The relative raxes at which 0 + CS +CO + S populates individual vibrational levels of CO have been determined (a) from infrared chemiluminescence esperiments, and (b) by using a cw CO laser to measure CO vibrational distibutions produced when mixtures of CS2 + O2 are flash photolysed.
Vibrational excitation of CO from the reaction C + O2
โ Scribed by E.A. Ogryzlo; J.P. Reilly; B.A. Thrush
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- English
- Weight
- 209 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
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
The reaction of CH2, particularly the ground electronic state triplet CH2 [l], with 0 2 is known to be very fast. The effectiveness of the reactions involving both singlet (lCH2) and triplet (3CH2) methylene was most dramatically demonstrated by the drastic effects of O2 on CO laser emissions in bot
The infrared emission observed from Hz0 or Co, when added to discharged oxygen containing Oz(r Zg> and C&(lA ) is shown to arise from their vibrational excitation in the quenching of Oz(\* $'). There was no ev&nce that O$'X> is quenched to the ground state rather than to the ' 4 state.