Abstract

Using a DFB laser diode at 1509.3 nm the OH(v = 1) formed in the reaction O(1D) + H2O was detected by absorption at the transition (v = 3)←(v = 1). The advantage of the method is the ability to obtain reliable data on absolute concentrations of vibrationally excited radicals. The spectrum of transient absorption near Q(3/2) line of 2Π3/2 term was recorded. At a pressure of 8 Torr He, the rotation distribution was found to be in thermal equilibrium. The yields of OH(v = 1) and OH(v = 2) in the chemical reaction were determined. The rate constants of vibrational relaxation of OH(v = 1) on H2O and SF6 were measured.

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