Organic contaminants degradation by modification carbon felt derived from Mn, Fe layered double hydroxide cathode

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.

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Publication Details

Journal
Vietnam Journal of Catalysis and Adsorption
Published
2025-09-30
DOI
https://doi.org/10.62239/jca.2025.040
Primary Topic
Water Quality Monitoring and Analysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Organic contaminants degradation by modification carbon felt derived from Mn, Fe layered double hydroxide cathode

Nguyễn Nhật Huy, N. Q. Vinh, N. N. Loi, Phan Quang Thang et al.
Vietnam Journal of Catalysis and Adsorption
Water Quality Monitoring and Analysis
article

Organic contaminants degradation by modification carbon felt derived from Mn, Fe layered double hydroxide cathode

Nguyễn Nhật Huy, N. Q. Vinh, N. N. Loi, Phan Quang Thang, Nguyen Trung Dung, B. Ha
article en

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.

Vietnam Journal of Catalysis and AdsorptionVol. 14(3)
Vietnam National University Ho Chi Minh City (VN), Le Quy Don Technical University (VN), Ho Chi Minh City University of Technology (VN), Vietnam Academy of Science and Technology (VN)
National Foundation for Science and Technology Development
Openalex Percentile: Top 65%
Water Quality Monitoring and Analysis
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Organic contaminants degradation by modification carbon felt derived from Mn, Fe layered double hydroxide cathode — Nguyễn Nhật Huy, N. Q. Vinh, et al. · Vietnam Journal of Catalysis and Adsorption (2025) | TGRS Research Map | TGRS