Corrosion Protection of Aluminum Alloy 2024-T3 by Vanadate Conversion Coatings

CORROSION ◽  
2004 ◽  
Vol 60 (3) ◽  
pp. 284-296 ◽  
Author(s):  
H. Guan ◽  
R. G. Buchheit

Abstract In this paper, the formation, chemistry, morphology, and corrosion protection of a new type of inorganic conversion coating is described. This coating, referred to as a vanadate conversion coating (VCC), forms on aluminum alloy substrates in a matter of minutes during simple immersion in aqueous vanadate-based solutions at ambient temperatures. VCCs are yellow in color and conformal across the surface of aluminum alloy 2024-T3 (AA2024-T3 [UNS A92024]) substrates. Auger electron sputter depth profiles and x-ray absorption near-edge spectroscopy show that VCCs formed by a 3-min immersion are 300 nm to 500 nm thick and consist of a mixture of vanadium oxides and other components in the coating bath. In anodic polarization experiments conducted in aerated chloride solutions, VCCs increase the pitting potential and decrease the rate of oxygen reduction. When characterized by electrochemical impedance spectroscopy, VCCs demonstrate a low-frequency impedance between 1 MΩ-cm2 and 2 MΩ-cm2 after 24 h exposure to aerated 0.5 M sodium chloride (NaCl) solutions. In salt spray testing conducted according to ASTM B117, VCCs suppress formation of large pits for more than 168 h. VCCs also appear to be self-healing. Analysis of solution in contact with VCCs by inductively coupled plasma emission spectroscopy indicates that vanadate is released into solution upon exposure. Vanadium deposits were identified by x-ray microchemical analysis on a bare alloy substrate held in close proximity to a vanadate conversion-coated surface, and corrosion resistance of this bare surface was observed to increase during exposure. An important component of VCC formation appears to involve inorganic polymerization of V5+, which leads to the buildup of a film that passivates the surface and inhibits corrosion.

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
N. Kumar ◽  
A. Jyothirmayi ◽  
R. Subasri

A hybrid sol synthesized from an acid-catalyzed hydrolysis and condensation reaction of 3-glycidoxypropyltrimethoxysilane (GPTMS) and zirconium n-propoxide was used as a matrix nanocomposite sol. To this sol, 0.01 M Ce3+ was added as an inhibitor to provide a self-healing coating system. The effect of an atmospheric air plasma surface pretreatment of aluminum alloy substrates prior to coating deposition of Ce3+-doped/undoped GPTMS-ZrO2 sol was studied with respect to corrosion protection. Coatings were generated by a dip coating technique employing a withdrawal speed of 5 mm/s and thermally cured at 130° C for 1 h. The coated Al surfaces were characterized using potentiodynamic polarization studies and electrochemical impedance spectroscopy. They were also subjected to accelerated corrosion testing using neutral salt spray test with 5% NaCl solution after creating an artificial scratch for more than 200 hours to assess the self-healing ability of coatings. It was observed that cerium (III) doping was effective for corrosion protection during long-term exposure to the electrolyte solution, and a plasma surface pretreatment of substrates prior to coating deposition of Ce3+-doped coatings improved the adhesion of coatings that provides enhanced corrosion protection along with self-healing ability exhibited in case of damages/scratches caused in the coating.


Metals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 337
Author(s):  
Ewa Wierzbicka ◽  
Marta Mohedano ◽  
Endzhe Matykina ◽  
Raul Arrabal

REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) regulations demand for an expedient discovery of a Cr(VI)-free alternative corrosion protection for light alloys even though the green alternatives might never be as cheap as current harmful technologies. In the present work, flash- plasma electrolytic oxidation coatings (FPEO) with the process duration < 90 s are developed on AZ31B alloy in varied mixtures of silicate-, phosphate-, aluminate-, and fluoride-based alkaline electrolytes implementing current density and voltage limits. The overall evaluation of the coatings’ anticorrosion performance (electrochemical impedance spectroscopy (EIS), neutral salt spray test (NSST), paintability) shows that from nine optimized FPEO recipes, two (based on phosphate, fluoride, and aluminate or silicate mixtures) are found to be an adequate substitute for commercially used Cr(VI)-based conversion coating (CCC). The FPEO coatings with the best corrosion resistance consume a very low amount of energy (~1 kW h m−2 µm−1). It is also found that the lower the energy consumption of the FPEO process, the better the corrosion resistance of the resultant coating. The superb corrosion protection and a solid environmentally friendly outlook of PEO-based corrosion protection technology may facilitate the economic justification for industrial end-users of the current-consuming process as a replacement of the electroless CCC process.


2012 ◽  
Vol 75 (1-2) ◽  
pp. 8-13 ◽  
Author(s):  
J. Carneiro ◽  
J. Tedim ◽  
S.C.M. Fernandes ◽  
C.S.R. Freire ◽  
A.J.D. Silvestre ◽  
...  

2016 ◽  
Vol 710 ◽  
pp. 216-221 ◽  
Author(s):  
Wagner Izaltino Alves Dos Santos ◽  
Isolda Costa ◽  
Célia Regina Tomachuk

New treatments for replacement of chromate require lower toxicity and corrosion protection. This study aims to investigate the influence of the combination of a Ce conversion coating (CCCe) with glycol molecules on the corrosion resistance of the AA2024-T3 clad (AA1230). The corrosion resistance of surface treated and untreated samples was evaluated by electrochemical techniques (electrochemical impedance spectroscopy, polarization tests and open circuit potential). These tests were complemented by salt spray tests to accelerate the corrosive effects of weathering. The surfaces were analyzed after corrosion tests by scanning electron microscopy with X-ray energy dispersive detector (SEM - EDX). The results of the CCCe samples in combination with glycol were compared with that of the surface with chromate layer and the results showed that the CCCe treatment is a candidate for replacement of chromating with the advantage that it does not generate toxic residues. The self-healing capacity of the new treatment tested was indicated by the increased formation of corrosion products deposition on top of Fe rich intermetallis in the AA1230 clad with time of exposure to the electrolyte.


2021 ◽  
Vol 8 ◽  
Author(s):  
Wen Zhu ◽  
Furui Chen ◽  
Youbin Luo ◽  
Zhijun Su ◽  
Wenfang Li ◽  
...  

In this study, a vanadium (V) and tannic acid-based composite conversion coating (VTACC) was prepared on 6063 aluminum alloy (AA6063) to increase its corrosion resistance. The surface morphology and compositions of the VTACCs were characterized using scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), and X-ray photoelectron spectroscopy (XPS). The corrosion resistance of the coatings was investigated by linear polarization and electrochemical impedance spectra (EIS). The self-healing ability of the coating was detected by SEM, EDS, and scanning vibrating electrode technique (SVET) measurements. The coating mainly consisted of metal oxides, including Al2O3, VO2, V2O3, and V2O5, and metal organic complexes (Al and V-complexes). The electrochemical measurement results indicated that the best corrosion resistance of VTACC was acquired when the treatment time was 12 min. Furthermore, because a new coating with vanadium rich oxide was developed on the scratch area, artificial scratch VTACC surfaces were repaired after several days of immersion in 3.5-wt% NaCl solution.


2021 ◽  
Vol 8 ◽  
Author(s):  
Peter Rodič ◽  
Sandrine Zanna ◽  
Ingrid Milošev ◽  
Philippe Marcus

This study aimed to synthesise and characterise two types of sol-gel acrylic coatings: one based on Si and the other based on Si and Zr. These coatings, which served as a barrier for corrosion protection of aluminium, were synthesised by sol-gel methodology using silicon precursors tetraethyl orthosilicate and organically modified silicon precursor 3-methacryloxypropyltrimethoxysilane, without and with the addition of zirconium(IV) n-propoxide chelated with methacrylic acid. The synthesis process was followed using real-time Fourier transform infrared spectroscopy, which confirmed the condensation reactions of Si–O–Si and Si–O–Zr networks, depending on the sol type. This was reflected in the composition of the coating as well, as shown by X-ray photoelectron spectroscopy. The coating topography, thickness and morphology were analysed using focused ion beam scanning electron microscopy. X-ray photoelectron spectroscopy was employed to follow the degradation of acrylic coatings upon immersion in sodium chloride solution. Corrosion properties, evaluated using electrochemical impedance spectroscopy in 0.1 M NaCl, confirmed high barrier protection of coated aluminium with acrylic coatings based on Si and even better for coating based on Si with Zr. The more durable corrosion protection of the latter was also confirmed by salt spray testing.


Metals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 89
Author(s):  
Wei Yuan ◽  
Qian Hu ◽  
Jiao Zhang ◽  
Feng Huang ◽  
Jing Liu

This study modified graphene oxide (GO) with hydrophilic octadecylamine (ODA) via covalent bonding to improve its dispersion in silicone-modified epoxy resin (SMER) coatings. The structural and physical properties of ODA-GO were characterized by field-emission scanning electron microscopy (FE-SEM), X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and contact angle tests. The ODA-GO composite materials were added to SMER coatings by physical mixing. FE-SEM, water absorption, and contact angle tests were used to evaluate the physical properties of the ODA-GO/SMER coatings, while salt spray, electrochemical impedance spectroscopy (EIS), and scanning Kelvin probe (SKP) methods were used to test the anticorrosive performance of ODA-GO/SMER composite coatings on Q235 steel substrates. It was found that ODA was successfully grafted onto the surfaces of GO. The resulting ODA-GO material exhibited good hydrophobicity and dispersion in SMER coatings. The anticorrosive properties of the ODA-GO/SMER coatings were significantly improved due to the increased interfacial adhesion between the nanosheets and SMER, lengthening of the corrosive solution diffusion path, and increased cathodic peeling resistance. The 1 wt.% ODA-GO/SMER coating provided the best corrosion resistance than SMER coatings with other amounts of ODA-GO (including no addition). After immersion in 3.5 wt.% NaCl solution for 28 days, the low-frequency end impedance value of the 1 wt.% ODA-GO/SMER coating remained high, at 6.2 × 108 Ω·cm2.


Metals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 930
Author(s):  
Juan Jesús Alba-Galvín ◽  
Leandro González-Rovira ◽  
Francisco Javier Botana ◽  
Maria Lekka ◽  
Francesco Andreatta ◽  
...  

The selection of appropriate surface pretreatments is one of the pending issues for the industrial application of cerium-based chemical conversion coatings (CeCC) as an alternative for toxic chromate conversion coating (CrCC). A two-step surface pretreatment based on commercial products has been successfully used here to obtain CeCC on AA2024-T3 and AA7075-T6. Specimens processed for 1 to 15 min in solutions containing CeCl3 and H2O2 have been studied by scanning electron microscopy coupled with energy-dispersive X-ray analysis (SEM-EDX), glow discharge optical emission spectroscopy (GDOES), potentiodynamic linear polarization (LP), electrochemical impedance spectroscopy (EIS), and neutral salt spray (NSS) tests. SEM-EDX showed that CeCC was firstly observed as deposits, followed by a general coverage of the surface with the formation of cracks where the coating was getting thicker. GDOES confirmed an increase of the CeCC thickness as the deposition proceed, the formation of CeCC over 7075 being faster than over 2024. There was a Ce-rich layer in both alloys and an aluminum oxide/hydroxide layer on 7075 between the upper Ce-rich layer and the aluminum matrix. According to LP and EIS, CeCC in all samples offered cathodic protection and comparable degradation in chloride-containing media. Finally, the NSS test corroborated the anti-corrosion properties of the CeCC obtained after the commercial pretreatments employed.


Polymers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1578 ◽  
Author(s):  
Haijuan Yang ◽  
Qiufeng Mo ◽  
Weizhou Li ◽  
Fengmei Gu

An organic coating is commonly used to protect metal from corrosion, but it is prone to failure due to microcracks generated by internal stress and external mechanical action. The self-healing and self-lubricating achieved in the coating is novel, which allows an extension of life by providing resistance to damage and repair after damage. In this study, a new approach to microencapsulating bifunctional linseed oil with polyurethane shell by interfacial polymerization. Moreover, the self-healing and self-lubricating coatings with different concentrations of microcapsules were developed. The well-dispersed microcapsules showed a regular spherical morphology with an average diameter of ~64.9 μm and a core content of 74.0 wt.%. The results of the salt spray test demonstrated that coatings containing microcapsules still possess anticorrosion, which is improved with the increase of microcapsules content, after being scratched. The results of electrochemical impedance spectroscopy showed a |Z|f=0.01Hz value of 104 Ω·cm2 for pure epoxy coating after being immersed for 3 days, whereas the coating with 20 wt.% microcapsules was the highest, 1010 Ω·cm2. The results of friction wear showed that the tribological performance of the coating was enhanced greatly as microcapsule concentration reached 10 wt.% or more, which showed a 86.8% or more reduction in the friction coefficient compared to the pure epoxy coating. These results indicated that the coatings containing microcapsules exhibited excellent self-healing and self-lubricating properties, which are positively correlated with microcapsules content.


2017 ◽  
Vol 22 (2) ◽  
pp. 17
Author(s):  
Karín Paucar Cuba ◽  
Hugo Rojas Flores ◽  
Abel Vergara Sotomayor

El estudio de la resistencia a la corrosión del anodizado de una aleación de aluminio (AA6063) en ácido sulfúrico a diferentes tiempos de anodizado: 30, 45 y 60 min. se realizó usando la espectroscopia de impedancia electroquímica (EIE) y el ensayo de niebla salina ácida. (ASTM B287). Los datos obtenidos por EIE y su correlación con los circuitos equivalentes más apropiados permitieron determinar los parámetros asociados a la capa porosa y a la capa barrera del óxido protector formado sobre la superficie del aluminio en estudio. La exposición de las muestras anodizadas durante 250h a una niebla salina ácida permitió observar variaciones en su masa. De los resultados obtenidos por EIE y las pérdidas de masa de las muestras anodizadas se estableció que la película de anodizado de 45 minutos mostró una mayor resistencia a la corrosión en comparación con la obtenida a 60 y 30 min., respectivamente. Palabras clave.- Aluminio, Anodizado, Impedancia electroquímica, Niebla salina ácida. ABSTRACTThe study of the corrosion resistance of anodized on aluminum alloy (AA6063) in sulfuric acid to different times: 30, 45 and 60 min. was performed using electrochemical impedance spectroscopy (EIS) and the acid salt spray test (ASTM B287). The EIS’data and its correlation with the most appropriate equivalent circuits allowed to determine the parameters associated with the porous layer and the oxide layer protective barrier formed on the aluminum surface under study. Exposure of the samples anodized for a 250h salt spray acid allowed to observe changes in their mass. From the results obtained by EIS and the mass losses of the anodized samples was established that the anodized film of 45 minutes showed higher corrosion resistance compared to that obtained at 60 and 30 min, respectively. Keywords.- Aluminum, Anodized, Electrochemical impedance, Acid salt spray.


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