SearcharxivSearch

arXiv · 1503.03720

A contact model for sticking of adhesive meso-particles

Abstract

The interaction between visco-elasto-plastic and adhesive particles is the subject of this study, where "meso-particles" are introduced, i.e., simplified particles, whose contact mechanics is not taken into account in all details. A few examples of meso-particles include agglomerates or groups of primary particles, or inhomogeneous particles with micro-structures of the scale of the contact deformation, such as core-shell materials. A simple, flexible contact model for meso-particles is proposed, which allows to model the bulk behavior of assemblies of many particles in both rapid and slow, quasi-static flow situations. An attempt is made to categorize existing contact models for the normal force, discuss all the essential mechanical ingredients that must enter the model (qualitatively) and finally solve it analytically. The model combines a short-ranged, non-contact part (resembling either dry or wet materials) with an elaborate, visco-elasto-plastic and adhesive contact law. Using energy conservation arguments, an analytical expression for the coefficient of restitution is derived in terms of the impact velocity (for pair interactions or, equivalently, without loss of generality, for quasi-static situations in terms of the maximum overlap or confining stress). Adhesive particles (or meso-particles) stick to each other at very low impact velocity, while they rebound less dissipatively with increasing velocity, in agreement with previous studies. For even higher impact velocities an interesting second sticking and rebound regime is reported. The low velocity sticking is due to non-contact adhesive forces, the first rebound regime is due to stronger elastic and kinetic energies with little dissipation, while the high velocity sticking is generated by the non-linearly increasing, history dependent plastic dissipation and adhesive contact force.

Explore related subjects

Keep this discovery

BibTeXRIS

Abhinendra Singh, Vanessa Magnanimo, Stefan Luding. 2015-03-12. A contact model for sticking of adhesive meso-particles. https://arxiv.org/abs/1503.03720

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Slow Dynamics and the Geometry of Jammed Packings

Saddle points in the energy landscape of granular packings dominate the discrete steepest descent dynamics and ultimately determine the path that an out of mechanical equilibrium packing will follow and the resulting stable minimum that it will find. The saddle points that ultimately determine the resulting minima tend to be low-index saddle points. For models with an analytic energy landscape, such as the $p$-spin model, the steepest descent minimization path is affected by higher-index saddle points, which pull the system towards saddle points of decreasing index before arriving at the minima. Here, we examine the steepest descent minimization path of granular packings and compare them to the $p$-spin model. We show that the granular packing steepest descent minimization paths act like their smooth energy landscape counterparts and get attracted by saddle points. The index versus time curves for all models follow a shifted, stretched exponential. We further show that the shape parameter for the granular packings is unchanged when the energy landscape is modified to become analytic (Gaussian potential in a harmonic well) or non-local (Mari-Krzakala-Kurchan). The $p$-spin, on the other hand, has a significantly larger shape parameter. The reason is not due to the dimensionality, packing fraction, nonanalyticity, or the locality of the Hamiltonian of the models. The exact reason for the discrepancy in the shape parameter is \st{still} an unsolved mystery.

cond-mat.soft

A Phase-Field Study of Desiccation Crack Pattern Maturation under Drying-Wetting Cycles

The characteristic intersection angle of the desiccation crack relaxes from near \ang{90} toward \ang{120} under repeated drying--wetting cycles. However, the theoretical understanding of this relaxation is insufficient, especially the modeling of the drying--wetting cycles. Here we introduce a phase-field model of desiccation fracture, extending the model proposed in previous studies by adding crack healing and a scar effect left by past cracks. By repeating drying--wetting cycles in a finite element simulation, we find that the angle distribution develops a growing peak near \ang{120} as the cycle number increases, consistent with experiments. The standard deviation of the intersection angle from \ang{120} relaxes exponentially with a characteristic time of about 2.85 cycles. These results are consistent with experiments, except that the characteristic time is slightly smaller than the experimental value. Crack energy dominates the total energy and also relaxes exponentially with nearly the same characteristic cycle as the angle relaxation. This decay is driven mainly by a shortening of the effective crack length rather than a change in effective fracture toughness.

cond-mat.soft

Kinetics of ferritin crystal formation and melting in acoustically levitated droplets

Understanding protein crystallization pathways is essential for controlling crystallization in structural biology, materials science, and pharmaceutical applications. Classical nucleation theory does not fully capture crystallization processes for several proteins, including ferritin. Here, we combine acoustic levitation with small- and wide-angle X-ray scattering (SAXS and WAXS) to monitor ferritin crystallization in evaporating aqueous polyethylene glycol (PEG) solutions. Acoustic levitation rapidly drives the droplets through a broad range of protein and polymer concentrations, enabling time-resolved measurements of crystallization during evaporation. The scattering data show that ferritin crystals form during evaporation and subsequently lose their crystalline order upon further dehydration. Varying the PEG molecular weight switches between distinct crystallization pathways: one dominated by attractive protein-protein interactions and another dominated by repulsive interactions and excluded-volume effects. Furthermore, we find that lower molecular weight PEG (1000 g/mol) suppresses the dehydration-induced loss of crystalline order observed for higher molecular weight PEG (6000 g/mol), providing a simple strategy for improving protein crystal stability.

cond-mat.soft