4.7 Article

Hydrothermal synthesis of CuCoFe layered double hydroxide and its performance in the degradation of antibiotics: Influencing factors, degradation pathways, and reaction mechanism

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ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2023.110127

Keywords

Hydrothermal; CuCoFe-LDH; Antibiotics; PMS activation; Superoxide; Singlet oxygen

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In this study, the CuCoFe-LDH catalyst was synthesized by hydrothermal method and used for degrading levo-floxacin (LFX) using peroxymonosulfate (PMS) activation. Various factors influencing the degradation of LFX were systematically investigated. The CuCoFe-LDH/PMS system showed high efficiency in removing LFX over a wide pH range and could effectively degrade different groups of antibiotics.
In this study, the CuCoFe-LDH catalyst was synthesized by hydrothermal method and applied to degrade levo-floxacin (LFX) by peroxymonosulfate (PMS) activation. The physicochemical properties of the synthesized samples were analyzed by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Brunauer-Emmett-Teller (BET), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA). The influence of various factors such as catalyst system, pH, catalyst content, PMS, pH, and coexisting ions on the degradation of LFX was system-atically investigated. The results showed that after 10 min, 94.57 % of LFX was decomposed under the conditions of 200 mg/L of catalyst, 500 mg/L of PMS, 10 mg/L of LFX, and pH 7.0. Besides, the CuCoFe-LDH/PMS system can effectively remove LFX over a wide pH range from 3.5 to 9.0. Both radical superoxide (O2 & BULL;-) and non-radical singlet oxygen (1O2) were major reactive oxygen species in the CuCoFe-LDH/PMS system. Mass spectrometry identified 16 major degradation products of LFX, and 38.43 % of LFX was mineralized after 30 min of reaction. Besides, the CuCoFe-LDH/PMS system had the ability to effectively degrade different groups of antibiotics (e.g., fluoroquinolone, tetracycline, and sulfonamide). The mechanism of PMS activation by CuCoFe-LDH and the LFX degradation pathway were proposed. Finally, testing the reusability of CuCoFe-LDH in LFX degradation showed that a decrease of nearly 7 % occurred after five consecutive cycles, suggesting its stability for practical applications.

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