Laser-induced fluorescence detection of HCO in a low-pressure flame

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We report the first laser-induced fluorescence measurement of the formyl radical, HCO, in a flame environment. A methane/oxygen flame =1.03, was burned at 5.8 Torr. The (0,0,2) vibrational level of thestate (which in emission forms the hydrocarbon flame bands) was excited at 245 nm. Dispersed fluorescence spectra confirmed the identification. Profiles of HCO, OH and temperature were determined using LIF. Spectroscopic aspects, including line assignments, interferences from OH and O2, and further information needed for quantitative measurements, are discussed. A flame model shows the correct ordering for the appearance of these radicals (as well as CH and singlet CH2) as a function of height, but predicts all species to arise later in the flame than measured.

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      The formyl radical (HCO) has for a long time been recognized as a good indicator of the flame front, as its concentration was found to be temporally and spatially correlated with the local HR rate [5,11]. The first HCO fluorescence detection in a combustion environment was performed in a methane/oxygen flame (ϕ = 1.02) at low pressure (5.8 Torr) by excitating the QR0 (J = 9) line in the (0, 0, 2)–(0, 0, 0) band of the B–X system near 244 nm, and the fluorescence emission from 276 nm to 284 nm was collected [12]. In further studies [11,13], two-dimensional HCO PLIF detection has been reported under various flame conditions by exciting the rotational transitions in the B–X (0, 0, 0)–(0, 0, 0) band near 258 nm with a conventional Nd:YAG/Dye laser system.

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