由重复脉冲纳秒放电激发的稀薄的空气混合物中温度和羟自由基的生成/衰减的测量
Measurements of Temperature and Hydroxyl Radical Generation/Decay in Lean Fuel-Air Mixtures Excited by a Repetitively Pulsed Nanosecond Discharge
关键词:荧光;动力学;激光;低温;混合物
摘 要:OH Laser Induced Fluorescence (LIF) and picosecond (ps), broadband Coherent Anti-Stokes Raman Spectroscopy (CARS) are used for time-resolved temperature and time-resolved, absolute OH number density measurements in lean H2-air, CH4-air, C2H4-air, and C3H8-air mixtures in a nanosecond (ns) pulse discharge cell/plasma flow reactor. The premixed fuel air flow in the reactor, initially at T0 = 500 K and P = 100 torr, is excited by a repetitive ns pulse discharge in a plane-to-plane geometry (peak voltage 28 kV, discharge gap 10 mm, estimated pulse energy 1.25 mJ/pulse), operated in burst mode at 10 kHz pulse repetition rate. In most measurements, burst duration is limited to 50 pulses, to preclude plasma-assisted ignition. The discharge uniformity in air and fuel air flows is verified using sub-ns-gated images (employing an intensified charge-coupled device camera). Temperatures measured at the end of the discharge burst are in the range of T = 550 600 K, using both OH LIF and CARS, and remain essentially unchanged for up to 10 ms after the burst. Time-resolved temperature measured by CARS during plasmaassisted ignition of H2-air is in good agreement with kinetic model predictions. Based on CARS measurement, vibrational nonequilibrium is not a significant factor at the present conditions. Time-resolved, absolute OH number density, measured after the discharge burst, demonstrates that OH concentration in C2H4-air, C3H8-air, and CH4 is highest in lean mixtures. In H2-air, OH concentration is nearly independent of the equivalence ratio. In C2H4-air and C3H8-air, unlike in CH4- air and in H2-air, transient OH-concentration overshoot after the discharge is detected. In C2H4-air and C3H8-air, OH decays after the discharge on the time scale of 0.02 0.1 ms, suggesting little accumulation during the burst of pulses repeated at 10 kHz. In CH4-air and H2-air, OH concentration decays within 0.1 1.0 ms and 0.5 1.0 ms, respectively, showing that it may accumulate during the burst.