Thermodynamic properties and diffusion of water plus methane binary mixtures

被引:20
|
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 | 2014年 / 140卷 / 10期
关键词
MOLECULAR-DYNAMICS ENSEMBLE; PRESSURE PHASE-EQUILIBRIA; TRANSITION-METAL HALIDES; AQUEOUS-SOLUTIONS; HEAT-CAPACITY; STATISTICAL THERMODYNAMICS; TEMPERATURE-DEPENDENCE; SELF-DIFFUSION; MOLAR COMPRESSIBILITIES; HYDROPHOBIC HYDRATION;
D O I
10.1063/1.4867282
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
Thermodynamic and diffusion properties of water + methane mixtures in a single liquid phase are studied using NVT molecular dynamics. An extensive comparison is reported for the thermal pressure coefficient, compressibilities, expansion coefficients, heat capacities, Joule-Thomson coefficient, zero frequency speed of sound, and diffusion coefficient at methane concentrations up to 15% in the temperature range of 298-650 K. The simulations reveal a complex concentration dependence of the thermodynamic properties of water + methane mixtures. The compressibilities, heat capacities, and diffusion coefficients decrease with increasing methane concentration, whereas values of the thermal expansion coefficients and speed of sound increase. Increasing methane concentration considerably retards the self-diffusion of both water and methane in the mixture. These effects are caused by changes in hydrogen bond network, solvation shell structure, and dynamics of water molecules induced by the solvation of methane at constant volume conditions. (c) 2014 AIP Publishing LLC.
引用
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页数:10
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