Thin-Film Composite Membranes Interlayered with Amphiphilic MoS2 Nanosheets via Controllable Interfacial Polymerization for Enhanced Desalination Performance

Polyamide (PA)-based nanofiltration (NF) membranes have demonstrated extensive applications for a sustainable water–energy–environment nexus. A rational control of interfacial polymerization (IP) is highly efficacious to enhance NF separation performance yet remains a technical challenge. Herein, we...

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Veröffentlicht in:Environmental science & technology 2024-07, Vol.58 (26), p.11855-11863
Hauptverfasser: Wang, Dong, Yuan, Shideng, Zhang, Na, Wang, Ziming, Zhu, Junyong, Wang, Zhining
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Sprache:eng
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Zusammenfassung:Polyamide (PA)-based nanofiltration (NF) membranes have demonstrated extensive applications for a sustainable water–energy–environment nexus. A rational control of interfacial polymerization (IP) is highly efficacious to enhance NF separation performance yet remains a technical challenge. Herein, we proposed a regulation strategy of constructing amphiphilic molybdenum disulfide/cetyltrimethylammonium bromide interlayer atop the Kevlar hydrogel substrate. The amphiphilic nanosheet interlayered NF membrane exhibited a crumpled PA surface with an elevated cross-linking degree of 76.9%, leading to an excellent water permeance (16.8 L m–2 h–1 bar–1) and an impressive Na2SO4 rejection (99.1%). Meanwhile, the selectivity coefficient of Na2SO4/NaCl of the optimized TFC membrane reached 91, surpassing those of the recently reported NF membranes. Moreover, the optimized membrane exhibited a desirable rejection of over 90% against Mn2+ and Cu2+ in actual textile wastewater. Importantly, the underlying NF membrane formation mechanism was elucidated via both experiments and molecular simulations. The synchronous control of mass and heat transfer of IP process offers a new methodology for the state-of-the-art membrane fabrication, which opens more avenues in softening of brackish water and purification of industrial wastewater containing heavy metal ions.
ISSN:0013-936X
1520-5851
1520-5851
DOI:10.1021/acs.est.4c04063