Lopez Carlos G, Richtering Walter
Institute of Physical Chemistry , RWTH Aachen University , Landoltweg 2 , 52056 Aachen , Germany.
J Phys Chem B. 2019 Jul 5;123(26):5626-5634. doi: 10.1021/acs.jpcb.9b03044. Epub 2019 Jun 20.
We report viscosity data of nonentangled sodium polystyrene sulfonate (NaPSS) in salt-free aqueous solution as a function of polymer concentration ( c) and degree of polymerization ( N). Different empirical equations are examined and found not to describe the semidilute solution viscosity over a wide concentration range and/or to yield values of [η] that do not match dilute solution measurements. Deviations from the scaling prediction of η ∝ c (Fuoss' law) are observed at high concentrations. Specifically, we find η ≈ N c e in the semidilute regime, which agrees with the scaling prediction only for c ≲ 0.02 M. The viscosity data presented in this study and in earlier reports show a high degree of consistency. A comparison with diffusion measurements for NaPSS in salt-free solution by Oostwal and co-workers suggests that the disagreement between the scaling theory and experiments does not arise solely from the concentration dependence of the monomeric friction coefficient.
我们报告了无盐水溶液中未缠结的聚苯乙烯磺酸钠(NaPSS)的粘度数据,该数据是聚合物浓度(c)和聚合度(N)的函数。我们研究了不同的经验方程,发现它们在较宽的浓度范围内无法描述半稀溶液的粘度,和/或得出的特性粘度值与稀溶液测量值不匹配。在高浓度下观察到与η ∝ c的标度预测(福斯定律)存在偏差。具体而言,我们发现在半稀区域η ≈ N c e,仅在c ≲ 0.02 M时才与标度预测相符。本研究和早期报告中给出的粘度数据显示出高度的一致性。与奥斯特瓦尔及其同事对无盐溶液中NaPSS的扩散测量结果进行比较表明,标度理论与实验之间的不一致并非仅源于单体摩擦系数的浓度依赖性。