Convective dissolution of CO2 in saline aquifers: Progress in modeling and experiments

被引:252
作者
Emami-Meybodi, Hamid [1 ]
Hassanzadeh, Hassan [1 ]
Green, Christopher P. [2 ]
Ennis-King, Jonathan [2 ]
机构
[1] Univ Calgary, Dept Chem & Petr Engn, Schulich Sch Engn, Calgary, AB T2N 1N4, Canada
[2] CSIRO, Energy Flagship, Clayton, Vic 3169, Australia
基金
加拿大自然科学与工程研究理事会;
关键词
CO2; dissolution; Natural convection; Solubility trapping; Saline formations; sequestration; CARBON-DIOXIDE SEQUESTRATION; BUOYANCY-DRIVEN CONVECTION; AQUEOUS NACL SOLUTIONS; EX-SITU DISSOLUTION; DIFFUSIVE NATURAL-CONVECTION; RAYLEIGH-NUMBER CONVECTION; DEVELOPING THERMAL FRONT; SATURATED POROUS LAYER; VARIABLE-DENSITY FLOW; LONG-TERM STORAGE;
D O I
10.1016/j.ijggc.2015.04.003
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The dissolution of carbon dioxide (CO2) in deep saline aquifer water is recognized as one of the fundamental mechanisms in the subsurface for storing significant quantities of CO2. One fundamental physical effect of CO2 dissolution is the slight increase in water density in the layer in contact with the buoyant free-phase CO2 plume. Under specific conditions, this may lead to gravitational instability and the onset of free convection, significantly accelerating the dissolution of the free-phase CO2 by bringing CO2 in contact with a larger volume of aquifer water. It is also feasible to enhance CO2 dissolution using engineering methodologies such as injecting water on top of the plume of CO2. The objective of this review is to provide a perspective on the progress in modeling and experimental observations of physical aspects of CO2 dissolution in deep saline aquifers. We review the published research efforts concerning the physical effects of CO2 dissolution in formation water, the conditions under which process can be accelerated either naturally, such as by free convection, or by use of engineering methodologies, and the effects of CO2 dissolution on CO2 storage. Finally, we discuss areas in need of further research. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:238 / 266
页数:29
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