Wear 268 (2010) 59–66 Contents lists available at ScienceDirect Wear journal homepage: www.elsevier.com/locate/wear Subsurface shear instability and nanostructuring of metals in sliding S. Tarasov ∗ , V. Rubtsov, A. Kolubaev Institute of Strength Physics & Materials Science SB RAS, Academicheskii, 2/4, Tomsk, Russia a r t i c l e i n f o Article history: Received 15 July 2008 Received in revised form 10 April 2009 Accepted 18 June 2009 Available online 26 June 2009 Keywords: Sliding Shear instability Strain localization Nanostructuring Viscous flow Numerical simulation a b s t r a c t Dry sliding wear conditions were used to obtain a 500 m-thick layer of nanosize grains on copper samples. As shown, this layer reveals a flow behavior pattern similar to that of a viscous non-Newtonian fluid. Four structurally different zones were found in the longitudinal cross-sections of samples below the worn surface. Upper two of them are nanocrystalline and consist of many ∼1 m-thick sublayers, which show either laminar or turbulent flow behavior. These sublayers demonstrate different levels of elasticity as compared to each other and may be related to an interplay between work-hardening and thermal softening. Lower two zones undergo usual plastic deformation and severe fragmentation without viscous mass transfer. High level of Young’s modulus in the fragmentation zone is evidence of insufficient thermal softening at that depth. We believe that viscous flow zones are the result of shear instability and subsequent shear deformation developed in subsurface layers due to thermal softening. Numerical study has been carried out to simulate friction-induced deformation and shear instability under conditions close to the experiment. As shown, such a situation is possible when deformation-generated heat is taken into account. Another interesting result relates to the sublayers’ strain rate distribution. It was found that 1 m-thick sublayers may show either high strain rate gradient or zero strain rate as a function of depth below the worn surface. The latter case means that a pack of layers may exist and behave like an elastic body in ductile medium. © 2009 Elsevier B.V. All rights reserved. 1. Introduction One of the most interesting and intriguing problems in tribology is structural changes in materials in sliding contact. These changes may be responsible for mild-to-catastrophic wear mechanism transition and is a very complex phenomenon while its main contributing factors are plastic deformation and friction-generated heat. When a ductile material slides against a harder one, the subsurface layers of the ductile material undergo plastic deformation and may even form a thick layer of severely deformed and even nanocrystalline metal. The depth of such a layer is determined both by the contact stress and the temperature dependence of the material’s yield point. It is a problem to observe in situ the strain stages in subsurface layers of metals in sliding since the deformation goes through all the stages in a very fast manner and in most cases we can observe only the final stage of this process without any intermediate states. Also these deformation stages do not necessarily coincide with those found in stress–strain compression diagrams of a corresponding metal. Nanostructuring in sliding wear is a fundamental problem that is receiving increased attention but no satisfying models have been ∗ Corresponding author. Tel.: +7 382 2 286815; fax: +7 382 2 492576. E-mail address: [email protected] (S. Tarasov). 0043-1648/$ – see front matter © 2009 Elsevier B.V. All rights reserved. doi:10.1016/j.wear.2009.06.027 developed. The mechanism of deformation which serves to produce nanocrystalline grains under condition of sliding wear and temperature gradients is not fully understood. Studies into such a phenomenon would help to gain better understanding of the nanostructuring in deformation since the severity of deformation is a function of depth below the worn surface. Another problem is deformational behavior of the nanostructured layers in sliding together with its effect on the tribological parameters such as coefficient of friction and wear rate. It is reported elsewhere [1] that nanocrystalline materials obtained by severe plastic deformation demonstrate high diffusivity for interstitial and impurity atoms, which may fully modify the tribology behavior of the sample. There are several mechanisms suitable for nanostructuring in sliding [2–4], but one of the most plausible ones is a shear instability mechanism [5,6]. This mechanism implies fast (almost adiabatic) shear deformation under conditions of thermal softening. However, it neglects all previous deformation stages and one of the most important ones is a stage of plastic strain localization. We do not fully understand how and why the shear instability happens at the microstructural scale. This work has been devoted to both experimental and numerical verification of shear instability mechanisms by studying structural fragmentation, mechanisms for the formation of structurally fragmented layer, and its morphology and flow behavior during sliding 60 S. Tarasov et al. / Wear 268 (2010) 59–66 Table 1 Chemical composition of the tool steel disk. G (MPa) y (MPa) Gpl (MPa) ◦ ◦ ◦ ◦ ◦ 20 C 1000 C 20 C 1000 C 20 C 1000 C 41,500 29,300 4 2 70 3.5 in the absence of mechanical intermixing of metals at the worn surface. 2. Experimental details Samples in the form of Ø5 mm and 20 mm length pins were cutoff the Ø5 mm commercial copper rods using a lathe tool. Chemical composition of copper was as follows—Cu: min 99.9%; Fe: 0.005 (wt.%); Ni: 0.002%; S: 0.004%; As: 0.002%; Pb: 0.005%; Zn: 0.004%; Ag: 0.003%; O: 0.05%; Sb: 0.002%; Bi: 0.001%; Sn: <0.002%. The pins’ end surfaces were ground manually and gently to remove the lathe grooves and then used in wear test. Vertical pin-on-disk sliding tester 2169 UMT-1 (Tochpribor, Ivanovo) was used to test three samples simultaneously against a counterface of Ø320 mm 64 HRc tool steel disk (see Table 1). These samples were brought in the unlubricated sliding contact and then loaded stepwise to achieve nominal contact stress of 0.5 MPa. On finishing the test, the samples were mounted in Wood’s metal and sectioned using an abrasive wheel rotating at 1000 rpm with water cooling in a diametric plane parallel to the sliding direction, manually ground, polished with corundum abrasive papers followed by diamonds pastes of grades 2 and 1.0 m and etched in 10% NH4 OH for metallography. Microstructure of the worn samples was characterized using both an optical and a differential-interferential (DIC) contrast microscope Axiovert 200 MAT (Carl Zeiss) as well as an AFM instrument Solver Pro 47H (NT-MDT, Zelenograd) with atomic force acoustic microscopy (AFAM). This technique allows mapping the surfaces so that the brightness signal is proportional to the Young’s modulus magnitudes as determined from the stiffness of a probe/sample contact. The resolution of this method is higher than that of the basic contact AFM mode. It is a very helpful, simple and reliable method to detect the nanosize grains by the local difference in elasticity between the grain body and boundary. Also both Young’s modulus and nanohardness numbers have been determined using a CSEM Nanohardness tester (Oliver & Pharr method [7]). (kg/m3 ) , W/(m K) c, J/(kg K) 8900 395 386 ◦ parallel to the sliding direction while zone II is a place of intense structural fragmentation [8,9]. Morphological specificity of zones III and IV is that they both consist of <1 m-thick sublayers (Fig. 3). Such a stratification originates from their flow behavior under shear stress. The AFAM image of zone IV material in Fig. 4a shows that those sublayers are composed mainly of <100 nm horizontally elongated grains but nearly equiaxial >200 nm grains may be found too—Fig. 4b. The AFAM image of the zone II/III interface in Fig. 5b shows that the Young’s modulus magnitudes of zone II are higher those of zone III. It is conceivable that since zone II material is rheologically immobile, heavily fragmented and accumulates elastic strain from high dislocation density. Moreover, the sublayers of zone IV may flow at different speeds and also be either softened or hardened. Nanoindentation experiments carried out according to the Oliver & Pharr method [7] provide support to this point of view (Fig. 6). Fig. 1. Time dependence of friction moment for two different sliding regimes: (1) mild wear and (2) catastrophic wear (scuffing). 3. Results Time dependencies of the friction coefficient are shown in Fig. 1 for two different wear modes. Dependence 1 corresponds to relatively stable sliding and mild wear, which resulted in no structural changes other than subsurface metal grains rotated and elongated with respect to the sliding direction. The result of sliding under conditions of regime 2 was a 300–500 m-thick nanocrystalline layer having a clear interface separating it from the underlying material (Fig. 2). Structurally, this layer may be divided into four zones as follows: plastic deformation and texturized grain zone I; intense fragmentation zone II; “turbulent” flow zone III (may be absent) and finally, “laminar” flow zone IV (Fig. 2). Let us note that we just use these terms by drawing an analogy with the flow of very viscous fluid. Zones I and II may be called also by usual deformation zones whereas both III and IV are the viscous flow zones. One may see that both strain and fragmentation gradually grow starting from the deepest layers of zone I to the fragmentation zone II until an interface between zones II and IV (III) is formed as a result of shear instability. Zone I is characterized by crystallographic rotation of the grains with respect to shear stress so that {1 1 1} planes become Fig. 2. Optical micrograph of the plastic deformation zones in a longitudinal crosssection of copper sample worn against tool steel counterface (0.6 m s−1 , 0.5 MPa): (I) plastic strain zone; (II) fragmentation zone; (III) turbulent flow zone; (IV) laminar flow zone. S. Tarasov et al. / Wear 268 (2010) 59–66 61 Fig. 3. Optical micrograph (differential-interferential contrast) micrographs of zone III/II interface. Fig. 5. AFM (a) and AFAM (b) images of zone IV/II interface. The brighter zones in the AFAM image correspond to those of higher Young’s modulus. Fig. 4. AFAM images of nanocrystalline layer: (a) elongated nanocrystalline grains and (b) equiaxial grains. Fig. 6. Nanohardness (1) and Young’s modulus (2) vs. depth below the worn surface. (I) Plastic strain zone; (II) fragmentation zone; (III) turbulent flow zone; (IV) laminar flow zone. Curves 1 and 2 are the least square approximation lines. 62 S. Tarasov et al. / Wear 268 (2010) 59–66 Generally, the distribution of nanohardness numbers qualitatively coincides with that of the Young’s modulus except for zone III, where the nanohardness peak has been found. The distribution of the nanohardness numbers and Young modulus’ magnitudes across zone IV show a peak, which may originate from a higher stress level sublayer (Fig. 6). One may see that apart from the peaks, the mean level of the Young’s modulus is the same for zones I and IV whereas the nanohardness levels are different. According to the Oliver & Pharr method, the Young’s modulus is determined from the unloading portion of the indentation curve, therefore nanocrystalline material of zone III is deformed in a manner that allows no far-range elastic stress accumulation. On the contrary, the fragmented structure of zone II material shows the highest level of Young’s modulus of 140 GPa. An explanation may be given in terms of an interplay between processes of hardening and softening in different zones [10]. The hardening is considered as a process of accumulating dislocations at the grain boundaries while softening is provided by annihilation of dislocations at the grain boundaries activated by the friction-generated heat. Deformation behavior of nanocrystalline material in zone IV (III) dramatically differs from that of zones I and II. Such a mass transfer mechanism looks like flow of a very viscous non-Newtonian fluid. However, unlike the fluid, this layer is really composed of smaller sublayers which may flow at different rates with respect to each other. The most suitable deformation mechanism may be grain-boundary slipping (GBS) with the only specificity that slipping mainly occurs at the sublayer interfaces. Taking into account the grain size in zone IV one may suggest that deformation is controlled also by diffusion-assisted grain-boundary processes. Zone II material structure is composed of grains’ fragments having almost the same size as zone IV grains, however, no shear instability is observed below the zone IV/II interface because of insufficient thermal softening. It follows from the contrast of the AFAM image in Fig. 5b that zone II shows high level of elasticity that may be related to high level of far-range elastic inner stress exerted by subgrain boundaries saturated with numerous defects and strain localization bands [10]. The most intense fragmentation occurs when two strain localization bands cross each other [11]. Such a crossing may serve as a place where first nanocrystalline grains nucleate and provoke shear instability by activating grainboundary slipping mechanism. The result is generation of a shear band in subsurface layers of the ductile sample [9]. 4. Model description and numerical simulations It seems that a reason for the layered structure formation is macroscopic stress and strain distributions across the subsurface layer of materials in sliding contact. Plastic flow in subsurface layers of metal in sliding contact that may result in generation of layers parallel to the sliding direction can be simulated within the framework of a dynamic one-dimensional sliding contact model described elsewhere [6,12–13]. This model can be called a macroscopic one in the sense that it does not account distinctly for both microstructure and deformation mechanism of the medium but operates by its macroscopic characteristics only. The model describes friction process occurring on a single contact spot, which is formed when a ductile micropin slides over an absolutely rigid counterbody at the constant velocity Vc . The micropin of height hsample is assembled of many uniform thickness layers—Fig. 7. The counterbody exerts both contact stress P and shear stress from the friction force P (where is the friction coefficient) to the pin’s topmost layer. The bottom layer is rigidly fixed on the base. All the layers are assumed to be absolutely rigid and have equal lengths L and thicknesses hlayer . The layer material is characterized by the density , heat conductivity , uniaxial yield point y , shear modulus G and “plastic” shear modulus Gpl , which characterizes the work-hardening susceptibility of the material. Additionally, each layer is characterized by the coordinate x and travel velocity V. It is assumed in this model that the micropin may experience the shear deformation when its composing layers displace with respect to each other in the direction parallel to the worn surface. As suggested, each layer may interact only with its closest neighbors. Two neighboring layers are counted as a unit of shear deformation. We do not consider explicitly the compression of the sample under normal stress P in this model assuming it to be constant over the micropin’s height and equal to the normal stress in the contact area. The normal stress level is considered in computing a plasticity criterion. To determine the shear stress level for a couple of layers, we use an elastic–plastic response function which is described in detail elsewhere [12]. As shown schematically in Fig. 8, this function serves to establish a relation between the shear stress and the shear strain in a couple of layers. Its parameters are as follows: elastic and plastic moduli Gc and G cpl , maximal elastic strain el and equilibrium shear eq . The magnitude of el is a maximum shear strain at which the material still retains its elasticity, eq is the total plastic shear strain accumulated from the deformation onset. The line portion AB in Fig. 6 shows elastic deformation mode while portions DA and BC denote plastic deformation with linear hardening. Also we use a deformational plasticity criterion with this model. A cross-over from elastic to elastic–plastic deformation occurs for a couple of layers when the strain magnitude becomes higher the maximum elastic strain at the current temperature within this couple, i.e. > el . At the beginning of the computation procedure, the layer couple’s properties are set to be the mean values of those belonging to the layers. In further computations, the couple’s properties are changed so that both Gc and G cpl values are corrected for the current temperature at each time step. In addition to the temperature dependence, the values of eq and el depend also on the previous deformation history of the given couple of layers. The onset value of maximum elastic deformation 0el corresponds to the undeformed material and may be determined according to Ref. [14] with the use of the von Mises criterion for plain deformation. Such an approach allows us to take into consideration the fact that two types of stress are applied to the micropin within the framework of the one-dimensional problem, namely, normal and shear. Before the simulations, we calculated the starting values of maximum elastic strain for each layer coupled within √ the possible temperature range as follows: 0el = y 2 − P 2 / 3Gc . A special procedure of the response function modification is applied in this model to take into account all previous history of both deformation and temperature changes. This modification procedure allows consideration of two competing and concurrent processes such as work-hardening and thermal softening as well as thermal stress relieving and irreversible plastic deformation. Details on the response function modification procedure are given elsewhere [12]. To determine the temperature field in the micropin, we were looking for a solution of the one-dimensional friction heat problem. The calculation lattice nodes were placed at the layer interfaces. For simplicity, we assumed that both heat conductivity and capacity did not depend on the temperature. When modeling the single contact, we considered that its life is rather short, therefore, the depth of the heat propagation below the worn surface is not larger the micropin’s height and the temperature at S. Tarasov et al. / Wear 268 (2010) 59–66 63 Fig. 7. Schematic of the modeling system. Fig. 8. The response function shape. the micropin/base interface is constant and equal to the starting. It is assumed that the heat generated on the worn surface is distributed in equal portions between the sample and counterbody, therefore, the heat release power transmitted to the sample is determined as 0.5PVc − V1 |, where 0.5 stands for the heat flux distribution; |Vc − V1 | is an absolute value of sample/counterbody sliding velocity; V1 is the sample’s top layer velocity. Earlier [6,13] we used this model to show that subsurface plastic shear strain as high as tens of percents and even higher may develop during sliding for contact times being on the order of 1 × 10−4 s. It is rather severe deformation and most of its energy is released in the form of heat in the bulk of subsurface layer. This heat would change greatly both the heat dissipation regime and materials’ deformation behavior. The drawback of the mentioned above model is that it takes into account the heat generated only on the sliding surface. In this work we improve the model by introducing the heat generated in the subsurface layer due to its plastic deformation. This model implies that if a couple of layers experience shear deformation during some moment of time, it simultaneously generates some quantity of heat. We assume that the plastic deformation work fully transforms into the heat, therefore the quantity of heat released in a couple of layers per a time interval was made equal to the mechanical work spent for plastic deformation of that couple. During the simulation, we first determine the temperature fields for all procedure steps. Then, the response function parameters of each layer couple are modified in accordance with the temperature and deformation prehistory. At the next stage, we integrate the system of classic motion equations applied to the micropin, determine coordinates and velocities of each layer and, finally, obtain the shear strain magnitudes. On doing so, we find the heat release power at the worn surface as well as power of the internal (subsurface) heat sources and use the results to calculate the temperature for the next moment of time. To estimate the lifetime tc of a contact spot of length L, let us invoke a simple approximation tc = L/Vc . Changing the procedure time tc , we can change the spot lifetime in the same way and carry out simulation for contact spots of different sizes. The simulation was carried out for the 500 m contact spot and typical sliding velocity 1 m s−1 , which gives us the contact duration tc = 5 × 10−4 s. The friction coefficient was = 0.5 which is not an unexpected value for unlubricated sliding test of metals. It was shown experimentally in this work that the thickness of plastically deformed layer (total thickness of zones I through IV) may achieve 600–700 m and thickness of zone IV (III) sublayers is about 1 m (Fig. 3). Taking it into account for simulations, we assume the micropin’s height to be 1000 m, and compose it of one thousand 1 m-thick layers. Thus, a zone of interest to us in which the plastic shear is developed contains at least several hundreds of layers. The thickness of the model micropin’s layers corresponds to the minimal thickness of the experimentally found sublayer. We believe it is an adequate assumption to describe the behavior of the material within the framework of the proposed here macroscopic approach. The starting temperature for simulation was 20 ◦ C, normal contact stress 51.8 MPa (Table 2). The objective was to observe the plastic shear strain development in the subsurface layers of the material and, therefore, the shear stress magnitude was adjusted to produce only elastic strain Table 2 Physical constants of model material. G (MPa) Gpl (MPa) y (MPa) 20 ◦ C 1000 ◦ C 20 ◦ C 1000 ◦ C 20 ◦ C 1000 ◦ C 41,500 29,300 4 2 70 3.5 (kg/m3 ) , W/(m K) c, J/(kg K) 8900 395 386 64 S. Tarasov et al. / Wear 268 (2010) 59–66 Fig. 9. Time dependence of ratio between current yield point and its onset value for n different moments of time. 1–1 × 10−5 s; 2–3 × 10−5 s; 3–5 × 10−5 s; 4–1.5 × 10−4 s. for the given friction coefficient and temperature during the very first moment of time. During the very first moment of time, the shear stress at the sliding surface is kept below the yield point so the sample will undergo only elastic deformation. As time has passed, the subsurface layer heats up and then starts reducing its yield point level. The ratio between the current yield point and its onset value is shown in Fig. 9 for different moments of time. As long as the stress magnitude is kept below the yield point, the maximum of temperature and, therefore, the maximum of thermal softening are found at the very surface of the sample (see curve 1, Fig. 9). However, when the shear stress magnitude overcomes the yield point, there occurs a local shear stress instability in the form of adiabatic plastic shear (Fig. 9, curve 2). This deformation act produces the heat that will further elevate the local temperatures in already softened layer and thus enhance the softening. At the same time, the yield point must grow due to work-hardening. As shown by modeling, those two competing processes result in keeping the yield point approximately constant (Fig. 9). Curves 3 and 4 have their minimums in the form of plateaus, which correspond to one and the same yield point level, being approximately equal to the actual shear stress level. The plateau describes behavior of heat softened and then plastically deformed and work-hardened material. The curve portions on the right of the plateau relate to only elastically deformed material, which, however, is softened to some of its depth. Heat generated on the worn surface together with heat effect of deformation serves to elevate the mean temperature in the subsurface layer, thermal softening and plastic deformation of progressively deeper layers (curves 3 and 4, Fig. 9). The length of plateau at curves 3 and 4 (Fig. 9) coincides with the plasticized layer thickness for the given moment of time. Fig. 10 shows development of both shear strain (Fig. 10a) and layer velocity (Fig. 10b) in the sample. It is clear (Fig. 10a) that both the plasticized layer thickness and accumulated plastic strain steadily grow with time. However, the layer velocity distribution curves in Fig. 10b demonstrate that plastic deformation in subsurface layer is not a stationary process both in space and time. With time, the plasticized layer thickness grows and the subsurface strain develops two types of layer velocity distributions. High layer velocity gradient portions of the curves in Fig. 10b relate to shear instability behavior and intense plastic deformation. Another type of behavior is expected at the plateau portions, where layer velocity gradient is zero and a whole pack of equal layer velocity layers is formed and move in parallel to the sliding direction. As shown in Fig. 11, these packs consist of five and more sublayers. This pack is composed of layers capable of only elastic deformation Fig. 10. Plastic shear strain (a) and layer velocity (b) as function of depth below the worn surface for different moments of time. 1–8.18 × 10−5 s; 2–1.463 × 10−4 s; 3–2.9 × 10−4 s; 4–4.03 × 10−4 s; 5–4.874 × 10−4 s. with respect to each other. Such a formation moves as an elastic solid body through the plasticized medium. The number of zones of both types may vary during the deformation; zones may change their thickness, migrate down from the surface and then come back. For instance, on passing 8.18 × 10−5 s since the beginning of the sliding we can see at least three zones: two of them are the shear instability zones and between them is the 5 m-thick elastic pack (Fig. 10b, curve 1). The next deformation stage shows already three instability zones and two elastic packs (Fig. 10b, curve 2). Later we Fig. 11. Plastic shear strain vs. time at fixed depth of 100 m below the surface. S. Tarasov et al. / Wear 268 (2010) 59–66 can see two shear instability zones separated by the elastic pack (Fig. 10b, curve 3). Generally, the number of both packs and plastic shear zones is increased with the whole layer thickness as well as the elastic pack mean thickness. Zones of both types never stop migrating, disappearing and appearing again during sliding (Fig. 10b, curves 4 and 5) and therefore the time-dependent accumulation of plastic shear strain within the plasticized layer occurs non-uniformly. The time dependence of shear strain at the 100 m depth below the surface is shown in Fig. 11. Horizontal line portions E1, E2, E3, E4 and E5 denote the time intervals within which only elastic packs are migrating in material at his depth. The sloped line portions P1, P2, P3, P4 and P5 correspond to the time intervals of intense plastic deformation. One may see from Fig. 11 that subsurface layer deformation is a cyclic process when plastic shear time interval is followed by the interval of no plastic deformation. The mean time period of such a process is ≈5 × 10−6 s, which is five times longer of time needed for the elastic shear wave to travel down from the surface to the bottom and back. Also this period is two times longer as compared to the period of the observed elastic oscillations of the whole sample. The strain rate in the plastic deformation intervals is as follows: ≈3.2 × 102 s−1 in P1 interval and up to ≈ 2.5 × 102 s−1 in P5 interval. Mean shear strain rate for the total time as shown in Fig. 11 is ≈2.2 × 102 s−1 . It is important that alternating horizontal and sloped portions of the strain curve are found not only for some specific depth. The results of simulations show that such a behavior is typical for the total plasticized layer thickness when elastic strain time intervals alternate with plastic shear ones. 5. Discussion Both the morphology of the nanocrystalline layer and specificity of its flow at the interface enable a suggestion that the most feasible mechanism for formation of such a layer is a mechanism that includes both formation and relative displacement of zone II fragments with respect to each other. Strain localization and structural fragmentation of material in zones I and II may be considered a precursor stage of the shear instability which is necessary to provide a degree of structural fragmentation suitable for launching the shear instability mechanism. Using the speckle decorrelation technique, we studied kinetics of strain localization and shear instabilities in subsurface layers of ductile metals in sliding [11]. It was shown that there are three stages of strain development in subsurface layers of metal in sliding. Fig. 10 shows a time-scan of strain zone development in a longitudinal cross-section of the sample. Stage 1 is characterized by the strain zones travelling across the sample’s longitudinal cross-section at the speed equal to the speed of sliding. At the stage 2 the zones may slow down and even stop (localize) at some place in a sample. This stage is marked by the growing slope of initially vertical areas in Fig. 10. Stage 2 is a stage when strain localization bands are formed below the worn surface and intense fragmentation is initiated in the sites where these bands cross each other [11]. One may say this is a process of zone II nucleation and growth. Finally, the strain zones may start travel again at the sliding speed (stage 3), thus marking the moment of shear instability (Fig. 12). The result of shear instability was nanostructuring in thin subsurface layer and a sharp interface between the layer and the base metal. It is our view that generation of such a nanocrystalline layer is similar to the generation of a shear band in severely deformed metal under condition of thermal softening by friction heat. Microstructurally this softening means that the grain fragments formed by severe deformation undergo recovery and even 65 Fig. 12. Development of plastic strain localization and shear instability in subsurface layers of copper–zinc alloy. Arrow shows a direction of strain localization zone displacement. L is the sample’s longitudinal cross-section width. Sliding speed 5 mm/min. recrystallization, thus reducing effect of work-hardening and forming the nanosize grains suitable for grain-boundary slipping (GBS). The definitive role played both by kinetics of lattice and boundary dislocations in the deformation of nanocrystalline materials has been demonstrated in Ref. [10]. It has been shown that dislocations may either accumulate in the grains or annihilate at the grain boundaries thus reducing the effect of their accumulation. In addition to the grain boundaries (Fig. 2), the sliding-induced nanocrystalline material shows sublayer boundaries (Fig. 3). It was shown earlier that friction-induced nanocrystalline material shows self-affine geometry in some structure scales [15], which is believed to originate from its layered structure. This self-affine geometry suggests self-consistent mode of sublayer deformation similar to that obtained in numerical simulation. The sublayers (or a pack of sublayers) undergo shear deformation with respect to each other along the sublayer boundaries. However, it was shown by numerical simulations that the sublayers demonstrate a wide range of strain rates. It was established also that shear instability fronts may travel across the longitudinal cross-section of the sample thus creating conditions for the lessened fragmentation of source structure and layered structure formation. The results of numerical simulations provide support for the earlier suggestion that shear stress and strain distribution will determine the layered structure formation. It turned out that these distributions are non-uniform both in time and depth below the surface and really can be the reason for development of the layered structure. It is plausible that slow sublayers are more prone to accumulate dislocations. The faster sublayers generate more heat during deformation, since the dislocations are expelled to the sublayer boundaries and annihilate there. The slower sublayers play the role of strain localization bands in the nanocrystalline material. 6. Summary The microstructure and mechanical characteristics of frictiongenerated nanocrystalline copper layer were investigated. The results of experiments were consistent with the results of numerical simulations carried out on the assumption that shear instability is controlled by competing processes of thermal softening and work-hardening. We develop a macroscopic numerical simulation approach, which allows us to study a material response to severe deformation under reasonable test conditions. Strain-induced structural changes in subsurface layers of metal have been examined and it is demonstrated that shear instability develops in a severely deformed zone composed of fine grain fragments due to the thermal softening. This mechanism is responsible for the generation of a 500 m-thick nanocrystalline layer, which, in its turn, consists of numerous <1 m-thick sublayers having 66 S. Tarasov et al. / Wear 268 (2010) 59–66 different elasticity levels depending on their strain rate. Such a layered structure suggests a viscous flow mechanism of deformation during sliding similar to that of non-Newtonian fluid or a granular medium that has great influence on the mild-to-catastrophic wear mechanism transition. Acknowledgements The present work has been carried out according to Project No. 3.6.1.2 of SB RAS basic research Program 3.6.2 and Project 3.6.2.1 of SB RAS basic research Program 3.6.1 of as well as supported by the Russian Fund for Basic Research (Grant No. 06-08-00200a). References [1] Yu.R. Kolobov, R.Z. Valiev, et al., Grain Boundary Diffusion and Properties of Nanostructured Materials, Cambridge International Science Publishing, 2007, p. 250. [2] D.A. Rigney, Transfer, mixing and associated chemical and mechanical processes during the sliding of ductile materials, Wear 245 (2000) 1–9. [3] D. Shakhvorostov, K. Pohlmann, M. Scherge, Structure and mechanical properties of tribologically induced nanolayers, Wear 260 (4–5) (2006) 433–437. [4] L. 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