Cottet H, Gareil P, Theodoly O, Williams C E
Laboratoire d'Electrochimie et de Chimie Analytique, Ecole Nationale Supérieure de Chimie de Paris, France.
Electrophoresis. 2000 Nov;21(17):3529-40. doi: 10.1002/1522-2683(200011)21:17<3529::AID-ELPS3529>3.0.CO;2-2.
This work focuses on the understanding of the electrophoretic behavior of flexible chains of polystyrenesulfonates (PSSs) in free solution. It deals mainly with the variation of the electrophoretic mobility with (i) the polymerization degree (N) of fully sulfonated PSSs and (ii) the sulfonation rate of randomly sulfonated PSSs. In both cases, the electrophoretic mobility was modeled following a semi-empirical approach which involves parameters retaining a physical meaning. Fully sulfonated PSS oligomers, having a length smaller than or similar to the Debye length, exhibit a particular electrophoretic behavior, in-between that observed for multicharged small molecules and that for polyelectrolytes. The electrophoretic mobility of these oligomers increases strongly with N, which is attributed to a hydrodynamic coupling between monomers. Then the mobility is maximum for an N of about 10, for which the PSS oligomers are still in a rod-like conformation. Afterwards, as N increases and the PSSs are larger than the Debye length, the electrophoretic mobility decreases slowly until it reaches a constant value corresponding to the free-draining behavior. Next, the electrophoretic behavior of long PSS (N about 1,200) differing in their sulfonation rates was investigated. The effective charge rates were determined independently by conductimetric measurements and the mobilities were modeled as a function of the sulfonation rate. The PSS behavior observed was compared to the one previously reported for classical polyelectrolytes having hydrophilic backbones, such as copolymers of poly(acryamide-coacrylic acid). A specific behavior has been pointed out for these partially sulfonated PSSs, which is attributed to the hydrophobicity of their backbone. Finally, it is shown that separations of PSSs of different sulfonation rates can be obtained with electrolytes containing an anionic surfactant or methanol.
这项工作聚焦于理解聚苯乙烯磺酸盐(PSSs)柔性链在自由溶液中的电泳行为。它主要研究电泳迁移率随以下因素的变化:(i)全磺化PSSs的聚合度(N),以及(ii)随机磺化PSSs的磺化率。在这两种情况下,电泳迁移率都采用半经验方法进行建模,该方法涉及具有物理意义的参数。长度小于或近似于德拜长度的全磺化PSS低聚物表现出一种特殊的电泳行为,介于多电荷小分子和聚电解质所观察到的行为之间。这些低聚物的电泳迁移率随N强烈增加,这归因于单体之间的流体动力学耦合。然后,对于N约为10时迁移率最大,此时PSS低聚物仍处于棒状构象。此后,随着N增加且PSSs大于德拜长度,电泳迁移率缓慢下降,直至达到对应于自由排水行为的恒定值。接下来,研究了磺化率不同的长PSS(N约为1200)的电泳行为。通过电导测量独立确定有效电荷率,并将迁移率建模为磺化率的函数。将观察到的PSS行为与先前报道的具有亲水性主链的经典聚电解质(如聚(丙烯酰胺 - 共丙烯酸)共聚物)的行为进行了比较。已指出这些部分磺化PSSs的特定行为,这归因于其主链的疏水性。最后,结果表明,使用含有阴离子表面活性剂或甲醇的电解质可以实现不同磺化率PSSs的分离。