Comparative study on corrosion protection properties of electroless Ni‐P‐ZrO2 and Ni‐P coatings on AZ91D magnesium alloy

Electroless Ni‐P‐ZrO₂ and Ni‐P coatings on AZ91D magnesium alloy were prepared, and their corrosion protection properties were compared in this paper. The potentiodynamic curves and electrochemical impedance spectroscopy (EIS) of the coated magnesium alloy in 3.5% NaCl solution showed that the corrosion performance of Ni‐P‐ZrO₂ composite coating was superior to that of Ni‐P coating. The same conclusion was obtained with salt spray and immersion tests. The corrosion morphologies of two kinds of coatings with various immersion time intervals in 3.5% NaCl solution indicated that most corrosion products concentrated on the nodules boundaries of Ni‐P coating and blocked corrosion pit was the main corrosion form. For the Ni‐P‐ZrO₂ coating, tortuous nodules boundaries were not the weak sites of the coating and corrosion initiated from the nickel phosphor alloy around the nanometer powders. Open corrosion pits occurred on the composite coating surface, and the coating was corroded gradually. Thus, the Ni‐P‐ZrO₂ coating exhibited better corrosion protection property to magnesium alloy substrate than Ni‐P coating.     

Impedance spectroscopy studies of electroless Ni–P matrix,Ni–W–P,Ni–P–ZrO2, and Ni–W–P–ZrO2 coatings exposed to 3.5% NaCl solution

Ni–P matrix, ternary Ni–W–P and Ni–P–ZrO₂ coatings, and quaternary Ni–W–P–ZrO₂ coatings were deposited using electroless method from a glycine bath. Their corrosion resistance was evaluated by electrochemical impedance spectroscopy (EIS) for various immersion times in a 3.5% NaCl solution. From among the investigated coatings, the ternary Ni–W–P coatings show the highest resistance to corrosion in the first hour of exposure to the 3.5% NaCl medium. An addition of ZrO₂ adversely affects the performance of both the Ni–P coatings and the Ni–W–P coatings. For all the coatings, including the ones containing tungsten, a marked decrease in pore resistance (R_por) over time is observed. This means that their corrosion resistance and capacity to protect the substrate decline. On the other hand, after 24 h immersion in the 3.5% NaCl solution the Ni–W–P coating shows the highest low‐frequency impedance modulus (|Z|_{f = 0.01 Hz}). As regards corrosion resistance, the Ni–P coatings and the Ni–W–P coatings perform best.     

Laser nanocrystallisation and corrosion behaviour of electroless Ni–W–P coating with high phosphorus content

This paper reports an investigation of microstructural characteristics in electroless Ni–3·9W–13·4P (wt.%) coating by laser nanocrystallisation using a quantitative X–ray diffraction (XRD) method and scanning electron microscopy (SEM) with energy dispersive X–ray spectroscopy (EDX). The corrosion resistance of the coatings before and after laser treatment has been evaluated in 0·5 M H₂SO₄ solution by potentiodynamic polarisation and electrochemical impedance spectroscopy (EIS) techniques. The results show that the laser treatment improves the corrosion resistance of the coatings. The corrosion mechanism has been studied and correlated to the microstructural characteristics including volume fraction of I_Ni3P/I_total, microstrain, and the crystallite size of the Ni and Ni₃P phases.     

Synthesis and passivation behavior of electroless Ni–P‐CNT composite coating

Carbon nanotubes (CNTs) have high chemical stability, unique hollow nanotube structure, and are believed to be ideal materials for fabricating composites. In this study, Ni–P and Ni–P‐CNT composite coatings were fabricated by electroless plating. Scanning electron microscopy was used to characterize the coatings. The corrosion behavior of Ni–P and Ni–P‐CNT coated samples were evaluated by polarization curves and electrochemical impedance spectroscopy in 3.5 wt% NaCl and 0.1 M H₂SO₄ aqueous solutions at room temperature. The results indicated that incorporation of CNTs in the coating significantly increased corrosion resistance. The role of CNTs in improvement of corrosion resistance of the coating was also discussed.     

The corrosion behaviour of Fe-15Mn-7Si-9Cr-5Ni shape memory alloy

The corrosion behaviour of Fe-15Mn-7Si-9Cr-5Ni (mass%) shape memory alloy at 25 °C in 0.5 M H₂SO₄ and 3.5% NaCl solutions has been studied using potentiodynamic polarization and electrochemical impedance techniques. Three different microstructures viz., single-phase γ, γ-δ and γ-Fe₅Ni₃Si₂, were produced by heat-treating the alloy in different equilibrium phase fields. The corrosion behaviour in 0.5 M H₂SO₄ solution is almost same for all three microstructures, barring a slight difference in the passivation range. Although, the passivation current in 0.5 M H₂SO₄, is in the same range as that of SS 304, the critical current required for onset of passivation is almost three orders higher and the passivation range is much shorter. In 3.5% NaCl solution the corrosion behaviour of all three microstructures of the Fe-15Mn-7Si-9Cr-5Ni shape memory alloy was that of general dissolution without passivity or localized attack (pitting). The best corrosion resistance in both H₂SO₄ and NaCl solutions is shown by the single-phase γ microstructure.     

Corrosion Performance of Laser Posttreated Cold Sprayed Titanium Coatings

The recent development of cold spray technology has made possible the deposition of highly reactive, oxygen sensitive materials, such as titanium, without significant chemical reaction of the powder, modification of particle microstructure and with minimal heating of the substrate. However, the presence of interconnected pathways (microscale porosity) within the deposit limits the performance of the metallic coating as an effective barrier to corrosion and substrate attack by corrosive media is usually inevitable. The aim of the present study was to investigate the effects of processing, including a postspray laser treatment, on the deposit microstructure and corrosion behavior. Commercially pure titanium (CP Ti) was deposited onto a carbon steel substrate, using a commercial cold spray system (CGT^TM Kinetiks^? 4000) with preheated nitrogen as both the main process gas and the powder carrier gas. Selected coatings were given a surface melting treatment using a commercial 2 kW CO₂ laser (505 Trumpf DMD). The effect of postdeposition laser treatment on corrosion behavior was analyzed in terms of pore structure evolution and microstructural changes. Optical microscopy, scanning electron microscopy, and x-ray diffraction were employed to examine the microstructural characteristics of the coatings. Their corrosion performance was investigated using electrochemical methods in 3.5 wt.% NaCl (ASTM G5-94 (2004)). As-sprayed titanium coatings could not provide favorable protection to the carbon steel substrate in the aerated NaCl solution, whereas the coatings with laser-treated surfaces provided barrier-like properties.     

Electrochemical corrosion behavior of electroless Ni–P coating in NaCl and H2SO4 solutions

Electrochemical corrosion behavior of electroless Ni–P coating in NaCl and H₂SO₄ solutions were studied by potentiodynamic polarization curves and electrochemical impedance spectra techniques, as well as the corrosion morphology was characterized. The results indicate that electroless Ni–P coating with about 25 µm is stable in 30 days immersion in NaCl solution. Although it was corroded with prolonged immersion days, the corrosive medium has not penetrated through the coating. During the H₂SO₄ concentration ranging from 5 to 10%, the corrosion current density of electroless Ni–P coating increased due to the intensified anodic dissolution process; in 15% H₂SO₄ solution, electroless Ni–P coating shows obvious anodic passivation effect.     

Corrosion of alloys and their diffusion aluminide coatings by KCl:K2SO4 deposits at 650 °C in air

P91 ferritic‐martensitic steel, 17Cr–13Ni and alloy 800 austenitic stainless steels and Inconel 617 alloy have been aluminised to form Fe₂Al₅, (Fe,Ni)Al and Ni₂Al₃ aluminide coatings. These alloys and their corresponding coatings were subjected to corrosion in air by 50:50 mol/mol K₂SO₄/KCl deposits at 650 °C for 300 h. With the exception of the Inconel 617 alloy, significant metal losses (>180 µm) were recorded. These losses were planar for P91 alloy but involved internal corrosion for the two austenitic steels. The (Fe,Ni)Al and NiAl coatings on the austenitic steels and the Inconel 617 alloy were significantly corroded via intergranular and internal chloridation–sulphidation–oxidation. In contrast, the Fe₂Al₅ coating on the P91 alloy coating was virtually unattacked. For the alloys, the relative extents of corrosion damage can be explained in terms of the stability and volatility of metal chlorides formed. For the coatings, STEM/EDS analyses enable clear linkages to be made between the presence and number of Cr‐rich particles on coating grain boundaries and the corrosion damage observed for the coatings.     

Electrochemical corrosion behaviors and protective properties of Ni–Co–TiO2 composite coating prepared on sintered NdFeB magnet

In this paper, a protective Ni–Co–TiO₂ composite coating was prepared on the sintered NdFeB magnet by direct current electrodeposition. The surface morphologies, microstructure, and chemical composition of the composite coating were studied using scanning electron microscope (SEM), X‐ray diffraction (XRD), and energy dispersive spectroscopy (EDS), respectively. The surface morphologies and microstructure analysis showed that the composite coating possessed cauliflower‐like grain colonies, and formed face‐centered cubic (fcc) solid solution. The electrochemical corrosion behaviors of the composite coating in 0.5 mol/L H₂SO₄, 0.6 mol/L NaOH, 0.6 mol/L Na₂SO₄, and neutral 3.5 wt% NaCl solutions were evaluated by potentiodynamic polarization measurements and electrochemical impedance spectroscopy (EIS), showing good protection for NdFeB magnet. In order to further investigate the protective properties of the composite coating for NdFeB magnet and the practicability of the composite coating, the long‐term immersion test was carried out in neutral 3.5 wt% NaCl solutions using EIS. The results of long‐term corrosion test showed that the Ni–Co–TiO₂ composite coating could provide long‐term protection in neutral 3.5 wt% NaCl solutions for NdFeB magnet.     

Effect of plasma surface treatment and heat treatment ambience on mechanical and corrosion protection properties of hybrid sol-gel coatings on aluminum

Hybrid sol-gel coatings derived from a base catalyzed hydrolysis of tetraethylorthosilicate and methyltriethoxysilane were deposited on aluminum substrates by a dip coating technique. Some of the coatings were deposited on substrates whose surfaces were pre-treated using atmospheric-air plasma prior to coating in order to study the effect of surface activation by plasma pre-treatment. The coated substrates were heat treated in different ambiences like air, flowing N₂ and vacuum to see the effect of heat treatment ambience on the properties of the coatings. Characterization of the coatings after heat treatment was carried out with respect to coating thickness, pencil scratch hardness, adhesion, water contact angle and their microstructure. Corrosion testing for all the coatings was carried out by electrochemical polarization measurements as well as electrochemical impedance spectroscopy in 3.5% NaCl solution for 1 h exposure time to investigate on their corrosion resistance. Coating thicknesses ranging from 1 μm-5 μm were obtained by varying the withdrawal speeds. Heat treatment in a controlled atmosphere with low oxygen content was seen to improve the hydrophobicity of coated surface, as measured by water contact angles (20^o — air; 71^o — N₂; 95^o — vacuum), thereby improving the corrosion resistance. Surface pre-treatment using open-air plasma was seen to improve the adhesion of the sol-gel coatings thus making it possible to obtain adherent and thick coatings in a single dip coating process. Both the methods of processing the coatings reduced the corrosion rate of aluminum from 1.95 mpy to 0.004 mpy in case of coatings densified in nitrogen and to 0.00068 mpy for coatings deposited on a plasma treated substrate and densified in air.     

Ni/Cu定向结构涂层在不同浓度H2SO4中的耐蚀性能

为了研究Cu元素对Ni基合金定向结构涂层耐腐蚀性能的影响,向Ni60合金粉末中添加了5%Cu(质量分数,下同),制备了定向结构Ni60/Cu复合涂层。采用电化学试验和浸泡试验,评估了涂层在不同浓度H₂SO₄溶液中的电化学腐蚀特性和浸泡腐蚀性能,探讨了涂层在不同浓度H₂SO₄溶液中的腐蚀行为。结果表明,涂层在不同浓度H₂SO₄溶液中的腐蚀均表现为活化-钝化-过钝化的过程,电化学阻抗谱在整个时间常数内具有典型的容抗特征,H₂SO₄溶液浓度从5%增至80%时,电荷转移电阻先减小后增大,涂层的耐腐蚀性呈现先降低后升高的趋势。随着H₂SO₄溶液浓度的增加,涂层表面的腐蚀程度先加剧后逐渐减缓,且在H₂SO₄溶液浓度为40%时,腐蚀电位移至最负,腐蚀电流密度增至最大。但在H₂SO₄溶液浓度达到80...     

Corrosion Properties of Cold-Sprayed Tantalum Coatings

Cold spraying enables the production of pure and dense metallic coatings. Denseness (impermeability) plays an important role in the corrosion resistance of coatings, and good corrosion resistance is based on the formation of a protective oxide layer in case of passivating metals and metal alloys. The aim of this study was to investigate the microstructural details, denseness, and corrosion resistance of two cold-sprayed tantalum coatings with a scanning electron microscope and corrosion tests. Polarization measurements were taken to gain information on the corrosion properties of the coatings in 3.5 wt.% NaCl and 40 wt.% H₂SO₄ solutions at room temperature and temperature of 80 °C. Standard and improved tantalum powders were tested with different spraying conditions. The cold-sprayed tantalum coating prepared from improved tantalum powder with advanced cold spray system showed excellent corrosion resistance: in microstructural analysis, it showed a uniformly dense microstructure, and, in addition, performed well in all corrosion tests.     

Corrosion and tribocorrosion behaviour of thermally sprayed ceramic coatings on steel

This research aims at investigating the corrosion and tribocorrosion behaviour of thermally sprayed ceramic coatings deposited on steel specimens and exposed to a 3.5% NaCl solution. The coatings have been prepared by plasma spraying Cr₂O₃ and Al₂O₃/13% TiO₂ powders on a Ni/20% Cr bond coating. Combined wear-corrosion conditions have been achieved by sliding an alumina antagonist on the lateral surface of coated steel cylinders, during their exposure to the aggressive solution.Polarization resistance values monitored during 3 days exposures and polarization curves recorded at the end of the immersion period show that both coatings only partially protect steel substrate from corrosion. Sliding conditions (under 2 N load and 20 rpm or 10 N and 100 rpm) induce a limited increase of the substrate corrosion rates, likely as a consequence of an increase in the defect population of the ceramic coatings.On Cr₂O₃-coated specimens, tribocorrosion is more severe at 10 N and 100 rpm, while on Al₂O₃/13% TiO₂-coated specimens, a stronger corrosion attack is achieved at 2 N and 20 rpm. Profilometer analysis and wear track observations by optical and scanning electron microscopes evidence that on both coatings abrasion of the surface asperities produce both a surface polishing effect and, at high loads, the formation of a tribofilm, more continuous on Al₂O₃/13% TiO₂. On this coating the tribofilm reduces the amount of surface defects and limits the corrosion attack to a certain extent.     

Microstructural characterisation and corrosion behaviour of electroless Ni–W–P deposits of mixed nanocrystalline/amorphous structures

Abstract

An investigation has been undertaken of the influence of the mixed nanocrystalline and amorphous microstructure on the corrosion behaviour of electroless Ni–5·5W–6·5P (wt-%) deposits on steel substrates. The effects of annealing temperature on microstructure evolution were investigated. The corrosion behaviour of the deposits was evaluated by potentiodynamic polarisation in 0·5M H₂SO₄ solution and EIS measurements in 3·5%NaCl solution. Relationships between the microstructure and corrosion mechanisms of the as plated and the annealed deposits were considered by reference to microstructural information, including degree of crystallisation, grain sizes of both nickel and Ni₃P phases, porosity development, microstrains and residual stresses.     

Annealing effects on the intermetallic compound formation of cold sprayed Ni,Al coatings

The annealing of Ni and Al coatings under various conditions on substrates fabricated by a cold gas dynamic spray process (CDSP) were investigated. The powder particles were accelerated through a standard De Laval-type nozzle with air used as the main carrying gas. The coatings were annealed at 450–550 °C in either argon or air atmospheres for 4 h. In the case of Ni coatings during annealing both in argon and air atmospheres, intermetallic compound layers such as Al₃Ni and Al₃Ni₂ were observed at the interfaces between the Ni coating and Al substrate. Also, the intermetallic layer formation of Al₃Ni and Al₃Ni₂ at the interfaces depended on the solid-state diffusion and the annealing temperature. The intermetallic compound AlNi was obtained at the interface of Al coating on a Ni substrate by low-temperature annealing under the melting temperature.     

Effects of Al and Ni doping on oxidation and corrosion resistance of electrophoretic deposited YSZ coatings

Yttria-stablized zirconia (YSZ)/(Ni,Al) coatings were deposited on Inconel 600 alloy substrate by the electrophoretic deposition combined with vacuum sintering technique. The effects of isothermal oxidation at 1100 °C on the composition of the coatings and the crack healing were investigated, and the corrosion resistance of the coatings in 3.5% NaCl (mass fraction) solution was also studied. The results showed that the cracks on the coating gradually healed up with the increase of the isothermal oxidation time. During isothermal oxidation process, the coating composed of Ni₃Al was transformed to α-Al₂O₃ particulates. The α-Al₂O₃ particulates can seal the defects such as pores and cracks, and meanwhile prevent the oxygen diffusion into the coatings. The polarization curves and EIS results indicated that the coatings oxidized for 40 h had a more positive corrosion potential, higher breakdown potential, higher impedance module at low frequency and much lower corrosion current density compared with YSZ coated and uncoated Inconel 600 alloys.     

Corrosion behavior of thermal-sprayed WC cermet coatings in SO4 2− environment

A series of the electrochemical and long-term corrosion tests was carried out in a 3.5 wt% Na2SO4 solution on thermal-sprayed WC-17Co and WC-10Co-4Cr cermet coatings in order to examine the effect of composition of binder materials on the corrosion behavior. The results reveal that the overall corrosion resistance of the WC-17Co coating is inferior to that of the WC–Co–Cr coatings due to the corrosion of binder materials which induce WC particles to fall off. CoO and WO3 oxide films form on the surface of WC-17Co coating in Na2SO4 solution electrochemical corrosion process, which will protect the coating in the process of corrosion. Cr2O3 oxide film formed on the WC-10Co-4Cr coating surface has a strong hindered role to corrosion. The corrosion mechanism of WC-17Co coating in Na2SO4 solution is entire corrosion of Co matrix, while it is film-hole corrosion mechanism for WC-10Co-4Cr coating.     

Aluminium depletion in NiCrAlY bond coatings by hot corrosion as a function of projection system

Three different projection system are used to prepare NiCrAlY bond coats over metallic substrates: atmospheric plasma spray (APS), high velocity oxyfuel (HVOF) and high frequency pulse detonation (HFPD). These coatings were tested in hot corrosion experiments with sprayed Na₂SO₄ at 1000 °C for 20 and 100 h experiments in air. Coatings surface composition after thermal treatment was characterised by XRD and SEM. Cross section of coatings were analysed by SEM-EDX. A relationship between microstructural characteristics of initial coatings and final performance in hot corrosion was found in terms of porosity percentage: plasma sprayed coatings present higher percentage of porosity compared to HVOF and HFPD projection systems for the same composition and Al is heavily consumed in interparticle oxidation. This Al depletion in turn involves intrinsic chemical failure and surface layer is comprised by a porous spinel of mixed oxides. On the other hand, high energy projection systems produce dense coatings allowing the Al migration to external alumina layer, particularly in the case of HVOF coating.     

Deposition and corrosion resistance of electroless Ni-PCTFE-P nanocomposite coatings

The present work deals with the process of electroless deposition and electrochemical corrosion behavior of nickel-polychlorotrifluoroethylene-phosphorous (Ni-PCTFE-P) nanocomposite coatings. The process of autocatalytic-catalytic reduction of Ni in nickel sulfate and sodium hypophosphate solution with PCTFE suspended particles has been employed for the formation of the electroless Ni-PCTFE-P composite coatings. Surface morphology and composition of the composite coatings are characterized by scanning electron microscopy (SEM), energy dispersive X-ray (EDX) measurements and X-ray diffraction (XRD) analysis. Corrosion behavior of coatings is evaluated using open-circuit potential (E_OCP) measurements, electrochemical impedance spectroscopy (EIS) and polarization techniques in 3.5 wt.% NaCl solution. The study reveals significant shift in corrosion potential towards the noble direction, decrease in corrosion current density, increase in charge transfer resistance and decrease in double‐layer capacitance values with the incorporation of PCTFE particles in the Ni-P matrix. The significant improvement in corrosion resistance observed for Ni-PCTFE-P nanocomposite coatings (25.3 kΩ cm²) compared to Ni-P (16 kΩ cm²) could have resulted from the microstructural differences of pure Ni-P with Ni-PCTFE-P nanocomposite coatings.     

Study of structure and corrosion resistance of Fe-based amorphous coatings prepared by HVAF and HVOF

Fe-based amorphous coatings with a composition of Fe_49.7Cr₁₈Mn_1.9Mo_7.4W_1.6B_15.2C_3.8Si_2.4 have been prepared on a mild steel substrate by High velocity air fuel (HVAF) and High velocity oxygen fuel (HVOF) processes. The microstructure and corrosion resistance in 3.5 wt.% NaCl solution of the coatings prepared by the two processes were comparatively studied. It was found that the two coatings exhibit dense structure with the porosity of 0.4% and compact bonding with the substrate. However, HVOF coating contains higher oxygen content than HVAF coating, resulting from the formation of significant oxide contours between the partially melted particles in HVOF process. Electrochemical polarization tests and electrochemical impedance spectroscopy (EIS) analysis indicate that the HVAF coating has better corrosion resistance than the HVOF coating. The preferential corrosion along the oxide contours thus providing efficient diffusion channels for electrolyte accounts for the poor corrosion resistance in HVOF coating. The present results demonstrate that HVAF with less cost can be a promising spray process to fabricate the Fe-based amorphous coating for industrial applications.