Effects of Fuel Doping and Fuel Chemistry on Soot Formation in Co-flow Laminar Diffusion Flames at Elevated Pressures


Book Description

Effects of fuel doping and fuel chemistry on soot formation were studied in laminar diffusion flames at elevated pressures. Soot spectral emission is used to obtain radial temperature, soot volume fraction, and soot yield profiles. This thesis first investigated addition of 0%-40% ethanol in ethylene flames at 3-10 bar. 10% ethanol-doped flames didn't exhibit measurable soot synergy, whereas 20%-40% ethanol displayed lower soot yields. Secondly, 7.5% of benzene, cyclo-hexane and n-hexane was added into methane flames at 1.4-10 bar. Pressure dependence of sooting propensity is lowest for benzene. Thirdly, 3% of m-xylene and n-octane was mixed with methane at 1.4-10 bar. m-Xylene doped methane flames produced highest soot yields but lowest pressure dependency in soot yields. Results indicate that pressure dependence of highly sooting aromatics weakens compared to that of less sooting n-alkanes at high pressures.







Soot Formation in Co-flow and Counterflow Laminar Diffusion Flames of Fuel Mixtures


Book Description

In the formation process of soot in the flames of even-carbon-numbered fuels, acetylene and its derivatives are suspected to be dominant. The addition of an odd-carbon-numbered fuel into these flames introduces methyl radicals and/or C3 chemistries, which are believed to (de)activate certain chemical pathways towards the production of soot. The resultant soot formation rate of the mixture could be higher than the sum of the respective rates of the mixture components, i.e., synergistic effect.In this work, the mixtures of butane isomers, ethylene-butane isomers, and propane-butane isomers were studied on a co-flow and a counterflow burner. Chemical effects were isolated from those of thermal and dilution by mixing isomers and comparing the mixtures including one isomer to those including the counterpart. Line of sight attenuation (LOSA) and laser-light extinction techniques were used for measuring soot volume fraction. The results provide information on synergistic effects in soot formation for the fuels used.







Soot Formation in Non-premixed Laminar Flames at Subcritical and Supercritical Pressures


Book Description

An experimental study was conducted using axisymmetric co-flow laminar diffusion flames of methane-air, methane-oxygen and ethylene-air to examine the effect of pressure on soot formation and the structure of the temperature field. A liquid fuel burner was designed and built to observe the sooting behavior of methanol-air and n-heptane-air laminar diffusion flames at elevated pressures up to 50 atm. A non-intrusive, line-of-sight spectral soot emission (SSE) diagnostic technique was used to determine the temperature and the soot volume fraction of methane-air flames up to 60 atm, methane-oxygen flames up to 90 atm and ethylene-air flames up to 35 atm. The physical flame structure of the methane-air and methane-oxygen diffusion flames were characterized over the pressure range of 10 to 100 atm and up to 35 atm for ethylene-air flames. The flame height, marked by the visible soot radiation emission, remained relatively constant for methane-air and ethylene-air flames over their respected pressure ranges, while the visible flame height for the methane-oxygen flames was reduced by over 50 % between 10 and 100 atm. During methane-air experiments, observations of anomalous occurrence of liquid material formation at 60 atm and above were recorded. The maximum conversion of the carbon in the fuel to soot exhibited a strong power-law dependence on pressure. At pressures 10 to 30 atm, the pressure exponent is approximately 0.73 for methane-air flames. At higher pressures, between 30 and 60 atm, the pressure exponent is approximately 0.33. The maximum fuel carbon conversion to soot is 12.6 % at 60 atm. For methane-oxygen flames, the pressure exponent is approximately 1.2 for pressures between 10 and 40 atm. At pressures between 50 and 70 atm, the pressure exponent is about -3.8 and approximately -12 for 70 to 90 atm. The maximum fuel carbon conversion to soot is 2 % at 40 atm. For ethylene-air flames, the pressure exponent is approximately 1.4 between 10 and 30 atm. The maximum carbon conversion to soot is approximately 6.5 % at 30 atm and remained constant at higher pressures.







Conjugate Heat Transfer and Sooting Propensity of Ethanol for Laminar Coflow Diffusion Flames at Elevated Pressures


Book Description

The effect of sooting propensity of various compositions of methane and ethanol fuel in laminar diffusion flames at elevated pressures was analyzed numerically. Simulations of laminar diffusion flames comprised of pressure conditions up to 20 atm and composition of ethanol and methane fuel ranging from pure methane to pure ethanol. For all fuel compositions evaluated, the total carbon mass flow rate was maintained at a constant value of 0.458 mg/s. Soot formation and soot yield were corroborated against measured data and demonstrated well agreement with trends for pressure and fuel composition. For elevated pressure, fuel compositions with higher ethanol content yield higher peak soot concentrations, however at lower pressures synergistic effects result to soot concentration decreasing with ethanol content for ethanol dominant fuel mixtures. Finally, the effect of conjugate heat transfer and modification in burner wall geometry were evaluated which exhibited improved trends and overall results.




The Effect of Elevated Pressure on Soot Formation in a Laminar Jet Diffusion Flame


Book Description

Soot volume fraction (f[subscript sv]) is measured quantitatively in a laminar diffusion flame at elevated pressures up to 25 atmospheres as a function of fuel type in order to gain a better understanding of the effects of pressure on the soot formation process. Methane and ethylene are used as fuels; methane is chosen since it is the simplest hydrocarbon while ethylene represents a larger hydrocarbon with a higher propensity to soot. Soot continues to be of interest because it is a sensitive indicator of the interactions between combustion chemistry and fluid mechanics and a known pollutant. To examine the effects of increased pressure on soot formation, Laser Induced Incandescence (LII) is used to obtain the desired temporally and spatially resolved, instantaneous f[subscript sv] measurements as the pressure is incrementally increased up to 25 atmospheres. The effects of pressure on the physical characteristics of the flame are also observed. A laser light extinction method that accounts for signal trapping and laser attenuation is used for calibration that results in quantitative results. The local peak f[subscript sv] is found to scale with pressure as p[superscript 1.2] for methane and p[superscript 1.7] for ethylene.




Fuel Structure and Pressure Effects on the Formation of Soot Particles in Diffusion Flames


Book Description

Studies emphasizing the effects of fuel concentration and operating pressure on the formation of soot particles have been conducted in a series of laminar diffusion flames. These experiments have shown that fuel concentration has a measurable effect on the amount of soot formed in the flame. However, a simple, constant proportionality between the fuel concentration and soot volume fraction has not been found to apply for the range of flow conditions studied. This observation is believed to be a result of flame residence time and diffusion effects which mitigate the consequences of reduced initial fuel concentration. Comparisons with simple laminar diffusion flame models are currently being used to investigate the relationship between initial fuel concentration and local flame concentration fields. Similar studies of soot formation in laminar diffusion flames as a function of operating pressure have also been completed for ethene, ethane and propene fuel species. Keywords: Soot formation, Soot particles, Diffusion flames. (JES).