Intro To PVT
Intro To PVT
• Differential Liberation
• Viscosity tests
Each of these tests is described below in detail both for oil and retrograde gas.
Oil
Relative Volume
About 100 cm3 of the reservoir fluid are transferred to the PVT cell at constant pressure at
mono-phasic conditions.
The cell is heated from ambient temperature (Ta) to reservoir temperature (Tr). The
volume increase (δV) of the sample due to heating is taken into account.
1 ∂V
α=
V ∂T p
Then the pressure of the cell is decreased stepwise and the new volume of the sample at
each pressure step is recorded. From these volumetric data the compressibility of the
reservoir fluid is calculated:
1 ∂V
c=
V ∂p T
Retrograde Gas
The dew point pressure (pD) is determined by visual observation in a window cell. This
observation is subsequently checked by extrapolating the liquid deposit curve.
Specific volumes or densities at dew point pressure are calculated from the molecular
composition of the fluid and the gas equation. The total volume of the fluids in the cell is
recorded at each step and is reported as Vr to give the pressure-volume relationship.
For this type of studies special type of equipment has to be used that enables to visually
observe the appearance of the first gas bubble or of the first liquid drop.
The cell consists of two high-pressure cylinders having a large diameter, connected
through a narrow section (about 17-mm long and 3.5-mm diameter). This section is
fitted with two sapphire windows for visual observations of retrograde liquid deposition
and its volumetric measurements. The upper cell is fitted with a piston and the bottom
cell is in contact with mercury.
Hydrocarbon
liquid interface
Convex
Mercury
Interface
It is possible to observe the hydrocarbon liquid meniscus even when the liquid deposit is
as low as 0.006 cm3. As soon as hydrocarbon liquid starts to fill, a concave meniscus of
the hydrocarbon liquid phase can be observed just touching the convex mercury
interface the space between the wall of the narrow tube and the convex mercury
interface. This will be a clear indication of the dew formation. Thus visually observed
dew point is recorded. Furthermore, since small volumes as low as 0.01 cm3 (exactly
0.007 cm3) can be measured, the dew point pressure can confirmed by extrapolating
the liquid deposit curve (vs. pressure) down to zero liquid volume.
The position of the piston as well as the liquid level can be adjusted with the dual pump.
This enables to position either the hydrocarbon liquid interface or the mercury meniscus
in the middle of the window, without changing the system pressure. A magnified image
of the window is seen through a video camera and a TV screen.
The use of large volumes in the cell (e.g. over 2000 cm3) can minimise the error
associated with the measurement; The experimental system allows the accurate
measurement of retrograde liquid deposits volume down to 0.01 cm3. The accuracy of
the dew point pressure measurement is + or - 5 psia;
pV
z=
nRT
where:
p = pressure
n = number of moles
R = gas constant
When the pressure of the cell is reduced to a value below pB, the gas cap that is formed
is pushed out from the cell to a gasometer. The remaining fluid is subsequently depleted
down to the next pressure step.
The liberated gas is analysed by gas chromatography for molecular composition, and
gas viscosity; gas gravities are calculated from the molecular composition.
The following parameters are measured or calculated from other sets of data:
Oil density is computed at a given pressure step, using the mass of gas liberated at that
pressure and the mass of oil at previous stage and the volume ratios measured during the
DL experiment.
Composite Vaporisation
The composite vaporisation study for an oil is the most suitable laboratory test for
determining Formation Volume Factors (Bo, Bg) and Solution GOR (Rs) to be used for
reservoir engineering calculations. A differential liberation study is performed at
reservoir temperature at each step of which a small volume of the remaining equilibrium
liquid is produced, in the laboratory, through selected separation conditions to yield
stock tank oil. It is called composite vaporisation as it combines differential liberation
with flash separator test. In fact, in this way, the continuous process through which the
oil is produced at the surface during reservoir depletion is simulated stepwise.
On liquid phase:
• Separator GOR, Stock tank GOR, separator and stock tank gas analysis.
On gas phase:
• Gas volume at indicated pressure and at standard conditions to calculate Rs, z and
Bg.
It is considered that this process simulates closely the actual depletion that takes place in
a gas condensate reservoir where only gas is produced, the condensate deposit stays in
the pores of the formation and the total hydrocarbon pore volume remains constant
regardless of pressure.
The technical descriptions of the state of art apparatus used for this study are as follows:
Injection Pump Rate Rated for 10,000 psia with min. counts of 0.01 cm3.
At each equilibrium step, the following parameters are measured on the produced well
stream:
Gas molecular composition, liquid content (GPM) and cumulative liquid recovery.
Fluid volume at cell conditions and at standard conditions (this allows to compute true z-
factor) and cumulative produced fluid (percentage of initial fluid). Retrograde liquid
deposit (RLD) curve (reported as a percentage of total fluid volume at pD).
rld = +3.1842 X+1.2238*9 -4.2725 X+1.2238*6 -2.3992 X+1.2238*3 +1.647 X+1.2238 +1.8381
p
X=
3162
The viscosity of the reservoir fluid is measured at downhole temperature, or at any other
specified temperature, from initial reservoir pressure down to atmospheric pressure.
During this study, below pB, viscosity is measured on the liquid phases, which are
obtained following a differential vaporisation approach.
A rolling ball type of viscometer or a capillary tube one is used for the viscosity study.
The reservoir fluid sample is transferred to the viscometer at an elevated pressure, to
ensure mono-phasic transfer.
Viscosity of gas phase is calculated from liberated gas given by differential vaporisation
Usually, 4 single stage separation tests are performed at four different pressures and the
same separator temperature.
299 2.06 83.9 302.0 224 40.3 203 36.6 427 76.9
157 1.08 83.9 302.0 301 54.3 102 18.4 403 72.7
15 0.10 83.9 302.0 406 73.1 406 73.1
Pressure Temperature Separator liquid density Tank liquid density Tank liquid density at
std. conditions
299 2.06 83.9 302.0 0.769 769 0.816 816 0.816 816
157 1.08 83.9 302.0 0.782 782 0.817 817 0.817 817
15 0.10 83.9 302.0 0.800 800 0.818 818 0.818 818
Shrinkage Factor:
Separator
liquid Flash to
composition atmospheric
conditions
Check pB or
pD and p-V
curve Reservoir
fluid
composition
Reservoir
fluid
composition
Differential Constant
Viscosity Separation
vaporisation mass
determination tests Expansion
3 separator 3 separator
liquid gas
samples samples
Check pB’s
and p-V.
curves 3 separator
gas
Flash to compositions
atmospheric
conditions
Separator Dew
liquid point
composition check
Reservoir
fluid
composition
Constant Constant
volume mass
depletion Expansion
Constant Reservoir
volume fluid
depletion composition
Differential Constant
Viscosity Separation mass
vaporisation determination tests Expansion
Oilphase, Aberdeen.