Tailoring the molecular structure of crosslinked polymers for pervaporation desalination

Polymer crosslinking imbues chemical stability to thin films at the expense of lower molecular transportation rates. Here in this work we deployed molecular dynamics simulations to optimise the selection of crosslinking compounds that overcome this trade-off relationship. We validated these simulati...

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Published inNature communications Vol. 11; no. 1; pp. 1461 - 9
Main Authors Xue, Yun Long, Huang, Jin, Lau, Cher Hon, Cao, Bing, Li, Pei
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 19.03.2020
Nature Publishing Group
Nature Portfolio
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Summary:Polymer crosslinking imbues chemical stability to thin films at the expense of lower molecular transportation rates. Here in this work we deployed molecular dynamics simulations to optimise the selection of crosslinking compounds that overcome this trade-off relationship. We validated these simulations using a series of experiments and exploited this finding to underpin the development of a pervaporation (PV) desalination thin-film composite membrane with water fluxes reaching 234.9 ± 8.1 kg m −2 h −1 and salt rejection of 99.7 ± 0.2 %, outperforming existing membranes for pervaporation and membrane distillation. Key to achieving this state-of-the-art desalination performance is the spray coating of 0.73 μm thick crosslinked dense, hydrophilic polymers on to electrospun nanofiber mats. The desalination performances of our polymer nanocomposites are harnessed here in this work to produce freshwater from brackish water, seawater and brine solutions, addressing the key environmental issue of freshwater scarcity. Polymer crosslinking in desalination membranes adds stability on the cost of molecular transportation rates through the membrane. Here the authors tailor crosslinking of desalination membranes to overcome the stability and transport trade-off, and demonstrate a pervaporation desalination thin-film composite membrane with high water flux.
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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-020-15038-w