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.     

Tribological properties of spark-plasma-sintered ZrO2(Y2O3)-CaF2-Ag composites at elevated temperatures

Spark-plasma sintering is employed to synthesize self-lubricating ZrO₂(Y₂O₃) matrix composites with different additives of CaF₂ and Ag as solid lubricants by tailoring the composition and by adjusting the sintering temperature. The friction and wear behavior of ZrO₂(Y₂O₃) matrix composites have been investigated in dry sliding against an alumina ball from room temperature to 800 °C. The effective self-lubrication at different temperatures depends mainly on the content of various solid lubricants in the composites. The addition of 35 wt.% Ag and 30 wt.% CaF₂ in the ZrO₂(Y₂O₃) matrix can promote the formation of a well-covered lubricating film, and effectively reduce the friction and wear over the entire temperature range studied. The friction coefficients at low temperatures were at a minimum value for the composite containing 35 wt.% of silver. At this silver concentration, low and intermediate temperature lubricating properties are greatly improved without affecting high-temperature lubrication by the calcium fluoride in ZrO₂(Y₂O₃) matrix composites. The worn surfaces and transfer films formed during wear process have been characterized to identify the synergistic lubrication behavior of CaF₂ and Ag lubricants at different temperatures.     

Microstructure and tribological characteristics of ZrO2–Y2O3 ceramic coatings deposited by laser-assisted plasma hybrid spraying

ZrO₂–Y₂O₃ ceramic coatings were deposited on AISI 304 stainless steel by both a low-pressure plasma spraying (LPPS) and a laser-assisted plasma hybrid spraying (LPHS). Microstructure and tribological characteristics of ZrO₂–Y₂O₃ coatings were studied using an optical microscope, a scanning electron microscope, and an SRV high-temperature friction and wear tester. The LPHS coatings exhibit distinctly reduced porosity, uniform microstructure, high hardness and highly adhesive bonding, although more microcracks and even vertical macrocracks seem to be caused in the LPHS coatings. The ZrO₂ lamellae in the LPHS coatings before and after 800°C wear test consist mainly of the metastable tetragonal (t′) phase of ZrO₂ together with small amount of c phase. The t′ phase is very stable when it is exposed to the wear test at elevated temperatures up to 800°C for 1 h. The friction and wear of the LPHS coatings shows a strong dependence on temperature, changing from a low to a high wear regime with the increase of temperature. At low temperatures, friction and wear of the LPHS coatings is improved by laser irradiation because of the reduced connected pores and high hardness in contrary to the LPPS coating. However, at elevated temperatures, the friction and wear of the LPHS coatings is not reduced by laser irradiation. At room temperature, mild scratching and plastic deformation of the LPHS coatings are the main failure mechanism. However, surface fatigue, microcrack propagation, and localized spallation featured by intersplat fracture, crumbling and pulling-out of ZrO₂ splats become more dominated at elevated temperatures.     

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.     

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.     

Dry sliding wear mechanism for P/M austenitic stainless steels and their composites containing Al2O3 and Y2O3 particles

Austenitic stainless steels are used in applications demanding general corrosion resistance at room or moderate operating temperatures. However, their use is often limited by the relative softness of these materials and their suceptibility to wear and galling. The present investigation deals with the dry sliding wear behaviour of two P/M austenitic stainless steels (AISI 304L and 316L) and their composites containing two different ceramic particles (Al₂O₃ and Y₂O₃) and two different sintering activators (BN and B₂Cr). Unlubricated pin-on-disc wear tests were carried out. Wear mechanisms were analysed by means of scanning electron microscopy and X-ray diffraction. A plastic deformation and particle detachment wear mechanism was revealed. Plasticity during sliding induced an austenite to martensite transformation. The presence of ceramic particles (Al₂O₃ and Y₂O₃) and sintering activators (B₂Cr, BN) improved significantly the wear resistance (especially the combination Al₂O₃ and B₂Cr). Ceramic particles limited plastic deformation while sintering activators decreased final porosity.     

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.     

Tribological Properties of Spark-Plasma-Sintered ZrO2(Y2O3)–Al2O3–Ba x Sr1?x SO4 (x?=?0.25, 0.5, 0.75) Composites at Elevated Temperature

Self-lubricating ZrO₂(Y₂O₃)–Al₂O₃–Ba _x Sr_1−x SO₄ (x = 0.25, 0.5, 0.75) composites have been fabricated by spark plasma sintering (SPS) method. The tribological properties have been evaluated using a high-temperature friction and wear tester at room temperature and 760 °C in dry sliding against alumina ball. The composites exhibit distinct improvements in effectively reducing friction and wear, as compared to the unmodified ZrO₂(Y₂O₃)–Al₂O₃ ceramics. The ZrO₂(Y₂O₃)–Al₂O₃–Ba _x Sr_1−x SO₄ (x = 0.25, 0.5, 0.75) composites have great low and stable friction coefficients of less than 0.15 and wear rates in the order of 10^− 6mm³/Nm at 760 °C. Delamination is considered as the dominating wear mechanism of the composites at room temperature. At elevated temperature, the formation and effective spreading of Ba _x Sr_1−x SO₄ (x = 0.25, 0.5, 0.75) lubricating films during sliding play an important role in the reduction of the friction and wear.     

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.     

Lubrication of Si3N4 and Al2O3 in water with and without addition of silane coupling agents in the range of 0.05–0.10 mol/l

To improve water lubrication of ceramics at a lower sliding velocity, the effect of the addition of silane coupling agents was investigated. Si₃N₄ and Al₂O₃ were slid against themselves in water with and without the addition of silane coupling agents in amounts ranging from 0.05 to 0.10 mol/l. Silane coupling agents containing one or more amino groups were effective in reducing the friction of Si₃N₄ and Al₂O₃ in water. Si₃N₄ also showed significant wear reduction but not Al₂O₃. However, the addition of a silane coupling agent containing an epoxy group increased both friction and wear of Si₃N₄. Improved lubricative characteristics of Si₃N₄ in water and in silane coupling agent solutions were obtained when Si₃N₄ contained smaller amounts of sintering additives. The adsorption behaviour of a silane coupling agent on ceramics was examined using both Fourier transform infrared spectroscopy and thin layer chromatography to clarify the interaction between the silane coupling agent and the ceramics. The role of polysiloxane film formation on ceramics is discussed to demonstrate the lubrication properties of ceramics.     

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.     

Wear behaviour of Al/(Al2O3p+SiCp) hybrid composites

In this study, dry sliding metal–metal and metal–abrasive wear behaviours of the aluminium matrix hybrid composites produced by pressure infiltration technique were investigated. These composites were reinforced with 37 vol% Al₂O₃ and 25 vol% SiC particles and contained up to 8 wt% Mg in their matrixes. While matrix hardness and compression strength increased, amount of porosity and impact toughness decreased with increasing Mg content of the matrix. Metal–metal and metal–abrasive wear tests revealed that wear resistance of the composites increased with increasing Mg addition. On the other hand, abrasive resistance decreased with increasing test temperature, especially above 200 °C.     

Friction and wear of MgO single crystals on sintered Al2O3 in vacuum

Experiments were carried out on the wear of MgO single crystals on sintered Al₂O₃ using a pin-on-disk type machine in a vacuum chamber. Minimum values of friction and wear with a smooth wear surface were found in the range 10^?2–10⁰ Torr; these were shifted to higher values and/or to poor vacuum with increasing sliding velocities. High wear rates in a high vacuum were due to repeated micro brittle fractures because of adhering wear fragments. Low wear rates in a poorer vacuum were caused by the tearing off of the laminated surface film by plastic flow.     

Friction–wear behavior and tribochemical reactions of different ceramics in HFC-134a gas

The friction and wear properties of the ionic ceramics Al₂O₃ and ZrO₂, and the covalent ceramics Si₃N₄ and SiC rubbing against an Al₂O₃ ball in vacuum (10⁻⁵ Pa) and in CF₃CH₂F (HFC-134a) gas at 10⁴ Pa were investigated using a ball-on-disk type tribometer. Without exposure to air, the surface composition and chemical state of the wear tracks and debris on the disks were determined with X-ray photoelectron spectroscopy (XPS). It is found that HFC-134a gas significantly reduces the friction and wear of all the ceramic couples, and that the ionic ceramic pairs show lower friction and wear. On the other hand, metal fluorides and/or fluorine-containing organic compounds are detected on the sliding surfaces. The differences in the friction–wear behavior of the ceramics rubbing in HFC-134a gas may be due to the products of tribochemical reactions, which are dependent on the bond type of the ceramics.     

High-temperature tribological properties of strontium sulfate films formed on zirconia-alumina, alumina and silicon nitride substrates

In our present study, Al₂O₃, (ZrO₂–3 mol% Y₂O₃)–39.6 mass% Al₂O₃ and Si₃N₄ substrates coated with SrSO₄ and SrSO₄–10 mass% Ag films were prepared, and the friction and wear properties of these specimens were investigated using a reciprocating ball-on-disk tribometer in the temperature range from room temperature to 1073 K in air. It was clarified that (ZrO₂–3 mol% Y₂O₃)–39.6 mass% Al₂O₃ substrates coated with chemically precipitated SrSO₄ particles and the substrates coated with SrSO₄–10 mass% Ag films prepared by mechanically grinding and annealing at 1073 K for 3.6 ks exhibited low friction coefficients and low wear rates at all the testing temperatures. In addition, the average friction coefficients of Si₃N₄ substrates were reduced above 673 K by coating with chemically precipitated SrSO₄ particles.     

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.     

Effect of ZrO2 Nanoparticles Additive on the Tribological Behavior of Multialkylated Cyclopentanes

Monodisperse ZrO₂ nanoparticles with a particle size of about 6–7 nm and low volatile multialkylated cyclopentanes (MACs) lubricant were prepared and characterized. The effect of ZrO₂ nanoparticles as additive on the friction and wear behavior of MACs base oil was investigated. The friction and wear performance of 2 wt% ZrO₂ nanoparticles + MACs was evaluated using an Optimal SRV oscillating friction and wear tester, with a steel ball sliding against the same steel counterpart disc. Results indicate that the wear resistance and load-carrying capacity of MACs base oil were markedly raised and its friction coefficient changed little when 2 wt% ZrO₂ nanoparticles were added to it.     

Tribological performance of MoS2---B2O3 compacts

A recent investigation suggests that selected oxides perform well as additives in molybdenum disulphide (MoS₂) because of their ability to soften at asperity contacts with the result that the solid lubricant can attain and retain a preferred tribological orientation.This research determined the effectiveness of boric oxide (B₂O₃), when used as an additive in MoS₂, for substrate temperatures ranging from 21°C to 316°C. This range was used to allow the asperity contact temperature to vary below and above the softening point of B₂O₃. It was found that a moderate friction coefficient and high wear, which is attributed to the additive acting abrasively, occurred when the asperity contact temperature was well below the softening point of the oxide. When the asperity contact temperature neared the softening point of the oxide, the friction coefficient increased dramatically and wear volume was reduced. It is postulated that B₂O₃ acted adhesively at the interface resulting in a higher coefficient of friction, and wear decreased due to an attainment of a preferred orientation by the MoS₂. For asperity contact temperatures significantly above the softening point of B₂O₃, the friction coefficient returned to about the same value as for temperatures below the softening point. It is speculated that wear continued to increase moderately because of localized melting of the B₂O₃, permitting the MoS₂ to be removed from the interface. These observations support a hypothesis that an additive, such as boric oxide, can soften as the asperity contact temperature approaches the softening point temperature of the additive so that the overall tribological conditions may be improved resulting in reduced interfacial wear. Significant changes in temperature, load or sliding velocity would, of course, dramatically alter the wear characteristics observed at the interface.     

The influence of the composition of nanostructural PSZ powders on ceramics wear

The results of tribological testing of ceramics with the composition ZrO₂ + Al₂O₃, ZrO₂ + Y₂O₃, and ZrO₂ + Y₂O₃ + Al₂O₃ made of nanostructural powders are presented. The nanopowders have been obtained by chemical precipitation from solutions of zirconium and yttrium chloride salts. The studies have been carried out as applied to machine parts: drawing dies and bearing plugs. The dependence of the wear of friction pairs on the composition of the ceramics is shown.