In Situ Molecular Spectroscopic Evidence for CO2 Intercalation into Montmorillonite in Supercritical Carbon Dioxide

被引:105
|
作者
Loring, John S. [1 ]
Schaef, Herbert T. [1 ]
Turcu, Romulus V. F. [1 ]
Thompson, Christopher J. [1 ]
Miller, Quin R. S. [1 ]
Martin, Paul F. [1 ]
Hu, Jianzhi [1 ]
Hoyt, David W. [1 ]
Qafoku, Odeta [1 ]
Ilton, Eugene S. [1 ]
Felmy, Andrew R. [1 ]
Rosso, Kevin M. [1 ]
机构
[1] Pacific NW Natl Lab, Richland, WA 99352 USA
关键词
SOCIETY SOURCE CLAYS; X-RAY; BASE-LINE;
D O I
10.1021/la301136w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interaction of anhydrous supercritical CO2 (scCO(2)) with both kaolinite and similar to 1W (i.e., close to but less than one layer of hydration) calcium-saturated montmorillonite was investigated under conditions relevant to geologic carbon sequestration (50 degrees C and 90 bar). The CO2 molecular environment was probed in situ using a combination of three novel high-pressure techniques: X-ray diffraction, magic angle spinning nuclear magnetic resonance spectroscopy, and attenuated total reflection infrared spectroscopy. We report the first direct evidence that the expansion of montmorillonite under scCO(2) conditions is due to CO2 migration into the interlayer. Intercalated CO2 molecules are rotationally constrained and do not appear to react with waters to form bicarbonate or carbonic acid. In contrast, CO2 does not intercalate into kaolinite. The findings show that predicting the seal integrity of caprock will have complex dependence on clay mineralogy and hydration state.
引用
收藏
页码:7125 / 7128
页数:4
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