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Enhanced Photocatalytic Degradation of Herbicide 2,4-Dichlorophenoxyacetic Acid Using Sulfated CeO[sub.2]

The present study presents the results obtained from evaluating the photocatalytic behavior of a series of sulfated CeO[sub.2] materials in the photocatalytic degradation of the herbicide 2,4-dichlorophenoxyacetic acid. The CeO[sub.2] photocatalytic support was prepared using the precipitation synth...

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Bibliographic Details
Published in:Catalysts 2024-09, Vol.14 (9)
Main Authors: Rodríguez, Carlos, Castañeda, Claudia, Sosa, Edwin, Martínez, José J, Mancipe, Sonia, Rojas, Hugo, Tzompantzi, Francisco, Gómez, Ricardo
Format: Article
Language:English
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Summary:The present study presents the results obtained from evaluating the photocatalytic behavior of a series of sulfated CeO[sub.2] materials in the photocatalytic degradation of the herbicide 2,4-dichlorophenoxyacetic acid. The CeO[sub.2] photocatalytic support was prepared using the precipitation synthesis method. Subsequently, the support was wetly impregnated with different contents of sulfate ions (0.5, 1.0, and 2.0 wt.%). The materials were characterized using X-ray diffraction, nitrogen physisorption, infrared spectroscopy, diffuse reflectance UV–Vis spectrophotometry, and thermal analysis. The characterization results showed that the sulfation of the material promoted an increase in the surface area and a decrease in the average size of the crystallites. Likewise, it was possible to demonstrate the surface sulfation of the support through bidentate coordination of the sulfate groups to the semiconductor metal. Concerning photoactivity, the convenience of the surface modification of CeO[sub.2] was confirmed because the sulfate groups acted as capturers of the electrons generated during the photocatalytic process, reducing the frequency of recombination of the charge carriers and allowing the availability of the gaps to favor the degradation reaction of the contaminant. Finally, it was evident that a percentage of 1.0 wt.% of the sulfate anion is the optimal content to improve the photocatalytic properties of CeO[sub.2].
ISSN:2073-4344
2073-4344
DOI:10.3390/catal14090594