RUO Home

Repositorio Institucional de la Universidad de Oviedo

View Item 
  •   RUO Home
  • Producción Bibliográfica de UniOvi: RECOPILA
  • Artículos
  • View Item
  •   RUO Home
  • Producción Bibliográfica de UniOvi: RECOPILA
  • Artículos
  • View Item
    • español
    • English
JavaScript is disabled for your browser. Some features of this site may not work without it.

Browse

All of RUOCommunities and CollectionsBy Issue DateAuthorsTitlesSubjectsxmlui.ArtifactBrowser.Navigation.browse_issnAuthor profilesThis CollectionBy Issue DateAuthorsTitlesSubjectsxmlui.ArtifactBrowser.Navigation.browse_issn

My Account

LoginRegister

Statistics

View Usage Statistics

RECENTLY ADDED

Last submissions
Repository
How to publish
Resources
FAQs

Peroxydisulfate activation by cerium (iv) oxide-supported palladium (pd/ceo2) for bisphenol a oxidation and e. Coli inactivation from aquatic matrices

Author:
Ioannidi, A. A.; Bampos, G.; Antonopoulou, M.; Oulego Blanco, PaulaUniovi authority; Mantzavinos, D.; Frontistis, Z.
Publication date:
2024
Publisher version:
http://dx.doi.org/10.1016/j.jece.2023.111851
Citación:
Journal of Environmental Chemical Engineering, 12(1), (2024); doi:10.1016/j.jece.2023.111851
Abstract:

In this study, a series of Pd/CeO2 catalysts were synthesized, characterized, and evaluated for the activation of persulfate and the degradation of the micropollutant, bisphenol A (BPA). The efficiency followed a volcano-type behavior with respect to Pd loading, and the 0.25% wt. Pd/CeO2 exhibited the highest catalytic activity. However, this activity strongly depended on the operating conditions. The system was able to degrade 500 μg/L BPA in less than 30 min, and the removal was favored at near neutral pH (6.2). Scavenging experiments highlighted the role of superoxide and singlet oxygen, followed by sulfate radicals. The efficiency was found to be stable across several cycles, despite a slight decrease in the first cycle. The removal of BPA decreased with the complexity of the water matrices, showing the need for system optimization under real conditions. Five transformation products were identified using UHPLC/TOF-MS and their ecotoxicity was estimated using ECOSAR. Intriguingly, the system was capable of inactivating 99.99% of 2.4 × 105 CFU/mL E. coli, in less than 210 min making it an appealing alternative technology for the simultaneous inactivation of pathogens and degradation of micropollutants in environmental systems.

In this study, a series of Pd/CeO2 catalysts were synthesized, characterized, and evaluated for the activation of persulfate and the degradation of the micropollutant, bisphenol A (BPA). The efficiency followed a volcano-type behavior with respect to Pd loading, and the 0.25% wt. Pd/CeO2 exhibited the highest catalytic activity. However, this activity strongly depended on the operating conditions. The system was able to degrade 500 μg/L BPA in less than 30 min, and the removal was favored at near neutral pH (6.2). Scavenging experiments highlighted the role of superoxide and singlet oxygen, followed by sulfate radicals. The efficiency was found to be stable across several cycles, despite a slight decrease in the first cycle. The removal of BPA decreased with the complexity of the water matrices, showing the need for system optimization under real conditions. Five transformation products were identified using UHPLC/TOF-MS and their ecotoxicity was estimated using ECOSAR. Intriguingly, the system was capable of inactivating 99.99% of 2.4 × 105 CFU/mL E. coli, in less than 210 min making it an appealing alternative technology for the simultaneous inactivation of pathogens and degradation of micropollutants in environmental systems.

URI:
https://hdl.handle.net/10651/73716
ISSN:
2213-3437
DOI:
10.1016/j.jece.2023.111851
Patrocinado por:

European Union (European Social Fund-ESF) through the Operational Programme "Human Resources Development, Education and Lifelong Learning"

Collections
  • Artículos [37549]
Files in this item
Métricas
Compartir
Exportar a Mendeley
Estadísticas de uso
Estadísticas de uso
Metadata
Show full item record
Página principal Uniovi

Biblioteca

Contacto

Facebook Universidad de OviedoTwitter Universidad de Oviedo
The content of the Repository, unless otherwise specified, is protected with a Creative Commons license: Attribution-Non Commercial-No Derivatives 4.0 Internacional
Creative Commons Image