Non-equilibrium Kinetics of the Transformation of Liquids into Physical Gels

Abstract

A major stumbling block for statistical physics and materials science has been the lack of a uni- versal principle that allows us to understand and predict elementary structural, morphological, and dynamical properties of non-equilibrium amorphous states of matter. The recently-developed non- equilibrium self-consistent generalized Langevin equation (NE-SCGLE) theory, however, has been shown to provide a fundamental tool for the understanding of the most essential features of the transformation of liquids into amorphous solids, such as their aging kinetics or their dependence on the protocol of fabrication. In this work we focus on the predicted kinetics of one of the main fingerprints of the formation of gels by arrested spinodal decomposition of suddenly and deeply quenched simple liquids, namely, the arrest of structural parameters associated with the morpho- logical evolution from the initially uniform fluid, to the dynamically arrested sponge-like amorphous material. The comparison of the theoretical predictions (based on a simple specific model system), with simulation and experimental data measured on similar but more complex materials, suggests the universality of the predicted scenario.

4 figures

References in corpus (2)

• Theoretical perspective on the glass transition and amorphous materials
• Colloidal Gels: Equilibrium and Non-Equilibrium Routes

Cited by in corpus (6)

• Waiting-time dependent non-equilibrium phase diagram of simple glass- and gel-forming liquids
• From sub-aging to hyper-aging in structural glasses
• Phase separation and dynamical arrest of protein solutions dominated by short-range attractions
• Non-Equilibrium View of the Amorphous Solidification of Liquids with Competing Interactions
• Non-equilibrium Onsager-Machlup theory
• Structural relaxation, dynamical arrest and aging in soft-sphere liquids