Phase behavior of
hydrocarbon fluids in nanopores is different
from that observed in a PVT cell due to the confinement effect. While
scholars have established various models for studying the phase behavior
in nanopores, the authors often ignore the effect of pore geometries,
which can significantly affect the critical fluid properties in shale
nanopores. In this study, we extend the Soave-Redlich-Kwong equation
of state (SRK EOS) using potential theory and establish models of
critical property shift, considering pore geometries, adsorption,
and water film. Our research shows that the critical property shifts,
considering fluid adsorption, begin at r
p ≤ 10 nm and are seriously strengthened with nanopore radius
reduction. The extended SRK EOS is applied to compute phase diagrams
of the 50% C1–50% nC10 mixture at different pore sizes and find that the thickness of adsorption
and water film causes a depression in the P–T diagram and that
the bubble point pressure is lower in cylindrical pores. At pressures
above 6 MPa, the irreducible water saturation and pore geometries
greatly impact the vapor–liquid ratio. This study is significant
for evaluating residual oil distribution and studying fluid flow laws
in shale reservoirs.