Search

The survivability of two thermographic phosphors, YAG:Pr3+ and SMP:Sn2+ ((Sr,Mg)3(PO4)2:Sn2+), in a combustion environment is studied in the post-flame regime of a premixed propane/air flame. While the laser-induced luminescence of YAG:Pr3+ can be exploited for in situ temperature measurements in the exhaust gas above the flame, there is no in situ detectable luminescence for SMP:Sn2+ for any reaction conditions within the stability limits of the flame. The phosphor particles are recaptured above the flame and ex situ analyzed for chemical or structural changes using microscopic analysis (SEM/EDX) and x-ray diffraction. The microscopic analysis of post-flame YAG:Pr3+ does not show any alteration, whereas morphology and chemical composition of SMP:Sn2+ have been modified upon passing through the reaction zone, which is responsible for the loss of its luminescence properties. [ABSTRACT FROM AUTHOR]

In many scientific communities, the definition of standardized experiments has enabled major progress in process understanding. The investigation of the spray-flame synthesis of nanoparticles at a well-defined standard burner by experiment and simulation makes it possible to produce a comprehensive data set with various established and novel measuring methods. In this work, we introduce the design of the SpraySyn burner as a new standard for a free-jet type burner that offers well-defined and simulation-friendly boundary conditions and geometries as well as accessibility for optical diagnostics. A combustible precursor solution is fed through a centrally located capillary and aerosolized with an oxygen dispersion gas flow. The spray flame is stabilized by a premixed flat methane/oxygen pilot flame fed via a porous bronze matrix surrounded by a stabilizing nitrogen coflow emanating through the same porous matrix, providing easy-to-calculate boundary conditions for simulations. This burner design enables the use of a wide choice of solvents, precursors, and precursor combinations. Best-practice operating instructions and parameters are given, and large-eddy simulations are performed demonstrating the suitability of the SpraySyn burner for computational fluid dynamics simulations. For ensuring reproducible operation across labs, we define a consumer-camera-based flame characterization scheme for the quantitative assessment of the flame geometry such as flame length, diameter, tilt angle, and photometric distribution of visible chemiluminescence along the center axis. These parameters can be used for benchmarking the pilot and spray flame by each user of the SpraySyn burner with the reference flames. [ABSTRACT FROM AUTHOR]

The measurement of soot and soot precursors is important for understanding the formation of soot particles in flames. In this paper, we use the difference between laser-induced incandescence (LII) and two-dimensional extinction measurements to assess the contribution of soot precursors to the extinction measurement. LII measurements are performed with a high spatial resolution of 100 µm to determine the soot volume fraction ( f) in a laminar ethylene/air non-premixed flame at the standard Gülder conditions. While LII is specific to mature soot only, the extinction data represent attenuation due to mature and young soot (absorption and elastic scattering) and also absorption by soot precursors. The difference between the two measurements indicates the contribution of soot precursors and allows a determination of the maturity of soot. This is important knowledge for those using extinction techniques to measure soot concentration, as the contribution from soot precursors may lead to an overestimation of the mature soot concentration. Further, regions with high soot-precursor concentrations, which lead to soot formation, can be identified. [ABSTRACT FROM AUTHOR]

Abstract: In practical flames such as gas turbine combustors, spatially-integrated OH∗ chemiluminescence (CL) is frequently used as a heat release rate (HRR) indicator – which has been questioned by some authors to be restricted to flames of a limited range of equivalence ratios and low Reynolds numbers – while in lab flames the approach of combined detection of OH and H2CO via LIF is an accepted diagnostic technique. Even when using specialized optics with limited acceptance angle the first method is spatially integrating while the second one allows for spatially resolved imaging. In the present work we retrieved simultaneously HRR-based information via both techniques from the same spatial flame volume, i.e., OH∗–CL radiation is collected exclusively from within the light sheet volume cutting through the flame for LIF imaging. Turbulent premixed swirl flames were investigated with a thermal power up to 30kW to shed light on the still unresolved question if correlations exist between signal intensities derived from both methods in turbulent flames. Measurements were performed in methane/air flames with Reynolds numbers between 6900 and 10,000, equivalence ratios between 0.8 and 1.2, and with a replacement of 20vol% of methane by hydrogen. Although scatter plots of HRR vs. CL intensities cluster in certain regions depending on flame conditions, their large scatter shows that correlations are weak, probably caused by flame stretch and curvature. Depending on flame conditions, correlation coefficients to characterize the scatter plots range between 0.45 and 0.81. [Copyright &y& Elsevier]

The in-situ and localized observation of heat release in turbulent flames is important for the validation of computational modeling of turbulent flows with combustion. In the present work we obtain localized information on heat release rate (HRR) by the commonly accepted technique of the simultaneous and single-shot planar imaging of OH and CHO concentrations by laser-induced fluorescence (LIF). Additionally, we combine this with the simultaneous line-of-sight and temporally resolved chemiluminescence detection of OH, spatially integrated within the flame volume, interrogated by the laser sheets used for the HRR imaging technique. The combined diagnostic methods are demonstrated for a swirl-stabilized, premixed turbulent methane/air flame of 30-kW thermal power, and they show the existence of correlations between both HRR-sensitive diagnostic techniques. [ABSTRACT FROM AUTHOR]

A detailed comparison has been conducted between chemiluminescence (CL) species profiles of OH, CH, and C, obtained experimentally and from detailed flame kinetics modeling, respectively, of atmospheric pressure non-premixed flames formed in the forward stagnation region of a fuel flow ejected from a porous cylinder and an air counterflow. Both pure methane and mixtures of methane with hydrogen (between 10 and 30 % by volume) were used as fuels. By varying the air-flow velocities methane flames were operated at strain rates between 100 and 350 s, while for methane/hydrogen flames the strain rate was fixed at 200 s. Spatial profiles perpendicular to the flame front were extracted from spectrograms recorded with a spectrometer/CCD camera system and evaluating each spectral band individually. Flame kinetics modeling was accomplished with an in-house chemical mechanism including C-C chemistry, as well as elementary steps for the formation, removal, and electronic quenching of all measured active species. In the CH/air flames, experiments and model results agree with respect to trends in profile peak intensity and position. For the CH/H/air flames, with increasing H content in the fuel the experimental CL peak intensities decrease slightly and their peak positions shift towards the fuel side, while for the model the drop in mole fraction is much stronger and the peak positions move closer to the fuel side. For both fuel compositions the modeled profiles peak closer to the fuel side than in the experiments. The discrepancies can only partly be attributed to the limited attainable spatial resolution but may also necessitate revised reaction mechanisms for predicting CL species in this type of flame. [ABSTRACT FROM AUTHOR]

Abstract: The combustion of stoichiometric Ethyl-hexyl-nitrate (EHN)-doped n-heptane/oxygen/argon and (EHN)-doped n-heptane/air mixtures, respectively, was investigated in a low-pressure burner with a molecular-beam mass spectrometer and ignition delay-time (τ ign) measurements were performed in a high-pressure shock tube. The experiments with the low-pressure flame were used for the determination of the flame structure including concentration profiles of reactants, products and important intermediates in the flame. The shock tube experiments provided τ ign for a temperature range of 690K⩽ T ⩽1275K at a pressure of 40±2 bar for stoichiometric and lean mixtures under engine relevant conditions. A chemical mechanism for n-heptane/EHN mixtures was developed from an automatically generated mechanism for n-heptane by manually adding reactions to describe the influence of EHN. This mechanism was validated against the shock-tube data for various temperatures, levels of EHN-doping and equivalence ratios by homogeneous reactor calculations. The ignition delay times predicted by the model agree well with the shock tube results for a large range of temperatures, equivalence ratios and EHN concentrations. The influence of EHN onto ignition delay was largest in the low-temperature regime (770–1000K). Numerical analysis suggests that the prevalent reason for the ignition-enhancing effect of EHN is the formation of highly reactive heptyl radicals by thermal decomposition of EHN. Due to this comparatively simple and generic mechanism, EHN is expected to have a similar ignition-enhancing effect also for other hydrocarbon fuels. [Copyright &y& Elsevier]

The iron-atom concentration distribution as well as the gas-phase temperature was measured via laser-induced fluorescence (LIF) during iron-oxide nanoparticle synthesis in a low-pressure hydrogen/oxygen/argon flame reactor using ironpentacarbonyl (Fe(CO)5) as precursor. Temperature measurements based on multi-line NO-LIF imaging are used to correct for temperature-dependent ground-state populations. The concentration measurement is calibrated based on line-of-sight absorption measurements. The influence of the precursor on the flame is observed at precursor concentrations larger than 70 ppm as the flame front moves closer to the burner surface with increasing Fe(CO)5 concentration. [ABSTRACT FROM AUTHOR]

We present and apply a methodology for the single-shot measurement of absolute concentrations of the OH-radical in a turbulent, premixed natural gas/air flame. The method is based on a combination of detailed numerical simulations of the turbulent flame and an experimental approach using planar laser-induced fluorescence (LIF). The numerical simulation is used to predict LIF intensities. It shows the existence of a sharp correlation between the LIF signal after excitation of the A-X(3,0) P2(8) transition near 248.45 nm and OH concentrations for a wide range of conditions, including stationary and instationary laminar flames of different strain rates, with different models to treat molecular transport and different degrees of heat loss. This correlation allows the transformation of measured OH-LIF intensity images into absolute OH concentration maps. [ABSTRACT FROM AUTHOR]

Abstract. Within the TECFLAM group a standard swirl burner is investigated, both experimentally using optical and probe measurements and by simulations using different modeling attempts. The present study is focused on the laser-based investigation of the NO distribution within the reacting flow field of a strongly swirling, confined 150-kW natural gas flame. Simultaneous quantitative measurements of NO- and OH-concentration fields by laser-induced fluorescence imaging (LIF) and temperature distribution (Rayleigh scattering) are performed. Mixing properties of the unburned gases are investigated tot the isothermal and the combusting flow using tetrahydrothiophene (THT) as a new fluorescing tracer. These measurements show which areas are sufficiently mixed allowing for the application of planar Rayleigh thermometry. Areas where THT-LIF interferes with OH-LIF detection am localized and omitted from data evaluation. The data is analyzed yielding global scalar fields for comparison with model simulations and correlations between the different measured scalars are investigated showing an almost linear correlation of NO concentration and temperature within the swirl flame whereas no apparent correlation between NO and OH concentration was found. [ABSTRACT FROM AUTHOR]

Abstract: Olivine, LiFePO4 is a promising cathode material for lithium-ion batteries due to its low cost, environmental acceptability and high stability. Its low electric conductivity prevented it for a long time from being used in large-scale applications. Decreasing its particle size along with carbon coating significantly improves electronic conductivity and lithium diffusion. With respect to the controlled formation of very small particles with large specific surface, gas-phase synthesis opens an economic and flexible route towards high-quality battery materials. Amorphous FePO4 was synthesized as precursor material for LiFePO4 by flame spray pyrolysis of a solution of iron acetylacetonate and tributyl phosphate in toluene. The pristine FePO4 with a specific surface from 126–218 m2 g−1 was post-processed to LiFePO4/C composite material via a solid-state reaction using Li2CO3 and glucose. The final olivine LiFePO4/C particles still showed a large specific surface of 24 m2 g−1 and were characterized using X-ray diffraction (XRD), electron microscopy, X-ray photoelectron spectrocopy (XPS) and elemental analysis. Electrochemical investigations of the final LiFePO4/C composites show reversible capacities of more than 145 mAh g−1 (about 115 mAh g−1 with respect to the total coating mass). The material supports high drain rates at 16 C while delivering 40 mAh g−1 and causes excellent cycle stability. [Copyright &y& Elsevier]

• Investigation of iron pentacarbonyl-doped low-pressure H 2 /O 2 /Ar flames by MBMS. • Evaluation of a chemical reaction mechanism for iron pentacarbonyl. • Ion chemistry of iron pentacarbonyl. • Iron hydroxides and iron oxides. • Ion sampling from flames. The information of the gas phase kinetics are relevant for the development of detailed reaction mechanisms as well as for process design and control in flame synthesis. In this study, the decomposition of iron pentacarbonyl and the reaction pathways towards iron oxide clusters and particles in laminar H 2 /O 2 /Ar low-pressure synthesis flames are investigated. Gas-phase species are analyzed by photoionization and electron ionization mass spectrometry. The extraction of a representative sample from the particle-laden flow of a synthesis flame by an intrusive sampling technique for the analysis is challenging, because iron-intermediate species can condense easily. Cations can be extracted from the flame with a high efficient ion sampling technique that results in high sensitivity. Iron-containing cations provide evidence of the presence of key intermediates, e.g., Fe(OH) 2 , Fe(OH) 3 , Fe 2 O 3 , and larger Fe-O-clusters which are the dominant intermediates with respect to particle formation and need to be considered in future gas-phase reaction mechanisms. [ABSTRACT FROM AUTHOR]