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Synergistic oxidation induced by underwater bubbling plasma and diatomite-CoFeO activated peroxymonosulfate for the degradation of ciprofloxacin hydrochloride. | LitMetric

Synergistic oxidation induced by underwater bubbling plasma and diatomite-CoFeO activated peroxymonosulfate for the degradation of ciprofloxacin hydrochloride.

Environ Pollut

School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300350, China. Electronic address:

Published: May 2024

Underwater bubbling plasma (UBP) coupled with diatomite-CoFeO (Dt-CFO) activated peroxymonosulfate (PMS) was proposed for the degradation of ciprofloxacin hydrochloride (CIP) in this work. The catalyst sample of Dt-CFO with large specific surface area, rich active sites and excellent magnetic property was prepared by the hydrothermal method and systematically characterized to investigate its material properties. The combination of UBP and Dt-CFO activated PMS (UBP/Dt-CFO/PMS) showed excellent synergy with the synergistic factor of 1.98, and reached the CIP degradation percentage of 94.7%, which corresponded to the kinetic constant of 0.097 min. Dt-CFO with the diatomite content of 30 wt% achieved the best catalytic activity in the reaction system. Higher catalyst and PMS dose, peak voltage, pulse frequency and lower initial CIP concentration were beneficial for CIP removal. The addition of Cl, HCO, SO and humic acid suppressed CIP degradation, while NO had no effect on CIP removal. The Dt-CFO composite exhibited excellent reusability and low leaching metal amount, demonstrating its good stability. SO·, ·OH, ·O, O, e, O and HO were the active species confirmed to be involved in CIP degradation. The redox circles of ≡ Co(Ⅱ)/≡Co(Ⅲ) and ≡ Fe(Ⅱ)/≡Fe(Ⅲ) on Dt-CFO surface and the plasma-induced physicochemical effects dominated PMS activation. The decomposition process of CIP was explored through fluorescence spectra. Three degradation pathways were inferred, and the toxicity analysis showed the toxicity of CIP solution weakened after discharge treatment.

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http://dx.doi.org/10.1016/j.envpol.2024.123891DOI Listing

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