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Characterization of Fe(3)O(4) Nanoparticles for Applications in Catalytic Activity in the Adsorption/Degradation of Methylene Blue and Esterification

The aim of this study is to evaluate the applicability of the catalytic activity (CA) of the Fe(3)O(4) magnetic system in the adsorption/degradation of methylene blue and esterification. The thermal decomposition method allowed the preparation of Fe(3)O(4) nanoparticles. The crystallites of the Fe(3...

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Detalles Bibliográficos
Autores principales: Hernandez, Juan Sebastian Trujillo, Aragón-Muriel, Alberto, Corrales Quintero, Willinton, Castro Velásquez, Juan Camilo, Salazar-Camacho, Natalia Andrea, Pérez Alcázar, German Antonio, Tabares, Jesús Anselmo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9781974/
https://www.ncbi.nlm.nih.gov/pubmed/36558109
http://dx.doi.org/10.3390/molecules27248976
Descripción
Sumario:The aim of this study is to evaluate the applicability of the catalytic activity (CA) of the Fe(3)O(4) magnetic system in the adsorption/degradation of methylene blue and esterification. The thermal decomposition method allowed the preparation of Fe(3)O(4) nanoparticles. The crystallites of the Fe(3)O(4) structural phase present an acicular form confirmed by X-ray diffraction. Transmission electron microscopy results identified the acicular shape and agglomeration of the nanoparticles. Mössbauer spectroscopy showed that the spectrum is composed of five components at room temperature, a hyperfine magnetic field distribution (HMFD), two sextets, a doublet, and a singlet. The presence of the HMFD means that a particle size distribution is present. Fluorescence spectroscopy studied the CA of the nanoparticles with methylene blue and found adsorption/degradation properties of the dye. The catalytic activity of the nanoparticles was evaluated in the esterification reaction by comparing the results in the presence and absence of catalyst for the reaction with isobutanol and octanol, where it is observed that the selectivity for the products MIBP and MNOP is favored in the first three hours of reaction.