Oxy-CO2 reforming of methane to syngas over CoOx/MgO/SA-5205 catalyst
The oxy-CO2 methane reforming reaction (OCRM) has been investigated over CoOx supported on a MgO precoated highly macroporous silica-alumina catalyst carrier (SA-5205) at different reaction temperatures (700-900 deg C), O2/CH4 ratios (0.3-0.45) and space velocites (20,000-100,000cc/g/h). The reactio...
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Published in | Fuel (Guildford) Vol. 85; no. 17-18; pp. 2484 - 2488 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Elsevier
01.12.2006
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Subjects | |
Online Access | Get full text |
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Summary: | The oxy-CO2 methane reforming reaction (OCRM) has been investigated over CoOx supported on a MgO precoated highly macroporous silica-alumina catalyst carrier (SA-5205) at different reaction temperatures (700-900 deg C), O2/CH4 ratios (0.3-0.45) and space velocites (20,000-100,000cc/g/h). The reaction temperature had a profound influence on the OCRM performance over the CoO/MgO/SA-5205 catalyst; the methane conversion, CO2 conversion and H2 selectivity increased while the H2/CO ratio decreased markedly with increasing reaction temperature. While the O2/CH4 ratio did not strongly affect the CH4 and CO2 conversion and H2 selectivity, it had an intense influence on the H2/CO ratio. The CH4 and CO2 conversion and the H2 selectivity decreased while the H2/CO increased with increasing space velocity. The O2/CH4 ratio and the reaction temperature could be used to manipulate the heat of the reaction for the OCRM process. Depending on the O2/CH4 ratio and temperature the OCRM process could be operated in a mildly exothermic, thermal neutral or mildly endothermic mode. The OCRM reaction became almost thermoneutral at an OCRM reaction temperature of 850 deg C, O2/CH4 ratio of 0.45 and space velocity of 46,000cc/g/h. The CH4 conversion and H2 selectivity over the CoO/MgO/SA-5205 catalyst corresponding to thermoneutral conditions were excellent: 95% and 97%, respectively with a H2/CO ratio of 1.8. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0016-2361 1873-7153 |
DOI: | 10.1016/j.fuel.2006.04.013 |