Enhanced low-concentration phosphate adsorption using magnetic UiO-66@Fe3O4 composite with potential linker exchange
A magnetic FenUiO-66 adsorbent was created to achieve high phosphate adsorption capacity. The incorporation of Fe3O4 facilitated the precipitation and growth of UiO-66 during crystallization, resulting in a shift towards a multilayer heterogeneous distribution of adsorption sites. The increased Fe3O...
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Veröffentlicht in: | Chemosphere (Oxford) 2024-09, Vol.364, p.143126, Article 143126 |
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Sprache: | eng |
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Zusammenfassung: | A magnetic FenUiO-66 adsorbent was created to achieve high phosphate adsorption capacity. The incorporation of Fe3O4 facilitated the precipitation and growth of UiO-66 during crystallization, resulting in a shift towards a multilayer heterogeneous distribution of adsorption sites. The increased Fe3O4 content notably enhanced the magnetic properties of FenUiO-66, while negligibly affecting its adsorption performance. The Fe1.5UiO-66 demonstrated exceptional phosphate adsorption capacity (136.54 mg/g), outstanding selectivity, and sustained reusability, with an 80% removal efficiency after nine cycles of treating actual water. The mechanism of phosphate adsorption by FenUiO-66 involved electrostatic attraction, ligand exchange, and linker exchange. Notably, while linker exchange significantly contributed to high adsorption capacity, it resulted in irreversible damage to the FenUiO-66 crystal. These unequivocal findings will serve as a solid foundation for further research and underline the critical role of linkers in the process of phosphate adsorption.
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•Magnetic MOF for phosphate adsorption realized via synthesis of UiO-66 on Fe3O4.•Fe3O4 changed adsorption mode of UiO-66 with sufficient adsorption capacity.•Linker exchange created defects to improve phosphate adsorption for first use.•Linker exchange cause irreversible structural damage and decrease reusability.•High performance remained after repeatedly treating actual water. |
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ISSN: | 0045-6535 1879-1298 1879-1298 |
DOI: | 10.1016/j.chemosphere.2024.143126 |