Abstract

A series of methane adsorption isotherms were measured at 35.4°C, 50.6°C, and 65.4°C at pressures up to 15.0MPa for eight dried, overmature Lower Silurian–Upper Ordovician shale samples collected from the Sichuan Basin with TOC values in the range of 1.87–5.74%. The measured maxima of excess adsorption capacity of methane range from 1.25 to 2.50cm3/g rock at 65.4°C; the maxima are slightly enhanced at 35.4°C, but all are positively correlated with total organic carbon (TOC). Both the supercritical Dubinin–Radushkevich (SDR)- and Langmuir-based excess adsorption models were found to represent the experimental excess adsorption isotherms equally well within the experimental range. The temperature-dependent densities of adsorbed methane resulting from the parameter fit of the SDR-based excess adsorption model are in the range of 297–415mg/cm3; for the Langmuir-based excess adsorption model, the adjusted densities range from 386mg/cm3 to 1027mg/cm3 and most of them are much larger than the liquid density of methane at its boiling point (424mg/cm3). Nevertheless, the maxima of absolute methane adsorption capacity fitted by both models are not significantly different and are linearly correlated. One of the contributors to the uncertainty of the gas-in-place estimation in geological conditions is the inconsistent utilization of experimental excess sorption data as “absolute sorption” values, particularly at high pressures. However, the choice of adsorption model itself (Langmuir- or SDR-based) and the fitting procedure, assuming either constant or temperature-dependent adsorbed phase density and maximum sorption capacity, do not significantly affect the estimated GIPs for the geological system studied here with depths of less than 4000m.

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