Diffusion of aqueous solutions of ionic, zwitterionic, and polar solutes

被引:9
|
作者
Teng, Xiaojing [1 ]
Huang, Qi [1 ]
Dharmawardhana, Chamila Chathuranga [1 ]
Ichiye, Toshiko [1 ]
机构
[1] Georgetown Univ, Dept Chem, Washington, DC 20057 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2018年 / 148卷 / 22期
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
RANGE; 0.1-35; MPA; BIOMOLECULAR SIMULATIONS; KINEMATIC VISCOSITY; UREA SOLUTIONS; FORCE-FIELD; WATER; DYNAMICS; PRESSURE; PROTEINS; ASSOCIATION;
D O I
10.1063/1.5023004
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 properties of aqueous solutions of ionic, zwitterionic, and polar solutes are of interest to many fields. For instance, one of the many anomalous properties of aqueous solutions is the behavior of water diffusion in different monovalent salt solutions. In addition, solutes can affect the stabilities of macromolecules such as proteins in aqueous solution. Here, the diffusivities of aqueous solutions of sodium chloride, potassium chloride, tri-methylamine oxide (TMAO), urea, and TMAO-urea are examined in molecular dynamics simulations. The decrease in the diffusivity of water with the concentration of simple ions and urea can be described by a simple model in which the water molecules hydrogen bonded to the solutes are considered to diffuse at the same rate as the solutes, while the remainder of the water molecules are considered to be bulk and diffuse at almost the same rate as pure water. On the other hand, the decrease in the diffusivity of water with the concentration of TMAO is apparently affected by a decrease in the diffusion rate of the bulk water molecules in addition to the decrease due to the water molecules hydrogen bonded to TMAO. In other words, TMAO enhances the viscosity of water, while urea barely affects it. Overall, this separation of water molecules into those that are hydrogen bonded to solute and those that are bulk can provide a useful means of understanding the short-and long-range effects of solutes on water. Published by AIP Publishing.
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页数:7
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