Rate cocfticicnts for the collisiona! quenching of Of (' a,) by NO and CO, at 2-8 torr and 300 K have been determined. X-NO = (2.48 t 0.23) X lo-" cm3 moleculc~' s-' anzkCOz = (2.56 5 0.12) X IO-" cm3 moleculc~ s-l.
Collisional quenching of chlorine (32P12) by H2, D2, CO, O2, N2 and CO2
โ Scribed by S.A. Sotnichenko; V.Ch. Bokun; A.I. Nadkhin
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 712 KB
- Volume
- 153
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
The quenching of electronically excited chlorine atoms, CI( 3 'PI ?). by several gases has been studied using a small gain laser pulse method, based on photochemical Cl and I lasers, operating on spin-orbit transitions 2P,,Z,F+*P3,Z,F... The quenching efliciencies for HZ, D,, CO, and SF6 are shown to be high and it is suggested that quenching occurs via near-resonant electronic to vibration-rotation (E-V,R) energy transfer. Also the collisional broadening parameters of the 2P, ,?,,:, >-2P3,2,F. =z line of Cl for a number of atoms and molecules have been measured.
๐ SIMILAR VOLUMES
Collisional deactivation processes of the CO\* A 2TI( u= I ) state are investigated by a time-resolved laser-induced fluorescence technique.Theoverallquenchingrateconstantsaredeterminedtobe (9.lfl.O)xlO-", (1.3~0.1)~10-", (1.1~0.1)~10-9, (1.9+ 0.1 )X 10m9, and (1.5 kO.1) X 10m9 cm' molecule-' s-',
lL11c coefficrents for coll1s1on~1 removal of Ott D) by SLY atnlosplrertc gases have been measured by momtormg the appearance of O(3P) followng photolvtlc productlon of O(' D) The measured values, x"hI 2 SJ, m units of IO-" cm3 molccule-' s-l arc k-0, = ?? 8 5 :! 3, k~~ = 2 52 ? 0.25, k-co, = 10 4 +
Reccivcd 11 May 1973 Rxte constants are reported for collisional quenching ot K'(4p'P) and K'(5p'P) by H20, CFq, and CA+. TRc X;'(+p'P) Or K'(Sp\*P) is produced by photodissociation of K1 vapor nt 2450 A or 1925 A. respectively.
A photoacoustic method is used under such experimental conditions that the (01'0) level ofC02 gas is not in e@li%rinrn with the other vibrational Ievck The rate mnsta.ntsk;o characterizing the CO2 (01'0) collisional deactivation by Nz, CO aad 02 are measured directly.
Collisional deactivation rate constants of CO+ A 'fI(v=O and 2) by He, Ne. Ar, N,, and CO have been determined by using a time-resolved laser-induced fluorescence technique. The results were combined with the previously determined Y= 1 rate constants to obtain an interesting u dependence of the rate