4.7 Article

Enhanced monovalent anion selectivity of poly(2,6-dimethyl-1,4-phenylene oxide)-based amphoteric ion exchange membranes having rough surface

期刊

JOURNAL OF MEMBRANE SCIENCE
卷 661, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.memsci.2022.120911

关键词

Mono-/bi-valent anion separation; Side-chain-type structure; PPO; Amphoteric ion exchange membrane; Electrodialysis

资金

  1. National Natural Science Foundation of China [21878273, 22008214]
  2. Natural Science Foundation of Zhejiang Province, China [LQ20B060005]
  3. Key Research and Development Program of Zhejiang Province, China [2021C03170]
  4. Key Special Projects for 2020 Science and Technology Boosting the Economy from Ministry of Industry and Information Technology of China

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Amphoteric ion-exchange membranes have been prepared for ion separation in this study. The optimized membrane shows good separation performance and may provide guidance for the design of advanced ion-exchange membranes.
Amphoteric polyelectrolytes have been used as the materials for the high-performance ion-exchange membranes applied in redox flow battery and electrodialysis (ED) etc. In this work, four amphoteric ion-exchange membranes (AIEMs) based on sodium 1-propanesulfonate-3-methylimidazole (MIm-PS) and 1-butylimidazole (BIm) deco-rated poly(2,6-dimethyl-1,4-phenylene oxide) have been prepared for mono-/bi-valent anion separation by using the electrodialyzer. The optimized AIEM has a low surface area resistance of 5.79 omega.cm(2). During the ED testing, at 2.5 mA.cm(-2), the perm-selectivity (P-SO4(2-Cl-) ) tested in a binary mixture of 0.05 M NaCl and 0.05 M Na2SO4, achieves the value of 16.12 at 30th min, which is significantly higher than that of anion-exchange membrane (1.68) as the reference. This superior separation performance has been further verified by the perm-selectivity of 55.5, tested in a single solution of 0.05 M NaCl or 0.05 M Na2SO4. The high perm-selectivity results from the electrostatic repulsion difference of mono-/bi-valent ions against the negatively-charged -SO(3)(- )groups, accompanying with pore-size sieving effect resulting from the smaller ion cluster space of 0.261 nm. It is interesting to find that AIEMs show the increased ion flux values of Cl-/SO42-, though the presence of the negatively-charged -SO3- groups, which is possibly related to the convex particle-like surface that increasing the effective surface area for ions passing. This work may provide a reference to guide the architectural design of advanced mono-valent anion-selective IEMs.

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