A pragmatic
technique has been developed to experimentally and
theoretically quantify the nonequilibrium phase behavior of alkane
solvent(s)–CO2–heavy oil systems under reservoir
conditions. Experimentally, constant-composition expansion tests have
been conducted for alkane solvents–CO2–heavy
oil systems at constant-volume expansion rates with a PVT setup to
simultaneously measure volume and pressure change of the aforementioned
systems. Theoretically, mathematical formulations have been developed
to quantify the amount of the evolved gas as a function of time based
on the real gas equation, while mathematical models on compressibility
and density of the oleic phase mixed with the entrained gas (i.e.,
foamy oil) are respectively formulated. The required equilibrium time
and exponential coefficients associated with gas-bubble growth are
determined once the deviation between the experimentally measured
pressure–volume profile and the theoretically calculated one
has been minimized. In addition to effectively capturing the main
features of foamy oil during expansion processes, its nonequilibrium
fluid properties (i.e., compressibility and density) are determined
as a function of the amount of the entrained gas in the liquid phase.
For compressibility, a sudden change is located at the pseudobubble
point pressure rather than at the thermodynamic bubble point pressure
at which gas bubbles start to form. The density of the foamy oil is
then found to decline at different rates when pressure is decreased
from its initial value to the pseudobubble point pressure. For CO2–heavy oil systems (binary system), the difference
between the pseudobubble point pressure and the maximum pressure after
the pseudobubble point pressure shows a monotonic decline, whereas,
for CO2–C3H8–heavy
oil systems (ternary system), it reaches a peak with an increase in
temperature.