Green decomposition of organic dyes using octahedral molecular sieve Manganese Oxide catalysts

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dc.contributor.author King’ondu, Cecil K.
dc.contributor.author Sriskandakumar, Thamayanthy
dc.contributor.author Opembe, Naftali
dc.contributor.author Chen, Chun-Hu
dc.contributor.author Morey, Aimee
dc.contributor.author Suib, Steven L.
dc.date.accessioned 2015-04-14T11:52:36Z
dc.date.available 2015-04-14T11:52:36Z
dc.date.issued 2009
dc.identifier.citation J. Phys. Chem. A, 2009, 113 (8), pp 1523–1530 en_US
dc.identifier.uri http://pubs.acs.org/doi/abs/10.1021/jp807631w
dc.identifier.uri http://repository.seku.ac.ke/handle/123456789/1159
dc.description DOI: 10.1021/jp807631w en_US
dc.description.abstract The catalytic degradation of organic dye (methylene blue, MB) has been studied using green oxidation methods (tertiary-butyl hydrogen peroxide, TBHP, as the oxidant with several doped mixed-valent and regular manganese oxide catalysts in water) at room and higher temperatures. These catalysts belong to a class of porous manganese oxides known as octahedral molecular sieves (OMS). The most active catalysts were those of Mo6+- and V5+-doped OMS. Rates of reaction were found to be first-order with respect to the dye. TBHP has been found to enhance the MB decomposition, whereas H2O2 does not. Reactions were studied at pH 3−11. The optimum pH for these reactions was pH 3. Dye-decomposing activity was proportional to the amount of catalyst used, and a significant increase in catalytic activity was observed with increasing temperature. X-ray diffraction (XRD), energy dispersive spectroscopy (EDX), and thermogravimetric analysis (TGA) studies showed that no changes in the catalyst structure occurred after the dye-degradation reaction. The products as analyzed by electrospray ionization mass spectrometry (ESI-MS) showed that MB was successively decomposed through different intermediate species. en_US
dc.language.iso en en_US
dc.title Green decomposition of organic dyes using octahedral molecular sieve Manganese Oxide catalysts en_US
dc.type Article en_US


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