Diffusion of ions in supercritical water: Dependence on ion size and solvent density and roles of voids and necks

被引:19
作者
Chakraborty, Debashree [1 ]
Chandra, Amalendu [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Kanpur 208016, Uttar Pradesh, India
关键词
Molecular dynamics; Ion diffusion; Supercritical water; Voids; Necks; MOLECULAR-DYNAMICS SIMULATION; DIELECTRIC FRICTION; AQUEOUS-SOLUTIONS; ELECTROLYTE-SOLUTIONS; TEMPERATURE-DEPENDENCE; SOLVATION STRUCTURE; PAIR; MOBILITY; MODEL; NACL;
D O I
10.1016/j.molliq.2011.05.006
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 have performed molecular dynamics simulations of alkali metal (Li+, Na+, K+, Rb+, Cs+) and halide (F-, Cl-, Br-, I-) ions in supercritical water at 673 K. The calculations were done for water at three different densities of 1.0, 0.7 and 0.35 g cm(-3) to investigate the effects of solute size on the diffusion of ions in supercritical water. On increase of ion size, we observe a maximum for diffusion of ions in supercritical water of higher densities (1.0 and 0.7 g cm(-3)). However, no such maximum is found for ion diffusion in the supercritical water of low density (0.35 g cm(-3)) or for diffusion of neutral solutes at all densities. These results are analyzed in terms of passage through voids and necks present in supercritical water. Correlations of the observed diffusion behavior with the sizes of ions and voids present in the systems are discussed. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:12 / 19
页数:8
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