Laboratoire d'Electrochimie, Corrosion et de Valorisation Energétique (LECVE), Faculté de Technologie, Université A. MIRA , Bejaia 06000, Algérie.
Université du Maine, IMMM UMR CNRS 6283 , Avenue Olivier Messiaen, 72085 Le Mans, Cedex 5, France.
J Phys Chem B. 2017 Feb 2;121(4):867-875. doi: 10.1021/acs.jpcb.6b11237. Epub 2017 Jan 19.
Self-assembly in aqueous solutions of an amphiphilic comblike polyelectrolyte (80C12) that consists of a polystyrene (PS) backbone onto which quaternary ammonium pendant moieties have been grafted has been investigated by light scattering and cryo-transmission electron microscopy measurements in the presence of KCl and methylviologen dication (MV) under conditions mimicking those for electrochemical measurements. Polymer chains self-assemble within branched cylindrical micelles that display viscoelastic properties, characterized by a relaxation time of 4 s. To tune this time, 80C12 was mixed with a polyoxyethylene nonionic surfactant (Brij CE). Relatively increasing the amount of the latter leads to a decrease in the relaxation time of the 80C12 solution. Correlatively, electrochemical experiments with a rotating disk electrode show a transition of the mass transport rate, which deviates from the classical Newtonian behavior in the same velocity domain. This result generalizes what has been already observed with solutions of linear polymers of high molecular weight and wormlike micelles based on surfactants subjected to elongational deformations. Moreover, the critical times derived from rheological and electrochemical experiments display the same trend.
在存在 KCl 和甲紫二阳离子(MV)的条件下,通过光散射和低温透射电子显微镜测量研究了由接枝了季铵盐侧基的聚苯乙烯(PS)主链组成的两亲梳状聚合物(80C12)在水溶液中的自组装。聚合物链在具有粘弹性质的支化圆柱胶束内自组装,其弛豫时间为 4 秒。为了调节这个时间,可以将 80C12 与聚氧乙烯非离子表面活性剂(Brij CE)混合。相对增加后者的量会导致 80C12 溶液的弛豫时间降低。相应地,使用旋转圆盘电极进行的电化学实验显示质量传输速率发生了转变,这偏离了在相同速度范围内的经典牛顿行为。这一结果推广了已经观察到的具有高分子量线性聚合物溶液和基于表面活性剂的蠕虫状胶束在受到拉伸变形时的情况。此外,从流变学和电化学实验得出的临界时间显示出相同的趋势。