Thermodynamic interpretation of the scaling of the dynamics of supercooled liquids
R. Casalini, U. Mohanty, C. M. Roland
Abstract
The recently discovered scaling law for the relaxation times, tau=f(T,Vg), where T is temperature and V the specific volume, is derived by a revision of the entropy model of the glass transition dynamics originally proposed by Avramov [I. Avramov, J. Non-Cryst. Solids 262, 258 (2000).]. In this modification the entropy is calculated by an alternative route, while retaining the approximation that the heat capacity is constant with T and P. The resulting expression for the variation of the relaxation time with T and V is shown to accurately fit experimental data for several glass-forming liquids and polymers over an extended range encompassing the dynamic crossover. From this analysis, which is valid for any model in which the relaxation time is a function of the entropy. we find that the scaling exponent g can be identified with the Gruneisen constant.
Create a lesson
Related papers
Nonparametric multiscale modeling of boundary lubrication: hexadecane in highly pressurized gold asperity contacts
Hannes Holey, Michael Moseler, Peter Gumbsch et al.
Asymmetric Ions in Solution are Similar to Active Brownian Particles
Setare Mostajabi Sarhangi, Dmitry V. Matyushov
Influence of twist direction and large deformation on soft material torsional contact
Yucai Hu, Pengfei Li, Michele Ciavarella et al.
Phase transitions and microphases in elastomers. II. Anisotropy-driven morphologies
Manu Mannattil, David Andelman, Haim Diamant
Comparing non-local granular fluid continuum models for silo discharge: Toward clogging prediction
Y. Zhou, Y. Wang, M. Li et al.
Residual semi-crystalline particles released during enzymatic degradation of plastics
Michael Schindler, Ludwik Leibler