Tribological Behavior of Plasma-Sprayed Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-20 wt.%TiO<Subscript>2</Subscript> Coating

Al₂O₃-20 wt.% TiO₂ ceramic coatings were deposited on the surface of Grade D steel by plasma spraying of commercially available powders. The phases and the microstructures of the coatings were investigated by x-ray diffraction and scanning electron microscopy, respectively. The Al₂O₃-20 wt.% TiO₂ composite coating exhibited a typical inter-lamellar structure consisting of the γ-Al₂O₃ and the Al₂TiO₅ phases. The dry sliding wear behavior of the coating was examined at 20 °C using a ball-on-disk wear tester. The plasma-sprayed coating showed a low wear rate (~4.5 × 10^?6 mm³ N^?1 m^?1), which was <2% of that of the matrix (~283.3 × 10^?6 mm³ N^?1 m^?1), under a load of 15 N. In addition, the tribological behavior of the plasma-sprayed coating was analyzed by examining the microstructure after the wear tests. It was found that delamination of the Al₂TiO₅ phase was the main cause of the wear during the sliding wear tests. A suitable model was used to simulate the wear mechanism of the coating.     

Tribocorrosion Behavior of Fe-Based Amorphous Composite Coating Reinforced by Al<Subscript>2</Subscript>O<Subscript>3</Subscript> in 3.5% NaCl Solution

Although corrosion and friction/wear behavior of Fe-based amorphous coatings and their composites has been extensively studied during the past decade, there is very limited work related to tribocorrosion behavior. In this paper, the tribocorrosion behavior of a Fe-based amorphous composite coating reinforced with 20 wt.% Al₂O₃ particles was investigated in a 3.5% NaCl solution on a ball-on-disk tester and was compared to the monolithic amorphous coating and 316L stainless steel (SS). The results showed that the amorphous composite coating exhibited the highest tribocorrosion resistance among the three materials tested, as evidenced by the lowest coefficient of friction (~0.3) and tribocorrosion wear rate (~1.2 × 10^?5 mm³/N·m). In addition, potentiodynamic polarization measurements before and during tribocorrosion testing demonstrated that corrosion resistance of the amorphous composite coating was not influenced so much by mechanical loading compared to the amorphous coating and the 316L SS. Observations on the worn surface revealed a corrosion-wear- and oxidational-wear-dominated tribocorrosion mechanism for the composite coatings. The excellent tribocorrosion resistance of the composite coating results from the effect of chemically stable Al₂O₃ phase which resists oxidation and delamination during sliding, along with poor wettability with corrosive NaCl droplets.     

ZM5镁合金无铬前处理化学镀镍层的性能

采用优化的Na4P2O7+Na2SO4+NaNO3体系的化学蚀刻无铬前处理化学镀镍工艺,在ZM5镁合金上制备Ni-P镀层。利用扫描电镜、能谱仪、X射线衍射仪分析镀层的微观形貌、成分和相结构。通过电化学方法和摩擦磨损试验评价了镀层的耐蚀性和耐磨性。结果表明:无铬前处理工艺制备的镀层中P的质量分数为12.90%。与ASTM标准的含铬前处理工艺得到的镀层的耐蚀性和耐磨性相比,无铬前处理得到的镀层的自腐蚀电位为-0.506V,腐蚀电流密度为2.132×10-6 A/cm2,接近ASTM工艺含铬前处理得到的镀层的耐蚀性能;同时其磨损率为3.056×10-4 mg/s,与ASTM工艺的1.778×10-3 mg/s相比,其抗摩擦磨损性能明显优于含铬前处理的镀层。无铬前处理化学镀镍显著提高了ZM5镁合金的耐蚀性和耐磨性。     

电解液成分对等离子体电解氧化TC4合金腐蚀行为和摩擦学性能的影响（英文）

在TC4合金表面制备4种典型等离子体电解氧化(PEO)涂层,研究电解质组成对PEO涂层腐蚀行为和摩擦学性能的影响。结果表明,PEO涂层的腐蚀行为和摩擦学性能与电解质成分密切相关。在含NaH₂PO₂的电解液中制备的PEO涂层由于内氧化膜较致密而具有最好的耐蚀性能,而在含NaAlO₂的电解液中制备的PEO涂层由于含有Al₂O₃而具有最好的摩擦学性能。为制备具有良好耐蚀性和耐磨性的PEO涂层,以NaH₂PO₂和NaAlO₂为电解液主要成分制备了复合PEO涂层。     

Manufacturing and Properties of High-Velocity Oxygen Fuel (HVOF)-Sprayed FeVCrC Coatings

This paper studies the microstructure, sliding wear behavior and corrosion resistance of high-velocity oxygen fuel (HVOF)-sprayed FeVCrC-based coatings. Various process parameters were tested to evaluate their effects on the coating properties, which were also compared to those of HVOF-sprayed NiCrBSi and Stellite-6 coatings. The Fe alloy coatings are composed of flattened splats, originating from molten droplets and consisting of a super-saturated solid solution, together with rounded particles, coming from partially unmolten material and containing V- and Fe-based carbide precipitates. All process parameters, apart from “extreme” settings with excess comburent in the flame, produce dense coatings, indicating that the feedstock powder is quite easily processable by HVOF. These coatings, with a microhardness of 650-750 HV_0.3, exhibit wear rates of ≈2 × 10^?6 mm³/(Nm) in ball-on-disk tests against sintered Al₂O₃ spheres. They perform far better than the reference coatings, and better than other Fe- and Ni-based alloy coatings tested in previous research. On the other hand, the corrosion resistance of the coating material (tested by electrochemical polarization in 0.1 M HCl solution) is quite low. Even in the absence of interconnected porosity, this results in extensive, selective damage to the Fe-based matrix. This coating material is therefore unadvisable for severely corrosive environments.     

Corrosion and wear resistance of AZ31 Mg alloy treated by duplex process of magnetron sputtering and plasma electrolytic oxidation

In order to improve the wear and corrosion resistance of AZ31 magnesium alloy, a magnetron-sputtered Al layer with a thickness of 11 μm was firstly applied on the alloy, and then treated by plasma electrolytic oxidation (PEO) in an aluminate and silicate electrolytes, respectively. The performance of PEO coatings was investigated by dry sliding wear and electrochemical corrosion tests. The aluminate coating exhibits excellent wear resistance under both 10 and 20 N loads. The silicate coating only shows low wear rate under 10 N, but it was destroyed under 20 N. Corrosion tests show that the Al layer after magnetron sputtering treatment alone cannot afford good protection to the Mg substrate. However, the duplex layer of PEO/Al can significantly improve the corrosion resistance of AZ31 alloy. Electrochemical tests show that the aluminate and silicate coatings have corrosion current densities of ∼1.6×10⁻⁶ and ∼1.1×10⁻⁶ A/cm², respectively, which are two orders lower than that of the un-coated AZ31 alloy. However, immersion tests and electrochemical impedance spectroscopy (EIS) show that the aluminate coating exhibits better long-term corrosion protection than silicate coating.     

Effect of NaOH on plasma electrolytic oxidation of A356 aluminium alloy in moderately concentrated aluminate electrolyte

Plasma electrolytic oxidation(PEO) of cast A356 aluminum alloy was carried out in 32 g/L NaAlO₂ with the addition of different concentrations of NaOH. The stability of the aluminate solution is greatly enhanced by increasing the concentration of NaOH. However, corresponding changes in the PEO behaviour occur due to the increment of NaOH concentration. Thicker precursor coatings are required for the PEO treatment in a more concentrated NaOH electrolyte. The results show that the optimal NaOH concentration is 5 g/L, which improves the stability of storage electrolyte to about 35 days, and leads to dense coatings with high wear performance (wear rate: 4.1×10⁻⁷ mm³·N⁻¹·m⁻¹).     

纳米Si3N4 对TC4钛合金微弧氧化层微观结构和性能的影响

在基电解液中加入氮化硅纳米颗粒,对TC4钛合金进行微弧氧化（MAO）处理,研究了Si₃N₄浓度对微弧氧化层表面形貌、耐蚀性和耐磨性的影响。添加Si₃N₄的MAO层呈现多孔结构,当Si₃N₄浓度为1 g/L时,涂层厚度最大,且经过7 d的酸腐蚀试验,该涂层的耐蚀性良好,腐蚀速率最低,约为0.057 mg·cm^-2·d^-1。随着Si₃N₄的加入,MAO涂层的抗菌性能先升高后降低。当Si₃N₄的添加量为1 g/L时,该MAO层的抗菌性能最好。Si₃N₄的加入能明显提高涂层在模拟海水中的耐磨性。当Si₃N₄的添加量为3和4 g/L时,所得涂层的摩擦系数低且稳定,且添加3 g/L Si₃N₄制备来的MAO涂层表现出优异的耐磨性。     

Friction and wear mechanisms in MoS2/Sb2O3/Au nanocomposite coatings

Fundamental phenomena governing the tribological mechanisms in sputter deposited amorphous MoS₂/Sb₂O₃/Au nanocomposite coatings are reported. In dry environments the nanocomposite has the same low friction coefficient as pure MoS₂ (～0.007). However, unlike pure MoS₂ coatings, which wear through in air (50% relative humidity), the composite coatings showed minimal wear, with wear factors of ～1.2–1.4 × 10^?7 mm³ Nm^?1 in both dry nitrogen and air. The coatings exhibited non-Amontonian friction behavior, with the friction coefficient decreasing with increasing Hertzian contact stress. Cross-sectional transmission electron microscopy of wear surfaces revealed that frictional contact resulted in an amorphous to crystalline transformation in MoS₂ with 2H-basal (0 0 0 2) planes aligned parallel to the direction of sliding. In air the wear surface and subsurface regions exhibited islands of Au. The mating transfer films were also comprised of (0 0 0 2)-oriented basal planes of MoS₂, resulting in predominantly self-mated “basal on basal” interfacial sliding and, thus, low friction and wear.     

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.     

Oxidation and Hot Corrosion Behavior of Plasma-Sprayed MCrAlY–Cr<Subscript>2</Subscript>O<Subscript>3</Subscript> Coatings

The oxidation and hot corrosion behavior of two atmospheric plasma-sprayed NiCoCrAlY–Cr₂O₃ and CoNiCrAlY–Cr₂O₃ coatings, which are primarily designed for wear applications at high temperature, were investigated in this study. The two coatings were exposed to air and molten salt (75%Na₂SO₄–25%NaCl) environment at 800 °C under cyclic conditions. Oxidation and hot corrosion kinetic curves were obtained by thermogravimetric technique. X-ray diffraction analysis and scanning electron microscopy with energy-dispersive x-ray spectrometry were employed to characterize the coatings’ microstructure, surface oxides, and composition. The results showed that both coatings provided the necessary oxidation resistance with oxidation rates of about 1.03 × 10^?2 and 1.36 × 10^?2 mg/cm² h, respectively. The excellent oxidation behavior of these two coatings is attributed to formation of protective (Ni,Co)Cr₂O₄ spinel on the surface, while as-deposited Cr₂O₃ in the coatings also acted as a barrier to diffusion of oxidative and corrosive substances. The greater presence of Co in the CoNiCrAlY–Cr₂O₃ coating restrained internal diffusion of sulfur and slowed down the coating’s degradation. Thus, the CoNiCrAlY–Cr₂O₃ coating was found to be more protective than the NiCoCrAlY–Cr₂O₃ coating under hot corrosion condition.     

Ti-Cr-B-N coatings prepared by pulsed cathodic-arc evaporation of ceramic TiCrB target produced by SHS

The method of pulsed cathodic-arc evaporation of composite targets based on self-propagating high-temperature synthesis has been applied for the first time to prepare nanocomposite coatings in the Ti-Cr-B-N system. The influence of the deposition-process parameters on the coating structure and properties has been studied. Structural investigations have been carried out using X-ray diffraction analysis, transmission and scanning electron microscopy, glow-discharge optical-emission spectroscopy, and optical profilometry. The coating properties have been determined by nanoindentation and tribological tests. The results of the study show that the coatings mainly consist of highly dispersed fcc phase based on Ti(Cr)N in the form of crystallites 1–2 nm in size; in addition, amorphous BNx phase has been found to exist in the coatings. The coatings obtained under optimal conditions have the following parameters: hardness 20–24 GPa, friction coefficient ～0.6, and reduced wear about 2 × 10^?6 mm³ N^?1 m^?1.     

TiN, TiN gradient and Ti/TiN multi-layer protective coatings on Uranium

Single-layer TiN, gradient TiN and multi-layer Ti/TiN coating were deposited on silicon and uranium substrates by means of arc ion plating technique. The main phase in the single-layer TiN coating was TiN with a (111) preferred orientation. Ti and TiN were observed in the TiN gradient coating and Ti/TiN multi-layer coatings. The single-layer TiN coating has demonstrated the best wear resistance among the three coatings. Compared with the bare U substrate, the corrosion potential E_corr of the multi-layer Ti/TiN coatings is increased by 580 mV, and the corrosion current density I_corr is decreased at least by two orders of magnitude. The multi-layer Ti/TiN coatings possessed the highest corrosion resistance among the three coating in a 0.5 μg/g Cl⁻ solution.     

不同纳米WS2含量Ni-P-Ti N-WS_(2)复合化学镀层的制备及其摩擦学性能EI北大核心CSCD

Ni-P-TiN化学复合镀层具有比Ni-P镀层更高的硬度和耐磨性,但其表面粗糙度大,与对偶件之间的摩擦因数高,应用潜力受到限制。通过在化学镀液中添加不同用量的纳米WS_(2)颗粒和固定用量的TiN颗粒,在低碳钢表面制备Ni-P-TiN-WS_(2)复合镀层。采用X射线能谱仪(EDS)、扫描电子显微镜(SEM)和X射线衍射仪(XRD)对镀层的化学成分(质量分数)、表面形貌及微观结构进行表征,并利用球盘式摩擦磨损试验机测试复合镀层的摩擦磨损性能。结果表明:纳米WS_(2)颗粒与纳米TiN颗粒的共沉积可使镀层表面更加致密、平整。随着镀液中纳米WS_(2)用量的增加,复合镀层的硬度先减小后增大,与氮化硅陶瓷球的摩擦因数则先升后降,磨损率显著下降,耐磨性增强。镀液中纳米WS_(2)粉末的用量为2.5 g/L时复合镀层的摩擦学性能最佳。纳米WS_(2)颗粒的加入及用量优化可显著改善复合镀层的综合性能,可为发展高耐磨低摩擦因数的先进涂层提供借鉴。     

TC4钛合金表面沉积CrSiN/SiN纳米多层膜在3.5%NaCl溶液中的腐蚀磨损性能

为了研究纳米多层膜的耐腐蚀性能以及腐蚀磨损机理,采用离子源辅助磁控溅射在TC4钛合金表面制备不同调制周期的CrSiN/SiN纳米多层膜。使用扫描电子显微电镜、能谱仪表征涂层的微观结构、腐蚀形貌以及元素分布;使用划痕仪、纳米压痕仪、维氏硬度计测量涂层的膜基结合力、硬度、弹性模量及断裂韧性,采用电化学工作站以及销盘磨损仪测量涂层耐腐蚀性和腐蚀磨损性。结果表明:调制周期为90 nm与360 nm时涂层耐腐蚀性能较好,腐蚀电流密度分别为1.31×10~(-8)A·cm~(-2)和1.20×10~(-8)A·cm~(-2)。此外,调制周期为45nm时,涂层硬度及弹性模量最大,分别为(22.5±0.6)GPa和(226.4±6.3)GPa,且腐蚀磨损率最低,为9.67×10~(-7)mm~3·N~(-1)·m~(-1)。多层膜结构显著改善了TC4钛合金的耐腐蚀及腐蚀磨损性能。     

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.     

Mechanical and tribological properties of plasma-sprayed Cr3C2-NiCr, WC-Co, and Cr2O3 coatings

Mechanical properties such as Young’s moduli and fracture toughness of plasma-sprayed Cr₃C₂-NiCr, WC-Co and Cr₂O₃ coatings were measured. The tribological properties of the three kinds of coatings were investigated with a block-on-ring self-mated arrangement under water-lubricated sliding. Furthermore, the influences of the mechanical properties on the tribological properties of the coatings were also examined. It was found that the Young’s moduli, bend strengths and fracture toughness of the coatings were lower than the corresponding bulk materials, which may be attributed to the existence of pores and microcracks in the coatings. Among the three kinds of coatings, the magnitude of wear coefficients, in decreasing order, is Cr₃C₂-NiCr, WC-Co and Cr₂O₃, and the wear coefficient of Cr₂O₃ coating was less than 1 × 10⁻⁶mm³N⁻¹m⁻¹. The wear mechanisms of the coatings were explained in terms of microcracking and fracturing, and water deteriorated wear performance of the coatings. The higher the fracture toughness and the lower the porosity and length of microcracking of the coating, the more the wear-resistance of the coating.     

淫羊藿苷含量对Mg/UMAO/CS/IC涂层性能的影响

为了研究淫羊藿苷含量对镁/超声微弧氧化/壳聚糖/淫羊藿苷（Mg/UMAO/CS/IC）涂层性能的影响,并提高纯镁的耐蚀性,采用电泳沉积（EPD）和UMAO技术在纯镁基体上制备Mg/UMAO/CS/IC涂层。采用扫描电子显微镜（SEM）、X射线衍射（XRD）、原子力显微镜（AFM）和傅立叶变换红外光谱（FTIR）对涂层的特征进行分析。对不同样品在模拟体液中进行了电化学阻抗和动电位极化的腐蚀行为研究。结果表明：当IC含量为0.4 g/L时CS/IC层具有较好的封孔效果。添加不同IC含量的Mg/UMAO/CS/IC涂层均由Mg、MgO、CS和Mg₂SiO₄组成。不同IC含量涂层的自腐蚀电流密度（i_corr）比Mg至少都低一个数量级,能为镁基底提供更有效的保护。IC含量为0.4 g/L时Mg/UMAO/CS/IC涂层的耐蚀性更好,自腐蚀电流密度（1.667×10^-6 A/cm²）最小。Mg/UMAO/CS/IC涂层可有效解决纯镁在临床骨内固定应用上降解过快的问题。     

大气等离子喷涂TiB2-316L不锈钢基复合涂层及其耐磨性能

分别采用高能球磨制备了TiB2含量(质量分数)为10%的316L不锈钢基复合粉,高能球磨与喷雾干燥造粒工艺制备了TiB2含量(质量分数)为40%的316L不锈钢基复合粉,大气等离子喷涂制备相应的TiB2-316L不锈钢基金属陶瓷涂层与316L不锈钢涂层.室温下采用高速环块磨损试验研究TiB2-316L不锈钢基金属陶瓷涂层的磨损特性.采用X射线衍射分析涂层物相,扫描电镜分析喷涂粉末、涂层结构和摩擦副磨损表面形貌.结果表明,大气等离子喷涂两种制粉工艺获得的316L不锈钢基TiB2复合粉能获得较耐磨的316L不锈钢基TiB2复合涂层,耐磨性高于316L不锈钢涂层,且TiB2在复合涂层中增强涂层耐磨性的原因是TiB2颗粒在涂层316L韧性基体中充当强化相,且TiB2在摩擦接触处摩擦氧化形成的氧化产物具有自润滑特性,能减少涂层的磨损量.     

用优化的双电解液制备AZ91D镁合金微弧氧化膜(英文)

在含有Na2SiO3、NaAlO2、Na2B4O7、NaOH、C3H8O3和C6H5Na3O7的电解液中,采用交流脉冲电源对AZ91D镁合金进行微弧氧化处理。利用SEM、膜层测厚仪、EDS和XRD分别研究膜层的表面和截面微观形貌、厚度、成分及相结构。利用交流阻抗和动电位极化曲线试验测量膜层在3.5%NaCl中性溶液中的耐蚀性能。结果表明,正交试验得到的双电解液成分为15g/LNa2SiO3、9g/LNaAlO2、2g/LNa2B4O7、3g/LNaOH、5mL/LC3H8O3和7g/LC6H5Na3O7。经过微弧氧化处理而得到的膜层较致密,其腐蚀电流密度较镁合金基体的降低了2个数量级,自腐蚀电位提高了近73mV。EIS结果认为膜层的耐蚀性取决于内部致密层。微弧氧化膜主要组成元素为Mg、Al、O和Si,主要组成相为MgO、Mg2SiO4和MgAl2O4。