论文标题
在动力学和宏观水平上的多粒子气体建模
Polytropic gas modelling at kinetic and macroscopic levels
论文作者
论文摘要
在本文中,我们考虑了在两个不同的设置中描述多原子气体的连续类型的动力学模型,该模型与用于定义宏观量的功能空间的不同选择相对应。这样的模型引入了一个连续变量,该变量应捕获与具有多个原子的分子的更复杂结构相关的所有现象,例如碰撞中的内部自由度。特别是,我们提供了这两种设置的直接比较,并在重新分配分配函数并重新重新重新截止分配函数后显示它们的等价性。然后,我们专注于动力学模型,最近证明了严格的存在和独特性导致空间均匀情况的独特性。使用该分析中提出的横截面以及最大熵原理,我们建立了六个和14个场的宏观模型。在六个时刻的情况下,我们计算了确切的,非线性的生产项,并证明了其与扩展热力学的总一致性,因为它满足了整个模型有效性范围内的熵残差不平等。此外,对于第四瞬间模型,我们提供了新的表达方式,以在线性化的环境中放松时间和传输系数,这两者都与剪切粘度对温度的依赖性相匹配,以及与PrandTL数量的理论值相同,在室温范围内的转化模式和旋转模式均与较高的计算相同。
In this paper, we consider the kinetic model of continuous type describing a polyatomic gas in two different settings corresponding to a different choice of the functional space used to define macroscopic quantities. Such a model introduces a single continuous variable supposed to capture all the phenomena related to the more complex structure of a molecule having more than one atom, such as internal degrees of freedom in a collision. In particular, we provide a direct comparison of these two settings, and show their equivalence after the distribution function is rescaled and the cross section is reformulated. We then focus on the kinetic model for which the rigorous existence and uniqueness result in the space homogeneous case is recently proven. Using the cross section proposed in that analysis together with the maximum entropy principle, we establish macroscopic models of six and fourteen fields. In the case of six moments, we calculate the exact, nonlinear, production term and prove its total agreement with extended thermodynamics, as it satisfies the entropy residual inequality on the whole range of model validity. Moreover, for the fourteen moments model, we provide new expressions for relaxation times and transport coefficients in a linearized setting, that yield both matching with the experimental data for dependence of the shear viscosity upon temperature and a satisfactory agreement with the theoretical value of the Prandtl number, on the room temperature range when only translational and rotational modes of molecules are taken into account, as much as on higher temperatures when vibrational modes appear as well.