Synergism between anodic oxidation with diamond anodes and heterogeneous catalytic photolysis for the treatment of pharmaceutical pollutants

The mineralization of diclofenac and acetaminophen has been studied by single anodic oxidation with boron-doped diamond (AO-BDD) using an undivided electrolysis cell, by single heterogeneous catalytic photolysis with titanium dioxide (HCP-TiO) and by the combination of both advanced oxidation proces...

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Detalles Bibliográficos
Autores: Peralta-Hernández, Juan Manuel, Rosa Juárez, Catalina de la, Buzo-Muñoz, Vianey, Páramo-Vargas, Javier, Cañizares Cañizares, Pablo, Rodrigo Rodrigo, Manuel Andrés
Tipo de recurso: artículo
Fecha de publicación:2016
País:España
Institución:Universidad de Castilla-La Mancha
Repositorio:RUIdeRA. Repositorio Institucional de la UCLM
OAI Identifier:oai:ruidera.uclm.es:10578/29173
Acceso en línea:http://hdl.handle.net/10578/29173
Access Level:acceso abierto
Palabra clave:Ingeniería Química
Oxidación anódica
Fotólisis catalítica heterogénea
Diclofenaco
Paracetamol
Diamante dopado con boro
Dióxido de titanio
Descripción
Sumario:The mineralization of diclofenac and acetaminophen has been studied by single anodic oxidation with boron-doped diamond (AO-BDD) using an undivided electrolysis cell, by single heterogeneous catalytic photolysis with titanium dioxide (HCP-TiO) and by the combination of both advanced oxidation processes. The results show that mineralization can be obtained with either single technology. The type of functional groups of the pollutant does not influence the results of the single AO-BDD process, but it has a significant influence on the results obtained with HCP-TiO. A clear synergistic effect appears when both processes are combined showing improvements in the oxidation rate of more than 50% for diclofenac and nearly 200% for acetaminophen at the highest current exerted. Results obtained are explained in terms of the production of oxidants on the surface of BDD (primarily peroxodisulfate) and the later homogeneous catalytic light decomposition of these oxidants in the bulk. This mechanism is consistent with the larger improvement observed at higher current densities, for which the production of oxidants is promoted.