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dc.creatorKomissarov, Anatoly V.en_US
dc.creatorHeaven, M. C.en_US
dc.date.accessioned2006-06-15T20:11:14Z
dc.date.available2006-06-15T20:11:14Z
dc.date.issued2001en_US
dc.identifier2001-RC-11en_US
dc.identifier.urihttp://hdl.handle.net/1811/20116
dc.description$^{a}$Work supported by Air Force Office of Scientific Research.en_US
dc.descriptionAuthor Institution: Fachbereich 9, Anorganische Chemie, Emory University; Department of Chemistry, Emory Universityen_US
dc.description.abstractMetastable $NCl(a^{1}\Delta)$ is a promising energy carrier for use in chemically driven iodine lasers. The present studies of NCl kinetics were conducted in support of efforts to develop an NCl(a)/I laser system. Photolysis of $N_{3}Cl$ was used to generate NCl for spectroscopic and kinetic measurements. The kinetics of NCl in the ground and excited electronic states was studied by means of time-resolved direct absorption and emission measurements. Rate constants for removal of NCl(a) by $O_{2}$, $H_{2}$, $Cl_{2}$, $I_{2}$, $ClN_{3}$ and self-annihilation $(NCl(a)+NCl(a))$ were determined. The reaction of NCl(a) with $I_{2}$ and energy transfer from NCl(a) to I were examined using photolysis of $N_{3}Cl/I_{2}$ and $N_{3}Cl/CH_{2}I_{2}$ mixtures, respectively. Time-resolved fluorescence from $I^{*}$ was used to follow the reaction and transfer kinetics. Kinetic models were developed to simulate the $I^{*}$ time histories. The models, which were anchored by the NCl removal rate constants, were used to explore the kinetics of secondary photoproducts. The relevance of the results to NCl/I transfer lasers will be discussed.en_US
dc.format.extent205509 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleKINETIC SPECTROSCOPY OF $NCl^{a}$en_US
dc.typearticleen_US


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