Photosensitivity of ferrate(VI) in tetracycline degradation: role of solar irradiation and reactive species

The purpose of this study was to investigate the photosensitivity of hexavalent ferrate(VI) [Fe(VI)] and identify its main reactive species during pollutant degradation under solar irradiation. Using tetracycline hydrochloride (TC) as the target pollutant, the degradation efficiency of Fe(VI) was evaluated under dark, simulated solar, natural sunlight, and ultraviolet (UV) conditions. The degradation efficiency reached 81.4% under simulated solar, 80.3% under natural solar, and 76.7% under UV, versus 73.24% in the dark. The results demonstrated that compared with the UV-Fe(VI) process, the solar-Fe(VI) process achieved a higher TC degradation rate. Singlet oxygen was identified as the main reactive species responsible for enhancing the efficiency of Fe(VI)-mediated TC degradation under solar irradiation. Furthermore, visible light exerted no significant promotional effect on the self-decomposition of Fe(VI), whereas UV light significantly accelerated this process.

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Publication Details

Journal
Environmental Technology
Published
2026-04-07
DOI
https://doi.org/10.1080/09593330.2026.2648630
Primary Topic
Advanced oxidation water treatment
Type
article
Field-Weighted Citation Impact
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article

Photosensitivity of ferrate(VI) in tetracycline degradation: role of solar irradiation and reactive species

Linhao Fan, Naidong Zhang, Jiarui Xu
Environmental Technology
Advanced oxidation water treatment
article

Photosensitivity of ferrate(VI) in tetracycline degradation: role of solar irradiation and reactive species

Linhao Fan, Naidong Zhang, Jiarui Xu
article en

Abstract

The purpose of this study was to investigate the photosensitivity of hexavalent ferrate(VI) [Fe(VI)] and identify its main reactive species during pollutant degradation under solar irradiation. Using tetracycline hydrochloride (TC) as the target pollutant, the degradation efficiency of Fe(VI) was evaluated under dark, simulated solar, natural sunlight, and ultraviolet (UV) conditions. The degradation efficiency reached 81.4% under simulated solar, 80.3% under natural solar, and 76.7% under UV, versus 73.24% in the dark. The results demonstrated that compared with the UV-Fe(VI) process, the solar-Fe(VI) process achieved a higher TC degradation rate. Singlet oxygen was identified as the main reactive species responsible for enhancing the efficiency of Fe(VI)-mediated TC degradation under solar irradiation. Furthermore, visible light exerted no significant promotional effect on the self-decomposition of Fe(VI), whereas UV light significantly accelerated this process.

Environmental TechnologyVol. 47(12)
Dalian Maritime University (CN)
Openalex Percentile: Top 33%
Advanced oxidation water treatment
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