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通过 1H NMR 光谱研究 Nafion 膜中水分的水合过程和旋转动力学分析。

Analysis of the hydration process and rotational dynamics of water in a Nafion membrane studied by 1H NMR spectroscopy.

机构信息

Institute for Chemical Research, Kyoto University, Uji, Kyoto, Japan.

出版信息

Anal Chem. 2013 Aug 6;85(15):7581-7. doi: 10.1021/ac401653v. Epub 2013 Jul 25.

Abstract

(1)H NMR spectroscopy is employed to reveal the hydration process of a Nafion membrane by measuring both the chemical shift and the spin-lattice relaxation time. In a former study, the hydration process was suggested to comprise two steps: the molecular adsorption of water on the sulfonic acid groups and wetting with liquid water. The present study has revealed the first step can further be divided into two steps. By introducing a new experimental technique, the quantitatively reliable NMR measurements of protons ((1)H) of water involved in the polymer membrane are realized. In addition, a new analytical procedure is developed using a reciprocal concentration on a saturation-adsorption model, and the hydration is clearly revealed to have three individual steps. Both the chemical shift and the relaxation time plots against the reciprocal concentration exhibit three linear parts with apparently different slopes. Of great interest is that the initial hydration is divided into two stages: the first hydration is a very strong adsorption of water probably on the hydroxyl group of the sulfonic acid group, and the second one is a relatively weak adsorption on another site of the sulfonic acid group. The third hydration is readily assigned to excess bulk (liquid-like) water as expected. These adsorption processes are readily correlated with the rotational motion of water by converting the spin-lattice relaxation time to the rotational correlation time.

摘要

(1)NMR 光谱用于通过测量化学位移和自旋晶格弛豫时间来揭示 Nafion 膜的水合过程。在以前的研究中,水合过程被认为包括两个步骤:水分子在磺酸基团上的分子吸附和与液态水的润湿。本研究表明,第一步可以进一步分为两个步骤。通过引入一种新的实验技术,实现了对聚合物膜中质子((1)H)参与的定量可靠的 NMR 测量。此外,使用饱和吸附模型的倒数浓度开发了一种新的分析程序,清楚地表明水合作用有三个单独的步骤。化学位移和弛豫时间与倒数浓度的关系图显示出三个线性部分,斜率明显不同。有趣的是,初始水合作用分为两个阶段:第一阶段是水的强吸附,可能是在磺酸基团的羟基上,第二阶段是磺酸基团上的另一个位置的相对较弱的吸附。第三阶段水合作用很容易被分配给多余的体相(液态)水,这是预期的。这些吸附过程很容易与水的旋转运动相关联,方法是将自旋晶格弛豫时间转换为旋转相关时间。

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