Modificación superficial de fieltro de grafito con nanopartículas de magnetita Fe3O4 para su uso en un sistema electro-Fenton

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In this work, an electro-Fenton system was manufactured for the degradation of aromatic-type contaminants in aqueous pollutants and the simultaneous generation of electrical energy. The system consisted in two chambers (anode and cathode) separated by a Nafion membrane. The electrical energy was gen...

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Detalles Bibliográficos
Autor: Calderón Zavaleta, Sandy Luz
Formato: tesis de maestría
Fecha de Publicación:2019
Institución:Pontificia Universidad Católica del Perú
Repositorio:PUCP-Institucional
Lenguaje:español
OAI Identifier:oai:repositorio.pucp.edu.pe:20.500.14657/167852
Enlace del recurso:http://hdl.handle.net/20.500.12404/14907
Nivel de acceso:acceso abierto
Materia:Nanopartículas
Soluciones (Química)
Contaminantes
Electroquímica
https://purl.org/pe-repo/ocde/ford#1.04.00
Descripción
Sumario:In this work, an electro-Fenton system was manufactured for the degradation of aromatic-type contaminants in aqueous pollutants and the simultaneous generation of electrical energy. The system consisted in two chambers (anode and cathode) separated by a Nafion membrane. The electrical energy was generated by anodic oxidation of glucose catalyzed by gold. The cathode was made of graphite felt modified on its surface with magnetite nanoparticles (Fe3O4NPs/GFoxi). The magnetite nanoparticles were impregnated on graphite felt by means of a layer-by-layer self-assembled method that uses polydiallyldimethylammonium chloride (PDDA) as a polyelectrolyte. In the anodic chamber, a graphite felt surface modified with gold nanoparticles (AuNPs/GF) was used. The nanoparticles were deposited on the surface of this electrode by electrochemical deposition. The electro-Fenton system generated an average output power of 550 mW m-2, which served as a power supply for carry out pollutant degradation process. This system led to the degradation of 0.35 mmol L-1 of hydrogen potassium phthalate (model pollutant) attaining 73.7% of COD decay during 23 h of treatment at pH 3.
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