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Spectrum of hydrodynamic volumes and sizes of macromolecules of linear polyelectrolytes versus their charge density in salt-free aqueous solutions

机译:水动力学体积和线性聚电解质大分子大小的尺寸与其在无盐水溶液中的电荷密度

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摘要

Molecular characteristics of statistical copolymers based on hydrophilic poly(N-methyl-N-vinylacetamide) have been monitored throughout the entire possible range of charge density from 1.5 to 39 mol%. Different trends in the dependence of intrinsic viscosity on the average charge density of polymer chains at minimal ionic strength were revealed. A new parameter, l(qq)/A(bare), describing this behavior was proposed (l(qq) is the average distance between the neighboring charges along the chain, and A(bare) is the statistical segment length of a non-charged homologue). For polyelectrolyte chains, this parameter allows the regions of charge density values where electrostatic long-range or short-range interactions dominate to be indicated. Two homologous series of copolymers were characterized by methods of molecular hydrodynamics under conditions of suppressed charge effects. Intrinsic viscosity in salt-free solutions characterizing an individual macromolecule was estimated by a method proposed earlier.
机译:在整个可能的电荷密度范围内监测基于亲水性聚(N-甲基-N-乙烯基乙酰胺)的统计共聚物的分子特性。揭示了在最小离子强度下聚合物链的平均电荷密度的特性粘度依赖性的不同趋势。提出了一种新的参数L(QQ)/ a(裸),描述该行为(L(QQ)是沿着链条的相邻电荷之间的平均距离,而a(裸)是非 - 的统计段长度带电的同源物)。对于聚电解质链,该参数允许指示静电远程或短距离相互作用的电荷密度值区域。通过在抑制电荷效应的条件下,通过分子流体动力学的方法表征两种同源共聚物。通过提前提出的方法估算了表征单个大分子的无盐溶液中的固有粘度。

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