Formation of electronically excited oxygen atoms in the reactions of argon(3P0,2) and xenon(3P2) atoms with oxygen molecules

1982 ◽  
Vol 86 (14) ◽  
pp. 2765-2769 ◽  
Author(s):  
John Balamuta ◽  
Michael F. Golde
Keyword(s):  
Electronically Excited ◽  
Excited Oxygen ◽  
Oxygen Atoms

Reactive scattering of ground-state and electronically excited oxygen atoms on a liquid hydrocarbon surface

1997 ◽  
Vol 108 ◽  
pp. 387-399 ◽  
Author(s):  
Donna J. Garton ◽  
Timothy K. Minton ◽  
Michele Alagia ◽  
Nadia Balucani ◽  
Piergiorgio Casavecchia ◽  
...  
Keyword(s):  
Ground State ◽  
Liquid Hydrocarbon ◽  
Reactive Scattering ◽  
Electronically Excited ◽  
Excited Oxygen ◽  
Oxygen Atoms

The collisional quenching of electronically excited oxygen atoms, O(21D2), by the gases NH3, H2O2, C2H6, C3H8, and C(CH3)4, using time-resolved attenuation of atomic resonance radiation

1976 ◽  
Vol 54 (11) ◽  
pp. 1765-1770 ◽  
Author(s):  
I. S. Fletcher ◽  
D. Husain
Keyword(s):  
Resonance Radiation ◽  
Recent Measurement ◽  
Absolute Rate ◽  
Collisional Quenching ◽  
Time Resolved ◽  
Excited Atoms ◽  
Electronically Excited ◽  
Hartley Band ◽  
Excited Oxygen ◽  
Oxygen Atoms

A kinetic study of electronically excited oxygen atoms, O(21D2), is presented. These optically metastable species were generated by repetitive pulsed irradiation in the Hartley-band continuum and monitored photoelectrically in absorption by time-resolved attenuation of resonance radiation at λ = 115.2 nm (O(31D20)←O(21D2). Absolute rate constants for the collisional quenching of O(21D2) are reported for the gases NH3, H2O2, C2H6 C3H8, and C(CH3)4. These are found to be respectively (in units of 10−10 cm3 molecule−1 S−1 at 300 K), 6.3 ± 0.7, 5.2 ± 0.6, 7.3 ± 0.8, 9.5 ± 1.0, and 12.3 ± 1.3. With the exception of a recent measurement for NH3• these data represent the first absolute measurements for these quenching gases. Further, a general comparison is made between absolute rate measurements using this technique and recent work by Schiff and co-workers using time-resolved emission at λ = 630 nm (O(21D2) → O(23P2)) in order to monitor the excited atoms.

Branching ratios for electronically excited oxygen atoms formed in the reaction of N+ with O2 at 300 K

1986 ◽  
Vol 84 (4) ◽  
pp. 2158-2166 ◽  
Author(s):  
Andrew O. Langford ◽  
Veronica M. Bierbaum ◽  
Stephen R. Leone
Keyword(s):  
Branching Ratios ◽  
Electronically Excited ◽  
Excited Oxygen ◽  
Oxygen Atoms

Excited State Chemistry in the Stratosphere

1974 ◽  
Vol 52 (8) ◽  
pp. 1452-1464 ◽  
Author(s):  
R. J. Cvetanović
Keyword(s):  
Excited State ◽  
Excited States ◽  
Chemical Behavior ◽  
Molecular Fragments ◽  
Electronically Excited ◽  
Excited Oxygen ◽  
Oxygen Atoms

Potential involvement of excited states of molecules and molecular fragments in the chemistry of the stratosphere is discussed, with particular emphasis on the chemical behavior of electronically excited oxygen atoms.

Collisional quenching of electronically excited oxygen atoms, O(1D): temperature dependence of some rate coefficients

1976 ◽  
Vol 5 (3) ◽  
pp. 173
Author(s):  
G.E. Street ◽  
C.J. Howard ◽  
A.L. Schmeltekopf ◽  
J.A. Davidson ◽  
C.M. Sadowsky ◽  
...  
Keyword(s):  
Temperature Dependence ◽  
Rate Coefficients ◽  
Collisional Quenching ◽  
Electronically Excited ◽  
Excited Oxygen ◽  
Oxygen Atoms

Collision Integrals for Interactions Between Oxygen Atoms and Ions in Electronically Excited States

2006 ◽  
Author(s):  
Annarita Laricchiuta ◽  
Mario Capitelli ◽  
Roberto Celiberto ◽  
Claudine Gorse ◽  
Domenico Bruno ◽  
...  
Keyword(s):  
Excited States ◽  
Collision Integrals ◽  
Electronically Excited States ◽  
Electronically Excited ◽  
Oxygen Atoms
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