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dc.creatorSmith, Gregory P.en_US
dc.creatorCrosley, David R.en_US
dc.date.accessioned2006-06-15T14:39:01Z
dc.date.available2006-06-15T14:39:01Z
dc.date.issued1981en_US
dc.identifier1981-MF'-1en_US
dc.identifier.urihttp://hdl.handle.net/1811/11537
dc.descriptionAuthor Institution:en_US
dc.description.abstractEnergy transfer from specific rotational levels (quantum Number $N^{\prime}$;) of $v^{\prime}=1$ of the $A^{2}\Sigma ^{+}$ state of the hydroxyl radical has been studied. The environment is the burnt gases ($\sim 70% N_{2}$) of a $Ch_{4/air}$ flame at $T=1900$ K and atmospheric pressure. A tunable laser populates seven individual levels in the range $N^{\prime}=1$ to 16, and rotationally resolved fluorescence measurement are made with a scanning monochromator. The energy transfer rate is found to decrease with increasing $N^{\prime}$. The rotational population distribution for molecules transferred into $v^{\prime}=0$ is thermal-like ($T\sim 2200 $K) for an initial N `=1,5 and 10 in v `=1 but much hotter ($T\sim3400 $K) for an initial N `=13-16. The ratio of the rate of rotational energy transfer within v `=1, to the quenching rate, decreases rapidly over the range N `=13 to 16, which spans the predissociation limit. A definite propensity for transfer to nearby levels, and for maintaining, spin component ($F_{1} vs F_{2}$), is exhibited during rotational relaxation of the levels of high N`.en_US
dc.format.extent87276 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleENERGY TRANSFER OF $OH(A^{2} \Sigma ^{+},v`=1)$ IN FLAME GASESen_US
dc.typearticleen_US


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