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Development of the gas phase laser induced phosphorscence technique and soot measurements in flame using laser induced incandescenceLawrence, Martin January 2013 (has links)
Thermometry measurements were carried out using planar laser induced phosphorescence in conjunction with thermographic phosphors in heated turbulent jets and laminar flames in order to further develop the technique for usage in flames. Two dimensional thermometry measurements are essential to improve the understanding of combustion processes, as temperature governs soot pyrolysis, leading to soot formation. Two particular thermographic phosphors, BAM and YAG:Dy were tested and compared and it was found that they were unsuitable for gas phase flame thermometry measurements. Soot volume fraction measurements were carried out using planar two colour laser induced incandescence in gaseous and liquid fuel flames. The gas fuel flames were diluted with nitrogen, carbon dioxide and hydrogen individually and then with nitrogen and hydrogen together, as well as carbon dioxide and hydrogen together, separately. Results revealed the dilution effects of the gases on the soot formation process, where increasing nitrogen percentage in the flow decreased SVF, carbon dioxide reduced it further and hydrogen showed no marked difference. Biodiesels were compared with each other and with diesel in a wick burner in order to analyse their compositional effects on soot. Biodiesel composition was measured using gas chromatography. The sooting tendencies of the biodiesels were as expected, fuels with a longer average carbon chain length and a higher degree of unsaturation were found to produce more soot than shorter, more saturated fuels. Diesel was sootier than all of the biofuels tested, due to containing aromatics and a lower oxygen content. A pilot study was also done, where the performance and emissions of biofuels and biofuel-diesel blends were tested in a gas turbine engine, in order to relate the investigation to real world situations.
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Evaluation of Zinc Oxide: Gallium for High-Speed Thermographic Phosphorescence During Impact StudiesPatrick B Moore (10452029) 06 May 2021 (has links)
Thermographic phosphors
are useful compounds to determine temperature, due to their luminescence
characteristics being a function of temperature. In this research, Zinc Oxide: Gallium
was evaluated for its ability to measure the temperature of an impact event in
a drop weight apparatus. Different solids loadings of the phosphor were placed
in a sylgard binder and these samples were then excited by a 355 nm laser as
they were impacted. Images of the event were captured through two separate
filters with a high-speed camera, from which intensity ratios were formed.
These intensity ratios correlated to a temperature, revealing the change in
temperature of the sample throughout the impact. Initial testing at a
repetition rate of 500 kHz provided insignificant data, due to difficulties
with timing. The whole impact event was not able to be captured, and the
imprecise timing of the drop did not allow for imaging of a specific area of
the impact. Moving to a slower repetition rate of 50 kHz, the entire impact was
captured on the high-speed camera, showing three separate areas of interest.
The first section of this area was where the impact was first initiated,
resulting in a temperature increase. Next, there was a temperature decrease,
where the energy from the drop weight transitioned to deforming, rather than
heating the sample. Lastly, there was a final temperature rise when the sample
was fully compressed, but the impact was still occurring. This trend presented
itself in all of the samples, supporting the idea that when combined with the
intensity ratio method, ZnO:Ga embedded in a sylgard binder is an appropriate
method to determine the temperature changes in a high-speed impact event.
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Analyse de la topologie des flammes prémélangées swirlées confinées / Analysis of the topology of premixed swirl-stabilized confined flamesGuiberti, Thibault 04 February 2015 (has links)
Ce travail porte sur la stabilisation de flammes prémélangées et swirlées de mélanges combustibles méthane/hydrogène/air avec différents taux de dilution d’azote et de dioxyde de carbone. Une tige centrale permet de stabiliser des flammes pour de faibles nombres de swirl. Le sommet de la flamme interagît éventuellement avec les parois de la chambre de combustion. L’objectif ces travaux est d’améliorer la connaissance des mécanismes qui gouvernent la stabilisation et la topologie de ces flammes. Ces travaux démontrent que le nombre de swirl, la composition du mélange combustible, la géométrie de la chambre de combustion ainsi que les conditions aux limites thermiques ont une grande influence sur la forme prise par la flamme. Le dispositif expérimental permet de modifier la forme et la taille de la chambre de combustion, le diamètre du tube d’injection et le nombre de swirl. Des conditions opératoires propices aux transitions de forme de flamme sont ensuite étudiées pour différentes configurations de brûleur. Une caractérisation expérimentale fouillée d’un point de fonctionnement est réalisée grâce à la Fluorescence Induite par Laser sur le radical Hydroxyle (OH-PLIF), la Vélocimétrie par Images de Particules (PIV) et la Phosphorescence Induite par Laser de phosphores sensibles à la température (LIP). Une base de donnée de l’écoulement et des conditions aux limites associées est obtenue sans et avec combustion. Les mécanismes qui contrôlent les transitions de formes de flamme sont ensuite analysés lorsque la flamme interagit avec les parois de la chambre de combustion. L’influence de la composition du mélange combustible, de la vitesse débitante et du nombre de swirl est caractérisée et il est démontré que la transition d’une flamme en V vers une flamme en M est déclenchée par un retour de flamme dans la couche limite le long d’une des parois latérales de la chambre de combustion. Les nombres sans dimension contrôlant ces transitions sont identifiés et un modèle de prévision de la forme de ces flammes est développé. La physique déterminant les transitions de forme de flammes est différente lorsque celles-ci n’interagissent pas avec les parois de la chambre de combustion. En utilisant le signal de chimiluminescence OH* et la OH-PLIF, il est montré que la teneur en hydrogène dans le combustible a une grande influence sur la forme de flamme. L’utilisation de la LIP et de thermocouples a également permis de montrer que les conditions aux limites thermiques jouent un rôle prépondérant sur la forme de flamme. Les effets combinés de l’étirement et des pertes thermiques sont examinés par l’utilisation conjointe de la PIV et de la OH-PLIF. Il est montré que les limites d’extinction de flammes pauvres prémélangées sont réduites par les pertes thermiques et que la transition d’une flamme en M vers une flamme en V est consécutive à l’extinction du front de flamme situé dans la couche de cisaillement externe du jet soumis à un étirement trop important. Ces expériences sont complétées par une analyse de la dynamique de ces flammes. Des modulations de la vitesse débitante à basse fréquence et à haute amplitude modifient la forme de flamme. La stabilisation de flammes CH4/H2/air diluées par du N2 ou du CO2 est finalement examinée. La zone de recirculation produite par la tige centrale permet d’alimenter la base de la flamme avec des gaz brûlés chauds et de stabiliser des flammes fortement diluées. Augmenter la fraction molaire de diluant dans le combustible réduit l’intensité de lumière émise par le radical OH*. Il est également montré que la composition du diluant a un impact sur le champ de température des gaz brûlés et des surfaces de la chambre de combustion. La dilution par du CO2 augmente les pertes thermiques par rayonnement des gaz brûlés. Cela réduit l’efficacité de la chambre de combustion équipée de quatre parois transparentes. [...] / This work deals with the stabilization of premixed turbulent swirling flames of methane/hydrogen/air combustible mixtures with different dilution rates of nitrogen and carbon dioxide. A central bluff body helps stabilizing the flames at low swirl numbers. The flame tip eventually impinges the combustor peripheral wall. The general objective is to gain understanding of the mechanisms governing the stabilization and the topology of these flames. It is found that the swirl number, the combustible mixture composition, the geometry of the combustor, and the thermal boundary conditions have a strong impact on the shape taken by these flames. The experimental setup used to characterize flames topologies is first described. Flames prone to topology bifurcations are selected and are studied for different arrangement of the combustor when the combustion chamber shape and size, the injection tube diameter, and swirl number are varied. One operating condition is fully characterized under non-reactive and reactive conditions using Planar Hydroxyl Laser Induced Fluorescence (OH-PLIF), Particle Imaging Velocimetry (PIV), and Laser Induced Phosphorescence of thermographic phosphors (LIP) to generate a detailed database of the flow and the corresponding boundary conditions. An analysis is then conducted to understand the mechanisms controlling shape bifurcations when the flame interacts with the combustor peripheral wall. Effects of the combustible mixture composition, the bulk flow velocity, and the swirl number are analyzed. It is shown that the transition from a V to an M flame is triggered by a flashback of the V flame tip in the boundary layer of the combustor peripheral wall. Dimensionless numbers controlling these transitions are identified and a simplified model is developed to help the prediction of the flame shapes. The physics of these shape bifurcations differs when the flame does not interact with the combustor wall. The large influence of the hydrogen enrichment in the fuel on the flame shape is analyzed using flame chemiluminescence and OH-PLIF. LIP and thermocouple measurements demonstrate that the thermal boundary conditions still have a strong impact on the flame topology. The combined effects of strain and heat losses are investigated using joint OH-PLIF and PIV experiments. It is shown that flammability limits of premixed flames are reduced due to heat losses and the transitions from M to V shaped flames is consecutive to localized extinctions of flame front elements located in the outer shear layer of the jet flow that are submitted to large strain rates. These experiments are completed by an analysis of the dynamics of methane/hydrogen/air flames. It is shown that low frequency and high amplitude velocity modulations generated by a loudspeaker alter the shape taken by these flames. The stabilization of methane/hydrogen/air flames diluted by nitrogen and carbon dioxide is finally examined. It was possible to stabilize swirled flames featuring important dilution rates due to the presence of the bluff body, installed on the axis of the injection tube. The recirculation zone behind this element supplies hot burnt gases to the flame anchoring point. Using OH* chemiluminescence imaging, it is shown than increasing the molar fraction of diluent in the fuel reduces the light emission from excited OH* radicals. The influence of dilution on the flame chemistry is emphasized with experiments conducted at a fixed thermal power and fixed adiabatic flame temperature. It is also demonstrated that the composition of the diluent has a strong influence on the temperature field of the burnt gases and of the combustor wall surfaces. Dilution with carbon dioxide increases radiative heat losses from the burnt gases in comparison to dilution with nitrogen. This penalizes the combustor efficiency equipped with four transparent quartz walls. [...]
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