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Article: Symmetrically recombined nanofibers in a high-selectivity membrane for cation separation in high temperature and organic solvent

TitleSymmetrically recombined nanofibers in a high-selectivity membrane for cation separation in high temperature and organic solvent
Authors
Issue Date2019
Citation
Journal of Materials Chemistry A, 2019, v. 7, n. 34, p. 20006-20012 How to Cite?
AbstractDevelopment of polymeric cation exchange membranes (CEMs) with high thermostability and resistance to organic solvents is an urgent challenge for materials chemistry and a major problem for industrial application. Herein, we report a novel CEM design, which symmetrically recombines poly(p-phenylene terephthalamide) nanofibers and 2,5-diaminobenzenesulfonic acid based on amide hydrolysis and amide condensation reaction for ion separation in high temperature and organic solvent aqueous applications. The resulting membrane (10 μm thickness) exhibited greater thermodynamic and electrochemical properties than the common commercial CEMs. Attributed to the membrane's specific structure, size sieving, and electrostatic repulsion effects, the resulting membrane showed a more selective separation of monovalent cations in electrodialysis. Moreover, it has demonstrated exceptional desalination at high temperature (as high as 100 °C) and organic solvent aqueous environments (as high as 80% acetone solution), which had not been previously reported in electrodialysis. The resulting membrane combines the benefits of nano-materials and a specific structure design allowing for electrodialysis in high temperature and organic solvent aqueous application environments.
Persistent Identifierhttp://hdl.handle.net/10722/327976
ISSN
2021 Impact Factor: 14.511
2020 SCImago Journal Rankings: 3.637
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhao, Yan-
dc.contributor.authorQiu, Yangbo-
dc.contributor.authorMai, Zhaohuan-
dc.contributor.authorOrtega, Emily-
dc.contributor.authorShen, Jiangnan-
dc.contributor.authorGao, Congjie-
dc.contributor.authorVan Der Bruggen, Bart-
dc.date.accessioned2023-06-05T06:53:04Z-
dc.date.available2023-06-05T06:53:04Z-
dc.date.issued2019-
dc.identifier.citationJournal of Materials Chemistry A, 2019, v. 7, n. 34, p. 20006-20012-
dc.identifier.issn2050-7488-
dc.identifier.urihttp://hdl.handle.net/10722/327976-
dc.description.abstractDevelopment of polymeric cation exchange membranes (CEMs) with high thermostability and resistance to organic solvents is an urgent challenge for materials chemistry and a major problem for industrial application. Herein, we report a novel CEM design, which symmetrically recombines poly(p-phenylene terephthalamide) nanofibers and 2,5-diaminobenzenesulfonic acid based on amide hydrolysis and amide condensation reaction for ion separation in high temperature and organic solvent aqueous applications. The resulting membrane (10 μm thickness) exhibited greater thermodynamic and electrochemical properties than the common commercial CEMs. Attributed to the membrane's specific structure, size sieving, and electrostatic repulsion effects, the resulting membrane showed a more selective separation of monovalent cations in electrodialysis. Moreover, it has demonstrated exceptional desalination at high temperature (as high as 100 °C) and organic solvent aqueous environments (as high as 80% acetone solution), which had not been previously reported in electrodialysis. The resulting membrane combines the benefits of nano-materials and a specific structure design allowing for electrodialysis in high temperature and organic solvent aqueous application environments.-
dc.languageeng-
dc.relation.ispartofJournal of Materials Chemistry A-
dc.titleSymmetrically recombined nanofibers in a high-selectivity membrane for cation separation in high temperature and organic solvent-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/c9ta07416c-
dc.identifier.scopuseid_2-s2.0-85071726122-
dc.identifier.volume7-
dc.identifier.issue34-
dc.identifier.spage20006-
dc.identifier.epage20012-
dc.identifier.eissn2050-7496-
dc.identifier.isiWOS:000483565400040-

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