Perrin Jean-Christophe, Lyonnard Sandrine, Guillermo Armel, Levitz Pierre
Structures et Propriétés d'Architectures Moléculaires, UMR 5819 (CEA-CNRS-UJF), DRFMC/SPrAM, CEA-Grenoble, 38054 Grenoble Cedex 9, France.
J Phys Chem B. 2006 Mar 23;110(11):5439-44. doi: 10.1021/jp057433e.
The dynamic behavior of water within two types of ionomer membranes, Nafion and sulfonated polyimide, has been investigated by field-cycling nuclear magnetic relaxation. This technique, applied to materials prepared at different hydration levels, allows the proton motion on a time scale of microseconds to be probed. The NMR longitudinal relaxation rate R(1) measured over three decades of Larmor angular frequencies omega is particularly sensitive to the host-water interactions and thus well-suited to study fluid dynamics in restricted geometries. In the polyimide membranes, we have observed a strong dispersion of R(1)(omega) following closely a 1/square root omega law in a low-frequency range (correlation times from 0.1 to 10 micros). This is indicative of a strong interaction of water with "interfacial" hydrophilic groups of the polymeric matrix (wetting situation). Variations of the relaxation rates with water uptake reveal a two-step hydration process: solvation and formation of disconnected aqueous clusters near polar groups, followed by the formation of a continuous hydrogen bond network. On the contrary, in the Nafion we observed weak variations of R(1)(omega) at low frequencies. This is typical of a nonwetting behavior. At early hydration stages, R(1)(omega) evolves logarithmically, suggesting a confined bidimensional diffusion of protons in the microsecond time range. Such an evolution is lost at higher swelling where a plateau related to three-dimensional diffusion is observed.
通过场循环核磁共振弛豫研究了两种离聚物膜(Nafion和磺化聚酰亚胺)中水的动态行为。该技术应用于在不同水合水平下制备的材料,能够探测微秒时间尺度上的质子运动。在三个数量级的拉莫尔角频率ω范围内测量的核磁共振纵向弛豫率R(1)对主体-水相互作用特别敏感,因此非常适合研究受限几何结构中的流体动力学。在聚酰亚胺膜中,我们观察到在低频范围(相关时间从0.1到10微秒)R(1)(ω)有强烈的色散,紧密遵循1/√ω定律。这表明水与聚合物基体的“界面”亲水基团有很强的相互作用(湿润情况)。弛豫率随吸水量的变化揭示了一个两步水合过程:在极性基团附近溶剂化并形成不相连的水簇,随后形成连续的氢键网络。相反,在Nafion中,我们在低频下观察到R(1)(ω)的变化较弱。这是非湿润行为的典型特征。在早期水合阶段,R(1)(ω)呈对数变化,表明质子在微秒时间范围内存在受限的二维扩散。在更高的溶胀度下这种变化消失,观察到与三维扩散相关的平台期。