Effects of modifying Ni/Al2O3 catalyst with cobalt on the reforming of CH4 with CO2 and cracking of CH4 reactions
Alumina supported nickel (Ni/Al2O3), nickel–cobalt (Ni–Co/Al2O3) and cobalt (Co/Al2O3) catalysts containing 15% metal were synthesized, characterized and tested for the reforming of CH4 with CO2 and CH4 cracking reactions. In the Ni–Co/Al2O3 catalysts Ni–Co alloys were detected and the surface metal...
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Published in | International journal of hydrogen energy Vol. 39; no. 22; pp. 11462 - 11472 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier Ltd
24.07.2014
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Alumina supported nickel (Ni/Al2O3), nickel–cobalt (Ni–Co/Al2O3) and cobalt (Co/Al2O3) catalysts containing 15% metal were synthesized, characterized and tested for the reforming of CH4 with CO2 and CH4 cracking reactions. In the Ni–Co/Al2O3 catalysts Ni–Co alloys were detected and the surface metal sites decreased with decrease in Ni:Co ratio. Turnover frequencies of CH4 were determined for both reactions. The initial turnover frequencies of reforming (TOFDRM) for Ni–Co/Al2O3 were greater than that for Ni/Al2O3, which suggested a higher activity of alloy sites. The initial turnover frequencies for cracking (TOFCRK) did not follow this trend. The highest average TOFDRM, H2:CO ratio and TOFCRK were observed for a catalyst containing a Ni:Co ratio of 3:1. This catalyst also had the maximum carbon deposited during reforming and produced the maximum reactive carbon during cracking. It appeared that carbon was an intermediate product of reforming and the best catalyst was able to most effectively crack CH4 and oxidize carbon to CO by CO2.
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•Initial TOFDRM for Ni–Co/Al2O3 were larger due to Ni–Co alloy sites.•Most active Ni–Co/Al2O3 catalyst, 75Ni25Co/Al2O3, contains a Ni:Co ratio of 3:1.•Average TOFDRM, TOFCRK and H2:CO ratio maximum for 75Ni25Co/Al2O3.•Carbon deposited appears to be an intermediate product.•75Ni25Co/Al2O3 appears to crack methane and oxidize carbon most effectively. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2014.05.058 |