Observations on the effectiveness of some surface treatments of mineral particles and inorganic compounds from Armenia as the fillers in polyphenylene sulfide for tribological performance

This is a general study in which a number of minerals and inorganic compounds from Armenia were investigated for their effectiveness as the fillers in polyphenylene sulfide (PPS) for tribological performance. The minerals studied were tuff, bentonite, and travertine, and inorganic compounds MoO₃ and MoO₂. The filled polymer specimens were prepared by compression molding and tested for tribological behavior in the pin-on-disk sliding configuration. The particulate fillers included many variations in terms of the size (micro and nano) and surface treatment. Friction and wear test results revealed that MoO₂ and nano size bentonite particles were effective in improving the wear resistance. The lowest steady state wear rate in this study was observed for PPS+7% MoO₂ (50 nm)+5% PTFE composite, and MoO₂-filled composites had generally lower coefficients of friction than that of the unfilled PPS. From the wear plots, filler abrasiveness, and transfer film studies, it was concluded that the abrasion by filler was mostly responsible for the detrimental wear behavior. The wear behavior has been discussed in terms of the abrasion by filler and transfer film uniformity, texture, thickness, and coverage. The effects of particulate size and surface treatment are also included in the discussion. In view of the results reported for these fillers in formaldehyde and dioxolane copolymer (CFD) and the observations in this study, it is felt that the fillers from Armenia with the exception of tuff and MoO₃ have considerable appeal for further investigation using other innovative surface treatments for fillers.     

Effect of transfer film structure, composition and bonding on the tribological behavior of polyphenylene sulfide filled with nano particles of TiO2, ZnO, CuO and SiC

The tribological behavior of polyphenylene sulfide (PPS) filled with inorganic nano particles was studied. The fillers investigated were TiO₂, ZnO, CuO and SiC whose sizes varied from 30 to 50 nm. The polymer composites were compression molded with varying proportions of these fillers. Wear and friction tests were performed in a pin-on-disk configuration at a sliding speed of 1.0 m/s, nominal pressure of 0.65 MPa, and counterface roughness of 0.10 μm Ra. The polymer composite pins slid against hardened tool steel counterfaces. The transfer films of the composite materials formed on the counterfaces during sliding were studied by optical microscopy and X-ray photoelectron spectroscopy (XPS) and the adhesion between the transfer film and counterface was measured in terms of the peel strength. It was found that the wear rate of PPS decreased when TiO₂ and CuO were used as the fillers but increased with ZnO and SiC fillers. The optimum wear resistance was obtained with 2 vol.% CuO or TiO₂. These filled composites had the coefficients of friction lower than that of the unfilled PPS. The wear behavior of the composites is explained in terms of the topography of transfer film and adhesion of transfer film to the counterface as observed from peel strength studies. There is a good correlation observed between the transfer film-counterface bond strength and wear resistance.     

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.     

Friction and wear of polyphenylene sulfide composites filled with micro and nano CuO particles in water-lubricated sliding

The tribological behavior of polyphenylene sulfide (PPS) composites filled with micro and nano CuO particles in water-lubricated sliding condition were studied. Pin-on-disk sliding tests were performed against a steel counterface of surface roughness 0.09–0.11 μm. The lubrication regimes were established from friction data corresponding to various combinations of loads and sliding speeds. Later experiments were performed using the sliding speed of 0.5 m/s and contact pressure of 1.95 MPa, which corresponded to boundary lubrication regime. Micro CuO particles as the filler were effective in reducing the wear of PPS but nano CuO particles did not reduce wear. The steady state wear rate of PPS-30 vol.% micro CuO composite was about 10% of that of unfilled PPS and the coefficient of friction in this case was the lowest. The examination of the topography of worn pin surfaces of nano CuO-filled PPS by SEM revealed grooving features indicating three-body abrasion. The transfer films formed on the counterfaces during sliding were studied by optical microscopy and AFM. The wear behavior of the composites in water-lubricated sliding is explained using the characteristics of worn pin surfaces and transfer films on the counterface.     

Friction of some commercial polymer-based bearing materials against steel

Cylindrical test pins of some commercial polymer-based bearing materials (comprising two nylons 6, a filled nylon 6/6, a filled ultra-high molecular weight polyethene (uhmwpe) and three polyurethanes) were rotated, in dry conditions and at constant load and sliding speed, on circular tracks on stationary discs of steel gauze and abrasive paper.Wear against run-in steel gauze was proportional to the sliding time (distance), with the specific wear rate, v_sp, (wear volume per unit area per unit sliding distance) varying with the nominal pressure, p, according to v_sp = Kp^α. Values of K and α are presented enabling comparison of the fatigue wear of the materials at various loads against steel (or a counterface with rounded asperities) in non-transfer film conditions. Nylon 6 showed the least wear and the polyurethanes showed the greatest wear, up to pressures of 3.43 MN m⁻² (500 lbf in⁻²).With abrasive paper, the circular path became progressively clogged with transfer films and wear debris, and the wear volume, ΔW, diminished with time, t, throughout the test duration, following the relationship ΔW = Dt^c, where both c and D are functions of the wear path diameter. c appears to be related to the film transfer capability of the polymer. The best overall abrasive wear resistance (in transfer film conditions) was exhibited by the filled uhmwpe, followed by two polyurethanes. Nylon 6 showed relatively poor abrasion resistance under these conditions. The mechanical properties indicate, with one exception, a similar ranking order for non-transfer film conditions     

Friction and wear properties of rice husk ceramics under dry condition

The friction and wear behaviors of rice husk (RH) ceramics, prepared by carbonizing the mixture of rice husk and phenol resin at 900 °C in N₂ gas environment, sliding against high carbon chromium steel (JIS SUJ2), austenitic stainless steel (JIS SUS304), and Al₂O₃ under dry condition were investigated using a ball-on-disk tribometer. The test results show that the friction coefficient of RH ceramics takes very low values 0.05–0.08 and 0.06–0.11 sliding against SUJ2 and SUS304, respectively, and much higher values around 0.14–0.23 against Al₂O₃. It was also shown that SUJ2 provides the lowest specific wear rate values below 10⁻⁹ mm²/N, while, those of SUS304 and Al₂O₃ mostly stayed between 10⁻⁹ to 10⁻⁸ mm²/N range. The worn surfaces of counterparts were observed with optical microscopy and analyzed using cross-sectional transmission electron microscopy with energy dispersive X-ray spectroscopy and electron diffraction. It was suggested that the tribological behaviors of RH ceramics are closely related with the formation of a transferred film, consisted of amorphous silica and carbon particles, on a counterpart surface. The transferred film was formed readily on SUJ2 balls, whereas for SUS304 the presence of the film was subject of the sliding conditions. Moreover, formation of the transferred film could not be detected on Al₂O₃ counterparts.     

Sliding friction and wear performance of Ti6Al4V in the presence of surface-capped copper nanoclusters lubricant

The friction and wear properties of Ti₆Al₄V sliding against AISI52100 steel ball under different lubricative media of surface-capped copper nanoclusters lubricant—Cu nanoparticles capped with O,O′-di-n-octyldithiophosphate (Cu-DTP), rapeseed oil and rapeseed oil containing 1 wt% Cu-DTP was evaluated using an Optimol SRV oscillating friction and wear tester. The wear mechanism was examined using scanning electron microscopy (SEM) and X-ray photoelectron spectrosmeter (XPS). Results indicate that Cu-DTP can act as the best lubricant for Ti₆Al₄V as compared with rapeseed oil and rapeseed oil containing 1 wt% Cu-DTP. The applied load and sliding frequency obviously affected the friction and wear behavior of Ti₆Al₄V under Cu-DTP lubricating. The frictional experiment of the Ti₆Al₄V sliding against AISI52100 cannot continue under the lubricating condition of rapeseed oil or rapeseed oil containing 1 wt% Cu-DTP when the applied load are over 100 N. Surprisingly, the frictional experiment of Ti₆Al₄V sliding against AISI52100 steel can continue at the applied load of 450 N under Cu-DTP lubricating. The tribochemical reaction film containing S and P is responsible for the good wear resistance and friction reduction of Ti₆Al₄V under Cu-DTP at the low applied load. However, a conjunct effect of Cu nanoparticle deposited film and tribochemical reaction film containing S and P contributes to the good tribological properties of Ti₆Al₄V under Cu-DTP at the high-applied load.     

Investigation of the Transition State in the Wear of Polyphenylene Sulfide Sliding Against Steel

The effect of sliding variables, including counterface roughness, sliding speed, and contact pressure, on the run-in state of wear and friction was studied. Sliding was performed in the pin-on-disk configuration with a polyphenylene sulfide (PPS) pin resting on the flat steel counterface. Some experiments were also run to study the effect of air cooling and heating. Optical microscopy and scanning electron microscopy were used to study the shape and size of the wear debris, worn pin surface, and the transfer film formed on steel counterfaces. It was found that friction and wear in the run-in state were significantly affected by the sliding variables studied and their influence was closely related to the development of a transfer film during the run-in state. If the transfer film developed during initial sliding, the coefficient of friction increased and wear rate decreased. The wear rate in the run-in state increased with the increase in initial counterface roughness and there was an optimal counterface roughness of 0.06 m Ra for minimum steady state wear rate. A higher applied load led to a higher wear rate in the run-in state but that was not the case with steady state wear rate.     

The friction and wear properties of nanometre SiO2 filled polyetheretherketone

Nanometre SiO₂ filled-polyetheretherketone (PEEK) composite blocks with different filler proportions were prepared by compression moulding. Their friction and wear properties were investigated on a block-on-ring machine by running a plain carbon steel (AISI 1045 steel) ring against the composite block. The morphologies of the wear traces and the transfer film were observed by scanning electron microscopy (SEM). It was found that nanometre SiO₂ filled-PEEK exhibited considerably lower friction coefficient and wear rate in comparison with pure PEEK. The lowest wear rate was obtained with the composite containing 7.5 wt.% SiO₂. The SEM pictures of the wear traces indicated that with the frictional couple of carbon steel ring/composite block (fillec with 7.5 wt.% filler), a thin, uniform, and tenacious transfer film was formed on the ring surface. It was inferred that the transfer film contributed largely to the decreased friction coefficient and wear rate of the filled PEEK composites.     

Sliding wear characteristics of gas boronized steel

The wear characteristics and the mechanism of sliding wear of boronized steel under unlubricated conditions were studied. Characteristic wear curves of FeB and Fe₂B boride layers formed on SAE 1045 steel were similar in form. The maximum wear rates were obtained under a sliding velocity of 0.30 m s^?1 for FeB specimens and 0.50 m s^?1 for Fe₂B specimens. Under such conditions both mechanical wear caused by scratching and oxidative wear occurred. Under conditions of mild wear the wear loss was caused mainly by oxidative wear. Under conditions of heavy wear destruction of the sliding surface was caused by thermal stress. The wear debris was composed principally of iron oxides (α Fe₂O₃, Fe₃O₄) formed by oxidative wear, α iron and borides (FeB, Fe₂B) produced by mechanical wear and B₂O₃ produced by the preferential oxidation of boron in the boride layer.     

The effect of sliding time and speed on the wear of composite materials

The friction and wear properties of an Al 201 alloy and a unidirectionally oriented graphite fiber-aluminum matrix composite (T50-Al 201) were investigated. The experiments were conducted on a pin-on-disc type friction machine. The diameter of the pin was 0.22 cm and the load 4.46 N. The sliding velocity varied between 0.17 and 0.43 m s^?1. The disc counterface was of commercially pure iron. It has been found that the friction coefficient μ and the wear rate W_L of the composite material decrease as the sliding time is increased until a steady state value is reached. The steady state wear rate is proportional to the reciprocal of the sliding speed in accord with a recently proposed model. Scanning electron microscopy and Auger electron spectroscopy observations indicate that the high initial values of μ and W_L are due to a high degree of matrix adhesion to the counterface accompanied by fiber breaking and transfer. The low steady state values of μ and W_L are due to the formation of a film that impedes adhesion and confers some degree of self-lubrication. It is suggested that the observed variation of W_L with sliding speed is related to changes in the degree of subsurface damage as the velocity is varied.     

Further investigation on the tribological behavior of Al2O3–20Ag20CaF2 composite at 650°C

The friction and wear behaviors of the self‐lubricating Al₂O₃–20Ag20CaF₂ disk against an Al₂O₃ pin pair have been investigated over a broad load range from 1 to 30 N and sliding velocities from 0.084 to 1 m/s at 650^°C. Four typical wear modes have been identified and the wear mode map was constructed to illustrate the influence of load and speed on the friction coefficient and wear rate. The results showed the effective self‐lubricating region (II) (continuous lubricating film) is almost independent of sliding speed, and mainly dependent on the load. It is suggested that the plastic deformation and plastic flow during sliding play an important role in the formation of the self‐lubricating film on the sliding surface. Furthermore, the worn surface in the region (II) (continuous lubricating film) was found to be much softer than the original surface and the distribution of Vickers hardness became more uniform due to the presence of the lubricating film on the worn surface. This revised version was published online in July 2006 with corrections to the Cover Date.     

Tribochemical effects on the friction and wear behaviors of diamond-like carbon film under high relative humidity condition

Friction and wear behaviors of diamond-like carbon (DLC) film in humid N₂ (RH-100%) sliding against different counterpart ball (Si₃N₄ ball, Al₂O₃ ball and steel ball) were investigated. It was found that the friction and wear behaviors of DLC film were dependent on the friction-induced tribochemical interactions in the presence of the DLC film, water molecules and counterpart balls. When sliding against Si₃N₄ ball, a tribochemical film that mainly consisted of silica gel was formed on the worn surface due to the oxidation and hydrolysis of the Si₃N₄ ball, and resulted in the lowest friction coefficient and wear rate of the DLC film. The degradation of the DLC film catalyzed by Al₂O₃ ball caused the highest wear rate of DLC film when sliding against Al₂O₃ ball, while the tribochemical reactions between DLC film and steel ball led to the highest friction coefficient when sliding against steel ball.     

Tribological characteristics of polycrystalline Magnéli-type titanium dioxides

The results presented in this paper have clarified experimentally, that titania-based Magnéli-phases (Ti₄O₇/Ti₅O₉ and Ti₆O₁₁) with (121)-shear planes exhibit more anti-wear properties than lubricious (low-frictional) properties. The results for dry sliding indicate that the coefficients of friction lie in the range of 0.1–0.6 depending on sliding speed and ambient temperature. The COF decreased with increasing temperature (T= 22–800°C) and increasing sliding speed (υ= 1−6 m/s). The dry sliding wear rate was lowest for the Al₂O₃ at 1 m/s at 800°C with values of 1.7 × 10−8 and 6.4 × 10−8 mm³/N m, comparable to boundary/mixed lubrication, associated with a high dry frictional power loss of 30 W/mm². The running-in wear length and, more important, the wear rate decreased under oscillating sliding tests with increasing relative humidity. The contact pressure for high-/low-wear transition increased under oscillating sliding tests with increasing relative humidity. At room temperature and a relative humidity of 100% the steady-state wear rate under dry oscillating sliding for the couple Al₂O₃/Ti₄O₇–Ti₅O₉ was lower than 2 × 10−7 mm³/N m and therefore inferior to the resolution of the continuous wear measurement sensor. TEM of wear tracks from oscillating sliding revealed at room temperature a work-hardening as mechanism to explain the running-in behavior and the high wear resistance. The hydroxylation of titania surfaces favours the high-/low-wear transition. This revised version was published online in August 2006 with corrections to the Cover Date.     

Tribological Sensitivity of PTFE/Alumina Nanocomposites to a Range of Traditional Surface Finishes

Wear tests were performed with polytetrafluoroethylene (PTFE) + Al ₂ O ₃ nanocomposites on various manufactured surfaces to determine whether or not the wear resistance of these nanocomposites is a strong function of surface preparation. Four different surface finishes of grade 304 stainless steel counterfaces were used: electropolished (R _q = 88 nm), lapped (R _q = 161 nm), wet-sanded (R _q = 390 nm), and dry-sanded (R _q = 578 nm). PTFE + Al ₂ O ₃ nanocomposites made from powders of roughly 2-20 μm PTFE (matrix) and ～44 nm Al ₂ O ₃ (filler) were prepared at filler weight percentages of 0, 1, 5, and 10% and tested on each surface finish. Additionally, 5 wt% 44-nm nanocomposites were compared to identically prepared 5 wt% 80- and 500-nm Al ₂ O ₃ filled PTFE composites on each surface. Friction coefficients were between 0.12 and 0.19 and wear rates decreased from K = 810 × 10^{? 6} mm ³ /(Nm) for the 5 wt% 500-nm alumina-filled PTFE on the dry-sanded surface to K = 0.8 × 10^{? 6} mm ³ /(Nm) for the 5 wt% 80-nm filled composite on the lapped surface. It was found that the minimum wear rate occurred on the lapped counterface for every composite, and the wear rate is a strong function of the transfer film thickness and morphology.     

Coupled Effect of Filler Content and Countersurface Roughness on PTFE Nanocomposite Wear Resistance

In tests of PTFE with 2.9% volume content alpha-phase alumina nanoparticles (40 or 80 nm) in sliding reciprocation against polished steel, wear rates of ~10⁻⁷ mm³/Nm were measured which is four orders-of-magnitude lower than unfilled PTFE and two orders-of-magnitude lower than with microparticles (0.5 or 20 μm) of more conventional filler size. This was similar to that previously reported in unidirectional sliding, and did not vary greatly with stroke of reciprocation. For a microfilled PTFE, the wear rate gradually increased towards that of unfilled PTFE as filler content was reduced, whereas nanofilled PTFE maintained relatively constant ~10⁻⁷ mm³/Nm to filler contents as low as 0.18% before reverting towards the rapid wear rate of unfilled PTFE. Lightly filled nanocomposites depend upon low countersurface roughness to maintain such low wear rate, and with increasing roughness the wear rate was found to transition at a critical value to a wear rate of ~10⁻⁵ mm³/Nm. Nanocomposites with higher filler contents were able to retain the low wear rates against rougher countersurfaces, as the critical roughness at which this wear resistance was lost tended to increase with the square of the filler content. Upon encountering extremely high countersurface roughness in the range R _a = 6–8 μm, nanocomposites at each filler content eventually increased in wear rate to ~10⁻⁴ mm³/Nm. The steel countersurface did not appear to play an important role in the extreme wear resistance of these alumina nanofilled PTFE composites, as comparable performance was also displayed against alumina countersurfaces.     

Abrasive wear of some commercial polymers

Cylindrical test pins of some commercial polymer-based bearing materials (comprising two nylons 6, a filled nylon 6/6, a filled ultra-high molecular weight polyethene (uhmwpe) and three polyurethanes) were rotated, in dry conditions and at constant load and sliding speed, on circular tracks on stationary discs of steel gauze and abrasive paper.Wear against run-in steel gauze was proportional to the sliding time (distance), with the specific wear rate, v_sp, (wear volume per unit area per unit sliding distance) varying with the nominal pressure, p, according to v_sp = Kp^α. Values of K and α are presented enabling comparison of the fatigue wear of the materials at various loads against steel (or a counterface with rounded asperities) in non-transfer film conditions. Nylon 6 showed the least wear and the polyurethanes showed the greatest wear, up to pressures of 3.43 MN m^?2 (500 lbf in^?2).With abrasive paper, the circular path became progressively clogged with transfer films and wear debris, and the wear volume, ΔW, diminished with time, t, throughout the test duration, following the relationship ΔW = Dt^c, where both c and D are functions of the wear path diameter. c appears to be related to the film transfer capability of the polymer. The best overall abrasive wear resistance (in transfer film conditions) was exhibited by the filled uhmwpe, followed by two polyurethanes. Nylon 6 showed relatively poor abrasion resistance under these conditions. The mechanical properties indicate, with one exception, a similar ranking order for non-transfer film conditions     

Friction and wear behaviour of plasma-sprayed Cr2O3 coatings against steel in a wide range of sliding velocities and normal loads

This study investigates the influence of sliding speed and normal load on the friction and wear of plasma-sprayed Cr₂O₃ coatings, in dry and lubricated sliding against AISI D2 steel. Friction and wear tests were performed in a wide speed range of 0.125–8 m/s under different normal loads using a block-on-ring tribometer. SEM, EDS and XPS were employed to identify the mechanical and chemical changes on the worn surfaces. A tangential impact wear model was proposed to explain the steep rising of wear from the minimum wear to the maximum wear. The results show that the wear of Cr₂O₃ coatings increases with increasing load. Secondly, there exist a minimum-wear sliding speed (0.5 m/s) and a maximum-wear sliding speed (3 m/s) for a Cr₂O₃ coating in dry sliding. With the increase of speed, the wear of a Cr₂O₃ coating decreases in the range 0.125–0.5 m/s, then rises steeply from 0.5 m/s to 3 m/s, followed by a decrease thereafter. The large variation of wear with respect to speed can be explained by stick-slip at low speeds, the tangential impact effect at median speeds and the softening effect of flash temperature at high speeds. Thirdly, the chemical compositions of the transfer film are a-Fe₂O₃ in the speed range 0.25–2 m/s, and FeO at 7 m/s. In addition, the wear mechanisms of a Cr₂O₃ coating in dry sliding versus AISI D2 steel are adhesion at low speeds, brittle fracture at median speeds and a mixture of abrasion and brittle fracture at high speeds. Finally the lubricated wear of Cr₂O₃ coating increases sharply from 1 to 2.8 m/s.     

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.