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Typical commercial pulsed dye laser systems used in the generation of narrowband, tunable ultraviolet radiation for planar laser-induced fluorescence (PLIF) imaging are optimized for either high (∼5-10  kHz) repetition rates at comparatively low ultraviolet pulse energies (hundreds of microjoules) or high-output pulse energies (>10  mJ) at comparatively low repetition rates (∼10  Hz). In this work we use a frequency-doubled Nd:YAG burst-mode laser to pump a custom dye laser system for high pulse energies and repetition rates of 7.5, 10, and 20 kHz at 566 nm. The frequency-doubled output of over 2.2 mJ/pulse at 283 nm, which can be used for PLIF imaging of combustion radicals, is an order of magnitude higher per pulse energy as compared with continuously pulsed dye laser systems and is ∼3× higher in overall efficiency than a burst-mode optical parametric oscillator at similar wavelengths. The influence of repetition rate, pump energy, and dye concentration on the output conversion efficiency and pulse-to-pulse stability of the current system is discussed.

The paper presents simultaneous high-speed (7.5 kHz) planar laser-induced fluorescence (PLIF) of formaldehyde (CHO) and the hydroxyl-radical (OH) for visualization of the flame structure and heat release zone in a non-premixed unsteady CH/O/N flame. For this purpose, a dye laser designed for high-speed operation is pumped by the second-harmonic 532 nm output of a Nd:YAG burst-mode laser to produce a tunable, 566 nm beam. After frequency doubling a high-energy kHz-rate narrowband pulse train of approximately 2.2 mJ/pulse at 283 nm is used for excitation of the OH radical. Simultaneously, CHO is excited by the frequency-tripled output of the same Nd:YAG laser, providing a high-frequency pulse train over 10 ms in duration at high pulse energies (>100 mJ/pulse). The excitation energies enable signal-to-noise ratios (SNRs) of ~10 and ~60 for CHO and OH PLIF, respectively, using a single high-speed intensified CMOS camera equipped with an image doubler. This allows sufficient SNR for investigation of the temporal evolution of the primary heat release zone and the local flame structure at kHz rates from the spatial overlap of the OH- and CHO-PLIF signals.

1-methylnaphthalene (1-MN) is a widely used laser-induced fluorescence (LIF) tracer for planar imaging of mixture formation and temperature distributions in internal combustion (IC) engines. As the LIF measurement results can be biased by partial tracer oxidation, the conversion of 1-MN and the base fuel isooctane is analyzed in a calibration cell. First, measurements using supercontinuum laser absorption spectroscopy (SCLAS) are presented in order to quantify the conversion by detection of the produced H2O mole fraction. A single mode fiber (SMF) coupled setup is presented, with the fiber core acting as entrance slit of a Czerny-Turner spectrometer. Dependencies on residence time and global air-fuel ratio are presented at pressures up to 1.5 MPa and temperatures up to 900 K, at which distinct tracer and fuel consumption is observed. Signal loss due to intense beam steering was partially compensated using a self-stabilizing double-pass setup with a retroreflector.