Removal of arsenic() from water by 2D zeolitic imidazolate framework-67 nanosheets
Ultrathin two-dimensional (2D) porous materials, which can efficiently capture harmful pollutants from aqueous solutions are highly desired yet scarcely reported. Herein, 2D zeolitic imidazolate framework-67 porous nanosheets (ZIF-67-NS) were first applied as a promising adsorbent for arsenic( iii )...
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Veröffentlicht in: | Environmental science. Nano 2020-11, Vol.7 (11), p.3616-3626 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Ultrathin two-dimensional (2D) porous materials, which can efficiently capture harmful pollutants from aqueous solutions are highly desired yet scarcely reported. Herein, 2D zeolitic imidazolate framework-67 porous nanosheets (ZIF-67-NS) were first applied as a promising adsorbent for arsenic(
iii
) removal from water. An ultrathin structure was observed for the as-prepared ZIF-67-NS with an average thickness of 1.3 nm. The resulting ZIF-67-NS shows outstanding water stability in alkaline conditions. Owing to the unique dimensionality, ZIF-67-NS exhibited a significantly higher adsorption capacity (516 mg g
−1
) and faster uptake kinetics (2 h) toward As(
iii
) than its 3D bulk-type counterpart (ZIF-67-NB). The superior adsorption performance in the ultrathin ZIF-67-NS is attributed to the coordinatively unsaturated Co(
ii
) atoms, which are open sites dominating adsorption, as evidenced by X-ray photoelectron and Fourier transform infrared spectroscopy. On the other hand, the phase transformation in ZIF-67-NB was observed from the 3D bulk structure to the 2D layered structure during the As(
iii
) absorption. Lastly, ZIF-67-NS can be efficiently regenerated with few losses in the adsorption capacity after 3 cycles. Overall, this work represents a practical case of As(
iii
) removal by a 2D crystalline porous material and demonstrates its potential for the development of 2D nanomaterial adsorbents.
Ultrathin 2D metal-organic framework nanosheets can efficiently and rapidly capture arsenate from water. |
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ISSN: | 2051-8153 2051-8161 |
DOI: | 10.1039/d0en00851f |