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Shock-induced ignition for a two-step chain-branching kinetics model

机译:两步链支化动力学模型的激振点火

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The ignition of reactive materials by a shock wave, when the chemistry is governed by chain-branching kinetics, is investigated using a combination of high activation temperature asymptotics and numerical simulations. A two-step chemical model is used. The first step is a thermally neutral induction time, representing chain initiation and chain branching, which has a temperature-sensitive Arrhenius form of the reaction rate. At the end of the induction time is a transition point where the fuel is instantaneously converted into chain radicals. The second step is a temperature-insensitive exothermic reaction, representing chain recombination. It is found that the initiation process is qualitatively different from that for a temperature-sensitive one-step reaction considered previously. Three different cases, when the rate of heat release is slow, comparable and fast compared to the initial induction time, are considered. In each case ignition first occurs at the piston and the transition point (which marks the end of the induction zone and the start of the main heat release zone) initially propagates away from the piston at subsonic speeds, so that pressure and temperature disturbances from the exothermic region overtake the transition path and accelerate it. For rapid rates of heat release, a secondary shock is very promptly formed near the piston, which is subsequently amplified into a strong detonation propagating through the induction zone behind the leading shock. However, unlike for one-step kinetics the formation of the secondary shock does not involve quasisteady weak detonations. For moderate rates of heat release a secondary shock still eventually forms at the front of the disturbed region of the induction zone behind the leading shock, but a detonation is not formed until after the collision of the shocks. When the rate of heat release is slow, the transition point is continuously accelerated, but its speed remains subsonic until disturbances due to the heat release overtake the shock. No secondary shock forms for this case, completely unlike the case for one-step kinetics. (C) 2002 American Institute of Physics. [References: 37]
机译:当化学反应受链支化动力学支配时,利用高活化温度渐近线和数值模拟相结合的方法研究了反应波对反应材料的点燃。使用两步化学模型。第一步是热中性诱导时间,代表链引发和链支化,其反应速率具有温度敏感性阿伦尼乌斯形式。在感应时间结束时,是一个过渡点,在该过渡点处,燃料立即转化为链自由基。第二步是对温度不敏感的放热反应,代表链重组。发现引发过程在质量上与先前考虑的对温度敏感的一步反应不同。考虑三种不同的情况,即放热速率与初始诱导时间相比缓慢,可比且较快。在每种情况下,点火都首先在活塞上发生,并且过渡点(标志着感应区的末端和主要放热区的起点)首先以亚音速传播离开活塞,因此来自活塞的压力和温度扰动放热区超过过渡路径并加速它​​。为了快速释放热量,在活塞附近会非常迅速地形成二次冲击,随后会放大为强烈的爆炸声,并通过引导冲击后面的感应区传播。但是,不同于一步动力学,二次冲击的形成并不涉及准稳态的弱爆轰。对于适度的热量释放,最终仍会在感应区域的受干扰区域的前部引导声之后形成二次电击,但直到电击发生后才形成爆炸。当放热速度缓慢时,过渡点会持续加速,但其速度将保持亚音速,直到因放热引起的干扰超过了冲击为止。在这种情况下,不会形成二次冲击,这完全不同于单步动力学的情况。 (C)2002美国物理研究所。 [参考:37]

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