Linear polyelectrolytes in tetravalent salt solutions

被引:38
|
作者
Hsiao, PY [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Engn & Syst Sci, Hsinchu 300, Taiwan
来源
JOURNAL OF CHEMICAL PHYSICS | 2006年 / 124卷 / 04期
关键词
D O I
10.1063/1.2155484
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 effect of adding tetravalent salt of different sizes to a solution of linear and flexible polyelectrolytes is investigated by molecular dynamics simulations. Upon the addition of salt, a chain reexpansion takes place, following a well-known collapsed conformation. The degrees of collapse and reexpansion increase with ion size. In the solution, tetravalent counterions replace monovalent ones and condense onto the chains. The condensation for small ions displays a profile different from that for large ones. In a high-salt region, ions can form layering orders around a polyelectrolyte and locally overcompensate the charge inside. Consequently, the integrated charge distribution reveals an oscillatory behavior away from a chain. By studying the radial distribution function between monomers on different polyelectrolytes, like-charge attraction between chains is demonstrated. This attraction is a prerequisite to chain aggregation or precipitation. The results show a strong dependence of salt concentration and ion size on the properties of polyelectrolyte solutions. (c) 2006 American Institute of Physics.
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页数:10
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