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DOUBLE SCREENING IN POLYELECTROLYTE SOLUTIONS - LIMITING LAWS AND CROSSOVER FORMULAS

机译:电解质溶液的双重筛选-极限定律和交叉公式

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We have derived general expressions for the Helmholtz free energy of a polyelectrolyte solution and the average size of a labeled chain as functions of polyelectrolyte concentration, salt concentration, and the strengths of excluded volume and electrostatic interaction all varying from very low to very high. We have shown that the bare excluded volume interaction and the electrostatically screened Coulomb interaction between any two segments are both screened by the presence of polyelectrolyte chains at nonzero concentrations. The screening length associated with this excluded volume screening is a function of Debye length and the entropy of the connected polymer and consequently depends on the polyelectrolyte concentration differently at different salt concentrations. By treating the correlation of the monomer density fluctuations, we have derived integral equations coupling the effective interaction between any two segments and the effective step length of a labeled chain. In the limit of the excluded volume screening length and the effective step length being independent of wave vectors, they are related by algebraic equations. These equations reduce to scaling laws with numerical prefactors for semidilute and concentrated polyelectrolyte solutions. Our development provides limiting laws and analytical interpolation formulas for the excluded volume screening length, effective step length, free energy of the polyelectrolyte solution, and the average size of a chain for various polyelectrolyte concentrations in an isotropic solution and for arbitrary strengths of excluded volume and electrostatic interactions. The excluded volume screening leads to an attractive component in the effective potential interaction at intermediate distances between two segmental charges of the same sign. The strength and range of the attractive potential are determined by the concentrations of the polyelectrolyte and the various ions. (C) 1996 American Institute of Physics. [References: 45]
机译:我们已经得出了聚电解质溶液的亥姆霍兹自由能和标记链的平均大小与聚电解质浓度,盐浓度以及排除体积和静电相互作用强度的函数的一般表达式,其范围从非常低到非常高。我们已经表明,通过两个非零浓度的聚电解质链的存在,可以筛选任何两个片段之间的裸露的体积相互作用和静电筛选的库仑相互作用。与该排除的体积筛选有关的筛选长度是德拜长度和所连接的聚合物的熵的函数,因此在不同的盐浓度下取决于聚电解质的浓度不同。通过处理单体密度波动的相关性,我们导出了积分方程,该方程耦合了任意两个链段之间的有效相互作用以及标记链的有效步长。在排除体积筛选长度和有效步长与波矢无关的范围内,它们与代数方程式相关。这些方程式可简化为具有数字预因子的比例定律,适用于半稀释和浓缩聚电解质溶液。我们的发展为排除体积筛选长度,有效步长,聚电解质溶液的自由能以及各向同性溶液中各种聚电解质浓度以及排除体积和浓度的任意强度提供了限制律和分析插值公式。静电相互作用。排除的体积筛选导致在相同符号的两个分段电荷之间的中间距离处的有效电位相互作用中具有吸引力的成分。吸引力的强度和范围由聚电解质和各种离子的浓度决定。 (C)1996年美国物理研究所。 [参考:45]

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