INFLUENCE OF MACHINING ON FRICTION AND WEAR OF LUBRICATED CERAMICS IN SLIP-ROLLING CONTACTS

The slip-rolling friction and wear tests were performed in a twin disc tribometer of the Amsler-type at a Hertzian pressure of 3 GPa over 2 million revolutions. Paraffinic oil with no additives was used as lubricant. The ceramics were machined with different processes, resulting in different surface roughness (i.e., rough and fine honed, rough and fine ground, rough and fine lapped, and rough and fine polished). Ceramic materials like HIP-Si₃N₄, S-SiC, HIP-ZrO₂, and GPS-Si₃N₄-TiN were investigated as self-mated couples. This paper summarizes the results. Si₃N₄, Si₃N₄-TiN, and ZrO₂ generally exhibit a small wear coefficient in the range of 10^-9 mm³/Nm in paraffinic oil and their wear coefficients correlate with the initial surface roughness and the material removal rate. The lowest wear coefficients were exhibited by ZrO₂- With a reduction of the Hertzian pressure to 1.5 GPa, S-SiC exhibits the same tribological behavior as the other ceramics.     

Sliding speed-temperature wear transition maps for Si3N4/iron alloy couples

The superior high temperature resistance of silicon nitride (Si₃N₄) based ceramics makes them suitable for tribological applications above room temperature or in high speed unlubricated sliding. There are some published works on the wear behaviour of Si₃N₄/metal alloys. However, experimental data are shown in a form that is not of direct use for engineers involved in materials selection. In the present work, Si₃N₄ pins were tested against tool steel and grey cast iron on a pin-on-disc tribometer. Ceramics were produced by hot-pressing and tested without lubrication at variable temperature and sliding speed. SEM/EDS and XRD analysis were used for chemical and microstructural characterisation of worn surfaces and wear debris. At low speeds (0.05–0.5 m s⁻¹) and room temperature, Si₃N₄ surfaces are polished-like due to a combination of humidity-assisted tribo-oxidation and abrasive action of very fine wear debris. At high sliding speeds (2–3.5 m s⁻¹), as well as for temperatures in the range 400–600°C, an extensive coherent tribolayer mainly composed by iron oxides spreads over the ceramic surfaces. Polishing and protection by adherent tribolayers are the mechanisms responsible for observed severe and mild wear regimes, respectively. Wear maps are constructed showing the transition of wear regimes in Si₃N₄/iron alloys contacts determined by constant flash temperature curves. Equations for calculation of bulk and flash contact temperatures in tribocontacts between dissimilar materials are deduced.     

Friction and wear properties of CN<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>/SiC in water lubrication

Amorphous carbon nitride coatings (a-CN_x) were deposited on SiC disk by ion beam assisted deposition (IBAD). The tribological behavior of a-CN_x coating sliding against SiC ball in water was investigated and compared with that of SiC/SiC system at room temperature. The influences of testing conditions on friction coefficient and specific wear rate of both kinds of tribopairs were studied. The worn surfaces on disks were observed by scanning electron microscope (SEM). The results indicate that the running-in period of a-CN_x/SiC was shorter than that of SiC/SiC system in water. At a sliding velocity of 120 mm/s, the mean steady-state friction coefficients of SiC/SiC (0.096) was higher than that of a-CN_x/SiC (0.05), while at 160 mm/s, lower friction coefficient (0.01) was obtained for SiC/SiC in water. With an increment of normal load, the mean steady-state friction coefficients after running-in first decreased, reaching a minimum value, and then increased. For self-mated SiC, the specific wear rate of SiC ball was a little higher than that of SiC disk, while for a-CN_x/SiC, the specific wear rate of SiC ball were 10 times smaller than that of a-CN_x coating. Furthermore, the specific wear rate of SiC ball sliding against a-CN_x coating was reduced by a factor up to 100~1000 in comparison to that against SiC in water. The wear mechanism of SiC/SiC system in water is related to micro-fracture of ceramic and instability of tribochemical reaction layer. Conversely, wear mechanism for a-CN_x/SiC is related to formation and transfer of easy-shear friction layer.     

干摩擦工况下Si3N4/PTFE配副材料摩擦磨损特性与转移膜形成分析

为使全陶瓷轴承在干摩擦工况下可靠运转,选用四氟乙烯(PTFE)材质的保持架为全陶瓷轴承提供润滑.利用Rtec销/盘摩擦磨损试验机,以PTFE盘与氮化硅(Si3 N4)销为摩擦副,研究Si3 N4/PTFE在不同载荷和转速条件下的摩擦磨损性能,通过SEM对Si3 N4表面的转移膜形貌进行观察,分析转移膜形成原因.结果表明...     

The effects of iron particles on the friction and wear mechanisms of ceramics in ethanol

For the combinations of an Si₃N₄ pin and five kinds of ceramic disk (SiC, Si₃N₄, Al₂O₃, ZrO₂, TiC), a friction and wear test was carried out in ethanol and in ethanol containing iron particles (1 wt.%, average diameter d = 200 nm, D = 12 μm under cohered condition) under a load in the range 5.88–11.50 N, at a sliding velocity of 0.138–0.196 m s⁻¹. A topographical analysis was also performed on the microasperities of the wear surfaces to estimate the behavior of the iron particles, and the degree of surface damage. As a result, the following facts were found. (1) The addition of iron particles in ethanol decreased both the wear rates of SiC and TiC disks and the mating pins, and also decreased the wear rate of the Al₂O₃ disk but increased that of the mating pin. The addition increased the wear rates of both ZrO₂ and Si₃N₄ disks and the mating pins. (2) The average coefficients of friction with the addition of iron particles were greater than those without iron particles. (3) The wear rates of pin and disk depended on the topographies of wear surfaces and the wear index Γ.     

A study of the friction and wear performance of MoSx thin films produced by ion beam enhanced deposition and magnetron sputtering

MoS_x thin films were deposited by ion beam enhanced deposition (IBED) and magnetron sputtering (MS) onto the surface of IBEN Si₃N₄ and TiN thin films. The friction and wear performances of thin films and 52100 steel were compared using an SRV model reciprocating testing machine. The results showed that all MoS_x films exhibit good tribological behavior. The MS MoS_x thin film has better wear resistance and the IBED MoS_x film has a longer wear life. The wear resistance of IBED Si₃N₄ and TiN thin film plus MoS_x film is 3–4 times and 8–20 times that of single IBED Si₃N₄ and TiN thin films and 52100 steel respectively. The analyses indicate that the difference in friction and wear performance between the two kinds of MoS_x thin film is determined by the x value of MoS_x, its microstructure and the atom mixing effect at the interface.     

The comparisons of sliding speed and normal load effect on friction coefficients of self-mated Si3N4 and SiC under water lubrication

The effects of sliding speed and normal load on friction coefficients of self-mated Si₃N₄ and SiC sliding in water after running-in in water were investigated with pin-on-disk apparatus at sliding speeds of 30 to 120 mm/s, normal loads of 1 to 14 N in ambient condition. The results showed that, after running-in in water, for two kinds of self-mated ceramics, friction coefficient increases with both decreasing sliding speed and increasing normal load when normal load is larger than a critical normal load. Friction coefficient was independent of normal load when normal load is smaller than the critical load. The lubrication film of Si₃N₄ under water lubrication exhibited larger load carrying capacity than that of SiC did. Stribeck curves indicated that, for self-mated Si₃N₄ ceramics, hydrodynamic lubrication will change into boundary lubrication abruptly when the sommerfeld number is less than a critical value; while for self-mated SiC ceramics, hydrodynamic lubrication will change into mixed lubrication and then into boundary lubrication gradually when the sommerfeld number is below critical value.     

Ionic Liquid Lubrication Effects on Ceramics in a Water Environment

Ionic liquids were studied to determine their effectiveness as boundary lubricant additives for water. The chemical and tribochemical reactions that govern their behavior were probed to understand lubrication mechanisms. Under water lubricated conditions, silicon nitride ceramics are characterized by a running-in period of high friction, during which time the surface is modified causing a dramatic decrease in friction and wear. Two mechanisms have been proposed to explain the friction and wear behavior. Si₃N₄ sliding against itself may result in tribochemical reactions that form a hydrated silicon oxide layer on the surface of the sliding contact. This film has been suggested to mediate friction and wear. Others have suggested that tribo-dissolution of SiO₂ results in an ultra smooth surface and after a running-in period of high wear, the lubrication mode becomes hydrodynamic. The goal of this study was to examine the effects that ionic liquids have on the friction and wear properties of Si₃N₄, in particular their effects on the running-in period. Tribological properties were evaluated using pin-on-disk and reciprocating tribometers. The tribological conditions of the tests were selected to produce mixed/hydrodynamic lubrication. The relative lubrication mode between mixed and hydrodynamic was controlled by the initial surface roughness. Solutions containing 2 wt% ionic liquids were produced for testing purposes. Chemical analysis of the sliding surfaces was accomplished with X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). The test specimens were 1 in diameter Si₃N₄ disks sliding against 1/4 in Si₃N₄ balls. The addition of ionic liquids to water resulted in dramatically reduced running-in periods for silicon nitride from thousands to the hundreds of cycles. Proposed mechanisms include the formation of BF_x and PF_x films on the surface and creation of an electric double layer of ionic liquid.     

The Difference in Running-In Period and Friction Coefficient Between Self-Mated Si3N4 and SiC Under Water Lubrication

Running-in periods and friction coefficients of SiC and Si₃N₄ sliding against themselves under water lubrication were investigated with a pin-on-disk apparatus at sliding speed of 120 mm/s and a normal load of 5 N under ambient conditions. It was found that the running-in period of self-mated Si₃N₄ is much shorter than that of self-mated SiC, and also that the steady-state friction coefficient of self-mated Si₃N₄ was lower (0.0035) than that of self-mated SiC (0.01). The difference in mechanism was analyzed from the point of view of electronic structure and surface chemistry.     

Fretting wear behavior of TiB2-based materials against bearing steel under water and oil lubrication

Lubricated fretting tests in water and paraffin oil were performed with a monolithic TiB₂, a TiB₂-based cermet with 16 vol.% Ni₃(Al, Ti) binder, a sialon–TiB₂ (60/40) composite and a ZrO₂–TiB₂ (70/30) composite against ball bearing grade steel. Based on the measured friction and wear data, the ranking of the investigated fretting couples was evaluated. Furthermore, the morphological investigations of the worn surfaces and transfer layers are carried out and the wear mechanisms for the investigated friction couples are elucidated. While fretting in water, experiments revealed that tribochemical reactions, coupled with mild abrasion, played a major role in the wear behavior of the studied material combinations. ZrO₂–TiB₂ (70/30)/steel wear couple has been found to have the highest fretting wear resistance among the different tribocouples under water lubrication. Under oil lubrication, extensive cracking of the paraffin oil at the fretting contacts, caused by tribodegradation, leads to the deposition of a carbon-rich lubricating layer, which significantly reduced friction and wear of all the investigated tribosystems.     

Ceramic-ceramic composite materials with improved friction and wear properties

Dry friction and wear tests were performed with self-mated couples of SiC containing 50% TiC, Si₃N₄---BN, SiC---TiB₂ and Si₃N₄ with 32% TiN at room temperature and 400°C or 800°C.Under room temperature conditions, the friction coefficient of the couple SiC---TiC/SiC---TiC is only half of that of the couple SiC/SiC and the wear is one order of magnitude smaller. At 400°C, it exceeds the friction coefficient of SiC/SiC except at the highest sliding velocity of 3 m s⁻¹. At lower sliding velocities the wear coefficient of SiC---TiC/SiC---TiC is lower than that of SiC/SiC.The couple Si₃N₄---TiN/Si₃N₄---TiN exhibits high friction coefficients under all test conditions. At room temperature the wear volume of the self-mated couples of Si₃N₄ and Si₃N₄---TiN after a sliding distance of 1000 m is similar, but Si₃N₄---TiN shows a running-in behaviour. At 800°C the wear coefficient of Si₃N₄---TiN/Si₃N₄---TiN is approximately two orders of magnitude smaller than that of Si₃N₄/Si₃N₄, and equal to those at room temperature. At 22°C the addition of BN reduces the friction of Si₃N₄. The wear coefficient is independent of sliding velocity and the self-mated couples showing running-in. Friction and wear increase with increasing temperature. The wear coefficient of SiC---TiB₂ above 0.5 m s⁻¹ at 400°C is advantageously near 10⁻⁶ mm³ (Nm)⁻¹. With the other test conditions the wear behaviour is similar to SSiC.     

Si_3N_4陶瓷旋转超声磨削加工的表面摩擦特性

为了探索结构陶瓷材料在摩擦过程中表面形貌的变化规律及其对摩擦特性影响,分析了摩擦过程中材料的接触过程及力学关系,并对旋转超声磨削加工的Si3N4陶瓷试样开展了摩擦表面形貌、摩擦因数等特性的试验研究。首先根据接触特点和材料特性,基于分形理论推导出接触面总载荷计算公式,基于该公式建立了结构陶瓷摩擦因数分形模型。分析结果表明:当初始表面轮廓分形维数分别为1.4,1.45,1.5和1.55时,摩擦因数与摩擦后表面轮廓分形维数呈类似正态分布曲线。然后通过旋转超声磨削加工的Si3N4陶瓷试样面面接触摩擦试验,研究了摩擦后陶瓷材料表面微观形貌和摩擦因数变化规律,分析了各因素对摩擦因数的影响。试验结果表明:产生微观裂纹是Si3N4陶瓷摩擦后表面微观形貌的显著特点;温度值等于160℃是Si3N4陶瓷摩擦因数由下降转为上升的拐点;当施加载荷为360N和往复频率为80Hz时,摩擦因数最大。得到的结果为通过表面形貌控制提高结构陶瓷耐磨性能提供了技术支撑。     

Micro- and macro-tribological properties of SiC ceramics in sliding contact

Surface properties of single-crystalline and polycrystalline silicon carbide (SiC) specimens were measured using atomic force/friction force microscopy, Auger electron spectroscopy and nano-indentation techniques. Running-in behavior during sliding tests in vacuum was studied on self-mated SiC pairs as a function of surface quality produced by machining. Tribological mechanisms were analyzed in short-time tests using a high-resolution micro-tribometer and then were related to results obtained from macro-tribological tests in humid air and in the presence of distilled water. Information on the structure, chemical composition and properties of SiC surfaces resulting from measurements on the nanoscale can be very useful for explaining tribological performance under far different operating conditions such as in vacuum or air, with contact areas ranging from diameters of a few nanometers to one millimeter and initial applied contact pressure from about 1 MPa to 3 GPa. Friction and wear mechanisms are discussed as functions of surface composition and roughness, vacuum and humidity of air.     

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.     

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.     

On the Tribological Behaviour of SiC and Alumina Mated Against Different Steels Under Dry Sliding Conditions

There have been several studies regarding the tribological behaviour of ceramics such as SiC and alumina mated against steels or self-mated. Nevertheless, only little is known about possible tribochemical reactions when ceramics are mated against steels. In the present study, ceramic pins made of SiC (EKasicF) or alumina (F99.7) respectively were tested under dry sliding conditions against different steel disc counter bodies using a pin-on-disc tribometer. The different ceramics showed significant differences in their tribological behaviour, i.e., coefficient of friction and wear amount. Especially, the SiC couples showed significant differences in the wear amounts while these were quite similar for the alumina couples. The wear behaviour of the SiC couples is discussed in more detail. A correlation between chromium content of the steel discs was found for the SiC couples. The surfaces of selected specimens were analysed by Auger-Electron-Spectroscopy (AES). Wear for the SiC couples was mainly attributed to tribochemical reactions as far as the steel disc was containing the alloying element chromium in considerable amount. Furthermore, a simple wear schematic is proposed.     

Investigation of wear mechanism of SiC particulate-reinforced Al-20Si-3Cu-1Mg aluminium matrix composites under dry sliding and water lubrication

Unreinforced Al-20Si-3Cu-1Mg (ASCM) aluminium alloy and SiC particle reinforced Al-20Si-3Cu-1Mg (ASCM-SiC) aluminium matrix composites were fabricated by powder metallurgy (). The samples were slid against 4Cr13 stainless steel in a reciprocal friction tester under a load of 25 N to 175 N and sliding velocity of 0.3 to 1.2 m s⁻¹ at ambient conditions. The results show that SiC particulate-reinforced aluminium matrix composites possess good wear resistance at dry sliding and less wear resistance under water lubrication. Ploughing wear is the dominant wear mechanism at dry sliding and tribochemical wear is dominant under water lubrication. SEM, AES and XPS were used to examine the wear morphology and surface chemistry.     

Tribochemical Effects on Tribological Properties of Self-Mated Zirconia Ceramic in HFC-134a Gas

Tribochemical effects on the tribological properties of self-mated zirconia ceramic in CF₃CH₂F (HFC-134a) were investigated using a ball-on-disk type environmental tribometer. The friction chamber of the tribometer was attached to a micro-spot X-ray Photoelectron Spectrometer (XPS) for ensuring that surface analysis be conducted without exposuring the frictional surfaces to air. It was found that HFC-134a gas was an effective lubricant for zirconia ceramic, especially at a pressure higher than 10³ Pa. The products of tribochemical reactions between zirconia and HFC-134a molecules were detected. The amount and chemical state of the tribochemical products seemed to control the tribological behaviors. Thus, the role of tribochemical products on the tribological properties of zirconia in HFC-134a gas at 10⁴ Pa was studied in detail under applied loads of 0.6–5.0 N and sliding speed of 0.04–0.35 m/s. It was found that severe tribochemical reactions occurred at low speeds and high loads. The formation of ZrF₄ accelerated the chemical wear of zirconia, and raised the friction. Zirconia ceramic is suitable for use at moderate load and sliding speed under a reactive environment.     

Influence of Surface Roughness on the Transfer Film Formation and Frictional Behavior of TiC/a-C Nanocomposite Coatings

Influence of surface roughness on the friction of TiC/a-C nanocomposite coatings while sliding against bearing steel balls in humid air was examined by detailed analyses of the wear surfaces and the wear scar on the ball counterparts by atomic force microscopy, optical, and confocal microscopy. It was observed that the surface roughness of the coatings essentially determines the wear behavior of the ball counterpart, which consequently influences the transfer film formation. A rough coating causes abrasive wear of the steel ball during the running-in period, which impedes the formation of a stable transfer film and leads to higher values of coefficient of friction (CoF). Moreover, the CoF does not show a decreasing trend after the running-in period, although the roughness of the coating was greatly reduced. Replacing the worn ball with a new one after the running-in period yields lower CoF values similar to that observed for a smooth coating. In both of the cases, no wear of the steel ball occurs and a stable transfer film forms and effectively covers the contact area. The influence of the wear debris on the formation of the transfer film is also discussed.     

Tribological behaviour of alumina sliding on several kinds of materials

Friction and wear behaviour of alumina sliding on various materials (nickel, copper, titanium, aluminium, alumina) were investigated experimentally. Pin-on-disc tests were conducted in air at various relative humidity levels (RHL). The results show that the influence of humidity depends on the material of the couples. Tribological behaviour of alumina sliding on very reactive metals such as titanium and aluminium is not influenced by RHL. In contrast, the friction coefficient and wear mechanism of nickel and copper are strongly affected by adsorbed films of water vapour. Nickel implanted with boron was also studied. The friction and wear of implanted surfaces are drastically reduced due to a lowering of the nickel surface reactivity. The tribological behaviour of the Al₂O₃/Al₂O₃ couple is also sensitive to RHL. The variation of friction coefficient and wear of this system are discussed in terms of tribochemical reactions and crack propagation.