论文标题
相对渗透性作为固定过程:不混溶的位移中的能量波动
Relative permeability as a stationary process: energy fluctuations in immiscible displacement
论文作者
论文摘要
相对渗透性通常用于模拟通过多孔材料的不混溶流体流动。在这项工作中,我们从能源的保护中得出了相对渗透率的关系,假设该系统在大长度上是非癌性的,并且依靠在时空和时间上平均来均质化行为。获得明确的标准以定义固定条件:(1)在时间平均间隔内对系统状态进行广泛衡量的净变化; (2)进入系统中的净能量输入为零,这意味着系统上完成的工作率必须与去除热量的平衡; (3)由于内部能量波动的贡献,没有进行净工作。然后根据直接数值模拟评估结果。在稳态流期间观察到动态连通性,这是基于欧拉的特征进行定量评估的。我们表明,即使在低毛细管数($ \ Mathsf {ca} \ sim1 \ times10^5 $)的稳态流动期间,典型的流程过程也会探索多个连接状态。每个连接状态的停留时间都是根据时间和空间平均值捕获的。当术语独立考虑时,能量波动的分布被证明是多模式和非高斯的。但是,我们证明它们的总和为零。考虑到适当选择热力学驱动力,我们表明传统的相对渗透率关系足以模拟具有复杂孔隙尺度动力学的系统中的能量耗散,从而通常会改变流体连接途径的结构。
Relative permeability is commonly used to model immiscible fluid flow through porous materials. In this work we derive the relative permeability relationship from conservation of energy, assuming that the system to be non-ergodic at large length scales and relying on averaging in both space and time to homogenize the behavior. Explicit criteria are obtained to define stationary conditions: (1) there can be no net change for extensive measures of the system state over the time averaging interval; (2) the net energy inputs into the system are zero, meaning that the net rate of work done on the system must balance with the heat removed; and (3) there is no net work performed due to the contribution of internal energy fluctuations. Results are then evaluated based on direct numerical simulation. Dynamic connectivity is observed during steady-state flow, which is quantitatively assessed based the Euler characteristic. We show that even during steady-state flow at low capillary number ($\mathsf{Ca}\sim1\times10^5$), typical flow processes will explore multiple connectivity states. The residence time for each connectivity state is captured based on the time-and-space average. The distribution for energy fluctuations is shown to be multi-modal and non-Gaussian when terms are considered independently. However, we demonstrate that their sum is zero. Given an appropriate choice of the thermodynamic driving force, we show that the conventional relative permeability relationship is sufficient to model the energy dissipation in systems with complex pore-scale dynamics that routinely alter the structure of fluid connected pathways.