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At least 361 records · Page 20

Understanding Composition, Formation, and Aging of Organic Aerosols in Wildfire Emissions via Combined Mountain Top and Airborne Measurements

Wildfires are an important source of global aerosols that have pronounced impacts on regional air quality and global climate. A major component of wildfire emissions is organic, including primary organic aerosols (POA) and large amounts of gases that can be oxidized to form secondary organic aerosols (SOA). The environmental impacts of wildfire emissions are strongly correlated with the chemical, optical, and microphysical properties of biomass-burning organic aerosols (BBOA), which are dependent, in a complex manner, on combustion and atmospheric aging processes. Here we discuss results from recent field and laboratory studies aimed at understanding the chemical composition, formation, and evolution of BBOA in wildfire emissions. Comprehensive analysis of a large number of fresh and aged (up to days of aging) fire plumes originating in the Pacific Northwest region of the United States reveals that the enhancement of BBOA mass concentrations relative to the enhancement of the sum of CO and CO2 in wildfire smokes is primarily driven by combustion efficiency, whereas the composition and properties of the BBOA are strongly influenced by atmospheric oxidation and other aging processes. These results shed light on organic aerosol formation and transformation in biomass burning emissions.

54 ENVIRONMENTAL SCIENCES↗

Effect of fuel nitrogen and hydrogen content on emissions in hydrocarbon combustion

The results of an investigation of the effect of operating conditions and fuel properties on emission for the two-stage combustion of fuels with significant organic nitrogen content are presented. The way in which the emissions of nitrogen oxides and carbon monoxide are affected by the decreased hydrogen content and the increased organic nitrogen content of coal-derived fuels is discussed. Limited measurements of smoke from the rich-lean combustion of simulated syncrude fuels indicate relatively high smoke emissions in spite of the very lean second-stage burning. This fact, together with the high observed carbon monoxide emissions, suggests that trade-offs will be necessary between the conditions that minimize NOx and those that control CO and smoke emissions.

Bittker, D. A.↗

Validated CFD Model for Multimode Gasoline Compression Ignition Engine

A validated CFD model for the multimode combustion engine developed under the DOE funded project DE-EE0008478 (Co-optimized Mixed-Mode Engine and Fuel Demonstrator for Improved Fuel Economy while Meeting Emissions Requirements). It incorporates advanced physics-based fuel surrogate models for thermophysical properties and reaction kinetics. The combustion modes include spark ignition (SI), low temperature combustion (LTC), and compression ignition (CI). The real fuel model was validated for RON60, RON70, RON80, RON90, and two biofuel blends. The validation cases can be found in https://doi.org/10.2172/1887341.

02 PETROLEUM↗

Resolving Mixtures of Soot Characterized by SP-AMS Spectra Using a Latent Dirichlet Allocation Model

Soot produced by detonation or combustion events exhibits different chemical properties depending on the fuel, device construction, and environmental conditions in which the event occurs. These properties can be useful for defining relevant signatures for probabilistically identifying the different types of events that occurred, based on the soot that is produced from these events. However, it is rare to observe samples of soot from a detonation or combustion that are not contaminated by outside particles. In this paper, we present a method for resolving mixtures of soot to determine the contributions of sources that may be present in samples of recovered soot. We use Latent Dirichlet Allocation to describe the generative process for a sample of recovered soot, and use Variational Bayesian Inference to learn about the parameters associated with the generative model. We demonstrate the utility of this method by considering real samples of mixtures of soot under various frameworks to show that the model is able to identify the different components present in a sample of soot as well as their mixing proportions.

54 ENVIRONMENTAL SCIENCES↗

Flame Radiation, Structure, and Scalar Properties in Microgravity Laminar Fires

Results from microgravity combustion experiments conducted in the Zero Gravity Research Facility (ZGF) 5.18 second drop facility are reported. The results quantify flame radiation, structure, and scalar properties during the early phase of a microgravity fire. Emission mid-infrared spectroscopy measurements have been completed to quantitatively determine the flame temperature, water and carbon dioxide vapor concentrations, radiative emissive power, and soot concentrations in microgravity laminar methane/air, ethylene/nitrogen/air and ethylene/air jet flames. The measured peak mole fractions for water vapor and carbon dioxide are found to be in agreement with state relationship predictions for hydrocarbon/air combustion. The ethylene/air laminar flame conditions are similar to previously reported results including those from the flight project, Laminar Soot Processes (LSP). Soot concentrations and gas temperatures are in reasonable agreement with similar results available in the literature. However, soot concentrations and flame structure dramatically change in long-duration microgravity laminar diffusion flames as demonstrated in this report.

Feikema, Douglas↗

Study of photoluminescence properties of CaAl{sub 2}O{sub 4}: Eu{sup 2+} prepared by combustion synthesis method

Eu{sup 2+} doped alkaline earth metals such as strontium aluminate, calcium aluminate and barium aluminate prepared by using modified combustion synthesis method at 600°C with Urea as fuel. Crystal structure is determined by using XRD and the sample confirmation by using the FTIR. The effect of the host material on the photoluminescence (PL) and phosphorescence properties were studied by using the Hitachi F-7000 spectrofluorimeter equipped with a 450W Xenon lamp, in the range 200-650 nm. The emission spectra of Eu{sup 2+} range from 450 to 500 nm in the Blue to aqua region and the transition 4f{sup 7}-4f{sup 6} 5d{sup 1}. The observed emission in CaAl{sub 2}O{sub 4} is 440 nm.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Luminescence properties of ZnMoO{sub 4}:Eu{sup 3+}:Y{sup 3+} materials synthesized by solution combustion synthesis method

The Zn{sub (1-x-y)}MoO{sub 4}:Eu{sup 3+}{sub (x)}: Y{sup 3+}{sub (y)} (x = 1 mol% and y = 1 or 2 mol%) compounds were prepared by combustion synthesis method. The crystal structure of the samples was identified by X-ray diffraction (XRD). The photoluminescence properties were investigated and it is observed that the co-doping of Y{sup 3+} enhances the luminescence emission intensity of ZnMoO{sub 4}:Eu{sup 3+} material. The Y{sup 3+} acts as a sensitizer in the ZnMoO{sub 4}:Eu{sup 3+} lattice. The particle size is calculated from XRD data by using Scherer Equation. The particles has been found in the range of 30-40 nm.

36 MATERIALS SCIENCE↗

Combustion technology overview

An overview of combustor technology developments required for use of broadened property fuels in jet aircraft is presented. The intent of current investigations is to determine the extent to which fuel properties can be varied, to obtain a data base of combustion - fuel quality effects, and to determine the trade-offs associated with broadened property fuels. Subcomponents of in-service combustors such as fuel injectors and liners, as well as air distributions and stoichiometry, are being altered to determine the extent to which fuel flexibility can be extended. Finally, very advanced technology consisting of new combustor concepts is being evolved to optimize the fuel flexibility of gas turbine combustors.

Niedzwiecki, R. W.↗

Effect of broad properties fuel on injector performance in a reverse flow combustor

The effect of fuel type on the performance of various fuel injectors was investigated in a reverse flow combustor. Combustor performance and emissions are documented for simplex pressure atomizing, spill flow, and airblast fuel injectors using a broad properties fuel and compared with performance using Jet A fuel. Test conditions simulated a range of flight conditions including sea level take off, low and high altitude cruise, as well as a parametric evaluation of the effect of increased combustor loading. The baseline simplex injector produced higher emission levels with corresponding lower combustion efficiency with the broad properties fuel. There was little or not loss in performance by the two advanced concept injectors with the broad properties fuel. The airblast injector proved to be especially insensitive to fuel type.

Raddlebaugh, S. M.↗

Effects of molar expansion ratio of fuels on engine efficiency

Fuel properties have a strong impact on the efficiency of internal combustion engines. Contrary to other physical and thermochemical fuel properties, the molar expansion ratio is normally ignored. Molar expansion ratio is the ratio of number of moles of the products to the reactants. In this work, the impact of the fuel’s molar expansion ratio on engine efficiency is investigated. Findings are based on simulations of a spark ignition engine using different fuels (standard fuels and user-defined fuels) and different dilution ratios. Simulations without heat transfer and friction were performed first. The combustion then takes place at top dead center with a very short combustion duration to approach the ideal Otto cycle. The heat transfer and friction were then added step by step. From this analysis, it could be concluded that the heat loss and friction work decrease as molar expansion ratio increases. The gross indicated and brake thermal efficiencies thus increase. User-defined fuels with different molar expansion ratio, but the same physical and thermochemical properties were then employed. The simulated results showed that the brake thermal efficiency increases by around 1.15% with an increase in molar expansion ratio of 0.02 compared to a fuel with a molar expansion ratio of unity. Lastly, the simulation was also done with air and exhaust gas recirculation dilution.

42 ENGINEERING↗

Structural and optical properties of chromium doped zinc oxide nanoparticles synthesized by sol-gel method

Nanosized Cr-doped ZnO nano particles were synthesized by facile sol-gel auto combustion method. The structural and optical properties of Cr-doped ZnO nanoparticles have been investigated by XRD and UV-Vis spectroscopy at room temperature for 0% to 8% concentration. X-ray diffraction analysis reveals that the Cr-doped ZnO crystallizes in a single phase polycrystalline nature with wurtzite lattice. With every % of doping, the peaks are shifting scarcely and doping of Cr is possible up to 7%. After that, the last peak vanishes, that signifies its structure is transmuted from 8% doping. The average crystallite size decreases with increase in Cr concentration (i.e. 28.9 nm for 0% to 25.8 nm for 8%). The UV-Vis spectra of the nanoparticles betoken an incrementation in the band gap energy from 3.401, 3.415, 3.431, 3.437,3.453, 3.514,3.521, 3.530 and 3.538 eV respectively, for 0,1, 2, 3, 4, 5, 6, 7 and 8 % doping concentration.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Dielectric and magnetic properties of microwave-absorbing FeAl x O y catalysts fabricated via solution combustion synthesis

Iron-based alumina (FeAl x O y ) nanocomposites are microwave-absorbers and catalysts, which makes them promising for emerging microwave-assisted thermocatalytic technologies. Solution combustion synthesis (SCS) has been used to synthesize FeAl x O y powders, and prior work has demonstrated that adjusting SCS parameters significantly changes phase composition and specific surface area of the products. However, it is unclear how synthesis parameters affect their microwave-absorbing properties, which are essential for optimizing microwave-assisted technologies. To address this challenge, in the present work, twelve different FeAl x O y products were synthesized at different combinations of the SCS parameters such as two fuels (citric acid and glycine), two heating modes (hotplate and muffle furnace), and three Fe:Al molar ratios (2:1, 1:1, 1:2). Dielectric and magnetic properties of the products were characterized using a network analyzer and a vibrating sample magnetometer. Based on the measured permittivity and permeability, penetration depth and reflection loss were calculated as a function of frequency and bed thickness. The products were heated by microwaves at 2.45 GHz and then examined with X-ray diffraction (XRD) analysis. For all products, the magnetic saturation was lower than for bulk iron oxides because of the small crystallite size and aluminum substitution. The use of glycine induced high dielectric losses and enabled fast microwave-heating rates compared to citric acid. Higher Fe:Al ratio also led to higher dielectric and magnetic losses. With glycine fuel, SCS in a furnace induced larger penetration depth and lower microwave absorption than SCS on a hotplate. The minimization of reflected power was more sensitive to the thickness of the product bed than to the frequency of the electromagnetic field. Post-heating XRD analysis revealed different phase transformations in the FeAl x O y powders depending on the SCS parameters. As a result, an FeAl x O y material, synthesized via incipient wetness impregnation, lacked magnetic losses and did not heat well as compared to the SCS products.

Combustion synthesis↗

Correlation Between Structural, Magnetic and Dielectric Properties of Microwave Sintered Ni-Zn-Al Nanoferrites

A series of diamagnetic aluminum (Al{sup 3+}) substituted Ni-Zn Nanoferrites have been synthesized using sol-gel auto combustion route. Structural, magnetic, and dielectric properties were systematically studied and reported with respect to Al{sup 3+} substitution in host Fe{sup 3+} ions. X-ray diffraction (XRD) and infrared spectroscopy (IR) measurements confirm the presence of Al{sup 3+} ions at both A and B sites. Cation distribution proposed from XRD and IR correlates with magnetic and dielectric results. It is observed that Al{sup 3+} ions are distributed in to tetrahedral and octahedral sub-lattices. The saturation magnetization varies between 58.5 and 44.2 emu/g with increasing Al{sup 3+} substitution. This decrease in magnetization is ascribed to presence of the non-collinear spin (canted spin) structure in octahedral sub-lattice. Dielectric constant decreased and a significant improvement in AC resistivity is observed with Al{sup 3+} substitution. The observed variations are accounted on the basis of cation distribution in spinel ferrite.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Influence of Combustion Conditions on Yields of Solvent-Extractable Anhydrosugars and Lignin Phenols in Chars: Implications for Characterizations of Biomass Combustion Residues

Anhydrosugars, such as levoglucosan and its isomers (mannosan, galactosan), as well as the solvent-extractable lignin phenols (methoxylated phenols) are thermal degradation products of cellulose/hemicellulos and lignin, respectively. These two groups of biomarkers are often used as unique tracers of combusted biomass inputs in diverse environmental media. However, detail characterization of the relative proportion and signatures of these compounds in highly heterogeneous plant-derived chars/charcoals are still scarce. Here we conducted a systematic study to investigate the yields of solvent-extractable anhydrosugars and lignin phenols in twenty-five lab-made chars produced from different plant materials under different combustion conditions. Solvent extractable anhydrosugars and lignin phenols were only observed in chars formed below 350 C and yields were variable across different combustion temperatures. The yields mannosan (M) and galactosan (G) decreased more rapidly than those of levoglucosan (L) under increasing combustion severity (temp. and duration), resulting in variable L/M and L/(M+G) ratios, two diagnostic ratios often used for identification of combustion sources (e.g. hardwoods vs. softwoods vs. grasses). On the other hand, the results of this study suggest that the ratios of the major solvent-extractable lignin phenols (vanillyls (V), syringyls (S), cinnamyls (C)) provide additional source reconstruction potential despite observed variations with combustion temperature. We thus propose using a property property plot (L/M vs. S/V) as an improved means for source characterization of biomass combustion residues. The L/M-S/V plot has shown to be effective in environmental samples (soil organic matter, atmospheric aerosols) receiving substantial inputs of biomass combustion residues.

09 BIOMASS FUELS↗

Effects of the preparation processes on structural, electronic, and optical properties of LaHoO{sub 3}

Highlights: • The preparation of LaHoO{sub 3} by combustion and hydrothermal techniques was performed. • The crystal structure and characterization of the synthesized oxides were carried out. • The lattice distortions have effects on Raman, luminescence and optical band gap. • Electronic properties and band structure have been carried out by DFT method. • Sample prepared by hydrothermal process gives higher emission intensities. - ABSTRACT: Lanthanum holmium oxide (LaHoO{sub 3}) was synthesized using combustion and hydrothermal processes in order to compare the effects of preparation method on structural, electronic, and optical properties. For this purpose, the as-prepared samples were characterized with infrared spectroscopy, Raman scattering, X-ray diffraction, and scanning electronic microscopy. The Rietveld refinements structure of as-prepared samples show that lattice distortions and volume expansion were obtained for LaHoO{sub 3} synthesized with hydrothermal method compared to combustion process. The luminescence properties were investigated upon 488 and 750 nm laser excitations. The emission curves show the presence of characteristic Ho{sup 3+} transitions with a higher emission intensity for a sample prepared by hydrothermal method than the one obtained by combustion process. The structures properties effects on the band structure and the density of states were realized via generalized gradient approximation functional with Hubbard correction. The lattice distortions were found to have effects on Raman, luminescence and optical band gap.

36 MATERIALS SCIENCE↗

A Review on Biomass Torrefaction Process and Product Properties

Biomass Torrefaction is gaining attention as an important preprocessing step to improve the quality of biomass in terms of physical properties and chemical composition. Torrefaction is a slow heating of biomass in an inert or reduced environment to a maximum temperature of approximately 300 C. Torrefaction can also be defined as a group of products resulting from the partially controlled and isothermal pyrolysis of biomass occurring in a temperature range of 200-280 C. Thus, the process can be called a mild pyrolysis as it occurs at the lower temperature range of the pyrolysis process. At the end of the torrefaction process, a solid uniform product with lower moisture content and higher energy content than raw biomass is produced. Most of the smoke-producing compounds and other volatiles are removed during torrefaction, which produces a final product that will have a lower mass but a higher heating value. The present review work looks into (a) torrefaction process and different products produced during the process and (b) solid torrefied material properties which include: (i) physical properties like moisture content, density, grindability, particle size distribution and particle surface area and pelletability; (ii) chemical properties like proximate and ultimate composition; and (iii) storage properties like off-gassing and spontaneous combustion.

09 BIOMASS FUELS↗

Structure and Early Soot Oxidation Properties of Laminar Diffusion Flames

Soot is an important unsolved problem of combustion science because it is present in most hydrocarbon-fueled flames and current understanding of the reactive and physical properties of soot in flame environments is limited. This lack of understanding affects progress toward developing reliable predictions of flame radiation properties, reliable predictions of flame pollutant emission properties and reliable methods of computational combustion, among others. Motivated by these observations, the present investigation extended past studies of soot formation in this laboratory, to consider soot oxidation in laminar diffusion flames using similar methods. Early work showed that O2 was responsible for soot oxidation in high temperature O2-rich environments. Subsequent work in high temperature flame environments having small O2 concentrations, however, showed that soot oxidation rates substantially exceeded estimates based on the classical O2 oxidation rates of Nagle and Strickland-Constable and suggests that radicals such as O and OH might be strong contributors to soot oxidation for such conditions. Neoh et al. subsequently made observations in premixed flames, supported by later work, that showed that OH was responsible for soot oxidation at these conditions with a very reasonable collision efficiency of 0.13. Subsequent studies in diffusion flames, however, were not in agreement with the premixed flame studies: they agreed that OH played a dominant role in soot oxidation in flames, but found collision efficiencies that varied with flame conditions and were not in good agreement with each other or with Neoh et al. One explanation for these discrepancies is that optical scattering and extinction properties were used to infer soot structure properties for the studies that have not been very successful for representing the optical properties of soot. Whatever the source of the problem, however, these differences among observations of soot oxidation in premixed and diffusion flames clearly must be resolved. Motivated by these findings, the present study undertook measurements of soot and flame properties within the soot oxidation region of some typical laminar diffusion flames and exploited the new measurements to identify soot oxidation mechanisms for these conditions. Present considerations were limited to the early stages of soot oxidation (carbon consumption less than 70%) where reactions at the surface of primary soot particles dominate the process, rather than the later stages when particle porosity and internal particle oxidation become important as discussed by Neoh et al.

El-Leathy, A. M.↗