Reconstruction of three-dimensional chemiluminescence images with a maximum entropy deconvolution algorithm.

Three-dimensional (3D) images of flame emission are reported using a single direction of optical access. A Cassegrain system was designed with narrow depth of field. Images from this system are dominated by emission from the focused object plane with defocused contributions from out-of-plane structures. Translation of one mirror in the system allows for scanning the object plane through the flame. Images were taken at various depths to create a family of images. Reconstruction of the 3D flame structure was accomplished using a maximum entropy algorithm adapted for use with 3D imaging. Spatial resolution in the direction of imaging is examined using laminar flames with variable offset.

Technique of laser calibration for wavelength-modulation spectroscopy with application to proton exchange membrane fuel cell measurements.

A diode laser sensor was developed for partial pressure and temperature measurements using a single water vapor transition. The Lorentzian half-width and line intensity of the transition were calibrated for conditions relevant to proton exchange membrane (PEM) fuel cell operation. Comparison of measured and simulated harmonics from wavelength-modulation spectroscopy is shown to yield accuracy of +/-2.5% in water vapor partial pressure and +/-3 degrees C in temperature despite the use of a single transition over a narrow range of temperatures. Collisional half-widths in air or hydrogen are measured so that calibrations can be applied to both anode and cathode channels of a PEM fuel cell. An in situ calibration of the nonlinear impact of modulation on laser wavelength is presented and used to improve the accuracy of the numerical simulation of the signal.

Comparison of line-peak and line-scanning excitation in two-color laser-induced-fluorescence thermometry of OH.

Two-line laser-induced-fluorescence (LIF) thermometry is commonly employed to generate instantaneous planar maps of temperature in unsteady flames. The use of line scanning to extract the ratio of integrated intensities is less common because it precludes instantaneous measurements. Recent advances in the energy output of high-speed, ultraviolet, optical parameter oscillators have made possible the rapid scanning of molecular rovibrational transitions and, hence, the potential to extract information on gas-phase temperatures. In the current study, two-line OH LIF thermometry is performed in a well-calibrated reacting flow for the purpose of comparing the relative accuracy of various line-pair selections from the literature and quantifying the differences between peak-intensity and spectrally integrated line ratios. Investigated are the effects of collisional quenching, laser absorption, and the integration width for partial scanning of closely spaced lines on the measured temperatures. Data from excitation scans are compared with theoretical line shapes, and experimentally derived temperatures are compared with numerical predictions that were previously validated using coherent anti-Stokes-Raman scattering. Ratios of four pairs of transitions in the A2Sigma+<--X2Pi (1,0) band of OH are collected in an atmospheric-pressure, near-adiabatic hydrogen-air flame over a wide range of equivalence ratios--from 0.4 to 1.4. It is observed that measured temperatures based on the ratio of Q1(14)/Q1(5) transition lines result in the best accuracy and that line scanning improves the measurement accuracy by as much as threefold at low-equivalence-ratio, low-temperature conditions. These results provide a comprehensive analysis of the procedures required to ensure accurate two-line LIF measurements in reacting flows over a wide range of conditions.

Two-point time-series measurementsof hydroxyl concentration in a turbulent nonpremixed flame.

Quantitative two-point hydroxyl time-series measurements have been performed in a turbulent nonpremixed flame by using two-point picosecond time-resolved laser-induced fluorescence. The current diagnostic system has been improved from its preliminary version to address optical aberrations and fluorescence lifetime fluctuations. In particular, with a newly designed collection system, the aberration-limited blur spot is reduced from 6 mm to 180 microm. Additional photon-counting channels enable the recovery of absolute OH concentrations through a triple-bin integration method. The present research represents what we believe to be the first application of this two-point technique to turbulent flames. Two independent schemes have been applied to remove uncorrelated noise in the derived two-point statistics. We show that optical aberrations can have a significant effect on space-time correlations. However, the sampling rate and fluctuations in the fluorescence lifetime barely affect the spatial autocorrelation function and thus the integral length scale. Such length scales for hydroxyl are found to rise linearly with increasing axial distance at peak [OH] locations. Along the jet centerline, the integral length scale varies slightly below the flame tip but increases rapidly above the flame tip. In addition, the OH length scale demonstrates the same trend as the OH time scale along the jet centerline, but the opposite trend at peak [OH] locations.

Two-point time-series measurements of minor-species concentrations in a turbulent nonpremixed flame.

We report a technique that is capable of making simultaneous two-point time-series measurements of minor-species concentrations in turbulent flames. The experimental setup, which incorporates picosecond time-resolved laser-induced fluorescence, has a spatial resolution of less than 250 microm and a temporal resolution of less than 100 micros, which spatially and temporally resolve microscales in many turbulent flows. Two-point time-series data are given for a standard turbulent nonpremixed flame at Re= 10,000, including a discussion of potential implications.