Abstract
Abstract Because of the confinement effects in shale formations, fluid flow is different compared to conventional reservoirs. The interactions between the fluid molecules and porous wall inside nanopores play such an important role that can change the phase behavior of the fluids. The fluids in shale reservoirs are usually stored in two forms, free fluids and adsorbed fluids. The region where free fluids are stored has negligible fluid-wall interactions while the region for adsorbed fluids is under strong pore wall influence. The current available equations of state cannot capture the phase behavior of the adsorbed phase in porous media due to the ignorance of the fluid-wall interactions. This paper discussed the effects of the fluid-wall interactions on fluid phase behavior from a modeling of of view. The production from shale reservoirs in the US has shifted from gas windows to condensate windows and oil windows recently due to low natural gas price. Liquid-rich shales, such as Barnett, Eagle Ford, and Marcellus are brought more attentions than ever before. Thus, it is critical to understand the fluid phase behavior and properties and their impacts on production in the condensate systems. Our work focuses on the predictions of fluid critical property change and fluid density change inside nanoporous media. Simplified Local-Density theory for single component coupled with modified Peng-Robinson Equation of State was used to predict the density profiles of dry gas (pure methane) in confined pores. The model was then extended to mixtures for the study of condensate systems. Our results showed that due to the fluid-wall interactions, the fluid density is not uniformly distributed across the pore. The fluid density is higher near the wall than that in the center region of the pore. It also showed that depending on fluid types, temperature, pressure and pore sizes, the fluid density profile would change. The pore size range we focused on was from 2 nm to 10 nm. In order to present the condensate system, a synthetic mixture of 75% methane and 25% n-butane is used. It is found that fluid composition is not uniform across the pore. Heavier component (n-butane) tends to accumulate near the wall while lighter component (methane) would like to stay in the center region of the pore. For a 10 nm wide pore, the composition of n-butane of the synthetic mixture can be as high as 66% close to the pore wall.
Published Version
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