Open AccessQuenching rate coefficients for O + ( 2 P) derived from middle ultraviolet airglow
Author(s) -
Stephan A. W.,
Meier R. R.,
Dymond K. F.,
Budzien S. A.,
McCoy R. P.
Publication year - 2003
Publication title -
journal of geophysical research: space physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/2002ja009540
Subject(s) - airglow , thermosphere , photoionization , excited state , quenching (fluorescence) , atomic physics , analytical chemistry (journal) , physics , ionosphere , chemistry , atmospheric sciences , ionization , ion , fluorescence , optics , geophysics , quantum mechanics , chromatography
O + ( 2 P) is produced in the sunlit thermosphere primarily by photoionization of atomic oxygen. Thermospheric atomic oxygen concentrations can be inferred from measurements of airglow produced near 732.0 nm by the transition of this excited state to the 2 D state and at 247.0 nm by the transition to the 4 S ground state. The accuracy of these concentrations depends on the accuracy of the important chemical reaction rates used in the airglow model, including quenching of O + ( 2 P). We obtain coefficients for the quenching of O + ( 2 P) by O and N 2 by modeling rocket and satellite limb measurements of thermospheric middle ultraviolet (MUV) airglow at 247.0 nm. We derive a reaction rate for N 2 of 1.8 × 10 −10 cm 3 s −1 , which is lower than the value obtained by other airglow studies but in agreement with laboratory measurements. We obtain a best fit value for the O reaction rate of 5.0 × 10 −11 cm 3 s −1 , with an upper limit of 8.4 × 10 −11 cm 3 s −1 . The value of the O reaction rate determined by fits to 172 altitude profiles of the 247.0 nm emission shows a strong correlation with the magnitude of the excitation g factor. However, the airglow profile above 260 km favors the upper limit we have identified.