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Two-scale models pose a promising approach in simulating reactive flow and transport in evolving porous media. Classically, homogenized flow and transport equations are solved on the macroscopic scale, while effective parameters are obtained from auxiliary cell problems on possibly evolving reference geometries (micro-scale). Despite their perspective success in rendering lab/field-scale simulations computationally feasible, analytic results regarding the arising two-scale bilaterally coupled system often restrict to simplified models. In this paper, we first derive smooth-dependence results concerning the partial coupling from the underlying geometry to macroscopic quantities. Therefore, alterations of the representative fluid domain are described by smooth paths of diffeomorphisms. Exploiting the gained regularity of the effective space- and time-dependent macroscopic coefficients, we present local-in-time existence results for strong solutions to the partially coupled micro-macro system using fixed-point arguments. What is more, we extend our results to the bilaterally coupled diffusive transport model including a level-set description of the evolving geometry.

This paper presents a model of coagulation in electrolyte solutions. In this paper, the coagulation process is modeled according to DLVO-theory, which is an atomistic theory. On the other hand, we describe the dynamics in the electrolyte solutions by the Poisson-Nernst-Planck system, which is a continuum model. The contribution of this paper is to include the atomistic description of coagulation based on DLVO-theory in the continuum Poisson-Nernst-Planck system. Thereby, we involve information from different spatial scales. For this reason, the presented model accounts for the short-range interactions and the long-range interactions, which drive the coagulation process. Furthermore, many-body effects are naturally included as the resulting model is a continuum model.

This paper presents a thermodynamically consistent model for multicomponent electrolyte solutions. The first part of this paper derives the general governing equations for nonequilibrium systems within the theory of nonequilibrium thermodynamics. Here, we consider electrolyte solutions as general mixtures of charged constituents. Furthermore, in this part of the paper we combine the general theory of nonequilibrium thermodynamics with the well-known splittings of the entropy and the energy into a pure substance part and a part due to mixing. Thereby, we successfully establish evolution equations for both parts. Furthermore, we derive for both parts explicit expressions of the respective entropy production rates. Hence, we provide an approach that allows to study the entropy of mixing independently of the pure substance entropy and vice versa. This is of great value, in particular for a better understanding of the complex phenomena due to mixing in multicomponent systems. In the second part of this paper, we close the system of general balance equations by applying constitutive laws. This is the crucial step in the modeling procedure. ...

This paper analytically investigates the Darcy-Poisson-Nernst-Planck system. This system is a mathematical model for electrolyte solutions. In this paper, we consider electrolyte solutions, which consist of a neutral fluid and multiple suspended charged chemical species with arbitrary valencies. We prove global existence and uniqueness of weak solutions in two space dimensions.

This paper analytically investigates the Darcy-Poisson-Nernst-Planck system. This system is a mathematical model for electrolyte solutions. In this paper, we consider electrolyte solutions, which consist of a neutral fluid and two suspended oppositely charged chemical species with arbitrary valencies z_1 > 0 > z_2. We prove global existence and uniqueness of weak solutions in two space dimensions and three space dimensions. So far, most of the existence results have been proven for symmetric electrolyte solutions. These solutions consist of a neutral fluid and two suspended charged chemical species with symmetric valencies +/-z. As many electrolyte solutions in biological applications and hydrodynamical applications are not symmetric, the presented extension of the previous existence results is an important step.

We investigate the influence of multiscale aggregation and deposition on the colloidal dynamics in a saturated porous medium. At the pore scale, the aggregation of colloids is modeled by the Smoluchowski equation. Essentially, the colloidal mass is distributed between different size clusters. We treat these clusters as different species involved in a diffusion-advection-reaction mechanism. This modeling procedure allows for different material properties to be varied between the different species, specifically the rates of diffusion, aggregation, deposition as well as the advection velocities. We apply the periodic homogenization procedure to give insight into the effective coefficients of the upscaled model equations. Benefiting from direct access to microstructural information, we capture by means of 2D numerical simulations the effect of aggregation on the deposition rates recovering this way both the blocking and ripening regimes reported in the literature.

We perform the periodic homogenization (i.e. $\eps\to 0$) of the non-stationary Stokes-Nernst-Planck-Poisson system using two-scale convergence, where $\eps$ is a suitable scale parameter. The objective is to investigate the influence of \textsl{different boundary conditions and variable choices of scalings in $\eps$} of the microscopic system of partial differential equations on the structure of the (upscaled) limit model equations. Due to the specific nonlinear coupling of the underlying equations, special attention has to be paid when passing to the limit in the electrostatic drift term. As a direct result of the homogenization procedure, various classes of upscaled model equations are obtained., Comment: 29 pages, 1 figure