Changes in Pore Structure and Connectivity Induced by CO2 Injection in Carbonates: a Combined Pore-Scale Approach

被引:61
作者
Gharbi, Oussama [1 ]
Bijeljic, Branko [1 ]
Boek, Edo [2 ]
Blunt, Martin J. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Earth Sci & Engn, London SW7 2AZ, England
[2] Imperial Coll London, Dept Chem Engn, London SW7 2AZ, England
来源
GHGT-11 | 2013年 / 37卷
关键词
reactive transport; carbonates; pore scale; tomograpghy; wormholes; ELEVATED-TEMPERATURE; DISSOLUTION KINETICS; CALCITE; RATES; SEQUESTRATION; PH; DISPOSAL; PRESSURE; AQUIFER; DIOXIDE;
D O I
10.1016/j.egypro.2013.06.455
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
We investigate at the pore scale fluid-rock interactions that occur in the context of carbon dioxide (CO2) storage in saline carbonate aquifers. Brine saturated with super critical CO2 is injected into two carbonate samples (Estaillades limestone and an aquifer sample) at typical storage conditions (9MPa and 50 degrees C). Dry high resolution micro-computed tomography scans are obtained prior to and after the experiments and the pore structure, connectivity and computed flow fields are compared using image analysis and pore-scale modeling techniques. We perform direct simulations of transport properties and velocity fields on the 3D scans and we extract representative pore-throat networks to compute average coordination number and assess changes in pore and throat size distributions. In this study, we experimentally mimic near wellbore region conditions by injecting fluids at relatively high flow rates. For high Peclet and Damko hler numbers, experimental observations confirm the formation of highly conductive channels i.e wormholes. A significant increase in porosity and permeability is found with fewer pore and throats after dissolution while the average coordination number does not change significantly. Flow becomes concentrated in the wormhole regions after reactions although a very wide range of velocities is still observed. (c) 2013 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:5367 / 5378
页数:12
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