Enhanced Photocatalytic Degradation of Herbicide 2,4-Dichlorophenoxyacetic Acid Using Sulfated CeO2

Author:

Rodríguez Carlos1ORCID,Castañeda Claudia1ORCID,Sosa Edwin1ORCID,Martínez José J.1ORCID,Mancipe Sonia1,Rojas Hugo1ORCID,Tzompantzi Francisco2ORCID,Gómez Ricardo2ORCID

Affiliation:

1. Grupo de Catálisis, Escuela de Ciencias Químicas, Universidad Pedagógica y Tecnológica de Colombia UPTC, Avenida Central del Norte 39-115, Tunja 150003, Boyacá, Colombia

2. Grupo de Ecocatálisis, Universidad Autónoma Metropolitana-Iztapalapa, Av. San Rafael Atlixco No. 186, Ciudad de México 09340, Mexico

Abstract

The present study presents the results obtained from evaluating the photocatalytic behavior of a series of sulfated CeO2 materials in the photocatalytic degradation of the herbicide 2,4-dichlorophenoxyacetic acid. The CeO2 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 CeO2 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 CeO2.

Publisher

MDPI AG

Reference46 articles.

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