Search arXivSearch

arXiv · 2602.20443

Dynamic fragmentation of residually stressed solids: From microscopic instabilities to universal scaling

Abstract

The dynamic fragmentation of residually stressed solids involves a complex interplay between stored elastic energy, stress wave propagation, and crack instabilities. In this work, we investigate the fracture mechanics of chemically toughened glass through high-velocity projectile impact experiments and a novel micromechanical network model. We rigorously incorporate residual stress into the discrete lattice framework via a prescribed inelastic strain (eigenstrain) distribution, formulated as equivalent body and surface forces to ensure mesh-independent fracture paths. Our experiments and simulations demonstrate that while the fracture topology shifts from coarse to fine with increasing impact energy, the cumulative fragment size distribution consistently follows an exponential decay. Crucially, we reveal a universal scaling law: fragment size distributions from diverse loading conditions and stress profiles collapse onto a single master curve when normalized by the mean fragment area. Furthermore, the model elucidates the determinants of fragmentation, showing that the resulting fragment size is governed not only by the magnitude of residual stress but also by the steepness of the stress gradient. At the microscopic scale, we identify a mechanism for dynamic instability where non-sequential bond breaking ahead of the crack tip leads to apparent local crack speeds exceeding the Rayleigh wave speed ($c_r$). These arrested micro-branches, analogous to the Burridge-Andrews mechanism, provide a physical explanation for the "tongue-like" features and hackle zones observed in post-mortem fractography.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Vineet Dawara, Koushik Viswanathan. 2026-02-24. Dynamic fragmentation of residually stressed solids: From microscopic instabilities to universal scaling. https://arxiv.org/abs/2602.20443

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

KEEP EXPLORING

Related papers

Deformation and organization of droplet-encapsulated soft beads

Many biological, culinary, and engineering processes lead to the co-encapsulation of several soft particles within a liquid interface. In these situations the particles are bound together by the capillary forces that deform them and influence their biological or rheological properties. Here, we introduce an experimental approach to encapsulate a controlled number of soft beads within aqueous droplets in oil. These droplet-encapsulated gels are manipulated in a deformable microfluidic device to merge them and modify the liquid fraction. In the dry limit the contact surface between the hydrogels is found to be determined by the elastocapillary number $E_c$, with the contact radius following a $E_c^{1/3}$ dependence, indicating that the deformation increases for soft or small particles. When multiple beads are co-encapsulated within a single droplet they can be arranged into linear or three-dimensional aggregates that remain at a local energy minimum.

cond-mat.soft

Flexoelectricity-driven softening of bend elasticity leads to spontaneous chiral symmetry breaking in a polar fluid

The origin of the recently observed spontaneous chiral symmetry breaking in polar fluids composed of achiral molecules is an unsolved problem, raising fundamental questions about how heliconical structures emerge in such systems. Here, we investigate the pretransitional fluctuations leading to the formation of the spontaneously chiral twist-bend ferroelectric nematic phase using dielectric spectroscopy, light scattering, and small-angle X-ray scattering. We observe simultaneous softening of the bend elastic constant and the emergence of a collective dielectric mode on approaching the transition. By developing a theoretical model, we show that these phenomena are signatures of a flexoelectricity-driven transition arising from the coupling between electric polarization and bend deformation.

cond-mat.soft

Taylor dispersion in a soft tube

Diffusion of a solute along a tube is enhanced by hydrodynamic flow, a phenomenon known as Taylor dispersion. In microfluidic applications, the compliance of the tube boundaries modifies the hydrodynamic flow and thus solutal transport. Here, we develop the theory of solutal dispersion in a soft, axisymmetric tube where the tube walls respond to the hydrodynamic pressure through a Winkler response. By deriving the modified macro-transport equation for the solutal concentration dynamics based on multiple-time-scale analysis, we explore the influence of softness on solutal transport for steady and pulsatile configurations. Our main finding is that softness enhances the effective advection velocity and dispersion coefficient, which might have practical implication in biology and microfluidic technology.

cond-mat.soft