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Non-equilibrium effects on thermal ignition using hard sphere molecular dynamics

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Abstract The present study addresses the role of molecular non-equilibrium effects in thermal ignition problems. We consider a single binary reaction of the form A+B → C+C. Molecular dynamics calculations were performed… Click to show full abstract

Abstract The present study addresses the role of molecular non-equilibrium effects in thermal ignition problems. We consider a single binary reaction of the form A+B → C+C. Molecular dynamics calculations were performed for activation energies ranging between RT and 7.5RT and heat release of 2.5RT and 10RT. The evolution of up to 10,000 particles was calculated as the system undergoes a thermal ignition at constant volume. Ensemble averages of 100 calculations for each parameter set permitted to determine the ignition delay, along with a measure of the stochasticity of the process. A well behaved convergence to large system sizes is also demonstrated. The ignition delay calculations were compared with those obtained at the continuum level using rates derived from kinetic theory: the standard rate assuming that the distribution of the speed of the particles is the Maxwell–Boltzmann distribution, and the perturbed rates by Prigogine and Xhrouet [1] for an isothermal system, and Prigogine and Mahieu [2] for an energy releasing reaction, obtained by the Chapman–Enskog perturbation procedure. The molecular results were found in very good agreement with the latter at high activation energies (low temperature), confirming that non-equilibrium effects promote the formation of energetic particles that serve as seeds for subsequent reaction events: i.e., molecular hot spots. This effect was found to lower the ignition delay by up to 30%. At low activation energies (high temperatures), the ignition delay obtained from the standard equilibrium rate was found to be up to 60% longer than the molecular calculations. This effect is due to the rapidity of the reactive collisions that do not allow the system to equilibrate. For this regime, none of the perturbation solutions obtained by the Chapman–Enskog procedure were valid. This study thus clearly shows the importance of non-equilibrium effects in thermal ignition problems, for most activation energies of practical interest. These non-equilibrium effects are discussed in the context of hydrogen auto-ignition at low temperatures. The auto-catalytic loops of H2O2 and HO2 controlling the thermal ignition process, which have both high energy release production of these species subsequently involved in high activation reactions of these species, can be mostly impacted by hotspot non-equilibrium effects.

Keywords: non equilibrium; equilibrium effects; thermal ignition; effects thermal; ignition

Journal Title: Combustion and Flame
Year Published: 2019

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