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Enhanced Mono/Divalent Ion Separation via Charged Interlayer Channels in Montmorillonite-Based Membranes.
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- Additional Information
- Source:
Publisher: American Chemical Society Country of Publication: United States NLM ID: 0213155 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1520-5851 (Electronic) Linking ISSN: 0013936X NLM ISO Abbreviation: Environ Sci Technol Subsets: MEDLINE
- Publication Information:
Publication: Washington DC : American Chemical Society
Original Publication: Easton, Pa. : American Chemical Society, c1967-
- Subject Terms:
- Abstract:
Efficient mono- and divalent ion separation is pivotal for environmental conservation and energy utilization. Two-dimensional (2D) materials featuring interlayer nanochannels exhibit unique water and ion transport properties, rendering them highly suitable for water treatment membranes. In this work, we incorporated polydopamine/polyethylenimine (PDA/PEI) copolymers into 2D montmorillonite (MMT) nanosheet interlayer channels through electrostatic interactions and bioinspired bonding. A modified laminar structure was formed on the substrate surface via a straightforward vacuum filtration. The electrodialysis experiments reveal that these membranes could achieve monovalent permselectivity of 11.06 and Na + flux of 2.09 × 10 -8 mol cm -2 s -1 . The enhanced permselectivity results from the synergistic effect of electrostatic and steric hindrance effect. In addition, the interaction between the PDA/PEI copolymer and the MMT nanosheet ensures the long-term operational stability of the membranes. Theoretical simulations reveal that Na + has a lower migration energy barrier and higher migration rate for the modified MMT-based membrane compared to Mg 2+ . This work presents a novel approach for the development of monovalent permselective membranes.
- Contributed Indexing:
Keywords: 2D channel; MMT nanosheet; electrodialysis; electrostatic effect; monovalent permselectivity
- Accession Number:
1302-78-9 (Bentonite)
0 (Ions)
- Publication Date:
Date Created: 20240219 Date Completed: 20240306 Latest Revision: 20240306
- Publication Date:
20240306
- Accession Number:
10.1021/acs.est.3c08853
- Accession Number:
38373279
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