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At least 1,279 records · Page 71

Preliminary results of a determination of temperatures of flames by means of K-band microwave attenuation

The temperature effects on the attenuation of K-band microwaves, at a frequency of 26,500 plus or minus 30 megacycles per second, through natural-gas and propane flames containing added alkali halide salts, were investigated over a temperature range from 1900 to 2500 K. The preliminary data of this investigation indicated that the attenuation varies appreciably with the sodium-line-reversal temperatures of the flames and is independent of the particular hydrocarbon fuels that were used for temperature sources and of the particular halide components of the compounds used in the concentrations employed to produce easily measurable attenuation. A reproducibility of plus or minus 25 K was obtainable.

RESEARCH EQUIPMENT AND TECHNIQUES↗

Theory of flame propagation

The mechanism of flame propagation has been qualitatively formulated. In accordance with this formulation, the chemical reaction initiated in some layer brings about an increase in the temperature; because of the heat conduction, the temperature is raised in the neighboring layer where in turn the chemical reaction is initiated. In this manner the flame is propagated.

THEORIES - FLAME-PROPAGATION↗

Emulation of Condensed Fuel Flames Using a Burning Rate Emulator (BRE) in Microgravity

The Burning Rate Emulator (BRE) is a gaseous fuel burner developed to emulate the burning of condensed phase fuels. The current study details several tests at the NASA Glenn 5-s drop facility to test the BRE technique in microgravity conditions. The tests are conducted for two burner diameters, 25 mm and 50 mm respectively, with methane and ethylene as the fuels. The ambient pressure, oxygen content and fuel flow rate are additional parameters. The microgravity results exhibit a nominally hemispherical flame with decelerating growth and quasi-steady heat flux after about 5 seconds. The BRE burner was evaluated with a transient analysis to assess the extent of steady-state achieved. The burning rate and flame height recorded at the end of the drop are correlated using two steady-state purely diffusive models. A higher burning rate for the bigger burner as compared to theory indicates the significance of gas radiation. The effect of the ambient pressure and oxygen concentration on the heat of gasification are also examined.

flames↗

Direct numerical simulation of temporally evolving luminous jet flames with detailed fuel and soot chemistry

Direct numerical simulations of 2D temporally-evolving luminous turbulent ethylene-air jet diffusion flames are performed using a high-order compressible Navier-Stokes solver. The simulations use a reduced mechanism derived from a detailed ethylene-air chemical kinetic mechanism that includes the reaction pathways for the formation of polycyclic aromatic hydrocarbons. The gas-phase chemistry is coupled with a detailed soot particle model based on the method of moments with interpolative closure that accounts for soot nucleation, coagulation, surface growth through HACA mechanism, and oxidation. Radiative heat transfer of CO{sub 2}, H{sub 2}O, and soot is treated by solving the radiative transfer equation using the discrete transfer method. This work presents preliminary results of radiation effects on soot dynamics at the tip of a jet diffusion flame with a particular focus on soot formation/oxidation.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗

Reduced chemistry model calibration using unsteady flames with repetitive extinction and ignition

In this paper, combustion in a narrow channel with an imposed temperature gradient is used to calibrate a reduced chemical mechanism. The focus is placed on unsteady flames with repetitive extinction and ignition (FREI) at high pressure. The reduced mechanism follows a hybrid approach, combining a small fuel-dependent submechanism with a detailed fuel-independent submechanism for the core species chemistry. The fuel-dependent submechanism consists of three species and nine reactions describing both the low and high-temperature fuel decomposition pathways. The sensitivity of the extinction and ignition locations to the fuel-dependent reactions is assessed and multiple reactions are found to affect the FREI behavior. The sensitive reactions are calibrated following a Bayesian approach. The calibrated reduced model is compared to a detailed model and good agreement in ignition delay times and laminar flame speeds is observed. Finally, this illustrates the potential of a micro flow reactor with a controlled temperature profile to test fuels, calibrate chemical models, and infer kinetic data.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Ignition, Flame Propagation, and End-Gas Autoignition Studies of Natural Gas/EGR Blends in a Rapid Compression Machine

The development of high efficiency, spark ignited natural gas engines is currently limited by engine knock at high power density (at high compression ratio and/or elevated boost pressures) and misfire (at lean conditions and/or high exhaust gas recirculation levels). The knock and misfire limits are further confounded by the wide variety in fuel reactivity observed in “pipeline quality” natural gas. In this study, a rapid compression machine (RCM) was used to characterize the effects of variation in natural gas fuel reactivity and exhaust gas recirculation (EGR) on homogeneous ignition delay, flame propagation rate and end-gas autoignition (EGAI) propensity for stoichiometric natural gas/oxidizer/EGR blends. Pipeline quality natural gas with variable reactivity (68 < Methane Number < 95) was simulated using mixtures of methane, ethane, and propane. EGR was simulated with mixtures of Ar, CO2, CO, and NO. EGR substitution rates were varied from 0 to 30 mass percent. Ignition delay period under homogeneous autoignition conditions was measured at compressed pressures of 24.0 to 33.1 bar and compressed temperatures of 667 to 980 K. Flame propagation rate and EGAI propensity was measured at spark-ignition pressures of 29.9 to 32.9 bar and temperatures of 721 to 782 K.

Ignition Delay, Flame Propagation Rate, Rapid Comp↗

Synthesis of modified graphene oxide and its improvement on flame retardancy of epoxy resin

ABSTRACT In this work, the small molecule with double‐phosphaphenanthrene structure was successfully grafted on the surface of graphene oxide (GO), which is called functionalized graphene oxide (FGO). The introduction of FGO improved the poor interfacial compatibility between graphene and epoxy matrix. And FGO could be used as the highly effective flame retardant. The thermogravimetric analysis results showed a significant improvement in the char yield of cured FGO/EP. When the content of FGO was 3 wt %, the limiting oxygen index value reached 30.4%. At the same time, the three‐point bending and thermomechanical tests confirmed that the mechanical properties of the epoxy resin composites were improved. Based on the char analyses of SEM images and Raman spectroscopy, the flame retardant could promote the formation of a stable carbon layer. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137 , 47710.

Wu, Wenqian↗

A DNS evaluation of mixing models for transported PDF modelling of turbulent nonpremixed flames

Transported probability density function (TPDF) approaches are well suited to modelling turbulent, reacting, variable density flows. One of the main challenges to the successful deployment of TPDF methods is accurately modelling the unclosed molecular mixing term. This study examines three of the most widely used mixing models: the Interaction by Exchange with the Mean (IEM), Modified Curl (MC) and Euclidean Minimum Spanning Tree (EMST) models. Direct numerical simulation (DNS) data-sets were used to provide both initial conditions and inputs needed over the course of the runs, including the mean flow velocities, mixing frequency, and the turbulent diffusion coefficient. The same chemical mechanism and thermodynamic properties were used, allowing the study to focus on the mixing model. The simulation scenario was a one-dimensional, nonpremixed, turbulent jet flame burning either a syngas or ethylene fuel stream that featured extinction and reignition. This test scenario was selected because extinction and reignition phenomena are sensitive to the mixing model. Three DNS cases were considered for both the syngas and ethylene cases with a parametric variation of Reynolds and Damköhler numbers, respectively. Extinction events became more popular with increasing Reynolds number in the syngas cases and with decreasing Damköhler number in the ethylene cases. The model was first tested with the mixing frequency defined from the dissipation rate and variance of mixture fraction. With this definition, for the syngas cases this study finds that the TPDF method is successful at predicting flame extinction and reignition using all three mixing models for the relatively lower and intermediate Reynolds number cases, but that all models under-predict reignition in the relatively higher Reynolds number case. In the ethylene fuelled cases, only the EMST mixing model correctly predicts the reignition event for the two higher Damköhler number cases, yet, in the lowest Damköhler number case the EMST model over-predicts reignition and the IEM and MC models under-predict it. Mixing frequency was then modelled based on the turbulence frequency and a model constant $C_{\phi}$, the ratio of scalar to mechanical mixing rates. The DNS cases were reexamined with this definition and the findings suggested that the optimal value for $C_{\phi}$ is mixing model and case dependent. In particular, it was found in the ethylene case considered that reignition could be achieved with the IEM and MC models by adjusting the value of $C_{\phi}$.

42 ENGINEERING↗

The C 5 chemistry preceding the formation of polycyclic aromatic hydrocarbons in a premixed 1-pentene flame

We report the formation of small polycyclic aromatic hydrocarbons (PAHs) and their precursors can be strongly affected by reactions of C5 species. For improving existing combustion mechanisms for small PAH formation, it is therefore valuable to understand the fuel-specific chemistry of C5 fuels. To this end, we provide quantitative isomer-resolved species profiles measured in a laminar premixed ( Φ = 1.8) low-pressure (4 kPa) flame of 1-pentene with photoionization molecular-beam mass spectrometry (PI-MBMS) using tunable synchrotron vacuum-ultraviolet (VUV) radiation. These experimental results are accompanied with numerical simulations, starting from models from the literature by Wang et al. [JetSurF version 2.0 (2010)] and Healy et al. [Energy Fuels 24 (2010) 1521–1528] that were developed for different fuels, but which include 1-pentene as an intermediate, and by Narayanaswamy et al. [Combust. Flame 157 (2010) 1879–1898] focusing on the small PAH chemistry. Taking observed discrepancies between experimental results and simulations into consideration, a mechanism for C 5 chemistry was newly developed including PAH formation pathways, and its performance analyzed in detail. Special emphasis was placed on the initial fuel consumption of 1-pentene as well as on formation pathways of small aromatics. The mechanisms show differences regarding fuel decomposition and hydrocarbon growth reactions. These contribute to noticeable differences between the simulations with different models on one hand, and deviations between model predictions and experimental results on the other. While the new model presents overall satisfactory capabilities to predict the mole fraction profiles of common combustion intermediates, the predictive capability of the literature models was not fully satisfying for some intermediate species, including C 4 H 6 , C 7 H 8 , and C 10 H 8 . Lastly, the results indicate that the fuel-specific C 5 reaction routes as well as the mechanism for small PAH formation need further investigation.

1-PenteneAlkene combustion↗

Temperature measurements in heavily-sooting ethylene/air flames using synchrotron x-ray fluorescence of krypton

High-fidelity temperature field measurements have been made for several heavily-sooting ethylene/air flames that have historically been challenging environments for conventional optical diagnostics. These challenges have largely been overcome here, in this study, by conducting x-ray fluorescence (XRF) measurements of a Kr fluorescent agent in the hard x-ray regime (15 keV). The current methodology presents a more economical diagnostic than a previously reported implementation of the Kr-XRF method, by limiting seeding of the expensive fluorescent agent to only the fuel stream flows. Detailed reacting flow simulations have been used to interpret experimental signals by tracking the mole fraction of the fluorescent agent in the flow field. Simulated Kr densities are in excellent agreement with measurements throughout the flow field. Temperature measurements of the flow field also agree well with simulations and recent literature studies. However, uncertainties in the measurements become increasingly large downstream of the burner surface as the krypton fraction drops due to mixing of the fuel and co-flow streams. Additionally, we demonstrate that soot particles in the heavily sooting flames studied do not impede the Kr-XRF measurements.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Fish energy budget under ocean warming and flame retardant exposure

Highlights: • Energy proportion spent for growth dominated the mode of energy allocation (56–68%). • Energy channelled for R was around 26%, followed by excretion (F: 4–16%; U: 2–3%). • Energy budget parameters were significantly affected by warming and BDE-209 exposure. • Higher levels occurred under warming conditions: for weight, protein, ash and RGR. • Higher levels occurred under both stressors: for FE, AER, RMR and K{sub 1}. Climate change and chemical contamination are global environmental threats of growing concern for the scientific community and regulatory authorities. Yet, the impacts and interactions of both stressors (particularly ocean warming and emerging chemical contaminants) on physiological responses of marine organisms remain unclear and still require further understanding. Within this context, the main goal of this study was to assess, for the first time, the effects of warming (+ 5 °C) and accumulation of a polybrominated diphenyl ether congener (BDE-209, brominated flame retardant) through dietary exposure on energy budget of the juvenile white seabream (Diplodus sargus). Specifically, growth (G), routine metabolism (R), excretion (faecal, F and nitrogenous losses, U) and food consumption (C) were calculated to obtain the energy budget. The results demonstrated that the energy proportion spent for G dominated the mode of the energy allocation of juvenile white seabream (56.0–67.8%), especially under the combined effect of warming plus BDE-209 exposure. Under all treatments, the energy channelled for R varied around 26% and a much smaller percentage was channelled for excretion (F: 4.3–16.0% and U: 2.3–3.3%). An opposite trend to G was observed to F, where the highest percentage (16.0 ± 0.9%) was found under control temperature and BDE-209 exposure via diet. In general, the parameters were significantly affected by increased temperature and flame retardant exposure, where higher levels occurred for: i) wet weight, relative growth rate, protein and ash contents under warming conditions, ii) only for O:N ratio under BDE-209 exposure via diet, and iii) for feed efficiency, ammonia excretion rate, routine metabolic rate and assimilation efficiency under the combination of both stressors. On the other hand, decreased viscerosomatic index was observed under warming and lower fat content was observed under the combined effect of both stressors. Overall, under future warming and chemical contamination conditions, fish energy budget was greatly affected, which may dictate negative cascading impacts at population and community levels. Further research combining other climate change stressors (e.g. acidification and hypoxia) and emerging chemical contaminants are needed to better understand and forecast such biological effects in a changing ocean.

54 ENVIRONMENTAL SCIENCES↗

Chemiluminescence-based multivariate sensing of local equivalence ratios in premixed atmospheric methane-air flames

Chemiluminescence emissions from OH*, CH*, C2, and CO2 formed within the reaction zone of premixed flames depend upon the fuel-air equivalence ratio in the burning mixture. In the present paper, a new partial least square regression (PLS-R) based multivariate sensing methodology is investigated and compared with an OH*/CH* intensity ratio-based calibration model for sensing equivalence ratio in atmospheric methane-air premixed flames. Five replications of spectral data at nine different equivalence ratios ranging from 0.73 to 1.48 were used in the calibration of both models. During model development, the PLS-R model was initially validated with the calibration data set using the leave-one-out cross validation technique. Since the PLS-R model used the entire raw spectral intensities, it did not need the nonlinear background subtraction of CO2 emission that is required for typical OH*/CH* intensity ratio calibrations. An unbiased spectral data set (not used in the PLS-R model development), for 28 different equivalence ratio conditions ranging from 0.71 to 1.67, was used to predict equivalence ratios using the PLS-R and the intensity ratio calibration models. It was found that the equivalence ratios predicted with the PLS-R based multivariate calibration model matched the experimentally measured equivalence ratios within 7%; whereas, the OH*/CH* intensity ratio calibration grossly underpredicted equivalence ratios in comparison to measured equivalence ratios, especially under rich conditions ( > 1.2). The practical implications of the chemiluminescence-based multivariate equivalence ratio sensing methodology are also discussed.

Cross validation↗

NO{sub 2} gas sensing of flame-made Pt-loaded WO{sub 3} thick films

Unloaded WO{sub 3} and 0.25–1.0 wt% Pt-loaded WO{sub 3} nanoparticles for NO{sub 2} gas detection were synthesized by flame spray pyrolysis (FSP) and characterized via X-ray diffraction (XRD), scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HRTEM). The BET surface area (SSA{sub BET}) of the nanoparticles was measured by nitrogen adsorption. The NO{sub 2} sensing properties of the sensors based on unloaded and Pt-loaded WO{sub 3} nanoparticles were investigated. The results showed that the gas sensing properties of the Pt-loaded WO{sub 3} sensors were excellent to those of the unloaded one. Especially, 0.25 wt% Pt-loaded WO{sub 3} sensor showed highest response to NO{sub 2} than the others at low operating temperature of 150 °C. - Graphical abstract: The response of 0.25 wt% Pt-loaded WO3 sensor was 637 towards NO{sub 2} concentration of 10 ppm at 150 °C. - Highlights: • Unloaded and Pt-loaded WO{sub 3} nanoparticles for NO{sub 2} gas detection were synthesized by flame spray pyrolysis (FSP). • Gas sensing properties of the Pt-loaded WO{sub 3} sensors were excellent to those of the unloaded one. • 0.25 wt% Pt-loaded WO{sub 3} sensor showed highest response to NO{sub 2} at low operating temperature of 150 °C.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Harnessing biomass-derived reinforcements for sustainable flame-resistant composite

Bio-based composites containing natural fiber reinforcements have been integral to developing innovative, low-cost, and low-energy technologies for transportation applications in marine, automotive, and other industries. The low density of natural fibers gives these materials a high specific stiffness and strength, which can lead to significant weight savings in composites. This study focused on a specialty type of wood fiber treated with boric acid (≤ 7%) sourced from Northern White Pine in the USA, marketed as TimberFill. TimberFill is a high aspect ratio, fibrillated wood fiber that is produced commercially for wood fiber insulation; it is chemically treated to improve both its flame retardance and water resistance. In the present study, TimberFill was processed into non-woven mats using a process akin to papermaking and then infiltrated with epoxy resin. Biochar from wood waste was also incorporated into the epoxy resin as a low-cost filler and functional additive. The effects of biochar concentration on composites’ flame retardance (17% improvement in burn rate), thermal conductivity (improved by 9%), and mechanical performance (33% improvement in modulus) are herein presented. Additionally, it explores the plasticizing effect of the boric acid used in the treatment of TimberFill on the thermal and mechanical properties of the resulting composites, specifically on the thermal expansion coefficient.

Joshy, Joslin [ORNL]↗

Combustion of Silane-Hydrogen-Nitrous oxide Mixtures: Analysis of Laminar Flame Propagation and Condensed Products

The laminar burning rate, the explosion pressure, and the pressure rise coefficient have been measured for silane-nitrous oxide-argon mixtures using the spherically expanding flame technique in a constant volume combustion chamber. For these three parameters, the values obtained were higher than for hydrogen-nitrous oxide-argon and typical hydrocarbon-based mixtures. As an example, a maximum burning rate of 1800 g/m 2 s was measured at 101 kPa, whereas under similar conditions, a maximum burning rate around 950 g/m 2 s has been reported for hydrogen-nitrous oxide-argon mixtures. Here, the condensed combustion products formed in the silane-nitrous oxide-argon flames were sampled and characterized using electron micrograph, electronic diffraction, energy-dispersive spectroscopy, and X-ray powder diffraction. For all equivalence ratios, silica spherical particles with a mean diameter in the range 200-300 nm were observed. In addition, for mixtures with Φ ≥2.2, silicon nanowires were formed. X-ray diffraction experiments showed that the silicon nanowires are composed of a material referred to as “metal silicon” characterized by a cubic structure (lattice parameter: a = 5.425 Å) with the Fm-3m space group.

42 ENGINEERING↗

Chemical insights into ethyl acetate flames from experiment and kinetic modeling: Laminar burning velocity, speciation and NO$_x$ emission

Oxygenated fuels, such as alcohols, ethers, and esters, are promising alternatives to conventional fuels. These fuels can help reduce detrimental emissions like carbon monoxide and unburned hydrocarbons and enhance octane ratings. Among these oxygenates, ethyl acetate (EA), a small alkyl ester sourced from biomass, emerges as a clean, promising energy carrier. It serves as a surrogate fuel to facilitate investigations into the combustion behaviours of biodiesel. Despite its importance, the literature knowledge of EA combustion characteristics is limited. Therefore, this study aims to broaden the knowledge of the combustion behaviour of this type of oxygenated fuel compound. In this study, we measured the laminar burning velocities of EA by employing a heat flux burner and a closed combustion vessel over the equivalence ratios of 0.7 – 1.7, pressures of 1 – 10 bar and temperatures ranging from 353 – 423 K. Further, we also measured the NOx emissions in exhaust gas of the premixed flames fueled by EA/air for the first time over the equivalence ratio of 0.8 – 1.2. Additionally, we employed a non-premixed counterflow flame setup for extensive characterisation of species and their concentration under diverse conditions encompassing various strain rates and oxygen concentrations. Finally, we utilized these newly measured data to construct and validate a detailed kinetic model developed as part of this work. The newly developed model will help characterize the combustion properties of EA.

30 DIRECT ENERGY CONVERSION↗

Analysis of soot formation from aviation fuels in laminar counterflow flames

Combustion emissions from aviation contribute to the formation of condensation trail (contrail) that can lead to the formation of anthropogenic cirrus clouds. Ice particles that form contrails are observed to have a linear correlation with soot particle number density. Synthetic aviation fuels (SAFs) offer a promising route to mitigate the production of soot particles while also increasing energy security. Although studies have focused on combustion and spray behavior, the detailed investigation of soot formation processes for different jet fuels and their impact on models for computational fluid dynamics (CFD) applications is not well understood. Moreover, experimental measurements of soot for canonical flames using Synthetic aviation fuels (SAF) for model validation remain scarce. To address this, we use employed the Lawrence Livermore National Laboratory (LLNL) detailed soot model based on the discrete sectional method. Additionally, we develop two reduced chemical mechanisms for Jet-A and Alcohol-to-Jet (C1) that are suitable for turbulent flame simulations and couple them with the Hybrid Method of Moments (HMOM). The detailed and reduced model frameworks are validated against experimental measurements of soot volume fraction (ƒ ν ) from a counterflow burner experiment previously reported in the literature. Given the good agreement between modeling results and experimental measurements for the (1) spatial distribution of ƒ ν and (2) the non-linear variation of peak ƒ ν with strain rate, we further investigate the modeled sub-processes (nucleation, condensation, surface growth, and oxidation) using the LLNL model to analyze the assumptions in the reduced model framework. Furthermore, the results indicate a significant contribution from resonant radicals to the surface growth of soot particles, which are not accounted for in the current implementation of HMOM and could help reconcile soot predictions by the reduced model with observations.

Counterflow↗

Distribution of copper, silver and gold during thermal treatment with brominated flame retardants

Highlights: • Copper, silver and gold during thermal treatment with brominated flame retardants. • Distribution of copper, silver and gold during thermal processing. • Thermodynamic considerations of the bromination reactions. - Abstract: The growing consumption of electric and electronic equipment results in creating an increasing amount of electronic waste. The most economically and environmentally advantageous methods for the treatment and recycling of waste electric and electronic equipment (WEEE) are the thermal techniques such as direct combustion, co-combustion with plastic wastes, pyrolysis and gasification. Nowadays, this kind of waste is mainly thermally treated in incinerators (e.g. rotary kilns) to decompose the plastics present, and to concentrate metals in bottom ash. The concentrated metals (e.g. copper, precious metals) can be supplied as a secondary raw material to metal smelters, while the pyrolysis of plastics allows the recovery of fuel gases, volatilising agents and, eventually, energy. Indeed, WEEE, such as a printed circuit boards (PCBs) usually contains brominated flame retardants (BFRs). From these materials, hydrobromic acid (HBr) is formed as a product of their thermal decomposition. In the present work, the bromination was studied of copper, silver and gold by HBr, originating from BFRs, such as Tetrabromobisphenol A (TBBPA) and Tetrabromobisphenol A-Tetrabromobisophenol A diglycidyl ether (TTDE) polymer; possible volatilization of the bromides formed was monitored using a thermo-gravimetric analyzer (TGA) and a laboratory-scale furnace for treating samples of metals and BFRs under an inert atmosphere and at a wide range of temperatures. The results obtained indicate that up to about 50% of copper and silver can evolve from sample residues in the form of volatile CuBr and AgBr above 600 and 1000 °C, respectively. The reactions occur in the molten resin phase simultaneously with the decomposition of the brominated resin. Gold is resistant to HBr and remains unchanged in the residue.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗