Experimental and Modeling Study of Methane Adsorption onto Partially Saturated Shales

被引:35
作者
Wang, Lu [1 ,2 ]
Wan, Jiamin [2 ]
Tokunaga, Tetsu K. [2 ]
Kim, Yongman [2 ]
Yu, Qingchun [1 ]
机构
[1] China Univ Geosci Beijing, Sch Water Resources & Environm, Beijing, Peoples R China
[2] Lawrence Berkeley Natl Lab, Energy Geosci Div, Berkeley, CA USA
关键词
methane adsorption; moisture; shale; NORTHEASTERN BRITISH-COLUMBIA; CARBON-DIOXIDE ADSORPTION; HIGH-PRESSURE METHANE; SORPTION CAPACITY; GAS SHALE; MOLECULAR SIMULATION; WATER-ADSORPTION; ACTIVATED CARBON; CLAY-MINERALS; QAIDAM BASIN;
D O I
10.1029/2017WR020826
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Shale gas equilibrates through gas-liquid-solid interactions in reservoirs, but the role of moisture is rarely investigated. To determine how adsorbed water influences methane behavior, three carboniferous shale samples from the Qaidam Basin, China, were humidified at five levels up to a relative humidity of 89%, and their methane capacities at pressures up to 12 MPa were studied. The experimental results indicate that two water-related mechanisms, "water blocking for methane transport" and "surface competition for gas-solid interaction," are primarily responsible for the methane capacity variations. A compositional comparison suggests that a high abundance of clay minerals plays a favorable role in methane migration by retaining water in interlayer pores. Based on the experimental data, an optimized method for calculating the adsorption amount based on an approximation of density distribution is proposed. The model predicts the average thickness of the adsorption layer and the adsorbed methane density distribution on the surface at a given pressure. The methane adsorption layer "thins" in a stepped pattern by up to 45% in the presence of water, with little further change observed at relative humidities greater than 75% in the studied samples.
引用
收藏
页码:5017 / 5029
页数:13
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