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Updated: Sep 27, 2025

Author Spotlight: Functionalizing Metal-Organic Frameworks: Advancements, Challenges, and the Power of Post-Synthetic Ligand Exchange
Published on: June 23, 2023
Effective defluoridation of water using nanosized UiO-66-NH2 encapsulated within macroreticular polystyrene anion
Wenxiang Ni1, Haoran Dai1, Guanwen Ding1
1Collaborative Innovation Center of Atmospheric Environment and Equipment Technology, Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, School of Environmental Science and Engineering, Nanjing University of Information Science & Technology, 219 Ningliu Road, Nanjing, 210044, China.
Abstract:
Environmental concerns associated with the efficient defluoridation of contaminated water remain a substantial challenge. In this work, a new nanocomposite, UiO-66-NH2@PS+, was successfully fabricated via in situ precipitation of a water-stable metal-organic framework (UiO-66-NH2) inside a commercial polystyrene anion exchanger PS+. The as-formed nanocomposite UiO-66-NH2@PS+ was characterized using various morphological methods, which demonstrated that nanosized UiO-66-NH2 was homogenously dispersed within the inner pores of PS+. Batch adsorption experiments indicated that UiO-66-NH2@PS+ exhibited outstanding adsorption performance for fluoride over a broad pH range of 3.0-8.0. The saturated adsorption capacity of fluoride at 298 K was 27.5 and 32.8 mg/g for pH 6.5 and 4.5 with the adsorbent dosage of 0.5 g/L and initial concentration of 5-80 mg/L. Moreover, the utilization rate of active adsorption sites of UiO-66-NH2 was greatly improved after encapsulation. The XPS study indicated that the integrated effects of specific inner-sphere coordination and ligand exchange between fluoride and UiO-66-NH2 might be the dominant adsorption mechanism. Fixed-bed tests indicated that the UiO-66-NH2@PS+ column could successively produce clean water with bed volumes of 350 and 70 ([F-] <1.5 mg/L) from simulated fluoride-pollution water at pH 4.5 and 8.0, with a liquid velocity of 20 mL/h, and an empty bed contact time (EBCT) of 15 min, which was higher than that of the other materials. In addition, the exhausted UiO-66-NH2@PS+ was regenerated and reused for 5 times through complete regeneration, highlighting the potential feasibility of defluorination in practical applications.
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