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首页> 外文期刊>Geoscientific Model Development >A coupling alternative to reactive transport simulations for long-term prediction of chemical reactions in heterogeneous COsub2/sub storage systems
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A coupling alternative to reactive transport simulations for long-term prediction of chemical reactions in heterogeneous COsub2/sub storage systems

机译:反应输运模拟的耦合替代方案,用于长期预测异构CO 2 存储系统中的化学反应

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摘要

Fully coupled, multi-phase reactive transport simulations of CO2 storage systems can be approximated by a simplified one-way coupling of hydrodynamics and reactive chemistry. The main characteristics of such systems, and hypotheses underlying the proposed alternative coupling, are (i) that the presence of CO2 is the only driving force for chemical reactions and (ii) that its migration in the reservoir is only marginally affected by immobilisation due to chemical reactions. In the simplified coupling, the exposure time to CO2 of each element of the hydrodynamic grid is estimated by non-reactive simulations and the reaction path of one single batch geochemical model is applied to each grid element during its exposure time. In heterogeneous settings, analytical scaling relationships provide the dependency of velocity and amount of reactions to porosity and gas saturation. The analysis of TOUGHREACT fully coupled reactive transport simulations of CO2 injection in saline aquifer, inspired to the Ketzin pilot site (Germany), both in homogeneous and heterogeneous settings, confirms that the reaction paths predicted by fully coupled simulations in every element of the grid show a high degree of self-similarity. A threshold value for the minimum concentration of dissolved CO2 considered chemically active is shown to mitigate the effects of the discrepancy between dissolved CO2 migration in non-reactive and fully coupled simulations. In real life, the optimal threshold value is unknown and has to be estimated, e.g. by means of 1-D or 2-D simulations, resulting in an uncertainty ultimately due to the process de-coupling. However, such uncertainty is more than acceptable given that the alternative coupling enables using grids of the order of millions of elements, profiting from much better description of heterogeneous reservoirs at a fraction of the calculation time of fully coupled models.
机译:CO 2 存储系统的全耦合多相反应输运模拟可以通过简化的水动力和反应化学的单向耦合来近似。此类系统的主要特征以及所提出的替代耦合基础的假设是:(i)CO 2 的存在是化学反应的唯一驱动力,以及(ii)其在储层中的迁移由于化学反应,固定化仅受固定化的影响很小。在简化耦合中,通过非反应性模拟来估算流体动力网格中每个元素在CO 2 中的暴露时间,并在其网格化过程中将单个批地球化学模型的反应路径应用于每个网格元素。接触时间。在非均质环境中,解析比例关系提供了速度和反应量对孔隙度和气体饱和度的依赖性。在均质和非均质环境中,对启发于Ketzin试验地点(德国)的盐水中CO 2 注入进行TOUGHREACT全耦合反应输运模拟分析,证实了全耦合预测的反应路径网格中每个元素的仿真显示出高度的自相似性。在非反应性和完全耦合模拟中,显示了被认为具有化学活性的最低溶解CO 2 浓度阈值可减轻溶解CO 2 迁移之间差异的影响。在现实生活中,最佳阈值是未知的,必须进行估算,例如通过一维或二维仿真,最终由于工艺去耦而导致不确定性。但是,考虑到替代耦合能够使用数百万个元素的网格,这种不确定性是可以接受的,这得益于在完全耦合模型的计算时间的一小部分时间内对非均质油藏的更好描述。

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