Marie-Julie Dalbe

Aggregation of frictional particles due to capillary attraction

Capillary attraction between identical millimeter-sized spheres floating at a liquid-air interface and the resulting aggregation are investigated at low Reynolds number. We show that the measured capillary forces between two spheres as a function of distance can be described by expressions obtained using the Nicolson approximation at low Bond numbers for far greater particle sizes than previously assumed. We find that viscous hydrodynamic interactions between the spheres needs to be included to describe the dynamics close to contact. We then consider the aggregates formed when a third sphere is added after the initial two spheres are already in contact. In this case, we find that linear superposition of capillary forces describes the observed approach qualitatively but not quantitatively. Further, we observe an angular dependence of the structure due to a rapid decrease of capillary force with distance of separation, which has a tendency to align the particles before contact. When the three particles come into contact, they may preserve their shape or rearrange to form an equilateral triangle cluster-the lowest-energy state-depending on the competition between attraction between particles and friction. Using these observations, we demonstrate that a linear particle chain can be built from frictional particles with capillary attraction.

Rate-dependent elastic hysteresis during the peeling of pressure sensitive adhesives

The modelling of the adherence energy during peeling of Pressure Sensitive Adhesives (PSA) has received much attention since the 1950s, uncovering several factors that aim at explaining their high adherence on most substrates, such as the softness and strong viscoelastic behaviour of the adhesive, the low thickness of the adhesive layer and its confinement by a rigid backing. The more recent investigation of adhesives by probe-tack methods also revealed the importance of cavitation and stringing mechanisms during debonding, underlining the influence of large deformations and of the related non-linear response of the material, which also intervenes during peeling. Although a global modelling of the complex coupling of all these ingredients remains a formidable issue, we report here some key experiments and modelling arguments that should constitute an important step forward. We first measure a non-trivial dependence of the adherence energy on the loading geometry, namely through the influence of the peeling angle, which is found to be separable from the peeling velocity dependence. This is the first time to our knowledge that such adherence energy dependence on the peeling angle is systematically investigated and unambiguously demonstrated. Secondly, we reveal an independent strong influence of the large strain rheology of the adhesives on the adherence energy. We complete both measurements with a microscopic investigation of the debonding region. We discuss existing modellings in light of these measurements and of recent soft material mechanics arguments, to show that the adherence energy during peeling of PSA should not be associated to the propagation of an interfacial stress singularity. The relevant deformation mechanisms are actually located over the whole adhesive thickness, and the adherence energy during peeling of PSA should rather be associated to the energy loss by viscous friction and by rate-dependent elastic hysteresis.

Intermittent stick-slip dynamics during the peeling of an adhesive tape from a roller.

We study experimentally the fracture dynamics during the peeling at a constant velocity of a roller adhesive tape mounted on a freely rotating pulley. Thanks to a high speed camera, we measure, in an intermediate range of peeling velocities, high frequency oscillations between phases of slow and rapid propagation of the peeling fracture. This so-called stick-slip regime is well known as the consequence of a decreasing fracture energy of the adhesive in a certain range of peeling velocity coupled to the elasticity of the peeled tape. Simultaneously with stick slip, we observe low frequency oscillations of the adhesive roller angular velocity which are the consequence of a pendular instability of the roller submitted to the peeling force. The stick-slip dynamics is shown to become intermittent due to these slow pendular oscillations which produce a quasistatic oscillation of the peeling angle while keeping constant the peeling fracture velocity (averaged over each stick-slip cycle). The observed correlation between the mean peeling angle and the stick-slip amplitude questions the validity of the usually admitted independence with the peeling angle of the fracture energy of adhesives.

Strong dynamical effects during stick-slip adhesive peeling

We consider the classical problem of the stick-slip dynamics observed when peeling a roller adhesive tape at a constant velocity. From fast imaging recordings, we extract the dependence of the stick and slip phase durations on the imposed peeling velocity and peeled ribbon length. Predictions of Maugis and Barquins [in Adhesion 12, edited by K. W. Allen, Elsevier ASP, London, 1988, pp. 205-222] based on a quasistatic assumption succeed to describe quantitatively our measurements of the stick phase duration. Such a model however fails to predict the full stick-slip cycle duration, revealing strong dynamical effects during the slip phase.

Multiscale Stick-Slip Dynamics of Adhesive Tape Peeling

Using a high-speed camera, we follow the propagation of the detachment front during the peeling of an adhesive tape from a flat surface. In a given range of peeling velocity, this front displays a multiscale unstable dynamics, entangling two well-separated spatiotemporal scales, which correspond to microscopic and macroscopic dynamical stick-slip instabilities. While the periodic release of the stretch energy of the whole peeled ribbon drives the classical macro-stick-slip, we show that the micro-stick-slip, due to the regular propagation of transverse dynamic fractures discovered by Thoroddsen et al. [Phys. Rev. E 82, 046107 (2010)], is related to a high-frequency periodic release of the elastic bending energy of the adhesive ribbon concentrated in the vicinity of the peeling front.

Path (un)predictability of two interacting cracks in polycarbonate sheets using Digital Image Correlation

Crack propagation is tracked here with Digital Image Correlation analysis in the test case of two cracks propagating in opposite directions in polycarbonate, a material with high ductility and a large Fracture Process Zone (FPZ). Depending on the initial distances between the two crack tips, one may observe different complex crack paths with in particular a regime where the two cracks repel each other prior to being attracted. We show by strain field analysis how this can be understood according to the principle of local symmetry: the propagation is to the direction where the local shear - mode KII in fracture mechanics language - is zero. Thus the interactions exhibited by the cracks arise from symmetry, from the initial geometry, and from the material properties which induce the FPZ. This complexity makes any long-range prediction of the path(s) impossible.