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Crosslinked polyethersulfone membranes for organic solvent nanofiltration in polar aprotic and halogenated solvents.
- Source :
-
Journal of Membrane Science . Dec2022, Vol. 663, pN.PAG-N.PAG. 1p. - Publication Year :
- 2022
-
Abstract
- Organic solvent nanofiltration is a promising and more sustainable alternative to classic separation processes in multiple industries; however, proposed materials for polymeric membranes with high solvent stability mostly utilize unique or expensive polymers, or are fabricated by complex methods. Herein, a facile method is presented to fabricate crosslinked polyethersulfone membranes with remarkable stability in halogenated and polar aprotic solvents. After preparing the membranes by the conventional non-solvent-induced phase inversion process, a multidentate aromatic amine embedded in the polysulfone underwent diazotization/dediazonization to effectively crosslink the polymer matrix. Membrane performance was easily adjusted from ultra-to nanofiltration via the polymer fraction. The performance of the crosslinked polyethersulfone nanofiltration is similar to the state-of-the-art solvent stable membranes. A weeklong filtration experiment in dimethylformamide and chloroform underlines the membranes' excellent stability. Overall, the range of solvent stability and state-of-the-art performance, combined with high accessibility and scalability, make the presented membranes an ideal platform material. [Display omitted] • Intricately crosslinked PES membranes are prepared via dediazonization • The crosslinked membranes have excellent stability in a wide range of solvents • Membrane performance is preserved even in halogenated and polar aprotic solvents • Selectivity is easily adjustable from the UF to NF range • The presented procedure has a high potential for scalable SRNF membrane manufacture [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03767388
- Volume :
- 663
- Database :
- Academic Search Index
- Journal :
- Journal of Membrane Science
- Publication Type :
- Academic Journal
- Accession number :
- 159822198
- Full Text :
- https://doi.org/10.1016/j.memsci.2022.120963