9 research outputs found
The turbulent burning velocity of iso-octane/air mixtures
Turbulent burning velocities of iso-octane air mixtures have been measured for expanding flame kernels within a turbulent combustion bomb. High speed schlieren images were used to derive turbulent burning velocity. Turbulent velocity measurements were made at u’ = 0.5, 1.0, 2.0, 4.0, 6.0 m/s, equivalence ratios of 0.8, 1.0, 1.2, 1.4 and pressures of P = 0.1, 0.5, 1.0 MPa. The turbulent burning velocity was found to increase with time and radius from ignition, this was attributed to turbulent flame development. The turbulent burning velocity increased with increasing rms turbulent velocity, and with pressure; although differences were found in the magnitude of this increase for different turbulent velocities. Generally, raising the equivalence ratio resulted in enhanced turbulent burning velocity, excepting measurements made at the lowest turbulent velocity. The results obtained in this study have been compared with those evaluated for a number turbulent burning velocity correlations and the differences are discussed
Experimental observations on the influence of hydrogen atoms diffusion on laminar and turbulent premixed burning velocities
Measurements of the laminar and turbulent burning velocity of premixed hydrogen–air, n-hexane–air and n-octane–air flames were made and compared to corresponding measurements of deuterium–air, n-hexane-d14–air and n-octane-d18–air flames performed at identical initial conditions. Experiments were conducted in a constant volume, optically accessed vessel, at elevated initial pressure and temperature of 0.5 MPa and 360 K, for a range of equivalence ratios. Burn rate data was determined via schlieren imaging of flames. It was found that the isotope effect accounted for an average reduction of 20% in the laminar burn rate of alkanes. Similarly, deuterium was measured to burn around 30% slower than hydrogen at the range of equivalence ratios explored. The isotope effect on burn rate was significantly reduced under turbulence. The difference between the turbulent burn rates of the deuterated alkanes and their normal alkane counterparts were measured to be approximately 10%. The difference between the turbulent burn rates of deuterium and hydrogen was even smaller. Nonetheless, the laminar burn rate ranking was maintained under turbulence for all fuels and conditions explored, thus suggesting a degree of influence of radical transport and chemistry under turbulent burning
Turbulent burning rates of gasoline components, Part 2-Effect of carbon number
Experimental measurements of turbulent and laminar burning velocities have been made for premixed hydrocarbon–air flames of straight chain molecules of increasing carbon number (from n-pentane to n-octane). Measurements were performed at 0.5 MPa, 360 K and rms turbulent velocities of 2 and 6 m/s, for a range of equivalence ratios. The laminar burning velocities were used to interpret the turbulent data, but were also found to be broadly in line with those of previous workers. At lean conditions the turbulent burning velocity was measured to be similar between the four alkanes studied. However, at rich conditions there were notable differences between the turbulent burn rates of the fuels. The equivalence ratio of the mixtures at which the maximum burning velocities occurred in the turbulent flames was richer than that under laminar conditions. The equivalence ratio of the peak turbulent burning velocity was found to be a function of the carbon number of the fuel and the turbulent intensity and became gradually fuel rich with increases in each of these values
Turbulent burning rates of methane and methane-hydrogen mixtures
Methane and methane-hydrogen (10%, 20% and 50% hydrogen by volume) mixtures have been ignited in a fan stirred bomb in turbulence and filmed using high speed cine schlieren imaging. Measurements were performed at 0.1 MPa (absolute) and 360 K. A turbulent burning velocity was determined for a range of turbulence velocities and equivalence ratios. Experimental laminar burning velocities and Markstein numbers were also derived. For all fuels the turbulent burning velocity increased with turbulence velocity. The addition of hydrogen generally resulted in increased turbulent and laminar burning velocity and decreased Markstein number. Those flames that were less sensitive to stretch (lower Markstein number) burned faster under turbulent conditions, especially as the turbulence levels were increased, compared to stretch-sensitive (high Markstein number) flames
Fundamentals of high-energy spark ignition with lasers
An experimental study of laser-induced spark ignition of flammable, gaseous premixtures is reported, with theoretical interpretations. Ignition was in an explosion bomb, equipped with four variable-speed fans that facilitated the study of quiescent and isotropic turbulent conditions. Good optical access enabled the progress of plasma fronts, shock waves, igniting kernels, and propagating flames to be recorded with high-speed schlieren photography. A focused beam from a Q-switched Nd:YAG laser initiated electrical breakdown, with plasma energies between 85 and 200 mJ. Probabilities of breakdown were found for air and isooctane-air mixtures over ranges of pressures and temperatures. Blast-wave theory applied to shock-wave trajectories enabled initial plasma conditions to be inferred. This suggested electron temperatures of over 10 5 K and very high pressures. Calculated values of the absorption coefficient for the laser beam energy show these plasma properties to be commensurate with the observed energy and size. The ensuing rarefaction wave creates toroidal rings at the leading and trailing edges of the plasma. The former decays more rapidly and a third lobe of the kernel is generated that moves towards the laser. In flammable mixtures this enhances the flame spread. Laminar flame speeds are overdriven by this gasdynamic effect, as well as by the high energy of the plasma, to such an extent that the flame speed decays from elevated values as the flame stretch decreases, contrary to the increases that occur with normal flames with positive Markstein numbers. The extent to which turbulence narrows the ignition limits is found experimentally. For mixtures close to the lean flammability limit, strong gasdynamic flows induced by laser ignition can stretch the flames to extinction and narrow the ignition limits. If a flame becomes established, eventually the third lobe disappears as the initial gas dynamic effects decay and are overwhelmed by the imposed flow fields. Nevertheless, the overdrive effects persist for some time and overdriven flames were observed in regimes where normal flames would have quenched
The Influence of Simulated Residual and NO Concentrations on Knock Onset for PRFs and Gasolines
Laminar burning velocities of three C3H6O isomers at atmospheric pressure
Laminar flames of three C3H6O isomers (propylene oxide, propionaldehyde and acetone), representative of cyclic ether, aldehyde and ketone species important as intermediates in oxygenated fuel combustion, have been studied experimentally and computationally. Most of these flames exhibited a non-linear dependency of flame speed upon stretch rate and two complementary independent techniques were adopted to provide the most reliable burning velocity data. Significant differences in burning velocity were noted for the three isomers: propylene oxide + air mixtures burned fastest, then propionaldehyde + air, with acetone + air flames being the slowest; the latter also required stronger ignition sources. Numerical modelling of these flames was based on the Konnov mechanism, enhanced with reactions specific to these oxygenated fuels. The chemical kinetics mechanism predicted flame velocities in qualitative rather than quantitative agreement with the measurements. Sensitivity analysis suggested that the calculated flame speeds had only a weak dependency upon parent fuel-specific reactions rates; however, consideration of possible break-up routes of the primary fuels has allowed identification of intermediate compounds, the chemistry of which requires a better definition
Laminar burning behaviour of biomass gasification-derived producer gas
In the currently reported work, a mixture of H2, CO and N2 (21:24:55 vol%) has been considered as representative of the producer gas coming from gasification of lignocellulosic biomass. Laminar burning velocities have been determined, with simultaneous study of the effects of flame stretch rate and instabilities. Experimentally determined laminar burning velocities derived from schlieren flame images, over a range of equivalence ratios, have been compared with those determined using the CHEMKIN code. Good agreement obtained for 1 bar flames, but significant differences were observed for high pressure cellular flames. Markstein numbers were also derived from the experimental data and corresponding Lewis numbers were calculated. Hydrogen thermo-diffusive effects tended to destabilise lean flames, while the CO content resulted in laminar burning velocity peaking at very high equivalence ratios. The peak burning rate of producer gas proved faster than those of conventional fuels, such as isooctane and methane