Formation of corrosion resistant plasma electrolytic oxidation coatings on aluminium alloy with addition of sodium tungstate species

Plasma electrolytic oxidation (PEO) coatings were formed in silicate based electrolytes without and with the addition of sodium tungstate on AA?6063 aluminium alloy. Microstructure, composition and corrosion resistance of PEO coatings were investigated by scanning electron microscopy, X-ray diffraction and electrochemical impedance spectroscopy and potentiodynamic polarisation test respectively. The effects of additive sodium tungstate were examined. The results showed that the additive containing PEO coatings were of dense structure with additional phase (WO₃) and of less cracks than the additive free PEO coating. In addition, additive containing coatings were of better corrosion resistance than the additive free PEO coating, which was confirmed by electrochemical impedance spectroscopy and potentiodynamic polarisation tests. Furthermore, long time immersion test revealed that the PEO coated alloy with the addition of 12?g?L^??1 sodium tungstate maintained high impedance over 82?h in 3.5?wt-%NaCl, while the PEO coating without additive was unable to protect the substrate after such long time immersion.     

Investigation of wear and corrosion resistance of nanocomposite coating formed on AZ31B Mg alloy by plasma electrolytic oxidation

Ceramic-WC coatings were prepared on AZ31 B Mg alloy by plasma electrolytic oxidation (PEO) from a phosphate based bath containing suspended tungsten carbide nanoparticles at various process times. Scanning electron microscope results indicated that increase of coating time and incorporation of tungsten carbide into the ceramic coating during the PEO process led to a decrease in the number and diameter of coating pores. Phase analysis showed that the nanocomposite coating was composed of MgO, Mg₃(PO₄)₂ and WC. Tribological properties and corrosion behaviour of uncoated AZ31 B Mg alloy and ceramic coatings were evaluated using a pin-on-disc tribometer and potentiodynamic polarisation technique in 3.5% NaCl solution, respectively. The wear and electrochemical tests showed that wear and corrosion resistance of ceramic-WC nanocomposite coatings were better than ceramic only ones. In addition, wear and corrosion behaviour of coatings improved with increasing the coating time.     

IFHANAL-3 Inhibited Chromate-Free Conversion Coatings on V95T2 Aluminum Alloy

Alloys in the Al–Cu–Mg–Zn system are known to be characterized with high corrosion resistance in both atmospheric and aqueous media. It was earlier demonstrated that the alkaline chromate-free converting composite IFHANAL-3 enabled one to produce coatings with protective properties not inferior to those of conventional chromate coatings on a number of aluminum alloys, including that of grade V95 with different thermal treatment. The present work was devoted to studies of the effect of different complexing agents on the oxidation process and protective properties of coatings on V95T2 alloy. The studied modifying dopants decrease the concentrations of different oxides in the composition of conversion coatings, thus facilitating the adsorption of corrosion inhibitors and improvement of their protective properties. The decrease of the oxidation temperature in the solution of IFHANAL-3 modified with inhibitors of the azol type does not ly affect protective properties of the formed coatings.     

Formation of bioactive anticorrosion coatings on resorbable implants by plasma electrolytic oxidation

Calcium phosphate coatings (Ca/P = 1.61) containing magnesium oxide MgO and hydroxyapatite Ca₁₀(PO₄)₆(OH)₂ accelerating the growth of bone tissue have been prepared by the method of plasma electrolytic oxidation (PEO) on MA8 magnesium alloy. The phase and element compositions, morphology, and anticorrosion properties of coatings were investigated. Such PEO layers were found to essentially reduce the corrosion rate of magnesium alloy (polarization resistance being increased by two orders). This makes it possible to consider the formed PEO coatings as likely anticorrosion layers for medical bioresorbable implants.     

Non-chromate conversion coatings on A7075 aluminum alloy after various thermal treatment

The article discusses the studies of formation and protective properties of conversion coatings on A7075 aluminum alloy after various thermal treatment, obtained in alkaline conversion solutions. It is demonstrated, that filling of the coatings formed in the developed IFKhANAL-3 non-chromate conversion solution ting composition, in solutions of corrosion inhibitors sharply increases their protecting ability in chloride-containing mediums. The results of corrosion tests in salt-spray chamber evidence that the protective properties of such coatings are similar to those of chromate coatings.     

Environmentally assisted cracking behaviour of plasma electrolytic oxidation coated AZ31 magnesium alloy

Abstract

A wrought AZ31 magnesium alloy was plasma electrolytic oxidation (PEO) coated in phosphate and silicate based alkaline electrolytes. The effect of these PEO coatings on the stress corrosion cracking (SCC) behaviour of the alloy was investigated by slow strain rate tensile (SSRT) tests in ASTM D1384 solution. The untreated and PEO coated AZ31 magnesium alloy specimens were found to be susceptible to SCC, despite the fact that the PEO coatings offered an excellent general corrosion resistance. The results of the polarisation tests on the untreated AZ31 alloy specimen after prolonged immersion in ASTM D1384 electrolyte suggested the formation of a film on the surface constituted by the corrosion products. The cracking of this film and the evolution/ingress of hydrogen at these defective sites during the SSRT tests in the corrosive environment was believed to be responsible for the SCC of the untreated alloy. Similarly, the cracking of the PEO coatings during the SSRT test, the consequent exposure of the underneath magnesium alloy substrate and the associated electrochemical reactions were attributed as reasons for the SCC of the PEO coated specimens. The transgranular mode of fracture in all the cases avowed that the hydrogen induced cracking was the mechanism of SCC.     

The effect of MEVVA ion implantation of Zr on the corrosion behaviour of PVD TiN coatings

The use of TiN coatings as corrosion barriers is limited by the presence of defects such as pin-holes. In this study Zr ions were implanted into PVD deposited TiN coatings at varying doses, to improve the corrosion resistance. The corrosion behaviour was assessed in saline environments using linear polarisation techniques and the corroded surface of the coatings characterised using XPS and SEM. Overall, ion implantation resulted in an increase in the coating’s corrosion resistance. Protection was attributed to closure of existing pin-holes and the formation of various nitrides, oxides and oxynitrides of Ti and Zr.     

铝合金稀土磷化与铬磷化比较

采用电化学测试、全浸腐蚀试验和结合力测试,研究了6061铝合金铬磷化处理和以稀土为添加剂的磷酸盐处理所形成的化学转化膜的工艺性能。动力学研究表明,两者的成膜过程是不相同的。极化曲线测试结果显示,在弱极化区范围内,两者抗蚀性能相近,而在强极化区,铬磷化转化膜的抗蚀性优于以稀土为添加剂的磷酸盐化学处理所形成的转化膜,全浸腐蚀试验有类似的结果。结合力测试结果则表明,以稀土为添加剂的磷酸盐化学处理所形成的转化膜与有机涂层间的结合力要优于铬磷化转化膜。     

Evaluation of corrosion inhibition performance of silica sol–gel layers deposited on galvanised steel

The present work reports a comparative investigation of the electrochemical behaviour of some new types of silica sol–gel coatings with enhanced corrosion resistance deposited on electrolytically or thermally (hot-dip) zinc-coated steel. The coatings were rendered hydrophobic by silylation. Dichlorodimethylsilane or trimethylchlorosilane were used as silylating agents and cetyltrimethylammonium bromide or Pluronic PE 10300, as templating agents. The morpho-structural and optical properties of compact and mesoporous silica coatings were characterised with different methods. The corrosion behaviour of the coatings was evaluated by open circuit potential measurements, Tafel interpretation of the polarisation curves and electrochemical impedance spectroscopy. Both silylating agents improve significantly the corrosion resistance of both porous and compact coatings by reducing the corrosion current density with at least one order of magnitude. The possibility to use the porous structure of the coatings as corrosion inhibitor carriers was explored by loading of mesoporous silica layers with 1H-benzotriazole.     

Effect of Cr3+- based conversion films on the corrosion behaviour of electrodeposited composite ternary zinc alloys with embedded carbon nanotubes

ABSTRACT

Composite ternary zinc-based alloys Zn-Ni-P and Zn-Fe-P containing embedded multi-walled carbon nanotubes (CNT) were obtained electrochemically. They were treated additionally in an environmentally friendly chemical conversion solution for passivation based on Cr³⁺-compound. The surface morphology, chemical and phase composition of the coatings after their treatment in the passivating solution were determined by SEM, EDS and XRD analysis respectively. The corrosion behaviour of composite alloy deposits both with or without additional conversion film (CF) was investigated in a model corrosion medium of 5% NaCl using selected methods such as potentodynamic polarisation (PD) curves, electrochemical impedance spectroscopy (EIS) and polarisation resistance (R_p) measurements. The changes in the surface morphology and phase composition of the corrosion tested samples were determined by SEM and XRD analysis. The corrosion studies indicated that the presence of a CF leads to a delay in the anodic dissolution process during the polarisation.     

Triode plasma nitriding and PVD coating: A successful pre-treatment combination to improve the wear resistance of DLC coatings on Ti6Al4V alloy

Diamond-like carbon (DLC) coatings have found great applicability in the automotive industry because of their low friction coefficient and high wear resistance. Nevertheless, their tribological performance can be greatly reduced on soft substrates such as titanium alloys. The hard DLC coating cannot usually follow elastic and plastic deformation of the substrate without failing. In order to overcome this property mismatch between hard coating and soft substrate, triode plasma nitriding was applied as a pre-treatment to improve the mechanical properties of the Ti6Al4V alloy and further enhance the load support for the DLC coating. DLC and multilayered TiN/DLC, CrN/DLC CrAlN/DLC coatings were deposited onto “standard” and plasma nitrided Ti6Al4V substrates. Triode plasma nitriding increased the load-bearing capacity of the coating/substrate system, as higher critical adhesion loads were recorded for DLC coatings on plasma nitrided Ti6Al4V substrates. This treatment also reduced the wear rate of the DLC coating/substrate. Further load support and lower wear rates were achieved by using TiN, CrN and CrAlN as intermediate layers on plasma nitrided Ti6Al4V substrates.     

Investigation of Plasma Electrolytic Oxidation (PEO) coatings on a Zr-2.5Nb alloy using high temperature/pressure autoclave and tribological tests

A Plasma Electrolytic Oxidation (PEO) process was used to produce thin oxide coatings on a Zr-2.5 wt% Nb alloy. Effects of current density on surface morphologies and wear properties of PEO coatings were investigated and compared to the uncoated substrate and a commercially used black oxide coating. Corrosion properties at ambient and high temperature/pressure conditions were studied using potentiodynamic polarization tests and autoclave tests, respectively. Up to 30-day autoclave experiments were carried out in an aqueous condition of 300 °C and 10 MPa in 0.05 M LiOH solutions. It was found that most of the micro-pores which were produced during the PEO treatment were closed after the autoclave experiments. PEO coatings had larger weight gains in the first 10 exposure days than the black oxide coating. However, after 10 days, the corrosion rate of black oxide coating accelerated and exhibited a similar weight gain to PEO coatings after 30 days. PEO coatings prepared at low current densities had lower weight gains. Although the black oxide coating exhibited a good corrosion resistance, it had a much lower wear resistance than the PEO coatings. Compared with the uncoated substrate, all PEO coatings had a higher corrosion resistance, lower weight gain during autoclave tests and better wear resistance.     

Corrosion resistance of Ti–6Al–4V alloy with nitride coatings in Ringer’s solution

The corrosion behaviour of Ti–6Al–4V alloy with nitride coatings was investigated in Ringer’s solution at 36 and 40 °С. Nitride coatings of different composition, thickness and surface quality were formed because of changing nitrogen partial pressure from 1 to 10⁵ Ра and nitriding temperature from 850 to 900 °С. Results shown that nitride coatings improve anticorrosion properties of alloy at both solution temperatures. Corrosion resistance of alloy increases with the content increase of TiN phase in nitride coating. With increase of temperature from 36 to 40 °С the corrosion resistance of alloy is determined significantly by quality of nitride coating.     

Electrochemical corrosion behaviour and surface morphology of electrodeposited zinc,zinc–cobalt and their composite coatings

Abstract

The electrochemical behaviour as well as the surface morphology characteristics of electrodeposited Zn and Zn-Co (≈3 wt-%) alloy coatings on low carbon steel samples, with and without included nanoparticles of organic co-polymers in their structure, are discussed. Their corrosion resistance and protective properties were studied in a model corrosion medium, 5 wt-% NaCl, using electrochemical methods such as polarisation resistance (R _p) measurements and potentiodynamic (PD) polarisation curves. Scanning electron microscopy (SEM) was performed to examine the surface morphology changes of the samples before and after the corrosion treatment. Some conclusions are drawn about the influence and importance of the organic nanoparticles on the corrosion behaviour of the coatings presented.     

Effects of pre-treatments on the corrosion properties of electroless Ni-P layers deposited on AlMg2 alloy

Amorphous Ni-P layers with 8-10 wt.% phosphorus were deposited by sodium hypophosphite onto AlMg2 type aluminium alloy substrates after different pre-treatments. Prior to the electroless nickel-phosphorus (ENP) deposition in an acetate and lactic acid based nickel bath, the widely applied Zn (zincate) or Ni displacement (Ni strike) pre-treatments for aluminium substrates as well as a non-conventional surface conditioning one (soaking in a warm solution containing only hypophosphite and lactic acid) were all tested and their effects evaluated on the corrosion and other properties of the Ni-P layers developed right afterwards. The surface morphology and structure of the ENP layers were characterized by scanning electron microscopy and X-ray diffraction analysis. Polarization resistances were measured in 0.5 mol dm^− 3 Na₂SO₄ solution at pH 3. Compared to the direct electroless plating on the bare aluminium alloy AlMg2, it was found, that the hypophosphite adlayer (hypophosphite immersion pre-treatment) have also increased the corrosion resistance as the displacement pre-coatings, but without decreasing the deposition rate unlike conventional displacement methods. In the studied ENP deposition systems the decrease of corrosion rate could mainly be attributed to the lower microporosity and smoother morphology of the nickel-phosphorus coatings.     

Corrosion properties of anodic oxide coatings on Ti–6Al–4V in simulated body solution

Abstract

Anodic oxide coatings were synthesised on Ti–6Al–4V substrates using aqueous electrolytes containing dissolved calcium and phosphorus. Different coatings were produced by varying the time of synthesis. Inherent features of the coatings were studied by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). Uniform corrosion, electrochemical polarisation and ac impedance tests were performed in simulated body fluid (SBF). Small amounts of calcium and phosphorus are deposited from the electrolyte on to the coating and their levels increase with increasing duration of synthesis. Maximum values of porosity and thickness are obtained for oxides coated for 3 h. Coatings produced from shorter times showed very good resistance to the attack of SBF.     

Preparation and characterization of duplex PEO/MoC coatings on Mg-Li alloy

A combined PEO and chemical conversion process was employed to fabricate duplex plasma electrolytic oxidation/molybdate conversion (PEO/MoC) coating on the surface of Mg-Li alloy. The microstructure and composition of the composite coatings were investigated by SEM, EDX, XRD and XPS. The anti-corrosion properties of duplex PEO/MoC coatings were evaluated by potentiodynamic polarization and EIS. The duplex PEO/MoC coating was composed of crystalline NaMgF₃, Mg₂SiO₄, MoO₃ and MgO. Spherical-like microparticles accumulated and dispersed uniformly on the surface of the PEO coating. The corrosion resistance for Mg-Li alloy was improved by using a combination of plasma electrolytic oxidation and chemical conversion.     

The electrochemical behaviour of Ti‐13Nb‐13Zr alloy in various solutions

The electrochemical behaviour of a near‐β Ti‐13Nb‐13Zr alloy for the application as implants was investigated in various solutions. The electrolytes used were 0.9 wt% NaCl solution, Hanks' solution and a culture medium known as minimum essential medium (MEM) composed of salts, vitamins and amino acids, all at 37 °C. The electrochemical behaviour was investigated by the following electrochemical techniques: open circuit potential measurements as a function of time, electrochemical impedance spectroscopy (EIS) and determination of polarisation curves. The obtained results showed that the Ti alloy was passive in all electrolytes. The EIS results were analysed using an equivalent electrical circuit representing a duplex structure oxide layer, composed of an inner barrier layer, mainly responsible for the alloy corrosion resistance, and an outer and porous layer that has been associated to osteointegration ability. The properties of both layers were dependent on the electrolyte used. The results suggested that the thickest porous layer is formed in the MEM solution whereas the impedance of the barrier layer formed in this solution was the lowest among the electrolytes used. The polarisation curves showed a current increase at potentials around 1300 mV versus saturated calomel electrode (SCE), and this increase was also dependent on the electrolyte used. The highest increase in current density was also associated to the MEM solution suggesting that this is the most aggressive electrolyte to the Ti alloy among the three tested solutions.     

Organic-magnesium complex conversion coating on AZ91D magnesium alloy

An organic-magnesium complex conversion (OMCC) coating on AZ91D magnesium alloy was obtained by treating in a solution containing organic compounds. SEM, FESEM and XPS were used to examine the surface morphology, thickness and structure of the conversion coatings. The results show that the continuous and uniform conversion coating is deposited on AZ91D alloy and the main component of the coatings is organic compound containing benzene ring, which forms a chemical bond with magnesium. The polarization measurement and salt spray test show that the corrosion resistance of the conversion coating is much higher than that of traditional chromate conversion coating.     

Corrosion resistant coatings based on synergistic effects of alkaline etching and molybdate treatment for AZ31D magnesium alloy

Eco-friendly, non-toxic protective coatings deposited from molybdate–based solutions have been developed as undercoat thin-films (for subsequent organic top coats) for AZ31D magnesium alloy. Direct treatment of Mg AZ31D substrates with molybdate–based solutions has no significant effect on the overall surface resistance (charge transfer resistance). Alkaline etching of Mg AZ31D surfaces using KOH solution prior to molybdate conversion coating showed significant enhancement in the corrosion resistances The optimum conditions of alkaline etching and molybdate treatment steps have been determined. The total surface resistance was improved from 2.1?×?10³ Ω.cm² (for as-polished AZ31D) to be 3.2?×?10³ Ω.cm² for the alkaline etched samples followed by 10?g?L^?1 molybdate treatment. The resistance to localised corrosion (pitting and crevice) improved significantly after applying the alkaline etching step. Molybdate–based coatings formed on Mg AZ31D exhibited a network of flower-like and needle-like protective molybdenum oxide structures which are belived to be responsible for the improvement in the pitting and crevice corrosion resistance. They impede the corrosive media from reaching the bare metal and hence improve the pitting and crevice corrosion resistances. This simple eco-friendly, low-toxicity pretreatment approach seems very promising and effective for improving the corrosion resistance of magnesium alloys in chloride containing solutions.