Catalytic oxidative desulfurization of 4,6-dimethyl dibenzothiophene by phosphotungstic acid loaded on Al2O3, V2O5, and ZrO2 oxides

Ma Elena Manríquez, Ana Laura Ortiz, Martín Trejo-Valdez, Laura V. Castro, Emma Ortiz-Islas

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

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Resumen

This work reports the synthesis, characterization, and catalytic testing of ZrO2, V2O5, and Al2O3 that have been loaded with two amounts of phosphotungstic acid for the catalytic oxidative desulfurization of 4,6-dimethyl dibenzothiophene as a reaction test model to reduce the sulfur content in diesel. The catalysts were synthesized through the impregnation of individual oxides with a solution of the heteropolyacid to 3% and 3.5% mol with respect to the metal in each oxide. The materials were characterized by x-ray diffraction, infrared and Raman spectroscopy, nitrogen adsorption–desorption technique, scanning electron microscopy, and x-ray photoelectron spectroscopy. The acidity of the catalysts was determined by potentiometry by titration of the catalysts with pyridine. The reaction test is considered a viable alternative, because it is performed at ambient temperature and pressure. This reaction can be conducted in the liquid–liquid, liquid–solid, or triphasic phase using oxidants and catalysts. In this study, dimethyl dibenzothiophene was used as the sulfur species in diesel and as the molecule for evaluating catalyst activity. Acetonitrile was the solvent, and hydrogen peroxide was the oxidizing agent. Al2O3-based catalysts had the highest surface area and acidity among all catalysts. Catalytic activity was affected by the type of support and the heteropolyacid content. As the level of heteropolyacid increased, the catalytic activity rose. Other factors that influenced catalytic activity were the catalyst's surface area, acidity, and morphology. The catalytic activity improved when the acidity and surface area in the catalysts increased. For V2O5, empty spaces were observed, favoring adsorption of the reactants.

Idioma originalInglés
Páginas (desde-hasta)1523-1539
Número de páginas17
PublicaciónReaction Kinetics, Mechanisms and Catalysis
Volumen135
N.º3
DOI
EstadoPublicada - jun. 2022
Publicado de forma externa

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