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cc-by-nc-nd (c) Elsevier, 2020
Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/165140

In-situ dosage of Fe2+ catalyst using natural pyrite for thiamphenicol mineralization by photoelectro-Fenton process

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The degradation of the antibiotic thiamphenicol has been studied by photoelectro-Fenton (PEF) process with UVA light using pyrite particles as catalyst source. Pyrite is a sulfide mineral that naturally acidifies the reaction medium and releases Fe2+, thus promoting the effective generation of ¿OH from Fenton's reaction. The assays were made in an IrO2/air-diffusion cell, which yielded similar results to a boron-doped diamond (BDD)/air-diffusion one at a lower cost. In dark conditions, electro-Fenton (EF) process showed an analogous ability for drug removal, but mineralization was much poorer because of the large persistence of highly stable by-products. Their photolysis explained the higher performance of PEF. Conventional homogeneous PEF directly using dissolved Fe2+ exhibited a lower mineralization power. This suggests the occurrence of heterogeneous Fenton's reaction over the pyrite surface. The effect of current density and drug content on pyrite-catalyzed PEF performance was examined. The drug heteroatoms were gradually converted into SO42-, Cl- and NO3- ions. Nine aromatic derivatives and two dichloroaliphatic amines were identified by GC-MS, and five short-chain carboxylic acids were detected by ion-exclusion HPLC. A reaction route for thiamphenicol mineralization by PEF process with continuous H2O2 and Fe2+ supply on site is proposed.

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THIAM, Abdoulaye, et al. In-situ dosage of Fe2+ catalyst using natural pyrite for thiamphenicol mineralization by photoelectro-Fenton process. Journal of Environmental Management. 2020. Vol. 270, num. 110835. ISSN 0301-4797. [consulted: 18 of June of 2026]. Available at: https://hdl.handle.net/2445/165140

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