Dipolar origin of the gas-liquid coexistence of the hard-core 1:1 electrolyte model
arXiv:cond-mat/0208080 · doi:10.1103/PhysRevE.66.041204
Abstract
We present a systematic study of the effect of the ion pairing on the gas-liquid phase transition of hard-core 1:1 electrolyte models. We study a class of dipolar dimer models that depend on a parameter R_c, the maximum separation between the ions that compose the dimer. This parameter can vary from sigma_{+/-} that corresponds to the tightly tethered dipolar dimer model, to R_c --> infinity, that corresponds to the Stillinger-Lovett description of the free ion system. The coexistence curve and critical point parameters are obtained as a function of R_c by grand canonical Monte Carlo techniques. Our results show that this dependence is smooth but non-monotonic and converges asymptotically towards the free ion case for relatively small values of R_c. This fact allows us to describe the gas-liquid transition in the free ion model as a transition between two dimerized fluid phases. The role of the unpaired ions can be considered as a perturbation of this picture.
16 pages, 13 figures, submitted to Physical Review E
References in corpus (1)
Cited by in corpus (7)
- Avoiding unphysical kinetic traps in Monte Carlo simulations of strongly attractive particles
- Ion association in low-polarity solvents: comparisons between theory, simulation, and experiment
- Ultrasoft primitive model of polyionic solutions: structure, aggregation, and dynamics
- Computer simulations of the restricted primitive model at very low temperature and density
- Ion pairing in model electrolytes: A study via three particle correlation functions
- Liquid-gas separation in colloidal electrolytes
- Is it possible to overheat ice? The activated melting of TIP4P/Ice at solid-vapor coexistence