Unavailable / Thesis (Master, Chemical Engineering) -- Queen's University, 2013-08-02 23:11:16.825

Call number: LD2668 .T4 1957 G72 / Master of Science

"This study investigates the interaction of micron- sized coal particles entrained into lean methane €“ air premixed flames. In a typical axisymmetric burner, coal particles are made to naturally entrain into a stream of the premixed reactants using an orifice plate setup. Pittsburgh seam coal dust, with three particle sizes in the range of 0 to 25 µm, 53 to 63 µm, and 75 to 90 µm is used. The effects of different coal dust concentrations (10 €“ 300 g/m3) at three lean equivalence ratios, ϕ (methane-air) of 0.75, 0.80 and 0.85 on the laminar burning velocity are determined experimentally. The laminar burning velocity of the coal dust-methane-air mixture is determined by taking a shadowgraph of the resulting flame and using the cone-angle method. The results show that the addition of coal dust in methane-air premixed flame reduces the laminar burning velocity at particle size of 53 to 63 µm and 75 to 90 µm. However, burning velocity promotion is observed for 0 to 25 µm particles at ϕ = 0.80. Two competing effects are assumed involved in the process. The first is burning velocity promotion effect that the released volatile increases the gaseous mixture equivalence ratio and thus the burning velocity. The second is the heat sink effect of the coal particles to reduce the flame temperature and accordingly the burning velocity. A mathematical model is developed based on such assumption and it can successfully predict the change of laminar burning velocity at various dust concentration. Furthermore, the implication of this study to coal mine safety is discussed."

No description available.

The primary objectives of the described research were to examine the underlying physical phenomena occurring during flame/obstacles interactions in various chambers of low L/D ratio and to develop a new empirical equation for explosion venting. A literature review suggested that the propagating flame/obstacle interactions in enclosures with large L/D ratio (&gt 2) result in flame acceleration and subsequent pressure build-up during a gas explosion. However, the interactions in practical situations with small L/D &lt 2 were not extensively studied. In this thesis the first investigation involved the flame interaction with different single and multiple obstacles in a 1/20th model of real enclosure. Results provided the basis for flame propagation, local flame displacement speed probability density functions (pdfs), mean flame velocity and explosion pressure. The second investigation of the study involved the flame interaction with multiple bars within chambers of different L/D ratios. The results provided mean flame velocities on each stage, as a function of nondimensional time, and pressure developments as a function of L/D ratio. The final investigation is associated with gas explosion venting. The predictive ability between existing models on explosion venting and experimental results obtained in this thesis were undertaken and found to be deficient. Consequently a new empirical model for predicting explosion venting was developed. The new model was validated with experimental data published in literature.

In this thesis, a range of TiO2-based photocatalysts and cobalt-based Fischer-Tropsch (FT) catalysts were developed and synthesised via the one-step Flame Spray Pyrolysis(FSP). The work starts with the demonstration of bare TiO2 nanoparticles synthesis with controlled characteristics such as specific surface areas, crystallite sizes and anatase content. A comparative study was carried out by benchmarking with commercial Degussa P25 TiO2. The FSP TiO2 was shown to be more efficient in mineralising pollutants requiring direct charge transfer such as the saccharides, while P25 was better for mineralising alcoholic and aromatic compounds. Both catalysts were equally as active in mineralising carboxylic acids. Upon identifying the optimal synthesis of bare TiO2, an in situ co-precipitation of highly dispersed Pt on TiO2 was carried out in the flame. Deposition of Pt resulted in enhanced photocatalytic performance as a result of efficient charge trappings. It is highlighted here the inter-relationship between Pt oxidation states and the TiO2photocatalysis of carboxylic acid, alcohol and aromatic compounds. Depending on the mineralisation path adopted by the model organic compounds, they were shown to have direct influence on the Pt oxidation states. These oxidation states in turn affect the mineralisation rates of the organic compounds. Substitutional-doping of TiO2 with Fe(III) with tunable bandgap was also possible by FSP synthesis. The high temperature synthesis coupled with rapid quenching resulted in 5 times higher solubility limit (Fe/Ti = 0.05) than that previously reported in the literature. Under visible light irradiation, FSP-made Fe-TiO2 improved the photocatalytic mineralisation of oxalic acid by more than 6 times, with respect to P25 and FSP TiO2. Furthermore, the photocatalyst was reusable over a number of repetitions with minimal leaching or loss in activity. The last part of the work concerns the development of bare and Ru-doped Co-ZrO2 catalysts, where cobalt was finely dispersed within the zirconia matrix. Doping of Ru enhanced significantly the reducibility of cobalt, reducing even the embedded cobalt beneath the zirconia surface. It also increased the extent of CO-chemisorption and as such, enhanced the FT activity. This is the first time, catalysts of such type is synthesised and tested for FT reaction.

For natural gas combustion, there is a large amount of experience in the gas turbine industry. However, much of the design work is based on costly combustion tests due to insufficient accuracy of existing prediction tools for data such as emissions and effects due to fuel composition. In the present work, Computational Fluid Dynamics (CFD) approach is used to study partially premixed combustion in the 3rd generation DLE (Dry Low Emission) burner that is used in SGT-700 and SGT-800 gas turbines. The fuels that are studied here are natural gas and enriched hydrogen fuel. The CFD models which are used in this work are an axisymmetric and a 3D model and the softwares are ANSYS CFX and ANSYS FLUENT. One of the main objectives of this thesis is the study of flame shape and NOx emission in hydrogen enriched combustion. In the first study of the present work, effect of adding hydrogen to non-preheated gas combustion was investigated and the results were compared with the available measurement data. Calculated laminar burning velocity with CANTERA showed a good agreement with the experimental and numerical references. Also, the accuracy of generated flamelet libraries in CFD tools to calculate adiabatic flame temperature was compared with different available tools. Results showed good agreement between available tools for the ranges of interest. In addition, flame shape and NOx prediction was studied in the gas turbine burner. Adding hydrogen to the fuel increased significantly turbulent burning velocity and OH distribution in the domain. The effect of hydrogen on the central stagnation point was studied and the simulation results did not show a significant effect on the stagnation point location. Beside the flame shape, this study showed that although the CFD NOx prediction tools in ANSYS CFX and ANSYS FLUENT predict the trend of NOx and the flame propagation in the right manner, in order to use as a reliable prediction tool in the gas turbine industry they need to be improved.

The major objectives of this research were to examine the bioaccumulation parameters [depuration rates (kd), half life (t1/2) and biomagnification factor (BMF)] of individual isomers of hexabromocyclododecane (HBCD, C12H18Br6) in fish and to test the hypothesis of in vivo bioisomerization. This was done by exposing three groups of juvenile rainbow trout (Oncorhynchus Mykiss) to food fortified with known concentrations of an individual diastereoisomer (α, β, γ) for 56 days (uptake phase) followed by 112 days (depuration phase) of unfortified food. A fourth group of fish were exposed to unfortified food for the duration of the experiment. Fish (n=4) from all four aquaria were sacrificed on days 0, 7, 14, 56, 63, 70, 112 and 168 and muscle tissue was extracted and analyzed for diastereoisomer concentrations by high performance liquid chromatography tandem mass spectrometry (LC/MS/MS). Bioaccumulation of the γ diastereoisomer was linear during the uptake phase while the α and β diastereoisomers were found to increase exponentially with respective doubling times of 14.1 and 20.5 days. Both the β and γ diastereoisomers followed first order depuration kinetics with calculated t1/2’s of 94 ± 25 and 84 ± 51 (± 1 × standard error) days, respectively. The BMF for the α diastereoisomer (BMF = 4.1) was one and a half times greater than the β-diastereoisomer (BMF = 2.6) and about one fifth larger than the γ-diastereoisomer (BMF = 3.6). The large BMF for the α diastereoisomer is consistent with this diastereoisomer dominating higher trophic level organisms in wildlife. Although the BMF of the β diastereoisomer suggests that it will biomagnify, because it is present in small quantities in commercial mixtures it is rarely detected in environmental samples. Results from these studies also provide evidence of bioisomerization of the β and γ diastereoisomers. Most importantly, the α diastereoisomer which was recalcitrant to bioisomerization by juvenile rainbow trout in this study and known to be the dominant diastereosiomer in fish, was bioformed from both the β and γ diastereoisomers. To our knowledge, this is the first report of bioisomerization of a halogenated organic pollutant in biota. / May 2006

This thesis describes an experimental investigation of the flame transfer function between flow disturbances and heat release oscillations in lean, premixed combustors. This research effort was motivated by the fact that modern gas turbines, operating fuel-lean to minimize exhaust emissions, are susceptible to self-excited combustion oscillations. These instabilities generally occur when the unsteady combustion process couples with the acoustic modes of the combustion chamber. The resultant flow and structural vibrations can substantially reduce hot section part life. As such, avoiding operating regimes where high dynamics occur often requires operating at lower power outputs and/or higher pollutant emissions than the turbine is otherwise capable. This work demonstrated nonlinearities in the chemiluminescence response at large amplitude velocity oscillations in a turbulent, swirling flame. It is observed that the nonlinear flame response can exhibit a variety of behaviors, both in the shape of the response curve and the forcing amplitude at which nonlinearity is first observed depending on the operating conditions of the combustor. The phase between the flow oscillations and heat release is also seen to have substantial amplitude dependence. In addition, the interactions between the fundamental frequency and the higher and subharmonics of the measured signals can significantly influence the flame as well as the frequency response of the system. The nonlinear flame dynamics are governed by different mechanisms in different frequency and flowrate regimes. Three mechanisms, vortex rollup, unsteady flame liftoff, and parametric instability, are identified to influence the nonlinear flame response in these combustors. Analysis of the results shows that the mechanisms responsible for nonlinearity in the flame response are influenced by the Strouhal number, the mean velocity at the combustor dump plane, and the ratio of the oscillating velocity amplitude to the laminar flame speed.

A variety of materials were used to fabricate nanocoatings using layer-by-layer (LbL) assembly to reduce the flammability of cotton fabric. The most effective brominated flame retardants have raised concerns related to their toxicity and environmental impact, which has created a need for alternative flame retardant chemistries and approaches. Polymer nanocomposites typically exhibit reduced mass loss and heat release rates, along with anti-dripping behavior, all of which are believed to be due to the formation of a barrier surface layer. Despite these benefits, the viscosity and modulus of the final polymeric material is often altered, making industrial processing difficult. These challenges inspired the use of LbL assembly to create densely layered nanocomposites in an effort to produce more flame-retardant coatings. Laponite and montmorillonite (MMT) clay were paired with branched poly(ethylenimine) to create thin film assemblies that can be tailored by changing pH and concentration of aqueous deposition mixtures. Both films can be grown linearly as a function of layers deposited, and they contained at least 70 wt percent of clay. When applying these films to cotton fabric, the individual fibers are uniformly coated and the fabric has significant char left after burning. MMT-coated fabric exhibits reduced total heat release, suggesting a protective ceramic surface layer is created. Small molecule, POSS-based LbL thin films were also successfully deposited on cotton fabric. With less than 8 wt percent added to the total fabric weight, more than 12 wt percent char remained after microscale combustion calorimetry. Furthermore, afterglow time was reduced and the fabric weave structure and shape of the individual fibers were highly preserved following vertical flame testing. A silica-like sheath was formed after burning that protected the fibers. Finally, the first intumescent LbL assembly was deposited on cotton fabric. SEM images show significant bubble formation on fibers, coated with a 0.5 wt percent PAAm/1 wt percent PSP coating after burning. In several instances, a direct flame on the fabric was extinguished. The peak HRR and THR of coated fabric has 30 percent and 65 percent reduction, respectively, compared to the uncoated control fabric. These anti-flammable nanocoatings provide a relatively environmentally-friendly alternative for protecting fabrics, such as cotton, and lay the groundwork for rendering many other complex substrates (e.g., foam) flame-retardant without altering their processing and desirable mechanical behavior.