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In relation to this article, we declare that there is no conflict of interest.
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Received September 7, 2000
Accepted January 16, 2001
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Conversion of Methane to Higher Hydrocarbons in Pulsed DC Barrier Discharge at Atmospheric Pressure

Clean Tech. Res. Center, KIST, P.O. Box 131, Cheongryang, Seoul 130-650, Korea 1Dept. of Chem. Eng., Kwangwoon Univ., Wolgyedong, Nowonku, Seoul 139-701, Korea
nabk@kist.re.kr
Korean Journal of Chemical Engineering, March 2001, 18(2), 196-201(6), 10.1007/BF02698459
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Abstract

Conversion of methane to C2/C3 or higher hydrocarbons in a pulsed DC barrier discharge at atmospheric pressure was studied. Non-equilibrium plasma was generated in the barrier discharge reactor. In this plasma, electrons which had sufficient energy collided with the molecules of methane, which were then activated and coupled to C2/C3 or higher hydrocarbons. The effect of the change of applied voltage, pulse frequency and methane flow rate on methane_x000D_ conversion, selectivities and yields of products was studied. Methane conversion to higher hydrocarbons was about 25% as the maximum. Ethane, propane and ethylene were produced as primary products, including a small amount of unidentified C4 hydrocarbons. The selectivity and yield of ethane as a main product came to about 80% and 17% as the highest, respectively. The selectivities of ethane and ethylene were influenced not by the change of pulse frequency but by the change of applied voltage and methane flow rate. However, in case of propane, the selectivity was independent of those condition changes. The effect of the packing materials such as glass and Al2O3 bead on methane conversion was also considered, showing that Al2O3 played a role in enhancing the selectivity of ethane remarkably as a catalyst.

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