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Article: Highly permeable and highly selective ultrathin film composite polyamide membranes reinforced by reactable polymer chains

TitleHighly permeable and highly selective ultrathin film composite polyamide membranes reinforced by reactable polymer chains
Authors
KeywordsThin film composite membrane
Ultrathin rejection layer
Interfacial polymerization
Divalent to monovalent salts selectivity
Reactable substrate
Issue Date2019
PublisherAcademic Press. The Journal's web site is located at http://www.elsevier.com/locate/jcis
Citation
Journal of Colloid and Interface Science, 2019, v. 552, p. 418-425 How to Cite?
AbstractThis study reports highly permeable ultrathin film composite (uTFC) membranes whose rejection layer was reinforced by polymer chains during the interfacial polymerization of trimesoyl chloride (TMC) and m-phenylenediamine (MPD) to achieve enhanced salt rejection. A rejection layer of approximately 20 nm was formed at an MPD concentration of 0.01 wt%. This reinforced membrane had a water permeability of about 16.7 L/(m2 h bar), while exhibiting an improved divalent salt (Na2SO4) to monovalent salt (NaCl) selectivity compared with the control TFC membrane without reinforcement (3.44 vs. 1.06). The role of the reactable polymer chains in interfacial polymerization was discussed as MPD adsorbent and reactant, according to the measurements by quartz crystal microbalance and X-ray photoelectron spectroscopy. This work provides a new pathway for the design and construction of uniform ultrathin layers as well as the preparation of high performance separation membranes.
Persistent Identifierhttp://hdl.handle.net/10722/272863
ISSN
2021 Impact Factor: 9.965
2020 SCImago Journal Rankings: 1.538
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYao, Z-
dc.contributor.authorYang, Z-
dc.contributor.authorGuo, H-
dc.contributor.authorMa, X-
dc.contributor.authorDong, Y-
dc.contributor.authorTang, CY-
dc.date.accessioned2019-08-06T09:17:59Z-
dc.date.available2019-08-06T09:17:59Z-
dc.date.issued2019-
dc.identifier.citationJournal of Colloid and Interface Science, 2019, v. 552, p. 418-425-
dc.identifier.issn0021-9797-
dc.identifier.urihttp://hdl.handle.net/10722/272863-
dc.description.abstractThis study reports highly permeable ultrathin film composite (uTFC) membranes whose rejection layer was reinforced by polymer chains during the interfacial polymerization of trimesoyl chloride (TMC) and m-phenylenediamine (MPD) to achieve enhanced salt rejection. A rejection layer of approximately 20 nm was formed at an MPD concentration of 0.01 wt%. This reinforced membrane had a water permeability of about 16.7 L/(m2 h bar), while exhibiting an improved divalent salt (Na2SO4) to monovalent salt (NaCl) selectivity compared with the control TFC membrane without reinforcement (3.44 vs. 1.06). The role of the reactable polymer chains in interfacial polymerization was discussed as MPD adsorbent and reactant, according to the measurements by quartz crystal microbalance and X-ray photoelectron spectroscopy. This work provides a new pathway for the design and construction of uniform ultrathin layers as well as the preparation of high performance separation membranes.-
dc.languageeng-
dc.publisherAcademic Press. The Journal's web site is located at http://www.elsevier.com/locate/jcis-
dc.relation.ispartofJournal of Colloid and Interface Science-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectThin film composite membrane-
dc.subjectUltrathin rejection layer-
dc.subjectInterfacial polymerization-
dc.subjectDivalent to monovalent salts selectivity-
dc.subjectReactable substrate-
dc.titleHighly permeable and highly selective ultrathin film composite polyamide membranes reinforced by reactable polymer chains-
dc.typeArticle-
dc.identifier.emailYang, Z: zheyang8@hku.hk-
dc.identifier.emailGuo, H: guohao7@hku.hk-
dc.identifier.emailTang, CY: tangc@hku.hk-
dc.identifier.authorityYang, Z=rp02847-
dc.identifier.authorityGuo, H=rp02772-
dc.identifier.authorityTang, CY=rp01765-
dc.description.naturepostprint-
dc.identifier.doi10.1016/j.jcis.2019.05.070-
dc.identifier.pmid31151019-
dc.identifier.scopuseid_2-s2.0-85066245196-
dc.identifier.hkuros299806-
dc.identifier.volume552-
dc.identifier.spage418-
dc.identifier.epage425-
dc.identifier.isiWOS:000481566500043-
dc.publisher.placeUnited States-
dc.identifier.issnl0021-9797-

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