Synergetic effect of plasma/catalysis hybrid system for CH4 removal

被引:23
作者
Baylet, A. [1 ]
Marecot, P. [1 ]
Duprez, D. [1 ]
Jeandel, X. [2 ]
Lombaert, K. [3 ]
Tatibouet, J. M. [1 ]
机构
[1] Univ Poitiers, LACCO, UMR CNRS 6503, F-86022 Poitiers, France
[2] API FR CTL L47 2 61 1, Direct Avants Projets Environm Mecan, F-91510 Lardy, France
[3] API FR CTL L16 1 41 1, Direct Ingn Mat, F-91510 Lardy, France
关键词
Methane; Carbon monoxide; Non-thermal plasma discharge; Monolith; Palladium; DIELECTRIC-BARRIER DISCHARGE; CARBON-DIOXIDE; LA2O3/GAMMA-AL2O3; CATALYST; METHANE CONVERSION; PARTIAL OXIDATION; LOW-TEMPERATURE; PLASMA REACTOR; SYNTHESIS GAS; HYDROCARBONS; ACTIVATION;
D O I
10.1016/j.apcatb.2011.10.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Methane abatement from rich gas mixture was performed in a plasma-catalyst reactor. The inlet concentration of CH4 varied from 0.15 to 1 vol.% of the total flow rate. Influences of different parameters such as temperature, gas composition and catalyst were investigated. The catalyst was an alumina wash-coated monolith made of cordierite containing 0.15 wt% of palladium and 15 wt% of Al2O3. The plasma was generated by means of a high voltage monopolar excitation. The higher the energy density, the higher the methane conversion. For plasma experiments carried out without catalyst, the CH4 conversion reached a maximum of 33% for 1 vol.% CH4 and 49% for 0.3 vol.% CH4 in a N-2/O-2/CO2/H2O gas mixture (75/18.7/4/2 vol.%) at 200 degrees C and 1823 J L-1. Carbon monoxide (CO) was observed to be the main product. The CO yield reached 29% and 49% for 1 and 0.3 vol.% CH4, respectively. Moreover, experiments performed with a hybrid plasma-catalytic reactor showed two different behaviours depending on the catalyst location. In POST-plasma position, the presence of the catalyst did not modify the methane conversion but oxidized CO into CO2. In IN-plasma position, the catalyst inhibited the methane conversion by decreasing the plasma volume between electrodes but oxidized CO into CO2. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:31 / 36
页数:6
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