Copper and sulphur co-doped titanium oxide nanoparticles with enhanced catalytic and photocatalytic properties

Copper and sulphur co-doped titanium oxide nanoparticles have been prepared by the sol–gel method to develop versatile catalysts exhibiting enhanced catalytic and photocatalytic properties. Structural, morphological, chemical composition, and optical characterizations of the synthesized titanium oxi...

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Detalles Bibliográficos
Autores: Ortiz-Bustos, Josefa, Gómez-Ruiz, Santiago, Mazario, Jaime, Domine, Marcelo E., del Hierro, Isabel, Pérez, Yolanda
Tipo de recurso: artículo
Fecha de publicación:2020
País:España
Institución:Universidad Rey Juan Carlos
Repositorio:BURJC-Digital. Repositorio Institucional de la Universidad Rey Juan Carlos
OAI Identifier:oai:burjcdigital.urjc.es:10115/42013
Acceso en línea:https://pubs.rsc.org/en/content/articlelanding/2020/cy/d0cy01041c
https://hdl.handle.net/10115/42013
Access Level:acceso embargado
Palabra clave:Co-doped-TiO2
photocatalysis
catalysis
ciprofloxacin degradation
oxidation of thioanisole
Descripción
Sumario:Copper and sulphur co-doped titanium oxide nanoparticles have been prepared by the sol–gel method to develop versatile catalysts exhibiting enhanced catalytic and photocatalytic properties. Structural, morphological, chemical composition, and optical characterizations of the synthesized titanium oxide nanoparticles have been carried out in order to study the effect of incorporating copper and sulphur on the catalytic and photocatalytic activities of TiO2 nanoparticles. Optimal incorporation of copper and sulphur to the titanium dioxide nanoparticles promotes the photocatalytic degradation of ciprofloxacin in water under irradiation of UV or visible light. Complete degradation of ciprofloxacin was achieved after 120 min with the 0.4% Cu–0.5% S–TiO2 photocatalyst using UV and in 90 min applying visible light. Cu–S–TiO2 nanoparticles also exhibit high activity (94–98% conversion) and excellent recyclability (with no loss of activity after 14 runs) in selective oxidation of thioanisole using H2O2 as an oxidant.