The Nanoscale Basis of CO2 Trapping for Geologic Storage

被引:109
|
作者
Bourg, Ian C. [1 ,2 ,3 ]
Beckingham, Lauren E. [3 ]
DePaolo, Donald J. [3 ]
机构
[1] Princeton Univ, Dept Civil & Environm Engn, Princeton, NJ 08544 USA
[2] Princeton Univ, Princeton Environm Inst, Princeton, NJ 08544 USA
[3] Lawrence Berkeley Natl Lab, Div Earth Sci, Berkeley, CA 94720 USA
关键词
CARBON-DIOXIDE STORAGE; REACTIVE-SURFACE-AREA; RELATIVE PERMEABILITY HYSTERESIS; MOLECULAR-DYNAMICS SIMULATION; X-RAY-DIFFRACTION; TOP-SEAL LEAKAGE; SUPERCRITICAL CO2; INTERFACIAL-TENSION; PORE-SCALE; IN-SITU;
D O I
10.1021/acs.est.5b03003
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Carbon capture and storage (CCS) is likely to be a critical technology to achieve large reductions in global carbon emissions over the next century. Research on the subsurface storage of CO2 is aimed at reducing uncertainties in the efficacy of CO2 storage in sedimentary rock formations. Three key parameters that have a nanoscale basis and that contribute uncertainty to predictions of CO2 trapping are the vertical permeability k(v) of seals, the residual CO2 saturation S-g,S-r in reservoir rocks, and the reactive surface area a(r) of silicate minerals. This review summarizes recent progress and identifies outstanding research needs in these areas. Available data suggest that the permeability of shale and mudstone seals is heavily dependent on clay fraction and can be extremely low even in the presence of fractures. Investigations of residual CO2 trapping indicate that CO2-induced alteration in the wettability of mineral surfaces may significantly influence S-g,S-r. Ultimately, the rate and extent of CO2 conversion to mineral phases are uncertain due to a poor understanding of the kinetics and fluids. Rapidly improving characterization techniques using X-rays and neutrons, and computing capability for simulating chemical interactions, provide promise for important advances.
引用
收藏
页码:10265 / 10284
页数:20
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