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Quenching of NO(D /sup 2/. sigma. /sup +/, E /sup 2/. sigma. /sup +/) formed by UV photodissociation of NOCl

Journal Article · · J. Chem. Phys.; (United States)
OSTI ID:5424803
The photodissociation of NOCl at 193 nm has resulted in vibrationally excited NO which was subsequently excited to the D(v = 5) and E(v = 0) states. The resulting fluorescence at 160--180 nm has been analyzed in terms of a kinetic model. Saturation of the photodissociation was observed at laser intensities above 2 MW/cm/sup 2/. The quenching rate constants of NO* by Ne, Ar, Kr, and Xe were determined to be k/sub Ne/ = (6.4 +- 1.6) x 10/sup -11/ cm/sup 3/ s/sup -1/, k/sub Ar/ = (1.7 +- 0.4) x 10/sup -10/ cm/sup 3/ s/sup -1/, k/sub Kr/ = (6.6 +- 1.7) x 10/sup -10/ cm/sup 3/ s/sup -1/, and k/sub Xe/ = (1.0 +- 0.2) x 10/sup -9/ cm/sup 3/ s/sup -1/. The quenching by NO and Cl was explained in terms of charge transfer mechanism and the corresponding rate constants were found to be: k/sub NO/ = (2.7 +- 0.6) x 10/sup -9/ cm/sup 3/ s/sup -1/ and k/sub Cl/ = (2.1 +- 0.5) x 10/sup -9/ cm/sup 3/ s/sup -1/.
Research Organization:
Department of Physics, University of Illinois at Chicago Circle, Chicago, Illinois 60680
OSTI ID:
5424803
Journal Information:
J. Chem. Phys.; (United States), Journal Name: J. Chem. Phys.; (United States) Vol. 76:9; ISSN JCPSA
Country of Publication:
United States
Language:
English