用介电弛豫光谱表征水合聚合物:连接相对介电常数,磺化聚砜的水态和盐输运性质

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Sean M. Bannon, Beatrice M. Tremblay, Andrew Boudreau, Nurshaun Sreedhar, Caroline Morin, Charles R. Leroux, Phu Phan, Abhishek Roy, Mou Paul* and Geoffrey M. Geise*, 
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引用次数: 0

摘要

磺化聚砜是一种很有前途的膜材料,用于分离和能量生成过程,这些过程依赖于膜来控制小分子(例如水和离子)的传输速率。水分子、离子和这些聚合物中的磺酸基之间的相互作用在控制这些运输速率方面起着关键作用,但关于这些磺化聚合物中的基本相互作用仍有很多未知。在这项研究中,我们使用介电弛豫光谱来表征磺化聚砜和Nafion中的水分子动力学。我们发现,带电的磺酸基以一种由磺酸基的浓度和性质(即共轭碱强度)控制的方式限制了水分子动力学(即,偶极运动的特征时间尺度的减少)。此外,我们制定策略,利用这些数据,以帮助模拟在磺化聚砜离子传输。这些结果可能有助于指导聚合物膜的工程策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterizing Hydrated Polymers via Dielectric Relaxation Spectroscopy: Connecting Relative Permittivity, State of Water, and Salt Transport Properties of Sulfonated Polysulfones

Sulfonated polysulfone is a promising membrane material for separation and energy generation processes that rely on membranes to control the rates of small-molecule (e.g., water and ions) transport. The interactions among water molecules, ions, and the sulfonate groups in these polymers play a key role in controlling these rates of transport, but much remains unknown about these fundamental interactions in sulfonated polymers. In this study, we used dielectric relaxation spectroscopy to characterize water molecule dynamics in sulfonated polysulfone and Nafion. We found that the charged sulfonate groups contribute to a restriction of water molecule dynamics (i.e., a reduction in the characteristic time scale of dipolar motions) in a manner that is governed by the concentration and nature (i.e., conjugate base strength) of the sulfonate group. Additionally, we develop strategies to use these data to aid in modeling ion transport in sulfonated polysulfone. These results may be useful to guide engineering strategies for polymeric membranes.

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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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