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Photocatalytic degradation of cefotaxime pharmaceutical compounds onto a modified nanocatalyst

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Abstract

The photocatalytic advanced oxidation process as treatment for the removal of cefotaxime pharmaceutical compounds was conducted onto a modified nanocatalyst. Using photocatalysis with hydrogen peroxide (H2O2) in advanced oxidation processes (AOPs) is a suitable and alternative method. Therefore, this study targeted acquiring insights into using ultraviolet (UV) light radiation sources with two types of nanocatalysts (i.e., TiO2 and TiO2/kaolin) to reduce cefotaxime contaminants. The characterization properties of both catalysts were determined using X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET), and Fourier-transform infrared spectroscopy (FT-IR). The study investigated the effects of the irradiation time (10–120 min), cefotaxime concentration (10–40 mg/L), TiO2 dose (0.05–0.2 g), and pH (4–8) on the decomposition cefotaxime. The highest degradation with pure TiO2 was obtained at a contact time of 90 min, cefotaxime concentration of 10 mg/L, TiO2 dose of 0.2 g, and a pH of 4, with a removal efficiency of almost 68%. The results indicated that cefotaxime can easily be oxidized with a TiO2/kaolin catalyst with a removal efficiency of approximately 99.8% when using a UV/H2O2 treatment. The UV/H2O2 oxidation was more effective and sustainable as well as being a promising technique for the treatment of cefotaxime in wastewater.

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Acknowledgements

The authors wish to thank the Department of Chemical Engineering, University of Technology- Iraq, Baghdad, Iraq, Mustansiriyah University/College of Engineering/Materials Engineering Department Baghdad-Iraq, and Department of Chemical and Petroleum Industries Engineering, Al-Mustaqbal University College, Babylon, Iraq.

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Correspondence to Talib M. Albayati.

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Abbood, N.S., Ali, N.S., Khader, E.H. et al. Photocatalytic degradation of cefotaxime pharmaceutical compounds onto a modified nanocatalyst. Res Chem Intermed 49, 43–56 (2023). https://doi.org/10.1007/s11164-022-04879-3

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