performed in phosphate buffer solutions at different potential scan rates and different potential ranges were carried out in order to evaluate the electrochemical behavior of the CPE-RuNP modified electrodes. From amperometric measurements performed at -0.1 V vs. Ag/AgCl, KClsat, the electrocatalytic efficiency toward H(2)O(2) reduction was evaluated and it was found in the range: 28.47% (CPE) < 94.81% (CPE-RuNP (2.5:1)) < 118.19 % (CPE-RuNP (2.5:3)) < 152.43% (CPE-RuNP (2.5:2), recommending the new electrodes as promising sensors for hydrogen peroxide detection.