Abstract

ZrⅣ-based metal–organic frameworks (MOFs)–featuring exceptional water stability, large surface area, and structural tunability–hold promise for efficient antibiotics adsorption from water. However, their inherent positive charge in neutral environments and the harsh conditions required for their synthesis hinder their effective removal of cationic antibiotics. To address this challenge, a green one-pot synthesis approach was proposed to fabricate phosphotungstic acid-functionalized MOF-808 (termed as PTA@MOF-808) at room temperature for elevated antibiotic adsorption. This approach not only leverages the strong electronegativity of PTA to improve electrostatic interactions and π-π stacking but also finely tailors the pore size of MOF-808, resulting in enhanced adsorption capacity of PTA@MOF-808. The influence of PTA loading, solution pH, and absorbent dosage on the performance of PTA@MOF-808 were studied in detail. Adsorption experiments demonstrated that PTA@MOF-808 outperformed unmodified MOF-808 in removing various positively charged antibiotics, with 5 % PTA@MOF-808 exhibiting maximum adsorption capacities of 548.1 mg g−1 and 482.9 mg g−1, for DOX and TCHC, respectively. The adsorption process followed the Langmuir isothermal model and the pseudo-second-order kinetic equation. Furthermore, the composite PTA@MOF-808 displayed excellent reusability after multiple adsorption–desorption cycles. These findings highlight the potential of PTA@MOF-808 as a promising absorbent for removing specific antibiotics from water, with significant implications for wastewater treatment.

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