摘要
The stability, versatility, and reusability of an adsorbent are of great significance to its practicability to remove antibiotics from water due to their universal residual. Herein, a magnetic composite of nano-iron wrapped by graphitic carbon in the carbonaceous matrix with hierarchical pores (Fe in /C-700) was constructed by one-step pyrolysis using Fe in /Zn-MOF as a precursor. Fe in /C-700 exhibited a core–shell structure and superparamagnetism behavior, which showed excellent chlortetracycline (CTC) adsorption with the maximum adsorption capacity of 546.5 mg/g. The adsorption process matched well with the pseudo-second-order kinetics model and Langmuir model, indicating chemisorption was likely contributed to the CTC adsorption. Electrostatic interaction, surface complexation, hydrogen bond, and π-π EDA interaction were the dominant driving forces. Cl - and SO 4 2- significantly enhanced the CTC adsorption due to the electrostatic attraction or hydrogen bond formed among Fe in /C-700, anions, and CTC. Fe in /C-700 maintained high adsorption capacities in the mixed antibiotic system (255.1, 143.3, and 169.6 mg/g for CTC, ciprofloxacin, and sulfamethoxazole), in actual water (372.9, 383.3, 390.6, and 366.7 mg/g for CTC in Pearl River water, lake water, tap water, and ultrapure water), and regeneration (366.7, 354.2, 360.4, 314.6, and 301.0 mg/g for CTC in five runs), indicating a promising reusable adsorbent for the remediation of antibiotics in water. These findings provide a feasible and straightforward strategy to synthesize high stable magnetic nanoparticles derived from MOFs.
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