The fractions of energy partitioned between a desorbed product molecule and a solid catalyst are calculated for two surfacecatalyzed reactions according to a simple statistical model. It is shown that the experimentally measured energy disposal in the oxidation of CO on Pt is, to a first approximati
Vibrational energy distribution of CO in the oxidation of C on Pt
β Scribed by Moris Kori; Bret L. Halpern
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 588 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
C'O.cw~t~d to its seventh vibrational level, is generated by C oxidation on Pt at 1000-1400 K. Analysis of its Fourier tran?torm IR emission spectrum suggestsa non-equilibrium,yct statistica1, vibrational distribution. A long-lived reaction complex mvolwng 2-3 Pt atoms 1s postulated.
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Tltc prcscnt study introduces ;I simplified method for :rcating vibrational-rot;ltionnl coupling during the collisionnl cschan~e of energy. This rorationnl couplinp modifies the vibrational cncrgy mismatch, wo and is a dominant cffcct, working to make the actu;ll energy mismatch smtilcr than the app
CO\*(A "ll-X 2P) emission produced from the C(2P) + O2 reaclm hss been observed al thermal cncrgy III a flowing afterdow apparatus. The relabve vIbrational population In the CO\*(A %I) state was dctcrrnmcd The avcngc fmctlon of VIbntional cncrgy dwrbulcd m CO+(A Zn).(/vJ. ws estimated to be 0.20 i 0