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Features in chemical kinetics. I. Signatures of self-emerging dimensional reduction from a general format of the evolution law

机译:化学动力学特征。一,从演化定律的一般形式看自发降维的特征

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Simplification of chemical kinetics description through dimensional reduction is particularly important to achieve an accurate numerical treatment of complex reacting systems, especially when stiff kinetics are considered and a comprehensive picture of the evolving system is required. To this aim several tools have been proposed in the past decades, such as sensitivity analysis, lumping approaches, and exploitation of time scales separation. In addition, there are methods based on the existence of the so-called slow manifolds, which are hyper-surfaces of lower dimension than the one of the whole phase-space and in whose neighborhood the slow evolution occurs after an initial fast transient. On the other hand, all tools contain to some extent a degree of subjectivity which seems to be irremovable. With reference to macroscopic and spatially homogeneous reacting systems under isothermal conditions, in this work we shall adopt a phenomenological approach to let self-emerge the dimensional reduction from the mathematical structure of the evolution law. By transforming the original system of polynomial differential equations, which describes the chemical evolution, into a universal quadratic format, and making a direct inspection of the high-order time-derivatives of the new dynamic variables, we then formulate a conjecture which leads to the concept of an "attractiveness" region in the phase-space where a well-defined state-dependent rate function ω has the simple evolution ω = -ω2 along any trajectory up to the stationary state. This constitutes, by itself, a drastic dimensional reduction from a system of N-dimensional equations (being N the number of chemical species) to a one-dimensional and universal evolution law for such a characteristic rate. Step-by-step numerical inspections on model kinetic schemes are presented. In the companion paper [P. Nicolini and D. Frezzato, J. Chem. Phys. 138, 234102 (2013)] this outcome will be naturally related to the appearance (and hence, to the definition) of the slow manifolds.
机译:通过降维来简化化学动力学描述对于实现复杂反应系统的精确数值处理特别重要,尤其是在考虑了刚性动力学并且需要全面了解演化系统的情况下。为了达到这个目的,在过去的几十年中已经提出了几种工具,例如灵敏度分析,集总方法和时标分离的开发。另外,存在基于所谓的慢流形的存在的方法,该慢流形是比整个相空间之一尺寸小的超表面,并且在初始快速瞬变之后在其附近发生慢速发展。另一方面,所有工具在某种程度上都包含着某种不可替代的主观性。关于等温条件下的宏观和空间均相反应系统,在这项工作中,我们将采用现象学方法从演化定律的数学结构中自我体现降维。通过将描述化学演化的多项式微分方程的原始系统转换为通用二次格式,并直接检查新动态变量的高阶时间导数,我们可以得出一个推论,得出相空间中“吸引”区域的概念,其中明确定义的与状态相关的速率函数ω沿任何轨迹直至平稳状态都具有简单的演化ω=-ω2。这本身就构成了从N维方程组(化学物种的数量为N)到这种特征速率的一维通用演化规律的大幅缩减。提出了对模型动力学方案的逐步数值检验。在随附的论文中[P. Nicolini和D.Frezzato,J.Chem。物理138,234102(2013)]这个结果自然会与慢速歧管的出现(因此,与定义)有关。

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