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X 射线微断层扫描技术在溶解过程中对孔隙率、渗透率和反应表面积变化的表征。

X-ray microtomography characterization of porosity, permeability and reactive surface changes during dissolution.

机构信息

Geosciences Montpellier, UMR 5243 CNRS, Universite Montpellier 2, Montpellier, France.

出版信息

J Contam Hydrol. 2011 Mar 1;120-121:45-55. doi: 10.1016/j.jconhyd.2010.07.004. Epub 2010 Jul 24.

Abstract

Numerical programs for simulating flow and reactive transport in porous media are essential tools for predicting reservoir properties changes triggered by CO(2) underground injection. At reservoir scale, meshed models in which equations are solved assuming that constant macroscopic properties can be defined in each cells, are widely used. However, the parameterization of the dissolution-precipitation problem and of the feedback effects of these processes on the flow field is still challenging. The problem arises from the mismatch between the scales at which averaged parameters are defined in the meshed model and the scale at which chemical reactions occur and modify the pore network geometry. In this paper we investigate the links between the dissolution mechanisms that control the porosity changes and the related changes of the reactive surface area and of the permeability. First, the reactive surface area is computed from X-ray microtomography data obtained before and after a set of dissolution experiments of pure calcite rock samples using distinctly different brine-CO(2) mixtures characterizing homogeneous to heterogeneous dissolution regimes. The results are used to validate the power law empirical model relating the reactive surface area to porosity proposed by Luquot and Gouze (2009). Second, we investigate the spatial distribution of the effective hydraulic radius and of the tortuosity, two structural parameters that control permeability, in order to explain the different porosity-permeability relationships observed for heterogeneous and homogeneous dissolution regimes. It is shown that the increase of permeability is due to the decrease of the tortuosity for homogeneous dissolution, whereas it is due to the combination of tortuosity decrease and hydraulic radius increase for heterogeneous dissolution. For the intermediate dissolution regime, identified to be the optimal regime for increasing permeability with small changes in porosity, the increase of permeability results from a large increase in the mean effective hydraulic radius of the sample.

摘要

用于模拟多孔介质中流动和反应传输的数值程序是预测 CO2地下注入引发的储层性质变化的重要工具。在储层尺度上,广泛使用在假设每个单元中都可以定义恒定宏观性质的网格模型来求解方程。然而,溶解-沉淀问题的参数化以及这些过程对流场的反馈效应仍然具有挑战性。该问题源于网格模型中定义平均参数的尺度与发生化学反应并改变孔隙网络几何形状的尺度之间的不匹配。在本文中,我们研究了控制孔隙率变化的溶解机制与相关的反应表面积和渗透率变化之间的联系。首先,从使用明显不同的盐水-CO2混合物进行的一组纯方解石岩样溶解实验前后获得的 X 射线微断层扫描数据计算反应表面积。结果用于验证 Luquot 和 Gouze(2009 年)提出的将反应表面积与孔隙率相关联的幂律经验模型。其次,我们研究了有效水力半径和迂曲度这两个控制渗透率的结构参数的空间分布,以解释在均匀和非均匀溶解条件下观察到的不同孔隙率-渗透率关系。结果表明,对于均匀溶解,渗透率的增加是由于迂曲度的降低所致,而对于非均匀溶解,渗透率的增加是由于迂曲度的降低和水力半径的增加共同作用所致。对于中间溶解条件,该条件被确定为在较小的孔隙率变化下增加渗透率的最佳条件,渗透率的增加是由于样品的平均有效水力半径的大幅增加所致。

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