Kulatilaka Waruna D, Patterson Brian D, Frank Jonathan H, Settersten Thomas B
Combustion Research Facility, Sandia National Laboratories, PO Box 969, Livermore, California 94551, USA.
Appl Opt. 2008 Sep 10;47(26):4672-83. doi: 10.1364/ao.47.004672.
Two-photon laser-induced fluorescence (TP-LIF) line imaging of atomic hydrogen was investigated in a series of premixed CH4/O2/N2, H2/O2, and H2/O2/N2 flames using excitation with either picosecond or nanosecond pulsed lasers operating at 205 nm. Radial TP-LIF profiles were measured for a range of pulse fluences to determine the maximum interference-free signal levels and the corresponding picosecond and nanosecond laser fluences in each of 12 flames. For an interference-free measurement, the shape of the TP-LIF profile is independent of laser fluence. For larger fluences, distortions in the profile are attributed to photodissociation of H2O, CH3, and/or other combustion intermediates, and stimulated emission. In comparison with the nanosecond laser, excitation with the picosecond laser can effectively reduce the photolytic interference and produces approximately an order of magnitude larger interference-free signal in CH4/O2/N2 flames with equivalence ratios in the range of 0.5< or =Phi< or =1.4, and in H2/O2 flames with 0.3< or =Phi< or =1.2. Although photolytic interference limits the nanosecond laser fluence in all flames, stimulated emission, occurring between the laser-excited level, H(n=3), and H(n=2), is the limiting factor for picosecond excitation in the flames with the highest H atom concentration. Nanosecond excitation is advantageous in the richest (Phi=1.64) CH4/O2/N2 flame and in H2/O2/N2 flames. The optimal excitation pulse width for interference-free H atom detection depends on the relative concentrations of hydrogen atoms and photolytic precursors, the flame temperature, and the laser path length within the flame.
利用波长为205nm的皮秒或纳秒脉冲激光激发,对一系列预混CH4/O2/N2、H2/O2和H2/O2/N2火焰中的原子氢进行了双光子激光诱导荧光(TP-LIF)线成像研究。测量了一系列脉冲能量下的径向TP-LIF分布,以确定12种火焰中每种火焰的最大无干扰信号水平以及相应的皮秒和纳秒激光能量。对于无干扰测量,TP-LIF分布的形状与激光能量无关。对于更高的能量,分布的畸变归因于H2O、CH3和/或其他燃烧中间体的光解以及受激发射。与纳秒激光相比,皮秒激光激发可以有效减少光解干扰,并在当量比范围为0.5≤Φ≤1.4的CH4/O2/N2火焰以及0.3≤Φ≤1.2的H2/O2火焰中产生大约大一个数量级的无干扰信号。尽管光解干扰限制了所有火焰中的纳秒激光能量,但在激光激发态H(n = 3)和H(n = 2)之间发生的受激发射是H原子浓度最高的火焰中皮秒激发的限制因素。纳秒激发在最富燃料(Φ = 1.64)的CH4/O2/N2火焰和H2/O2/N2火焰中具有优势。无干扰H原子检测的最佳激发脉冲宽度取决于氢原子和光解前体的相对浓度、火焰温度以及火焰内的激光路径长度。