The structure of stationary adiabatic premixed flames within porous inert media under intense interphase heat transfer is investigated using the asymptotic expansion method. For the pore sizes of interest for combustion in porous inert media, this condition is reached for extremely lean mixtures where lower flame velocities are found. The flame structure is analysed in three distinct regions. In the outer region (the solid-phase diffusion length scale), both phases are in local thermal equilibrium and the problem formulation is reduced to the one-equation model for the energy conservation. In the first inner region (the gas-phase diffusion length scale), there is local thermal non-equilibrium and two equations for the energy conservation are required. In this region, the gas-phase temperature at the flame is limited by the interphase heat transfer. In the second inner region (the reaction length scale), the chemical reaction occurs in a very thin zone where the highest gas-phase temperature is found. The results showed that superadiabatic effects are reduced for leaner mixtures, smaller pore sizes and smaller fuel Lewis numbers. The results also show that there is a minimum superadiabatic temperature for the flame propagation to be possible, which corresponds to the lean flammability limit for the premixed combustion in porous inert media. A parameter that universalizes the leading-order flame properties is identified and discussed.
In this work we propose a new method to decrease the heating time of droplets. Our model considers the heating process of magnetic nanofluid droplet, which was taken to an ambient atmosphere at high temperature and with an alternating magnetic field. Analytical solutions were obtained in systems governed by Brownian and/or low-barrier Néel relaxation ͑superparamagnetic regime͒. The droplet heating time was shown to scale with the reciprocal of the square of frequency ͑1 / f 2 ͒ at the low frequency regime. The droplet heating time was calculated as function of frequency for different particle sizes, coating layers, and relaxation mechanisms.
In this work, heating and vaporization of a liquid droplet with dispersed magnetic nanoparticles (ferrofluid) are analyzed. The ferrofluid droplet is in a quiescent inert gas phase with a temperature which is set down equal to, higher and lower than the liquid boiling temperature. Under these conditions, an alternating magnetic field is applied and, as a result, the magnetic nanoparticles generate heat by the Brownian relaxation mechanism. In this mechanism, the magnetic dipoles present a random orientation due to collisions between the fluid molecules and nanoparticles. The magnetic dipoles tend to align to the magnetic field causing rotation of the nanoparticles. Consequently the temperature increases due to the energy dissipated by the friction between the resting fluid and the rotating nanoparticles. Assuming a very large magnetic power and a uniform distribution of nanoparticles, the droplet core is uniformly heated. A thermal boundary layer is established in the liquid-phase adjacent to the droplet surface due to heat flux from the ambient atmosphere. The temperature profile inside the thermal boundary layer is obtained in appropriate time and length scales. In the present model, the ferrofluid droplet is heated up to its boiling temperature in a very short time. In addition, the combination of the heat generated by magnetic nanoparticles and heat conduction from gas phase results in a higher vaporization rate. Under specific conditions, the boiling temperature is achieved not at the surface but inside the thermal boundary layer. Moreover, the results point out that the thermal boundary layer depends directly on the vapor Lewis number but the vaporization rate reciprocally on it.
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