Quantitative 2D thermometry in turbulent sooting non-premixed flames using filtered Rayleigh scattering.

This paper demonstrates the application of a thermometry method in turbulent sooting non-premixed flames using filtered Rayleigh scattering (FRS). Fuel tailoring is used to establish a specific C2H2-based fuel mixture such that temperature can be determined accurately by a single FRS measurement over the entirety of mixture fraction space, or equivalently, for all relevant thermo-chemical states. Evaluation is performed in a hierarchy of flows to establish measurement precision and accuracy. Initial assessments in a series of heated fuel mixtures; non-sooting, near-adiabatic flat flames; and laminar non-premixed sooting flames show accuracy of the approach over a full range of expected temperatures and high single-shot measurement precision (e.g., 65

Evaluation of the Tenti S6 model for hydrocarbon fuels at elevated temperatures using filtered Rayleigh scattering measurements.

This Letter targets the assessment of the well-known Tenti S6 model for predicting the Rayleigh-Brillouin scattering (RBS) spectra of select gas-phase hydrocarbon fuels (CH4, C2H2, C2H4, C3H8, and C4H10) over a temperature range of 300 to 700 K. The Tenti S6 model is evaluated by comparing filtered Rayleigh scattering (FRS) measurements to synthetic FRS signals generated from the combination of the Tenti S6 output and an accurate iodine absorption filter model. The experimental and synthetic FRS results agree very well (<3% difference) over the full temperature range for CH4, C2H2, and C2H4, indicating accurate calculation of the RBS spectra. For C3H8 and C4H10, there are some large differences between the experimental and synthetic FRS results which cannot be resolved through tuning of bulk viscosity, internal heat capacity, or inclusion of vibrational degrees of freedom, suggesting the need for detailed measurements of the Rayleigh-Brillouin spectra.

Quantitative planar temperature imaging in turbulent non-premixed flames using filtered Rayleigh scattering.

The paper presents results demonstrating the application of filtered Rayleigh scattering (FRS) for quantitative temperature measurements within turbulent non-premixed jet flames. Through targeted fuel tailoring, i.e., the selection of a specific fuel mixture, temperature measurements are made under non-premixed fueling conditions with a single FRS measurement. For this to be feasible, the instantaneous measured FRS signal is uniquely proportional to the local temperature for all thermo-chemical states of the targeted fuel-oxidizer system. Simulated results using laminar, counterflow flame calculations show that for select CH4/H2/Ar fuel mixtures issuing into air, a unique relationship between the local FRS signal and temperature is achieved for all mixture fraction values over a full range of operating conditions from near-equilibrium to near-extinction flames. Furthermore, for the selected FRS-optimized fuel, the local mixture-averaged Rayleigh scattering cross section is nearly constant from fuel to oxidizer to products. Thus, traditional laser Rayleigh scattering (LRS) can be used to determine the temperature as a "standard" to which to compare and assess the FRS-based temperature results. Simultaneous LRS-FRS temperature measurements from Re=10,000, 20,000, and 30,000 turbulent non-premixed jet flames are presented that show good agreement between the two techniques in terms of instantaneous temperature fields and statistical quantities at various spatial locations within the flame. These results provide confidence that the current approach of FRS thermometry allows for accurate temperature measurements within the selected set of turbulent non-premixed flames.

Quantitative fuel vapor/air mixing imaging in droplet/gas regions of an evaporating spray flow using filtered Rayleigh scattering.

This Letter demonstrates the application of filtered Rayleigh scattering (FRS) for quantitative two-dimensional fuel vapor/air mixing measurements in an evaporating hydrocarbon fuel spray flow. Using the FRS approach, gas-phase measurements are made in the presence of liquid-phase droplets without interference. Effective suppression of the liquid-phase droplet scattering using FRS is enabled by the high spectral purity of the current Nd:YAG laser system. Simultaneous Mie-scattering imaging is used to visualize the droplet field and illustrate the droplet loading under which the FRS imaging is applied in the current spray flows. The initial quantification of the FRS imaging is based on calibration measurements from a flow cell of known fuel vapor/air mixtures, while future work targets the utilization of a Rayleigh-Brillouin spectral model for quantification of the FRS signals.

Spatial resolution-preserving retroreflection for gas-phase laser scattering measurements in turbulent flames using a phase-conjugate mirror.

This Letter reports on the demonstration of a stimulated Brillouin-scattering phase conjugate mirror (SBS-PCM) for multipass laser-based scattering measurements in turbulent flames. Retroreflective measurements using the SBS-PCM show substantial improvements in spatial-resolution preservation as compared to measurements using a conventional mirror as a multipass reflector. The results using the SBS-PCM indicate an insensitivity to large index-of-refraction gradients and preservation of the original spatial resolution as defined by the laser beam under reacting flow conditions. This approach offers the possibility of increasing signal-to-noise ratios within low-signal gas-phase measurements such as Rayleigh and Raman scattering.

Ultrahigh laser pulse energy and power generation at 10 kHz.

This Letter presents results from a new master-oscillator, power-amplifier pulse-burst laser system demonstrating ultrahigh pulse energies greater than 2.0 J/pulse at 1064 nm with interpulse separations of 100 µs (10 kHz) for burst durations of 100 pulses. Each pulse generates peak powers exceeding 130 MW and an average power of approximately 20 kW is generated over a 100-pulse-burst. Pulse energies decrease by less than 10% over a 100 sequential pulses, demonstrating negligible "droop" over long-duration pulse trains. Second-harmonic generation of 532 nm with conversion efficiency greater than 50% is demonstrated for 100-pulse-burst durations.

Separation of thiamin and its phosphate esters by capillary zone electrophoresis and its application to the analysis of water-soluble vitamins.

A capillary zone electrophoresis method for the separation and determination of thiamin and its phosphate esters (free thiamin, thiamin monophosphate, and thiamin pyrophosphate) was developed and optimized. The efficiency achieved with boric acid-sodium tetraborate decahydrate buffer (pH 8.24; 65-8 mM) at an applied potential of 30 kV gave the detection limit (S/N = 3) and the limit of quantitative measurement (S/N = 10) of thiamin and its phosphate esters ranging from 10(-4) to 6 x 10(-4) mM and from 6 x 10(-4) to 1.2 x 10(-3) mM, respectively. The effects of pH on separation and migration times of thiamin and its phosphate esters are described. The method was validated and applied to the quantitative determination of thiamin in commercial tablets containing both a massive and a normal dose of thiamin.

Rayleigh scattering cross sections of combustion species at 266, 355, and 532 nm for thermometry applications.

Rayleigh scattering cross sections are measured for nine combustion species (Ar, N2, O2, CO2, CO, H2, H2O, CH4, and C3H8) at wavelengths of 266, 355, and 532 nm and at temperatures ranging from 295 to 1525 K. Experimental results show that, as laser wavelengths become shorter, polarization effects become important and the depolarization ratio of the combustion species must be accounted for in the calculation of the Rayleigh scattering cross section. Temperature effects on the scattering cross section are also measured. Only a small temperature dependence is measured for cross sections at 355 nm, resulting in a 2-8% increase in cross section at temperatures of 1500 K. This temperature dependence increases slightly for measurements at 266 nm, resulting in a 5-11% increase in cross sections at temperatures of 1450 K.

Optimization of CH fluorescence diagnostics in flames: range of applicability and improvements with hydrogen addition.

This study quantifies the range of premixed flame conditions for which CH fluorescece diagnostics are applicable, and it shows that the CH fluorescence signal can be increased if some of the hydrocarbon fuel is replaced with hydrogen. The CH fluorescence signal is found to be adequate for fuel-air equivalence ratios (phi) as small as 0.85 for both methane-air and propane-air flames. The CH signal increases until a maximum at phi = 1.25 and phi = 1.35 for methane-air and propane-air flames, respectively, and then decreases for richer conditions. A strategy to increase the CH fluorescence signal and decrease interference from soot precursors is proposed by addition of the proper amount of hydrogen to the hydrocarbon fuel. Hydrogen addition reduces the background signal from soot precursors by as much as afactor of 10 and increases the CH fluorescence signal by as much as 80%. The normalized CH fluorescence measurements are compared with computations that utilize GRI-MECH 3.0 chemistry. Sources experimental uncertainties are discussed.