Bamboo-like MnO2â
Co3O4: High-performance catalysts for the oxidative removal of toluene.
J Environ Sci (China)
; 147: 617-629, 2025 Jan.
Article
en En
| MEDLINE
| ID: mdl-39003076
ABSTRACT
The manganese-cobalt mixed oxide nanorods were fabricated using a hydrothermal method with different metal precursors (KMnO4 and MnSO4·H2O for MnOx and Co(NO3)2â
6H2O and CoCl2â
6H2O for Co3O4). Bamboo-like MnO2â
Co3O4 (B-MnO2â
Co3O4 (S)) was derived from repeated hydrothermal treatments with Co3O4@MnO2 and MnSO4â
H2O, whereas Co3O4@MnO2 nanorods were derived from hydrothermal treatment with Co3O4 nanorods and KMnO4. The study shows that manganese oxide was tetragonal, while the cobalt oxide was found to be cubic in the crystalline arrangement. Mn surface ions were present in multiple oxidation states (e.g., Mn4+ and Mn3+) and surface oxygen deficiencies. The content of adsorbed oxygen species and reducibility at low temperature declined in the sequence of B-MnO2â
Co3O4 (S) > Co3O4@MnO2 > MnO2 > Co3O4, matching the changing trend in activity. Among all the samples, B-MnO2â
Co3O4 (S) showed the preeminent catalytic performance for the oxidation of toluene (T10% = 187°C, T50% = 276°C, and T90% = 339°C). In addition, the B-MnO2â
Co3O4 (S) sample also exhibited good H2O-, CO2-, and SO2-resistant performance. The good catalytic performance of B-MnO2â
Co3O4 (S) is due to the high concentration of adsorbed oxygen species and good reducibility at low temperature. Toluene oxidation over B-MnO2â
Co3O4 (S) proceeds through the adsorption of O2 and toluene to form O*, OH*, and H2C(C6H5)* species, which then react to produce benzyl alcohol, benzoic acid, and benzaldehyde, ultimately converting to CO2 and H2O. The findings suggest that B-MnO2â
Co3O4 (S) has promising potential for use as an effective catalyst in practical applications.
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Texto completo:
1
Base de datos:
MEDLINE
Asunto principal:
Oxidación-Reducción
/
Óxidos
/
Tolueno
/
Cobalto
/
Compuestos de Manganeso
Idioma:
En
Revista:
J Environ Sci (China)
Asunto de la revista:
SAUDE AMBIENTAL
Año:
2025
Tipo del documento:
Article