Subscriber access provided by CORNELL UNIVERSITY LIBRARY
Article
Improved oil reservoir sweep with viscoelastic surfactants Joris van Santvoort, and Michael Golombok Energy Fuels, Just Accepted Manuscript • DOI: 10.1021/acs.energyfuels.6b01932 • Publication Date (Web): 14 Sep 2016 Downloaded from http://pubs.acs.org on September 22, 2016
Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a free service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are accessible to all readers and citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.
Energy & Fuels is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.
Page 1 of 27
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Energy & Fuels
1
Improved oil reservoir sweep with viscoelastic
2
surfactants
3
Joris van Santvoortᵃ*, Michael Golombokᵃ ᵇ
4 5
ᵃ Technische Universiteit Eindhoven, 5612 AZ Eindhoven, The Netherlands
6
ᵇ Shell Global Solutions International B.V., 1031 HW Amsterdam, The Netherlands
7
*Corresponding author
8
1 ACS Paragon Plus Environment
Energy & Fuels
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
1
Abstract
2
Viscoelastic surfactant solutions increase oil recovery by selectively modifying the viscosity of
3
the injected displacing fluid in different zones of the reservoir. We demonstrate that flow
4
resistance in high permeability zones is increased whereas no significant change in viscosity
5
occurs in low permeability zones. This greatly reduces injected fluid losses via the high
6
permeability route. In two phase flow in sandstones, recovery increases by about 25%. Efficiency
7
also increases by a factor of 3 as shown by the large reduction in injected volume at
8
breakthrough. Consequently less fluid is lost through high permeability thief zones. Recovery is
9
increased in carbonates as well but the efficiency is depleted due to apparent changes in wetting.
10
The reduction in injected fluid before breakthrough has the potential to prolong the economical
11
lifespan of water wet reservoirs.
2 ACS Paragon Plus Environment
Page 2 of 27
Page 3 of 27
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
1
Energy & Fuels
1. Introduction
2
In secondary oil recovery water is injected into the reservoir to drive oil towards a
3
production well. Water-flooding typically yields 15-35% incremental absolute recovery of the
4
original oil in place (OOIP).1 This relatively low efficiency largely stems from reservoir
5
heterogeneity where high permeability zones and/or fractures cause preferential flow paths with
6
low flow resistance. These preferential paths act as ‘thief zones’ through which the bulk of the
7
displacing fluid flows.2 Oil in the low permeability layers is bypassed and becomes stranded.
8
Eventually breakthrough is reached via these high permeability zones and the injected fluid will
9
be produced from the reservoir. From this point most of the fluid injected into the reservoir does
10
not contribute to recovery. Nearly all of the water is lost through the thief zones without any
11
displacement of additional oil. Also there is an increase in water-cut at the producer which
12
increases post-processing costs. For these reasons many mature reservoirs become economically
13
unattractive and have a relatively short lifespan.3
14
Reservoir heterogeneity can be overcome by redirecting flow paths towards oil rich low
15
permeability zones (conformance control). Typically thief zones are blocked by injecting
16
polymeric gel or surfactant foam.4 The displacing fluid is subsequently diverted into the low
17
permeability layers sweeping the reservoir more effectively. This process is expensive and
18
relatively complicated since it requires extensive knowledge of the reservoir. Improper use can
19
permanently block low permeability layers and prevent oil production.5
20
In this study we investigate the use of viscoelastic surfactant (VES) solutions for
21
conformance control. These fluids have a unique rheological behavior which makes them
22
applicable as spatially self-regulating displacement fluids. Previous work showed that VES fluids
23
can adjust the flow in a heterogeneous reservoir to create a more uniform flow front.6,7 Most of
24
the previous work was single phase in homogeneous synthetic porous media. This paper focusses 3 ACS Paragon Plus Environment
Energy & Fuels
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
1
on oil displacement testing of VES fluids in real reservoir rock (carbonate and sandstone).
2
Section 2 explains the nature of VES fluids, their unique non-Newtonian behavior and the
3
potential for conformance control. The experimental process is outlined in section 3 and the
4
results are discussed in section 4.
5
2. Background
6
Enhanced oil recovery (EOR) strives to overcome the challenges associated with water-
7
flooding. Chemicals are typically added to the water to alter the properties and promote oil
8
mobilization. One particular class of chemicals in EOR are surfactants which are used for
9
reducing interfacial tension. However some categories of surfactants can also modify the
10
rheological behavior of the fluid in which they are dissolved. In particular, viscoelastic surfactant
11
solutions show non-Newtonian behavior.8,9 Worm-like micelles are formed at low concentration
12
in the presence of organic salts. They create a polymer-like complex network which alters the
13
structure of the fluid.10 Unlike polymers, worm-like micelles are not composed of unyielding
14
chains and can thus freely break and reform. The ability to self-heal gives them a significant
15
advantage during the injection stage into a reservoir where polymer might degrade.11
16
The use of VES fluids for mobility control in oil reservoirs has been investigated with
17
high-viscosity shear-thinning surfactant solutions.12 However, the rheological behavior of VES
18
fluids extends further than merely shear-thinning. When the surfactants are dissolved in a specific
19
dilute concentration range, they exhibit a unique shear-response. Experiments in Couette flow
20
showed that VES fluids can have a non-monotonic shear-thickening/shear-thinning response.13,14
21
The shear-thickening effect is caused by the formation of so-called shear induced structures (SIS)
22
associated with the worm-like micelles mentioned above. These long-range connections cannot
23
form under static conditions which explains the lower zero-shear viscosity.15 Once the shear rate
4 ACS Paragon Plus Environment
Page 4 of 27
Page 5 of 27
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Energy & Fuels
1
becomes too high the SIS structures are mechanically degraded and the viscosity drops (shear
2
thinning).
3
Pressure driven flow experiments show that viscosity is selectively increased in high
4
permeability zones. Darcy’s law (from which the apparent viscosity is derived) is, strictly
5
speaking, not valid for non-Newtonian fluids, however it can be applied to assess the apparent
6
deviation in response of the test fluid compared to the Newtonian base fluid in which the VES is
7
dissolved. We compare the flow velocities ( ) of base fluid (i.e. fluid such as water or brine into
8
which VES is dissolved) and the VES solutions velocity ( ) at identical pressure gradients
9
(figure 1) through a core of permeability . The reduction in flow rate represents a resistance
10 11
factor equivalent to the ratio of apparent to base fluid (brine) viscosities given by:15 =
=
(1)
12
Note that the resistance factor is different from the mobility ratio which is also used in EOR. The
13
mobility ratio uses the viscosity ratio between the displaced phase (oil) and the injected aqueous
14
phase to analyze the effect of viscous fingering.16 The resistance factor on the other hand gives
15
the added flow resistance when a non-Newtonian (in this case viscoelastic) fluid is used instead
16
of a conventional Newtonian fluid.
17
The resistance factor is used to compare flow resistance in high permeability ( ) and
18
low permeability ( ) cores. For Newtonian fluids = since the viscosity is constant and
19
thus independent of flow conditions. For VES fluids however it has previously been
20
demonstrated that > .17 This disparity in resistance factor between cores of different
21
permeability reduces the fluid lost through the preferential high permeability core. The resistance
22
factor cannot simply be calculated from a Couette sheared flow response which is at best
5 ACS Paragon Plus Environment
Energy & Fuels
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
1
indicative that a particular solution may be interesting for a test in permeable pressure driven
2
flow.
3
The resistance factor in pressure driven flow is thus not exclusively a result of the shear
4
response of the fluid.6 There are extra components such as viscoelastic effects which contribute to
5
the apparent viscosity. This effect has been extensively investigated for viscoelastic polymer flow
6
through porous media.18 Furthermore these viscoelastic contributions have been investigated in
7
flow through converging/diverging geometries19,20 and flow past confined cylinders.10 This work
8
concluded that at high flow rate the viscoelastic effect becomes dominant over the shear response
9
which enhances the apparent viscosity.
10
Previous work on VES fluids for conformance control showed that it is indeed possible to
11
utilize them to partially overcome reservoir heterogeneity. The surfactant cetyl ammonium
12
bromide (CTAB) in combination with an organic salt sodium salicylate (NaSal) shows the
13
desired behavior in porous flow.6 Hydrocarbons partially destroy worm-like micelles although
14
this can be overcome by increasing concentrations somewhat.21 The reservoir volumes where we
15
wish to increase viscosity i.e. those already swept highly permeable sections, are where the oil
16
content is already reduced to residual levels. These previous tests were performed in idealized
17
porous media made of sintered glass beads. The behavior of VES fluids for oil displacement in
18
real reservoir rock has not been investigated. In particular, as mentioned at the beginning of this
19
section, the surfactants have two effects – the desired selective viscous enhancement as well as
20
the more traditional EOR changes in interface tension. This means that the different wetting
21
responses of carbonates and sandstones are an issue and this is one of the key aspects of the
22
current study
23 24 6 ACS Paragon Plus Environment
Page 6 of 27
Page 7 of 27
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Energy & Fuels
1
3. Experiments
2
3.1
Materials
3
Two different types of porous rock cores are used to simulate a heterogeneous reservoir;
4
sandstone and carbonate. Sandstone rock is typically water-wet whereas carbonate rock is usually
5
oil-wet.22 The petrochemical properties of the different cores can be found in table 1. For both
6
sandstone and carbonate rock there are two cores with varying permeability to represent a
7
heterogeneous reservoir. The chemicals used for the experiments are a cationic surfactant cetyl tri-methyl
8 9
ammonium bromide (CTAB, ) and an organic salt sodium salicylate (NaSal,
!)
10
mentioned above. These were purchased from Sigma Aldrich at a purity of >99.0% and >99.5%
11
respectively. For two solutions synthetic seawater is used as a base fluid which was synthesized
12
by dissolving 3wt% sodium chloride (NaCl) in demineralized water. We denote a solution
13
containing " mM CTAB and # mM NaSal as an “"⁄#” solution. The following concentrations
14
were used: 2/2 and 6/4 in brine as well as 30/10 in demineralized water. The viscous response
15
and reproducibility of the different surfactant concentration VES fluids are tested in an Anton
16
Paar MCR 302 rheometer with a double gap measurement system. For two-phase experiments we
17
used decane ( ) with a purity of >99.0% purchased from Sigma Aldrich. The viscosity of
18
decane at room temperature is lower than the viscosity of the displacing phase. This reduces the
19
effect of viscous fingering and allows us to specifically target the effect of preferential flow.
20
3.2
Parallel core setup
21
The viscosifying potential of the VES fluids in a heterogeneous reservoir is simulated by
22
placing two cores of different permeability parallel to each other (figure 2). The reservoir rock
23
cores are placed inside the core-holder with a rubber sleeve wrapped around each. The sleeve is
24
radially pressurized to 6 bar by compressed air. This forces a tight seal between the rubber sleeve 7 ACS Paragon Plus Environment
Energy & Fuels
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
1
and the cores to ensure axial flow. The core-holders are positioned vertically in a controlled
2
temperature chamber to drive air out at the top and achieve maximum fluid saturation. VES fluid
3
is pumped through both cores by a dual piston QX 6000 HC Quizix pump (pump 1). The pressure
4
drop is measured by differential pressure transducers of type Rosemount 3051CD 4 (accuracy
5
0.1%). A second pump is used to saturate the cores with decane before performing a
6
displacement experiment. The effluent from both cores exits to fractional collectors.
7
Two distinct types of experiments can be performed using this setup. The first experiment
8
is performed to test the non-Newtonian response during single-phase flow of VES through
9
sandstone and carbonate cores of different permeability. During these experiments the cores are
10
tested individually. The second test is a parallel two-phase (VES and decane) displacement
11
experiment to test the recovery efficiency of the heterogeneous system.
12
Prior to each experiment the cores are placed in an oven at 250 ºC to ensure all fluids
13
inside the cores from previous experiments are evaporated. After the cores have cooled down
14
they are placed in the rubbers sleeves and positioned inside the core holder. The cores are then
15
flushed with CO to displace the air trapped inside the pores. Next, pump 1 saturates both cores
16
with brine. Then the brine permeability of the cores is determined by measuring the pressure drop
17
at 5 different flow rates and applying Darcy’s law. This is done before each experiment to ensure
18
the conditions have not changed due to prior experiments.
19
3.2.1
Single phase flow
20
The two cores represent two contrasting pathways in a reservoir between injector and
21
producer wells. One pathway is low resistance (high permeability) and the other is high resistance
22
(low permeability). For the single phase experiments, both cores are fully saturated with VES
23
without any hydrocarbon present. The pump is set to stepwise increase flow rate through each
8 ACS Paragon Plus Environment
Page 8 of 27
Page 9 of 27
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Energy & Fuels
1
core separately. At every point the resistance factor is calculated and the results of cores of
2
different permeability are compared (equation 1).
3
3.2.2
Hydrocarbon displacement
4
Prior to the displacement experiment, the brine filled cores are saturated with decane
5
injected from the top. During this saturation process effluent is collected and the displaced
6
volume of brine is a measure for the original oil in place (OOIP) inside both cores – denoted by
7
'(()* . After decane saturation the cores are left to soak for a period of 12 hours. Fluid is injected
8
into both cores simultaneously at identical pressure and decane is produced – a volume '(+, . The
9
recovery at any moment during the displacement process is:
10
/01
-. =
(2)
//23
11
-. is the combined hydrocarbon recovery from both cores. After break through, injected fluid
12
leaves the core as effluent. This effluent is primarily injected brine and no more oil is displaced.
13
Since flow rate will be highest in the high permeability core, this core will reach
14
breakthrough first. Note that the flow through this core continues until both cores have been fully
15
flushed. The injected fluid in the high permeability core does not contribute to the oil
16
displacement. The amount of injected fluid at any moment is represented by '45 . The volumes of
17
injection fluid used are often non-dimensionalised to the core pore volume 6'7,8 to give the
18
pore volumes of injected fluid
19
9'45 = φ:;<
(3)
=>1?
20
For this analysis 1 pore volume is defined as the combined void space of both cores. The results
21
are used to analyze the effectiveness of the VES fluids compared to a brine displacement. This is
22
particularly relevant when breakthrough is reached in both cores– we define this point as 9' ∗ .
23
Effective sweep of the parallel system of both cores is characterized by low values for 9' ∗ . 9 ACS Paragon Plus Environment
Energy & Fuels
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
1
4. Results and discussion
2
4.1 Single phase calibration
Page 10 of 27
3
The resistance factor (equation 1) of the 2/2 solution flowing through contrasting
4
permeability sandstone and carbonate cores is shown in figure 3. The 30 mD sandstone core has a
5
nearly constant resistance factor of = 2 (figure 3a). In this core the flow rate does not become
6
high enough for the VES fluid to become significantly viscoelastic. The 1600 mD sandstone core
7
on the other hand shows a clear increase in resistance to flow with pressure gradient caused by
8
the induced viscoelasticity of the fluid in that higher permeability rock sample. This leads to a
9
reduction in flow rate. For example, at 0.5 bar/m the flow rate of VES in the high permeability
10
core is reduced by = 10 compared to brine. By contrast, the flow of VES in the low
11
permeability core at 0.5 bar/m is reduced by only = 2 times compared to brine. Flow is thus
12
reduced more in the high permeability core decreasing the difference between the cores and
13
creating a more uniform flow profile.
14
The carbonate cores in single phase show similar results as the sandstone cores (figure
15
3b). Here the difference in permeability (20 mD vs 130 mD) is less. However there is still a
16
significant difference in resistance factor between the cores. At equal pressure gradient the
17
resistance factor in the 130 mD carbonate core is higher than in the 20 mD carbonate core. This
18
again leads to more flow reduction in the high permeability core which reduces the inequality in
19
flow rate between the cores. However we shall see below that differential wetting interferes with
20
this apparently favourable effect in carbonates. Note that the 130 mD carbonate core has a higher
21
resistance factor than the 1600 mD sandstone core. This can be attributed to differences in the
22
porosity of the cores. Carbonates have a wider range of pore sizes which increase the chance of
23
flow within the viscoelastic response region. That along with vugs and dead-end cavities lead to a
24
higher viscosifying effect even though the permeability is lower. 10 ACS Paragon Plus Environment
Page 11 of 27
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Energy & Fuels
1
The 2/2 solution clearly shows selective retardation in high permeability zones in single
2
phase. When applied to hydrocarbon displacement, previous work has shown that the
3
concentration of components needs to be increased in order to overcome lipophilic absorption
4
effects.7 6/4 solutions remained viscoelastic even when part of the surfactant molecules were
5
adsorbed into the hydrocarbon phase.7 Under only shear (in Couette flow) this solution is mostly
6
shear-thinning as shown in figure 4. By contrast, a 30/10 solution shows a more pronounced non-
7
monotonic initially shear-thickening and then shear thinning behavior. These solutions then form
8
the basis for subsequent two phase studies.
9
4.2 Hydrocarbon recovery
10
4.2.1 Sandstone
11
Figure 5 shows the hydrocarbon recovery -. as a function of injected pore volumes for
12
high and low permeability cores. For the brine base fluid case (grey diamonds), initially there is a
13
rapid increase in recovery due to the decane displaced from the high permeability core. The
14
recovery rate then drops significantly since the high permeability core is depleted and no longer
15
contributes to the total recovery. From this point on decane is predominantly recovered from the
16
low permeability core at a low rate. The high permeability core now serves as a thief zone
17
through which displacing fluid is lost. After injecting 10.3 PV of brine, breakthrough is reached
18
∗ in the low permeability core and both cores are fully flushed (i.e. 9'D,48 = 10.3).
19
Turning to the VES solutions, the 6/4 solution (open triangles) shows an improved
20
recovery curve compared to brine. The initial recovery curve is very similar since decane is
21
mainly displaced from the high permeability core. After breakthrough has occurred in the high
22
permeability core the local flow resistance gradually increases. This reduces fluid flow through
23
the high permeability core and thus less fluid is lost while flushing the low permeability core. The
24
30/10 solution shows an even better recovery curve. This is due to the increased surfactant 11 ACS Paragon Plus Environment
Energy & Fuels
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 12 of 27
1
concentration which results in faster formation of worm-like micelles in the presence of
2
hydrocarbons. As fig. 5 shows, the 30/10 solution required the least amount of PV to be fully
3
∗ ∗ ∗ flushed (i.e. 9'!/ < 9'I/ < 9'D,48 ).
4
Figure 6a shows that initially the resistance factor of the 6/4 solution is approximately
5
equal in both high and low permeability core. After enough VES is injected the resistance factor
6
in the high permeability core increases and selectively reduces the local flow rate. This effect is
7
gradual due to the adsorption of surfactants into the decane which become saturated when more
8
fluid is injected. We quantify this by α, the change of resistance factor per unit of injected pore
9
volume. Assigning the superscript hi and lo to high and low permeability rock respectively, we
10
note that at least in the beginning α !/ > α!/ ≈ αI/ ≈ αI/
11
There is reduced impact of hydrocarbon interaction for the 30/10 solution. More chemical
12
can be sacrificed in hydrocarbon interaction while leaving sufficient concentration to retain the
13
selective viscoelastic effect in high permeability rock. There are two effects here: first the high
14
permeability rock has reduced oil content due to prior flooding and secondly, there are more
15
surfactant molecules available to be “sacrificed” by hydrocarbon interaction while leaving
16
enough over to provide the flow induced viscoelastic effect.
17
4.2.2 Carbonate
18
Figure 7 shows the results of the displacement experiments in carbonate cores. We
19
compare these results with the sandstone core results (figure 5). Initial recovery rate is high
20
which is caused by decane displacement from the high permeability core. In contrast to sandstone
21
∗ cores, brine flooding requires the least amount of fluid to reach breakthrough. (9'D,48