Manganese ferrite solid nanospheres solvothermally synthesized as catalyst for peroxymonosulfate activation to degrade and mineralize para-nitrophenol: Study of operational variables and catalyst reutilization
MnFe2O4 solid nanospheres (MSN) were synthesized by a solvothermal method. The sample was then used as catalyst to activate potassium peroxymonosulfate (PMS) for the generation of sulfate (SO4.–) and hydroxyl (HO.) radicals to degrade and mineralize para-nitrophenol (PNP) in water. The aim of this w...
- Autores:
-
Mateus Montañez, Olga Lucia
Torres-Alcázar, Lucía
Lopez Ramon, Maria Victoria
Álvarez-Merino, Miguel Ángel
Moreno-Castilla, Carlos
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2021
- Institución:
- Universidad de Ciencias Aplicadas y Ambientales U.D.C.A
- Repositorio:
- Repositorio Institucional UDCA
- Idioma:
- eng
- OAI Identifier:
- oai:repository.udca.edu.co:11158/4204
- Acceso en línea:
- https://repository.udca.edu.co/handle/11158/4204
https://doi.org/10.1016/j.jece.2021.105192
- Palabra clave:
- Manganeso
Ferrita
Radicales (Química)
Peroxymonosulfate
Para-nitrophenol oxidation
Hydroxyl radicals
Catalizador
Oxidación
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode.es
Summary: | MnFe2O4 solid nanospheres (MSN) were synthesized by a solvothermal method. The sample was then used as catalyst to activate potassium peroxymonosulfate (PMS) for the generation of sulfate (SO4.–) and hydroxyl (HO.) radicals to degrade and mineralize para-nitrophenol (PNP) in water. The aim of this work was to study the influence of operational variables on the activity of the MSN catalyst to degrade and mineralize PNP, the PMS consumption kinetics, the leaching of metal ions, and the removal of nitrogen. Results showed that 100% of PNP (0.1 mM) was removed in MSN/PMS system by degradation within 7 h at a dosage of 4 mM of PMS, 0.5 g L−1 of MSN, 40 °C, and pH0 5.8. The reusability of the MSN catalyst was also studied, and a PNP degradation pathway was proposed. The PNP degradation followed a pseudo-first-order kinetic model and the activation energy obtained was 37.1 kJ/mol. Under the above standard reaction conditions, the catalyst showed a good performance after five catalytic runs, with a degradation efficiency that exceeded 98%, and removed around 70% of total organic carbon in each run. The excellent reusability and long-term stability was verified by the characterization of fresh and used catalysts. The sole degradation products were maleic and fumaric acids and nitrate and nitrite ions. |
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