Vacuum-Ultraviolet Photolysis of N2O. II. Deactivation of N2(A 3Σu+*rpar; and N2(B 3Πg)

Abstract
Quenching of N2(A 3Σu+) , produced during the photodissociation of N2O with 1470‐Å radiation, was studied using the NO γ‐band emission excited by the process N2(A 3Σu+) + NO → N2 + NO(A 2Σ+) as a monitor of N2(A 3Σu+) . The relative quenching efficiencies of NH3, C2H2, C2H4, NO, C2N2, N2O, O2, CO, CO2, H2 CH4, N2, Ar, and He are 2.6, 2.3, 2.2, 1, 0.8, 0.091, 0.054, 0.036, < 4 × 10−4,≤ 10−4, < 10−4, < 10−4, < 10−4, and < 10−4. At 1236 Å the B 3Πg state of N2 is produced in N2O photolysis and the variation of the intensity of N2O first positive emission with N20 pressure was used to evaluate the quenching rate of N2(B 3Πg) by N2O. The value obtained was 1.6 × 10−10 cm3 molecule−1·sec−1. Quenching efficiencies for other gases were determined relative to N2O and hence absolutely. The values obtained for NO, CO2, O2, CO, H2, N2, Ar, and He are ∼2.4 × 10−10, 1.5 × 10−10, 1.1 × 10−10, 8.5 × 10−11, 4.6 × 10−11, 2.7 × 10−11, 1.6 × 10−12, and 8 × 10−13 cm3 molecule−1·sec−1.