Competitive formation of NO, NO2, and O3 in an air-flowing plasma reactor: A central role of the flow rate

•Competitive formation of NO, NO2, and O3 was experimentally demonstrated in a surface dielectric discharge reactor.•The competitive chemical formation was achieved by only changing the gas flow rate.•The selective production of NO, NO2, and O3 with 85%, 99%, and 97% purities, respectively, is achie...

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Published inChemical engineering journal (Lausanne, Switzerland : 1996) Vol. 468; p. 143636
Main Authors Kim, Jinwoo, Lee, Hyungyu, Huh, Seong-Cheol, Bae, Jin Hee, Choe, Wonho, Han, Duksun, Park, Seungil, Ryu, Seungmin, Park, Sanghoo
Format Journal Article
LanguageEnglish
Published Elsevier B.V 15.07.2023
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Summary:•Competitive formation of NO, NO2, and O3 was experimentally demonstrated in a surface dielectric discharge reactor.•The competitive chemical formation was achieved by only changing the gas flow rate.•The selective production of NO, NO2, and O3 with 85%, 99%, and 97% purities, respectively, is achieved.•Zero-dimensional chemical modeling shows a good agreement with our experimental observation.•An accurate in-situ measurement of NO, NO2, and O3 was successfully carried out based on an NNLS algorithm. Beyond ozone (O3) generation, diverse applications of dielectric barrier discharge (DBD) have been developed. When using ambient air, one of the longstanding challenges of DBD reactors has been the selective production of nitric oxide (NO), nitrogen dioxide (NO2), and O3. In this work, we report the competitive formation of NO, NO2, and O3 in an air-flowing surface DBD reactor. The temporal evolution of each chemical species was obtained by using in situ optical absorption spectroscopy. The possibility to select the plasma-chemistry mode (i.e., NO–, NO2–, or O3-dominant conditions) by adjusting the gas flow rate of the reactor was demonstrated with constant temperature and input power. As the flow rate increased from 260 to 1380 standard cubic centimeters per minute, the dominant chemical species changed from NO to NO2 [the achieved purity of NO2/(NO + NO2 + O3) was 99%]. With even higher flow rates, O3 appeared and dominated in the reactor [O3/(NO + NO2 + O3) was nearly 100%]. The experimental results were compared with zero-dimensional modeling, and the reactions involving NO, NO2, and O3 were analyzed in depth. Our findings will provide great guidance for future studies and for plasma applications of DBD reactors.
ISSN:1385-8947
1873-3212
DOI:10.1016/j.cej.2023.143636