Methane Adsorption on Shale under Simulated Geological Temperature and Pressure Conditions

被引:394
作者
Rexer, Thomas F. T. [1 ,2 ]
Benham, Michael J. [3 ]
Aplin, Andrew C. [4 ]
Thomas, K. Mark [1 ,2 ]
机构
[1] Newcastle Univ, Sch Civil Engn & Geosci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Newcastle Univ, Sch Chem Engn & Adv Mat, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[3] Hiden Isochema Ltd, Warrington WA5 7TS, Cheshire, England
[4] Univ Durham, Sci Labs, Dept Earth Sci, Durham DH1 3LE, England
关键词
NORTHEASTERN BRITISH-COLUMBIA; MISSISSIPPIAN BARNETT SHALE; CRETACEOUS GAS SHALES; NORTH-CENTRAL TEXAS; CARBON-DIOXIDE; THERMODYNAMIC PROPERTIES; ABSOLUTE ADSORPTION; SORPTION ISOTHERMS; PORE STRUCTURE; BLACK SHALES;
D O I
10.1021/ef400381v
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
Shale gas is becoming an increasingly important energy resource. In this study, the adsorption of methane on a dry, organic-rich Alum shale sample was studied at pressures up to similar to 14 MPa and temperatures in the range 300-473 K, which are relevant to gas storage under geological conditions. Maximum methane excess uptake was 0.176-0.042 mmol g(-1) (125-30 scf t(-1)) for the temperature range of 300-473 K. The decrease in maximum methane surface excess with increasing temperature can be described with a linear model. An isosteric enthalpy of adsorption 19.2 +/- + 0.1 kJ mol(-1) was determined at 0.025 mmol g(-1) using the van't Hoff equation. Supercritical adsorption was modeled using the modified Dubinin-Radushkevich and the Langmuir equations. The results are compared with absolute isotherms calculated from surface excess and the pore volumes obtained from subcritical gas adsorption (nitrogen (78 K), carbon dioxide (273 and 195 K), and CH4 (112 K)). The subcritical adsorption and the surface excess results allow an upper limit to be put on the amount of gas that can be retained by adsorption during gas generation from petroleum source rocks.
引用
收藏
页码:3099 / 3109
页数:11
相关论文
共 56 条
[1]   Shale Gas-in-Place Calculations Part I: New Pore-Scale Considerations [J].
Ambrose, Ray J. ;
Hartman, Robert C. ;
Diaz-Campos, Mery ;
Akkutlu, I. Yucel ;
Sondergeld, Carl H. .
SPE JOURNAL, 2012, 17 (01) :219-229
[2]  
[Anonymous], 1993, CRC HANDBOOK OF CHEM
[3]  
[Anonymous], 1990, HANDBOOK OF COMPRESS
[4]  
[Anonymous], 2008, AUTOSORB VERSION 1 6
[5]   High-pressure adsorption of methane and carbon dioxide on coal [J].
Bae, Jun-Seok ;
Bhatia, Suresh K. .
ENERGY & FUELS, 2006, 20 (06) :2599-2607
[6]   Modeling of high-pressure adsorption isotherms above the critical temperature on microporous adsorbents: Application to methane [J].
Benard, P ;
Chahine, R .
LANGMUIR, 1997, 13 (04) :808-813
[7]   Methane and CO2 sorption and desorption measurements on dry Argonne premium coals:: pure components and mixtures [J].
Busch, A ;
Gensterblum, Y ;
Krooss, BM .
INTERNATIONAL JOURNAL OF COAL GEOLOGY, 2003, 55 (2-4) :205-224
[8]   CO2 as an adsorptive to characterize carbon molecular sieves and activated carbons [J].
Cazorla-Amoros, D ;
Alcaniz-Monge, J ;
de la Casa-Lillo, MA ;
Linares-Solano, A .
LANGMUIR, 1998, 14 (16) :4589-4596
[9]   The organic matter distribution and methane capacity of the lower Cretaceous strata of northeastern British Columbia, Canada [J].
Chalmers, Gareth R. L. ;
Bustin, R. Marc .
INTERNATIONAL JOURNAL OF COAL GEOLOGY, 2007, 70 (1-3) :223-239
[10]   Lower Cretaceous gas shales in northeastern British Columbia, Part II: evaluation of regional potential gas resources [J].
Chalmers, Gareth R. L. ;
Bustin, R. Marc .
BULLETIN OF CANADIAN PETROLEUM GEOLOGY, 2008, 56 (01) :22-61