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Decomposition of the Methylene Blue Dye Using Layered Manganese Oxide Materials Synthesized by Solid State Reactions

Acceso Abierto
ID Minciencias: ART-0000297640-190
Ranking: ART-ART_A2

Abstract:

The modulation in the synthesis parameters of layered manganese oxides allowed us to produce materials with different AC conductivities. These conductivities were correlated with the catalytic performance of the materials in the decomposition of methylene blue, as a model of electron transfer reactions. The manganese oxides were prepared by thermal reduction of KMnO 4 at 400°C and 800°C where one sample was heated at 1°C/min and the other was heated at 10°C/min. The materials were characterized by atomic absorption, average oxidation states of manganese, X-ray diffraction, thermogravimetric analysis, and scanning electron microscopy. The results indicate that, by increasing the synthesis temperature, both the lamellar arrangement and the crystal size increased, while the Mn 4+ amount in the material decreased. Furthermore, it was observed that as the conductivity increases for the materials, the catalytic performance also increases. Therefore, a direct correlation between the conductivity and catalytic performance can be established. For example, the layered manganese oxides material synthesized at 400°C, using a heating rate of 10°C/min, showed the highest AC conductivity and had the best performance in the degradation of methylene blue. Finally, we propose a general mechanism for understanding how manganese oxides behave as catalysts that produce oxidizing species from H 2 O 2 which degrades methylene blue. Our proposed mechanism takes into consideration the state of aggregation of the catalyst, the availability of Mn 4+ , and the electrical conductivity.

Tópico:

Supercapacitor Materials and Fabrication

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Citations: 16
16

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Información de la Fuente:

SCImago Journal & Country Rank
FuenteInternational Journal of Chemical Engineering
Cuartil año de publicaciónNo disponible
Volumen2018
IssueNo disponible
Páginas1 - 11
pISSN1687-806X
ISSNNo disponible

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