Amorphous glassy materials of diverse nature-concentrated emulsions, granular materials, pastes, molecular glasses-display complex flow properties, intermediate between solid and liquid, which are at the root of their use in many applications. A general feature of such systems, well documented yet not really understood, is the strongly nonlinear nature of the flow rule relating stresses and strain rates. Here we use a microfluidic velocimetry technique to characterize the flow of thin layers of concentrated emulsions, confined in gaps of different thicknesses by surfaces of different roughnesses. We find evidence for finite-size effects in the flow behaviour and the absence of an intrinsic local flow rule. In contrast to the classical nonlinearities of the rheological behaviour of amorphous materials, we show that a rather simple non-local flow rule can account for all the velocity profiles. This non-locality of the dynamics is quantified by a length, characteristic of cooperativity within the flow at these scales, that is unobservable in the liquid state (lower emulsion concentrations) and that increases with concentration in the jammed state. Beyond its practical importance for applications involving thin layers (for example, coatings), these non-locality and cooperativity effects have parallels in the behaviour of other glassy, jammed and granular systems, suggesting a possible fundamental universality.

A kinetic model for the elastoplastic dynamics of a jammed material is proposed, which takes the form of a nonlocal--Boltzmann-like--kinetic equation for the stress distribution function. Coarse graining this equation yields a nonlocal constitutive law for the flow, exhibiting as a key dynamic quantity the local rate of plastic events. This quantity, interpreted as a local fluidity, is spatially correlated with a correlation length diverging in the quasistatic limit, i.e., close to yielding. In line with recent experimental and numerical observations, we predict finite size effects in the flow behavior, as well as the absence of an intrinsic local flow curve.

International audienceIn this paper, we investigate the rheological behavior of jammed emulsions in microchannels on the basis of microvelocimetry techniques. We demonstrate that velocity profiles in this confined geometry cannot be accounted for by the bulk - Herschel-Bulkley - rheological flow curve measured independently in a rheometer. A strong dependence of the flow behavior on the confinement, pressure drop and surface roughness is evidenced, which cannot be described by classical rheological descriptions. We show that these behaviors can be rationalized on the basis of a non local rheological model, introducing the notion of local fluidity as a key rheological quantity. The model reproduces the experimental velocity profiles for any confinements and any surface nature. The non-locality is quantified by a length, z, characterizing the flow cooperativity of jammed emulsions, and typically of the order of several emulsion droplet diameters. We study the influence of volume fraction, droplet diameter, and emulsions polydispersity on this length