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- Publisher Website: 10.1021/acs.est.0c05387
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- PMID: 33185431
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Article: Cross-linked graphene oxide framework membranes with robust nano-channels for enhanced sieving ability
Title | Cross-linked graphene oxide framework membranes with robust nano-channels for enhanced sieving ability |
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Authors | |
Issue Date | 2020 |
Publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journal/esthag |
Citation | Environmental Science & Technology, 2020, v. 54 n. 23, p. 15442-15453 How to Cite? |
Abstract | It remains challenging for graphene oxide (GO) membranes to achieve highly efficient performance and sufficient stability for aqueous molecule/ion precise separations. Herein, a molecular-level rational structure design protocol was proposed to develop ceramic-based graphene oxide framework (GOF) membranes with significantly enhanced sieving performance and stability for efficient removal of salts and micropollutants. Via a molecular cross-linking strategy, interlayered nanochannels between GO nanosheets can be rationally designed, featuring precisely tailorable channel size, promising surface chemistries and remarkably robust stability suitable for aqueous separation. Due to a significantly decreased nanochannel size, cross-linking of TU (thiourea) molecule significantly improved monovalent salt rejection (95.6% for NaCl), outperforming existing state-of-the-art GO-based, commercial organic nanofiltration and emerging two-dimensional MoS2 membranes, while moderately decreasing water permeability. In comparison, the GOF membranes cross-linked with MPD (m-phenylenediamine) exhibited a simultaneous increase in permeability and rejection for both salts and micropollutants (21.0% and 53.3% enhancement for chloramphenicol (CAP) solution), breaking their conventional trade-off issue. Cross-linking mechanism indicates that more robust nanochannels were formed by stronger covalent bonds via dehydration condensation between amine (TU/MPD) and carboxyl groups (GO), and nucleophilic addition between amine (TU/MPD) and epoxy groups (GO). Molecule/ion separation mechanism involved size sieving (steric hindrance), electrostatic interaction, Donnan effect, and partial dehydration effect. This work provides a novel protocol for rationally designing size and surface chemistry of highly robust GO nanochannels at a subnanometer level to construct water-stable functional GOF membranes with enhanced sieving performance for water treatment applications. |
Persistent Identifier | http://hdl.handle.net/10722/306357 |
ISSN | 2023 Impact Factor: 10.8 2023 SCImago Journal Rankings: 3.516 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Yuan, B | - |
dc.contributor.author | Wang, M | - |
dc.contributor.author | Wang, B | - |
dc.contributor.author | Yang, F | - |
dc.contributor.author | Quan, X | - |
dc.contributor.author | Tang, C | - |
dc.contributor.author | Dong, Y | - |
dc.date.accessioned | 2021-10-20T10:22:28Z | - |
dc.date.available | 2021-10-20T10:22:28Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Environmental Science & Technology, 2020, v. 54 n. 23, p. 15442-15453 | - |
dc.identifier.issn | 0013-936X | - |
dc.identifier.uri | http://hdl.handle.net/10722/306357 | - |
dc.description.abstract | It remains challenging for graphene oxide (GO) membranes to achieve highly efficient performance and sufficient stability for aqueous molecule/ion precise separations. Herein, a molecular-level rational structure design protocol was proposed to develop ceramic-based graphene oxide framework (GOF) membranes with significantly enhanced sieving performance and stability for efficient removal of salts and micropollutants. Via a molecular cross-linking strategy, interlayered nanochannels between GO nanosheets can be rationally designed, featuring precisely tailorable channel size, promising surface chemistries and remarkably robust stability suitable for aqueous separation. Due to a significantly decreased nanochannel size, cross-linking of TU (thiourea) molecule significantly improved monovalent salt rejection (95.6% for NaCl), outperforming existing state-of-the-art GO-based, commercial organic nanofiltration and emerging two-dimensional MoS2 membranes, while moderately decreasing water permeability. In comparison, the GOF membranes cross-linked with MPD (m-phenylenediamine) exhibited a simultaneous increase in permeability and rejection for both salts and micropollutants (21.0% and 53.3% enhancement for chloramphenicol (CAP) solution), breaking their conventional trade-off issue. Cross-linking mechanism indicates that more robust nanochannels were formed by stronger covalent bonds via dehydration condensation between amine (TU/MPD) and carboxyl groups (GO), and nucleophilic addition between amine (TU/MPD) and epoxy groups (GO). Molecule/ion separation mechanism involved size sieving (steric hindrance), electrostatic interaction, Donnan effect, and partial dehydration effect. This work provides a novel protocol for rationally designing size and surface chemistry of highly robust GO nanochannels at a subnanometer level to construct water-stable functional GOF membranes with enhanced sieving performance for water treatment applications. | - |
dc.language | eng | - |
dc.publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journal/esthag | - |
dc.relation.ispartof | Environmental Science & Technology | - |
dc.rights | This document is the Accepted Manuscript version of a Published Work that appeared in final form in Environmental Science & Technology. copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/10.1021/acs.est.0c05387 | - |
dc.title | Cross-linked graphene oxide framework membranes with robust nano-channels for enhanced sieving ability | - |
dc.type | Article | - |
dc.identifier.email | Tang, C: tangc@hku.hk | - |
dc.identifier.authority | Tang, C=rp01765 | - |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1021/acs.est.0c05387 | - |
dc.identifier.pmid | 33185431 | - |
dc.identifier.scopus | eid_2-s2.0-85096550581 | - |
dc.identifier.hkuros | 326735 | - |
dc.identifier.volume | 54 | - |
dc.identifier.issue | 23 | - |
dc.identifier.spage | 15442 | - |
dc.identifier.epage | 15453 | - |
dc.identifier.isi | WOS:000596728600070 | - |
dc.publisher.place | United States | - |