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Rolling friction is of great importance for many applications, such as tires and conveyor belts. We study the rolling friction for hard cylinders rolling on flat rubber sheets. The rolling friction depends on the number of rolling cycles, the rolling speed, and the temperature. We show that when the rubber is cooled down below the glass transition temperature, the deformations of the rubber surface are frozen-in, resulting in a non-flat rolling track where uphill and downhill rolling movements strongly affect the rolling force. The experimental data are analyzed using the Persson rolling friction theory; good agreement with the experiments is obtained when the non-linear (strain-softening) properties of the viscoelastic modulus are taken into account.
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We discuss the origin of the breakloose (or static) friction force when an ice block is slid on a hard randomly rough substrate surface. If the substrate has roughness with small enough amplitude (of order a 1 nm or less), the breakloose force may be due to interfacial slip and is determined by the elastic energy per unit area, Uel/A0, stored at the interface after the block has been displaced a short distance from its original position. The theory assumes complete contact between the solids at the interface and that there is no elastic deformation energy at the interface in the original state before the application of the tangential force. The breakloose force depends on the surface roughness power spectrum of the substrate and is found to be in good agreement with experimental observations. We show that as the temperature decreases, there is a transition from interfacial sliding (mode II crack propagation, where the crack propagation energy GII = Uel/A0) to opening crack propagation (mode I crack propagation with GI the energy per unit area to break the ice-substrate bonds in the normal direction).
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We study the friction when rectangular blocks made from rubber, polyethylene, and silica glass are sliding on ice surfaces at different temperatures ranging from -40 to 0 °C, and sliding speeds ranging from 3 µm/s to 1 cm s-1. We consider a winter tire rubber compound both in the form of a compact block and as a foam with â¼10% void volume. We find that both rubber compounds exhibit a similar friction on ice for all studied temperatures. As in a previous study at low temperatures and low sliding speeds, we propose that an important contribution to the friction force is due to slip between the ice surface and ice fragments attached to the rubber surface. At temperatures around 0 °C (or for high enough sliding speeds), a thin pre-melted water film will occur at the rubber-ice interface, and the contribution to the friction from shearing the area of real contact is small. In this case, the dominant contribution to the friction force is due to viscoelastic deformations of the rubber by the ice asperities. The sliding friction for polyethylene (PE) and silica glass (SG) blocks on ice differs strongly from that of rubber. The friction coefficient for PE is â¼0.04-0.15 and is relatively weakly velocity dependent except close to the ice melting temperature where the friction coefficient increases toward low sliding speeds. Silica glass exhibits a similarly low friction as PE for T > -10 °C but very large friction coefficients (of order unity) at low temperatures. For both PE and SG, unless the ice track is very smooth, the friction force depends on the position x along the sliding track. This is due to bumps on the ice surface, which are sheared off by the elastically stiff PE and SG blocks, resulting in a plowing-type of contribution to the friction force. This results in friction coefficients, which locally can be very large â¼1, and visual inspection of the ice surface after the sliding acts show ice wear particles (white powder) in regions where ice bumps occur. Similar effects can be expected for rubber blocks below the rubber glass transition temperature, and the rubber is in the (elastically stiff) glassy state.
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Face masks are used to trap particles (or fluid drops) in a porous material (filter) in order to avoid or reduce the transfer of particles between the human lungs (or mouth and nose) and the external environment. The air exchange between the lungs and the environment is assumed to occur through the face mask filter. However, if the resistance to air flow through the filter is high some air (and accompanied particles) will leak through the filter-skin interface. In this paper I will present a model study of the side-leakage problem.
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Máscaras , Tamanho da PartículaRESUMO
When a crack propagates in a viscoelastic solid, energy dissipation can occur very far from the crack tip where the stress field may be very different from the [Formula: see text] singular form expected close to the crack tip. Most theories of crack propagation focus on the near crack tip region. Remarkable, here I show that a simple theory which does not account for the nature of the stress field in the near crack tip region results in a crack propagation energy in semiquantitative agreement with a theory based on the stress field in the near crack tip region. I consider both opening and closing crack propagation and show that for closing crack propagation in viscoelastic solids, some energy dissipation processes must occur in the crack tip process zone. The theory is illustrated by new experimental results for the adhesive interaction between a silica glass ball and a silicone rubber surface.
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I discuss fluid flow at the interface between solids with anisotropic roughness. I show that the Bruggeman effective medium theory and the critical junction theory give nearly the same results for the fluid flow conductivity. This shows that, in most cases, the surface roughness observed at high magnification is irrelevant for fluid flow problems such as the leakage of static seals, and fluid squeeze-out. The effective medium theory predicts that the fluid flow conductivity vanishes at the relative contact area A/A0 = 0.5 independent of the anisotropy. However, the effective medium theory does not solve the elastic contact mechanics problem but is based on a purely geometric argument. Thus, for anisotropic roughness the contact area may percolate at different values of A/A0 depending on the direction. We discuss how this may be taken into account in the effective medium and critical junction theories.
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We derive approximate mean field equations for the fluid flow between elastic solids with randomly rough surfaces including interfacial fluid slip and shear thinning. We present numerical results for the fluid flow and friction factors for realistic systems, in particular, we consider the case of an elastic cylinder with random surface roughness in relative sliding contact with a flat rigid (low-energy) counter-surface. We present experimental data for the sliding friction between rubber stoppers and glass barrels lubricated with baked-on silicone oil. We find that the frictional shear stress acting in the rubber asperity contact regions is nearly velocity independent for velocities in the 10-1000µm/s range, and very small [Formula: see text] MPa, while for bare glass in silicone oil [Formula: see text] is much larger and velocity dependent.
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We have developed a theory of air leakage at interfaces between two elastic solids with application to suction cups in contact with randomly rough surfaces. We present an equation for the airflow in narrow constrictions which interpolates between the diffusive and ballistic (Knudsen) air-flow limits. To test the theory, we performed experiments using two different suction cups, made from soft polyvinylchloride (PVC), in contact with sandblasted polymethylmethacrylate (PMMA) plates. We found that the measured time to detach (lifetime) of the suction cups was in good agreement with theory, except for surfaces with a root-mean-square (rms) roughness below ≈1 µm, where diffusion of plasticizer from the PVC to the PMMA surface caused blockage of critical constrictions. The suction cup volume, stiffness, and elastic modulus have a huge influence on the air leakage and hence the failure time of the cups. Based on our research we propose an improved biomimetic design of suction cups that could show improved failure times with varying degrees of roughness under dry and wet environments.
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There is growing interest in touchscreens displaying tactile feedback due to their tremendous potential in consumer electronics. In these systems, the friction between the user's fingerpad and the surface of the touchscreen is modulated to display tactile effects. One of the promising techniques used in this regard is electrostatic actuation. If, for example, an alternating voltage is applied to the conductive layer of a surface capacitive touchscreen, an attractive electrostatic force is generated between the finger and the surface, which results in an increase in frictional forces acting on the finger moving on the surface. By altering the amplitude, frequency, and waveform of this signal, a rich set of tactile effects can be generated on the touchscreen. Despite the ease of implementation and its powerful effect on our tactile sensation, the contact mechanics leading to an increase in friction due to electroadhesion has not been fully understood yet. In this paper, we present experimental results for how the friction between a finger and a touchscreen depends on the electrostatic attraction and the applied normal pressure. The dependency of the finger-touchscreen interaction on the applied voltage and on several other parameters is also investigated using a mean field theory based on multiscale contact mechanics. We present detailed theoretical analysis of how the area of real contact and the friction force depend on contact parameters, and show that it is possible to further augment the friction force, and hence the tactile feedback displayed to the user by carefully choosing those parameters.
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Equipamentos e Provisões Elétricas , Tato , Adesividade , Biomimética , Humanos , Modelos Teóricos , Pele , Propriedades de SuperfícieRESUMO
We study the temperature and velocity dependency of rolling friction. Steel and PMMA cylinders are rolled on sheets of nitrile butadiene rubber (NBR), with and without filler, and fluoroelastomer (FKM) with filler. Measurements of the rolling friction are performed for temperatures between -40 °C and 20 °C, and for velocities between 5 µm s-1 and 0.5 cm s-1. For the unfilled NBR, a smooth rolling friction master curve is obtained using the bulk viscoelastic frequency-temperature shift factor aT. For the filled rubber compounds, a small deviation from the bulk viscoelastic shift factor is observed at low temperatures. The experimental data are analyzed using an analytical theory of rolling friction. For the filled compounds, good agreement with theory is obtained when strain softening is included, which increases the rolling friction by a factor â¼2 for the filled FKM and â¼3 for the filled NBR compounds. For the unfilled NBR, the maximum of the rolling friction occurs at higher sliding speeds than predicted by the theory. We discuss the role of the adhesive (crack-opening) contribution to the rolling friction, and the role of frozen-in elastic deformations as the rubber is cooled down below the rubber glass transition temperature.
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Surface roughness has a huge influence on most tribology properties. Sandblasting is a standard way to produce surface roughness in a controlled and reproducible way. Sometimes the sandblasted surfaces are annealed to reduce the roughness and reduce the sharpness of the roughness. We study the nature of the surface roughness of sandblasted silica glass surfaces and how it is modified by annealing at different temperatures. The surface roughness decreases with increasing annealing temperature due to viscous flow of the glass driven by the surface tension. However, the skewness and kurtosis remain nearly unchanged. Optical pictures of the annealed glass surfaces exhibit cell-like structures (cell diameter ≈20-40 µm), which we interpret as micro-cracks. The concentration of micro-cracks increases with increasing annealing temperature. The micro-cracks result in a (advancing) water contact angle which decreases with increasing annealing temperature, which is opposite to what is expected from the theory if no micro-cracks would occur.
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Adhesion between a glass ball and a polydimethylsiloxane (PDMS) sample is dependent on the PDMS cross-link density, and the transformation of the material from the uncrosslinked liquid state to the fully crosslinked solid state is investigated in this study. The physical picture reflected a gradual transition from capillary forces driven contact mechanics to the classical Johnson-Kendall-Roberts (JKR)-type contact mechanics. PDMS was produced by mixing the base fluid and a cross-linker at a ratio of 10 : 1 and allowed to slowly cross-link at room temperature with simultaneous measurement of the ball-PDMS interaction force. The PDMS sample was in the liquid state during the first ≈16 hours, and in this case the ball-PDMS interaction was purely adhesive, i.e., no repulsive interaction was observed. Later at the PDMS gel-point the cross-linked PDMS clusters percolate, converting the fluid into a soft (fluid-filled) poroelastic solid. In the transition period, PDMS appears similar to pressure-sensitive adhesives. There we observe so-called "stringing" and permanent deformation of the material impacted by the ball. At room temperature, it takes more than â¼100 hours for PDMS to fully cross-link that can be confirmed by the comparison with the earlier-studied reference PDMS produced at elevated temperatures.
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We study the contact mechanics between 3 different tire tread compounds and a smooth glass surface in water. We study both adhesion and sliding friction at low-sliding speeds. For 2 of the compounds the rubber-glass contact in water is hydrophobic and we observe adhesion, and slip-stick sliding friction dynamics. For one compound the contact is hydrophilic, resulting in vanishing adhesion, and steady-state (or smooth) sliding dynamics. We also show the importance of dynamical scrape, both on the macroscopic level and at the asperity level, which reduces the water film thickness between the solids during slip. The experiments show that the fluid is removed much faster from the rubber-glass asperity contact regions for a hydrophobic contact than for a hydrophilic contact. We also study friction on sandblasted glass in water. In this case all the compounds behave similarly and we conclude that no dewetting occur in the asperity contact regions. We propose that this is due to the increased surface roughness which reduces the rubber-glass binding energy.
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I present a theory for ice friction for ice sliding on a hard randomly rough surface which includes ice melting-freezing (regelation), viscoelastic energy dissipation, and cavitation. The theory is an extension of earlier work by Weertman, Lliboutry, Nye, and Kamb. I present numerical results for surfaces with realistic surface roughness power spectra. I consider both airfilled and (pressurized) waterfilled cavities. The calculated frictional shear stresses are consistent with experimental observations for temperate glaciers.
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I develop a general mean-field theory for the influence of electrostatic attraction between two solids on the contact mechanics. I assume elastic solids with random surface roughness. I consider two cases, namely, with and without an electrically insulating layer between the conducting solids. The former case is important for, e.g., the finger-touch screen interaction. I study how the electrostatic attraction influences the adhesion and friction. For the case of an insulating layer, I find that when the applied nominal contact pressure is relatively small, as the applied voltage increases, there is a sharp increase in the contact area, and hence in the friction, at a critical voltage.
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There are two contributions to the friction force when a rubber block is sliding on a hard and rough substrate surface, namely, a contribution Fad = τf A from the area of real contact A and a viscoelastic contribution Fvisc from the pulsating forces exerted by the substrate asperities on the rubber block. Here we present experimental results obtained at different sliding speeds and temperatures, and we show that the temperature dependency of the shear stress τf, for temperatures above the rubber glass transition temperature Tg, is weaker than that of the bulk viscoelastic modulus. The physical origin of τf for T > Tg is discussed, and we propose that its temperature dependency is determined by the rubber molecule segment mobility at the sliding interface, which is higher than in the bulk because of increased free-volume effect due to the short-wavelength surface roughness. This is consistent with the often observed reduction in the glass transition temperature in nanometer-thick surface layers of glassy polymers. For temperatures T < Tg, the shear stress τf is nearly velocity independent and of similar magnitude as observed for glassy polymers such as PMMA or polyethylene. In this case, the rubber undergoes plastic deformations in the asperity contact regions and the contact area is determined by the rubber penetration hardness. For this case, we propose that the frictional shear stress is due to slip at the interface between the rubber and a transfer film adsorbed on the concrete surface.
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We study the adhesion between differently processed glass and filled bromobutyl rubber in dry conditions, in water, and in silicone oil. The boundary line between contact and non-contact in adhesion experiments can be considered as a mode I crack, and we show that viscoelastic energy dissipation, close to the opening (or closing) crack tip and surface roughness, strongly affects the work of adhesion. We observe strong adhesion hysteresis and, in contrast to the Johnson-Kendall-Roberts theory prediction for elastic solids, this results in a pull-off force (and work of adhesion) which depends on the loading force and contact time. In particular, for the system immersed in water and silicone oil, we register very weak adhesive bonding. For glass ball with baked-on silicone oil, the pull-off force is nearly independent of the contact time, but this is not observed for the unprocessed glass surface.
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Adhesion between glass and bromobutyl and polydimethylsiloxane elastomers is investigated. We show that viscoelastic energy dissipation close to the opening (or closing) crack tip, and surface roughness, strongly affect the work of adhesion. We observe strong adhesion hysteresis and we show, in contrast to the Johnson-Kendall-Roberts theory prediction for elastic solids, that this results in a pull-off force, and effective work of adhesion to be dependent on the maximum loading force.
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We study a simple contact mechanics model of the vertebrate cartilage, which includes (bulk) osmotic effects. The surface roughness power spectrum of a pig cartilage is obtained from the measured surface topography. Using the Reynolds equations with fluid flow factors, calculated using the Persson contact mechanics theory and the Bruggeman effective medium theory, we show how the area of contact and the average interfacial separation change with time. We found that in most cases the contact area percolates, resulting in islands of confined fluid which carry most of the external load. Most importantly, we find that the pressure in the area of real contact is nearly independent of the external load, and well below 1 MPa. This allows the surfaces in the area of "real contact", to be separated (at nanometer range separation distance) by osmotic repulsion, resulting in a very small (breakloose) friction force observed even after a long time of stationary contact.
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Cartilagem , Fenômenos Mecânicos , Modelos Biológicos , Animais , Fenômenos Biomecânicos , Elasticidade , Osmose , Propriedades de Superfície , SuínosRESUMO
We study the adhesion, friction and leak rate of seals for four different elastomers: Acrylonitrile Butadiene Rubber (NBR), Ethylene Propylene Diene (EPDM), Polyepichlorohydrin (GECO) and Polydimethylsiloxane (PDMS). Adhesion between smooth clean glass balls and all the elastomers is studied both in the dry state and in water. In water, adhesion is observed for the NBR and PDMS elastomers, but not for the EPDM and GECO elastomers, which we attribute to the differences in surface energy and dewetting. The leakage of water is studied with rubber square-ring seals squeezed against sandblasted glass surfaces. Here we observe a strongly non-linear dependence of the leak rate on the water pressure ΔP for the elastomers exhibiting adhesion in water, while the leak rate depends nearly linearly on ΔP for the other elastomers. We attribute the non-linearity to some adhesion-related phenomena, such as dewetting or the (time-dependent) formation of gas bubbles, which blocks fluid flow channels. Finally, rubber friction is studied at low sliding speeds using smooth glass and sandblasted glass as substrates, both in the dry state and in water. The measured friction coefficients are compared to theory, and the origin of the frictional shear stress acting in the area of real contact is discussed. The NBR rubber, which exhibits the strongest adhesion both in the dry state and in water, also shows the highest friction both in the dry state and in water.