Two-photon LIF imaging of atomic oxygen in flames with picosecond excitation

Abstract

Interference-free planar laser-induced fluorescence measurements of atomic oxygen are demonstrated in steady and unsteady laminar premixed methane flames. Two-dimensional LIF measurements of atomic oxygen present a challenge because of the relatively weak two-photon absorption cross-sections and the nonlinear dependence of the LIF signal on laser intensity. Previous two-photon LIF measurements of atomic oxygen in hydrocarbon flames using nanosecond laser excitation were complicated by significant interference from photolytically produced oxygen atoms. Recent results from line-imaging studies in our laboratory indicate that CO 2 is the dominant photolytic precursor. Here, we use picosecond excitation to image atomic oxygen with negligible photolytic interference. We demonstrate this capability in premixed CH 4/O 2/N 2 ( ϕ = 1.08 , X N 2 = 0.63 ) flames with an adiabatic flame temperature of 2480 K and an estimated peak O-atom mole fraction of 0.5%. Peak single-shot signal-to-noise ratios of 9 are achieved, and the estimated detection limit is approximately 80 ppm. Quantitative O-atom LIF measurements also require knowledge of the temperature-dependent quenching cross-sections, which are not currently available. The effects of collisional quenching on the O-atom LIF are predicted using two models for the temperature dependence of quenching cross-sections, and the results indicate that O-atom LIF signals can provide accurate measurements of O-atom profiles in flames. Measurements in an acoustically forced Bunsen flame illustrate the feasibility of using O-atom LIF to investigate flow–flame interactions.