Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/41409
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dc.contributor.authorRao, K S Rama-
dc.contributor.authorNarayana, K V-
dc.contributor.authorVenugopal, A-
dc.contributor.authorRao, V Venkat-
dc.contributor.authorMasthan, S Khaja-
dc.contributor.authorRao, P Kanta-
dc.date.accessioned2017-04-24T06:45:28Z-
dc.date.available2017-04-24T06:45:28Z-
dc.date.issued1996-08-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/41409-
dc.description656-659en_US
dc.description.abstractAmorphous and crystallite chromia catalysts have been prepared by in situ reduction of Cr(VI) oxide and by decomposition of Cr(NO3)3 respectively, characterized by several techniques and evaluated for dehydrogenation of cycIohexane to benzene. The catalysts are found to be mesoporous and macroporous with average pore diameters of 108 Å and 470 Å respectively. The surface area of amorphous chromia is found to be 5.2 times larger than that of crystalline chromia. In the reduced form, the oxygen chemisorption capacity of the former is 8.3 times higher than that of the latter. The ratio of the dehydrogenation rates over the two catalysts is also found to be almost equal to that of their O2 uptakes. The intrinsic activities of the two morphologies of chromia calculated on the-basis of irreversible O2 uptakes and the activities are found to be equal (3.61 x 10-1). All these observations suggest that the dehydrogenation of cyclohexane is a structure insensitive reaction on chromia catalysts.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.35A(08) [August 1996]en_US
dc.titleInfluence of method of preparation on pore structure and dehydrogenation activity of chromia catalystsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.35A(08) [August 1996]

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