The catalytic performance of modified hydroxyapatite nanoparticles, CaFeW(PO)(OH), was applied for the degradation of methylene blue (MB), fast green FCF (FG) and norfloxacin (NOR). XPS analysis pointed to the successful partial replacement of Ca by Fe. Under photo-electro-Fenton process, the catalyst CaFeWFe(PO)(OH) was combined with UVC radiation and electrogenerated HO in a Printex L6 carbon-based gas diffusion electrode. The application of only 10 mA cm resulted in 100% discoloration of MB and FG dyes in 50 min of treatment at pH 2.5, 7.0 and 9.0. The proposed treatment mechanism yielded maximum TOC removal of ∼80% and high mineralization current efficiency of ∼64%. Complete degradation of NOR was obtained in 40 min, and high mineralization of ∼86% was recorded after 240 min of treatment. Responses obtained from LC-ESI-MS/MS are in line with the theoretical Fukui indices and the ECOSAR data. The study enabled us to predict the main degradation route and the acute and chronic toxicity of the by-products formed during the contaminants degradation.
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http://dx.doi.org/10.1016/j.chemosphere.2024.142515 | DOI Listing |
Chemosphere
February 2025
São Carlos Institute of Chemistry, University of São Paulo, Avenida Trabalhador São Carlense, 400, São Carlos, 13566-590, Brazil. Electronic address:
The present work investigated the application of UVC combined with electrogenerated HO (UVC/e-HO) for BTA degradation using a Printex L6 carbon-based (PL6C) gas diffusion electrode (GDE). The studies were carried out by analyzing the influence of the current density, pH and initial BTA concentration in the contaminant degradation process. Under optimal conditions using 0.
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August 2024
Faculty of Exact Sciences and Technology - FACET, Federal University of Grande Dourados - UFGD, Rodovia Dourados-Itahum, Km 12, Dourados,MS, 79804-970, Brazil. Electronic address:
The catalytic performance of modified hydroxyapatite nanoparticles, CaFeW(PO)(OH), was applied for the degradation of methylene blue (MB), fast green FCF (FG) and norfloxacin (NOR). XPS analysis pointed to the successful partial replacement of Ca by Fe. Under photo-electro-Fenton process, the catalyst CaFeWFe(PO)(OH) was combined with UVC radiation and electrogenerated HO in a Printex L6 carbon-based gas diffusion electrode.
View Article and Find Full Text PDFChemosphere
March 2024
Centre of Natural and Human Sciences, Federal University of ABC. Rua Santa Adélia 166, Bairro Bangu, 09210-170, Santo André, SP, Brazil. Electronic address:
Hydrogen peroxide (HO) stands as one of the foremost utilized oxidizing agents in modern times. The established method for its production involves the intricate and costly anthraquinone process. However, a promising alternative pathway is the electrochemical hydrogen peroxide production, accomplished through the oxygen reduction reaction via a 2-electron pathway.
View Article and Find Full Text PDFWater Environ Res
January 2024
School of Environmental Science and Technology, Dalian University of Technology, Dalian, China.
In this study, a novel photocatalytic fuel cell electro-Fenton (PFC-EF) system was constructed using g-C N @N-TNA and Ag/CNT@CF as electrodes. The composition, structure, and morphology of the electrodes were obtained. The g-C N @N-TNA, with its 2.
View Article and Find Full Text PDFSci Total Environ
February 2024
Laboratori d'Electroquímica dels Materials i del Medi Ambient, Departament de Ciència de Materials i Química Física, Secció de Química Física, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona, Spain. Electronic address:
The decolorization and TOC removal of solutions of Acid Brown 14 (AB14) diazo dye containing 50 mg L of total organic carbon (TOC) have been first studied in a continuous-flow electrocoagulation (EC) reactor of 3 L capacity with Fe electrodes of ∼110 cm area each. Total loss of color with poor TOC removal was found in chloride, sulfate, and/or hydrogen carbonate matrices after 18 min of this treatment. The best performance was found using 5 anodes and 4 cathodes of Fe at 13.
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