摘要
The widespread use of antibiotics has led to their accumulation in water, posing serious environmental risks. Biochar has emerged as a promising adsorbent for antibiotic removal, but its performance is often limited by low capacity and slow kinetics, especially for high-molecular-weight antibiotics. In this study, a hierarchical porous Fe-supported biochar (HPFeBC) was synthesized via one-step pyrolysis of pine sawdust using Fe(NO 3 ) 3 as both activator and template. The obtained HPFeBC exhibited a well-interconnected pore structure with a high surface area (417.23 m 2 /g) and enhanced mesoporosity, significantly improving mass transfer and accessibility of adsorption sites. HPFeBC demonstrated exceptional adsorption performance for both low-molecular-weight antibiotic tetracycline (TC) and high-molecular-weight antibiotic tylosin (TYL), with maximum capacities of 361.23 mg/g and 173.61 mg/g, respectively. Notably, HPFeBC achieved rapid adsorption equilibrium within 5 mins for TC and 30 mins for TYL, far surpassing commercial adsorbents. The adsorption process followed the pseudo-second-order kinetics and the Freundlich isotherm model, and thermodynamic analysis confirmed the spontaneous and endothermic nature of adsorption. The adsorption mechanism involved pore filling, π-π interactions, hydrogen bonding, surface complexation, and limited redox reaction. HPFeBC also exhibited excellent stability over a wide pH range, strong anti-interference ability, and good reusability. Overall, the synthesis HPFeBC can act as an effective candidate for rapid and efficient removal of antibiotics from water.
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