Dependence of the dielectric constant of electrolyte solutions on ionic concentration - a microfield approach
arXiv:1208.5169 · doi:10.1103/PhysRevE.94.012611
Abstract
We present a novel microfield approach for studying the dependence of the orientational polarization of the water in aqueous electrolyte solutions upon the salt concentration and temperature. The model takes into account the orientation of the solvent dipoles due to the electric field created by ions, and the effect of thermal fluctuations. The model predicts a dielectric functional dependence of the form , where is the Langevin function, is the salt concentration, is the dielectric of pure water, is the dielectric of the electrolyte solution at the molten salt limit, and is the total excess polarization of the ions. The functional form gives a remarkably accurate description of the dielectric constant for a variety of salts and a wide range of concentrations.
Accepted for publication in Physical Review E
References in corpus (5)
- The Dielectric Constant of Ionic Solutions: A Field-Theory Approach
- Are Room Temperature Ionic Liquids Dilute Electrolytes?
- Differential capacitance of the electric double layer: The interplay between ion finite size and dielectric decrement
- Surface Tension of Electrolyte Interfaces: Ionic Specificity within a Field-Theory Approach
- Static dielectric properties of dense ionic fluids
Cited by in corpus (22)
- Underscreening in concentrated electrolytes
- Relaxation Behavior by Time-Salt and Time-Temperature Superpositions of Polyelectrolyte Complexes from Coacervate to Precipitate
- Dielectric Constant of Ionic Solutions: Combined Effects of Correlations and Excluded Volume
- Molecular Mean-Field Theory of Ionic Solutions: a Poisson-Nernst-Planck-Bikerman Model
- A comparison of classical interatomic potentials applied to highly concentrated aqueous lithium chloride solutions
- Transient electrohydrodynamic flow with concentration dependent fluid properties: modelling and energy-stable numerical schemes
- On the analogy between the restricted primitive model and capacitor circuits. Part II: A generalized Gibbs-Duhem consistent extension of the Pitzer-Debye-Hückel term with corrections for low and variable relative permittivity
- Reliable computational prediction of supramolecular ordering of complex molecules under electrochemical conditions
- Explicit Solvent Theory of Salt-Induced Dielectric Decrement
- Systematic incorporation of the ionic hard-core size into the Debye-Huckel theory via the cumulant expansion of the Schwinger-Dyson equations
- Sensing electrochemical signals using a nitrogen-vacancy center in diamond
- Mathematical Modeling of Microscale Biology: Ion Pairing, Dielectric Decrement, and Born Energy in Glycosaminoglycan Brushes
- Length scales in electrolytes
- Confining Eutectic Gallium Indium (eGaIn) in Expired Artificial Kidneys to Unveil Nanoporous Conductive Wires
- Electrochemistry, Ion Adsorption and Dynamics in the Double Layer: A Study of NaCl(aq) on Graphite
- On the properties of methanolic NaCl solution by molecular dynamics simulations
- Controlling the interfacial and bulk concentrations of spontaneously charged colloids in non-polar media
- Unified microscopic theory of equilibrium thermodynamics and ion association in aqueous and non-aqueous electrolytes with explicit hard-core size
- Computational modeling of biological nanopores
- Anomalous, Dielectrophoretic Transport of Molecules in Non-Electrolytes
- Effect of variable relative permittivity on the thermodynamics of asymmetric valency aqueous salts
- On the cause of Zeta potential of a charged vesicle. The extra- and intravesicular membrane charges contribute differently to the extra- and intravesicular potential