Synthesis, Characterization and Kinetic Evaluation of Manganese Oxide Nanoparticles for the H2O2 Catalytic Decomposition

Manuel D. Delgado Vigil, Centro de Investigacion en Materiales Avanzados S. C.
Francisco Paraguay Delgado, Centro de Investigacion en Materiales Avanzados S. C.
Virginia Collins Martínez, Centro de Investigacion en Materiales Avanzados S. C.
Alejandro López Ortiz, Centro de Investigacion en Materiales Avanzados S. C.

Abstract

Nanostructured manganese oxides were synthesized towards the catalytic decomposition of hydrogen peroxide. The effect of the type of precipitant (Na2CO3 and NH4OH) over the particle size and crystallographic phase was determined. Also, the influence of particle size and crystal phase over the catalytic activity was established. Characterization of the obtained nanoparticles was performed through XRD analysis, BET surface area and TEM microscopy. Catalytic activity was followed through gasometry of the oxygen evolution [H2O2(l) → H2O(l) + O2 (g)] at 25°C. Na2CO3 (Mn-1) and NH4OH (Mn-2) precipitants produced nanoparticles with average sizes of 5-10 nm and 20 nm, respectively. This result was attributed to higher pH stability of precipitant Na2CO3 during the synthesis process. XRD results revealed the presence of ß-MnO2, Mn5O8 and Mn3O4 crystal phase mixture for Mn-1 and Mn5O8 for Mn-2 catalyst. Catalytic activity resulted in intrinsic rate constants (kint = min-1m-2) of 5.2 and 2.3 for Mn-1 and Mn-2, respectively. The greater catalytic activity of Mn-2 catalyst was attributed to the presence of the Mn55O8 phase.

Recommended Citation

Delgado Vigil, Manuel D.; Paraguay Delgado, Francisco; Collins Martínez, Virginia; and López Ortiz, Alejandro (2008) "Synthesis, Characterization and Kinetic Evaluation of Manganese Oxide Nanoparticles for the H2O2 Catalytic Decomposition," International Journal of Chemical Reactor Engineering: Vol. 6: A5.
Available at: http://www.bepress.com/ijcre/vol6/A5

 
 
 
 

ISSN: 1542-6580 ©1999-2008 The Berkeley Electronic Press™ All rights reserved.

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