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首页> 外文期刊>Colloid and polymer science >Dilute-semidilute regime crossover in aqueous solutions of poly(acrylic acid)-sodium poly(styrene sulfonate) mixtures
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Dilute-semidilute regime crossover in aqueous solutions of poly(acrylic acid)-sodium poly(styrene sulfonate) mixtures

机译:聚(丙烯酸) - 聚(苯乙烯磺酸盐)混合物水溶液中稀型 - 半汇分制度交叉

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摘要

Overlap and entanglement formation in aqueous solutions of mixtures of poly(acrylic acid) (PAA) and sodium poly(styrene sulfonate) (PSS) have been studied by means of light scattering and viscometry in comparison with concentration transitions in solutions of the individual polyelectrolytes. In the presence of 0.1M HCl, PAA forms a complex with PSS due to ion-dipole interactions of carboxylic groups with polyanion sulfonic groups. In the overlap region, a single diffusion mode is split into fast and slow modes, with the average scattering intensity passing through a maximum. In the region of entanglement network formation, the third mode appears, which we interpret as an interaction mode. The concentration dependences of diffusion coefficients and viscosity of the considered systems coincide with the theoretical predictions of the scaling model of polyelectrolyte solutions. In semidilute regime, the viscosity of the complex significantly exceeds that of initial components, indicating strong structuring of the solution.
机译:通过光散射和粘度法研究了聚(丙烯酸)(PAA)和聚(苯乙烯磺酸盐)(苯乙烯磺酸钠)(PSS)的混合物水溶液中的重叠和缠结形成,与各个聚电解质的溶液中的浓度转变相比,粘度测定研究。在0.1M HCl的存在下,PAA由于羧基与聚沉砜基团的离子 - 偶极相互作用而形成与PS的复合物。在重叠区域中,单个扩散模式被分成快速和慢速模式,具有最大值的平均散射强度。在纠缠网络形成区域中,出现第三种模式,我们将其解释为交互模式。所考虑系统的扩散系数和粘度的浓度依赖性与聚电解质溶液的缩放模型的理论预测一致。在半径制度中,复合物的粘度明显超过初始组分的粘度,表明溶液的强大结构。

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