Laboratory Investigation of Enhanced Light-Oil Recovery by CO /flue Gas Huff-n-Puff Process
Laboratory Investigation of Enhanced Light-Oil Recovery by CO /flue Gas Huff-n-Puff Process
Temperature (° C) 15 20 68
Density (kg/m3) at 0.1 MPa 873.8 (30.3° API) 870.2 835.6*
Viscosity (mPa•s) at 0.1 MPa 12.4 10.4 3.04*
Basic sediment and water Trace
Oil molecular weight (g/g-mol) 224
* Estimated based on regression
TABLE 2: Properties of Elswick brine (produced water). total GOR, density, swelling factor, formation volume factor, and
viscosity of the liquid phase as a function of saturation pressure.
Property Value The saturation pressure of the reconstituted oil was determined to
be 10.2 MPa from isothermal pressure-volume expansion plots as
Density (kg/m3) @ 15° C 1,106.2 well as traditional Y-function plots.
@ 20° C 1,104.2
@ 60° C 1,084.6
@ 68° C 1,080.6* Oil-CO2 Mixture Phase Behaviour
Measurement Apparatus
Viscosity (mPa•s) @ 15° C 1.52 The experimental apparatus used for this study is a traditional
@ 20° C 1.33 PVT apparatus designed for operation at typical reservoir tempera-
@ 60° C 0.65 tures and pressures. A variable-volume high-pressure cell is placed
@ 68° C 0.57* in a thermostated oven. Fluids (oil and gas) are introduced into the
cell under pressure, and then mixed to achieve equilibrium at the
Refractive index @ 25° C 1.3584 desired temperature and pressure. Viscosities are measured by run-
ning the fluids at a constant rate through a capillary viscometer.
Conductivity (mS) @ 25° C 208 Fluid densities are measured in a high-pressure oscillating tube
pH @ 20° C 6.91
densitometer (Anton Paar DMA 512 P) at reservoir temperature.
A single-stage separator flash procedure is used to obtain the
Total dissolved solids (mg/L) GOR, composition, and formation volume/swelling factors. In this
@ 120° C 161,000 procedure, a sample of fluid from the cell is flashed directly down
@ 180° C 159,000 to atmospheric conditions. The liquid and gas portions resulting
from this process are collected separately. The weight and density
Major components in brine (mg/L)
of the liquid are measured, as well as the volume and composition
Chloride (Cl-) 90,400 of the gas. The results are used to calculate the composition, GOR,
Sulfate (SO42-) 2,300
etc., of the whole sample.
Sodium (Na+) 47,300
Potassium (K+) 870
Magnesium (Mg2+) 720 Huff-n-Puff PVT Procedure
Calcium (Ca2+) 3,010
The experiments carried out in this study were designed to sim-
Iron (Fe2+) < 0.1
< 0.8
ulate the sequence that occurs during a typical huff-n-puff process.
Barium (Ba2+) As mentioned in the introduction, typical huff-n-puff operations
Manganese (Mn2+) < 0.08
begin with carbonation or pressurization of the oil during the gas
* Estimated based on regression injection stage (huff). A soak period allows the gas to dissolve
into the oil. Finally, liberation or depressurization of the oil occurs
pressure-volume-temperature (PVT) study. The following PVT during the production stage (puff). Accordingly, the oil was satu-
properties of the reconstituted fluid were measured: GOR, vis- rated with injection gas in several steps of increasing pressure up to
cosity, density, and formation volume factor (FVF). a maximum value for the huff part of the process. The pressure was
The viscosity and density were measured over a range of pres- then reduced in a number of stages down to atmospheric condi-
sures, which made it possible to determine the value at saturation tions. At each step, the oil and gas were equilibrated, and the prop-
pressure by a short extrapolation. The equilibrium reservoir fluid erties of the oil and gaseous phases were measured as described in
properties are presented in Table 3. These properties include the the previous section.
TABLE 3: Equilibrium liquid properties during CO2 huff-n-puff at 68° C.
Composition (mol%)
Psat Equilib.
Description
(MPa) Phase N2 CO2 H2 S C1 C2 C3 iC4 nC4 iC5 nC5 C6+
Reservoir
10.2 - 1.6 0.4 0.0 19.3 6.8 7.1 1.2 4.0 1.8 2.1 55.8
fluid
Reservoir 11.5 Liquid 1.9 10.3 0.0 16.5 6.0 6.3 1.1 3.5 1.6 1.9 50.9
fluid-CO2 12.4 Liquid 1.9 17.7 0.0 14.4 5.3 5.8 1.2 3.4 1.6 1.9 46.7
mixtures 13.7 Liquid 1.5 27.6 0.0 12.1 4.6 5.2 0.9 3.1 1.4 1.7 41.7
huff cycle 15.7 Liquid 0.9 36.2 0.0 10.0 4.2 4.5 0.8 2.9 1.4 1.7 37.5
12.6 Liquid 0.9 34.9 0.0 10.0 4.3 4.6 0.9 2.9 1.4 1.7 38.5
Vapour 6.0 59.1 0.0 25.5 4.4 2.8 0.4 1.0 0.4 0.5 0.0
Reservoir 10.0 Liquid 0.4 31.2 0.0 8.6 4.4 4.9 0.9 3.0 1.4 1.7 43.5
fluid-CO2 Vapour 4.6 57.7 0.0 28.6 4.8 2.7 0.3 0.8 0.2 0.3 0.0
mixtures 7.1 Liquid 0.2 26.0 0.0 5.7 4.1 5.0 1.0 3.2 1.5 1.8 51.5
puff cycle Vapour 2.3 62.0 0.0 25.9 5.3 2.9 0.3 0.8 0.3 0.3 0.0
3.0 Liquid 0.1 13.9 0.0 1.8 3.1 4.8 1.0 3.2 1.6 1.9 68.6
Vapour 1.2 66.6 0.0 18.2 7.0 4.5 0.5 1.3 0.3 0.4 0.0
FIGURE 4: Mixture densities in Elswick recombined oil-CO2 FIGURE 5: Mixture viscosities in Elswick recombined oil-CO2
huff-n-puff. huff-n-puff.
The viscosities of CO2-oil mixtures during the huff and puff from 6,822 mPa⋅s for the recombined oil down to 226 mPa⋅s for the
stages are tabulated in Table 6 and plotted in Figure 5. As with CO2-saturated oil at 6.55 MPa. This should be taken into account
Table 5, the first lines of data in each set in Table 6 are the esti- when screening reservoirs for applicability of cyclic gas stimula-
mated values for the saturated fluid, and the remaining data are tion enhanced oil recovery.
measured for the undersaturated liquids. In all cases, the viscosity An interesting phenomenon is observed when the pressure is re-
increases with increasing pressure, as is expected. As with density duced: the viscosity remains low as gas is released from the liquid
(see Figure 4), the slopes of the pressure-viscosity plots are almost phase, and is consistently lower than the viscosity of the liquid
constant and do not vary appreciably with composition. phase of the huff cycle. This is a result of the oil-rich phase re-
From Figure 5, it is observed that the saturated oil-rich phase’s leasing methane preferentially to CO2 during pressure decrease,
viscosity decreases as it absorbs more CO2 during the huff cycle. so the residual liquid is relatively rich in CO2, which is an effec-
This is one of the main benefits of the CO2 huff-n-puff process, tive viscosity-reducing component. This is reinforced by the higher
wherein the reduced viscosity renders the oil more mobile. In the GORs during the puff cycle than during the huff, as shown in
present case, the Elswick recombined oil’s viscosity was reduced Figure 2; more dissolved gas results in lower viscosities.
from 1.7 mPa⋅s for the live oil to 1.0 mPa⋅s at the maximum satura-
tion pressure of 15.7 MPa. Huff-n-Puff Core Coreflooding Results
It should be mentioned that the viscosity-reduction effectiveness Laboratory coreflooding tests focused on investigating the in-
of CO2 is more pronounced with heavier, more viscous oils(8,10). fluence of the remaining oil saturation and drive gas composition
For example, Sayegh and Maini(8) reported a viscosity reduction on oil recovery efficiency for the huff-n-puff process. In total, three
28 Journal of Canadian Petroleum Technology
TABLE 6: Effect of pressure on viscosities of CO2-Elswick recombined oil – huff and puff cycles.
TABLE 7: Summary of huff-n-puff coreflood results (saturated with Elswick live oil).