Dielectric and structural properties of aqueous nonpolar solute mixtures

被引:6
|
作者
Shvab, I. [1 ]
Sadus, Richard J. [1 ]
机构
[1] Swinburne Univ Technol, Ctr Mol Simulat, Hawthorn, Vic 3122, Australia
来源
JOURNAL OF CHEMICAL PHYSICS | 2012年 / 137卷 / 12期
关键词
PRESSURE PHASE-EQUILIBRIA; MONTE-CARLO-SIMULATION; COMPUTER-SIMULATION; HYDROPHOBIC HYDRATION; MOLECULAR SIMULATION; RARE-GASES; AB-INITIO; PVT-DATA; WATER; METHANE;
D O I
10.1063/1.4753940
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The dielectric properties and molecular structure of water mixtures with different nonpolar solutes (methane and noble gases) are studied using molecular dynamics. The water-water, water-solute, and solute-solute interactions are calculated using the combination of a polarizable potential [J. Li, Z. Zhou, and R. J. Sadus, J. Chem. Phys. 127, 154509 (2007)] for water plus the Lennard-Jones potential. The effect of solute size and concentration on the solubility of the system, hydrogen bonding, dielectric constant, and dipole moment are investigated over a temperature range of 278-750 K and solute percentage mole fractions up to 30%. Solute particles affect the structure of water, resulting in the compression of oxygen-oxygen and oxygen-hydrogen radial distribution functions. The influence of the solute extends both to relatively low concentrations and high temperatures. The coordination numbers of aqueous solutions of the nonpolar solutes appear to be proportional to the size of the solute particles. Our study shows the destructive influence of the nonpolar solute on both the tetrahedral water structure and hydrogen bond formation at solute concentrations greater than 30%. The presence of nonpolar particles typically decreases both the dielectric constant and dipole moment. The decrease of dielectric constant and water dipole moment is directly proportional to the solute concentration and temperature. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4753940]
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页数:13
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