Critical conditions at liftoff limit of a laminar n-butane-air jet diffusion flame

The stability mechanism of laminar coflow jet diffusion flames in normal gravity has been studied computationally and experimentally. N-butane, the heaviest alkane in a gaseous state at ambient temperature and pressure, is used as the fuel since the reaction mechanism is similar to that of higher (liquid) hydrocarbons. The critical mean n-butane jet and coflowing air velocities at flame stability limits are measured using a small fuel tube burner (0.8 mm inner diameter). The time-dependent, axisymmetric numerical code with a detailed reaction mechanism (58 species and 540 reactions), molecular diffusive transport, and a radiation model, reveals a flame structure. A fuel-lean peak reactivity spot (i.e., reaction kernel), possessing the hybrid nature of diffusion-premixed flame structure at a constant temperature of ≈1560 K, is formed at the flame base and controls the flame stability. In a near-quiescent environment, the flame base resides below the fuel tube exit plane and thereby premixing is limited. As the coflowing air velocity is increased incrementally under a fixed fuel jet velocity, the flame base moves slightly above (≈1 mm) the burner exit and vigorous premixed combustion becomes prevailing. The local heat-release rate at the reaction kernel nearly doubles due to the increased convective oxygen flux (i.e., a blowing effect). The local Damköhler number, newly defined as a ratio of the square root of the local heat-release rate and the local velocity, decreases gradually first and drops abruptly at a critical threshold value and the flame base lifts off from the burner rim. The calculated coflow air velocity at liftoff is ≈0.38 m/s at the fuel jet velocity of 2 m/s, which is consistent with an extrapolated measured value of 0.41 m/s. This work has determined the critical Damköhler number at the stability limit quantitatively, for the first time, for laminar jet diffusion flames.     

Flame structure and flame spread rate over a solid fuel in partially premixed atmospheres

We have investigated the downward flame spread over a thin solid fuel. Hydrogen, methane, or propane, included in the gaseous product of pyrolysis reaction, is added in the ambient air. The fuel concentration is kept below the lean flammability limit to observe the partially premixing effect. Both experimental and numerical studies have been conducted. Results show that, in partially premixed atmospheres, both blue flame and luminous flame regions are enlarged, and the flame spread rate is increased. Based on the flame index, a so-called triple flame is observed. The heat release rate ahead of the original diffusion flame is increased by adding the fuel, and its profile is moved upstream. Here, we focus on the heat input by adding the fuel in the opposed air, which could be a direct factor to intensify the combustion reaction. The dependence of the flame spread rate on the heat input is almost the same for methane and propane/air mixtures, but larger effect is observed for hydrogen/air mixture. Since the deficient reactant in lean mixture is fuel, the larger effect of hydrogen could be explained based on the Lewis number consideration. That is, the combustion is surely intensified for all cases, but this effect is larger for lean hydrogen/air mixture (Le < 1), because more fuel diffuses toward the lean premixed flame ahead of the original diffusion flame. Resultantly, the pyrolysis reaction is promoted to support the higher flame spread rate.     

Effect of non-zero relative velocity on the flame speed of two-phase laminar flames

A numerical study of one-dimensional n-heptane/air spray flames is presented. The objective is to evaluate the flame propagation speed in the case where droplets evaporate inside the reaction zone with possibly non-zero relative velocity. A Direct Numerical Simulation approach for the gaseous phase is coupled to a discrete particle Lagrangian formalism for the dispersed phase. A global two-step n-heptane/air chemical mechanism is used. The effects of initial droplet diameter, overall equivalence ratio, liquid loading and relative velocity between gaseous and liquid phases on the laminar spray flame speed and structure are studied. For lean premixed cases, it is found that the laminar flame speed decreases with increasing initial droplet diameter and relative velocity. On the contrary, rich premixed cases show a range of diameters for which the flame speed is enhanced compared to the corresponding purely gaseous flame. Finally, spray flames controlled by evaporation always have lower flame speeds. To highlight the controlling parameters of spray flame speed, approximate analytical expressions are proposed, which give the correct trends of the spray flame propagation speed behavior for both lean and rich mixtures.     

Nonlinear hydrodynamic and thermoacoustic oscillations of a bluff-body stabilised turbulent premixed flame

Turbulent premixed flames often experience thermoacoustic instabilities when the combustion heat release rate is in phase with acoustic pressure fluctuations. Linear methods often assume a priori that oscillations are periodic and occur at a dominant frequency with a fixed amplitude. Such assumptions are not made when using nonlinear analysis. When an oscillation is fully saturated, nonlinear analysis can serve as a useful avenue to reveal flame behaviour far more elaborate than period-one limit cycles, including quasi-periodicity and chaos in hydrodynamically or thermoacoustically self-excited system. In this paper, the behaviour of a bluff-body stabilised turbulent premixed propane/air flame in a model jet-engine afterburner configuration is investigated using computational fluid dynamics. For the frequencies of interest in this investigation, an unsteady Reynolds-averaged Navier–Stokes approach is found to be appropriate. Combustion is represented using a modified laminar flamelet approach with an algebraic closure for the flame surface density. The results are validated by comparison with existing experimental data and with large eddy simulation, and the observed self-excited oscillations in pressure and heat release are studied using methods derived from dynamical systems theory. A systematic analysis is carried out by increasing the equivalence ratio of the reactant stream supplied to the premixed flame. A strong variation in the global flame structure is observed. The flame exhibits a self-excited hydrodynamic oscillation at low equivalence ratios, becomes steady as the equivalence ratio is increased to intermediate values, and again exhibits a self-excited thermoacoustic oscillation at higher equivalence ratios. Rich nonlinear behaviour is observed and the investigation demonstrates that turbulent premixed flames can exhibit complex dynamical behaviour including quasiperiodicity, limit cycles and period-two limit cycles due to the interactions of various physical mechanisms. This has implications in selecting the operating conditions for such flames and for devising proper control strategies for the avoidance of thermoacoustic instability.     

Measurements of local mixture fraction of reacting mixture in swirl-stabilised natural gas-fuelled burners

Local, time-dependent measurements of mixture fraction of the reacting mixture were obtained in a swirl-stabilised natural gas-fuelled, nominally non-premixed burner using the intensity of chemiluminescence from OH^∗ and CH^∗ radicals. The measurements quantified the mean, rms of fluctuations and probability density functions of local mixture fraction at the stabilisation region of the flame. In addition, the probability of flame presence and the degree of lean or rich versus stoichiometric reaction is reported. The burner was operated for three air flow Reynolds numbers (Re=18970, 29100 and 57600), at an overall equivalence ratio of 0.32, without and with imposed oscillations to the air flow of the burner at the resonance frequency of 350 Hz. Results show that combustion occurred in a partially premixed mode for all flow conditions, although fuel and air were injected separately in the reaction zone. The mean local mixture fraction was nearly stoichiometric at the base of the flame without imposed air oscillations, but with large fluctuations leading to around 80% of lean or rich reaction. The degree of non-stoichiometric reaction increased with axial distance from the burner exit and Reynolds number and lean reaction dominated. Imposed air oscillations led to lifted flames and increased the degree of non-stoichiometric reaction for Re=18970 and 29100, whereas the flame remained attached onto the injector for Re=57600 and little modification of the mixture fraction was observed.     

Response of non-premixed flames to bulk flow perturbations

This paper describes the dynamics of non-premixed flames responding to bulk velocity fluctuations, and compares the dynamics of the flame sheet position and spatially integrated heat release to that of a premixed flame. The space–time dynamics of the non-premixed flame sheet in the fast chemistry limit is described by the stoichiometric mixture fraction surface, extracted from the solution of the

-equation. This procedure has some analogies to premixed flames, where the premixed flame sheet location is extracted from the G = 0 surface of the solution of the G-equation. A key difference between the premixed and non-premixed flame dynamics, however, is the fact that the non-premixed flame sheet dynamics are a function of the disturbance field everywhere, and not just at the reaction sheet, as in the premixed flame problem. A second key difference is that the non-premixed flame does not propagate and so flame wrinkles are convected downstream at the axial flow velocity, while wrinkles in premixed flames convect downstream at a vector sum of the flame speed and axial velocity. With the exception of the flame wrinkle propagation speed, however, we show that that the solutions for the space–time dynamics of the premixed and non-premixed reaction sheets in high velocity axial flows are quite similar. In contrast, there are important differences in their spatially integrated unsteady heat release dynamics. Premixed flame heat release fluctuations are dominated by area fluctuations, while non-premixed flames are dominated by mass burning rate fluctuations. At low Strouhal numbers, the resultant sensitivity of both flames to flow disturbances is the same, but the non-premixed flame response rolls off slower with frequency. Hence, this analysis suggests that non-premixed flames are more sensitive to flow perturbations than premixed flames at O(1) Strouhal numbers.     

Effects of pressure on flame propagation in a premixture containing fine fuel droplets

Combustion experiments on fuel droplet–vapor–air mixtures have been performed with a rapid expansion apparatus which generates monodispersed droplet clouds with narrow diameter distribution using the condensation method. The effects of fine fuel droplets on flame propagation were investigated for ethanol droplet–vapor–air mixtures at various pressures from 0.2 to 1.0 MPa. A stagnant fuel droplet–vapor–air mixture, generated in a rapid expansion chamber, was ignited at the center of the chamber using an ignition wire. Spherical flame propagation under constant-pressure conditions was observed with a high-speed video camera and flame speed was measured. Total equivalence ratio, and the ratio of liquid fuel mass to total fuel mass, was varied from 0.6 to 1.4 and from zero to 56%, respectively. The mean droplet diameter of fuel droplet–vapor–air mixtures was set at 8.5 and 11 μm. It was found that the flame speed of droplet–vapor–air mixtures less than 0.9 in the total equivalence ratio exceeds that of premixed gases of the same total equivalence ratio at all pressures. The flame speed of fuel droplet–vapor–air mixtures decreases as the pressure increases in all total equivalence ratios. At large ratios of liquid fuel mass to total fuel mass, the normalized flame speed (the flame speed of droplet–vapor–air mixtures divided by the flame speed of the premixed gas with the same total equivalence ratio), increases with the increase in pressure for fuel-lean mixtures, and it decreases for fuel-rich mixtures. The outcome is reversed at small ratios of liquid fuel mass to total fuel mass; the normalized flame speed decreases with the increase in pressure for fuel-lean mixtures, and increases for fuel-rich mixtures. The results suggest that the increase in pressure promotes droplet evaporation in the preheat zone.     

Phenomenological model of chain-branching premixed flames

In this work, we introduce a global kinetic model that includes fuel, oxygen, products and two radical species involved in the reversible chain-branching, chain-propagation and chain-termination reactions. The model naturally extends the Zeldovich–Liñán and Zeldovich–Barenblatt–Dold models and can be used to describe both premixed and diffusion flames. Here it is applied to the problem of the deflagration wave propagation in the hydrocarbon fuel/air mixture with arbitrary equivalence ratio under the simplifying thermal-diffusive approximation. The conservation equations are solved numerically in order to obtain the velocity and structure of the combustion wave. It is demonstrated that the peak values of the adiabatic flame temperature and deflagration velocity are shifted towards the rich mixture composition if the reverse reactions of product decomposition are taken into account. The dependence of the flame speed and temperature on parameters of the system is analysed. The prospects of further investigation are discussed.     

Premixed flame oscillations in obstructed channels with both ends open

An initially laminar premixed flame front accelerates extremely fast and may even trigger a detonation when propagating in a semi-open obstructed channel (one end of the channel is closed; the flame is ignited at the closed end and moves towards the open one). However, industrial and laboratory conduits oftentimes have both ends open, or vented, with a flame ignited at one of these ends. The latter constitutes the focus of the present work. Specifically, premixed flame propagation through a comb-shaped array of obstacles, in-built in a channel with both ends open, is studied by means of computational simulation of the reacting flow equations with fully-compressible hydrodynamics and an Arrhenius chemical kinetics. The parametric study includes various blockage ratios and spacing as well as the thermal expansion ratios, with oscillations of the burning rate observed in the majority of the cases, which conceptually differs from fast flame acceleration in semi-open channels. Such a difference is devoted to the fact that while the entire flame-generated jet-flow is pushed towards a single exit in a semi-open channel, in a channel with two ends open, this jet-flow is distributed between the upstream and downstream flows, thereby moderating flame propagation. The flame oscillations are nonlinear in all cases where they are observed. The oscillation period grows with the blockage ratio but decreases with the thermal expansion. The present results also support the recent experiments, modeling and theory of flames in obstructed channels with both ends open, which all yielded steady or quasi-steady flame propagation prior to the onset of flame acceleration. Indeed, the present oscillations can be treated as the fluctuations around a quasi-steady solution.     

Effect of flame retardants on side-wall quenching of partially premixed laminar flames

A combined experimental and numerical investigation of partially premixed laminar methane-air flames undergoing side-wall quenching (SWQ) is performed. A well-established SWQ burner is adapted to allow the seeding of the main flow with additional gaseous products issued from a (secondary) wall inlet close to the flame’s quenching point. First, the characteristics of the partially premixed flame that quenches at the wall are assessed using planar laser-induced fluorescence measurements of the OH radical, and a corresponding numerical simulation with fully-resolved transport and chemistry is conducted. A boundary layer of enriched mixture is formed at the wall, leading to a reaction zone parallel to the wall for high injection rates from the wall inlet. Subsequently, in a numerical study, the wall inflow is mixed with dimethylmethylphosphonat (DMMP), a phosphor-based flame retardant. The DMMP addition allows the assessment of the combined effects of heat loss and flame retardants on the flame structure during flame-wall interaction. With an increasing amount of DMMP in the injected mixture, the flame stabilizes further away from the wall and shows a decrease in the local heat-release rate. Thereby, the maximum wall heat flux is significantly reduced. That results in a lower thermal load on the quenching wall. The flame structure analysis shows an accumulation of the intermediate species HOPO at the wall similar to the CO accumulation during the quenching of premixed flames without flame retardant addition. The study shows how the structure of a partially premixed flame is influenced by a wall that releases either additional fuel or a mixture of fuel and flame retardant. The insights gained from the canonical configuration can lead to a better understanding of the combined effects of flame retardants and heat losses in near-wall flames.     

Combustion of bimodal nano/micron-sized aluminum particle dust in air

The combustion of bimodal nano/micron-sized aluminum particles with air is studied both analytically and experimentally in a well-characterized laminar particle-laden flow. Experimentally, an apparatus capable of producing Bunsen-type premixed flames was constructed to investigate the flame characteristics of bimodal-particle/air mixtures. The flame speed is positively affected by increasing the mass fraction of nano particles in the fuel formulation despite the lower flame luminosity and thicker flame zone. Theoretically, the flames are assumed to consist of several different regimes for fuel-lean mixture, including the preheat, flame, and post flame zones. The flame speed and temperature distribution are derived by solving the energy equation in each regime and matching the temperature and heat flux at the interfacial boundaries. The analysis allows for the investigation of the effects of particle composition and equivalence ratio on the burning characteristics of aluminum-particle/air mixtures. Reasonable agreement between theoretical results and experimental data was obtained in terms of flame speed. The flame structure of a bimodal particle dust cloud may display either an overlapping or a separated configuration, depending on the combustion properties of aluminum particles at different scales. At low percentages of nano particles in the fuel formulation, the flame exhibits a separated spatial structure with a wider flame regime. At higher nano-particle loadings, overlapping flame configurations are observed.     

Further investigation on the enhancement of flame speed in vortex ring combustion

Enhancement of flame speed in vortex ring combustion has been investigated experimentally. The flame speed and the maximum tangential velocity for each vortex ring were simultaneously measured with a PIV system and a high speed camera. To vary the extent of the enhancement, methane/hydrogen mixtures were used. Furthermore, rich mixtures were used as a source of vortex ring so that the situation of the experiment and the results could be applied more directly to practical use. Results have confirmed that enhancement of flame speed does occur in vortex ring combustion of rich methane/hydrogen mixtures in air. The extent of the enhancement becomes larger as the hydrogen content is increased. The flame speed reaches about twice as high as the maximum tangential velocity for pure hydrogen. Based on momentum conservation across the flame, a simple equation on the ratio of the flame speed to the maximum tangential velocity has been obtained, which has shown that the flame speed enhancement can be explained successfully by considering the spherically expanding type premixed combustion behind the flame. The pressure rise of a spherically expanding type premixed flame can explain the flame speed enhancement observed in the present rich methane/hydrogen vortex ring combustion.     

Ethanol turbulent spray flame response to gas velocity modulation

A numerical investigation of the interaction between a spray flame and an acoustic forcing of the velocity field is presented in this paper. In combustion systems, a thermoacoustic instability is the result of a process of coupling between oscillations in heat released and acoustic waves. When liquid fuels are used, the atomisation and the evaporation process also undergo the effects of such instabilities, and the computational fluid dynamics of these complex phenomena becomes a challenging task. In this paper, an acoustic perturbation is applied to the mass flow of the gas phase at the inlet and its effect on the evaporating fuel spray and on the flame front is investigated with unsteady Reynolds averaged Navier-Stokes numerical simulations. Two flames are simulated: a partially premixed ethanol/air spray flame and a premixed pre-vaporised ethanol/air flame, with and without acoustic forcing. The frequencies used to perturb the flames are 200 and 2500 Hz, which are representative for two different regimes. Those regimes are classified based on the Strouhal number St = (D/U)f_f: at 200 Hz, St = 0.07, and at 2500 Hz, St = 0.8. The exposure of the flame to a 200 Hz signal results in a stretching of the flame which causes gas field fluctuations, a delay of the evaporation and an increase of the reaction rate. The coupling between the flame and the flow excitation is such that the flame breaks up periodically. At 2500 Hz, the evaporation rate increases but the response of the gas field is weak and the flame is more stable. The presence of droplets does not play a crucial role at 2500 Hz, as shown by a comparison of the discrete flame function in the case of spray and pre-vaporised flame. At low Strouhal number, the forced response of the pre-vaporised flame is much higher compared to that of the spray flame.     

Influence of micro-explosions on the stability of laminar premixed water-in-fuel emulsion spray flames

A model is presented for a one-dimensional laminar premixed flame, propagating into a rich, off-stoichiometric, fresh homogenous mixture of water-in-fuel emulsion spray, air and inert gas. Due to its relatively large latent heat of vaporisation, the water vapour acts to cool the flame that is sustained by the prior release of fuel vapour. To simplify the inherent complexity that characterises the analytic solution of multi-phase combustion processes, the analysis is restricted to fuel-rich laminar premixed water-in-fuel flames, and assumes a single-step global chemical reaction mechanism. The main purpose is to investigate the steady-state burning velocity and burnt temperature as functions of parameters such as initial water content in the emulsified droplet and total liquid droplet loading. In particular, the influence of micro-explosion of the spray’s droplets on the flame’s characteristics is highlighted for the first time. Steady-state analytical solutions are obtained and the sensitivity of the flame temperature and the flame propagating velocity to the initial water content of the micro-exploding emulsion droplets is established. A linear stability analysis is also performed and reveals the manner in which the micro-explosions influence the neutral stability boundaries of both cellular and pulsating instabilities.     

Turbulent flame propagation limits of polymethylmethacrylate particle cloud–ammonia–air co-combustion

Ammonia is a highly promising energy carrier for achieving a carbon-neutral society. The co-combustion of solid particle clouds–ammonia, in particular, is considered an efficient and feasible method of reducing carbon dioxide emissions. Understanding turbulent flame stabilization and extinguishment processes during the two-phase hybrid-mixture co-combustion of solid particle clouds–ammonia is essential for the co-combustion technology to be used in combustors. To the best of our knowledge, this is the first study to describe the turbulent flame propagation limits and associated mechanism on the co-combustion of solid particle clouds–ammonia–air. Turbulent flame propagation experiments on silica particle clouds–ammonia–air mixing combustion and polymethylmethacrylate (PMMA) particle cloud–ammonia–air co-combustion were conducted in this work using a novel fan-stirred constant-volume vessel to clarify the turbulent flame propagation limits and associate mechanism of solid particle cloud–ammonia–air co-combustion. Results showed that adding inert silica particles contracted the turbulent flame propagation limits of premixed ammonia–air mixtures. However, adding PMMA particles expanded and then contracted the turbulent flame propagation limits of a premixed ammonia–air mixture as the ammonia equivalence ratio increased from lean to rich. In the solid particle cloud–ammonia–air co-combustion, reactive particles induce two types of effects on the turbulent flame propagation limits of premixed ammonia–air mixtures: The local equivalence ratio increment effect is caused by adding volatile matter from preheated particles in the preheat zone of the flame front, and the heat sink negative effect is induced by the unburned particles.     

Dynamic behavior of a freely-propagating turbulent premixed flame under global stretch-rate oscillations

Dynamic features of a freely propagating turbulent premixed flame under global stretch rate oscillations were investigated by utilizing a jet-type low-swirl burner equipped with a high-speed valve on the swirl jet line. The bulk flow velocity, equivalence ratio and the nominal mean swirl number were 5 m/s, 0.80 and 1.23, respectively. Seven velocity forcing amplitudes, from 0.09 to 0.55, were examined with a single forcing frequency of 50 Hz. Three kinds of optical measurements, OH-PLIF, OH^* chemiluminescence and PIV, were conducted. All the data were measured or post-processed in a phase-locked manner to obtain phase-resolved information. The global transverse stretch rate showed in-phase oscillations centering around 60 (1/s). The oscillation amplitude of the stretch rate grew with the increment of the forcing amplitude. The turbulent flame structure in the core flow region varied largely in axial direction in response to the flowfield oscillations. The flame brush thickness and the flame surface area oscillated with a phase shift to the stretch rate oscillations. These two properties showed a maximum and minimum values in the increasing and decreasing stretch periods, respectively, for all the forcing amplitudes. Despite large variations in flame brush thickness at different phase angles, the normalized profiles collapse onto a consistent curve. This suggests that the self-similarity sustains in this dynamic flame. The global OH^* fluctuation response (i.e. response of global heat-release rate fluctuation) showed a linear dependency to the forcing velocity oscillation amplitudes. The flame surface area fluctuation response showed a linear tendency as well with a slope similar to that of the global OH^* fluctuation. This indicated that the flame surface area variations play a critical role in the global flame response.     

Stability and emissions control using air injection and H2 addition in premixed combustion

We experimentally study lean premixed combustion stabilized behind a backward-facing step. For a propane–air mixture, the lean blowout limit is associated with strong pressure fluctuation arising simultaneously with strong flame–vortex interactions, which have been shown to constitute the mechanism of heat release dynamics in this flow. A high-speed air jet, issuing from a small slot and injected perpendicular to the main flow near the step, is used to disrupt this mechanism. For momentum ratio of jet to main flow below unity, the jet dilutes the mixture, further destabilizing the flame or leading to complete blowout. Above unity, the flame becomes more stable, and the pressure oscillations are suppressed. Flow visualization and OH*/CH* chemiluminescence measurements show that a strong jet produces a more compact flame that is less driven by the wake vortex, anchored closer to the step, and deflected upwards away from the lower wall of the channel. This renders the flame less vulnerable to heat loss and strong strains, which improves its stability and extends the flammability limit. Adding hydrogen to the main fuel improves the flame stability over the entire range of the air jet mass flow, with better results for momentum ratio larger than 1; H₂ pulls the flame further upstream, away from the shear zone and the unsteady vortex. NO_x emission benefits from the air jet, while, with H₂ addition, NO_x concentration is higher in the products as the overall burning temperature rises. However, hydrogen addition enables extending the flammability limit further by increasing air supply in the primary stream, hence achieving lower NO_x. The study suggests a simpler, almost passive, multi-objective combustion control technique and indicates that hydrogen addition can be a successful in situ approach for NO_x reduction.     

Dynamics of an edge-flame in the corner region of two mutually perpendicular streams

The stabilization and dynamics of an edge-flame in the corner region of two mutually perpendicular streams, one of fuel and the other of oxidizer, is studied within the context of a diffusive-thermal model, with an imposed flow satisfying the Navier-Stokes equations. The formulation allows for non-unity Lewis numbers and finite rate chemistry with an Arrhenius dependence on temperature. Two flow configurations, corresponding to inlet velocity profiles of uniform speed and of constant strain, have been examined. The results identify the dependence of the flame standoff distance on the flow as well as on the properties of the mixture, including the Damköhler D and Lewis numbers. For high flow rates, or small enough D, sufficient pre-mixing occurs in front of the edge-flame, which consequently takes on a tribrachial structure consisting of two premixed branches, one lean and one rich, with a trailing diffusion flame sheet. For large D, however, there is no enough premixing and the chemical reaction occurs in a small kernel very close to the corner, much like a local thermal explosion; further downstream the reaction occurs along a diffusion flame sheet that extends along the symmetry axis. The present results also predict the onset of spontaneous oscillations when the Lewis numbers are sufficiently large provided the flow rate is sufficiently high, or D reduced below a critical value. Oscillations are first sustained when D is reduced below criticality, but depending on the flow conditions, they are either damped leading to flame re-stabilization, or amplified leading to blow-off.     

Combustion of partially premixed spray jets

Gas turbines, liquid rocket motors, and oil-fired furnaces utilize the spray combustion of continuously injected liquid fuels. In most cases, the liquid spray is mixed with an oxidizer prior to combustion, and further oxidizer is supplied from the outside of the spray to complete diffusion combustion. This rich premixed spray is called “partially premixed spray.” Partially premixed sprays have not been studied systematically although they are of practical importance. In the present study, the burning behavior of partially premixed sprays was experimentally studied with a newly developed spray burner. A fuel spray and an oxidizer, diluted with nitrogen, was injected into the air. The overall equivalence ratio of the spray jet was set larger than unity to establish partially premixed spray combustion. In the present burner, the mean droplet diameter of the atomized liquid fuel could be varied without varying the overall equivalence ratio of the spray jet. Two combustion modes with and without an internal flame were observed. As the mean droplet diameter was increased or the overall equivalence ratio of the spray jet was decreased, the transition from spray combustion only with an external group flame to that with the internal premixed flame occurred. The results suggest that the internal flame was supported by flammable mixture through the vaporization of fine droplets, and the passage of droplet clusters deformed the internal flame and caused internal flame oscillation. The existence of the internal premixed flame enhanced the vaporization of droplets in the post-premixed-flame zone within the external diffusion flame.     

A multi-zone chemistry mapping approach for direct numerical simulation of auto-ignition and flame propagation in a constant volume enclosure

A direct numerical simulation (DNS) coupling with multi-zone chemistry mapping (MZCM) is presented to simulate flame propagation and auto-ignition in premixed fuel/air mixtures. In the MZCM approach, the physical domain is mapped into a low-dimensional phase domain with a few thermodynamic variables as the independent variables. The approach is based on the fractional step method, in which the flow and transport are solved in the flow time steps whereas the integration of the chemical reaction rates and heat release rate is performed in much finer time steps to accommodate the small time scales in the chemical reactions. It is shown that for premixed mixtures, two independent variables can be sufficient to construct the phase space to achieve a satisfactory mapping. The two variables can be the temperature of the mixture and the specific element mass ratio of H atom for fuels containing hydrogen atoms. An aliasing error in the MZCM is investigated. It is shown that if the element mass ratio is based on the element involved in the most diffusive molecules, the aliasing error of the model can approach zero when the grid in the phase space is refined. The results of DNS coupled with MZCM (DNS-MZCM) are compared with full DNS that integrates the chemical reaction rates and heat release rate directly in physical space. Application of the MZCM to different mixtures of fuel and air is presented to demonstrate the performance of the method for combustion processes with different complexity in the chemical kinetics, transport and flame–turbulence interaction. Good agreement between the results from DNS and DNS-MZCM is obtained for different fuel/air mixtures, including H₂/air, CO/H₂/air and methane/air, while the computational time is reduced by nearly 70%. It is shown that the MZCM model can properly address important phenomena such as differential diffusion, local extinction and re-ignition in premixed combustion.