Pore–Scale Numerical Investigations of the Impact of Mineral Dissolution and Transport in Naturally Fractured Systems During CO2–Enriched Brine Injection

Jiahui You, K. Lee
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Abstract

CO2 storage and sequestration are regarded as an effective approach to mitigate greenhouse gas emissions. While injecting an enormous amount of CO2 into carbonate–rich aquifers, CO2 dissolves in the formation brine under the large pressure, and the subsequently formed CO2–enriched brine reacts with the calcite. Reaction–induced changes in pore structure and fracture geometry alter the porosity and permeability, giving rise to concerns of CO2storage capacity and security. Especially in the reservoir or aquifer with natural fractures, the fractures provide a highly permeable pathways for fluid flow. This study aims to analyze the acid–rock interaction and subsequent permeability evolution in the systems with complex fracture configurations during CO2 injection by implementing a pore–scale DBS reactive transport model. The model has been developed by expanding the functionality of OpenFOAM, which is an open–source code for computational fluid dynamics. A series of partial differential equations are discretized by applying the Finite Volume Method (FVM) and sequentially solved. Different fracture configurations in terms of fracture length, density, connection, and mineral components have been considered to investigate their impacts on the dynamic porosity–permeability relationship, dissolution rate, and reactant transport characteristics during CO2 storage. The investigation revealed several interesting findings. We found that calcium (Ca) concentration was low in the poorly connected area at the initial time. As CO2–enriched brine saturated the system and reacted with calcite, Ca started being accumulated in the system. However, Ca barely flowed out of the poor–connected area, and the concentration became high. Lengths of branches mainly influenced the dissolution rates, while they had slight impacts on the porosity–permeability relationship. While fracture connectivity had an apparent influence on the porosity–permeability relationship, it showed a weak relevance on the dissolution rate. These microscopic insights can help enhance the CO2 sealing capacity and guarantee environmental security.
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富co2注盐过程中天然裂缝体系中矿物溶解和运移影响的孔隙尺度数值研究
二氧化碳的储存和封存被认为是减少温室气体排放的有效途径。在向富碳酸盐含水层注入大量CO2的同时,CO2在高压下溶解于地层卤水中,随后形成的富CO2卤水与方解石发生反应。反应引起的孔隙结构和裂缝几何形状的变化改变了孔隙度和渗透率,引起了对二氧化碳储存能力和安全性的担忧。特别是在具有天然裂缝的储层或含水层中,裂缝为流体流动提供了高渗透率的通道。本研究旨在通过孔隙尺度的DBS反应输运模型,分析复杂裂缝构型体系在CO2注入过程中的酸岩相互作用及其后续渗透率演化。该模型是通过扩展OpenFOAM的功能开发的,OpenFOAM是计算流体动力学的开源代码。采用有限体积法对一系列偏微分方程进行离散,并对其进行顺序求解。考虑了不同的裂缝长度、密度、连接方式和矿物成分,研究了它们对CO2储存过程中动态孔渗关系、溶解速率和反应物输运特性的影响。调查显示了几个有趣的发现。我们发现钙(Ca)浓度在初始连接不良的区域较低。当富含co2的盐水使体系饱和并与方解石反应时,Ca开始在体系中积累。然而,Ca几乎没有流出连接差的区域,并且浓度变得很高。分支长度主要影响溶蚀速率,对孔渗关系影响较小。裂缝连通性对孔隙度-渗透率关系有明显影响,但对溶蚀速率的相关性较弱。这些微观的洞察可以帮助提高二氧化碳密封能力,保证环境安全。
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