A Simple New Way To Account for Free Volume in Glassy Dynamics: Model-Free Estimation of the Close-Packed Volume from PVT Data

Abstract

In this article we focus on the important role of well-defined free volume (V_free) in dictating the structural relaxation times, τ, of glass-forming liquids and polymer melts. Our definition of V_free = V – V_hc, where V is the total system volume, means the use of V_free depends on determination of V_hc, the system’s volume in the limiting closely packed state. Rejecting the historically compromised use of V_free as a dynamics-dependent fitting function, we have successfully applied a clear thermodynamics-based route to V_hc using the locally correlated lattice (LCL) model equation of state (EOS). However, in this work we go further and show that V_hc can be defined without the use of an equation of state by direct linear extrapolation of a V(T) high-pressure isobar down to zero temperature (T). The results from this route, tested on a dozen experimental systems, yield ln τ vs 1/V_free isotherms that are linear with T-dependent slopes, consistent with the general ln τ ∼ f(T) × (1/V_free) form of behavior we have previously described. This functional form also results by implementing a simple mechanistic explanation via the cooperative free volume (CFV) rate model, which assumes that dynamic relaxation is both thermally activated and that it requires molecular segmental cooperativity. With the degree of the latter, and thus the activation energy, being determined by the availability of free volume, the new route we demonstrate here for determination of V_free expands the potential for understanding and predicting local dynamic relaxation in glass-forming materials.