A link between viscosity and cation-anion contact pairs: Adventure on the concept of structure-making/breaking for concentrated salt solutions

被引:18
|
作者
Peng, Hong [1 ]
Nguyen, Anh, V [1 ]
机构
[1] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
关键词
Viscosity; TIP4P/2005; Cation anion interaction; Structure-making; Hydration shell; Molecular dynamics; MOLECULAR-DYNAMICS SIMULATION; LITHIUM-CHLORIDE SOLUTIONS; AQUEOUS IONIC-SOLUTIONS; COMPUTER-SIMULATION; ELECTROLYTE-SOLUTIONS; ALKALI-METAL; LIQUID WATER; BIOLOGICAL STRUCTURE; NEUTRON-DIFFRACTION; SODIUM-CHLORIDE;
D O I
10.1016/j.molliq.2018.04.145
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
We investigated structure properties of structure-making salts (LiCI, NaCl, and NaBr) and structure-breaking salts (KCI and KBr) solutions of 0.5 M to 4 M using TIP4P/2005 water model and OPLS ionic force fields. The viscosity results show a good trend with experimental values for all salts. For the water structure, the O-O number decreased with increasing salt concentrations but is independent of the salt types. There is an extra shoulder (Cl-O/LiCl) or no obvious low-point at the first minimum point of anion oxygen ROE patterns (Cl-O/NaCl and Br-O/NaBr) while two structure-breaking salts show a normal minimum point (Cl-O/KCI and Br-O/KBr). Additionally, we observed that the ratio (R-12) of primary and second shell cation-anion numbers showed a similar trend as the viscosity behaves with increasing salt concentration. For structure-making salts, values of R-12 increased with increasing salt concentrations while R-12 values of structure-breaking salts slightly decreased with concentration. These observations may indicate that the change in viscosity is due to the disturbance of cation-anion contact hydration pairs, not the free water hydrogen network. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 117
页数:9
相关论文
共 2 条