Abstract
In this study, the synergetic adsorption and Fenton-like degradation of tetracycline hydrochloride (TCH) by magnetic spent bleaching earth carbon (Mag-SBE@C) with H2O2 were developed and performed, with 91.5% of TCH degradation efficiency and 42.1% of TOC removal efficiency. The effects of the reaction parameters (temperature, initial pH, catalyst dosage, molar ratio of TCH to H2O2) on TCH degradation in Mag-SBE@C/H2O2 system were studied. Under the optimal conditions (temperature 41.1 °C, initial pH 4.89 and molar ratio of H2O2 to TCH 114.435) forecasted by response surface methodology (RSM), high TCH degradation efficiency (99%) was achieved. Also, four cycling tests were performed to confirm the excellent stability and regeneration ability of Mag-SBE@C in presence of H2O2. In addition, the characteristics of Mag-SBE@C after reaction are analyzed in details via scanning electron microscope (SEM), energy dispersive spectrometer (EDS), Brunner-Emmet-Teller (BET), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectrum (FTIR) and X-ray diffraction (XRD), and it was found that Fe3O4 nanoparticles on Mag-SBE@C surface acted as co-catalyst and participated in degradation and improved reaction efficiency, while its properties were not greatly changed. The quenching experiments showed that hydroxyl radicals on Mag-SBE@C surface (OHadsorption) were dominant in Mag-SBE@C/H2O2 system. Meanwhile, three possible TCH degradation pathways were given based on the possible intermediates determined by liquid chromatography quadrupole-time-of-flight mass spectrometry (LC-Q-TOF-MS/MS). Mag-SBE@C is an excellent heterogeneous Fenton-like catalyst, exhibiting greatly potential to antibiotics elimination.
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