Tungsten/bismuth – based catalysts for the degradation of 5-fluorouracil cytostatic drug in water by solar-LED photocatalysis
Yaah, Velma Beri Kimbi; Pastrana-Martínez, L. M.; Maldonado-Hódar, F. J.; Morales-Torres, S. (2025-03-17)
Yaah, Velma Beri Kimbi
Pastrana-Martínez, L. M.
Maldonado-Hódar, F. J.
Morales-Torres, S.
Elsevier
17.03.2025
Yaah, V. B. K., Pastrana-Martínez, L. M., Maldonado-Hódar, F. J., & Morales-Torres, S. (2025). Tungsten/bismuth – based catalysts for the degradation of 5-fluorouracil cytostatic drug in water by solar-LED photocatalysis. Environmental Technology & Innovation, 38, 104148. https://doi.org/10.1016/j.eti.2025.104148.
https://creativecommons.org/licenses/by/4.0/
© 2025 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
© 2025 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:oulu-202504232862
https://urn.fi/URN:NBN:fi:oulu-202504232862
Tiivistelmä
Abstract
A new series of photocatalysts, including WO₃, Bi₂O₃ and Bi₂WO₆, were prepared for the photo-oxidation of 5-Fluorouracil (5-FU) in water, as a model of cytostatic drug, under solar-LED irradiation. The materials were hydrothermally prepared under the same experimental conditions, and the effect of incorporating an activated carbon during the synthesis and further post-treatments in air or nitrogen atmosphere were investigated. All photocatalysts were thoroughly characterized by complementary techniques analyzing their morphologies and physicochemical properties, which differed based on the type of semiconductor used. In general, the addition of carbon led to an increased porosity (\(\text{S}_{\text{BET}}\)= 20–50 m²/g), a reduced band gap (Eg= 2.7–2.9 eV) and a lower crystallite size compared to the original semiconductor. The photocatalytic performance of the materials depended also on the thermal post-treatment, while N₂ treatment improved the efficiency of Bi-carbon composites, the air treatment did not influence the pure semiconductors. The 5-FU degradation varied as WO₃ (10 %) < Bi₂WO₆ (36 %) < Bi₂O₃ (68 %) after 100 min under solar-LED irradiation, while their corresponding carbon-metal composites always improved the performance. In particular, the conversion of 5-FU after 100 min of reaction was 64 % and 84 % for Bi₂WO₆-3C and Bi₂WO₆-3C-n, while the carbon-Bi₂O₃ composite achieved total photodegradation of 5-FU (\(k_{app}\)= 43.89 ×10⁻³ min⁻¹) after ∼100 min of reaction and under solar-LED irradiation.
A new series of photocatalysts, including WO₃, Bi₂O₃ and Bi₂WO₆, were prepared for the photo-oxidation of 5-Fluorouracil (5-FU) in water, as a model of cytostatic drug, under solar-LED irradiation. The materials were hydrothermally prepared under the same experimental conditions, and the effect of incorporating an activated carbon during the synthesis and further post-treatments in air or nitrogen atmosphere were investigated. All photocatalysts were thoroughly characterized by complementary techniques analyzing their morphologies and physicochemical properties, which differed based on the type of semiconductor used. In general, the addition of carbon led to an increased porosity (\(\text{S}_{\text{BET}}\)= 20–50 m²/g), a reduced band gap (Eg= 2.7–2.9 eV) and a lower crystallite size compared to the original semiconductor. The photocatalytic performance of the materials depended also on the thermal post-treatment, while N₂ treatment improved the efficiency of Bi-carbon composites, the air treatment did not influence the pure semiconductors. The 5-FU degradation varied as WO₃ (10 %) < Bi₂WO₆ (36 %) < Bi₂O₃ (68 %) after 100 min under solar-LED irradiation, while their corresponding carbon-metal composites always improved the performance. In particular, the conversion of 5-FU after 100 min of reaction was 64 % and 84 % for Bi₂WO₆-3C and Bi₂WO₆-3C-n, while the carbon-Bi₂O₃ composite achieved total photodegradation of 5-FU (\(k_{app}\)= 43.89 ×10⁻³ min⁻¹) after ∼100 min of reaction and under solar-LED irradiation.
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