Publications

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The collapse or merging of individual plumes of direct-injection gasoline injectors is of fundamental importance to engine performance because of its impact on fuel-air mixing. However, the mechanisms of spray collapse are not fully understood and are difficult to predict. The purpose of this work is to study the aerodynamics in the inter-spray region, which can potentially lead to plume collapse. High-speed (100 kHz) particle image velocimetry is applied along a plane between plumes to observe the full temporal evolution of plume interaction and potential collapse, resolved for individual injection events. Supporting information along a line of sight is obtained using simultaneous diffused back illumination and Mie-scatter techniques. Experiments are performed under simulated engine conditions using a symmetric eight-hole injector in a high-temperature, high-pressure vessel at the “Spray G” operating conditions of the engine combustion network. Indicators of plume interaction and collapse include changes in counter-flow recirculation of ambient gas toward the injector along the axis of the injector or in the inter-plume region between plumes. The effect of ambient temperature and gas density on the inter-plume aerodynamics and the subsequent plume collapse are assessed. Increasing ambient temperature or density, with enhanced vaporization and momentum exchange, accelerates the plume interaction. Plume direction progressively shifts toward the injector axis with time, demonstrating that the plume interaction and collapse are inherently transient.

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The effects of combustion on the strain rate field in turbulent premixed CH4/air Bunsen flames were investigated using simultaneous tomographic PIV and OH LIF measurements. Measurements were compared in three lean-to-stoichiometric flames that have different amounts of heat release and Damköhler numbers greater than unity. The extensive strain rate preferentially aligned with the flame normal in the reaction zone. The strength of this alignment increased with increasing heat release leading to highly extensive flame-normal strain rate. These effects are associated with the gas expansion normal to the flame surface which is largest for the stoichiometric flame. In the preheat zone the compressive strain rate exhibited a tendency to align with the flame normal while away from the flame front the flame the strain rate alignment was arbitrary in both the reactants and products. The flame-tangential strain rate was on average positive across the flame front implying that the turbulent strain rate field contributes to the enhancement of scalar gradients as in passive scalar turbulence.

We present a series of benchmark flames consisting of six partially-premixed piloted dimethyl ether (DME)/air jet flames. These flames provide an opportunity to understand turbulence-flame interactions for oxygenated fuels and to develop predictive models for these interactions using a canonical burner geometry. The development of accurate models for DME/air flames would establish a foundation for studies of more complex oxygenated fuels. The flames are stabilized on a piloted jet burner similar to that of the partially-premixed methane/air jet flames that have been studied extensively within the context of the TNF Workshop. This series of six jet flames spans jet exit Reynolds numbers, ReD, from 29,300 to 73,300 and stoichiometric mixture fractions, ξst, from 0.35 to 0.60. Flame conditions range from very low probability of localized extinction to a high probability of localized extinction and subsequent re-ignition. Measurements in the flames are compared at downstream locations from 5 to 25 diameters above the nozzle exit. Mean and fluctuating velocity components are measured using stereo particle image velocimetry (SPIV). Simultaneous laser-induced fluorescence (LIF) imaging of OH and CH2O provides insights into the distribution of these intermediate species in partially-premixed DME/air flames. OH LIF imaging is also combined with SPIV to investigate the strain rate field across the reaction zone.

Stabilization methods of turbulent flames often involve mixing of reactants with hot products of combustion. The stabilizing effect of combustion product enthalpy has been long recognized, but the role played by the chemical composition of the product gases is typically overlooked. We employ a counterflow system to pinpoint the effects of the combustion product stoichiometry on the structure of turbulent premixed flames under conditions of both stable burning and local extinction. To that end, a turbulent jet of lean-to-rich, CH4/O2/N2-premixed reactants at a turbulent Reynolds number of 1050 was opposed to a stream of hot products of combustion that were generated in a preburner. While the combustion product stream temperature was kept constant, its stoichiometry was varied independently from that of the reactant stream, leading to reactant-to-product stratification of relevance to practical combustion systems. The detailed structure of the turbulent flame front was analyzed in two series of experiments using laser-induced fluorescence (LIF): joint CH2O LIF and OH LIF measurements and joint CO LIF and OH LIF measurements. Results revealed that a decrease in local CH2O+OH and CO+OH reaction rates coincide with the depletion of OH radicals in the vicinity of the combustion product stream. These critical combustion reaction rates were more readily quenched in the presence of products of combustion from a stoichiometric flame, whereas they were favored by lean combustion products. As a result, stoichiometric combustion products contributed to a greater occurrence of local extinction. Furthermore, they limited the capacity of premixed reactants to ignite and of the turbulent premixed flames to stabilize. In contrast, lean and rich combustion products facilitated flame ignition and stability and reduced the rate of local extinction. The influence of the combustion product stream on the turbulent flame front was limited to a zone of approximately two millimeters from the gas mixing layer interface (GMLI) of the product stream. Flame fronts that were separated from the GMLI by larger distances were unaffected by the product stream stoichiometry.

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In turbulent flows, the interaction between vorticity, ω, and strain rate, s, is considered a primary mechanism for the transfer of energy from large to small scales through vortex stretching. The ω-s coupling in turbulent jet flames is investigated using tomographic particle image velocimetry (TPIV). TPIV provides a direct measurement of the three-dimensional velocity field from which ω and s are determined. The effects of combustion and mean shear on the ω-s interaction are investigated in turbulent partially premixed methane/air jet flames with high and low probabilities of localized extinction as well as in a non-reacting isothermal air jet with Reynolds number of approximately 13 000. Results show that combustion causes structures of high vorticity and strain rate to agglomerate in highly correlated, elongated layers that span the height of the probe volume. In the non-reacting jet, these structures have a more varied morphology, greater fragmentation, and are not as well correlated. The enhanced spatiotemporal correlation of vorticity and strain rate in the stable flame results in stronger ω-s interaction characterized by increased enstrophy and strain-rate production rates via vortex stretching and straining, respectively. The probability of preferential local alignment between ω and the eigenvector of the intermediate principal strain rate, s2, which is intrinsic to the ω-s coupling in turbulent flows, is larger in the flames and increases with the flame stability. The larger mean shear in the flame imposes a preferential orientation of ω and s2 tangential to the shear layer. The extensive and compressive principal strain rates, s1 and s3, respectively, are preferentially oriented at approximately 45° with respect to the jet axis. The production rates of strain and vorticity tend to be dominated by instances in which ω is parallel to the s1 - s2 plane and orthogonal to s3.

In this LDRD project, we developed a capability for quantitative high - speed imaging measurements of high - pressure fuel injection dynamics to advance understanding of turbulent mixing in transcritical flows, ignition, and flame stabilization mechanisms, and to provide e ssential validation data for developing predictive tools for engine combustion simulations. Advanced, fuel - efficient engine technologies rely on fuel injection into a high - pressure, high - temperature environment for mixture preparation and com bustion. Howe ver, the dynamics of fuel injection are not well understood and pose significant experimental and modeling challenges. To address the need for quantitative high - speed measurements, we developed a Nd:YAG laser that provides a 5ms burst of pulses at 100 kHz o n a robust mobile platform . Using this laser, we demonstrated s patially and temporally resolved Rayleigh scattering imaging and particle image velocimetry measurements of turbulent mixing in high - pressure gas - phase flows and vaporizing sprays . Quantitativ e interpretation of high - pressure measurements was advanced by reducing and correcting interferences and imaging artifacts.

Turbulent dimethyl ether (DME) jet flames provide a canonical flame geometry for studying turbulence-flame interactions in oxygenated fuels and for developing predictive models of these interactions. The development of accurate models for DME/air flames would establish a foundation for studies of more complex oxygenated fuels. We present a joint experimental and computational investigation of the velocity field and OH and CH2O distributions in a piloted, partially-premixed turbulent DME/air jet flame with a jet exit Reynolds number, ReD, of 29,300. The turbulent DME/air flame is analogous to the well-studied, partially-premixed methane/air jet flame, Sandia Flame D, with identical stoichiometric mixture fraction, ξst = 0.35, and bulk jet exit velocity, Vbulk = 45.9 m/s. Measurements include particle image velocimetry (PIV) and simultaneous CH2O and OH laser-induced fluorescence (LIF) imaging. Simulations are performed using a large eddy simulation combined with conditional moment closure (LES-CMC) on an intermediate size grid of 1.3 million cells. Overall, the downstream evolution of the mean and RMS profiles of velocity, OH, and CH2O are well predicted, with the largest discrepancies occurring for CH2O at x/D = 20-25. LES-CMC simulations employing two different chemical reaction mechanisms (Kaiser et al., 2000 [20] and Zhao et al., 2008 [21]) show approximately a factor of two difference in the peak CH2O mole fractions, whereas OH mole fractions are in good agreement between the two mechanisms. The single-shot LIF measurements of OH and CH2O show a wide range of separation distances between the spatial distributions of these intermediate species with gaps on the order of millimeters. The intermittency in the overlap between these species indicates that the consumption rates of formaldehyde by OH in the turbulent DME/air jet flame may be highly intermittent with significant departures from flamelet models.

The effects of combustion on the strain rate field in turbulent jets were studied using 10 kHz tomographic particle image velocimetry (TPIV). Measurements were performed in three turbulent jets: a well-studied, piloted partially-premixed methane/air jet flame, Sandia flame C, with low probability of localized extinction; a second piloted jet flame, analogous to flame C but with a reduced pilot flow rate and a high probability of localized extinction; and a non-reacting air jet. Since the jet exit Reynolds number of approximately 13000 was nearly identical in the three jets, differences in the strain rate fields were attributed to the effects of combustion. Spatiotemporal characteristics of the strain rate field were analyzed. Overall, the strain rate norm was larger in the flames than in the non-reacting jet with the most stable flame having the largest values. In all three jets, the compressive strain rate was on average the largest of the three principal strain rates. At high strain rates, the ratios of the compressive and extensive strain rate to the intermediate strain rate were similar to those found in isotropic incompressible turbulent flows. The three-dimensional velocity measurements were used to analyze the spatial distribution of strain rate clusters, defined as singly-connected groups of voxels where the strain rate magnitude exceeded a threshold value. The presence of a stable flame significantly attenuated the number of clusters of intermediate strain rate. Strain rate bursts, corresponding to sudden increases in the number of clusters, were identified in the three jets. Bursts in the non-reacting jet and the unstable flame contained up to twice as many clusters as in the stable flame. The temporal intermittency of intense strain rate clusters was analyzed using the time-series measurements. Clusters with strain rates greater than five times the standard deviation of the strain rate norm were highly intermittent.

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The University of Michigan and Sandia National Laboratories collaborated on the initial development of a compact single-camera approach for simultaneously measuring 3-D gasphase velocity and temperature fields at high frame rates. A compact diagnostic tool is desired to enable investigations of flows with limited optical access, such as near-wall flows in an internal combustion engine. These in-cylinder flows play a crucial role in improving engine performance. Thermographic phosphors were proposed as flow and temperature tracers to extend the capabilities of a novel, compact 3D velocimetry diagnostic to include high-speed thermometry. Ratiometric measurements were performed using two spectral bands of laser-induced phosphorescence emission from BaMg2Al10O17:Eu (BAM) phosphors in a heated air flow to determine the optimal optical configuration for accurate temperature measurements. The originally planned multi-year research project ended prematurely after the first year due to the Sandia-sponsored student leaving the research group at the University of Michigan.

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