Oxidation of acetylene by photocatalysis coupled with dielectric barrier discharge

被引:60
作者
Thevenet, F.
Guaitella, O.
Puzenat, E.
Herrmann, J.-M.
Rousseau, A.
Guillard, C. [1 ]
机构
[1] Univ Lyon 1, UMR 5634, CNRS, Lab Applicat Chim & Environm, F-69622 Villeurbanne, France
[2] Ecole Polytech, UMR 7648, CNRS, Lab Phys & Technol Plasmas, F-91120 Palaiseau, France
关键词
dielectric barrier discharge (DBD); non-thermal plasma; photocatalysis; advanced oxidation; VOC; NONTHERMAL PLASMA; INDOOR AIR; DECOMPOSITION; TIO2; ADSORPTION; ETHYLENE; BENZENE; WATER; VOCS; CONTAMINANTS;
D O I
10.1016/j.cattod.2007.01.057
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Volatile organic compound removal from air requires oxidative processes associating high carbon dioxide selectivity like photocatalysis with fast kinetics like non-thermal plasma. A specially designed coupling reactor has been used to investigate the interaction between photocatalysis and non-thermal plasma. Acetylene has been selected as a model molecule to evaluate oxidation efficiencies. After determining the oxidative efficiency of both techniques used separately, the coupling of plasma with titania photocatalyst has been performed. The influence of UV-irradiation of a photocatalyst placed inside the discharge by external lamps has been investigated. It is reported that photocatalysis leads to a complete mineralization of acetylene, whereas more than 50% of the carbon balance based on CO and CO2 is missing when plasma alone is performed. The presence of a porous material inside the discharge improves the initial removal rate of acetylene. It tends to favor the formation of adsorbed organic species, indicating that part of plasma reactivity is transferred to the adsorbed phase. Finally, the use of additional external UV-light is reported to improve the formation of carbon dioxide, means that photocatalysis can be usefully performed in an ionized gas. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:186 / 194
页数:9
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