Vibrational relaxation of NO(ν = 2, 3) by atomic oxygen
✍ Scribed by J.A. Dodd; S.M. Singleton; S.M. Miller; P.S. Armstrong; W.A.M. Blumberg
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 468 KB
- Volume
- 260
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
A two-laser, pump-probe arrangement has been used to measure room-temperature rate constants for the collision-induced relaxation of NO(v ~ 2, 3) by O atoms. The rate constants ko(o) are equal to (2.2 + 0.2) × 10-~t and (2.5 + 0.3) x 10 -11 cm 3 s -1 for v = 2 and 3, respectively. These values are significantly lower than previously measured values for v = 1, but are in accord with model predictions assuming the role of a metastable NO~ intermediate. The NO self-relaxation rate constants kNo(u) have been measured to be (3.2 + 0.3)X 10 -12 and (4.0 +_ 0.4)X 10 -t2 cm 3 s-I for v = 2 and 3, respectively, in reasonable agreement with published results.
📜 SIMILAR VOLUMES
A two-laser (IR overtone pump and UV laser-induced fluorescence probe) technique has been used to measure vibrational relaxation for NO(X \*II, v= 3) colliding with NO, 02, and CH4 at 295 K. The total removal rate coefficients are: (3.26 k 0.24) X 10-'2cm3s-'forNO,(1.46f0.15)~10-'3cm3s-'for02,and(1.
The vibrational relasation time for COz(v3) + O(3P) has been mcasurcd by Inscr fluorescence. The observed value, pCo2,0 = 0.21 \* 0.04 fiscc, is an order of mqniludc lower than the relaxation time for self-collisions.
Rate constants have been determined for the collisional de-excitation of HCl (v = 3, 2 and L) by CL
The rake constam [or NO+(u) vibrational relaxation by memsrable 02('A ) molecul& is round LO be (3+2)x10-" err? 5-l al room lemperanxc. in comras~ IO the lack of vibrational quenching of NO'(u) by ground-stale 02('X) molecules. [or which the quenching mLe constant <lo-" cm3 s-l. This suggests that N
A quasiciassieal tra&ctory study has been carried out to investigate the dynanlics of collisions between H f &(I G o C4) and D + Dz(l Q IJ is; 4), using the accurate Yates-Lester potential. Reaction is selectively enhanced by the vibrational excitation of the diitomic reagent, as judged by informati