Work

Enhanced visible-light-driven degradation of tetracycline via photocatalysis and photo-Fenton processes using B-TiO2/Fe3O4 composites

Year: 2025
Type: article
Abstract: The persistence of antibiotic pollutants in aquatic environments poses a significant threat to public health and ecosystems, driving the need for effective solar-driven water treatment technologies. This study synthesized and evaluated a series of black titanium oxide (B-TiO2) and B-TiO2/Fe3O4 composites for the visible-light-driven degradation of tetracycline, via photocatalysis and photo-Fenton processes. B-TiO2 was prepared through NaBH4-assisted reduction, introducing Ti3+ species and oxygen vacancies that narrowed the bandgap and enhanced visible-light absorption. Fe3O4 was incorporated via co-precipitation in varying proportions (12.5–50 wt%), generating heterostructures that improved charge separation and Fenton reaction. Comprehensive characterization by Transmission Electron Microscopy, x-ray Diffraction, Ultraviolet–Visible Diffuse Reflectance Spectroscopy and x-ray Photoelectron Spectroscopy confirmed the structural, optical, and surface chemical features responsible for enhanced photocatalytic activity. Photocatalytic degradation tests revealed that the composite sample B-TiO2 with 12.5% of Fe3O4 (BT-Fe12.5) exhibited the highest activity under visible light, attributed to improved light harvesting and heterojunction-assisted charge transfer. However, under photo-Fenton conditions, performance increased with Fe3O4 content, the composite sample B-TiO2 with 50% of Fe3O4 (BT-Fe50) achieving the highest rate constant (k = 0.02867 min−1) and shortest half-life (∼24 min), due to enhanced hydroxyl radical generation. This work demonstrates the synergistic mechanism and tunability of B-TiO2/Fe3O4 composites, highlighting their dual functionality and potential for cost-effective, sunlight-driven antibiotic removal from water.
Source: Nano Express
Language: English
Field: Energy
Open Access status: gold
Estimated APC paid: $2,185
OpenAlex ID: W4414229784
FWCI:
Cites: 69
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