Issue 0, 1976

Kinetic spectroscopy in the far vacuum ultraviolet. Part 2.—Fluorine atom resonance spectrometry and the measurement of F 2P atom concentrations

Abstract

A technique for the first atomic resonance detection of ground state F 2p52PJ atoms in a flow system is described. Collimated hole structures were used in place of windows to separate the lamp, flow tube and spectrometer. Resonance absorption measurements of the 3s–2p5 multiplet transition of F, between 95 and 98 nm, were used to obtain the first values for the oscillator strengths fik of the 97.39 nm 4P[fraction three-over-two]2P[fraction three-over-two] and the 97.77 nm 4P[fraction three-over-two]2P½ lines of these multiplets. The values, which have an estimated standard error of ±30 %, are : fik(97.39)= 4 × 10–5; fik(97.77)= 1 × 10–5.

Fluorine atom resonance fluorescence in the 3s2PJ–2p52PJ multiplet, and in one line of the 3s4PJ–2p52PJ multiplet, was observed for the first time; it was used to measure concentrations of [F 2PJ] atoms down to 1 × 1011 cm–3. Measurement of absolute [F2PJ] was by means of the rapid reactions (1) and (2), F + Br2 [graphic omitted] BrF + Br (1), F + Cl2→ ClF + Cl. (2), Attenuation of F atom resonance fluorescence was used to measure the rate constant k1 at 300 K. Combining this value with another (mass spectrometric) determination of k1, the mean value k1=(2.2 ± 1.1)× 10–10 cm3 molecule–1 s–1 from 298 to 300 K was obtained.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 2, 1976,72, 191-206

Kinetic spectroscopy in the far vacuum ultraviolet. Part 2.—Fluorine atom resonance spectrometry and the measurement of F 2P atom concentrations

P. P. Bemand and M. A. A. Clyne, J. Chem. Soc., Faraday Trans. 2, 1976, 72, 191 DOI: 10.1039/F29767200191

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