Choudhary, V. R. ; Mondal, K. C. ; Choudhary, T. V. (2006) Oxy-CO2 reforming of methane to syngas over CoOx/CeO2/SA-5205 catalyst Energy & Fuels, 20 (5). pp. 1753-1756. ISSN 0887-0624
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Official URL: http://pubs.acs.org/doi/abs/10.1021/ef060138o
Related URL: http://dx.doi.org/10.1021/ef060138o
Abstract
The oxy-CO2 methane reforming (OCRM) process has been investigated over the CoOx/CeO2/SA-5205 catalyst at varying reaction temperatures (750-900°C), O2/CH4 ratios (0.3-0.45), and space velocities (20000-100000 cm3/g/h). With an increasing OCRM reaction temperature, the contribution from the CO2 methane reforming reaction increased while that from methane combustion reactions decreased. Correspondingly, there was an increase in the H2/CO ratio and a sharp decrease in reaction exothermicity. At 900°C (gas hourly space velocity = 46000 cm3/g/h and O2/CH4 = 0.4), the OCRM reaction over the CoOx/CeO2/SA-5205 catalyst was mildly endothermic with >90% CH4 conversion, >95% H2 selectivity, and a H2/CO ratio of 1.63. CH4 conversion was relatively unaffected by the O2/CH4 ratio used in the OCRM reaction; however, CO2 conversion decreased on increasing the O2/CH4 ratio. While H2 selectivity was not significantly affected by the O2/CH4 ratio, the H2/CO ratio increased linearly with an increasing O2/CH4 ratio. The endothermicity of the reaction was found to decrease with an increasing CH4/O2 ratio, which can be explained on the basis of increased contribution from the methane partial oxidation reaction with an increasing O2/CH4 ratio.
Item Type: | Article |
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Source: | Copyright of this article belongs to American Chemical Society. |
ID Code: | 10329 |
Deposited On: | 04 Nov 2010 06:01 |
Last Modified: | 28 May 2011 10:55 |
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