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dc.creatorManzanares, Carlos E.en_US
dc.creatorLucas, Donalden_US
dc.creatorEwing, George E.en_US
dc.date.accessioned2006-06-15T14:07:43Z
dc.date.available2006-06-15T14:07:43Z
dc.date.issued1978en_US
dc.identifier1978-TG-02en_US
dc.identifier.urihttp://hdl.handle.net/1811/10647
dc.description$^{1}$ W. Calaway and G. Ewing, Chem. Phys. Lettr. 30, 485 (1975). $^{2}$ W. Calaway and G. Ewing, J. Chem. Phys. 63, 2892 (1975). $^{3}$ C. Manzanares and G. Ewing, J. Chem. Phys. (submitted for publication). Present address of Carlos Manzanares: Universidad Simon Bolivar, Departmento de Quimica, Sartenejas Baruta, Edo. Miranda, venezuela.""en_US
dc.descriptionAuthor Institution: Department of Chemistry, Indiana Universityen_US
dc.description.abstractFor the past several years we have conducted $experiments^{1,2,3}$ designed to investigate the storage, transfer and uses of vibrational energy in simple liquid systems. The liquids we have chosen for study are nitrogen or oxygen either neat or doped with small molecules such as $H_{2}, D_{2}, NO, CO, CO_{2}, N_{2}O, CH_{4}, CH_{4}$, or $CF_{4}$. In our experiments a Q-switched ruby laser is fired into the liquid producing vibrational excitation by Stimulated Ramon Scattering. The transfer or decay of vibrational excitation is monitored by either spontaneous Raman scattering or infrared luminescence. The lifetime of vibrational excitation of a molecule in these systems varies enormously. For $N_{2}{^{*}}$ in liquid nitrogen this time is of the order of seconds while for $CD_{4}{^{*}}$ in liquid nitrogen the time is of the order of $10^{-9}$ sec. The mechanisms for energy transfer in several of these systems will be discussed end models for understanding the vibrational lifetimes will be discussed.en_US
dc.format.extent141703 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleVIBRATIONAL ENERGY TRANSFER IN THE LIQUID STATEen_US
dc.typearticleen_US


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