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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
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Sol-flame synthesis of cobalt-doped TiO 2 nanowires with enhanced electrocatalytic activity for oxygen evolution reaction
Controllable doping of TiO 2 nanowires with cobalt using sol-flame method, which achieves significantly enhanced electrocatalytic activity for oxygen evolution reactions.
Emissions in short-gated ns/ps/fs-LIBS for fuel-to-air ratio measurements in methane-air flames
A study of short-gated 10 nanosecond (ns), 100 picosecond (ps), and 100 femtosecond (fs) laser induced breakdown spectroscopy (LIBS) was conducted for fuel-to-air ratio (FAR) measurements in an atmospheric Hencken flame. The intent of the work is to understand which emission lines are available near the optical range in each pulse width regime and which emission ratios may be favorable for generating equivalence ratio calibration curves. The emission spectra in the range of 550–800 nm for ns-LIBS and ps-LIBS are mostly similar with slightly elevated atomic oxygen lines by ps-LIBS. Spectra from fs-LIBS show the lowest continuum background and prominent individual atomic lines, though have significantly weaker ionic emission from nitrogen. A qualitative explanation based on assumed local thermodynamic equilibrium and electron temperatures calculated by the N I I ( 565 n m ) and N I I ( 594 n m ) emissions is presented. In studying line emission ratios for FAR calculation, it is found that H α <#comment/> ( 656 n m ) / N I I ( 568 n m ) is best for FAR measurements with ns-LIBS and remains viable for ps-LIBS, while H α <#comment/> ( 656 n m ) / O I ( 777 n m ) is optimal for the ps-LIBS and fs-LIBS cases. Due to low continuum background and short time delay for spectra collection, fs-LIBS is very promising for high-speed FAR measurements using short-gated LIBS.
Flame-Sampling Photoionization Mass Spectroscopy: Studies of Flame Chemistry with Sampling Photoionization Mass Spectrometry
Research focused on detailed studies of the complex combustion chemistry of oxygenated, bio-derived fuels. In particular, studies were done of the flame chemistry of simple methyl and ethyl esters chosen as surrogates for the long-chain esters that are primary constituents of biodiesel fuels. The principal goals of these studies were: (1) show how fuel-specific structural differences including degree of unsaturation, linear vs. branched chain structures, and methoxy vs. ethoxy functions affect fuel-destruction pathways, (2) understand the chemistry leading to potential increases in the emissions of hazardous air pollutants including aldehydes and ketones inherent in the use of biodiesel fuels, and (3) define the key chemical reaction mechanisms responsible for observed reductions in polycyclic aromatic hydrocarbons and particulate matter when oxygenated fuels are used as replacements for conventional fuels.
Interactions between Surface Chemistry and Gas-Phase Combustion: New Optical Tools for Probing Flame-Wall Interactions and the Heterogeneous Chemistry of Soot Growth and Oxidation in Flame. Final report
Some of the most stubborn and technologically critical problems in combustion are dominated by heterogeneous processes. While purely gas-phase combustion systems have been the subject of intense theoretical and experimental study, combustion phenomena occurring at interfaces are far less understood. This is partly caused by the lack of experimental approaches capable of probing locations very close to an interface, especially in the hostile environment of combustion. For laser-based optical techniques, measurements taken near interfaces are often complicated by laser scattering from the surface interfering with relatively weak signals. Further, for measurements intended to probe molecular species adsorbed at the interface between a gas-phase combustion reaction and a condensed phase material, signals are generally overwhelmed by contributions from the bulk phases, causing the small contribution from the interfacial molecular species to be undetectable. Our goal in this project has been to develop new optical tools for imaging chemical species, temperature, and surface species at and near surfaces or interfaces of relevance to combustion. We have placed focus on the development and refinement of ultrafast techniques such as femtosecond coherent Raman imaging and femtosecond/picosecond sum-frequency generation (SFG) scattering, as well as the models used to simulate such spectra under differing conditions of pressure and chemical speciation. The two physical phenomena initially targeted for study in this project were flamewall interactions, and the growth of particulates in flames.
Effect of Reynolds Number in Turbulent-flow Range on Flame Speeds of Bunsen-burner Flames
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Imaging Nanocarbon Materials: Soot Particles in Flames are Not Structurally Homogeneous
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An experimental and mechanistic study on the laminar flame speed, Markstein length and flame chemistry of the butanol isomers
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Flame structure and kinetic studies of carbon dioxide-diluted dimethyl ether flames at reduced and elevated pressures
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Determination of laminar flame speeds using stagnation and spherically expanding flames: Molecular transport and radiation effects
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Radiation-induced uncertainty in laminar flame speed measured from propagating spherical flames
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Numerical study of laminar flame speed of fuel-stratified hydrogen/air flames
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Premixed flame response to helical disturbances: Mean flame non-axisymmetry effects
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PAH formation in counterflow non-premixed flames of butane and butanol isomers
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Ignition and extinction of strained nonpremixed cool flames at elevated pressures
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Laminar flame speeds of stratified methane, propane, and n-heptane flames
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