Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/40329
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dc.contributor.authorLuo, Meng-fei-
dc.contributor.authorYuan, Xian-xin-
dc.contributor.authorZheng, Xiao-ming-
dc.date.accessioned2017-02-10T05:57:40Z-
dc.date.available2017-02-10T05:57:40Z-
dc.date.issued1998-11-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/40329-
dc.description1020-1023en_US
dc.description.abstractPalladium and platinum supported by CeO2, ZrO2 and AI2O3 have been prepared by conventional impregnation method. The effect of support on catalytic activity on oxidation of CO and methane has been studied. The activity of the supported Pd catalyst is much higher than that of the supported Pt catalyst. The catalytic activity depends on the nature of the support; the sequence for supported Pd and Pt catalyst being CeO2 > ZrO2 > Al2O3. For both CO and methane oxidation, Pd/CeO2 shows highest activity with a light-off temperature at 45° and 310°C respectively, with no apparent decay. This is mostly due to the superoxide species over CeO2 Pd/ZrO2, Pd/AI2O3 and Pt/CeO2 catalysts exhibit apparent deactivation. The heat-stability of Pd/CeO2 is inferior to Pd/AI2O3 catalyst, but the oxidation activity of Pd/CeO2), catalyst for CO and methane is higher than that of Pd/Al2O3, after calcination at 1200°C for 4h.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(11) [November 1998]en_US
dc.titleComplete oxidation of methane and carbon monoxide on supported palladium and platinum catalystsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.37A(11) [November 1998]

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