CuO/ZnFe2O4 heterostructure as efficient catalyst for NaBH4 - assisted reduction of Chloramphenicol

Submitting author affiliation:
University of Sciences, Hue University, Hue, Viet Nam

Beilstein Arch. 2026, 202620. https://doi.org/10.3762/bxiv.2026.20.v1

Published 26 Jun 2026

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Abstract

In this study, CuO/ZnFe2O4 heterostructure in the form of flower, consisting of CuO nanorods anchored on ZnFe2O4 microspheres, was successfully synthesized and evaluated for its catalytic reduction of chloramphenicol (CAP) in the presence of NaBH4. Structural and morphological analysis confirmed the successful formation of the heterostructure with enhanced contact between ZnFe2O4 and CuO. Compared to pure ZnFe2O4, the CuO/ZnFe2O4 catalyst exhibited significantly improved catalytic activity for CAP reduction. The reduction efficiency was strongly influenced by reaction conditions, with optimal performance achieved at pH 6, a catalyst dosage of 2.5 g/L, and a short reaction time of 20 minutes. The enhanced catalytic performance under mild, environmentally friendly conditions highlights the crucial role of CuO in promoting surface electron transfer and facilitating reduction. Kinetic analysis at room temperature revealed a shift from pseudo-first-order to zero-order kinetics throughout the reaction, suggesting surface-mediated catalysis. This evolution indicates that decatalysis is primarily governed by a surface-mediated Langmuir–Hinshelwood mechanism. Overall, the CuO/ZnFe2O4 heterostructure shows significant potential as an efficient catalyst for rapid CAP reduction under neutral conditions, offering a promising strategy for wastewater treatment. 

Keywords: ZnFe2O4, CuO, Chloramphenicol, catalytic, reduction, NaBH4

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When a peer-reviewed version of this preprint is available, this information will be updated in the information box above. If no peer-reviewed version is available, please cite this preprint using the following information:

Le, H. T.; Nguyen, H. T. T.; Le, V. Q.; Trinh, D. N.; Nguyen, C. D.; Le, N. T. T.; Tran, H. T. Beilstein Arch. 2026, 202620. doi:10.3762/bxiv.2026.20.v1

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