Contact of a spherical probe with a stretched rubber substrate

We report on a theoretical and experimental investigation of the normal contact of stretched neo-Hookean substrates with rigid spherical probes. Starting from a published formulation of surface Green's function for incremental displacements on a pre-stretched, neo-Hookean, substrate (L.H. Lee \textit{J. Mech. Phys. Sol.} \textbf{56} (2008) 2957-2971), a model is derived for both adhesive and non-adhesive contacts. The shape of the elliptical contact area together with the contact load and the contact stiffness are predicted as a function of the in-plane stretch ratios $\lambda_x$ and $\lambda_y$ of the substrate. The validity of this model is assessed by contact experiments carried out using an uniaxally stretched silicone rubber. for stretch ratio below about 1.25, a good agreement is observed between theory and experiments. Above this threshold, some deviations from the theoretical prediction are induced as a result of the departure of the mechanical response of the silicone rubber from the neo-Hokeean description embedded in the model

Effects of stretching on the frictional stress of rubber

In this paper, we report on new experimental results on the effects of in-plane surface stretching on the friction of Poly(DiMethylSiloxane) (PDMS) rubber with smooth rigid probes. Friction-induced displacement fields are measured at the surface of the PDMS substrate under steady-state sliding. Then, the corresponding contact pressure and frictional stress distributions are determined from an inversion procedure. Using this approach, we show that the local frictional stress $\tau$ is proportional to the local stretch ratio $\lambda$ at the rubber surface. Additional data using a triangular flat punch indicate that $\tau(\lambda)$ relationship is independent on the contact geometry. From friction experiments using pre-stretched PDMS substrate, it is also found that the stretch-dependence of the frictional stress is isotropic, i.e. it does not depend on the angle between stretching and sliding directions. Potential physical explanations for this phenomenon are provided within the framework of Schallamach's friction model. Although the present experiments are dealing with smooth contact interfaces, the reported $\tau(\lambda)$ dependence is also relevant to the friction of statistically rough contact interfaces, while not accounted for in related contact mechanics models

Poroelastic indentation of mechanically confined hydrogel layers

We report on the poroelastic indentation response of hydrogel thin films geometrically confined within contacts with rigid spherical probes of radii in the millimeter range. Poly(PEGMA) (poly(ethylene glycol)) methyl ether methacrylate), poly(DMA) (dimethylacrylamide) and poly(NIPAM) (\textit{N}-isopropylacrylamide) gel films with thickness less than 15 $\mu$m were grafted onto glass substrates using a thiol-ene click chemistry route. Changes in the indentation depth under constant applied load were monitored over time as a function of the film thickness and the radius of curvature of the probe using an interferometric method. In addition, shear properties of the indented films were measured using a lateral contact method. In the case of poly(PEGMA) films, we show that poroelastic indentation behavior is adequately described within the framework of an approximate contact model derived within the limits of confined contact geometries. This model provides simple scaling laws for the characteristic poroelastic time and the equilibrium indentation depth. Conversely, deviations from this model are evidenced for poly(DMA) and poly(NIPAM) films. From lateral contact experiments, these deviations are found to result from strong changes in the shear properties as a result of glass transition (poly(DMA)) or phase separation (poly(NIPAM)) phenomena induced by the drainage of the confined films squeezed between the rigid substrates

Role of uncrosslinked chains in droplets dynamics on silicone elastomers

We report an unexpected behavior in wetting dynamics on soft silicone substrates: the dynamics of aqueous droplets deposited on vertical plates of such elastomers exhibits two successive speed regimes. This macroscopic observation is found to be closely related to microscopic phenomena occurring at the scale of the polymer network: we show that uncrosslinked chains found in most widely used commercial silicone elastomers are responsible for this surprising behavior. A direct visualization of the uncrosslinked oligomers collected by water droplets is performed, evidencing that a capillarity-induced phase separation occurs: uncrosslinked oligomers are extracted from the silicone elastomer network by the water-glycerol mixture droplet. The sharp speed change is shown to coincide with an abrupt transition in surface tension of the droplets, when a critical surface concentration in uncrosslinked oligomer chains is reached. We infer that a droplet shifts to a second regime with a faster speed when it is completely covered with a homogeneous oil film

Elastic contact to nearly incompressible coatings -- Stiffness enhancement and elastic pile-up

We have recently proposed an efficient computation method for the frictionless linear elastic axisymmetric contact of coated bodies [A. Perriot and E. Barthel, J. Mat. Res. 19 (2004) 600]. Here we give a brief description of the approach. We also discuss implications of the results for the instrumented indentation data analysis of coated materials. Emphasis is laid on incompressible or nearly incompressible materials (Poisson ratio $\nu>0.4$): we show that the contact stiffness rises much more steeply with contact radius than for more compressible materials and significant elastic pile-up is evidenced. In addition the dependence of the penetration upon contact radius increasingly deviates from the homogeneous reference case when the Poisson ratio increases. As a result, this algorithm may be helpful in instrumented indentation data analysis on soft and nearly incompressible layers

Adhesive contact of model randomly rough rubber surfaces

We study experimentally and theoretically the equilibrium adhesive contact between a smooth glass lens and a rough rubber surface textured with spherical microasperities with controlled height and spatial distributions. Measurements of the real contact area $A$ versus load $P$ are performed under compression by imaging the light transmitted at the microcontacts. $A(P)$ is found to be non-linear and to strongly depend on the standard deviation of the asperity height distribution. Experimental results are discussed in the light of a discrete version of Fuller and Tabor's (FT) original model (\textit{Proceedings of the Royal Society A} \textbf{345} (1975) 327), which allows to take into account the elastic coupling arising from both microasperities interactions and curvature of the glass lens. Our experimental data on microcontact size distributions are well captured by our discrete extended model. We show that the elastic coupling arising from the lens curvature has a significant contribution to the $A(P)$ relationship. Our discrete model also clearly shows that the adhesion-induced effect on $A$ remains significant even for vanishingly small pull-off forces. Last, at the local asperity length scale, our measurements show that the pressure dependence of the microcontacts density can be simply described by the original FT model

Rate-dependent adhesion of viscoelastic contacts. Part II: Numerical model and hysteresis dissipation

In this paper, we propose a numerical model to describe the adhesive normal contact between a glass spherical indenter and a viscoelastic model rough substrate of PDMS material. The model accounts for dissipative process under the assumption that viscoelastic losses are localized at the (micro)-contact lines. Numerical predictions are then compared with experimental measurements, which show a strong adhesion hysteresis mostly due to viscous dissipation occurring during pull-off. This hysteresis is satisfactorily described by the contact model which allows to distinguish the energy loss due to material dissipation from the adhesion hysteresis due to elastic instability. Our analysis shows that the pull-off force required to detach the surfaces is strongly influenced by the detachment rate and the root mean square (rms) roughness amplitude, but it is almost unaffected by the maximum load from which unloading starts. Moreover, the increase in the length of the boundary line separating contact and non-contact regions, which is observed when moving from smooth to rough contacts, negligibly affects the viscous dissipation. Such increase is much less significant than the reduction in contact area, which therefore is the main parameter governing the strong decrease in the effective surface energy for the specific rough geometry considered in the present work

Weak non-linearities of amorphous polymer under creep

The creep behavior of an amorphous poly(etherimide) (PEI) polymer is investigated in the vicinity of its glass transition in a weakly non linear regime where the acceleration of the creep response is driven by local configurational rearrangements. From the time shifts of the creep compliance curves under increasing applied stresses in the range 1-15~\si{\mega\pascal}, we determine a macroscopic acceleration factor. At the start of creep, the stress is homogeneous and the macroscopic acceleration can be assimilated to that of the local rearrangements which is shown to vary as $f=e^{-(\sigma/Y)^n}$ with $n=2 \pm 0.2$, where $\sigma$ is the local stress and $Y$ is a decreasing function of compliance. This experimental result is in agreement with the recent theory of Long \textit{et al.} (\textit{Phys. Rev. Mat.} (2018) \textbf{2}, 105601 ) which predicts $n=2$. From a mean field approximation, we interpret the variation of $Y$ with compliance as the result of the development of stress heterogneities during creep

Transient sliding of thin hydrogel films: the role of poroelasticity

We report on the transient frictional response of contacts between a rigid spherical glass probe and a micrometer-thick poly(dimethylacrylamide) hydrogel film grafted onto a glass substrate when a lateral relative motion is applied to the contact initially at rest. From dedicated experiments with \textit{in situ} contact visualization, both the friction force and the contact size are observed to vary well beyond the occurrence of a full sliding condition at the contact interface. Depending on the imposed velocity and on the static contact time before the motion is initiated, either an overshoot or an undershoot in the friction force is observed. These observations are rationalized by considering that the transient is predominantly driven by the flow of water within the stressed hydrogel networks. From the development of a poroelastic contact model using a thin film approximation, we provide a theoretical description of the main features of the transient. We especially justify the experimental observation that the relaxation of friction force $F_t(t)$ toward steady state is uniquely dictated by the time-dependence of the contact radius $a(t)$, independently on the sliding velocity and on the applied normal load