Another resolution of the configurational entropy paradox as applied to hard spheres
Abstract
Recently, Ozawa and Berthier [J. Chem. Phys., 2017, 146, 014502] studied the configurational and vibrational entropies and from the relation for polydisperse mixtures of spheres. They noticed that because shall contain the mixing entropy per particle and shall not, the configurational entropy per particle shall diverge in the thermodynamic limit for continuous polydispersity due to the diverging . They also provided a resolution for this paradox and related problems-it relies on a careful redefining of and . Here, we note that the relation is essentially a geometric relation in the phase space and shall hold without redefining and . We also note that the total entropy per particle diverges with with continuous polydispersity as well. The usual way to avoid this and other difficulties with is to work with the excess entropy (relative to the ideal gas of the same polydispersity). Speedy [Mol. Phys., 1998, 95, 169] applied this approach to the relation above and wrote this relation as . This form has flows as well, because does not contain the term and the latter is introduced into instead. Here, we suggest that this relation shall actually be written as , where while and with standing for the de Broglie wavelength. In this form, all the terms per particle are always finite for and continuous when introducing a small polydispersity to a monodisperse system. We also suggest that the Adam-Gibbs and related relations shall in fact contain instead of .
Keywords
Cite
@article{arxiv.1706.09671,
title = {Another resolution of the configurational entropy paradox as applied to hard spheres},
author = {Vasili Baranau and Ulrich Tallarek},
journal= {arXiv preprint arXiv:1706.09671},
year = {2017}
}