Study of the Photocatalytic Activity of TiO2 and Fe2+ in the Activation of Peroxymonosulfate

González Quiles, Rodrigo ORCID: https://orcid.org/0000-0003-0268-8294, Andrés Almeida, Juan Manuel de ORCID: https://orcid.org/0000-0002-0654-5496 and Rodríguez Chueca, Jorge Jesús ORCID: https://orcid.org/0000-0001-9050-1682 (2021). Study of the Photocatalytic Activity of TiO2 and Fe2+ in the Activation of Peroxymonosulfate. "Water", v. 13 (n. 20); pp. 1-14. ISSN 2073-4441. https://doi.org/10.3390/w13202860.

Descripción

Título: Study of the Photocatalytic Activity of TiO2 and Fe2+ in the Activation of Peroxymonosulfate
Autor/es:
Tipo de Documento: Artículo
Título de Revista/Publicación: Water
Fecha: 13 Octubre 2021
ISSN: 2073-4441
Volumen: 13
Número: 20
Materias:
ODS:
Palabras Clave Informales: Coexisting chemicals; Degradation; Disinfection; Fresh-Water; Heterogeneous photocatalysis; Inactivation; Neutral pH; Peroxymonosulfate; PMS; Solar; Sulfate radicals; System; TiO 2; Tio2; UV radiation; UV-A
Escuela: E.T.S.I. Industriales (UPM)
Departamento: Ingeniería Química Industrial y del Medio Ambiente
Licencias Creative Commons: Reconocimiento - Sin obra derivada - No comercial

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Resumen

The increase in world population and human activities are leading to an increase in water stress in many regions of the planet, coupled with a decrease in the quality of water bodies. Advanced oxidation processes have demonstrated great potential for the reduction of almost any organic pollutant; however, it is necessary to intensify this type of treatment in order to reduce contact times and to reach a greater number of pollutants. The generation of sulfate radicals by activation of peroxymonosulfate (PMS) by divalent iron (Fe2+) and/or titanium dioxide (TiO2) were statistically studied to understand the role of these compounds as activators, using methylene blue as target pollutant because of its ease of handling and analysis. A factorial experimental design was used to study the influence of different variables (PMS, Fe2+, and TiO2) in the presence of UV-A or UV-C. There were relevant differences in the discoloration of methylene blue when analyzing the size of the effects and significance of the experiments, when UV-A or UV-C was used, being faster with UV-C. For instance, total discoloration of methylene blue was reached after 60 min with the system PMS/UV-C, while after 90 min only the 59% of methylene blue disappeared in presence of PMS/UV-A. Both Fe2+ and TiO2 in combination with PMS and UV increased the discoloration effect. So, in the presence of Fe2+, total discoloration of methylene blue was observed after 30 min in presence of UV-A, while this yield was reached in 7.5 min under UV-C. In the case of PMS/TiO2, it required 60 min under UV-A radiation to totally remove methylene blue, and around 15 min with UV-C. Statistically, the three variables were observed to have the main effect in combination with UV. Furthermore, the PMS/Fe2+ system has a significant interaction with UV-A and UV-C radiation, while the interaction of PMS/TiO2 was significant under UV-A, but with a negative effect under UV-C, or in other words the high elimination rates observed are achieved by the oxidation potential of UV-C, and the effect of PMS and TiO2 by itself.

Proyectos asociados

Tipo
Código
Acrónimo
Responsable
Título
Comunidad de Madrid
APOYO-JOVENES-X5PKL6-88-KZ46KU
IN_REUSE
Sin especificar
Intensification processes for reducing risks on water reuse

Más información

ID de Registro: 92450
Identificador DC: https://oa.upm.es/92450/
Identificador OAI: oai:oa.upm.es:92450
URL Portal Científico: https://portalcientifico.upm.es/es/ipublic/item/9438520
Identificador DOI: 10.3390/w13202860
URL Oficial: https://www.mdpi.com/2073-4441/13/20/2860
Depositado por: iMarina Portal Científico
Depositado el: 18 Dic 2025 11:41
Ultima Modificación: 15 Abr 2026 05:40