Tribochemical Behavior of Si3N4–hBN Ceramic Materials with Water Lubrication

The main objective of this article is to study the tribological behavior of Si₃N₄–hBN composites with different hexagonal boron nitride (hBN) volume fraction under distilled water lubrication. Water-lubricated sliding tests were carried out on a pin-on-disc tester, and Si₃N₄ was used as friction pair. The results showed that the addition of hBN to Si₃N₄ resulted in a severe decrease of the friction coefficient, from 0.35 for Si₃N₄ against Si₃N₄ to 0.01 for Si₃N₄-20% hBN against Si₃N₄ with drip-feed water lubrication; the friction coefficients of Si₃N₄–hBN/Si₃N₄ pairs sliding with full immersion water lubrication were as low as 0.01. The morphological and chemical characterization of the worn surfaces were conducted using scanning electron microscopy (SEM), laser scanning microscope, X-ray photoelectron spectroscopy (XPS). The analysis indicated that, with drip-feed water lubrication, hBN in Si₃N₄–hBN was spalled off during the wearing tests and spalling pits were formed on the wearing surface of Si₃N₄–hBN composites, then the wear debris were dropped into the pits and reacted with water, and thus a tribochemical film was formed on the wearing surface. The tribochemical film facilitated the wear surfaces of Si₃N₄–hBN and Si₃N₄ to smooth with drip-feed water lubrication, while the tribochemical remove facilitated the wear surfaces to smooth with full-immersion water lubrication.     

Influence of Sliding Speed on the Tribological Characteristics of Si3N4-hBN Ceramic Materials

The influence of sliding speed on the unlubricated tribological behaviors of silicon nitride–boron nitride (Si₃N₄-hBN) composites was investigated with two modes in air by a pin-on-disc tribometer. Using the upper disc–on–bottom pin test mode, as the sliding speed increased, the friction coefficient of the sliding pairs showed an upward trend; for example, from 0.18 at the sliding speed of 0.40 m/s to 0.54 at the sliding speed of 1.31 m/s for the Si₃N₄/Si₃N₄–20% hBN pair. The surface analysis indicated that a tribochemical film consisting of SiO₂ and H₃BO₃ formed on the wear surfaces of the Si3N4/Si3N4–20% hBN sliding pair at sliding speeds of 0.40 and 0.66 m/s. Moreover, the formation of this film lubricated the wear surfaces. At the sliding speed of 1.31 m/s, no tribochemical film formed on the wear surfaces, most likely due to the increase in surface temperature. In the upper pin–on–bottom disc test mode, the wear mechanism was dominated by abrasive wear, and no tribochemical products could be detected on the wear surfaces. The increase in sliding speed weakened the degree of abrasive wear, leading to a decrease in the friction coefficients.     

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.     

Silicon Nitride Boundary Lubrication: Lubrication Mechanism of Alcohols

This paper describes the lubrication mechanism of alcohols with silicon nitride under boundary lubrication conditions. Dynamic wear tests and static chemical reaction studies were conducted to study the chemical interaction between alcohols and silicon nitride. Direct evidence of chemical reactions occurring between alcohols and silicon nitride was collected. Gel-permeation-chromatography-graphite-furnace-atomic-absorption (GPC-GFAA) analysis detected the presence of high molecular weight (HMW), silicon-containing, metallo-organic compounds in the wearing contact. Secondary ion mass spectrometry (SIMS) analysis of the reaction products from wear tests revealed the formation of silicon alkoxides. These alkoxides subsequently reacted to form HMW products which had been independently verified as capable of lubricating silicon nitride surfaces. A two-ball collision test was used to verify the lubricating quality of the film generated from the wear test. A lubrication mechanism is proposed in which alcohols adsorb and react with the oxide/hydroxide layer of Si₃N₄ to produce a bonded surface silicon alkoxide. Subsequent tribochemical reactions prompted by the surface disruption from the wearing contact cause the formation of free silicon alkoxides. These species then proceed to form a variety of silicon-containing high molecular weight products that have demonstrable lubricating ability. This mechanistic understanding provides a framework of Si₃N₄ lubrication.     

Friction and wear behaviour of plasma sprayed WC–12Co coating sliding against Si3N4 under lubrication of ionic liquids

Abstract

The friction and wear behaviour of a WC–12Co coating prepared by plasma spraying sliding against a Si₃N₄ ceramic ball, under the lubrication of liquid paraffin and ionic liquids 1-methyl-3-butylimidazolium hexafluorophosphate and 1-methyl-3-hexylimidazolium hexafluorophosphate at room temperature, was investigated using an SRV tester. The morphology and elemental distribution of the worn coating surfaces were characterised by means of scanning electron microscopy (SEM) equipped with an energy dispersive X-ray analyser (EDXA) attachment, and the chemical state of typical elements in the boundary lubricating film on the worn coating surface was analysed by means of X-ray photoelectron spectroscopy (XPS). The SEM/EDXA analysis shows that phosphorus is uniformly distributed on the worn coating surface lubricated by ionic liquids. The XPS results also indicate that the boundary lubricating film is mainly composed of CoF₂ and PF_x and the tribochemical reaction products contribute to reducing the friction and wear of the plasma sprayed WC–12Co coating.     

Tribological behaviour of uni-directionally aligned silicon nitride against steel

Textured silicon nitride, where the β-Si₃N₄ grains were uni-directionally aligned, was fabricated and the effect of anisotropy in microstructure on tribological properties was investigated, compared with a conventional Si₃N₄. The wear tests were carried out for the tribopair of textured silicon nitride ceramic and steel using a block-on-ring tester without lubrication. For the textured Si₃N₄, tribological properties were evaluated in three directions with respect to the grain alignment; the plane normal to the grain alignment and in the directions parallel and perpendicular to the grain alignment in the side plane. The friction coefficient values of each specimen were of the same level under the same sliding conditions. The values of specific wear rate for the plane normal to the grain alignment were lower than those of the other specimens for all sliding conditions. It is considered that the high wear resistance of this plane was caused by restricted microfracture, such as grain dropping and minimal abrasion by wear debris. Both the friction coefficient and specific wear rate were decreased with increasing sliding speed and normal load because of the formation of lubricative FeO between the sliding surfaces.     

Ultra-low friction coefficient in alumina–silicon nitride pair lubricated with water

In a ball-on-disc wear test, an alumina ceramic body sliding against a silicon nitride ceramic body in water achieved an ultra-low friction coefficient (ULFC) of 0.004. The profilometer and EDX measurements indicated that the ULFC regime in this unmated Al₂O₃–Si₃N₄ pair was achieved because of the formation of a flat and smooth interface of nanometric roughness, which favored the hydrodynamic lubrication. The triboreactions formed silicon and aluminum hydroxides which contributed to decrease roughness and shear stress at the contact interface. This behavior enables the development of low energy loss water-based tribological systems using oxide ceramics.     

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.     

Comparison of the fretting wear of 100Cr6/100Cr6, Si3N4/Si3N4 and Si3N4/100Cr6 contacts in lubricated and dry conditions

The fretting wear behaviour of bearing steel against bearing steel, silicon nitride against silicon nitride, and silicon nitride against bearing steel, was investigated under lubricated and dry conditions. Amplitudes in the intermediate 5 to 50 μm range, and test durations from 10 to 360 min, were studied. Light microscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDS) were employed to determine the detailed nature of the friction and wear processes. In the silicon nitride against silicon nitride contact, brittle fracture of Si₃N₄ grains, and tribochemical reaction creating an amorphous layer on the mechanically damaged surface, were found. The main mechanism of fretting wear in the case of bearing steel against bearing steel contact was delamination. In the silicon nitride against bearing steel contact, chemical reactions predominated.     

Tribological Characterization of Several Silicon-Based Materials Under Ionic-Liquids Lubrication

The tribological behaviors of three silicon-based materials (low temperature silicon oxide (LTO), polysilicon (Poly Si) and silicon nitride (Si₃N₄) films) under ion liquids (ILs) lubrication have been investigated by varying the applied load and the sliding velocity. An atomic force microscope and a nanoindentor were used to characterize the deposited films, and the worn surfaces after frictional tests were analyzed by an optical microscope, a scanning electron microscope (SEM) with an energy dispersive spectrometer (EDS) and an X-ray photoelectron spectrometer (XPS). The results show the best lubricating properties of the IL lubricants are obtained at the intermediate load of 150 g for the three tribo-pairs. For the Si₃N₄/Si₃N₄ tribo-pair, the coefficients of friction (COFs) and the wear rates under ILs lubrication are larger than those under dry friction. The COF values decrease with sliding velocity, and the COFs of the Si₃N₄/Si₃N₄ tribo-pair are greater than the ones of the other two tribo-pairs (LTO/Si₃N₄ and Poly Si/Si₃N₄) at low velocities. The COF of 1-ethyl-3-methylimidazolium tetrafluoroborate is nearly 3 times larger than the other two IL lubricants (1-butyl-2,3-dimethylimidazolium tetrafluoroborate and N-butylpyridinium tetrafluoroborate) for the Si₃N₄/Si₃N₄ tribo-pair. The differences in COFs between the latter two lubricants for the three tribo-pairs are negligible. Different mechanisms of these results have been analyzed in the paper.     

Tribological Behavior of Si3N4-hBN Ceramic Materials without Lubrication under Different Test Modes

Unlubricated tribological behaviors of silicon nitride–boron nitride (Si ₃ N ₄ -hBN) composites were investigated with two test modes in air by using a pin-on-disc tribometer. Under upper-disc-on-bottom-pin test mode, the addition of hBN to Si ₃ N ₄ resulted in a significant decrease of the friction coefficient, from 0.54 for Si ₃ N ₄ against Si ₃ N ₄ to 0.19 for Si ₃ N ₄ -20% hBN against Si ₃ N ₄ . The surface analysis indicated that a tribochemical film consisting of SiO₂ and H ₃ BO ₃ was formed on the wear surfaces. The formation of tribochemical film might be attributed to the embedment of wear debris into the spalling pits on the wear surfaces of Si ₃ N ₄ -hBN specimen. The wear debris reacted with moisture in air, and the resultant tribochemical film lubricated the wear surfaces. Under upper-pin-on-bottom-disc test mode, the wear mechanism was dominated by abrasive wear, and no tribochemical products could be detected on the wear surfaces. A slight decrease of the friction coefficient, from 0.85 for Si ₃ N ₄ /Si ₃ N ₄ to 0.56 for Si ₃ N ₄ /Si ₃ N ₄ -30% hBN, was obtained, which might be attributed to the layered structure of hBN.     

Ionic liquid lubrication of electrodeposited nickel–Si3N4 composite coatings

Nano-Si₃N₄ particles were electrodeposited with nickel on copper substrate from a Ni bath. The friction and wear properties of the Ni/Si₃N₄ composite coating were evaluated while being lubricated with several various oils using a ball-on-disk sliding tester. The morphologies of the worn surfaces were observed using a scanning electron microscope. The chemical states of several typical elements on the worn surfaces were examined by means of X-ray photoelectron spectroscopy (XPS). Results indicated that the electrodeposited Ni/Si₃N₄ composition coating had excellent tribological properties while being lubricated with the ionic liquid. This was partly attributed to the high hardness of the electrodeposited nickel composite coating containing nano-sized Si₃N₄ and the tribochemical reaction between the lubricant and the sliding surface.     

Observation of delamination wear of lubricious tribofilm formed on Si3N4 during sliding against WC-Co in humidity air

Hot pressed silicon nitride that was exposed to high (90%) and low (32%) relative humidity was examined in ball-on-disc geometry against cemented carbide ball at various normal loads. The study indicated that Si₃N₄ tested at high R.H. gave less specific wear rate compared with Si₃N₄ at low R.H. The friction coefficient of Si₃N₄−WC-6% Co tribopairs was found in the range of 0.32–0.39 and 0.05–0.17 at low humidity and high humidity respectively. It is suggested that adsorbed moisture markedly affected the wear and friction properties of silicon nitride.Following the tests, SEM was used to elucidate the wear mechanism and particularly to delineate the effects of relative humidity on the wear and friction. SEM micrographs showed that the main wear mechanism at low relative humidity (32%) was caused by mechanical wear including abrasive grooves, large holes and polishing, whereas at high relative humidity (90%) the main mechanism was highly influenced by a tribochemical reaction related to the moisture adsorption from the environment. It is concluded that the removal of lubricious tribolayer was occurred by delamination induced crack propagation.     

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.     

Tribological behavior of RH ceramics made from rice husk sliding against stainless steel,alumina, silicon carbide,and silicon nitride

The tribological behavior of rice husk (RH) ceramics, a hard, porous carbon material made from rice husk, sliding against stainless steel, alumina, silicon carbide, and silicon nitride (Si₃N₄) under dry conditions was investigated. High hardness of RH ceramics was obtained from the polymorphic crystallinity of silica. The friction coefficients for RH ceramics disks sliding against Si₃N₄ balls were extremely low (<0.1), irrespective of contact pressure or sliding velocity. Transfer films from RH ceramics formed on Si₃N₄ balls. Wear-mode maps indicated that the wear modes were powder formation under all tested conditions, resulting in low specific wear rates (<5×10⁻⁹ mm²/N).     

Tribochemical aspects of silicon nitride ceramic sliding against stainless steel under the lubrication of seawater

Tribological behaviors of Si₃N₄ ceramic sliding against 316 stainless steel under seawater lubrication were investigated and compared with those under dry sliding and pure water lubrication. The results showed that SiO₂ colloidal particles were formed on the rubbing surface of Si₃N₄ due to the friction-induced chemical reaction of Si₃N₄ with H₂O, which were further aggregated into the silica gel with the assistance of ions in seawater. Because of the boundary lubrication of the silica gel layer, both the lowest friction coefficient and the smallest wear rates of Si₃N₄ and 316 steel were obtained in seawater.     

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.     

Lubrication of Silicon Nitride and Silicon Carbide by Water: Running in,Wear and Operation of Sliding Bearings

The purpose of this work was to establish the conditions for the operation and break-in of water-lubricated ceramic bearings. The experiments consisted of sliding 1/4 silicon nitride or—carbide balls against pre-polished disks of the same material in water until tribochemical wear generates smooth conformal surfaces that allow hydrodynamic lubrication (<0.002) by very thin water films. This running in was performed at various sliding speeds (0.01-4m/s) and loads (0.5-20N). The minimum sliding speed for low friction were 0.04m/s for silicon nitride and 0.5m/s for silicon carbide, much lower than for conventional bearings. The load carrying pressures were 60-80MPa, which is higher than the usually pressures of thrust bearings. The hydrodynamic fluid film thickness was estimated with a standard integration of Reynolds' equations modified for circular geometry, it was to be 5-15nm for silicon nitride, 25nm for silicon carbide. Operation over long distances (80km) allowed us to measure the wear rate during hydrodynamic lubrication; this was found to be <2×10^–11mm³/nm, a rate acceptable for industrial application. A novel method completed during this work allows the determination of the wear rate during run-in. It varies with sliding velocity for silicon nitride, from 1 to 6×10^–5mm³/nm; it is constant at 4×10^–6mm³/nm for silicon carbide.     

Dry and oil-lubricated sliding wear of Si<Subscript>3</Subscript>N<Subscript>4</Subscript> and Si<Subscript>3</Subscript>N<Subscript>4</Subscript>/BN fibrous monoliths

A high-temperature ball-on-flat tribometer was used to investigate dry and oil-lubricated friction and wear of sintered Si₃N₄ and Si₃N₄/hexagonal boron nitride (H-BN) fibrous monoliths. The friction coefficients of base Si₃N₄ flats sliding against Si₃N₄ balls were in the range of 0.6–0.8 for dry and 0.03–0.15 for lubricated sliding, and the average wear rates of Si₃N₄ were 10^–5 mm³ N^–1 m^–1 for dry sliding and 10^–10–10^–8 mm³ N ^–1m^–1 for lubricated sliding. The friction coefficients of Si₃N₄ balls against composite fibrous monoliths were 0.7 for dry sliding and 0.01–0.08 for lubricated sliding. The average specific wear rates of the pairs were of the same order as those measured for the conventional Si₃N₄ pairs. However, the fibrous monoliths, in combination with sprayed dry boron nitride, resulted in reduction in the lubricated friction coefficients of the test pairs and significant reduction in their wear rates. The most striking result of this study was that the coefficients of friction of the Si₃N₄/H-BN fibrous monolith test pair were 70–80 lower than those of either roughened or polished Si₃N₄ when tests were performed under oil-lubricated sliding conditions over long distances (up to 5000 m). The results indicated that Si₃N₄/H-BN fibrous monoliths have good wear resistance and can be used to reduce friction under lubricated sliding conditions.     

Tribological properties of γ-Y2Si2O7 ceramic against AISI 52100 steel and Si3N4 ceramic counterparts

Reciprocating ball-on-flat dry sliding friction and wear experiments have been conducted on single-phase γ-Y₂Si₂O₇ ceramic flats in contact with AISI 52100 bearing steel and Si₃N₄ ceramic balls at 5–15 N normal loads in an ambient environment. The kinetic friction coefficients of γ-Y₂Si₂O₇ varied in the range over 0.53–0.63 against AISI 52100 steel and between 0.51–0.56 against Si₃N₄ ceramic. We found that wear occurred predominantly during the running-in period and it almost ceased at the steady friction stage. The wear rates of γ-Y₂Si₂O₇ were in the order of 10^?4 mm³/(N m). Besides, wear debris strongly influenced the friction and wear processes. The strong chemical affinity between γ-Y₂Si₂O₇ and AISI 52100 balls led to a thick transfer layer formed on both contact surfaces of the flat and counterpart ball, which changed the direct sliding between the ball and the flat into a shearing within the transfer layer. For the γ-Y₂Si₂O₇/Si₃N₄ pair, a thin silica hydrate lubricant tribofilm presented above the compressed debris entrapped in the worn track and contact ball surface. This transfer layer and the tribofilm separated the sliding couple from direct contact and contributed to the low friction coefficient and wear rate.