Department of Chemistry, University of Massachusetts Boston, Boston, MA 02125, USA.
Phys Chem Chem Phys. 2018 Jun 13;20(23):15746-15752. doi: 10.1039/c8cp00905h.
The explosion limits of hydrogen-oxygen mixtures are macroscopic, temperature-pressure boundaries that divide the overall chemistry of hydrogen oxidation into slow-burning and explosive regimes. Here, we demonstrate that it is possible to recover the three chemical explosion limits of H2/O2 mixtures from nonequilibrium stochastic trajectories. This demonstration relies on the finding that, in explosive regimes, these trajectories have the quantitative features of a dynamical phase transition. Through computer simulations for both a generic and a reduced model for hydrogen oxidation, we find only one dominant reactive phase at temperatures below the explosion limits. At temperatures above the limits, however, a second phase transiently emerges from the chemistry. By locating the pseudo-critical temperature where two reactive phases are distinguishable, we construct all three explosion-limit boundaries for model hydrogen-oxygen mixtures of finite size.
氢氧混合物的爆炸极限是宏观的温度-压力界限,将氢气氧化的整体化学过程划分为缓慢燃烧和爆炸两个区域。在这里,我们证明了从非平衡随机轨迹中恢复 H2/O2 混合物的三个化学爆炸极限是可能的。这一证明依赖于这样一个发现,即在爆炸区域,这些轨迹具有动力学相变的定量特征。通过对通用和简化的氢气氧化模型的计算机模拟,我们发现,在爆炸极限以下的温度下,只有一种主要的反应相。然而,在极限以上的温度下,第二种相从化学过程中暂时出现。通过定位可以区分两种反应相的准临界温度,我们为有限尺寸的模型氢-氧混合物构建了所有三个爆炸极限边界。