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Article: Towards the fastest kinetics and highest uptake of post-functionalized UiO-66 for Hg2+ removal from water

TitleTowards the fastest kinetics and highest uptake of post-functionalized UiO-66 for Hg2+ removal from water
Authors
Issue Date9-Jun-2023
PublisherRoyal Society of Chemistry
Citation
Nanoscale, 2023, v. 15, n. 25, p. 10558-10566 How to Cite?
Abstract

Recent advances in adsorbents have improved the removal of mercury ions from wastewater. Metal-organic frameworks (MOFs) have been increasingly used as adsorbents due to their high adsorption capacity and ability to adsorb various heavy metal ions. UiO-66 (Zr) MOFs are mainly used because they are highly stable in aqueous solutions. However, most functionalized UiO-66 materials are unable to achieve a high adsorption capacity because of the undesired reactions that occur during post-functionalization. Herein, we report a facile post-functionalization method to synthesize a MOF adsorbent with fully active amide- and thiol-functionalized chelating groups, termed UiO-66-A.T. UiO-66-A.T. was synthesized via a two-step reaction by crosslinking with a monomer containing a disulfide moiety, followed by disulfide cleavage to activate the thiol groups. UiO-66-A.T. removed Hg from water with a maximum adsorption capacity of 691 mg g and a rate constant of 0.28 g mg min at pH 1. In a mixed solution containing 10 different heavy metal ions, UiO-66-A.T. has a Hg selectivity of 99.4%, which is the highest reported to date. These results demonstrate the effectiveness of our design strategy for synthesizing purely defined MOFs to achieve the best Hg removal performance to date among post-functionalized UiO-66-type MOF adsorbents.


Persistent Identifierhttp://hdl.handle.net/10722/338122
ISSN
2023 Impact Factor: 5.8
2023 SCImago Journal Rankings: 1.416
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLam, Yan Tsz Iris-
dc.contributor.authorYuan, Yufei-
dc.contributor.authorBang, Ki-Taek-
dc.contributor.authorChoi, Seon-Jin-
dc.contributor.authorShin, Dong-Myeong-
dc.contributor.authorLu, Dong-
dc.contributor.authorKim, Yoonseob-
dc.date.accessioned2024-03-11T10:26:25Z-
dc.date.available2024-03-11T10:26:25Z-
dc.date.issued2023-06-09-
dc.identifier.citationNanoscale, 2023, v. 15, n. 25, p. 10558-10566-
dc.identifier.issn2040-3364-
dc.identifier.urihttp://hdl.handle.net/10722/338122-
dc.description.abstract<p>Recent advances in adsorbents have improved the removal of mercury ions from wastewater. Metal-organic frameworks (MOFs) have been increasingly used as adsorbents due to their high adsorption capacity and ability to adsorb various heavy metal ions. UiO-66 (Zr) MOFs are mainly used because they are highly stable in aqueous solutions. However, most functionalized UiO-66 materials are unable to achieve a high adsorption capacity because of the undesired reactions that occur during post-functionalization. Herein, we report a facile post-functionalization method to synthesize a MOF adsorbent with fully active amide- and thiol-functionalized chelating groups, termed UiO-66-A.T. UiO-66-A.T. was synthesized via a two-step reaction by crosslinking with a monomer containing a disulfide moiety, followed by disulfide cleavage to activate the thiol groups. UiO-66-A.T. removed Hg<sup/> from water with a maximum adsorption capacity of 691 mg g<sup/> and a rate constant of 0.28 g mg<sup/> min<sup/> at pH 1. In a mixed solution containing 10 different heavy metal ions, UiO-66-A.T. has a Hg<sup/> selectivity of 99.4%, which is the highest reported to date. These results demonstrate the effectiveness of our design strategy for synthesizing purely defined MOFs to achieve the best Hg<sup/> removal performance to date among post-functionalized UiO-66-type MOF adsorbents.</p>-
dc.languageeng-
dc.publisherRoyal Society of Chemistry-
dc.relation.ispartofNanoscale-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleTowards the fastest kinetics and highest uptake of post-functionalized UiO-66 for Hg2+ removal from water-
dc.typeArticle-
dc.identifier.doi10.1039/D3NR01959D-
dc.identifier.scopuseid_2-s2.0-85163456177-
dc.identifier.volume15-
dc.identifier.issue25-
dc.identifier.spage10558-
dc.identifier.epage10566-
dc.identifier.eissn2040-3372-
dc.identifier.isiWOS:001005238000001-
dc.identifier.issnl2040-3364-

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