Hsiao Pai-Yi
Department of Engineering and System Science, National Tsing Hua University, Hsinchu 300, Taiwan, Republic of China.
J Chem Phys. 2006 Jan 28;124(4):044904. doi: 10.1063/1.2155484.
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.
通过分子动力学模拟研究了向线性柔性聚电解质溶液中添加不同大小的四价盐的效果。加入盐后,遵循众所周知的塌陷构象,链会发生重新膨胀。塌陷和重新膨胀的程度随离子大小而增加。在溶液中,四价抗衡离子取代单价离子并凝聚在链上。小离子的凝聚表现出与大离子不同的分布。在高盐区域,离子可以在聚电解质周围形成分层有序结构,并局部过度补偿内部电荷。因此,积分电荷分布显示出远离链的振荡行为。通过研究不同聚电解质上单体之间的径向分布函数,证明了链间的同电荷吸引。这种吸引是链聚集或沉淀的前提。结果表明盐浓度和离子大小对聚电解质溶液的性质有很强的依赖性。