Interfacial interactions between reservoir brine and CO2 at high pressures and elevated temperatures

被引:75
|
作者
Yang, DY [1 ]
Tontiwachwuthikul, P [1 ]
Gu, YG [1 ]
机构
[1] Univ Regina, Fac Engn, PTRC, Regina, SK S4S 0A2, Canada
关键词
D O I
10.1021/ef049792z
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
In this paper, an experimental technique has been developed to study the interfacial interactions of the reservoir brine-CO2 system at high pressures and elevated temperatures. Using the axisymmetric drop shape analysis (ADSA) for the pendant drop case, this new technique makes it possible to determine the interfacial tension (IFT) and visualize the interfacial interactions between the reservoir brine and CO2 under practical reservoir conditions. More specifically, the dynamic IFT between the reservoir brine and CO2 is measured as a function of pressure at two different temperatures. It is found that the dynamic IFT gradually reduces to a constant value, which is termed as the equilibrium IFT. The equilibrium IFT decreases as the pressure increases, whereas the same parameter increases as the temperature increases. The major interfacial interactions observed in this study include interface disappearance, the swelling effect, the shrinking effect, and wettability alteration. At an elevated temperature (T = 58degreesC), the pendant brine drop cannot be observed in the CO2 phase at a pressure of P greater than or equal to 12.238 MPa. It is also found that CO2 solubility in the brine phase, which is measured using the PVT system, approaches its maximum value under the same conditions. Further increases in pressure do not noticeably increase the CO2 solubility in the brine phase. The brine swelling effect is observed at all the pressures and temperatures tested, whereas the brine shrinking effect occurs only at high pressures and a lower temperature (T = 27degreesC). In addition, the wettability of the reservoir brine-CO2 system changes from the hydrophilic case to the hydrophobic case when the CO2 changes from the gas phase to the liquid phase.
引用
收藏
页码:216 / 223
页数:8
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