Effect of Tribofilm Formation on the Dry Sliding Friction and Wear Properties of Magnetron Sputtered TiAlCrYN Coatings

Nano-structured TiAlCrYN coatings, grown by unbalanced magnetron sputtering on various steel substrates, exhibited friction coefficients 0.6–0.8 and wear coefficients 10⁻¹⁶–10⁻¹⁵ m³ N⁻¹ m⁻¹ in dry sliding wear tests. This article reports comprehensive worn surface analyses using SEM, TEM, EDX, EELS and Raman spectroscopy. A ~80 nm thick tribofilm formed on the TiAlCrYN worn surface was found to have dense amorphous structure and homogeneous oxide composition of Cr_0.39Al_0.19Ti_0.20Y_0.01O_0.21. Viscous flow of the amorphous tribofilm was dominant in causing the high friction coefficient observed. The coatings showed combined wear mechanisms of tribo-oxidation and nano-scale delamination.     

Improved Substrate Protection and Self-Healing of Boundary Lubrication Film Consisting of Polydimethylsiloxane with Cationic Side Groups

The substrate protection and self-healing capability of a cationic polymer lubricant (CPL) on a silicon oxide surface were tested with a pin-on-disc tribometer and atomic force microscopy (AFM). CPL was made of low molecular weight polydimethylsiloxane (PDMS) containing covalently attached quaternary ammonium cations and iodide counter-anions. CPL was spin-coated on the silicon oxide surface to form a 3–4 nm thick bound-and-mobile lubricant layer. The CPL film capable of binding to the SiO₂ surface through ionic interactions is superior in substrate protection than the neutral PDMS film which cannot form the bound layer. The mobile component in the CPL film readily flows into the lubricant-depleted sliding contact region from the surrounding film. The self-healing capability of CPL via lateral flow is slightly enhanced in humid environments due to water uptake in the film. The 3–4 nm thick CPL film on silicon oxide takes 30–40 s to flow into a ~50 μm wide track, which corresponds to an apparent spreading rate of 2–3 × 10⁻¹¹ m²/s.     

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.     

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.     

Effect of Fluoride Content on Friction and Wear Performance of Ni<Subscript>3</Subscript>Al Matrix High-Temperature Self-Lubricating Composites

The self-lubricating composites Ni₃Al–BaF₂–CaF₂–Ag–Cr, which have varying fluoride contents, were fabricated by the powder metallurgy technique. The effect of fluoride content on the mechanical and tribological properties of the composites was investigated. The results showed that an optimal fluoride content and a balance between lubricity and mechanical strength were obtained. The Ni₃Al–6.2BaF₂–3.8CaF₂–12.5Ag–10Cr composite showed the best friction coefficients (0.29–0.38) and wear rates (4.2 × 10⁻⁵–2.19 × 10⁻⁴ mm³ N⁻¹ m⁻¹) at a wide temperature range (room temperature to 800°C). Fluorides exhibited a good reduced friction performance at 400 and 600°C. However, at 800°C, the formation of BaCrO₄ on the worn surface due to the tribo-chemical reaction at high temperatures provided an excellent lubricating property.     

Ni3Al Matrix Composite with Lubricious Tungstate at High Temperatures

Ni₃Al–Ag–BaF₂/CaF₂–W composites were fabricated by the powder metallurgy route, and their tribological properties over a wide temperature range, starting from room temperature up to 800 °C, were investigated. The Ni₃Al matrix composite with 15 wt% BaF₂/CaF₂ exhibited a favorable friction coefficient (range 0.3–0.4) and wear rate (0.2–6.2 × 10⁻⁴mm³ N⁻¹ m⁻¹). The formation of BaWO₄ and CaWO₄ with lubricity on the worn surface due to a tribo-chemical reaction at high temperatures provided excellent lubricating properties. The low friction coefficient over a broad temperature range could be attributed to the synergistic effect of Ag, BaF₂/CaF₂, BaWO₄, and CaWO₄.     

NiAl Matrix High-Temperature Self-Lubricating Composite

A high-temperature self-lubricating composite NiAl–Cr–Mo–CaF₂ was fabricated using the powder metallurgy technique, and the tribological behavior of the composite at a wide range of temperatures (room temperature to 1000 °C) was investigated. The results showed that the composite had a favorable friction coefficient of about 0.2 and an excellent wear resistance of about 1 × 10⁻⁵ mm³N⁻¹m⁻¹ at the high temperatures tested (800 and 1000 °C). The excellent self-lubricating performance was attributed to the formation of the glaze film on the worn surface consisting mainly of CaCrO₄ and CaMoO₄ as high-temperature solid lubricants.     

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 performance of PFPE and X-1P lubricants at head–disk interface. Part II. Mechanisms

This paper, with the concepts of hydrogen bonding interaction and tribo-emission, develops a new approach of the mechanism of perfluoropolyether (PFPE) lubricant degradation at the head–disk interface. The role of lubricant X-1P in tribological performance is also described. The mechanism is as follows: (1) at the interface, there exist hydrogen atoms with partial positive charge and oxygen atoms with partial negative charge; (2) hydrogen bonding interactions at the sliding interface result in high friction which depletes the lubricant film at some sites; (3) low energy electrons are emitted from the sites with solid–solid asperity contact, inducing C–O bond scission through the interaction of low-energy electrons with PFPE lubricant molecules. Carbon overcoat on Al₂O₃–TiC surface passivates the interaction between water and PFPE lubricant molecules. Hydrogen bonding interactions are minimized during the presence of lubricant X-1P. The new approach well explains experimental results in part I of the paper. This revised version was published online in July 2006 with corrections to the Cover Date.     

Multi-environmental lubrication performance and lubrication mechanism of MoS2/Sb2O3/C composite films

MoS₂–Sb₂O₃–C composite films exhibit adaptive behavior, where surface chemistry changes with environment to maintain the good friction and wear characteristics. In previous work on nanocomposite coatings grown by PVD, this type of material was called a “chameleon” coating. Coatings used in this report were applied by burnishing mixed powders of MoS₂, Sb₂O₃ and graphite. The solid lubricant MoS₂ and graphite were selected to lubricate over a wide and complementary range including vacuum, dry air and humid air. Sb₂O₃ was used as a dopant because it acts synergistically with MoS₂, improving friction and wear properties. The MoS₂–Sb₂O₃–C composite films showed lower friction and longer wear life than either single component MoS₂ or C film in humid air. Very or even super low friction and long wear-life were observed in dry nitrogen and vacuum. The excellent tribological performance was verified and repeated in cycles between humid air and dry nitrogen. The formation of tribo-films at rubbing contacts was studied to identify the lubricating chemistry and microstructure, which varied with environmental conditions. Micro-Raman spectroscopy and Auger electron spectroscopy (AES) were used to determine surface chemistry, while scanning electron microscopy and transmission electron microscopy were used for microstructural analysis. The tribological improvement and lubrication mechanism of MoS₂–Sb₂O₃–C composite films were caused by enrichment of the active lubricant at the contact surface, alignment of the crystal orientation of the lubricant grains, and enrichment of the non lubricant materials below the surface. Sb₂O₃, which is not lubricious, was covered by the active lubricants (MoS₂ – dry, C – humid air). Clearly, the dynamics of friction during environmental cycling cleaned some Sb₂O₃ particles of one lubricant and coated it with the active lubricant for the specific environment. Mechanisms of lubrication and the role of the different materials will be discussed.     

Tribological performance of PFPE and X-1P lubricants at head–disk interface. Part I. Experimental results

X-1P, a cyclic phosphazene lubricant, is studied and compared with polar perfluoropolyether (PFPE) lubricant Z-Dol. Contact angles of lubricants are measured on different solid surfaces. Contact start-stop (CSS), drag, and ball-on-flat tests are performed and the results are discussed. Drag tests under high vacuum are also performed and discussed. Experimental results show that lubricant X-1P exhibits lower static friction and higher durability than lubricant Z-Dol, especially at high humidity. Higher durability is also observed for X-1P under the high vacuum condition compared with lubricant Z-Dol. Diamond-like carbon (DLC) overcoat on the Al₂O₃–TiC slider surface lowers friction and prolongs durability, especially for lubricant Z-Dol at high humidity, whereas for X-1P, there is no benefit of DLC. X-1P as an additive shows some improvement in durability at high humidity as compared to lubricant Z-Dol. This revised version was published online in July 2006 with corrections to the Cover Date.     

Environmental Effects on the Tribology and Microstructure of MoS<Subscript>2</Subscript>–Sb<Subscript>2</Subscript>O<Subscript>3</Subscript>–C Films

The tribology of molybdenum disulfide (MoS₂)–Sb₂O₃–C films was tested under a variety of environmental conditions (ambient 50% RH, 10⁻⁷ Torr vacuum, 150 Torr oxygen, and 8 Torr water) and correlated with the composition of the surface composition expressed while sliding. High friction and low friction modes of behavior were detected. The lowest coefficient of friction, 0.06, was achieved under vacuum, while sliding in 8 Torr water and ambient conditions both yielded the highest value of 0.15. Water vapor was determined to be the environmental species responsible for high friction performance. XPS evaluations revealed a preferential expression of MoS₂ at the surface of wear tracks produced under vacuum and an increase in Sb₂O₃ concentration in wear tracks produced in ambient air (50% RH). In addition, wear tracks produced by sliding in vacuum exhibited the lowest surface roughness as compared to those produced in other environments, consistent with the picture of low friction originating from well-ordered MoS₂ layers produced through sliding in vacuum.     

Microstructure and Tribology of Spark Plasma Sintered Fe–Cr–B Metamorphic Alloy Powder

The spark plasma sintering (SPS) process was used to fabricate a bulk Fe–Cr–B alloy (known as Armacor M) from gas-atomized powders. The purpose of this work is to study the microstructure, hardness and tribology of this sintered bulk alloy. Post microstructure and mechanical characterizations were performed to investigate the effects of wear on the microstructure and mechanical properties. Microstructural analysis using X-ray diffraction (XRD), scanning electron microscope (SEM) and energy dispersive spectroscopy (EDS) showed that SPS successfully produced a fully dense bulk material containing 67 vol.% Cr_1.65Fe_0.35B_0.96 particles dispersed in 33 vol.% solid solution matrix consisting of Fe, Cr and Si. Using nanoindentation, the hardness of the Cr_1.65Fe_0.35B_0.96 particles and the matrix was found to be 24 and 6 GPa, respectively. From microindentation, the bulk hardness of the sintered alloy was 9.7 GPa (991 HV). Dry sliding wear testing under mild conditions (i.e., initial Hertzian mean contact pressure of 280 MPa) was conducted against a stainless steel pin. The steady state coefficient of friction against Armacor M was about 0.82. The wear of Armacor M proceeded primarily by adhesive and mild oxidative wear. The wear volume for Armacor M was 80% less than that of carbon steel and its wear rate was 5.53 × 10⁻⁶ mm³ N⁻¹ m⁻¹.     

A Wideband spectrometer for NMR studies

The design of a wideband decimeter-wave (200–900 MHz) spectrometer with a magnetic induction of up to ∼10 T is described. This spectrometer is intended for studying electronic-nuclear oscillations in antiferromagnets at low temperatures (4.2−1.3 K). Critical field H _c = 2.5 ± 0.3 T of a reorientation transition in a noncollinear antiferromagnet Mn₃Al₂Ge₃O₁₂ at temperature T ≈ 1.3 K was determined from a ⁵⁵Mn²⁺ NMR spectrum.     

Tribological properties of NiCr–Al2O3 cermet-based composites with addition of multiple-lubricants at elevated temperatures

The tribological properties of NiCr-40 wt% Al₂O₃ (NC40A) cermet-based composites containing SrSO₄ and other lubricant (graphite, MoS₂ and Ag) against alumina ball were evaluated to identify their self-lubrication mechanisms from room temperature to 800 °C. The composites demonstrated distinct improvements in effectively reducing friction and wear, as compared to NC40A cermet. The best results were observed for NC40A–10SrSO₄–10Ag composite, which exhibited satisfactory reproducibility of friction coefficient over a wide temperature range (200–800 °C) through high temperature cyclic friction tests due to the formation of synergistic lubricating films SrAl₄O₇, NiCr₂O₄ and Ag on the contact surface.     

Tribological Performance of Fe<Subscript>67</Subscript>B<Subscript>33</Subscript> Alloy Prepared by a Self-Propagating High-Temperature Synthesis Technique

A bulk Fe₆₇B₃₃ alloy was prepared by a self-propagating high-temperature synthesis technique that is convenient, low in cost, and capable of being scaled up for tailoring the bulk materials. The Fe₆₇B₃₃ alloy is composed of dendrites with the t-Fe₂B phase and eutectic matrix with the α-Fe and t-Fe₂B phases. The content of the dendrite t-Fe₂B is above 80 vol.%. The compressive fractured strength and Vickers microhardness are 3400 MPa and 12.4 GPa, respectively. The tribological performance of the Fe₆₇B₃₃ alloy is investigated under dry sliding and water lubricant against Si₃N₄ ceramic ball. The wear rates of the Fe₆₇B₃₃ alloy are of the magnitude of 10⁻⁵ to 10⁻⁴ mm³/m under water lubricant. It is lower than that of the Fe₆₇B₃₃ alloy under dry sliding (10⁻⁴ mm³/m). But both the friction coefficients are almost identical. Oxide layers form in both environments via different tribochemical mechanisms, which led to significant differences in wear behavior.     

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.     

Measurements and theoretical predictions of head/tape spacing over a flat-head

Experimental measurements and theoretical calculations of the head/tape spacing are presented for the self-acting subambient foil bearing phenomenon at the interface of a flexible tape and a flat surface (e.g., tape-head). The air entrained at the flat-head/tape interface forms a subambient pressure layer which creates suction on the tape to pull it down to contact the head. The head/tape spacing for flat-heads is measured with a commercially available, two-wavelength, digital interferometer by using transparent tape and Al₂O₃-TiC flat-heads. Measurements for a large array of tape speed, tension, wrap-angle values, and head-lengths are presented. The interferometric spacing measurements show that, in general, the tape contacts the flat-head in the central region of the head and forms displacement-bumps adjacent to the edges of the head in the upstream and downstream corners. Experiments also show that the length of the displacement-bump affects whether a central contact region will form. The length of the displacement-bump is proportional to tape tension and wrap angle and inversely proportional to tape speed. The experimental results compare favorably to results of a mathematical model of the flat-head/tape interface.     

Frictional Voltammetry with Copper

This paper presents an experimental study correlating frictional behavior with in situ voltammetry for a unidirectional sliding contact between a hemispherical tipped alumina probe and a flat rotating copper counterface (maximum Hertzian contact pressure of 68 MPa and sliding speed of 10 mm/s). The contact was immersed in an aqueous 0.1 M Na₂CO₃ solution (pH ∼11) where the copper counterface acted as the working electrode in a potentiostat controlled three-electrode cell; a coiled Pt wire was used as the counter electrode and a saturated calomel electrode (SCE) as the reference. Clear and reproducible trends were found between friction coefficient and published data suggesting the onset of particular redox reactions, graphically presented in a frictional voltammetry plot. At anodic potentials primarily associated with the formation of copper(I) oxide (Cu₂O) (V vs SCE ∼−0.25), the measured friction coefficient was in the range μ ∼0.4–0.5. At cathodic potentials primarily associated with the formation of CuO, Cu(OH)₂, and CuCO₃ (V vs SCE ∼−0.10), the friction coefficient transitions to the range μ ∼0.7–1.0. At sustained cathodic potentials associated with reduction of the native copper oxide, Cu₂O, (V vs SCE ∼−0.65), the friction coefficient is observed to fluctuate between μ ∼0.2 and 0.5, arguably a result of exposure of bare copper due to non-uniform reduction (fractional coverage) of Cu₂O.     

Disk Lubricant Additives,A20H and C2: Characteristics and Chemistry in the Disk Environment

Disk lubricant additives A20H and C2 are Fomblin Z type perfluoropolyether with the hydroxyl end-group, –O–CF₂–CH₂–OH, at one end, and the cyclo-triphosphazene end-group, R₅(PN)₃–O–, at the other end. Here, R is an m-trifluoromethyl-phenoxy group for A20H and a trifluoroethoxy group for C2. These additives were examined for miscibility with benzene, spin-off rate, water contact angle, and the diffusion rate over the carbon overcoat. It is revealed that A20H adheres to the carbon overcoat spontaneously. The attractive interaction arises from the charge–transfer type interaction between the aromatic rings of the phosphazene end and the graphitic regime of the carbon overcoat. No spontaneous adherence occurs between the lubricant C2 and the carbon overcoat. A TOF-SIMS study of disks coated with A20H and C2, respectively, with and without subsequent curing by short-UV (185 nm) was performed. It is revealed: (1) if presented with a low energy electron, the phenoxy groups of A20H readily undergo the dissociative electron capture, while the trifluoroethoxy group does not, and (2) photoelectrons generated by short-UV have little kinetic energy and the electron capture occurs only if an electrophilic molecular sector is in intimate contact with the carbon. Thus, in the case of disks coated with A20H, UV-curing results in detachment of a phenoxy group in contact with the carbon, generation of a radical center at the phosphorus atom and subsequent formation of a bona fide chemical bond between the phosphor and the carbon overcoat. No reaction of consequence occurs when disks coated with C2 are irradiated with short-UV.