Organic contaminants degradation by modification carbon felt derived from Mn, Fe layered double hydroxide cathode
Year: 2025
Type: article
Abstract: The traditional electro-Fenton (EF) process faced significant challenges, including a narrow pH range and poor catalyst reusability. The heterogeneous electro-Fenton (EF) process was a promising wastewater treatment technology because it generated H2O2 in situ and operated over a wide pH range without producing metal sludge. In this study, Mn-Fe layered double hydroxide (MnFe-LDH) electrodes were fabricated on carbon felt by an in situ hydrothermal method and were applied as cathodes for the heterogeneous electro-Fenton process to degrade organic pollutants, including antibiotics (oxytetracycline, levofloxacin, ciprofloxacin) and tartrazine dye. The surface morphology and structure of the catalyst were analysed by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and contact angle measurements. The results showed that 58.45–96.01% of the pollutants were decomposed under natural pH conditions after 120 minutes at a current intensity of 24 mA, pollutant concentration of 10 mg/L, and 50 mM Na2SO4 as the electrolyte. The MnFe-LDH/CF cathode demonstrated high durability and reusability. It could be applied in the electro-Fenton process to remove organic pollutants that were difficult to biodegrade in aqueous environments.
Authors: Bui Nguyen Thu Ha, Phan Quang Thang, Nguyen Nhat Huy, Nguyen Tien Loi, Nguyen Quang Vinh, Nguyen Trung Dung
Institutions: Hanoi University of Natural Resources and Environment, Graduate University of Science and Technology, Vietnam Academy of Science and Technology, Viện Khoa học công nghệ Năng lượng và Môi trường, Vietnam National University Ho Chi Minh City, Ho Chi Minh City University of Technology, Le Quy Don Technical University
Language: English
Subfield: Water Science and Technology
Field: Environmental Science
Domain: Physical Sciences
Open Access status: hybrid
Award: G5301756415
OpenAlex ID: W4415043300
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