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dc.contributor.authorDjaouani, Nedjwa
dc.contributor.authorMostefa, Lemerini
dc.contributor.authorOmar Sabbar, Dahham
dc.date.accessioned2018-12-08T04:53:47Z
dc.date.available2018-12-08T04:53:47Z
dc.date.issued2018-07
dc.identifier.citationInternational Journal of Nanoelectronics and Materials, vol.11(3), 2018, pages 271-282en_US
dc.identifier.issn1985-5761 (Printed)
dc.identifier.issn1997-4434 (Online)
dc.identifier.urihttp://dspace.unimap.edu.my:80/xmlui/handle/123456789/57578
dc.descriptionLink to publisher's homepage at http://ijneam.unimap.edu.myen_US
dc.description.abstractThe purpose of this work is to investigate the contribution of different chemical reactions that participate in NOx creation or reduction in N2/O2/H2O/CO2 mixed gas induced by negative corona discharge under different reduced electric field levels:100 - 200 Td (1Td=10−21 V.m2). The fundamental chemistry governing NOx evolution developed in this paper is based on a full set of processes regrouped in 200 selected chemical reactions involving 36 molecular, excited, atomic, and charged species. The density was calculated using the continuity equation while not the diffusion term, and the time analysis varied from 10−9 to 10−3s. The results of simulations show the role played by different chemical reactions on NOx conversion. It is shown that at 100 Td near 60% of NO can be removed by radical through the reaction NO + → + O2 and near 20% of NO2 and NO3 could be removed by radicals and through NO2 + → + O3 and NO3+ → N O2 respectively.en_US
dc.language.isoenen_US
dc.publisherUniversiti Malaysia Perlis (UniMAP)en_US
dc.subjectPlasma Chemistryen_US
dc.subjectRate Constanten_US
dc.subjectNox Conversionen_US
dc.subjectChemical Kineticen_US
dc.subjectGas Dischargeen_US
dc.titleNumerical Analysis of the Chemical Reactions Effects on NOx Conversion under Various Reduced Electric Fieldsen_US
dc.typeArticleen_US
dc.identifier.urlhttp://ijneam.unimap.edu.my
dc.contributor.urln.djaouani@yahoo.comen_US


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