Behaviour of MoDTC in DLC/DLC and DLC/steel contacts

Diamond-like carbon (DLC) coatings are beginning to be used on machine components parts because of their excellent friction and wear resistance properties. It is hence important to be able to formulate lubricants able to work effectively with these coatings. This requires knowledge of how the various surface-reactive additives generally employed in lubricants behave with DLCs. This paper compares the behaviour of seven types of DLC, a-C, a-C:H, a-C:H:W, a-C:H:WC, Si-DLC, ta-C, ta-C:H, lubricated with molybdenum dialkyldithiocarbamate (MoDTC) solution. It is found that a-C and a-C:H:WC give lower boundary friction than the other types of DLC. MoDTC improves the wear resistance of DLC/DLC contacts but appears to greatly degrade the wear resistance properties of some DLCs in DLC/steel contacts, even though Mo-derived tribofilms form on all DLCs.     

The influence of surface roughness on friction and wear of machine element coatings

The use of low friction coatings like amorphous carbon or metal-doped carbon coatings on machine elements is constantly increasing. Most often, a surface treatment, e.g. grinding and polishing or honing, is required for optimal performance of the coated machine element. This can be time consuming and costly.In this study, the effect of surface roughness on friction and sliding wear of two different coatings, one tungsten containing and one chromium containing coating, were examined using a ball-on-disc test. Ball bearing steel plates were grinded to different surface roughnesses and coated with the two different coatings.The friction was found to depend on surface roughness where the rougher surfaces gave higher friction coefficients. The wear rate for the a-C:W coating was found to be independent of the roughness, whereas the roughness had a strong influence on the wear rate for the a-C:Cr coating. This could partly be explained by a difference in wear mechanism, where fatigue wear was observed for the a-C:Cr coating but not for the a-C:W coating.     

Durability of ZDDP Tribofilms Formed in DLC/DLC Contacts

The tribological properties of diamond-like carbon (DLC) coatings have drawn much attention of OEMs and lubricant manufacturers in recent years. It is important to know whether conventional friction modifier and antiwear additives can form durable films and work as effectively with DLCs as they normally do on steel surfaces. In this study, the film-forming and friction properties of the antiwear additive ZDDP and the strength of tribofilms formed by this additive on five widely used DLC types, namely a-C:H, a-C:H:W, a-C:H:WC, Si-DLC and ta-C, have been investigated. It is found that ZDDP-derived tribofilms form on all the DLCs but exhibit different friction characteristics based on DLC type. With all DLCs, the amount of tribofilm elements measured after durability tests was less than that measured initially. Over 90 % of thiophosphate and 70 % of sulphide/sulphate were lost during durability tests. ZDDP tribofilms were found to be strongly adhered on Si-DLC and a-C:H compared with the other DLCs. The ZDDP tribofilms formed in DLC/DLC contact appear to be similar in structure to those formed in steel/steel contact but not to exhibit the antiwear performance seen in steel/steel contacts.     

Tribological properties of tribofilms formed from ZDDP in DLC/DLC and DLC/steel contacts

Diamond-like carbon coatings (DLCs) are considered to hold great promise for improvement in friction and wear resistance of engine parts. It is hence interesting to know whether conventional engine oil additives such as ZDDP can form tribofilms and reduce friction and wear in DLC contacts as effectively as they do in steel on steel contacts. This paper compares the behaviour with ZDDP of six different DLC coatings. It is seen that ta-C gives lower boundary friction than the other types while a-C:H gives better wear prevention. A ZDDP-derived tribofilm forms on all DLCs but a pad-like structure is seen only on W-DLC in DLC/DLC tribopairs.     

Tribological Behavior of TiC/a-C:H-Coated and Uncoated Steels Sliding Against Phenol–Formaldehyde Composite Reinforced with PTFE and Glass Fibers

Tribological experiments on phenol–formaldehyde composite reinforced with polytetrafluoroethylene (PTFE) and glass fibers were performed against 100Cr6 steel and TiC/a-C:H thin film-coated 100Cr6 steel. In both cases, the coefficient of friction increases with increasing sliding distance until a steady-state value is reached. Although the steady-state values of the coefficient of friction are very close and ultralow, the wear rate of the PTFE composite liner at a long sliding distance (1,000 m) is reduced when the steel ball is coated with the TiC/a-C:H coating. This behavior is mainly attributed to the smoother surface after long sliding and the improved wear resistance of TiC/a-C:H coating. PTFE transfer films are evident on the surfaces of the hard counterparts. The average thickness of the transfer film on TiC/a-C:H-coated surfaces is about 3.8 nm. On the surface of uncoated steel ball, a continuous but non-uniform transfer film of around 13.9 nm average thickness was found.     

Tribological properties of flame sprayed Fe–Ni–RE alloy coatings under reciprocating sliding

Fe–Ni–RE self-fluxing alloy powders were flame sprayed onto 1045 carbon steel. The tribological properties of Fe–Ni–RE alloy coatings under dry sliding against SAE52100 steel at ambient conditions were studied on an Optimol SRV oscillating friction and wear tester in a ball-on-disc contact configuration. Effects of load and sliding speed on tribological properties of the Fe–Ni–RE coatings were investigated. The worn surfaces of the Fe–Ni–RE alloy coatings were examined with a scanning electron microscopy(SEM) and an energy-dispersive spectroscopy(EDS). It was found that the Fe–Ni–RE alloy coatings had better wear resistance than the SAE52100 steel. An adhered oxide debris layer was formed on the worn surface in friction. Area of the friction layer varied with variety of sliding speed, but did not vary with load. The oxide layer contributed to decreased wear, but increased friction. Wear rate of the material increased with the load, but dramatically decreased at first and then slightly decreased the sliding speed. The friction coefficient of the material was 0.40-0.58, and decreased slightly with the load, but increased with sliding speed at first, and then tended to be a constant value. Wear mechanism of the coatings was oxidation wear and a large amount of counterpart material was transferred to the coatings.     

Compatibility of DLC coatings with formulated oils

In the present study, the tribological performance and compatibility of hydrogenated amorphous carbon coating (a-C:H) and metal-doped diamond-like carbon (DLC) coating (Me-C:H) with formulated oils under the boundary lubrication regime was investigated. The investigation employed ball-on-flat contact geometry in reciprocating sliding motion and six formulated oils (manual gearbox oil, automatic gearbox oil, hydraulic oil, compressor oil, and normal and high performance motor oil), with pure poly-alpha-olefin (PAO) oil used as a reference. In addition, DLC coatings behavior in diesel and gasoline fuel was evaluated.Compared with the uncoated steel surfaces a-C:H coatings give improved wear resistance in base PAO as well as in fully formulated oils and fuels. On the other hand, W-doped DLC coatings show the lowest steady-state friction under boundary lubrication, especially when using oils with high additive contents.     

Structure and water-lubricated tribological properties of Cr/a-C coatings with different Cr contents

The Cr containing amorphous carbon coatings (Cr/a-C) with varying Cr content were deposited using unbalanced magnetron sputtering. The results revealed that the chromium carbide nano-clusters were formed when the Cr content exceeded 4.9 at%. The critical load increased while the hardness decreased after the Cr element incorporation. Although the low Cr containing Cr/a-C coatings (≤4.9 at%) exhibited similar friction coefficient with a-C coatings, but the initial friction coefficient, running-in distance and wear rate of SUS440C balls all decreased. However, the Cr/a-C coatings with high Cr content (11.98–14.09 at%) would worsen the tribological properties because chromium carbides acted as abrasive wear particles during tribotests.     

Fatty Acid Adsorption on Several DLC Coatings Studied by Neutron Reflectometry

The application of diamond-like carbon (DLC) coatings on the contacts of mechanical systems is becoming widespread thanks to their excellent tribological properties. Numerous studies of DLC coatings have been reported over the past decade and, as a result, the understanding of their lubrication has improved. The tribological properties of boundary-lubricated contacts are drastically affected by adsorbed layers; however, due to the variety of lubricant additives and coating structures, no general adsorption mechanisms for DLC coatings have been put forward until now. This has, unfortunately, hindered improvements in their lubrication performance. Many of the essential physical properties of the adsorbed layers also remain undefined. In this work, we used neutron reflectometry to determine the thickness and the density of the adsorbed layers of fatty acid molecules on coatings of a-C, a-C:H, a-C:H:F and a-C:H:Si. The results showed that a 0.9-nm-thick layer adsorbed onto the a-C and a-C:H coatings. In contrast, both doped coatings, i.e. the a-C:H:F and a-C:H:Si, showed a poorer adsorption ability towards the fatty acid molecules than the a-C and a-C:H. Continuous adsorption layers were not detected on the a-C:H:F and a-C:H:Si; however, the possibility of adsorption in lower quantities cannot be ruled out.     

Dry friction and wear characteristics of nickel/carbon nanotube electroless composite deposits

Ni/carbon nanotube (Ni/CNTs) composite coatings were deposited on carbon steel plate by electroless deposition. The friction and wear properties were examined under dry sliding conditions using the ball-on-disk configuration. For reference, carbon steel plate was coated with Ni, Ni/SiC and Ni/graphite. The results show that the Ni/CNT coating has a microhardness value of 865 Hv, greater than for SiC reinforced composite deposits. The Ni/CNTs composite coating possesses not only a higher wear resistance but also a lower friction coefficient, resulting from their improved mechanical characteristics and the unique topological structure of the hollow nanotubes.     

Monitoring of Wear Characteristics of TiN and TiAlN Coatings at Long Sliding Distances

TiN and TiAlN thin hard coatings have been widely applied on machine components and cutting tools to increase their wear resistance. These coatings have different wear behaviors, and determination of their wear characteristics in high-temperature and high-speed applications has great importance in the selection of suitable coating material to application. In this article, the wear behavior of single-layer TiN and TiAlN coatings was investigated at higher sliding speed and higher sliding distances than those in the literature. The coatings were deposited on AISI D2 cold-worked tool steel substrates using a magnetron sputtering system. The wear tests were performed at a sliding speed of 45 cm/s using a ball-on-disc method, and the wear area was investigated at seven different sliding distances (36–1,416 m). An Al₂O₃ ball was used as the counterpart material. The wear evolution was monitored using a confocal optical microscope and surface profilometer after each sliding test. The coefficient of friction and coefficient of wear were recorded with increasing sliding distance. It was found that the wear rate of the TiAlN coating decreases with sliding distance and it is much lower than that of TiN coating at longer sliding distance. This is due to the Al₂O₃ film formation at high temperature in the contact zone. Both coatings give similar coefficient of friction data during sliding with a slight increase in that of the TiAlN coating at high sliding distances due to the increasing alumina formation. When considering all results, the TiAlN coating is more suitable for hard machining applications.     

Friction and wear measurements of laser-sintered and coated parts

The aim of this research is the investigation of surface properties, the measurements of friction coefficient and wear rate of laser-sintered and coated parts. The industrial background of this research is to prove applicability of laser-sintered prototype tools for injection moulding of fibre-reinforced polymers, furthermore to increase the wear resistance of unalloyed steel tools by laser coatings. The materials of the test specimens were laser-sintered phosphorous bronze and unalloyed steel. For increase of wear resistance we used hard Co-based and glassy-like Fe-based (FeB) coatings. As counter bodies we used polymers reinforced with short carbon and glass fibres. The laboratory model tests of selective laser-sintered parts were carried out on a pin-on-disk machine. In case of coated parts—with higher wear resistance—we used a cylinder-on-cylinder tribometer. The tribological properties were determined at different load and temperature conditions. The results of the investigation show that the friction coefficient and wear resistance of laser treated surfaces are good. The coefficient of friction of coated specimens is slightly less, but the wear rate is significantly less.     

碳基薄膜水润滑性能的研究进展

评述了碳基薄膜如类金刚石薄膜(DLC)和非晶氮化碳(a-CNx)薄膜水润滑的研究现状和进展。分析了第2元素加入和摩擦副材料对碳基薄膜在水中摩擦磨损特性的影响,探讨了碳基薄膜在水中的磨损机制。指出:氢化或氮化碳基薄膜的磨损率与摩擦副材料的水合反应有关,若摩擦副材料易于摩擦水合反应,碳基薄膜的磨损率很低;3种DLC薄膜在水中的磨损率与DLC的种类和对磨钢球材料无关,都在10-8mm3/(N.m)的数量级上变动;a-CNx/Si基非氧化物陶瓷摩擦副显示很低的摩擦因数和低的磨损率;在相同条件下,a-CNx薄膜比a-C薄膜更能显示优异的水润滑性能。     

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.     

Influence of humidity on the friction of diamond and diamond-like carbon materials

The friction of diamond and diamond-like carbon (DLC) materials was evaluated in reciprocating sliding wear testing under controlled relative humidity. The testing conditions were a displacement stroke of 100 μm, an oscillatory frequency of 8 Hz and a normal load of 2 N. The coefficient of friction of diamond and hydrogen-free DLC (a-C) coatings against a corundum sphere in the steady regime decreased with an increase in relative humidity. A water layer physisorbed at the interface between the mating surfaces played two major roles: acting as a lubricant and increasing the true area of contact. However, it was noticed that the friction coefficient of the hydrogenated DLC (a-C:H) coatings first increased and then decreased with increasing relative humidity in the steady state. There appeared to be a critical relative humidity for the a-C:H coatings, at which the steady-state friction reached the maximum value. The frictional behaviour of the a-C:H coatings also showed dependence on the wear test duration. The interaction between hydrogen and oxygen at the interface between the a-C:H coating and water layer was mainly responsible for such behaviour.     

Tribochemical effects on the friction and wear behaviors of a-C:H and a-C films in different environment

Friction and wear behaviors of hydrogenated amorphous carbon (a-C:H) and hydrogen-free amorphous carbon (a-C) films sliding against Si₃N₄ balls were investigated in different testing environments. The result showed that two films with extreme chemical disparity (one hydrogenated, and the other hydrogen free) showed distinct different friction and wear behaviors, and the friction and wear behaviors of the both films were strongly dependent on the environment. For a-C:H films, much low friction coefficient and wear rate were obtain in dry N₂. In the water and/or oxygen containing environments, the friction coefficient and wear rate of a-C:H films were obviously increased. On the contrary, a-C films only provided low friction coefficient and wear rate in the presence of water and/or oxygen in the test chamber. In dry N₂, the highest friction coefficient and wear rate were observed for a-C films. By investigating the worn surfaces of the films using XPS, it was proposed that the environment dependence of the friction and wear behaviors of the films was closely related with the friction-induced chemical interactions between the films and water and/or oxygen molecules. The specific roles of hydrogen, water and oxygen molecules and their tribochemical effects on the friction and wear mechanism of the films are discussed.     

Tribological Performance of Halogen-Free Ionic Liquids in Steel–Steel and DLC–DLC Contacts

The tribological performance of halogen-free ionic liquids at steel–steel and diamond-like carbon (DLC)–DLC contacts was investigated. Hydrogenated amorphous carbon (a-C:H) and tetrahedral amorphous carbon (ta-C) were used as test specimens. Friction tests were carried out on steel–steel, a-C:H–a-C:H, and ta-C–ta-C contacts by using a reciprocating cylinder-on-disk tribotester lubricated with two different types of halogen-free ionic liquids: 1-ethyl-3-methylimidazolium dicyanamide ([BMIM][DCN]) and 1-butyl-3-methylimidazolium tricyanomethanide ([BMIM][TCC]). From the results of friction tests, the ta-C–ta-C tribopair lubricated with [BMIM][DCN] or [BMIM][TCC] exhibited an ultralow friction coefficient of 0.018–0.03. On the other hand, ultralow friction was not observed at the steel–steel and a-C:H–a-C:H contacts. Measurements obtained with a laser scanning microscope and an atomic force microscope (AFM) showed that a chemical reaction film, derived from the ionic liquid lubricant used, was formed on the steel surfaces. However, this chemical reaction film was not observed on either of the DLC surfaces. The AFM results showed that there were high-viscosity products on the ta-C surfaces, that the wear tracks on the ta-C surfaces exhibited low frictional properties, and that the ta-C surfaces were extremely smooth after the friction tests. Based on these results, it was concluded that an ionic liquid–derived adsorbed film formed on the ta-C surface and resulted in the ultralow friction when lubricated with a halogen-free ionic liquid.     

Wear Resistance of Fine-Grained High Nitrogen Austenitic Stainless Steel Coated with Amorphous Carbon Films: The Soft X-ray Spectroscopy Approach

The wear resistance dependence on grain size of a high-nitrogen-alloyed austenitic stainless steels (HN) is investigated and compared to measurements for the same samples coated with amorphous carbon (a-C:H) and nitrogenated amorphous carbon (a-C:H(N)) films, deposited by means of plasma-enhanced chemical vapour deposition. A synergic effect between the grain refining and the film in the case of nitride amorphous carbon overcoats is observed in terms of increased low-friction performance duration. The temperature dependence of the wear resistance of a micro crystalline HN stainless steel coated with carbon films is also investigated. An overall decrease of the films' wear resistance is found with increasing temperature. Furthermore, a higher wear resistance is found in the a-C:H coated steel with respect to the a-C:H:N material. High-lateral-resolution photoemission microscopy reveals that inhomogeneities within the film after wear testing are correlated to an increase of the number of N-sp² C-bonded sites. The study of energy-distribution curves and high-lateral-resolution images on the nitrogenated samples shows that a modification of the surface chemistry occurs by mechanical action; in particular this implies that existing N-sp² C sites are beginning to cluster as temperature increases.     

Tribological Behavior of Nickel-Doped Diamond-Like Carbon Thin Films Prepared on Silicon Substrates via Magnetron Sputtering Deposition

In this study, nickel-doped diamond-like carbon (Ni-DLC) thin films were deposited on silicon (Si) substrates using a magnetron cosputtering system by varying DC power density applied to a Ni target at a fixed DC power density applied to a carbon (C) target. Their tribological properties were systematically investigated using a ball-on-disc microtribometer. The tribological results showed that increasing the DC power density applied to the Ni target more than 0.49 W/cm² significantly increased the friction and wear of the Ni-DLC films due to the degraded sp³-bonded cross-linking structures of the films. However, the much lower friction and wear of the Ni-DLC-coated Si samples than those of the uncoated Si sample implied that the Ni-DLC films could effectively prevent their Si substrates from wear. It could be concluded that the Ni-DLC films could be used as high wear-resistant coatings for micromold applications because their tribological properties were significantly influenced by the DC power density applied to the Ni target.     

Effects of film thickness and contact load on nanotribological properties of sputtered amorphous carbon thin films

The nanotribological properties of amorphous carbon (a-C) films of thickness in the range of 5-85 nm sputtered on Si(1 0 0) substrates were investigated with a surface force microscope (SFM), using a Berkovich diamond tip of nominal radius of curvature approximately equal to 200 nm and contact (normal) loads between 10 and 1200 μN. The dependence of the friction and wear behaviors of the a-C films on normal load and film thickness was studied in terms of nanomechanical properties, images of scratched surfaces, and numerical results obtained from a previous analytical friction model. The increase of the contact load caused the coefficient of friction to decrease initially to a minimum value and, subsequently, to increase to a maximum value, after which, it either remained constant or decreased slightly. The dominant friction mechanism in the low-load range was adhesion, while both adhesion and plowing mechanisms contributed to the friction behavior in the intermediate- and high-load ranges. Thinner (thicker) a-C films yielded higher (lower) friction coefficients for normal loads less than 50 μN (low-load range) and lower (higher) friction coefficients for normal loads greater than 150 μN (high-load range). Elastic and plastic deformation, microcracking, and delamination of the a-C films occurred, depending on the contact load and film thickness ranges. The reduced load-carrying capacity, relatively low effective hardness (strength) obtained with thinner films, and dominant friction and wear mechanisms at each load range illustrate the film thickness and contact load dependence of the nanotribological properties of the sputtered a-C films.