Abstract

Assessing unconventional petroleum resources, particularly shale gas reserve estimation, is challenging due to the adsorption phenomenon. This study presents a new method combining experimental and mathematical procedures to determine the absolute adsorption amount in shale samples. In the experimental section of this study, a new behavior was observed in the NMR decay time series of hydrocarbons in organic porous media. The fast section has a linear relationship with time rather than an exponential one. As a result, a Log-Exponential fit to these decay curves was proposed. Then the logarithmic portion was then used to estimate the absolute adsorbed amount. The method was validated against literature data and conventional methods.Based on this newly developed method, absolute adsorption isotherms were obtained for a Duvernay shale sample and activated carbon packs at pressures ranging from 0.77 MPa to 7 MPa. The model proved to be applicable and consistent with pressure variations. Methane in Duvernay shale exhibited adsorbed isotherm type V, with a methane adsorption capacity of 0.08 g per gram of Total Organic Content (TOC) at 6.24 MPa.In addition to absolute adsorption, the competitive adsorption of methane and CO2 was explored, which is critical for evaluating CO2-enhanced shale gas recovery and storage techniques. The injected CO2 resulted in the displacement of methane from smaller shale pores to larger ones.Adsorption and desorption experiments were conducted to investigate hysteresis. The new method was able to better describe the physical behavior of gaseous hydrocarbons in organic porous media. It was able to capture phase transition and critical pressure specific to organic porous media, which differ from non-organic porous media. This innovative approach enables the accurate characterization of shale reservoirs.

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