Vibrational deactivation studies of OH X 2Π (ν=1-5) by N2 and O2

被引:31
|
作者
D'Ottone, L [1 ]
Bauer, D [1 ]
Campuzano-Jost, P [1 ]
Fardy, M [1 ]
Hynes, AJ [1 ]
机构
[1] Univ Miami, Rosenstiel Sch Marine & Atmospher Sci, Div Marine & Atmospher Chem, Miami, FL 33149 USA
关键词
D O I
10.1039/b407297a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The deactivation kinetics of vibrationally excited OH X (2)Pi (nu=1-5) were studied using a pulsed laser photolysis-pulsed laser induced fluorescence technique. Temporal profiles of OH (nu) were obtained by exciting off-diagonal (Deltanu=-1,-3) transitions in the A-X band of OH and monitoring the diagonal, blue shifted fluorescence. Photolysis of O-3 at 266 nm was used to produce (OD)-D-1 which reacted rapidly with H-2, CH4 and H2O to produce OH (nu). Deactivation rate coefficients for OH (nu=1-5) with O-2 and N-2 and for OH (v=2,1) with O-3 were obtained. The deactivation rate coefficients show an exponential dependence on vibrational level for both O-2 and N-2, however O-2 is much more efficient.
引用
收藏
页码:4276 / 4282
页数:7
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