4.8 Article

Design of Zr-MOFs by Introducing Multiple Ligands for Efficient and Selective Capturing of Pb(II) from Aqueous Solutions

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AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c21546

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metal-organic frameworks; adsorption; heavy-metal ions; frontier molecular orbital; molecular electrostatic potential

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A novel metal-organic framework adsorbent (UiO-FHD) is developed, which efficiently and selectively captures lead ions by introducing multiple ligands. The maximum adsorption capacity of lead ions is 433.15 mg/g at pH 5. The adsorption process follows pseudo-second-order kinetic and Langmuir isotherm models, and appropriate temperature reduction facilitates the removal of Pb(II). Performance tests show that UiO-FHD maintains a high removal rate of 90.35% for Pb(II) after four consecutive adsorption-desorption cycles.
The existence of lead ions seriously affects the quality of many metal products in metallurgical enterprises. Currently, the various methods of lead-ion removal tried by researchers will affect valuable metals in the removal process, thus resulting in low economic efficiency. In this study, a novel metal- organic framework adsorbent (UiO-FHD) which efficiently and selectively captures lead ions is developed by introducing multiple ligands. The maximum adsorption capacity of lead ions is 433.15 mg/g at pH 5. The adsorption process accords with the pseudo-second-order kinetic and the Langmuir isotherm models at room temperature. Thermodynamic experiments indicate that the removal of Pb(II) is facilitated by appropriate temperature reduction. The performance tests indicate that UiO-FHD maintains a high removal rate of 90.35% for Pb(II) after four consecutive adsorption-desorption cycles. The distribution coefficient of lead ions (26.7 L/g) shows that UiO-FHD has excellent selective adsorption for lead ions. It is revealed that the chelation of the sulfhydryl groups and the electrostatic interaction of the hydroxyl groups are the dominant factors to improve the removal rate of Pb(II) by density functional theory calculations. This study clarifies the value of self-designed novel organic ligands in metal-organic framework materials that selectively capture heavy-metal ions.

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