Methane/ethane adsorption behavior in shale nanopore systems with mesopores and micropores: Evaluating micropore contribution

IF 2.8 3区 工程技术 Q3 CHEMISTRY, PHYSICAL Fluid Phase Equilibria Pub Date : 2024-12-25 DOI:10.1016/j.fluid.2024.114323
Wuquan Li , Jinrong Cao , Yunfeng Liang , Yoshihiro Masuda , Takeshi Tsuji , Kohei Tamura , Tomoaki Ishiwata , Daisuke Kuramoto , Toshifumi Matsuoka
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Abstract

Shale gas has garnered significant attention as a clean and high-quality fuel resource. Shale formations exhibit broad pore size distributions, with micropores (< 2 nm) and mesopores (2–50 nm), showing different gas sorption behaviors. The sorption behavior in kerogen nanopore systems with interconnected micropores and mesopores remains poorly understood. This study introduces three kerogen nanopore systems—low-density, middle-density, and high-density—each featuring a 7.5-nm mesopore and numerous micropores. Using Grand Canonical Monte Carlo (GCMC) simulations, the sorption behaviors of pure CH4, C2H6, and their mixture (9:1) across a range of pressures (1 MPa to 13 MPa) and temperatures (313.15 K, 323.15 K, and 333.15 K) were investigated. The study identified three Zones: Zone I for the free gas phase, Zone II for adsorption in mesopores, and Zone III for absorption in micropores. The sorption isotherms were calculated by integrating the adsorption amounts, normalized by measured pore volume in the mesopore domain, and absorption amounts, normalized by total organic content. The calculated excess sorption isotherms across different kerogen nanopore systems aligned with experimental results, allowing us to estimate the micropore contribution. We calculated the actual density profiles and estimated the adsorption density in micropores and those on mesopore walls, which can be used for field applications. The selectivity in three zones was compared across three kerogen nanopore systems, showing that it was not so significantly influenced by the pore geometry at all temperatures and pressures. The absolute absorption in micropores and the micropore contribution to the total absolute sorption (in percentage) align consistently with micropore volume across different kerogen nanopore systems, revealing a linear relationship with micropore volume. This research provides recommendations for laboratory experiments and offers valuable insights into the microscopic distribution of shale gas in nanopore systems, emphasizing the significance of micropores in addition to mesopores.

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Fluid Phase Equilibria
Fluid Phase Equilibria 工程技术-工程:化工
CiteScore
5.30
自引率
15.40%
发文量
223
审稿时长
53 days
期刊介绍: Fluid Phase Equilibria publishes high-quality papers dealing with experimental, theoretical, and applied research related to equilibrium and transport properties of fluids, solids, and interfaces. Subjects of interest include physical/phase and chemical equilibria; equilibrium and nonequilibrium thermophysical properties; fundamental thermodynamic relations; and stability. The systems central to the journal include pure substances and mixtures of organic and inorganic materials, including polymers, biochemicals, and surfactants with sufficient characterization of composition and purity for the results to be reproduced. Alloys are of interest only when thermodynamic studies are included, purely material studies will not be considered. In all cases, authors are expected to provide physical or chemical interpretations of the results. Experimental research can include measurements under all conditions of temperature, pressure, and composition, including critical and supercritical. Measurements are to be associated with systems and conditions of fundamental or applied interest, and may not be only a collection of routine data, such as physical property or solubility measurements at limited pressures and temperatures close to ambient, or surfactant studies focussed strictly on micellisation or micelle structure. Papers reporting common data must be accompanied by new physical insights and/or contemporary or new theory or techniques.
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