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dc.creatorTurrell, George C.en_US
dc.creatorJones, W. D.en_US
dc.creatorDecius, J. C.en_US
dc.date.accessioned2006-06-15T12:49:37Z
dc.date.available2006-06-15T12:49:37Z
dc.date.issued1957en_US
dc.identifier1957-B-7en_US
dc.identifier.urihttp://hdl.handle.net/1811/7599
dc.description$^{*}$Supported by the Office of Naval Research. $^{\dagger}$Present address, Metealf Research Laboratory, Brown University, Providence, Rhode Island. $^{\dagger}$Present address, Department of Chemistry, Cornell University, Ithaca, New York. $^{1}$R. N. Schwartz, Z. L. Slawsky, and K. F. Hertzfeld, J. Chem. Phys. 20, 1591 (1952).en_US
dc.descriptionAuthor Institution: Department of Chemistry, Oregon State Collegeen_US
dc.description.abstract“An infrared spectrophone for study of vibrational relaxation was developed and applied to the measurement of relaxation in carbon monoxide. CO was chosen for its theoretically predicted behaviour. Application of the $Schwartz-Slawsky-Herzfeld^{1}$ theory predicts a very long lifetime for pure CO, with a high dependence on reduced collision mass, low mass giving shorter lifetime. Special interest was directed toward $CO-H_{2}$ mixture, because of the predicted effect of $H_{2}$ and the fact that $H_{2}$ is an impurity in commercial CO. The lifetimes at room temperature for the collision $CO+$M, extrapolated to one atmosphere pressure of M. varied from 1.6 microseconds for $M=H_{2}$ to 190 microseconds for $M= CO$.”en_US
dc.format.extent90694 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleVIBRATIONAL RELAXATION IN CARBON MONOXIDE BY THE SPECTROPHONE $METHOD^{*}$en_US
dc.typearticleen_US


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