| Literature DB >> 27856058 |
Α Koltsakidou1, M Antonopoulou2, Ε Εvgenidou1, I Konstantinou3, A E Giannakas2, M Papadaki2, D Bikiaris1, D A Lambropoulou4.
Abstract
In the present study, the photocatalytic activity of TiO2-based photocatalysts toward degradation and mineralization of the anti-cancer drug 5-fluorouracil (5-FU) in aqueous phase was investigated under simulated solar and visible irradiation. Commercial TiO2 (P25) and N/S-doped TiO2 catalysts synthesized by a simple sol-gel method were used as photocatalysts. TiO2 P-25 was found to be the most photoactive catalyst for the removal of 5-FU, under simulated solar irradiation. Among N/S-doped TiO2 catalysts, the one with molar Ti:N/S ratio equal to 0.5 was the most efficient under simulated solar irradiation. In contrast, under visible irradiation the catalyst with equimolar Ti:N/S ratio showed the highest performance for the removal of 5-FU. Scavenging experiments revealed that HO radicals and h+ were the major reactive species mediating photocatalytic degradation of 5-FU using TiO2 P-25 and N/S-doped TiO2 catalysts, under simulated solar irradiation. On the other hand, the essential contribution of 1O2 and O2- in the degradation of 5-FU under visible light was proved. The transformation products (TPs) of 5-FU, were identified by LC-MS-TOF suggesting that defluorination followed by hydroxylation and oxidation are the main transformation pathways, under all the studied photocatalytic systems.Entities:
Keywords: 5-Fluorouracil; N/S-doped TiO(2) catalysts; Scavengers; TiO(2); Transformation products
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Year: 2016 PMID: 27856058 DOI: 10.1016/j.scitotenv.2016.08.208
Source DB: PubMed Journal: Sci Total Environ ISSN: 0048-9697 Impact factor: 7.963