Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/39862
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dc.contributor.authorLui, Meng-fei-
dc.contributor.authorZhong, Yi-jun-
dc.contributor.authorYuan, Xian-xin-
dc.contributor.authorZheng, Xiao-ming-
dc.date.accessioned2017-01-30T09:48:57Z-
dc.date.available2017-01-30T09:48:57Z-
dc.date.issued1998-01-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/39862-
dc.description41-44en_US
dc.description.abstractSupported CuO catalysts have been employed to investigate the catalytic combustion of acetonitrile, ethylenediamine and nitromethane. The catalytic activity depends on the nature of support. The difference in activity of supported CuO catalyst is because of the reducibility of CuO over catalyst, as confirmed by temperature programmed reduction (TPR) studies. When carbon atom in nitrogen-containing compound is oxidized totally to form CO2, N atom is oxidized to form N2, N2O and NO2. N2 selectivity in the case of nitromethane oxidation decreases monotonously with reaction temperature. However, N2 selectivity in the case of acetonitrile end ethylenediamine oxidation goes through a minimum. The possible reason of the minimum in N2 selectivity is that product NO2 and/or NO reacts with the -CN and -NH2 groups of acetonitrile and ethylenediamine molecule, and produces N2 at higher temperature. The N2 selectivity also depends on the nature of nitrogen-containing compound.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.37A(01) [January 1998]en_US
dc.titleCatalytic combustion of acetonitrile, ethylenediamine and nitromethane over supported CuO catalystsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.37A(01) [January 1998]

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