BackgroundCiprofloxacin (CIP) antibiotic, classified as an emerging organic contaminant, has caused an adverse impact on the ecological environment due to its persistence. MethodsIn this study, CIP was adsorbed on a novel nanocomposite using lanthanum ferrite spinel nanoparticles (LaFe2O4 NPs) dispersed on litchi shell-derived biochar supporter (BLF) with various loading ratios. The adsorption tests were conducted in batch mode to thoroughly investigate operational parameter effects. In addition, the adsorption kinetics, isotherms, and thermodynamics of CIP onto BLF at various temperatures were systematically studied. The as-synthesized adsorbent was thoroughly characterisized. Finally, CIP adsorption mechanisms onto BLF were revealed. Significant FindingsOur findings showed that the pristine biochar (PBC) was loaded by LaFe2O4, which resulted in more thorough carbonization, enhanced aromaticity, hydrophobicity, porosity, and enriched surface functional groups. The CIP adsorption onto BLF was the highest under optimal operational conditions of solution pH of 5.0, 3.0 g/L biochar dosage, and 50 mg/L initial CIP concentration. The pseudo-second order model best matched the CIP adsorption kinetics with high correlation coefficients of 0.9653-0.9939. The Langmuir model better described the adsorption behaviors of CIP on BLF, with a maximum adsorption capacity of 36.5 mg/g, which was greater than that on PBC by about 1.5 times. CIP adsorption on the BLF exhibited a spontaneous and endothermic nature. The primary mechanisms of CIP adsorption on the BLF were H-bonding and π-π interaction. In particular, La and Fe constituents in BLF functionally enhanced the CIP adsorption via the surface complexation mechanism. These findings illustrated that the BLF was a novel, feasible, and promising adsorbent for the effective removal of CIP antibiotics from water.
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