Issue 0, 1973

Kinetic investigation of electronically excited oxygen atoms, O(21D2), by time-resolved attenuation of atomic resonance radiation in the vacuum ultra-violet. Part 2.—Collisional quenching by the atmospheric gases N2, O2, CO, CO2, H2O and O3.

Abstract

The electronically excited oxygen atom. O(21D2), has been studied in absorption by time-resolved attenuation of the atomic resonance radiation at λ= 115.2 nm (31Do2→ 21D2). Absolute quenching coefficients for the removal of O(21D2) by the gases N2, O2, CO, CO2, H2O and O3 are reported.

These collisional processes are discussed within the context of the spin and orbital symmetry of reactants and products. A detailed comparison with previous laboratory and atmospheric measurements of these processes is presented.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 2, 1973,69, 927-938

Kinetic investigation of electronically excited oxygen atoms, O(21D2), by time-resolved attenuation of atomic resonance radiation in the vacuum ultra-violet. Part 2.—Collisional quenching by the atmospheric gases N2, O2, CO, CO2, H2O and O3.

R. F. Heidner, D. Husain and J. R. Wiesenfeld, J. Chem. Soc., Faraday Trans. 2, 1973, 69, 927 DOI: 10.1039/F29736900927

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