Electroless Ni-P and Ni-P-Al2O3 Nanocomposite Coatings and Their Corrosion and Wear Resistance

In an effort to utilize beneficial aspects of nanoparticles in providing corrosion and wear resistance, electroless Ni-P and Ni-P-Al₂O₃ nanocomposite coatings were produced. Alumina particles with various contents from 5 to 20 g/L in bath were co-deposited within Ni-P deposits on mild steel (ms) substrate. Coatings were characterized by scanning electron microscopy (SEM) for morphology, energy dispersive analysis of x-ray EDAX for analyzing elemental composition and x-ray diffractometry for investigating the structural changes of their components. Electrochemical and immersion measurements were used to analyze corrosion behavior of the coatings in 3.5% NaCl solution. Wear resistance of the coating was measured by pin-on-disc method. The results indicated that the Ni-P-Al₂O₃ coatings provide the high hardness as compare to the Ni-P coating. Corrosion and wear resistance of coatings is observed to be superior to that of ms. Corrosion protection properties of the coatings are found to be affected with continuous exposure to the electrolyte. Coating with high concentration of alumina is exhibiting high wear resistance than Ni-P coating. Wear mechanism in case of Ni-P coating appears to be adhesive type and seems to change to abrasive type on introduction of alumina.     

Corrosion Behavior and Microhardness of Ni-P-SiO<Subscript>2</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Nano-composite Coatings on Magnesium Alloy

In the present work, nano-composites of Ni-P-SiO₂-Al₂O₃ were coated on AZ91HP magnesium alloy. The surface morphology of the nano-composite coating was studied by field emission scanning electron microscopy (FESEM). The amount of SiO₂ in the coating was determined by energy-dispersive analysis of x-ray (EDX), and the crystalline structure of the coating was examined by x-ray diffractometer (XRD). All the experiments concerning the corrosion behavior of the coating carried out in 3.5 wt.% NaCl solution and evaluated by electrochemical impedance spectroscopy (EIS) and polarization technique. The results showed that an incorporation of SiO₂ and Al₂O₃ in Ni-P coating at the SiO₂ concentration of 10 g/Land 14 g/LAl₂O₃ led to the lowest corrosion rate (i _corr = 1.3 µA/cm²), the most positive E _corr and maximum microhardness (496 VH). Furthermore, Ni-P-SiO₂-Al₂O₃ nano-composite coating possesses less porosity than that in Ni-P coating, resulting in improving corrosion resistance.     

Effect of Feedstock Size and its Distribution on the Properties of Detonation Sprayed Coatings

The detonation spraying is one of the most promising thermal spray variants for depositing wear and corrosion resistant coatings. The ceramic (Al₂O₃), metallic (Ni-20 wt%Cr) , and cermets (WC-12 wt%Co) powders that are commercially available were separated into coarser and finer size ranges with relatively narrow size distribution by employing centrifugal air classifier. The coatings were deposited using detonation spray technique. The effect of particle size and its distribution on the coating properties were examined. The surface roughness and porosity increased with increasing powder particle size for all the coatings consistently. The feedstock size was also found to influence the phase composition of Al₂O₃ and WC-Co coatings; however does not influence the phase composition of Ni-Cr coatings. The associated phase change and %porosity of the coatings imparted considerable variation in the coating hardness, fracture toughness, and wear properties. The fine and narrow size range WC-Co coating exhibited superior wear resistance. The coarse and narrow size distribution Al₂O₃ coating exhibited better performance under abrasion and sliding wear modes however under erosion wear mode the as-received Al₂O₃ coating exhibited better performance. In the case of metallic (Ni-Cr) coatings, the coatings deposited using coarser powder exhibited marginally lower-wear rate under abrasion and sliding wear modes. However, under erosion wear mode, the coating deposited using finer particle size exhibited considerably lower-wear rate.     

Intermediate temperature tribological behavior of carbon nanotube reinforced plasma sprayed aluminum oxide coating

Tribological behavior of plasma sprayed carbon nanotube (CNT) reinforced aluminum oxide (Al₂O₃) composite coatings was examined at room temperature, 573 K and 873 K using tungsten carbide (WC) ball-on-disk tribometer. The weight loss due to wear of Al₂O₃ coating was found to be increasing with the temperature while Al₂O₃-CNT coating showed a decreasing trend in the weight loss with the temperature. Relative improvement in the wear resistance of Al₂O₃-CNT coating compared to Al₂O₃ coating was found to be 12% at room temperature which gradually increased to ∼ 56% at 573 K and ∼ 82% at 873 K. Protective layer as a result of tribo-chemical reaction was observed on the wear track of both of the coatings. The improvement in the wear resistance of Al₂O₃-CNT coating was attributed to three phenomena viz. (i) higher hardness at the elevated temperature as compared to Al₂O₃ coating, (ii) larger area coverage by protective film on the wear surface at the elevated temperature and (iii) CNT bridging between splats. The coefficient of friction (COF) of Al₂O₃ coating was nearly constant at room and elevated temperature whereas COF for Al₂O₃-CNT coating decreased at the elevated temperature (873 K).     

The use of Al-Al2O3 cold spray coatings to improve the surface properties of magnesium alloys

Pure Al and 6061 aluminium alloy based Al₂O₃ particle-reinforced composite coatings were produced on AZ91E substrates using cold spray. The strength of the coating/substrate interface in tension was found to be stronger than the coating itself. The coatings have corrosion resistance similar to that of bulk pure aluminium in both salt spray and electrochemical tests. The wear resistance of the coatings is significantly better than that of the AZ91 Mg substrate, but the significant result is that the wear rate of the coatings is several decades lower than that of various bulk Al alloys tested for comparison. The effect of post-spray heat treatment, the volume fraction of Al₂O₃ within the coating and of the type of Al powder used in the coatings on the corrosion and wear resistance was also discussed.     

Effects of the powder manufacturing method on microstructure and wear performance of plasma sprayed alumina-titania coatings

Three Al₂O₃-13wt.% TiO₂ powders, with the same chemical composition but different Al₂O₃-TiO₂ distribution patterns, are plasma sprayed and the resulting coatings are compared in terms of their phase composition, microstructure, hardness, crack growth resistance, and abrasive wear performance. It is demonstrated that the degree of mixing of the Al₂O₃ and TiO₂ ingredients in the feed powder has immense impact on the phase composition, microstructure, hardness, crack growth resistance, and abrasive wear performance of the coatings. A high degree of mixing of Al₂O₃ and TiO₂ in the powder state results in more uniform microstructure, higher hardness, higher crack growth resistance, and consequently better abrasive wear resistance of the coating.     

Wear mechanism of CrN/NbN superlattice coating sliding against various counterbodies

Wear properties of CrN/NbN superlattice coating deposited on the WC-12Co substrate was investigated while using 100Cr6 steel, SiC and Al₂O₃ ball as counterbodies for friction pairs. The value of friction coefficient and wear rate was lowest at ~ 0.01 and 2.6 × 10^− 7 mm³/Nm, respectively, when coating slides against Al₂O₃ ball. In contrast, friction coefficient and wear rate were increased while sliding with steel and SiC ball. The deviation in friction coefficient was described by mechanical and chemical properties of these balls. Hardness of Al₂O₃ and SiC ball was comparable but significant deviation in friction coefficient was observed. That is related to oxidation resistance of these balls which is high for Al₂O₃ compared to SiC ball as evident by Raman analysis of the wear track. However, hardness and oxidation resistance were low for steel ball which shows oxidational wear mechanism.     

Wear and corrosion resistance of AZ91 magnesium alloy coated by pulsed current electrodeposited Ni–Al2O3 nanocomposite

In this work, Ni and Ni–Al₂O₃ nanocomposite coatings were applied on AZ91 magnesium alloy using a pulse plating process and the corrosion resistance of coated samples was evaluated by means of the potentiodynamic polarisation method in 3.5?wt-% NaCl solution. Field emission scanning electron microscopy was employed to identify microstructure and morphology of the coatings. Vickers microhardness and pin-on-disc wear tests were also used to investigate mechanical properties of the coatings. The polarisation test revealed that the pure Ni coating on AZ91 along with the presence of nanoparticles were key factors leading to a reduction in the corrosion current density and the improvement of corrosion resistance so that the corrosion current density of 210.45?µA?cm^?2 for the substrate (AZ91) decreases to 31.92 and 1.54?µA?cm^?2 by applying pure Ni and Ni–Al₂O₃ nanocomposite coatings, respectively. Furthermore, Ni–Al₂O₃ nanocomposite coating increased the microhardness and wear resistance compared to the substrate up to 435 and 340%, respectively.     

The influence of SiO<Subscript>2</Subscript> and Al<Subscript>2</Subscript>O<Subscript>3</Subscript> nanoparticles on corrosion resistance enhancement of Ni–P on magnesium

In this study, the influence of adding SiO₂ and Al₂O₃ to Ni–P coated on magnesium substrate and the related corrosion resistance behavior were evaluated. The surface morphology of Ni–P–SiO₂–Al₂O₃ composite coating was investigated by field emission scanning electron microscopy (FESEM). The amount of Al₂O₃ and SiO₂ in the coating was measured by energy dispersive analysis of X-ray (EDX) and the corrosion behavior of coating was monitored by electrochemical impedance spectroscopy (EIS) and polarization techniques, showing the corrosion resistance of Ni–P–SiO₂–Al₂O₃ increases compare to Ni–P–SiO₂ and Ni–P–Al₂O₃. Furthermore, the microhardness of the coating was examined and the final hardness of Ni–P–SiO₂–Al₂O₃ reached 461 VH.     

镁合金表面化学镀 Ni-P 和 Ni-P-SiC 的对比

目的提高镁合金的耐磨性、耐蚀性,扩大其应用领域。方法采用"磷酸+钼酸铵酸洗→HF活化"的方法进行前处理,直接在AZ91D镁合金表面化学镀Ni-P合金镀层和Ni-P-SiC复合镀层。对两种镀层的表面和截面形貌、成分、结构、硬度、耐蚀性及耐磨性进行了系统比较。结果在Ni-P合金镀层中引入SiC粉末后,镀层的胞状颗粒细化,硬度提高至643HV,但其腐蚀电流密度有所增大。结论与Ni-P合金镀层相比,Ni-P-SiC复合镀层的耐蚀性有所下降,但耐磨性能大大提高。     

Wear and corrosion properties of plasma sprayed AI2O3 and Cr2O3 coatings sealed by aluminum phosphates

Plasma-sprayed aluminum oxide (AI₂O₃) and chromium oxide (Cr₂O₃) coatings were sealed by aluminum phosphates. Phosphates were formed throughout the coating, down to the substrate, and were verified by scanning electron microscopy and hardness measurements. The sealing increased the hardness of the coatings by 200 to 300 Vickers hardness (HV) units. Abrasion and erosion wear resistances were increased by the sealing treatment. Sealing also substantially closed the open porosity, as shown in electro-chemical corrosion tests. The sealed structures had good resistance against corrosion during 30 days of immersion in both acidic and alkaline solutions with pH values from 0 to 10. No decrease in abrasion wear resistance was observed after immersion.     

Corrosion Resistance of Copper Coatings Deposited by Cold Spraying

In the article, a study of corrosion resistance of copper and copper-based cermet (Cu+Al₂O₃ and Cu+SiC) coatings deposited onto aluminum alloy substrate using the low-pressure cold spraying method is presented. The samples were subjected to two different corrosion tests at room temperature: (1) Kesternich test and (2) a cyclic salt spray test. The selected tests were allowed to simulate service conditions typical for urban, industrial and marine environment. Examination of corroded samples included analysis changes on the coating surface and in the microstructure. The physicochemical tests were carried out using x-ray diffraction to define corrosion products. Moreover, microhardness and electrical conductivity measurements were conducted to estimate mechanical and physical properties of the coatings after corrosion tests. XRD analysis clearly showed that regardless of corrosion conditions, for all samples cuprite (Cu₂O) was the main product. However, in the case of Cu+Al₂O₃ cermet coating, chlorine- and sulfate-containing phases such as Cu₂Cl(OH)₃ (paracetamite) and Cu₃(SO₄)(OH)₄ (antlerite) were also recorded. This observation gives better understanding of the lowest microstructure changes observed for Cu+Al₂O₃ coating after the corrosion tests. This is also a justification for the lowest decrease in electrical conductivity registered after the corrosion tests for this coating.     

WC和Al2O3对氩弧熔覆FeAlCoCrCuTi0.4高熵合金涂层组织和耐冲蚀性能影响

利用氩弧熔覆技术制备了FeAlCoCrCuTi_0.4,WC/Al₂O₃-FeAlCoCrCuTi_0.4高熵合金涂层,并通过XRD,SEM,EDS,硬度测试和冲蚀磨损测试等方法,探究了WC和Al₂O₃的添加对FeAlCoCrCuTi_0.4高熵合金涂层显微组织和性能的影响.结果表明,通过氩弧熔覆技术所制备的合金涂层表面成形性良好,无孔洞、裂纹等缺陷产生,与基体呈高强度冶金结合.WC和Al₂O₃的添加对涂层稀释率的降低有显著作用.三种涂层都是主要由Bcc相（Fe-Cr固溶体）构成,晶粒以胞状树枝晶形式存在.添加WC后,晶粒细化明显,在各种强化作用下涂层硬度为685.8 HV.且WC和Al₂O₃的添加显著提高了涂层耐冲蚀磨损性能,耐磨性几乎可以达到FeAlCoCrCuTi_0.4高熵合金涂层的2倍.     

Hot Corrosion Performance of AlO-CrO/NiCoCrAlYTa and AlO/NiCoCrAlYTa Coatings Deposited by Atmospheric Plasma Spraying

AlO-CrO/NiCoCrAlYTa and AlO/NiCoCrAlYTa coatings were deposited on 316L stainless steel substrate using atmospheric plasma spraying, respectively, in order to improve the oxidation and corrosion resistance. The hot corrosion performance of the coatings at 700 and 900 °C were studied, and the detailed microstructures and phase composition of the coatings were analyzed using x-ray diffraction, scanning electron microscope with energy dispersive spectrometer, and transmission electron microscope. The results show that both coatings are structurally featured by slatted layers, consisting of amorphous phase, Cr₂O₃, Ni₃Al, and Al₂O₃. The hot corrosion resistance of AlO-CrO/NiCoCrAlYTa coating is better than that of AlO/NiCoCrAlYTa coating. This improvement is attributed to lower porosity and more compact Cr₂O₃ in AlO-CrO/NiCoCrAlYTa coating which performs better than Al₂O₃ in blocking further inward progress of corrosion and oxidization.     

Al2O3-ZrO2 mixed oxide composite incorporated aluminium rich zinc coatings for high wear resistance

Corrosion resistance and wear resistance are the two important parameters for high performance of zinc galvanic coating. In the present work, the improvement of these two characteristics was achieved by the incorporation of Al₂O₃-ZrO₂ mixed oxide composite in the coating. Al₂O₃-ZrO₂ mixed oxide composite was synthesized from ZrOCl₂·8H₂O. Aluminium rich zinc coatings with high sliding wear resistance was developed from a galvanic bath containing the mixed oxide. Based on the performance of the coating during physicochemical and electrochemical characterization, the concentration of mixed oxide composite in the bath was optimized as 0.50 wt% Al₂O₃-0.50 wt% ZrO₂. While rich in Al-metal content in the coating caused high corrosion resistance, the incorporation of the mixed oxide improved structural characteristics of the coating resulting in high wear resistance also. The coating was nonporous in nature and even the interior layers had high stability. The coatings have potential scope for high industrial utility.     

Effects of critical plasma spray parameter and spray distance on wear resistance of Al2O3-8 wt.%TiO2 coatings plasma-sprayed with nanopowders

Effects of plasma spraying conditions on wear resistance of nanostructured Al₂O₃-8 wt.%TiO₂ coatings plasma-sprayed with nanopowders were investigated in this study. Five kinds of nanostructured coatings were plasma-sprayed on a low-carbon steel substrate by varying critical plasma spray parameter (CPSP) and spray distance. The coatings consisted of fully melted region of γ-Al₂O₃ and partially melted region, and the fraction of the partially melted regions and pores decreased with increasing CPSP or decreasing spray distance. The hardness and wear test results revealed that the hardness of the coatings increased with increasing CPSP or decreasing spray distance, and that the hardness increase generally led to the increase in wear resistance, although the hardness and wear resistance were not correlated in the coating fabricated with the low CPSP. The main wear mechanism was a delamination one in the coatings, but an abrasive wear mode also appeared in the coating fabricated with the low CPSP. According to these wear mechanisms, the improvement of wear resistance in the coating fabricated with the low CPSP could be explained because the improved resistance to fracture due to the presence of partially melted regions might compensate a deleterious effect of the hardness decrease.     

Phase and Microstructure Evolution and Toughening Mechanism of a Hierarchical Architectured Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–Y<Subscript>2</Subscript>O<Subscript>3</Subscript> Coating under High Temperature

In recent years, numerous techniques have been developed to mimic nacre-like hierarchical architectures in order to improve the damage tolerance of materials. We present herein a simple strategy to fabricate such a hierarchical architectured Al₂O₃–Y₂O₃ composite coating via atmospheric plasma spraying. The evolution of the phase and microstructure of the Al₂O₃–Y₂O₃ composite coating were characterized under conditions of high-temperature exposure in air at 800-1350 °C. The hardness and porosity of several typical coatings were determined. In situ formation of dense hierarchical architectured Al₂O₃–YAG composite coating with improved hardness was achieved after heat treatment at 1350 °C. Compared with Al₂O₃ coating, elevated toughness was found for the hierarchical architectured Al₂O₃–YAG composite coating, which can be ascribed to the distribution of YAG phase that contributed to crack termination and deflection, and microbridging. After thermal aging treatment at 1350 °C, the hierarchical architectured Al₂O₃–YAG composite coating was quite stable after 100 h of thermal exposure. Furthermore, the Al₂O₃–Y₂O₃ composite coating exhibited superior sintering resistance compared with the Al₂O₃ coating.     

铝基表面等离子喷涂Al2O3-TiO2-Ta涂层的制备及防腐性能

采用等离子喷涂技术在铝基表面构建Al₂O₃-TiO₂涂层和Al₂O₃-TiO₂-Ta涂层。由于钽元素的引入,Al₂O₃-TiO₂-Ta涂层表面形貌更均匀、致密。同时钽金属具有极强的耐酸碱特性,因此,Al₂O₃-TiO₂-Ta涂层相对于Al₂O₃-TiO₂涂层具有更强的耐腐蚀性。Tafel曲线结果显示,Al₂O₃-TiO₂涂层使得基体的腐蚀电位仅正移了99.6 mV,Al₂O₃-TiO₂-Ta涂层使得铝基体腐蚀电位正移了208.9 mV。因此,由于耐蚀性极强的Ta金属的掺入,Al₂O₃-TiO₂涂层的防腐性得到了极大的增强,Al₂O₃-TiO₂-Ta涂层有效地防止铝合金腐蚀。     

Synthesis and characterization of hardness-enhanced multilayer oxide films for high-temperature applications

Multilayer oxide coatings consisting of amorphous Al₂O₃ and crystalline TiO₂ nanolayers have been deposited using reactive pulsed d.c. magnetron sputtering at different partial pressures of oxygen. Hardness enhancement has been observed in oxide multilayer coatings with amorphous Al₂O₃ as the majority component. These coatings had greater hardness-to-modulus ratios and showed greater resistance to wear over monolithic Al₂O₃ and TiO₂ majority phase multilayers. Multilayer films retain their high hardness up to ~ 800 °C in air; some hardness enhancement in the Al₂O₃ majority phase multilayer coating remains even after 1 h of air annealing at 1000 °C. The hardness decrease at elevated temperatures is due to the roughening of interfaces between nanolayers, which can be attributed to the annealing-driven change of crystallographic texture of TiO₂ layers.     

Microstructure and sliding wear behavior of pseudo-alloy PS45/CuAl8 composite coating sprayed by HVAA technique

A pseudo-alloy PS45/CuAl8 composite coating was sprayed on steel substrate by high-velocity activated arc spraying (HVAA) process. Its sliding wear behavior at room temperature was evaluated by M-2000 wear tester. For comparison, a single CuAl8 coating was also prepared and tested under the same conditions. It is found that the pseudo-alloy composite coating consists of α-Cu and γ-Ni metallic matrix phases together with homogenously distributed minor Al 2 O 3 , Cr 2 O 3 oxide phases. Moreover, pseudo-alloy coating possesses much better sliding wear resistance than CuAl8 coating due to the enhanced hardness and microstructural homogenization. Fatigue wear and abrasive wear are responsible for the wear-down mechanism of the pseudo-alloy coating.