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Título
Effect of dopants on the structure of titanium oxide used as a photocatalyst for the removal of emergent contaminants
Autor(es)
Palabras clave
Doped titanium oxide
Sol–gel method
Emerging contaminants removal
Photocatalysis
Clasificación UNESCO
2303 Química Inorgánica
Fecha de publicación
2017-09
Citación
A. Gil, A.M. García, M. Fernández, M.A. Vicente, B. González-Rodríguez, V. Rives, S.A. Korili,
Effect of dopants on the structure of titanium oxide used as a photocatalyst for the removal of emergent contaminants,
Journal of Industrial and Engineering Chemistry,
Volume 53,
2017,
Pages 183-191,
ISSN 1226-086X,
https://doi.org/10.1016/j.jiec.2017.04.024.
(https://www.sciencedirect.com/science/article/pii/S1226086X17302125)
Resumen
Photocatalysts composed of titanium dioxide modified with B, F, N and P have been synthesized, characterized and applied to the degradation of caffeine, diclofenac, ibuprofen and salicylic acid. The modified TiO2 samples were prepared by the sol–gel technique starting from titanium(IV) isopropoxide and using H3BO3, NH4F, N(C2H5OH)3 and H3PO4 as precursors of the modifiers, with the content varying between 0 and 5 wt%. Structural characterization was based on nitrogen physisorption at −196 °C, powder X-ray diffraction (PXRD), simultaneous thermogravimetric/differential thermal analysis (TG/DTA) and X-ray photoelectron spectroscopy (XPS). The structural properties of the modified TiO2 solids were significantly different depending on the nature and amount of modifiers and the calcination temperature. TiO2 in the anatase phase was obtained in all cases and was stable upon calcination at 400 °C. The photocatalytic degradation of caffeine, diclofenac, ibuprofen and salicylic acid by modified TiO2 was investigated under ultraviolet irradiation at 25 °C. The photocatalytic degradation behavior followed the order: caffeine > diclofenac = ibuprofen > salicylic acid. B-doped TiO2 was the most efficient catalyst in the degradation of these selected emerging contaminants.
URI
ISSN
1226-086X
DOI
10.1016/j.jiec.2017.04.024
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