Please use this identifier to cite or link to this item: https://repository.seku.ac.ke/handle/123456789/1179
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dc.contributor.authorKing’ondu, Cecil K.-
dc.contributor.authorNjagi, Eric C.-
dc.contributor.authorGenuino, Homer C.-
dc.contributor.authorDharmarathna, Saminda-
dc.contributor.authorSuib, Steven L.-
dc.date.accessioned2015-04-17T08:07:53Z-
dc.date.available2015-04-17T08:07:53Z-
dc.date.issued2012-04-
dc.identifier.citationApplied Catalysis A: General Volumes 421–422, 16 April 2012, Pages 154–160en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S0926860X12000725-
dc.identifier.urihttp://repository.seku.ac.ke/handle/123456789/1179-
dc.descriptiondoi:10.1016/j.apcata.2012.02.011en_US
dc.description.abstractAmorphous manganese oxide and binary copper manganese oxides were synthesized using the redox method, characterized, and tested in the catalytic oxidation of ethylene. The catalytic activity of the synthesized catalysts toward ethylene oxidation was high (100% conversion of 1.0% C2H4 at 200 °C with space velocity of View the MathML source and compared favorably with that of a commercial Hopcalite catalyst. The high catalytic activity was attributed a combination of factors including the poor crystallinity, the high surface areas (≥163 m2 g−1), porosity, presence of Mn4+ species, and compositional homogeneity of the synthesized copper manganese oxides. Incorporation of copper into the amorphous manganese oxide matrix significantly enhanced the catalytic activity of the resultant bimetallic oxides by increasing the reducibility and ease of removal of lattice oxygen species. The synthesized materials were characterized using FE-SEM, HR-TEM, BET, FAAS, XPS, and TPD methods.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectCatalytic oxidationen_US
dc.subjectCopper manganese oxideen_US
dc.subjectEthyleneen_US
dc.subjectVolatile organic compounds (VOCs)en_US
dc.titleCatalytic oxidation of ethylene at low temperatures using porous copper manganese oxidesen_US
dc.typeArticleen_US
Appears in Collections:School of Science and Computing (JA)

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