In soft amorphous materials, shear cessation after large shear deformation leads to structures having residual shear stress. The origin of these states and the distribution of the local shear stresses within the material is not well understood, despi
te its importance for the change in material properties and consequent applications. In this work, we use molecular dynamics simulations of a model dense non-Brownian soft amorphous material to probe the non-trivial relaxation process towards a residual stress state. We find that, similar to thermal glasses, an increase in shear rate prior to the shear cessation leads to lower residual stress states. We rationalise our findings using a mesoscopic elasto-plastic description that explicitly includes a long range elastic response to local shear transformations. We find that after flow cessation the initial stress relaxation indeed depends on the pre-sheared stress state, but the final residual stress is majorly determined by newly activated plastic events occurring during the relaxation process. Our simplified coarse grained description not only allows to capture the phenomenology of residual stress states but also to rationalise the altered material properties that are probed using small and large deformation protocols applied to the relaxed material.
We present simulations for the steady-shear rheology of a model adhesive dispersion. We vary the range of the attractive forces $u$ as well as the strength of the dissipation $b$. For large dissipative forces, the rheology is governed by the Weisenbe
rg number $ text{Wi}sim bdotgamma/u$ and displays Herschel-Bulkley form $sigma = sigma_y+ctext{Wi}^ u$ with exponent $ u=0.45$. Decreasing the strength of dissipation, the scaling with $text{Wi}$ breaks down and inertial effects show up. The stress decreases via the Johnson-Samwer law $Deltasigmasim T_s^{2/3}$, where temperature $T_s$ is exclusively due to shear-induced vibrations. During flow particles prefer to rotate around each other such that the dominant velocities are directed tangentially to the particle surfaces. This tangential channel of energy dissipation and its suppression leads to a discontinuity in the flow curve, and an associated discontinuous shear thinning transition. We set up an analogy with frictional systems, where the phenomenon of discontinuous shear thickening occurs. In both cases tangential forces, frictional or viscous, mediate a transition from one branch of the flowcurve with low tangential dissipation to one with large tangential dissipation.
We study the rheology of a soft particulate system where the inter-particle interactions are weakly attractive. Using extensive molecular dynamics simulations, we scan across a wide range of packing fractions ($phi$), attraction strengths ($u$) and i
mposed shear-rates ($dot{gamma}$). In striking contrast to repulsive systems, we find that at small shear-rates generically a fragile isostatic solid is formed even if we go to $phi ll phi_J$. Further, with increasing shear-rates, even at these low $phi$, non-monotonic flow curves occur which lead to the formation of persistent shear-bands in large enough systems. By tuning the damping parameter, we also show that inertia plays an important role in this process. Furthermore, we observe enhanced particle dynamics in the attraction-dominated regime as well as a pronounced anisotropy of velocity and diffusion constant, which we take as precursors to the formation of shear bands. At low enough $phi$, we also observe structural changes via the interplay of low shear-rates and attraction with the formation of micro-clusters and voids. Finally, we characterize the properties of the emergent shear bands and thereby, we find surprisingly small mobility of these bands, leading to prohibitely long time-scales and extensive history effects in ramping experiments.
