Study on the tribological behaviors of the phenolic composite coating filled with modified nano-TiO2

In order to overcome the disadvantages generated by the loosened nanoparticle agglomerates dispersed in polymer composite coatings, nano-TiO₂ particles are modified using trifluoracetic acid. The friction and wear properties of the phenolic coatings filled with different surface treated nano-TiO₂, sliding against AISI-C-52100 steel ring under dry sliding, were investigated on a MHK-500 wear tester. Owing to the effective improvement of their dispersibility in the phenolic coating, compared with the cases of untreated nano-TiO₂, the employment of modified nano-TiO₂ provided the phenolic coating with much better tribological performance. Worn surfaces of the untreated nano-TiO₂ or modified nano-TiO₂ filled phenolic coating and transfer films formed on the surface of the counterpart ring sliding against the composite coating were respectively investigated by SEM and optical microscope (OM), from which it is assumed that the optimal content of TiO₂ or TF-TiO₂ is able to enhance the adhesion of the transfer films to the surface of counterpart ring. As a result, the wear resistance of the phenolic composite coating filled with modified nano-TiO₂ was significantly enhanced, especially at extreme wear conditions, i.e. high contact pressures.     

Tribological properties of Ni3Al-Cr7C3 composite coating under water lubrication

The tribological properties of Ni₃Al-Cr₇C₃ composite coating under water lubrication were examined by using a ball-on-disc reciprocating tribotester. The effects of load and sliding speed on wear rate of the coating were investigated. The worn surface of the coating was analyzed using electron probe microscopy analysis (EPMA) and X-ray photoelectron spectroscopy (XPS). The results show the friction coefficient of the coating is decreased under water lubrication. The wear rate of the coating linearly increases with the load. At high sliding speed, the wear rate of the coating is dramatically increased and a large amount of the counterpart material is transferred to the coating worn surface. The low friction of the coating under water lubrication is due to the oxidizing of the worn surface in the wear. The wear mechanism of the coating is plastic deformation at low normal load and sliding speed. However, the wear mechanism transforms to microfracture and microploughing at high load with low sliding speed, and oxidation wear at high sliding speed. It is concluded that the contribution of the sliding speed to an increase in the coating wear is larger than that of the normal load.     

Tribological properties of ZrO2 (Y2O3)-Mo-BaF2/CaF2 composites at high temperatures

ZrO₂ (Y₂O₃) with different contents of BaF₂/CaF₂ and Mo were fabricated by hot pressed sintering, and the tribological behavior of the composites against SiC ceramic was investigated from room temperature to 1000 °C. It was found that the ZrO₂ (Y₂O₃)-5BaF₂/CaF₂-10Mo composite possessed excellent self-lubricating and anti-wear properties. The low friction and wear were attributed to enhanced matrix and BaMoO₄ formed on the worn surfaces.     

Tribological characteristics of low-pressure plasma-sprayed A12O3 coating from room temperature to 800 °C

The tribological characteristics of low-pressure plasma-sprayed (LPPS) Al₂O₃ coating sliding against alumina ball have been investigated from room temperature to 800 °C. These friction and wear data have been compared quantitatively with those of bulk sintered alumina to obtain a better understanding of wear mechanisms at elevated temperatures. The friction and wear of Al₂O₃ coating show a strong dependence on temperature, changing from a mild to a severe wear regime with the increase of temperature. The coefficient of friction at room temperature is approximately 0.17 to 0.42, depending on applied load. The tribochemical reaction between the coating surface and water vapor in the environment and the presence of the hydroxide film on the Al₂O₃ coating reduce the friction and wear at room temperature as contrasted to those of bulk sintered alumina. At intermediate temperatures, from 400 to 600 °C, the friction and wear behavior of Al₂O₃ coating depends on the inter-granular fracture and pull-out of Al₂O₃ grains. At above 700 °C, formation and deformation of fine grain layer, and abrasive wear in the form of removal of fine alumina grains further facilitate the friction and wear process of Al₂O₃ coating.     

Influence of Al2O3 reinforcement on the abrasive wear characteristic of Al2O3/PA1010 composite coatings

In the present study, the abrasive wear characteristics of Al₂O₃/PA1010 composite coatings were tested on the turnplate abrasive wear testing machine. Steel 45 (quenched and low-temperature tempered) was used as a reference material. The experimental results showed that when the Al₂O₃ particles have been treated with a silane coupling agent (γ-aminopropyl-triethoxysilane), the abrasive wear resistance of Al₂O₃/PA1010 composite coatings has a good linear relationship with the volume fraction of Al₂O₃ particles in Al₂O₃/PA1010 composite coatings and the linear correlation coefficient is 0.979. Under the experimental conditions, the size of Al₂O₃ particles (40.5-161.0 μm) has little influence on the abrasive wear resistance of Al₂O₃/PA1010 composite coatings. By treating the surface of Al₂O₃ particles with the silane coupling agent, the distribution of Al₂O₃ particles in PA1010 matrix is more homogeneous and the bonding state between Al₂O₃ particles and PA1010 matrix is better. Therefore, the Al₂O₃ particles make the Al₂O₃/PA1010 composite coatings have better abrasive wear resistance than PA1010 coating. The wear resistance of Al₂O₃/PA1010 composite coatings is about 45% compared with that of steel 45.     

Effects of anti-wear additives on friction and wear properties of Cr2O3 coating

The effects of some anti-wear additives on the friction and wear behaviour of plasma-sprayed Cr₂O₃ coating were investigated using a block-on-ring tester at ambient conditions. The results show that zinc dialkyldithiophosphate (ZDDP), tricesyl phosphate (TCP) and tributyl phosphate (TBP) significantly reduce the wear of Cr₂O₃ coating lubricated by paraffin oil. Additive concentrations as well as sliding time have great influence on the wear. The friction coefficient varies slightly with test conditions. The analysis by XPS of worn surfaces indicates that the wear resistance of these additives is due to the formation of tribochemical reaction films by reacting with Cr₂O₃ coatings.     

A study on friction and wear characteristics of nanometer Al2O3 /PEEK composites under the dry sliding condition

The friction and wear properties of the polyetheretherketone (PEEK) based composites filled with 5 mass% nanometer or micron Al₂O₃ with or without 10 mass% polytetrafluroethylene (PTFE) against the medium carbon steel (AISI 1045 steel) ring under the dry sliding condition at Amsler wear tester were examined. A constant sliding velocity of 0.42 m s⁻¹ and a load of 196 N were used in all experiments. The average diameter 250 μm PEEK powders, the 15 or 90 nm Al₂O₃ nano-particles or 500 nm Al₂O₃ particles and/or the PTFE fine powders of diameter 50 μm were mechanically mixed in alcohol, and then the block composite specimens were prepared by the heat compression moulding. The homogeneously dispersion of the Al₂O₃ nano-particles in PEEK matrix of the prepared composites was analyzed by the atomic force microscopy (AFM). The wear testing results showed that nanometer and micron Al₂O₃ reduced the wear coefficient of PEEK composites without PTFE effectively, but not reduced the friction coefficient. The filling of 10 mass% PTFE into pure PEEK resulted in a decrease of the friction coefficient and the wear coefficient of the filled composite simultaneously. However, when 10 mass% PTFE was filled into Al₂O₃/ PEEK composites, the friction coefficient was decreased and the wear coefficient increased. The worn scars on the tested composite specimen surfaces and steel ring surfaces were observed by scanning electron microscopy (SEM). A thin, uniform, and tenacious transferred film on the surface of the steel rings against the PEEK composites filled with 5 mass% 15 nm Al₂O₃ particles but without PTFE was formed. The components of the transferred films were detected by energy dispersive spectrometry (EDS). The results indicated that the nanometer Al₂O₃ as the filler, together with PEEK matrix, transferred to the counterpart ring surface during the sliding friction and wear. Therefore, the ability of Al₂O₃ to improve the wear resistant behaviors is closely related to the ability to improve the characteristics of the transfer film.     

The effect of Al2O3 on the friction performance of automotive brake friction materials

This study consists of two stages. In the first stage, bronze-based break linings were produced and friction-wear properties of them were investigated. In the second stage, 0.5%, 1%, 2% and 4% alumina (Al₂O₃) powders were added to the bronze-based powders and Al₂O₃ reinforced bronze-based break linings were produced. Friction–wear properties of the Al₂O₃ reinforced samples were aslo investigated and compared to those of plain bronze-based ones. For this purpose, friction coefficient and wear behaviour of the samples were tested on the grey cast iron disc. The hardness and density of the samples were also determined. Microstructures of the samples before and after the sintering and the worn surfaces of the wear specimens were examined using a scanning electron microscope (SEM). The sample compacted at 350 MPa and sintered at 820 °C exhibited the optimum friction–wear behaviour. With increase in friction surface temperature, a reduction in the friction coefficient of the samples was observed. The lowest reduction in the friction coefficient with increasing temperature was for the 2% and 4% Al₂O₃ reinforced samples. The SEM images of the sample indicated that increase in Al₂O₃ content resulted in adhesive wear. With increase in Al₂O₃ content, a reduction in mass loss of the samples was also observed. Overall, the samples reinforced with 2% and 4% Al₂O₃ exhibited the best results.     

Sliding wear characteristics of plasma-sprayed Al2O3 and Cr2O3 coatings against copper alloy under severe conditions

Al₂O₃ and Cr₂O₃ coatings were deposited by atmospheric plasma spraying and their tribological properties dry sliding against copper alloy were evaluated using a block-on-ring configuration at room temperature. It was found that the wear resistance of Al₂O₃ coating was superior to that of the Cr₂O₃ coating under the conditions used in the present study. This mainly attributed to its better thermal conductivity of Al₂O₃ coating, which was considered to effectively facilitate the dissipation of tribological heat and alleviate the reduction of hardness due to the accumulated tribological heat. As for the Al₂O₃ coating, the wear mechanism was plastic deformation along with some micro-abrasion and fatigue-induced brittle fracture, while the failure of Cr₂O₃ coating was predominantly the crack propagation-induced detachment of transferred films and splats spallation.     

Cr2N/CrN multilayer coatings for wood machining tools

The present paper describes results from a recent research project aimed at forming a wear resistant coating based on chromium on tools to wood machining. Cr₂N/CrN multilayer coatings deposited on HS6-5-2 steel substrates using cathodic arc evaporation were tested. These coatings were formed from 7 bilayers being ca. 340 nm thick and equally thick Cr₂N and CrN layers. For comparison, Cr₂N and CrN monolayer coatings were also prepared. Hardness measurements, indentation and scratch tests, friction and wear were performed to characterize the mechanical properties. The wear tracks and Rockwell indentations enable to assess wear mechanisms of the coatings. The results of the Cr₂N/CrN coatings investigated show high hardness: ca. about 22 GPa and a critical force being higher than 95 N and a low wear rate.The industrial tests of planer knives with Cr₂N/CrN multilayer coatings were carried out on a down-spindle milling machine to determine the durability of tools with wear resistant coatings for woodworking. These tools show increase of “life time” two times. Another positive feature of the use of such tools is the increase of the quality of wood surface machined when compared with uncoated tools.     

纳米Fe-Al/Cr_3C_2复合涂层及其抗高温腐蚀性能

制备纳米金属间化合物Fe-Al/Cr_3C_2复合涂层并测试其抗腐蚀性能,为利用热喷涂技术治理火电站易损部件腐蚀问题提供有效手段。运用自主研发的造粒系统,成功对高活性的纳米Fe-Al/Cr_3C_2复合喷涂粉体实施团聚造粒;运用高速火焰喷涂方法,在结构材料表面制备出了纳米Fe-Al/Cr_3C_2复合涂层,对比测试了微米、纳米Fe-Al/Cr_3C_2复合涂层的抗高温腐蚀性能,分别采用抛物线型和幂函数型对腐蚀动力学曲线进行拟合。纳米Fe-Al/Cr_3C_2复合喷涂材料的粒径由原始的50nm团聚到最终的114~178μm,团聚后的纳米颗粒呈圆形或椭圆形,各成分比例保持原始比例,团聚颗粒内部仍然保持纳米粉体状态;纳米Fe-Al/Cr_3C_2复合涂层表面致密、铺展均匀,截面元素过渡平缓、层片细小;运用幂函数方程对腐蚀动力学曲线的拟合效果更好。通过对腐蚀动力学拟合方程进行求导运算可推算出各复合涂层的腐蚀速率。团聚后的纳米颗粒满足热喷涂材料的相关要求,纳米Fe-Al/Cr_3C_2复合涂层的抗高温腐蚀性能显著高于微米Fe-Al/Cr_3C_2复合涂层。纳米Al、Cr优先氧化生成具有保护作用的氧化膜机理解释了纳米涂层抗高温腐蚀性能优异的原因。     

单层MoS2和WS2的太赫兹近场显微成像研究

采用太赫兹散射式扫描近场光学显微镜(THz s-SNOM)研究了化学气相沉积法制备的单层MoS₂和WS₂晶粒的太赫兹近场响应。在没有可见光激发时,未探测到可分辨的太赫兹近场响应,说明晶粒具有较低的掺杂载流子浓度。有可见光激发时,由于光生载流子的太赫兹近场响应,能够测得与晶粒轮廓完全吻合的太赫兹近场显微图。在相同的光激发条件下,MoS₂的太赫兹近场响应强于WS₂,反映了两者之间载流子浓度或迁移率的差异。研究结果表明,THz s-SNOM兼具超高的空间分辨率和对光生载流子的灵敏探测能力,对二维半导体材料和器件光电特性的微观机理研究具有独特的优势。     

Study on the tribological behavior of hybrid PTFE/cotton fabric composites filled with Sb2O3 and melamine cyanurate

The tribological behavior of the hybrid PTFE/cotton fabric composites filled with microsize Sb₂O₃ and melamine cyanurate (MCA) was investigated. It was found that the wear rate of the hybrid PTFE/cotton fabric composites decreased when Sb₂O₃ was used as the filler but increased with MCA filler. It was also observed that hybrid fillers (consists of Sb₂O₃ and MCA) had a wear reduction effect on the hybrid PTFE/cotton fabric composites at lower loads but increased the wear rate at higher loads. The wear behavior of the composites was explained in terms of the topography of worn surfaces and transfer film formed on the counterpart pin.     

Modelling particulate erosion–corrosion regime transitions for Al/Al2O3 and Cu/Al2O3 MMCs in aqueous conditions

Very little research effort has been directed at development of models of erosion–corrosion of composite materials. This is because, in part, the understanding of the erosion–corrosion mechanisms of such materials is poor. In addition, although there has been a significant degree of effort in the development of models for erosion of MMCs, there are still difficulties in applying such models to the laboratory trends on erosion rate.In this paper, the methodology for mapping erosion–corrosion processes in aqueous slurries was extended to particulate composites. An inverse rule of mixtures was used for the construction of the erosion model for the particulate MMCs. The corrosion rate calculation was evaluated with reference to the matrix material.The erosion–corrosion maps for composites showed significant dependency on pH and applied potential. In addition, the corrosion resistance of the matrix material was observed to affect the regime boundaries. Materials maps were generated based on the results to show the optimum composite composition for exposure to the environment.     

Characterization of nanoscale recording mark on Ge2Sb2Te5 film

We have fabricated nanoscale recording marks on Ge₂Sb₂Te₅ (GST) films with conductive atomic force microscope (AFM). GST films were deposited on glass or polyimide film with thickness of 150–200 nm by the rf–sputtering method. Through current–voltage (I–V) spectroscopy, good cantilevers for fabrication and characterization of nanoscale marks on GST were selected. A fresh and highly conductive tip showed voltage-switching characteristic in the I–V curve, where the threshold voltage was 1.6 V. Nanoscale dot and wire arrays of crystalline phases were successfully obtained by varying sample bias voltage from −10 to 10 V. With highly conductive tips, nanowires having full-width at half-maximum of 20 nm could be fabricated, whereas nanowires could not be fabricated with bias voltage below −2 V. The width of the nanoscale mark was increased by repetition of AFM lithography even with same applied voltage and lithography speed. For a thicker nanowire, the width measured in current-image (C-image) was observed to be 2 times of that measured in topography-image (T-image). This result supports that current sensing provides an image of phase-changed GST area with higher resolution than topography sensing.     

High-temperature tribological properties of spark-plasma-sintered Al2O3 composites containing barite-type structure sulfates

Al₂O₃–50BaSO₄–20Ag, Al₂O₃–50BaSO₄–10SiO₂, Al₂O₃–50(mass%)SrSO₄, Al₂O₃–50PbSO₄–5SiO₂, Al₂O₃–50BaSO₄ and Al₂O₃–50BaCrO₄ composites (mass%) were prepared by spark plasma sintering and their microstructure and high-temperature tribological properties were evaluated. Al₂O₃–50BaSO₄–20Ag composites (mass%) showed the lowest friction coefficients at the temperature ranging from 473 to 1073 K. Thin Ag film was observed on the wear tracks of the composites above 473 K. In addition, the friction coefficients of Al₂O₃ composites containing SrSO₄ and PbSO₄ were as low as those of Al₂O₃–BaSO₄ and Al₂O₃–BaCrO₄ composites at the temperatures up to 1073 K. The thin films formed on the wear tracks of the Al₂O₃–SrSO₄ composites were composed of Al₂O₃ and SrSO₄ phases, while the films formed on the wear tracks of the Al₂O₃–PbSO₄–SiO₂ composites consisted of Al₂O₃, PbSO₄ and SiO₂ phases.     

一种纤维锌矿结构CuInS2纳米化合物的合成方法

CuInS2(CIS)是重要的三元Ⅰ-Ⅲ-Ⅵ族直接带隙半导体化合物光伏材料。纤维锌矿CIS的铜和铟原子共享一个晶格,因此其在化学计量比调控方面更加灵活,对高效太阳能电池具有重要意义。在低温条件下,通过简单高效的热注入法合成了在常温下能稳定存在的纤维锌矿CIS纳米化合物,并通过X射线衍射仪(XRD)、扫描电子显微镜(SEM)、X射线光谱仪(EDX)和紫外可见分光光度计(UV)分别对其晶相、形貌、化学计量比和能带值进行了分析。结果表明:合成的CIS纳米化合物呈纤维锌矿结构;能带值为1.47eV,非常接近最佳能带值;呈六边形纳米盘状,纳米盘厚度约为10nm,直径约为100nm;Cu∶In∶S的化学计量比为1.70∶1∶2.94。     

Tribo-physical and tribo-chemical aspects of WC-based cermet/Ti3SiC2 tribo-pair at elevated temperatures

The tribological behaviors of tungsten carbide (WC) based cermet/Ti₃SiC₂ tribo-pair at elevated temperatures were investigated. Lead oxide (PbO) was added as a solid lubricant. The tribo-physical and tribo-chemical changes on sliding surfaces were studied in detail. The results indicated that adhesive and abrasive wear due to removal of metallic binder and pullout of grains were the dominant wear mechanisms at room temperature. At high temperature, tribo-physical changes (i.e. mechanical mixture or sintering) and tribo-chemical reactions including complex reaction and oxidations were induced by frictional heat combined with high environmental temperature. As a result PbWO₄ was formed as a reaction product and acted as a solid lubricant. PbWO₄ and tribo-oxides along with the physically changed layer on the sliding surfaces were favorable to reduce wear of both materials. At high temperature, the wear mechanism varied from adhesive and abrasive wear at room temperature to lubrication by tribo-layer containing PbWO₄, tribo-oxides, and sinters at high temperatures.     

A comparison of oxidation and oxygen substitution in MoS2 solid film lubricants

Significant advancements in the production of low friction, long wear life, sputter-deposited MoS₂ lubricant coatings have been made in the last decade. The introduction of multi-layered coatings, the establishment of careful controls on doping during DC and magnetron sputter deposition, and the implementation of ion assisted deposition have resulted in lubricants with substantially longer wear lives (up to a factor of ten greater than in the early 1980s) and lower sliding friction coefficients. A major research effort, designed to improve the performance of solid lubricants, involved a number of laboratories during this time period, resulting in these major breakthroughs. However, even with this concentrated effort, the typical investigation involved making an educated guess, based on previous experience, of the deposition conditions, target compositions, or post treatments that might be expected to provide improved performance of resulting coatings. One notable discovery during this time period was that typical MoS₂ films contain large quantities (up to 20 atom %) of oxygen substituted for sulfur in individual crystal lattices. In this paper we will compare the effects of this oxygen substitution with the effects of oxidation which involves a change in the oxidation number of the central molybdenum atoms within the crystals. A discussion of the relationship(s) between chemistry and coating structure and tribological performance will be presented with emphasis on defect chemistry and multiple phase interactions. Speculations on the role of coating chemistry in determining coating performance in applications such as in ball bearings will be presented.     

Wear-Resistant PTFE/SiO2 Nanoparticle Composite Films

Polytetrafluoroethylene (PTFE) is a polymer that is well known for its exceptional tribological properties and, as such, it is commonly used to reduce the coefficient of friction between surfaces. In recent years it has also been established that by incorporating nanoparticle fillers in PTFE, it is possible to extend the polymer's life by reducing its wear rate. Although much study has been placed on bulk PTFE, very little study has been focused on thin films. This article demonstrates that SiO ₂ nanoparticles can be used as a filler to significantly reduce the wear of PTFE thin films while also maintaining a low coefficient of friction. The wear resistance and coefficient of friction of PTFE/SiO ₂ composite films on stainless steel substrates were tested using a linear reciprocating tribometer and compared to pure PTFE films and bare stainless steel to evaluate the benefit of incorporating the SiO ₂ filler in the film. The composite films showed a significant improvement in wear resistance when compared to pure PTFE films. The coefficient of friction for the composite film remained low and stable during a 50 g normal load friction test for a duration of approximately 300 cycles, whereas that of PTFE showed an increasing trend at onset. In addition, of 1.7 and 3.3 wt% SiO ₂ concentrations in solution, 3.3 wt% SiO ₂ showed better performance, with a much higher wear resistance than that of 1.7% SiO ₂ after being subjected to a 1,000-cycle abrasive wear test.