Effects of a second phase on the tribological properties of Al2O3 and ZrO2 ceramics

The tribological properties of four different materials are investigated, tetragonal zirconia (Y-ZTP), Al₂O₃ dispersed in Y-TZP (ADZ), ZrO₂ dispersed in Al₂O₃ (ZTA) and Al₂O₃ (with 300 ppm MgO). These materials are used as a cylinder sliding against a plate of Y-TZP (TZ-3Y)). Compared to Y-TZP, the wear resistance of ADZ composites is increased by a factor of 4–10. At a contact pressure of 230 MPa, a wear transition for Y-TZP is observed from plastic deformation to microchipping and microfracture due to the high interfacial temperature (450°C–550°C) generated by frictional heating. Because of the higher elastic modulus, hardness and fracture toughness at high temperature, ADZ composites show better wear resistance and a higher transition contact pressure (over 400 MPa) under the present conditions. For Al₂O₃, the transition from mild to severe wear occurs when the contact pressure is changed from 250 to 400 MPa. For ZTA ceramics, the wear behaviour does not change because of the presence of a compressive layer due to the zirconia phase transformation during sliding.

In water the wear resistance for ADZ and ZY5 is almost two orders of magnitude higher than the results under dry conditions. Reduction of the interfacial temperature by using water and the formation of a hydroxide layer at the contact surface by the tribochemical reaction of water with the ceramic, as observed by XPS, gives a positive effect on wear resistance.     

Wear properties of two-phase Al2O3/ZrO2 (Y2O3) ceramics at temperatures from 296 to 1073 K

Reciprocating sliding friction experiments were conducted with various two-phase, directionally solidified Al₂O₃/ZrO₂ (Y₂O₃) pins sliding on B₄C flats in air at temperatures of 296, 873, and 1073 K under dry sliding conditions. Results indicate that all the Al₂O₃/ZrO₂ (Y₂O₃) ceramics, from highly Al₂O₃-rich to ZrO₂-rich, exceed the main wear criterion requirement of 10⁻⁶ mm³ N⁻¹ m⁻¹ or lower for effective wear-resistant applications. Particularly, the eutectics and Al₂O₃-rich ceramics showed superior wear properties. The composition and microstructure of Al₂O₃/ZrO₂ (Y₂O₃) ceramics played a dominant role in controlling the wear and friction properties. The controlling mechanism of the ceramic wear, friction, and hardness was an intrinsic effect involving the resistance to shear fracture of heterophase bonding and cohesive bonding and the interlocking microstructures at different scales in the ceramics.     

The tribological properties of YBa2Cu3O7 films in ambient environment

In the present study, high-T_c superconducting thin YBa₂Cu₃O₇ films and polysilicon films were prepared to investigate the initial sliding friction properties using a ball-on-flat tribometer when samples were moved against a sapphire ball or a steel ball in ambient environment. The surface topography was measured with atomic force microscope (AFM). After five times testing, the experimental results indicate that the friction coefficient of YBa₂Cu₃O₇ films is lower than that of polysilicon films when sliding against a sapphire ball and almost the same when sliding against a steel ball. In particular, the initial friction of YBa₂Cu₃O₇ films is more stable when sliding against a sapphire ball. However, the initial friction of polysilicon films fluctuates during a cycle period when sliding against a sapphire ball. They are both stable when sliding against a steel ball. Although, the surface profile of the YBa₂Cu₃O₇ film is rough and can be seen to be rougher than the polysilicon film, but the friction coefficient of the YBa₂Cu₃O₇ film is lower than that of polysilicon film. Also, although the topography of YBa₂Cu₃O₇ films changes during friction, the friction coefficients are stable. This clearly shows that the initial sliding friction of YBa₂Cu₃O₇ films under microfriction is stable. The observation signifies YBCO film is a good film to prevent stick–slip motion in ambient environment. The wear properties of YBa₂Cu₃O₇ films suggest that the superconducting outgrowths (CuO) are loose and they can be easily removed.     

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.     

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.     

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.     

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.     

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 load AFM friction and wear experiments on V2O5 thin films

High load friction and wear experiments by means of atomic force microscopy were carried out at the surface of highly (0 0 1) oriented vanadium oxide V₂O₅ thin films deposited on silicon by reactive magnetron sputtering. Microscopic friction coefficient was estimated for wide range of loads. The nature of surface wear due to multiple, high load scanning is presented and discussed.     

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.     

A comparative study on the microstructure and tribological properties of Si3N4 and TiN films produced by the IBED method

The tribological properties of Si₃N₄ and TiN thin films produced by ion beam enhanced deposition (IBED) were compared on a SRV friction and wear testing machine. The friction coefficient of all thin films shows a descending tendency with increase in load, and is lower than that of 52100 steel. All the IBED films show a much better wear resistance than 52100 steel, especially in the higher load and frequency ranges; it can reach six times that of the latter. In order to understand the reasons for their excellent properties, the microstructure, microhardness and bonding strength with the substrate were analysed by SEM, X-ray diffraction, Knoop hardness and scratching test methods separately. The results show that the TiN(1) film exhibits the best tribological properties, which are closely related with its greater hardness and bonding strength.     

Friction and wear properties of UHMWPE/Al2O3 ceramic under different lubricating conditions

Friction and wear behavior of ultra-high molecular weight polyethylene (UHMWPE) sliding against Al₂O₃ ceramic under dry sliding, and lubrication of fresh plasma, distilled water and physiological saline were investigated with a self-made pin-on-disk apparatus at 37±1°C. The worn surfaces were examined with a scanning electron microscope (SEM). The results show that the friction behavior of UHMWPE is very sensitive to its water absorption state. The wear rate of UHMWPE under dry sliding is the highest and under plasma lubrication is the lowest. The wear mechanisms are different under dry friction and various lubricating conditions.     

Tribological behavior of plasma sprayed Cr2O3-3%TiO2 coatings

Tribological behaviors of plasma-sprayed conventional and nanostructured Cr₂O₃-3%TiO₂ ceramic coatings (i.e., CC3T and NC3T, respectively) using pin on disc type dry sliding and pot type slurry erosion test were investigated in the present work. The experimental results indicated that there were two main wear mechanisms, plastic smearing and adhesive tearing, in the worn coatings under dry sliding. Plastic smearing corresponded to a lower average friction coefficient and wear rate, while adhesive tearing corresponded to higher values. The erosive environment selected for the slurry erosion experiments include 10, 20 and 30% of SiO₂ slurry concentrations in water with particle size 75-106 μm. The main damage mechanism observed in all the coatings submitted to slurry erosion were the formation and propagation of brittle cracks resulting in the detachment of coating surface material. Microstructural investigation was also carried to investigate the wear and erosion mechanism of the coatings using FE-SEM and EDS analysis. Properties like microhardness and porosity were also investigated for these coatings. Tribological performance of NC3T was better as compared to CC3T as observed in the present work.     

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.     

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.     

不同润滑条件下氧化铝陶瓷衬板的磨损机制

在干摩擦、水润滑、油润滑3种不同润滑条件下对氧化铝陶瓷进行摩擦磨损试验。利用SEM对磨损后的磨痕进行观察并进行显微组织结构分析,探讨不同介质下氧化铝陶瓷的磨损机制。结果表明:氧化铝陶瓷材料干摩擦条件下的磨损机制为大量的脆性剥落和大量的磨粒磨损,在水润滑条件下为较少的脆性剥落和轻微的磨粒磨损,在油润滑条件下为很少的脆性剥落和极微的磨粒磨损;液体润滑剂可使氧化铝陶瓷材料的磨损量大幅度降低,其中油润滑条件的减磨效果最为突出。     

Mechanical and tribological investigations of sol–gel derived SiO2 optical coatings

Sol–gel silica coatings were deposited on soda lime glass substrates by dip-coating. The silica films were amorphous, crack free, and smooth with an average roughness of less than 3 nm and thickness of 0.8–1.2 μm. Mechanical and tribological properties were investigated using nanoindentation, Taber abrasion and a polishing wear test. The hardness increased with increased thermal exposure from 2200 MPa for samples fired at 480 °C for 2 min to 3800 MPa for those fired at 560 °C for 14 min. In Taber abrasion, failure was due to penetration of the coatings by the abrasive particles of the Taber grinders, which caused scratches and subsequent delamination. For polishing wear experiments, hardness was inversely proportional to polishing wear rate. This suggests that hardness is a good indicator for the resistance of sol–gel silica coatings to polishing.     

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.     

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.     

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.