Novel Metal–Organic Framework (MOF) Based Composite Material for the Sequestration of U(VI) and Th(IV) Metal Ions from Aqueous Environment
The combination of magnetic nanoparticles and metal–organic frameworks (MOFs) has demonstrated their prospective for pollutant sequestration. In this work, a magnetic metal–organic framework nanocomposite (Fe3O4@AMCA-MIL53(Al) was prepared and used for the removal of U(VI) and Th(IV) metal ions f...
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Veröffentlicht in: | ACS applied materials & interfaces 2017-10, Vol.9 (41), p.36026-36037 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The combination of magnetic nanoparticles and metal–organic frameworks (MOFs) has demonstrated their prospective for pollutant sequestration. In this work, a magnetic metal–organic framework nanocomposite (Fe3O4@AMCA-MIL53(Al) was prepared and used for the removal of U(VI) and Th(IV) metal ions from aqueous environment. Fe3O4@AMCA-MIL53(Al) nanocomposite was characterized by TGA, FTIR, SEM-EDX, XRD, HRTEM, BET, VSM (vibrating sample magnetometry), and XPS analyses. A batch technique was applied for the removal of the aforesaid metal ions using Fe3O4@AMCA-MIL53(Al) at different operating parameters. The isotherm and kinetic data were accurately described by the Langmuir and pseudo-second-order models. The adsorption capacity was calculated to be 227.3 and 285.7 mg/g for U(VI) and Th(IV), respectively, by fitting the equilibrium data to the Langmuir model. The kinetic studies demonstrated that the equilibrium time was 90 min for each metal ion. Various thermodynamic parameters were evaluated which indicated the endothermic and spontaneous nature of adsorption. The collected outcomes showed that Fe3O4@AMCA-MIL53(Al) was a good material for the exclusion of these metal ions from aqueous medium. The adsorbed metals were easily recovered by desorption in 0.01 M HCl. The excellent adsorption capacity and the response to the magnetic field made this novel material an auspicious candidate for environmental remediation technologies. |
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ISSN: | 1944-8244 1944-8252 |
DOI: | 10.1021/acsami.7b10768 |