Post-synthesis introduction of dual functional groups in metal–organic framework for enhanced adsorption of moxifloxacin antibiotic

Highly effective removal of antibiotics from aqueous solution is of importance while still faces challenge. Herein, we report a novel metal-organic framework (MOF) adsorbent, MOF-808-SIPA (SIPA, 5-sulfoisophthalic acid), constructed via post-synthesis exchange strategy. On the basis, dual active groups including sulfonic acid and carboxyl groups are successfully introduced. The novel MOF-808-SIPA exhibits a high adsorption capacity of 287.1 mg g-1 for moxifloxacin hydrochloride (MOX·HCl), superior to that (174.6 mg g-1) of the pristine MOF-808-AA (AA, acetic acid). Besides, MOF-808-SIPA shows rapid adsorption equilibrium of ∼ 30 min, strong anti-interference ability from pH and inorganic ions, and feasible regeneration. The superiority renders MOF-808-SIPA a potential adsorbent for MOX removal. Density function theory (DFT) calculation and experiment confirm that H-bond interaction contributes largely to the excellent adsorption in MOF-808-SIPA. Our work provides a guideline for designing high-efficiency MOF-based adsorbent.