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Título

Effect of synthesis pH on the physicochemical properties of a synthesized Bi2WO6 and the type of substrate chosen, in assessing its photo-catalytic activities

AutorJaramillo-Páez, César; Navío, José A.; Hidalgo, M.C. CSIC ORCID
Palabras claveBismuth tungstate
Photocatalysis
Phenol
Dyes
Rhodamine B
TiO2(P25)
Fecha de publicación2020
EditorElsevier
CitaciónArabian Journal of Chemistry 13: 431- 443 (2020)
ResumenCrystalline orthorhombic BiWO powders were synthesized by a hydrothermal method from aqueous solutions of Bi(NO)·5HO and NaWO·2HO over a range of three selected pH values (2.0, 5.0 and 7.0), using NaOH as precipitating agent. The as-prepared catalysts were characterized by XRD, BET, FE-SEM, TEM, XPS and UV-vis spectroscopy. The effect of pH-synthesis on crystallinity, morphologies, surface area and optical absorption properties, were investigated. Although the pH has a marked influence on morphology, the nature of the precipitating agent (NaOH or TEA) also influences the morphology and surface structure composition, as it is observed in the present work. Three different probe molecules were used to evaluate the photo-catalytic properties under two illumination conditions (UV and Visible): Methyl Orange and Rhodamine B were chosen as dye substrates and Phenol as a transparent substrate. The photo-catalytic activities are strongly dependent not only on the pH used in the synthesis but also on the nature of the chosen substrate in assessing the photo-catalytic activities. Results were compared with those obtained when using TiO(P25, Evonik) in the same experimental conditions. The photo-catalytic activity of one of the synthesised samples has been evaluated by exposing a mixture of Rhodamine B and Phenol in water, to different illumination conditions. Our results provide new evidences about the issue of whether dyes are suitable substrates to assess the activity of a photo-catalyst.
Versión del editorhttp://dx.doi.org/10.1016/j.arabjc.2017.05.014
URIhttp://hdl.handle.net/10261/216508
DOI10.1016/j.arabjc.2017.05.014
Identificadoresdoi: 10.1016/j.arabjc.2017.05.014
issn: 1878-5352
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