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Structure of flexible and semiflexible polyelectrolyte chains in confined spaces of slit microanochannels

机译:狭缝微/纳通道狭窄空间中的柔性和半柔性聚电解质链的结构

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Understanding the behavior of a polyelectrolyte in confined spaces has direct relevance in design and manipulation of microfluidic devices, as well as transport in living organisms. In this paper, a coarse-grained model of anionic semiflexible polyelectrolyte is applied, and its structure and dynamics are fully examined with Brownian dynamics (BD) simulations both in bulk solution and under confinement between two negatively charged parallel plates. The modeling is based on the nonlinear bead-spring discretization of a continuous chain with additional long-range electrostatic, Lennard-Jones, and hydrodynamic interactions between pairs of beads. The authors also consider the steric and electrostatic interactions between the bead and the confining wall. Relevant model parameters are determined from experimental rheology data on the anionic polysaccharide xanthan reported previously. For comparison, both flexible and semiflexible models are developed accompanying zero and finite intrinsic persistence lengths, respectively. The conformational changes of the polyelectrolyte chain induced by confinements and their dependence on the screening effect of the electrolyte solution are faithfully characterized with BD simulations. Depending on the intrinsic rigidity and the medium ionic strength, the polyelectrolyte can be classified as flexible, semiflexible, or rigid. Confined flexible and semiflexible chains exhibit a nonmonotonic variation in size, as measured by the radius of gyration and end-to-end distance, with changing slit width. For the semiflexible chain, this is coupled to the variations in long-range bond vector correlation. The rigid chain, realized at low ionic strength, does not have minima in size but exhibits a sigmoidal transition. The size of confined semiflexible and rigid polyelectrolytes can be well described by the wormlike chain model once the electrostatic effects are taken into account by the persistence length measured at long length scale. (c) 2007 American Institute of Physics.
机译:了解聚电解质在密闭空间中的行为与微流体装置的设计和操作以及在生物体内的运输有着直接的关系。本文应用了一种阴离子半柔性聚电解质的粗颗粒模型,并通过布朗动力学(BD)模拟在本体溶液中以及在两个带负电荷的平行板之间的约束下,对其结构和动力学进行了全面研究。该建模基于连续链的非线性珠-弹簧离散化,并具有附加的远程静电,Lennard-Jones和成对的珠之间的流体动力学相互作用。作者还考虑了珠子和围墙之间的空间和静电相互作用。根据先前报道的关于阴离子多糖黄原胶的实验流变学数据确定相关的模型参数。为了进行比较,分别开发了具有零和有限固有持久性长度的柔性和半柔性模型。用BD模拟如实地描述了限制引起的聚电解质链的构象变化及其对电解质溶液筛选效果的依赖性。根据固有刚度和中等离子强度,聚电解质可分为柔性,半柔性或刚性。受限的柔性链和半柔性链在尺寸上呈非单调变化,如通过回转半径和端到端距离测量的那样,且缝隙宽度不断变化。对于半柔性链,这与远程键向量相关性的变化有关。以低离子强度实现的刚性链没有最小尺寸,但呈现出S形过渡。一旦通过长尺度测量的持久长度考虑到静电效应,蠕虫链模型就可以很好地描述受限的半柔性和刚性聚电解质的大小。 (c)2007年美国物理研究所。

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