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Enhanced Mono/Divalent Ion Separation via Charged Interlayer Channels in Montmorillonite-Based Membranes.
- Source :
-
Environmental science & technology [Environ Sci Technol] 2024 Mar 05; Vol. 58 (9), pp. 4415-4427. Date of Electronic Publication: 2024 Feb 19. - Publication Year :
- 2024
-
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 <superscript>+</superscript> flux of 2.09 × 10 <superscript>-8</superscript> mol cm <superscript>-2</superscript> s <superscript>-1</superscript> . 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 <superscript>+</superscript> has a lower migration energy barrier and higher migration rate for the modified MMT-based membrane compared to Mg <superscript>2+</superscript> . This work presents a novel approach for the development of monovalent permselective membranes.
- Subjects :
- Ions
Filtration
Bentonite
Water Purification methods
Subjects
Details
- Language :
- English
- ISSN :
- 1520-5851
- Volume :
- 58
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Environmental science & technology
- Publication Type :
- Academic Journal
- Accession number :
- 38373279
- Full Text :
- https://doi.org/10.1021/acs.est.3c08853