Molecular concept and experimental evidence of competitive adsorption of H2O, CO2 and CH4 on organic material

被引:245
作者
Gensterblum, Yves [1 ]
Busch, Andreas [2 ]
Krooss, Bernhard M. [1 ]
机构
[1] Univ Aachen, RWTH, Inst Geol & Geochem Petr & Coal, D-52056 Aachen, Germany
[2] Shell Global Solut Int BV, NL-2288 GS Rijswijk, Netherlands
关键词
Coal; Pre-adsorbed water; Sorption; Thermodynamics; Thermal maturity; CARBON-DIOXIDE ADSORPTION; SURFACE HETEROGENEITY; METHANE ADSORPTION; MESOPOROUS CARBONS; POROUS CARBONS; COAL; SIMULATION; SORPTION; WATER; MOISTURE;
D O I
10.1016/j.fuel.2013.07.014
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
Unconventional gas, such as shale gas or coalbed methane offers an attractive low-carbon solution and furthermore provides possibilities for CO2-storage and coevally for enhanced gas recovery. In order to better understand gas and water interaction with organic matter (natural coal) of different maturity we developed a molecular concept with experimental and literature support for sorption of CH4, CO2 and H2O on organic material over a broad range of thermal maturity (0.5-3.3% vitrinite reflectance). We present a conceptual model to explain CO2 and CH4 sorption in the presence of water on coal with varying coal maturity (from subbituminous to anthracite). Adsorption experiments have been performed on coals of different maturity at temperatures between 303 and 350 K, pressures up to 20 MPa and under dry and moisture-equilibrated conditions. With increasing coal maturity we find for both gases a linear sorption capacity trend for the moist and a more parabolic trend for the dry coal samples. Based on the differences in CH4 and CO2 sorption capacity on coals of different maturity as a function of moisture content we infer that oxygen-containing functional groups represent the primary sorption sites for which CO2 or CH4 compete with water molecules. The competitive interaction turns out to be a volumetric displacement independent of the gas type. A pore blocking mechanism could not be confirmed. Adsorbed molecules on anthracite are mobile within the adsorbed phase at low surface coverage. Additionally, restrictions in translational and vibrational movements of the sorbed gas molecules induced by adsorbed water molecules are observed. Therefore we conclude that sorbed molecules are more localised when water is present in the adsorbed phase, whereas at high surface coverage, the thermodynamic properties of adsorbed molecules are dominated by adsorbate-adsorbate interactions. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:581 / 588
页数:8
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