A compositional formulation for multiphase multicomponent reactive transport modelling of highly coupled systems

Author(s):  
Nicolas Seigneur ◽  
K. Ulrich Mayer

<p>In certain reactive transport applications, strong coupling between geochemical reactions and hydrodynamics exists. Dissolution and precipitation of minerals, such as the conversion between gypsum and anhydrite [1] or the precipitation of nesquehonite during CO<sub>2</sub> sequestration [2], as well as gas bubble formation [3] are geochemical processes which modify the multiphase flow dynamics, with direct feedback on reactive transport processes. In addition, heat generation induced by sulphide mineral oxidation can lead to significant increases in temperature [4], impacting flow, transport and geochemical reactions. In these instances, commonly used reactive transport modelling approaches, which rely on decoupling flow and reactive transport processes, have limitations. For density dependent or two-phase flow problems in the presence of a gas phase, the coupling between flow and reactive transport can be accounted for through a Picard iterative approach [3,5,6]. However, this approach is computationally expensive, involving the solution of nonlinear problems multiple times during each timestep, and convergence properties are often poor. More recently, a weak explicit coupling approach was developed to capture the impact of chemistry on flow by integrating water as a component and perform a volume balance calculation [7]. In the current work, a compositional approach is implemented into MIN3P-THCm, in which the flow variables (pressure, density) are expressed based on mass variables. Hence, this global implicit approach does not require solving the flow problem, but instead integrates groundwater flow processes directly into the reactive transport equations. We show that this approach yields very similar results to the commonly used approaches for single and two-phase flow. Finally, we show that, in highly coupled systems, not considering these coupled effects may lead to significant errors in simulating system evolution, highlighting the benefits of the newly developed approach.</p><p> </p><p>[1] Jowett, Cathles & Davis (1993). AAPG Bulletin, 77(3), 402-413.</p><p>[2] Harrison, Dipple, Power & Mayer (2015). Geochimica et cosmochimica Acta, 148, 477-495.</p><p>[3] Amos and Mayer (2006). Journal of contaminant hydrology, 87(1-2), 123-154.</p><p>[4] Lefebvre, Hockley, Smolensky & Gélinas (2001). Journal of contaminant hydrology, 52(1-4), 137-164.</p><p>[5] Henderson, Mayer, Parker, & Al (2009). Journal of contaminant hydrology, 106(3-4), 195-211.</p><p>[6] Sin, Lagneau and Corvisier (2017). Advances in Water Resources, 100, 62-77.</p><p>[7] Seigneur, Lagneau, Corvisier & Dauzères (2018). Advances in Water Resources 122, 355-366.</p>

2017 ◽  
Vol 99 ◽  
pp. 131-141 ◽  
Author(s):  
M. Carme Chaparro ◽  
Josep M. Soler ◽  
Maarten W. Saaltink ◽  
Urs K. Mäder

2021 ◽  
Author(s):  
Omar Chaabi ◽  
Emad W. Al-Shalabi ◽  
Waleed Alameri

Abstract Low salinity polymer (LSP) flooding is getting more attention due to its potential of enhancing both displacement and sweep efficiencies. Modeling LSP flooding is challenging due to the complicated physical processes and the sensitivity of polymers to brine salinity. In this study, a coupled numerical model has been implemented to allow investigating the polymer-brine-rock geochemical interactions associated with LSP flooding along with the flow dynamics. MRST was coupled with the geochemical software IPhreeqc. The effects of polymer were captured by considering Todd-Longstaff mixing model, inaccessible pore volume, permeability reduction, polymer adsorption as well as salinity and shear rate effects on polymer viscosity. Regarding geochemistry, the presence of polymer in the aqueous phase was considered by adding a new solution specie and related chemical reactions to PHREEQC database files. Thus, allowing for modeling the geochemical interactions related to the presence of polymer. Coupling the two simulators was successfully performed, verified, and validated through several case studies. The coupled MRST-IPhreeqc simulator allows for modeling a wide variety of geochemical reactions including aqueous, mineral precipitation/dissolution, and ion exchange reactions. Capturing these reactions allows for real time tracking of the aqueous phase salinity and its effect on polymer rheological properties. The coupled simulator was verified against PHREEQC for a realistic reactive transport scenario. Furthermore, the coupled simulator was validated through history matching a single-phase LSP coreflood from the literature. This paper provides an insight into the geochemical interactions between partially hydrolyzed polyacrylamide (HPAM) and aqueous solution chemistry (salinity and hardness), and their related effect on polymer viscosity. This work is also considered as a base for future two-phase polymer solution and oil interactions, and their related effect on oil recovery.


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