Cyclic Steam Injection into the Subsurface - … · Diplomarbeit Cyclic Steam Injection into the...
Transcript of Cyclic Steam Injection into the Subsurface - … · Diplomarbeit Cyclic Steam Injection into the...
Universitat Stuttgart - Institut fur WasserbauLehrstuhl fur Hydromechanik und Hydrosystemmodellierung
Prof. Dr.-Ing. Rainer Helmig
Diplomarbeit
Cyclic Steam Injection into the Subsurface
- solarthermal steam generation for
enhanced oil recovery
Submitted by
Christoph Klinginger
Matrikelnummer 2195007
Stuttgart, 26th January 2010
Examiners: Prof. Dr.-Ing. Rainer Helmig, Dr.-Ing. Holger Class
Supervisor: Dr.-Ing. Andreas Bielinski
Contents
1 Introduction 1
1.1 Global Energy Demand and the Resource Oil . . . . . . . . . . . . . . 1
1.2 Enhanced Oil Recovery through SAGD . . . . . . . . . . . . . . . . . . 2
1.3 Solarthermal Steam Generation for SAGD . . . . . . . . . . . . . . . . 4
1.4 Scope of this Work . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
2 Fundamentals of the Applied Model 6
2.1 Essential Terms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
2.1.1 Phases and Components . . . . . . . . . . . . . . . . . . . . . . 6
2.1.2 Primary Variables . . . . . . . . . . . . . . . . . . . . . . . . . . 6
2.1.3 Secondary Variables . . . . . . . . . . . . . . . . . . . . . . . . 7
2.1.4 State of Aggregation and Phase Change . . . . . . . . . . . . . 7
2.2 Flow and Transport Processes . . . . . . . . . . . . . . . . . . . . . . . 8
2.2.1 Advection and Buoyancy . . . . . . . . . . . . . . . . . . . . . . 8
2.2.2 Diffusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
2.2.3 Mass Transfer Processes . . . . . . . . . . . . . . . . . . . . . . 10
2.2.4 Thermal Convection . . . . . . . . . . . . . . . . . . . . . . . . 10
2.2.5 Thermal Conduction . . . . . . . . . . . . . . . . . . . . . . . . 10
2.3 Mathematical Formulations . . . . . . . . . . . . . . . . . . . . . . . . 11
2.3.1 Mass Balance Equation . . . . . . . . . . . . . . . . . . . . . . . 11
2.3.2 Energy Balance Equation . . . . . . . . . . . . . . . . . . . . . 12
2.4 The 2p1cni Model . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
2.5 MUFTE-UG: The Numerical Simulator . . . . . . . . . . . . . . . . . . 13
3 System Properties 15
3.1 Physical Properties of Water and Steam . . . . . . . . . . . . . . . . . 15
3.1.1 Density and Viscosity . . . . . . . . . . . . . . . . . . . . . . . . 15
3.1.2 Water Saturation Pressure . . . . . . . . . . . . . . . . . . . . . 15
3.1.3 Enthalpy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
3.2 Physical Properties of the Porous Medium . . . . . . . . . . . . . . . . 19
3.2.1 Heat Capacity . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
3.2.2 Porosity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
I
CONTENTS II
3.2.3 Absolute Permeability . . . . . . . . . . . . . . . . . . . . . . . 20
3.3 Composite Properties . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
3.3.1 Relative Permeability . . . . . . . . . . . . . . . . . . . . . . . . 20
3.3.2 Capillary Pressure . . . . . . . . . . . . . . . . . . . . . . . . . 21
3.3.3 Heat Conductivity . . . . . . . . . . . . . . . . . . . . . . . . . 22
4 Simulations 24
4.1 The Model . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
4.1.1 Definition of the Model Domain . . . . . . . . . . . . . . . . . . 24
4.1.2 Initial and Boundary Conditions . . . . . . . . . . . . . . . . . . 26
4.1.3 System Property Values . . . . . . . . . . . . . . . . . . . . . . 26
4.1.4 Conditions at the Injection Well . . . . . . . . . . . . . . . . . . 27
4.2 Continuous Steam Injection . . . . . . . . . . . . . . . . . . . . . . . . 30
4.2.1 The Injection Well . . . . . . . . . . . . . . . . . . . . . . . . . 30
4.2.2 Steam Chamber and Temperature Development . . . . . . . . . 31
4.3 Cyclic Steam Injection . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
4.3.1 The Injection Well . . . . . . . . . . . . . . . . . . . . . . . . . 35
4.3.2 Steam Chamber Growth . . . . . . . . . . . . . . . . . . . . . . 36
4.3.3 Temperature Development . . . . . . . . . . . . . . . . . . . . . 39
4.4 Comparison of the two Injection Routines . . . . . . . . . . . . . . . . 41
4.4.1 Steam Chamber Growth . . . . . . . . . . . . . . . . . . . . . . 41
4.4.2 Temperature Development . . . . . . . . . . . . . . . . . . . . . 44
4.5 Sensitivity Study . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
4.5.1 Absolute Permeability K . . . . . . . . . . . . . . . . . . . . . . 56
4.5.2 Porosity Φ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
4.5.3 Specific Heat Capacity of the Soil Grains csg . . . . . . . . . . . 58
4.5.4 Heat Conductivity λpm . . . . . . . . . . . . . . . . . . . . . . . 59
4.5.5 Capillary Pressure pc and Van Genuchten Parameter α . . . 60
4.5.6 Results of the Sensitivity Study . . . . . . . . . . . . . . . . . . 60
5 Summary 61
5.1 Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
5.2 Outlook . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
List of Figures
1.1 Schematic sketch of oil sand reservoir and well arrangement . . . . . . . 3
1.2 Schematic sketch of steam chamber growth . . . . . . . . . . . . . . . . 3
2.1 Phase diagram of water . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
2.2 Phase states and mass transfer processes considered in the 2p1cni model 13
2.3 The numerical simulator MUFTE-UG . . . . . . . . . . . . . . . . . . . 14
3.1 Water saturation pressure curve . . . . . . . . . . . . . . . . . . . . . . 16
3.2 Specific enthalpy of liquid water . . . . . . . . . . . . . . . . . . . . . . 17
3.3 h-T relation of saturated steam . . . . . . . . . . . . . . . . . . . . . . 18
3.4 h-p relation of saturated steam . . . . . . . . . . . . . . . . . . . . . . 19
3.5 Relative permeability-saturation relation . . . . . . . . . . . . . . . . . 21
3.6 Capillary pressure-saturation relation . . . . . . . . . . . . . . . . . . . 22
3.7 Heat conductivity of a fluid filled porous medium . . . . . . . . . . . . 23
4.1 Model domain for the simulations . . . . . . . . . . . . . . . . . . . . . 25
4.2 Data retrieval nodes within the model grid . . . . . . . . . . . . . . . . 25
4.3 Seasonal and daily injection cycle . . . . . . . . . . . . . . . . . . . . . 29
4.4 p, T and Sg at the injection node for continuous injection . . . . . . . . 30
4.5 Steam chamber growth for continuous injection . . . . . . . . . . . . . 32
4.6 T distribution for continuous injection . . . . . . . . . . . . . . . . . . 33
4.7 T and Sg underneath the overburden for continuous injection . . . . . . 34
4.8 p, T and Sg at the injection node for cyclic injection . . . . . . . . . . . 37
4.9 Steam chamber growth for cyclic injection . . . . . . . . . . . . . . . . 38
4.10 T distribution for cyclic injection . . . . . . . . . . . . . . . . . . . . . 40
4.11 Sg for continuous and cyclic injection after 5 years . . . . . . . . . . . . 42
4.12 Sg for continuous and cyclic injection after 4 years and 5 months . . . . 43
4.13 T for continuous and cyclic injection after 5 years . . . . . . . . . . . . 45
4.14 Low T areas for continuous and cyclic injection after 5 years . . . . . . 46
4.15 High T areas for continuous and cyclic injection after 5 years . . . . . . 47
4.16 Propagation of various T fronts for continuous and cyclic injection . . . 48
4.17 p at Node2 and Node3 for continuous and cyclic injection . . . . . . . . 50
4.18 p distribution for continuous and cyclic injection . . . . . . . . . . . . . 51
III
LIST OF FIGURES IV
4.19 Tsat distribution for continuous and cyclic injection . . . . . . . . . . . 52
4.20 Sg at Node2 and Node3 for continuous and cyclic injection . . . . . . . 53
4.21 Model domain for sensitivity analysis . . . . . . . . . . . . . . . . . . . 54
4.22 Heat conductivity-saturation relation for the sensitivity analysis . . . . 55
4.23 T front propagation for continuous and cyclic injection with varying K 56
4.24 T front propagation for continuous and cyclic injection with varying Φ 57
4.25 T front propagation for continuous and cyclic injection with varying csg 58
4.26 T front propagation for continuous and cyclic injection with varying λpm 59
4.27 T front propagation for continuous and cyclic injection with varying pc 60
List of Tables
2.1 Phase states and corresponding primary varibales for the 2p1cni model 8
4.1 Data nodes implemented in the model grid . . . . . . . . . . . . . . . . 26
4.2 System property values . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
4.3 System property values and range for the sensitivity analysis . . . . . . 55
V
Nomenclature
symbol meaning dimension
∆Q change of heat [J ]
∆U change of internal energy [J ]
∆Wv volume changing work [J ]
E extensive property
Fres resulting force [N ]
Glin linear Gravity number [−]
H enthalpy [J ]
K intrinsic permeability [m2]
Kob intrinsic permeability of overburden [m2]
Kf hydraulic conductivity [m/s]
Re Reynolds number [−]
Sα saturation of phase α [−]
Se effective water saturation [−]
Sw water saturation [−]
Sw,r residual water saturation [−]
T temperature [C]
Tinitial initial temperature [C]
Tsat water saturation temperature [C]
U internal energy [J ]
V volume [m3]
Vpores pore volume [m3]
Vtotal total bulk volume [m3]
csg specific heat capacity solid phase [J/kgK]
cp specific heat capacity at constant pressure [J/kgK]
cv specific heat capacity at constant volume [J/kgK]
d mean pore diameter [m]
d depth [m]
e intensive quantity corresponding to property E
g gravitational constant [m/s2]
VI
Nomenclature VII
g gravitational vector
h piezometric head [m]
h specific enthalpy [J/kg]
hα specific enthalpy of phase α [J/kg]
hg,sat specific enthalpy of saturated steam [J/kg]
hwet specific enthalpy of wet steam [J/kg]
hw,sat specific enthalpy of saturated water [J/kg]
kr relative permeability [−]
kr,α relative permeability of phase α [−]
kr,n relative permeability of non-wetting phase [−]
kr,s relative permeability of steam [−]
kr,w relative permeability of wetting phase [−]
m mass [kg]
m Van Genuchten parameter [−]
mgaseous mass gaseous component [kg]
mliquid mass liquid component [kg]
n Van Genuchten parameter [−]
n outer normal vector
p pressure [Pa]
pα pressure of phase α [Pa]
patm atmospheric pressure [Pa]
pc capillary pressure [Pa]
pg gas phase (steam) pressure [Pa]
pw water phase pressure [Pa]
pw,sat water saturation pressure [Pa]
qc mass source/sink term
qcond conductive heat flux [W/mK]
qh energy source/sink term
qs steam mass flux [kg/sm2]
s entropy [J/K]
t time [s]
u specific internal energy [J/kg]
uα specific internal energy of phase α [J/kg]
v flow velocity [m/s]
v Darcy velocity [m/s]
vα velocity of phase α [m/s]
va,α seepage velocity of phase α [m/s]
vs steam velocity [m/s]
x steam quality [−]
z height [m]
Nomenclature VIII
α Van Genuchten parameter [1/Pa]
α phase α
Γ boundary of control volume domain
λ heat conductivity [W/Km]
λf heat conductivity of fluid phase [W/Km]
λi heat conductivity of material i [W/Km]
λpm equivalent heat conductivity of the porous medium [W/Km]
λs heat conductivity of solid phase [W/Km]
µ dynamic viscosity [kg/ms]
µα dynamic viscosity of phase α [kg/ms]
µs dynamic viscosity of steam [kg/ms]
ν kinematic viscosity [m2/s]
Ω domain of control volume
Φ porosity [−]
Φob porosity of overburden [−]
% mass density [kg/m3]
%α mass density of phase α [kg/m3]
%w mass density of water [kg/m3]
%b mass density of a body b [kg/m3]
%f mass density of a fluid f [kg/m3]
%sg soil grain density [kg/m3]
subscript meaning
α referring to phase α
atm referring to atmospheric conditions
b referring to body b
f referring to fluid f
g referring to gas phase
i referring to material i
initial initial conditions
n referring to non-wetting phase
ob referring to overburden
pm referring to porous media
s referring to steam
sat referring to saturated conditions
sg referring to solid phase
w referring to water phase
wet referring to wet conditions
Chapter 1
Introduction
1.1 Global Energy Demand and the Resource Oil
According to the International Energy Agency (IEA), the worldwide economic
downturn since the end of 2008, has lead to a drop in the global energy demand,
accompanied by decreasing CO2 emissions and energy investments. However, this
is assumed to be a short-dated development. On current policies, the global energy
demand would quickly resume its longterm upward trend, once economic recovery is
underway (IEA (2009) [14]). The worldwide primary energy consumption in 2008
was estimated to be 11.29Gt of oil equivalent (BP (2009) [4]), oil being the biggest
primary energy source with around 34 % or an amount of 3.93 Gt.
With no major changes in government policies and measures, fossil fuels are going to
be the dominant source of primary energy in the near future. Oil will thereby remain
the largest single fuel source, although its share is assumed to drop from 34% in
2009 to 30% in 2030. The oil demand is projected to grow 1% per year from 85 mb/d
(million barrels per day) in 2008 to 105 mb/d in 2030 (IEA (2009) [14]). With the
conventional oil production of non OPEC countries assumed to peak around 2010,
and the oil reserves to production ratio (R/P) being estimated at 42 years, the so-called
non-conventional oil deposits become economically more interesting (the R/P ratio is
an indication for the period the reserve will last assuming a constant consumption rate).
Low viscous oil determined by a relatively good ability to flow, is usually re-
ferred to as conventional oil. While highly viscous oil and oil bound to oil sand and
oil shale, thus being immobile, is defined as non-conventional oil. For this reason, the
oil density can be used to differ between conventional and non-conventional oils. Oil
with a density below 10 API (or above 1 g/cm3) belongs to the non-conventional oils
(BGR (2009) [2]).
Such non-conventional oil deposits include bitumen from oil sand and heavy oil, of
which vast reserves and resources are found in Alberta, Canada and the Orinoco
tar belt in Venezuela (Butler (1991) [5]). According to the German Federal
1
1.2 Enhanced Oil Recovery through SAGD 2
Institute for Geosciences and Natural Resources (BGR), reserves are defined as the
deposits geologically detected with a high accuracy and economically and technically
producible. Resources, are the deposits geologically proved but currently economically
not producible, and the deposits which have not been approved but are geologically
expected in a certain region.
The total oil in place of the world’s oil sands alone, is assumed to be 462Gt, with
188 Gt defined as reserves and resources. The estimated total oil in place in the
Canadian oil sands is 272Gt, of which 110 Gt are claimed to be reserves and resources.
The estimated amount of oil in place in the Venezuelan heavy oil fields (which accounts
for more than 97 % of the total heavy oil) is 240Gt. Thereof, 54 Gt are defined as
reserves and resources (BGR (2009) [2]). The total potential, or estimated ultimate
recovery (EUR), of conventional oil is thought to be 400Gt, with a remaining potential
of 249Gt (reserves and resources combined).
These numbers indicate the enormous potential of the described non-conventional
reservoirs, even though one is advised not to directly compare between such numbers.
This is because different authors and institutions use different definitions of the
terms conventional and non-conventional oil deposits or reserves and resources.
Furthermore, the quality of the energy data provided by sources, such as governments
and companies, is not necessarily reliable due to low transparency, economical and
political interests, and know-how, as well as technical limitations.
1.2 Enhanced Oil Recovery through SAGD
Highly viscous oil, such as heavy oil or bitumen from oil sand, may be recovered using a
special method of the enhanced oil recovery technologies, called steam-assisted gravity
drainage (SAGD). It was developed, to remove the oil in a systematic manner, in order
to realise a more complete recovery of the reservoirs than achieved in common steam-
flooding processes. The steam-assisted gravity drainage process has since emerged as
the most effective and most promising in-situ technology for the recovery of heavy oil
and bitumen from oil sand, buried too deep for surface mining (Nasr et al. (1998)
[19]).
Gravity is naturally present in the reservoirs and is used as the main driving force to
effect the oil movement. This way, differential fingering, occuring when viscous oils are
moved by pushing with a less viscous fluid, can be avoided (Butler (1991) [5]). The
process of SAGD generally involves drilling paired horizontal wells close to the reser-
voir bottom, one well a short distance above the other (5 m to 10m). The so-called
well pair is drilled to the desired reservoir depth, where it continues horizontically for
500m to 700m. Several such well pairs, lying parallel to each other, are drilled into
the deposit near the reservoir bottom (see figure 1.1).
1.2 Enhanced Oil Recovery through SAGD 3
injection
35m
well length appr. 500 − 700m
production
horizontal distance appr. 100m
vertical distance5m
well pair, consisting of a production and injection well
reservoirthickness
400mreservoir depth
overburden
cross−sectional area for 2d simulations
low permeable
y
xz
Figure 1.1: Schematic 3D sketch of the typical well arrangement for SAGD in an oil
sand reservoir.
The top well of a well pair is used, to continuously inject steam into the oil sand for-
mation, creating a steam chamber. Thereby, the steam pressure is usually maintained
at a constant value throughout most of the process. The growing steam chamber is
surrounded by colder oil sand. At the interface between the steam front and the porous
medium, steam condenses, transferring heat to the surrounding medium. The heated,
less viscous oil near the condensation surface drains, due to gravitational forces, to the
bottom well, where it is produced (see figure 1.2). As the oil and steam condensates
drain downwards, the steam chamber grows upwards and sideways (Butler (1991)
[5]).
Heated oil flows to production well
Oil and condensate drain
Growing steam chamber
Continuous steaminjection
into chamber
continuously
Figure 1.2: Vertical 2D slice through an oil sand reservoir including two well pairs.
Schematic sketch of the steam chamber growth from the injection well, and the oil and
condensate flow down towards the production well (Butler (1991) [5]).
1.3 Solarthermal Steam Generation for SAGD 4
The most dominant features for a successful SAGD operation are the geology and the
reservoir properties. The reservoir’s average pay zone depth should be above 15 m,
and characterized by a good vertical communication without any thief zones. Often
SAGD operations are compromised by insufficient steam supply. However, as long as
the steam chamber can grow, the ultimate recovery of a SAGD operation can be in
the order of 60% to 70% (Jimenez (2008) [16]).
Reservoir conditions, the production strategy and the depth and quality of the
oil deposit define the steam injection rate, which in turn determines the steam
injection pressure. A steam injection rate of around 180 t/d (tonnes per day) per well
pair is assumed to be realistic. At a steam pressure of around 40 bar and a steam
quality of approximately 90%, this equals an energy amount of 473GJ.
Producing one barrel of oil using the SAGD technology, three barrels of water
and the energy equivalent of 1/3 of a barrel of oil is needed. According to BGR (2009)
[2], 80% to 90 % of the water can be reused, due to recycling processes.
1.3 Solarthermal Steam Generation for SAGD
As described earlier, the long-term trend of the global oil demand is expected to be
increasing, while no major new discoveries of conventional oil deposits are made. The
so induced rising oil price and the vast potential of non-conventional oil deposits, such
as oil sand, has made the depletion of these less traditional reservoirs more interesting.
For instance, bitumen production from the oil sand fields of Alberta, Canada has
almost doubled from the year 2000 to 2007, according to BGR (2009) [2]. This is
followed by an increasing demand for gas, to produce steam for enhanced oil recovery,
as most of the oil from the Alberta oil sands needs to be produced in-situ. The use
of increasingly large amounts of fossil fuel for steam generation presents a number of
economic and environmental problems. Common steam generators emit large amounts
of greenhouse gases, and the increasing demand for natural gas is feared to influence
the regional natural gas market.
The motivation for this work is thus, the idea of using the energy of solar radi-
ation to generate and inject the steam needed for enhanced oil recovery purposes.
Solarthermal power plants use point (solar tower) or line (solar trough) focusing
systems consisting of mirrors, to concentrate direct solar radiation in terms of heat.
The captured thermal energy is used to generate steam, which in turn is used to
produce electricity. While line focusing systems are determined by a concentration
factor of up to 80 and operating temperatures up to 350 C, the concentration achieved
with point focusing systems is higher, and thus is the temperature (Voss (2005) [22]).
Usually, the solar energy is absorbed by a heat storage fluid, such as oil or molten
1.4 Scope of this Work 5
salt. Unlike conventional solarthermal power plants, solarthermal steam generation
for enhanced oil recovery, would require steam at mid-level temperatures, directly
generated with no intermediate heat storage fluid, and thus enhancing the overall
thermal efficiency of the system (Kraemer et al. (2008) [17]).
The result of a solarthermal steam generation process would be an intermittent steam
injection rate, with higher injection rates in comparison to the traditional continuous
injection process (assumption of same total energy input). Assuming the reservoir
formation acts as a large thermal accumulator, work on the economical implications of
cyclic steam injection in the SAGD process by Birrel et al. [3] suggests, that the
effect of daily and seasonal variations on the average bitumen production is negligible.
Based on this assumption, a feasibility assessment of a solarthermal driven SAGD
process from both, a thermodynamic and economical point of view, is presented in
Kraemer et al. [17].
1.4 Scope of this Work
It needs to be understood, that the work presented here does not describe the influ-
ence of an intermittent steam injection process on the oil production. It is in fact a
hydrodynamical study, analysing and explaining the influence of a cyclic steam injec-
tion process on the steam chamber growth and the temperature distribution in the
geological formation. The component oil is thus neglected in this work.
The fundamentals of the applied model, which are specified in chapter 2, determine
the model, which is used to describe the flow and transport processes for the water
steam system. The system properties, which complement the conceptual model, are
characterized in chapter 3.
As specified in chapter 4, the non-isothermal water steam model is used to simulate a
continuous and, based on the assumption of a solarthermal steam generation, a cyclic
steam injection process into water saturated porous media. The steam chamber and
temperature front propagation within the reservoir is analysed for both injection rou-
tines. To understand the consequences of a cyclic injection routine, its influence on the
flow and transport patterns is compared to a continuous injection process.
A summary of the topic, results of this work and an outlook for future work related to
this topic is presented in chapter 5.
Chapter 2
Fundamentals of the Applied Model
2.1 Essential Terms
2.1.1 Phases and Components
Phases are homogeneous, immiscible matter, separated by a sharp interface
(e.g. Helmig (1997) [12]). A phase is characterized by continuous fluid properties.
Thus, it is possible for several liquid phases to exist in a porous medium, while only
one gaseous phase can be present. The term phase is furthermore used to describe a
substance’s state of aggregation (see section 2.1.4), such as gaseous, liquid and solid.
This is, however, not a sufficient enough description within the context of a multi-phase
system, as several liquid phases such as water and oil may exist within the pores.
The term components describes the constituents of a phase. These can be regarded as
the sole chemical substances, which influence the physical properties of a phase.
2.1.2 Primary Variables
Primary variables are parameters defining physical properties of a system, and are used
to describe the degrees of freedom of a thermodynamical system. They are needed for
a definite solution of the system of equations, which describes the applied model. The
choice of primary variables is not explicit. Hence, a different set of primary variables
may be chosen for the same system.
The non-isothermal water steam model discussed in this work, is described by two
equations (one mass and one energy balance). The two unknowns pressure p and tem-
perature T or pressure p(T ) and water saturation Sw (see equation 2.11 and 2.12) are
used as primary variables (see also table 2.1).
It is usually dinstinguished between extensive and intensive variables. Extensive vari-
ables depend on the size of a system. Examples are the volume V or the mass m. In
contrast, intensive variables are independent of the system’s size, such as the temper-
ature and the pressure.
6
2.1 Essential Terms 7
2.1.3 Secondary Variables
Secondary variables can be calculated from the primary variables, using constitutive
relationships and equations of state (e.g. Ochs (2006) [20]). These secondary pa-
rameters depend on the primary variables and help to describe the considered system
in detail. Examples are the density %, the viscosity µ, the capillary pressure pc, the
relative permeability kr, the specific enthalpy h, and the heat conductivity λ.
2.1.4 State of Aggregation and Phase Change
As mentioned before, a substance such as water may occur in different states of aggre-
gation. These phase states may be solid, liquid and gaseous. The component’s transfer
between different phases, due to the change of the thermodynamic state (e.g. by vapor-
ization, condensation), is called phase transition (e.g. Helmig (1997) [12]). A phase
diagram shows a substance’s state of aggregation as a function of state variables. Such
a phase diagram is given in figure 2.1, describing the phase state of water, depending
on the primary variables pressure and temperature.
pressure p [bar]
critical point
0.00612
1
221
triple point
0
solid
gaseous
liquid
100 374.25Temperature T [°C]
Figure 2.1: Schematic phase diagram of water for temperature and pressure.
The number of existing phases in a multi-phase system is not necessarily constant.
Displacement processes or mass transfer processes between the phases may result in a
phase state change from a single-phase to a multiphase system or vice versa (Helmig
(1997) [12]). Such a process is called a phase change and may be accompanied by a
switch of the primary variables that are necessary to describe the system.
2.2 Flow and Transport Processes 8
In the non-isothermal two-phase one-component model (2p1cni) used in this work,
water is the only component. Consequently, the total amount of primary variables
sufficient to describe the state of the system is two. Depending on the present phases
within the system, the used set of primary variables consists either of gas phase pressure
pg and water saturation Sw (two-phase system), or gas phase pressure pg and temper-
ature T (single-phase system) (Ochs (2006) [20]). This primary variable switch is
shown in table 2.1.
phase state present phases primary variables
1 water, gas pg(T), Sw
2 water pw, T
3 gas pg, T
Table 2.1: Phase states and corresponding set of primary variables for the 2p1cni
model.
2.2 Flow and Transport Processes
A steam injection process into water saturated porous media may be described by
a non-isothermal two-phase one-component system. Therefore, a description of the
various flow, transport and energetic processes, that have to be considered, is given in
the following section.
2.2.1 Advection and Buoyancy
The process of advection is associated with the movement of a quantity within the
vector field of a fluid. An example in porous media would be the transport of a compo-
nent’s concentration according to the fluid’s velocity field. Darcy’s Law, emerging from
a series of experiments in a permeameter column, describes the slow linear single-phase
flow through porous media on a macroscopic scale (Darcy (1856) [8]). It states:
v = −Kf grad(h). (2.1)
Here, v is the Darcy velocity, h is the piezometric head and Kf is the hydraulic con-
ductivity of water with
K = Kfµ
%g, (2.2)
where K is the absolute permeability, µ the dynamic fluid viscosity, % the fluid’s density
and g the gravitational constant.
Darcy’s Law is valid for seeping flow with a Reynolds number (Re) smaller than 1. The
2.2 Flow and Transport Processes 9
dimensionless Reynolds number in a porous medium describes the ratio of inertial to
viscous forces and is given by:
Re =dv
ν. (2.3)
Here, d is the mean pore diameter, v is the typical flow velocity and ν the kinematic
viscosity of the fluid.
To determine the advective flux within a multiphase system, Darcy’s Law has
to be extended for various phases α. The consideration of the phase density %α, the
phase pressure pα, the relative permeability kr,α of the phase, the phase’s dynamic
viscosity µα, the intrinsic permeability K and the gravitational vector g with the
constant g, yields the velocity of the individual phase vα:
vα = −kr,α
µα
K(grad(pα)− %αg
). (2.4)
The so-called Darcy velocity vα of the phase α refers to a flow through the total cross-
sectional area of the porous media. To calculate the actual particle speed, the porosity
Φ of the medium needs to be considered. This yields the seepage velocity va,α of the
phase α:
va,α =vα
Φ. (2.5)
The extended version of Darcy’s Law for multiphase systems, describes fluid flow pro-
cesses due to viscous (advection) and buoyant forces.
Buoyancy flow is caused by density differences within one phase (e.g. cold and hot
water) or between different phases (e.g. water and steam). It acts in the opposite di-
rection of gravitational forces.
Consequently, a balance of forces in vertical direction for a body with density %b,
submerged in a fluid with density %f yields:
Fres = buoyant forces− gravitational forces = (%b − %f) gV. (2.6)
In the case of steam injection into water saturated porous media this results in a
buoyant flow, driven by the high density difference between liquid water and steam. At
a pressure of 40 bar and a temperature of 250.35 C, the density of water is 798.37 kg/m3,
whereas the density of fully saturated steam is 20.09 kg/m3.
Therefore, buoyancy driven flow is suspected to play an important role in the context
of steam injection into water saturated porous media (Ochs (2006) [20]). Assuming
a hydrostatic pressure distribution in the system (h = p%g
+ z = const.), leads to the
pressure gradient in z-direction:
grad(pw) = %wg. (2.7)
Combining equation 2.7 with equation 2.4 for the Darcy velocity, results in the steam
velocity:
vs = −kr,s
µs
Kg (%w − %s) . (2.8)
2.2 Flow and Transport Processes 10
Equation 2.8 describes the buoyant flow of steam, in the opposite direction of the grav-
itational vector, driven by the density difference between steam and liquid water. The
comparison of equation 2.8 with equation 2.4 clearly indicates the difference between
advection and buoyancy.
2.2.2 Diffusion
The transport process of diffusion occurs continuously, independent of the fluid’s move-
ment. It originates from arbitrary Brownian movement of the molecules and corre-
sponds to the second law of thermodynamics which states, that the state of order of
any closed system decreases until equilibrium is reached (e.g. Ochs (2006) [20]).
As the system described only consists of the one component water, the process of
diffusion is neglected. This can be justified, as the influence of diffusion within one-
component systems is very small in comparison to multi-component systems (Corey
et al (2009) [7]).
2.2.3 Mass Transfer Processes
The multiphase one-component model described in this work, contains the two phases
water and steam. Both consist of the one present component water. A mass transport
between the phases, hence only occurs in terms of evaporation and condensation (see
figure 2.2).
2.2.4 Thermal Convection
The transport of thermal energy through bulk motion of a fluid is called thermal or
heat convection. Depending on its origin, it is distinguished between free and forced
convection. Forced convection is characterized by a fluid motion, that is induced by
external forces, such as during steam injection. Free or natural convection occurs
when temperature gradients, and respectively density differences, cause recirculation
processes within the fluid.
For most thermal recovery applications, forced convection is the dominant form of
heat transfer (Hong (1994) [13]). In porous media, the rate of heat transport through
convection is a function of the fluid-flow rate and the thermal properties of the fluid
and the reservoir. This type of thermal convection is described through an energy
balance on the flowing fluid, as the specific phase enthalpy is considered within the
advection term (see equation 2.12).
2.2.5 Thermal Conduction
Another important energy transfer process is thermal or heat conduction. Thermal
conduction is a diffusive process, caused by a temperature gradient. It is the result of
2.3 Mathematical Formulations 11
an energy transfer from high energetic molecules to less energetic ones. During steam
injection into a reservoir, thermal conduction is responsible for energy losses to the
overburden and the underlying strata (Hong (1994) [13]). It can also be an important
heat transfer process within the reservoir, when fluid flow velocities are small.
According to Fourier’s Law, one-dimensional stationary conductive heat transfer
is described by the following equation:
qcond = −λi grad(T ). (2.9)
The energy flux related to an area is given by qcond, with the unit J/s m2. The thermal
conductivity λi, is the ability of the material i to transmit heat. It is not only a material
property, but also depends on the geometry and composition of the system described,
as discussed in detail later.
2.3 Mathematical Formulations
In order to specify the depicted non-isothermal two-phase one-component system math-
ematically, the conservation laws of mass and energy are needed. In fluid dynamics,
the Reynolds Transport Theorem (RTT) is used to formulate these basic conservation
laws (see equation 2.10). It states that the total rate of change of an extensive system
property E equals the rate of change of its corresponding intensive quantity e within a
fixed control volume (CV), plus the net rate change across its boundaries (e.g. Ochs
(2006) [20]).dE
dt=
∫
Ω
∂(%e)
∂tdΩ +
∫
Γ
(%e)(v · n)dΓ. (2.10)
Using the RTT and considering an infinitesimal small CV, a differential formulation
for the conservation of a quantity E (e.g. mass) can be derived. A detailled description
of this process is given in Ochs (2006) [20]. The additional consideration of the pore
space and the phase saturation of the porous multiphase system, yields the balance
equations for each phase.
For the solution of the multiphase problem, the multiphase extension of Darcy’s
Law, as given in equation 2.4, is usually used to calculate the phase velocity vα
(e.g. Helmig (1997) [12]).
2.3.1 Mass Balance Equation
Based on the conservation law of mass, which states ∂%∂t
+ div(%v) = 0, the balance
of mass is formulated for each component, inserting equation 2.4 for the velocity v.
Consequently, any mass transfer from one phase to the other can be accounted for
(e.g. Class (2001) [6]).
2.3 Mathematical Formulations 12
In case of the depicted two-phase one-component model, the formulation of one mass
balance equation, for the one component water is necessary (e.g. Ochs (2006) [20]):
φ
∂∑α
(%αSα)
∂t︸ ︷︷ ︸accumulation term
−∑
α
div
%α
kr,α
µα
K(grad(pα)− %αg
)
︸ ︷︷ ︸advection term
− qc
︸︷︷︸source/sink term
= 0, α ∈ water, steam (2.11)
with the constant porosity Φ, phase density %α, phase saturation Sα, relative perme-
ability kr,α of phase α, dynamic viscosity µα of phase α, the intrinsic permeability K
and the phase pressure pα.
2.3.2 Energy Balance Equation
The first law of thermodynamics states, that in a physical process, energy can not be
lost but only be transferred from one state to another. In order to describe the energy
transfer in a multiphase system, the balance of energy is formulated, as it is done with
mass (e.g. Class (2001) [6]).
The change of a system’s internal energy ∆U equals the change of heat ∆Q across
the system boundaries plus the work ∆Wv done by change in volume. Assuming local
thermodynamic equilibrium, only one single energy balance equation is necessary to
describe the system (e.g. Ochs (2006) [20]).
φ
∂∑α
(%αSαuα)
∂t︸ ︷︷ ︸accumulation term fluid
+ (1− φ)∂ (%sgcsgT )
∂t︸ ︷︷ ︸accumulation term solid
− div(λpm grad(T )
)
︸ ︷︷ ︸conduction term
−∑
α
div
%αhα
kr,α
µα
K(grad(pα)− %αg
)
︸ ︷︷ ︸convection term
− qh
︸︷︷︸source/sink term
= 0 α ∈ water, steam (2.12)
2.4 The 2p1cni Model 13
In equation 2.12, radiation is neglected, uα is the specific internal energy of phase
α, hα is the specific enthalpy of phase α, %sg and csg are the soil grain den-
sity and the specific heat capacity of the solid medium, λpm is the equivalent heat
conductivity of the system (porous medium including fluids), and T is the temperature.
To solve the partial differential balance equations, the following closure relationships
are necessary:
− The sum of the phase saturations adds up to one:∑α
Sα = 1.
− The sum of the pressure of the wetting phase and the capillary pressure equals
the pressure of the non-wetting phase: pw + pc = pg.
2.4 The 2p1cni Model
For the process of steam injection into the water saturated subsurface, a heterogeneous
system, containing the two phases liquid water (water phase) and gaseous water (steam
phase), is assumed. Hence, a non-isothermal two-phase one-component model (2p1cni),
with each phase itself consisting of the one component water, is described in this work.
The occuring mass transfer processes for the system are shown in figure 2.2.
waterCondensation
Evaporation
water
water phase (liquid water) steam phase (gaseous water)
Figure 2.2: Mass transfer processes in the two-phase one-component (2p1cni) model
for the two phases water and steam.
2.5 MUFTE-UG: The Numerical Simulator
In this work, MUFTE-UG is used as the numerical simulator. It stands for Multiphase
Flow Transport and Energy Model on Unstructured Grids. As shown in figure 2.3,
it consists of two parts. The MUFTE part of the simulator describes the physical
problems and the discretisation method of the system (Helmig et al. (1998) [11]).
The UG part with its multigrid data structures, grid refinement techniques and the
numerical solvers deals with the partial differential equations (Bastian et al. (1997)
[1]). MUFTE-UG in this work, solves the problem of multi-phase one-component non-
isothermal flow processes in a geological formation.
2.5 MUFTE-UG: The Numerical Simulator 14
(Helmig et. al 1997, 1998)
(Bastian et. al 1997, 1998)(S. Lang, K. Birken, K. Johannsen et. al 1997)
- multigrid data structures- local grid refinement- solvers (multigrid, etc)
- parallelization- r,h,p-adaptive methods
- graphic representation- user interface
UG (Wittum, Bastian)
Interdisciplinary Center for Scientific Computing (IWR)
- problem description
- discretization methods- physical-mathematical models
- physical interpretation- refinement criteria- numerical schemes
- constitutive relationships
MUFTE (Helmig)
Institute for Hydraulic Engineering (IWS)
Figure 2.3: The numerical simulator MUFTE-UG
Chapter 3
System Properties
3.1 Physical Properties of Water and Steam
3.1.1 Density and Viscosity
The molar density of water is implemented after Panday et al. (1995) [21] and is
a function of temperature and pressure. While the density of the liquid water phase
is assumed to remain constant with changing temperature, the density of the gaseous
water phase (steam) decreases with increasing temperature. Increasing pressure pw,
respectively pg, results in an increase of density for both phases, water and steam.
The dynamic viscosity of water is only determined by the temperature. Unlike the
viscosity of the liquid water phase, which decreases with increasing temperature, that
of the steam phase increases (e.g. Helmig (1997) [12]).
3.1.2 Water Saturation Pressure
The water saturation pressure, or vapor pressure pw,sat is a function of temperature,
and is implemented in the model after the IFC report (IFC (1967) [15]). In terms of
a closed system, it describes the pressure of the gaseoues phase (steam) in equilibrium
with its liquid phase (water) at a certain temperature. It is the pressure, at which the
amount of condensing water molecules equals that of the evaporating ones (e.g. Faer-
ber (1997) [10]).
Figure 3.1 shows the water saturation pressure as a function of temperature, as imple-
mented in the model. The water saturation pressure-temperature relationship is used
to determine the occurence of a second phase within the model, accompanied by a
primary variable switch (for details see section 2.1.4).
For gas being the only phase present, and pg ≥ pw,sat, the water phase appears. For
water being the only phase present, and pg ≤ pw,sat, the gas phase appears.
15
3.1 Physical Properties of Water and Steam 16
Figure 3.1: Water saturation pressure depending on temperature. As implemented in
the model.
3.1.3 Enthalpy
The amount of energy within a system capable of doing mechanical work, is called
enthalpy H. It is defined as the sum of the system’s internal energy U and the volume
changing work pV (e.g. Helmig (1997) [12]). The division by the system’s mass yields
the specific enthalpy: h = u + p%.
The specific enthalpy of water is implemented after IFC (1967) [15]. While the spe-
cific enthalpy of gaseous water (steam) strongly depends on the volume changing work,
the definition of the specific enthalpy of liquid water often neglects this correlation, as
a result of the low compressibility of water: h ≈ u.
Figure 3.2 shows the specific enthalpy of liquid water depending on temperature (con-
stant pressure) and pressure (constant temperature). It is observed, that the specific
enthalpy of water is more dependent on temperature than on pressure.
3.1 Physical Properties of Water and Steam 17
(a) h-T relation of liquid water at constant p
(b) h-p relation of liquid water at constant T
Figure 3.2: Specific enthalpy of liquid water as a function of temperature at constant
pressure, and as a function of pressure at constant temperature. As implemented in
the model.
3.1 Physical Properties of Water and Steam 18
Defining the specific enthalpy of steam, it is theoretically distinguished between wet
steam, saturated steam and overheated steam. While wet and saturated steam are
determined through the parameters temperature T (p) and steam quality x, the specific
enthalpy of overheated steam is a function of T and p. The steam quality parameter
x is a mass ratio, defined as: x = mgaseous
mliquid+mgaseous.
Steam at boiling temperature, consisting of gaseous and liquid water (0.0 < x < 1.0)
is called wet steam. Steam at boiling temperature, containing 100% gaseous water
(x = 1.0) is called saturated steam. Steam that consists of 100 % gaseous water with
a temperature above boiling point is called overheated steam.
For the given process of steam injection into saturated porous media, it is high
quality wet steam occupying the pore space besides water. Overheated steam
would require higher temperatures. The specific enthalpy of wet steam hwet is
calculated, using hw,sat of saturated water and hg,sat of saturated steam at boiling
temperature, and combining it with the steam quality x: hwet = (1−x)·hw,sat+x·hg,sat.
The specific enthalpy of saturated steam as a function of temperature T , as im-
plemented in the model, is shown in figure 3.3. For more details see the Mollier
h,s-Diagram (Langeheinecke et al. (2003) [18]).
Figure 3.3: Specific enthalpy of saturated steam (x = 1.0) as a function of temperature.
As implemented in the model.
3.2 Physical Properties of the Porous Medium 19
Figure 3.3 indicates, that a pressure, respectively temperature increase only results in
an increased specific enthalpy for saturated steam up to a certain point. With pres-
sure, respectively temperature exceeding this point, a decrease in enthalpy is observed.
This is depicted schematically in figure 3.4. It is pointed out here, that the pressure,
respectively temperature to be exceeded for the enthalpy decrease depends on the
steam quality. With lower steam quality, a higher pressure, respectively temperature
is needed to cause the decline of the specific enthalpy. See the Mollier h,s-Diagram
(Langeheinecke et al. (2003) [18]) for more details.
pressure p [bar]
221critical point
saturated steamwet steam
saturated water
100°C
10
50
1
spec. enthalpy h [kJ/kg]
Figure 3.4: Schematic plot of the specific enthalpy of water as a function of pressure.
3.2 Physical Properties of the Porous Medium
3.2.1 Heat Capacity
The specific heat capacity of a material, is a measure of how much thermal energy
must be added to heat up 1 kg of the material by one Kelvin. The unit is kJ/kg K. The
heat capacity thus describes a substance’s ability to store heat. A body determined by
a high specific heat capacity stores heat well. In thermodynamics, it is distinguished
between the specific heat capacity cp at constant pressure, and cv at constant volume.
In terms of equation 2.12, the energy content of the fluid phase is calculated using
the specific internal energy u. The energy storage term of the solid phase however, is
calculated using the specific heat capacity of the soil grain material csg. As cp ≈ cv for
solid substances, a constant value, independent of pressure and temperature is used for
csg.
3.3 Composite Properties 20
3.2.2 Porosity
The porosity Φ is defined as the ratio between the pore volume and the total bulk
volume of the porous media: Φ = Vpores
Vtotal.
It is a measure of the volume not filled with soil grains but fluids, such as liquid water
and steam. It is furthermore distinguished between porosity and effective porosity,
which describes the pore space accessible for a fluid entering the porous medium.
3.2.3 Absolute Permeability
The absolute or intrinsic permeability K of a porous medium describes the resistance
that the material opposes to fluid flow. The unit is m2 or D, with 1 D ≈ 10−12 m2. As
given in equation 2.2, it is only dependent on the properties of the porous medium,
because it is correlated to the hydraulic conductivity Kf by including the fluid’s vis-
cosity and density. For the computation of multiphase flow as shown in equation 2.11,
the hydraulic conductivity is extended with the relative permeability kr,α of phase α
(e.g. Helmig (1997) [12]):
Kf = K kr,α%αg
µα
. (3.1)
While the intrinsic permeability K is solely a property of the soil grains, the relative
permeability is dependent on the fluid and the porous medium properties (for details
see section 3.3.1).
3.3 Composite Properties
Along the fluid and soil properties, additional parameters combining fluid and porous
medium properties are needed to describe the multiphase system. As these parameters
can neither be assigned solely to the porous medium, nor to the fluid occupying the
pore space, they are called composite properties here. They result from the interaction
between the fluid and the porous medium and are no conventional system properties.
Composite properties reflect the conceptual model, that is used to reproduce the system
behavior (Ochs (2006) [20]).
3.3.1 Relative Permeability
The relative permeability is a dimensionless number depending on the tortuosity of
the porous media, pore space geometry and phase saturation. It is used to scale the
intrinsic permeability (see equation 3.1), with the product of K and kr,α being called
the effective permeability of phase α (e.g. Helmig (1997) [12]). The introduction of
kr,α accounts for the fact, that in a multi-phase system, the presence of one phase in a
porous medium influences the flow of the other phase.
In the model, the relative permeability-saturation relations of the two phases water and
3.3 Composite Properties 21
steam are implemented after Van Genuchten, as shown in figure 3.5. With water
representing the wetting phase and steam being the non-wetting phase, the relative
permeabilities are calculated as follows:
kr,w =√
Se[1− (1− S1me )m]2
kr,n = (1− Se)13 [1− S
1me ]2m. (3.2)
The parameter m results from the definition of the effective water saturation Se as a
function of the capillary pressure pc after Van Genuchten:
Se(pc) =Sw − Sw,r
1− Sw,r
= [1 + (α · pc)n]m, (3.3)
with the water saturation Sw, the residual water saturation Sw,r, and m, n and α as
the three Van Genuchten parameters (see also section 3.3.2).
Figure 3.5: Relative permeability of the wetting phase (water) and of the non-wetting
phase (steam) as a function of the water saturation after Van Genuchten. As im-
plemented in the model.
3.3.2 Capillary Pressure
Considering two immiscible fluid phases in a state of equilibrium, a pressure difference
at the interface between the wetting and non-wetting phase occurs. It originates from
3.3 Composite Properties 22
molecular cohesion effects, which cause a surface tension at the interface. The resulting
pressure difference depends on the pore space geometry and the phase saturation, and
is called capillary pressure pc. In the model, it is calculated using the approach of Van
Genuchten (e.g. Class (2001) [6]), as depicted in figure 3.6.
pc =1
α(S
− 1m
e − 1)1n . (3.4)
With m = 1 − 1n, the two Van Genuchten paramaters α and n emerge. The pa-
rameter α describes the entry behaviour of the non-wetting phase, and the parameter
n describes the material’s uniformity, with a low value for n being associated with a
non-uniform material. The effective saturation Se is defined as given in equation 3.3.
Figure 3.6: Capillary pressure as a function of the water saturation after the approach
of Van Genuchten, with α set to 0.0028 1/Pa and n set to 4.0 . As implemented in
the model.
3.3.3 Heat Conductivity
The heat conductivity λ is a parameter combining fluid and soil grain properties with
respect to equation 2.12. It describes the averaged ability of the fluid filled porous
media to conduct heat. It is implemented after the approach of Somerton, as shown
in equation 3.5 (e.g. Class (2001) [6]).
λpm = λSw=0pm +
√Sw(λSw=1
pm − λSw=0pm ) (3.5)
3.3 Composite Properties 23
In this case, the definition of the effective heat conductivity λSw=1pm for the fully water
saturated and λSw=0pm for the fully steam saturated porous media is necessary. In terms
of steam, saturated steam with a steam quality of x = 1.0 is assumed. To obtain the
needed effective heat conductivities, an average of the heat conductivity λsg for the
soil grains and λf for the fluids (λSw=1pm for water and λSw=0
pm for steam) needs to be
determined. Here, the conservative method of the geometric mean is used:
λpm = λ(1−φ)sg · λφ
f . (3.6)
With λsg assumed to be 2.5 W/m · K (Quartz), the value of λSw=1f (liquid water) being
0.621 W/m K and that of λSw=0f (steam) being 0.051 W/m K . This yields a λpm as a
function of the water saturation calculated after equation 3.5, as shown in figure 3.7.
Figure 3.7: Heat conductivity as a function of water saturation. Approach of Somer-
ton, using the method of the geometric mean to calculate the effective heat conduc-
tivities for the fully water, and fully steam saturated porous media. As implemented
in the model.
Chapter 4
Simulations
Using a non-isothermal two-phase one-component model, described in Ochs (2006)
[20], steam injection into a water saturated system is simulated. The influence of a
cyclic injection routine on the steam chamber growth and the temperature distribution
within the porous medium is analysed, and compared to the process of a continuous
injection.
To determine the influence of the system properties on the simulation results, a
sensitivity study is carried out. Therefor, a set of porous medium and composite
properties, assumed to be most relevant for the depicted process, is chosen. Each
parameter is then seperately examined to determine its influence on the flow processes
in the geological formation.
4.1 The Model
4.1.1 Definition of the Model Domain
The development of the steam and temperature front along the horizontal injection
well, such as described in section 1.2, is assumed to be constant. Therefore, the steam
and temperature front development is depicted using a two-dimensional model, that
represents a vertical y-z slice through the inner reservoir area, with a thickness in x-
direction of 1m (see figure 1.1).
This results in the model domain shown in figure 4.1. The vertical model extension of
40m represents the full assumed reservoir height of 35 m, plus a 5m thick, low perme-
able overburden on top. The horizontal extension is chosen to include an equal area
to the left and right of the well pair, and is set to 120 m. This is, because the distance
between two well pairs of 100m leads to the assumption, that at 50m to the left and
right of the injection well, the steam front would link up with that of a neighbouring
well with the same injection routine.
Only the steam injection well (upper well of a well pair) is implemented in the model.
24
4.1 The Model 25
It is located 8 m above the reservoir bottom, in the middle of the reservoir at x = 60m
(see figure 4.1).
The grid discretization of the model domain is set to 0.5m, resulting in elements of
0.25m2. This allows for a satisfying computation speed, while providing reliable sim-
ulation results, and is the conclusion of simulations with different grid discretizations,
to analyse the grid sensitivity.
To retrieve detailed information on the system properties for certain areas within the
model domain, seven data nodes are implemented at various locations in the grid (see
figure 4.2 and table 4.1).
35m
120m
Sw(initial) = 1.0
400m belowsurface
hydrostatic pressure
distribution
hydrostatic pressure
distribution
left boundary:
injection well 8m above bottom boundary
reservoir
low permeable overburden 5m
p(y=360) = 37bar
p(y=400m) = 41bar
right boundary:
T (initial) and T (initial) and
y
x
top boundary: constant temperature and pressure
bottom boundary: no−flow conditions
T(initial) = 10°C
Figure 4.1: The model domain and its initial and boundary conditions as used for the
simulation of continuous and cyclic steam injection.
Figure 4.2: The model domain consisting of the permeable reservoir and the low per-
meable overburden. Locations of the data nodes implemented to retrieve information
on the system properties, as given in table 4.1.
4.1 The Model 26
designation x [m] y [m]
Node1 60.0 1.0
Node2 60.0 8.0
Node3 60.0 20.0
Node4 60.0 34.5
Node5 30.0 34.5
Node6 90.0 34.5
Node7 60.0 38.0
Table 4.1: Node names and coordinates of the seven nodes implemented in the model
grid.
4.1.2 Initial and Boundary Conditions
A reservoir depth of 400 m at the reservoir bottom is assumed. This determines the ini-
tial reservoir temperature and the pressure distribution (see figure 4.1), and is referring
to conditions found in the Canadian oil sand fields.
− The domain is assumed to be initially fully water saturated: Sw = 1.0.
− The initial reservoir pressure is given by a vertical hydrostatic pressure distribu-
tion, using p = patm + d · %w · g. With patm assumed to be 1.013 bar and d as the
total depth in meter.
− The initial temperature Tinitial is assumed to be 10 C. A vertical temperature
distribution, according to the geothermal temperature gradient (estimated to be
0.03 C/m), is neglected because of the reservoir being only 35m in height.
− The bottom boundary of the domain is determined by a no-flow condition. The
right, left and upper boundary of the domain is characterized by the temperature
and pressure of the initial situation. The definition of the upper boundary con-
dition in combination with the very low permeable overburden, accounts for the
fact, that while thermal energy can be lost from the reservoir into the overburden
by conduction, no relevant flux of water or steam into the overburden is possible.
4.1.3 System Property Values
The system properties described in detail in chapter 3 are either defined by a constant
value, or as a function of the primary variables, often including empirically derived
parameters. Only those properties, respectively parameters, associated with a constant
value are given in table 4.2. For details on the remaining parameters see chapter 3.
4.1 The Model 27
The porosity Φob and absolute permeability Kob are properties of the overburden and
account for the difference in permeability between the reservoir and overburden.
The values of the porosity and permeability of the reservoir are chosen to be rather
low in comparison to observed field data from Canadian oil sand fields. This is, to
account for the fact, that the presence of an oil phase in reality leads to a decrease
of the relative permeability of water. This procedure is random, but is considered to
be a first good approach to the problem. Furthermore, the sensitivity of the absolute
permeability is discussed in detail in section 4.5.1.
parameter value unit
specific heat capacity csg 850 J/kg K
porosity Φ 0.1 -
porosity Φob 0.05 -
absolute permeability K 40 mD
absolute permeability Kob 0.0001 mD
soil grain density %sg 2650 kg/m3
Van Genuchten parameter α 0.0028 1/Pa
Van Genuchten parameter n 4 -
residual saturation Sw,r of water and Sg,r of steam 0.0 -
Table 4.2: Values of the system properties.
4.1.4 Conditions at the Injection Well
The injection of steam into the model domain is realised by using a source term. Mass
and energy is injected at Node2 (see figure 4.2), and characterized by a mole and en-
thalpy flux (mol/s and J/s).
To analyse the influence of a solarthermal steam generation, respectively cyclic steam
injection, on the temperature and steam development in the subsurface, a cyclic injec-
tion process is compared to a continuous one. Two injection approaches, determined
by different injection conditions, are thus used.
On average, a daily injection of 0.3 t per meter well length (for details see chapter 1),
and a steam quality of approximately 90 % (x = 0.9) is assumed for both injection
routines.
For the continuous injection approach, this simply results in a mass and enthalpy flux
at the injection node of:
− 12.5 kg/hr
− 32875 kJ/hr.
4.1 The Model 28
For the cyclic injection approach based on solarthermal steam generation, the locally
available hours of direct solar radiation, which vary with the seasons, determine the
actual injection rate. For this work, statistical climate data for Edmonton in Alberta,
Canada has been used (Environment Canada (2009) [9]). The data suggests a
yearly average of approximately 6.3 hrs/d of bright sunshine. Based on an average daily
injection of 0.3 t/m, respectively 109.5 t/m per year, the mass and enthalpy flux for the
cyclic injection process is calculated to be approximately:
− 47.6 kg/hr
− 125238.1 kJ/hr.
A combination of two injection cycles determines the actual injection period for the
cyclic injection process, as a function of time. One describes the different seasons for
the given location of Edmonton (see figure 4.3(a)). The other represents the actual
daily injection window depending on the season (see figure 4.3(b)). As the possible
daily injection period varies with the seasons, so does the daily injected amount of
energy.
To guarantee the same energy input after one full seasonal cycle (12 months) for cyclic
injection as for continuous injection, the actual injection rates have been calculated as
described above. It is important to notice, that in case of cyclic injection, it is not the
actual injection rate changing with the seasons, but the duration of injection.
4.1 The Model 29
(a) Seasonal cycle
(b) Daily cycle
Figure 4.3: Seasonal distribution and daily injection window at the location of Edmon-
ton in Alberta, Canada, described by a sinusoidal function. Spring is represented by
the areas marked green, summer is marked orange, autumn is brown and winter is light
blue. The actual daily injection time is 3 hrs in winter, 6 hrs in spring and autumn,
and 10 hrs in summer.
4.2 Continuous Steam Injection 30
4.2 Continuous Steam Injection
As described in section 1.2, the application of steam assisted gravity drainage (SAGD)
for enhanced oil recovery purposes is based on the injection of high-pressure, high-
quality steam. The steam is usually produced by fossil fuel burning steam generators,
using gas, oil or LPG (liquified petroleum gas).
Such a steam generation process delivers a continuous steam injection rate, in case the
fossil fuel and water supply is sufficient.
4.2.1 The Injection Well
A constant mass and enthalpy flux is given at the injection well (see section 4.1.4).
Figure 4.4 shows a plot of the temperature, pressure and steam saturation versus time
at the injection node. It indicates, how a high injection pressure during the start-up
phase decreases over time, followed by a similar development of the temperature. The
steam saturation at the injection node is constant over the whole time.
Figure 4.4: Pressure, temperature and steam saturation at Node2 (injection node at
x = 60 m and y = 8 m) for a continuous injection process.
4.2 Continuous Steam Injection 31
4.2.2 Steam Chamber and Temperature Development
The steam chamber growth and the temperature front development from the injec-
tion well are analysed within the model domain. Therefore, steam saturation and
temperature are depicted for various time steps after the start of injection. Figure 4.5
and 4.6 show Sg, respectively the steam chamber growth, and T for the process of a
continuous injection after 3, 6, 9, 27, 30, 33, 51, 54, and 57 months.
Buoyant forces cause the steam to rise upwards from the injection well. Once the
low permeable overburden (indicated by the black horizontal line) is reached, steam
accumulates underneath it and the steam chamber growth is dominated by a horizontal
spreading underneath the overburden. To a smaller degree, this horizontal growth
is also observed in the middle of the steam chamber. The distribution of the steam
saturation within the steam chamber is rather homogeneous, with a higher steam
saturation around the injection well.
For the given injection rate, the development of the temperature front is mainly driven
by convection, and hence, basically follows the steam chamber growth. However,
due to conduction, a loss of thermal energy from the reservoir into the overburden is
observed.
Figure 4.7 shows the development of Sg and T at Node4, directly underneath the
overburden at x = 60 m and y = 34.5 m. A constant steam saturation and temperature
is observed, with the steam accumulating underneath the low permeable overburden.
A continuous injection rate results in a continuous growth of a steam chamber,
characterized by a homogeneous saturation distribution within the chamber, and a
similar development of the temperature front.
4.2 Continuous Steam Injection 32
Fig
ure
4.5:
Ste
amsa
tura
tion
Sg,re
pre
senti
ng
the
stea
mch
amber
grow
thfo
ra
conti
nuou
sin
ject
ion
pro
cess
ata
tim
eof
3,6,
9,27
,30
,33
,51
,54
,an
d57
mon
ths
afte
rth
est
art
ofin
ject
ion.
4.2 Continuous Steam Injection 33
Fig
ure
4.6:
Dis
trib
uti
onof
tem
per
ature
Tfo
ra
conti
nuou
sin
ject
ion
pro
cess
ata
tim
eof
3,6,
9,27
,30
,33
,51
,54
,an
d57
mon
ths
afte
rth
est
art
ofin
ject
ion.
4.2 Continuous Steam Injection 34
Figure 4.7: Temperature and steam saturation at Node4, directly underneath the over-
burden (x = 60 m and y = 34.5 m) for a continuous injection process.
4.3 Cyclic Steam Injection 35
4.3 Cyclic Steam Injection
The objective of the hydrodynamical study of cyclic steam injection into the subsurface
is the idea, to use solarthermal steam generation plants instead of fossil fuel burning
steam generators. The solarthermal plant would use direct solar radiation to generate
steam, and thus delivering a cyclic steam injection rate, depending on the daily available
hours of direct sunlight (see section 1.3 and 4.1.4).
4.3.1 The Injection Well
The injection rate determines the injection pressure, and consequently the steam
temperature. A cyclic injection routine, due to a solarthermal steam generation
process, thus results in a daily change between an injection and a non-injection
window, and the change of the daily injection duration with the seasons (see fig-
ure 4.3(b) and 4.3(a)). This injection routine determines the pressure, temperature
and saturation fluctuations obtained at the injection well.
Figure 4.8 depicts those oscillations at the injection node for one full seasonal cycle
(one year) for p, T and Sg in the fifth year of injection. The broad spectrum of the
data is the result of the daily shift between injection and non-injection phase. In the
model, the actual injection rate is the same for all seasons. The daily injection window
however, changes with the seasons, thus does the daily amount of injected steam (see
figure 4.3(b)).
It needs to be noticed, that in reality, the actual steam production and injection rate
may vary according to the daily and seasonal variation of the energy of the solar
radiation (assumption of sufficient water supply).
As shown in figure 4.8, the change from a short injection window to a long one
(e.g. spring to summer), results in more steam being injected into the steam chamber,
forcing it to grow faster. This causes a sudden pressure increase, which is reduced with
a growing steam chamber. The pressure fluctuations are followed by the temperature
oscillations, according to the water saturation pressure-temperature relation.
For a shift from a long to a short injection period (e.g. summer to autumn), a sudden
pressure decrease, followed by a temperature decline, is observed. This is because
an insufficient amount of steam is injected to obtain the expansion of the steam
chamber, causing steam to condense at the front, resulting in a near collapse of the
chamber. As water is more dense than steam, less pore volume is needed, resulting
in a pressure decline. With a then small, but slowly growing steam chamber, the
pressure rises again. The maximum pressure during injection, to which the injection
pressure generally converges, at the given injection rate, is approximately 44 bar.
The steam saturation at the injection well basically fluctuates within a given range,
according to the daily injection cycle, disregarding the change of seasons. An exception
is observed during the low-injection months of winter (see figure 4.8(c)). This is,
4.3 Cyclic Steam Injection 36
because the steam chamber diminishes as a consequence of the short injection window,
resulting in low steam saturations.
In the model, the steam injection is realised by defining a constant mass and
enthalpy flux. Hence, in the case of a cyclic injection process, the described injection
pressure fluctuations make it impossible to ensure a certain steam quality at the
injection node. This is, because a change in pressure would be accompanied with a
change of the specific steam enthalpy, with respect to a constant steam quality (see
figure 3.4). The change of the specific enthalpy is however assumed to be minor for a
steam quality of 90%. Thus, the needed adjustment of the steam enthalpy is neglected
in the model.
4.3.2 Steam Chamber Growth
Using a cyclic injection process, the steam chamber growth varies with time, depending
on the seasons. Figure 4.9 shows the steam saturation within the model domain at 3,
6, 9, 27, 30, 33, 51, 54, and 57 months after the start of injection. It indicates a fast
steam front propagation during the high-injection months (summer), while during low-
injection months (winter), the steam chamber is reduced in volume. This is because the
daily amount of injected steam varies with the seasons. It appears, the steam injection
during the seasons following summer, is not enough to sustain the steam chamber
extension reached during the summer months. The consequence is a hysteresis process,
resulting in a circular flush and drainage of the pores.
Furthermore, a rather heterogeneous steam saturation establishes within the steam
chamber, with layers of different saturations being observed. This layering of different
saturation areas is a result of the daily injection cycle, as the injected steam rises due to
buoyancy effects, leaving less saturated layers below during the non-injection period.
4.3 Cyclic Steam Injection 37
(a) p at Node2 (b) T at Node2
(c) Sg at Node2
Figure 4.8: Pressure, temperature and steam saturation at Node2 (injection node at
x = 60 m and y = 8 m) for a cyclic injection process.
4.3 Cyclic Steam Injection 38
Fig
ure
4.9:
Ste
amsa
tura
tion
Sg,
repre
senti
ng
the
stea
mch
amber
grow
thfo
ra
cycl
icin
ject
ion
pro
cess
ata
tim
eof
3,6,
9,
27,30
,33
,51
,54
,an
d57
mon
ths
afte
rth
est
art
ofin
ject
ion.
The
left
colu
mn
isduri
ng
sum
mer
,th
em
iddle
colu
mn
duri
ng
autu
mn,an
dth
eri
ght
colu
mn
duri
ng
win
ter.
4.3 Cyclic Steam Injection 39
4.3.3 Temperature Development
In case of a cyclic injection routine, the propagation of the temperature front does not
necessarily follow the steam chamber growth. Figure 4.10 indicates a fast temperature
front propagation during high-injection months, with large areas of high temperatures.
The temperature front propagation is mainly driven by convection, and hence follows
the steam chamber growth. During low-injection months however, the temperature
front keeps growing even though the steam chamber is reduced in size. The areas of
high temperatures are much smaller and restricted to the area close to the injection
well. The reason for this development is, that the temperature propagation is mainly
driven by conduction in these months. Hence, the thermal energy injected during high-
injection months is distributed within the reservoir during low-injection months.
The influence of conduction during low-injection months is also observed at the transi-
tion between the reservoir and the low permeable overburden. In summer months, the
heat lost into the overburden, is horizontally less spread than the temperature front
underneath it. This is, because the heat loss into the overburden is a result of the
rather slow process of conduction, while the horizontal spreading of the temperature
front underneath the overburden is driven by convection. In contrast, during winter
months, the main force driving the temperature propagation is conduction, leaving the
temperature front within the overburden and underneath it equally spread.
4.3 Cyclic Steam Injection 40
Fig
ure
4.10
:D
istr
ibuti
onof
tem
per
ature
Tfo
ra
cycl
icin
ject
ion
pro
cess
ata
tim
eof
3,6,
9,27
,30
,33
,51
,54
,an
d57
mon
ths
afte
rth
est
art
ofin
ject
ion.
The
left
colu
mn
isduri
ng
sum
mer
,th
em
iddle
colu
mn
duri
ng
autu
mn,
and
the
righ
tco
lum
n
duri
ng
win
ter.
4.4 Comparison of the two Injection Routines 41
4.4 Comparison of the two Injection Routines
To analyse the influence of a cyclic injection on the flow processes in the subsurface,
the steam chamber and temperature front propagation of the cyclic and continuous
steam injection routines are checked against each other. The two processes must be
compared at a point in time, determined by the same cumulative energy input. For
the way of injection described in section 4.1.4, this is given after one full seasonal cycle,
respectively after every 12 months. The point in time for the following comparison is
thus chosen to be after five full injection cycles, respectively five years.
4.4.1 Steam Chamber Growth
The propagation of the steam front is not found to be equal for both injection
approaches at one point in time, which is determined by the same cumulative energy
input. This is because of the varying influence of condensation in case of a cyclic
injection routine.
Figure 4.11 shows the steam saturation for the continuous and cyclic injection process
five years after the start of injection. A less horizontal steam chamber expansion
underneath the overburden, and a more heterogeneous steam saturation distribution
is observed in case of the cyclic injection. The steam chamber volume at the given
point in time is clearly bigger in case of the continuous injection.
However, it is pointed out, that with the cyclic injection process, the steam chamber
volume is decreasing in the second half of a full seasonal cycle (see figure 4.9). Thus,
the steam chamber expansion is more similar between the two approaches earlier
within the full injection cycle. This point in time though, would be characterized by
the cyclic cumulative energy input being higher than the continuous one. Figure 4.12
shows the steam saturation for the continuous and cyclic injection routine at the end
of the fifth summer, at a time of 4 years and 5 months after the start of injection.
For the case of a cyclic injection process, it clearly indicates, that the steam chamber
expansion at this point in time is similar to that of the continuous injection.
As the mobilisation of heavy oil is achieved with the reduction of the oil’s vis-
cosity due to the transfer of thermal energy (see section 1.2), it is not solely the steam
chamber growth influencing the enhanced oil recovery. In fact, the temperature front
propagation and the temperature distribution within the reservoir is assumed to be of
main interest for the production of heavy oil.
4.4 Comparison of the two Injection Routines 42
(a) Continuous injection
(b) Cyclic injection
Figure 4.11: Steam saturation Sg in the model domain for a continuous and cyclic
injection process, five years after the start of injection (after 5 full seasonal cycles).
4.4 Comparison of the two Injection Routines 43
(a) Continuous injection
(b) Cyclic injection
Figure 4.12: Steam saturation Sg in the model domain for a continuous and cyclic
injection process, four years and five months after the start of injection (after summer).
4.4 Comparison of the two Injection Routines 44
4.4.2 Temperature Development
It is observed, that the propagation of the temperature front is quite different between
the two injection routines. Figure 4.13 shows the temperature for a continuous and
cyclic injection process five years after the start of injection. For the case of a cyclic
injection, a smaller horizontal expansion of the high temperature front underneath the
overburden is observed. The propagation of the temperature front is thus different
between the two injection routines.
As the energy input is the same for both injection routines, the thermal energy must be
differently distributed in case of the cyclic process. Therefor, the temperature distribu-
tion within the formation is analysed. Figure 4.14 and figure 4.15 show the distribution
of low and high temperature areas within the model domain. It is observed, that while
the low temperature front is very similar for both injection routines, as shown in fig-
ure 4.14(a) and 4.14(b), the high temperature areas are differently distributed, as shown
in figure 4.15(a) and 4.15(b). In case of the continuous injection process, an increased
accumulation of thermal energy underneath the overburden is observed, while in case
of cyclic injection, the high temperature areas are more concentrated within the cen-
tral area around the injection well, which is also determined by a higher maximum
temperature.
The different distribution of high temperature areas between the two injection rou-
tines is shown more detailled in figure 4.16. It is observed, that while the depicted
245 C front has propagated further for the continuous process, the fronts of higher
temperatures are more developed for the cyclic injection routine, and higher overall
temperatures are reached.
4.4 Comparison of the two Injection Routines 45
(a) Continuous injection
(b) Cyclic injection
Figure 4.13: Temperature T in the model domain for a continuous and cyclic injection
process, five years after the start of injection (after 5 full seasonal cycles).
4.4 Comparison of the two Injection Routines 46
(a) Continuous injection
(b) Cyclic injection
Figure 4.14: Areas of low temperature T in the model domain for a continuous and
cyclic injection process, five years after the start of injection (after 5 full seasonal
cycles).
4.4 Comparison of the two Injection Routines 47
(a) Continuous injection
(b) Cyclic injection
Figure 4.15: Areas of high temperature T in the model domain for a continuous and
cyclic injection process, five years after the start of injection (after 5 full seasonal
cycles).
4.4 Comparison of the two Injection Routines 48
Fig
ure
4.16
:P
ropag
atio
nof
the
tem
per
ature
fron
tof
245 C
,24
8 C
,24
9 C
,an
d25
0 C
for
the
conti
nuou
san
dcy
clic
inje
ctio
n
pro
cess
,five
year
saf
ter
the
star
tof
inje
ctio
n(a
fter
5fu
llse
ason
alcy
cles
).
4.4 Comparison of the two Injection Routines 49
In summary, a differing temperature front propagation is observed, when comparing
the two injection routines. This is even though the cumulative energy input being the
same at the point of five years after the start of injection.
While the thermal energy is accumulated underneath the overburden in case of contin-
uous injection, the heat is more concentrated within the central area of the reservoir
in case of cyclic injection. This suggests, that the upward transport of thermal energy
due to buoyancy is less with a cyclic injection process. A smaller influence of buoyant
forces in turn, indicates a smaller volume of steam being present.
This observation may be explained by the cyclic injection routine itself. On the one
hand, as a cyclic injection results in the repetitive heating of the same porous media
area. This is, because the thermal energy transferred to the medium during injection
periods, is distributed throughout the formation during non-injection periods. On the
other hand, it seems likely, that the oscillation of the injection pressure, originating
from the cyclic injection routine, influences the propagation of the temperature front.
Figure 4.17(a) depicts the injection pressure oscillations of the cyclic injection routine
in comparison to the continuous injection, at the injection well. In case of a cyclic
process, the high pressure of the injection area propagates fast into the reservoir, re-
sulting in a higher pressure level within the reservoir for the main injection period (see
figure 4.17(b) and 4.18). As described in section 4.1.4, a pressure increase results in
an increase of the water saturation temperature according to figure 3.1. Hence, areas
of high pressure are characterized by a high water saturation temperature, as shown
in figure 4.19. In such areas, the energy needed to evaporate water, filling the pores, is
consequently more in case of the cyclic process relative to the continuous injection case.
As a result, less steam develops, which is indicated by lower steam saturations within
the formation (see figure 4.20). This suggests, that with cyclic injection, the amount
of thermal energy stored and transported with steam is less than with the continu-
ous process. Hence, the thermal energy within the hot water phase is proportionately
more with the cyclic steam injection process, which explains the fact, that the thermal
energy is less accumulated underneath the overburden, but more concentrated in the
central area of the reservoir.
4.4 Comparison of the two Injection Routines 50
(a) Node2
(b) Node3
Figure 4.17: Pressure at Node2 (x=60 m and y=8m) and Node3 (x=60m and y=20m)
in the fifth year of injection for the continuous and cyclic injection process.
4.4 Comparison of the two Injection Routines 51
(a)
51m
onth
saf
ter
star
tof
cont
inuo
usin
ject
ion
(b)
51m
onth
saf
ter
star
tof
cycl
icin
ject
ion
(c)
60m
onth
saf
ter
star
tof
cont
inuo
usin
ject
ion
(d)
60m
onth
saf
ter
star
tof
cycl
icin
ject
ion
Fig
ure
4.18
:P
ress
ure
pin
the
model
dom
ain
for
the
conti
nuou
san
dcy
clic
inje
ctio
npro
cess
,at
51m
onth
s(s
um
mer
)an
d60
mon
ths
afte
rth
est
art
ofin
ject
ion.
4.4 Comparison of the two Injection Routines 52
(a)
51m
onth
saf
ter
star
tof
cont
inuo
usin
ject
ion
(b)
51m
onth
saf
ter
star
tof
cycl
icin
ject
ion
(c)
60m
onth
saf
ter
star
tof
cont
inuo
usin
ject
ion
(d)
60m
onth
saf
ter
star
tof
cycl
icin
ject
ion
Fig
ure
4.19
:W
ater
satu
rati
onte
mper
ature
Tsa
tfo
rth
eco
nti
nuou
san
dcy
clic
inje
ctio
npro
cess
,at
51m
onth
s(s
um
mer
)an
d
60m
onth
saf
ter
the
star
tof
inje
ctio
n.
4.4 Comparison of the two Injection Routines 53
(a) Node2
(b) Node3
Figure 4.20: Steam saturation Sg at Node2 (x=60m and y=8m) and Node3 (x=60m
and y=20m) in the fifth year of injection for the continuous and cyclic injection process.
4.5 Sensitivity Study 54
4.5 Sensitivity Study
A sensitivity analysis is carried out to obtain an indication for the influence of various
system properties on the development of the temperature front for a steam injection
process. Therefor, five properties listed in table 4.3 are selected, and an upper and
lower boundary value is assumed (high and low value). For each parameter, simulation
runs determined by the high and low value are compared to the reference scenario,
given in table 4.3. The model domain of the sensitivity analysis is a section of the
model domain shown in figure 4.1. As the study only analyses the influence on
a short time scale (thus only the influence on the daily injection oscillation for a
cyclic injection process), the domain is given by a 20 mx20m box around an injection
well, which is located 5m above the reservoir bottom (see figure 4.21). The initial
temperature of the model domain is higher than for the domain given in figure 4.1, to
allow for a proper temperature front development within the short time of simulation
for the sensitivity study. The top, left and right domain boundary conditions are
those of hydrostatic pressure distribution and initial temperature.
The influence of the given parameters on the temperature front 1 C above ini-
tial temperature is analysed for a continuous and cyclic injection process, assuming
an injection rate of 0.5 t/d. For the cyclic injection, an injection window of 12 hrs/d, and
thus an actual injection rate twice that of the continuous process, is assumed. The
propagation of the temperature front is compared between the reference scenario, and
the high and low value scenario for each parameter (see figure 4.23 to 4.27). For the
cyclic injection, the point in time for the comparison is 14.5 d. For the continuous
injection it is 15 d. This allows for a comparison of the parameter’s influence between
the two processes, as the cumulative energy input is the same at these points in time.
low permeable overburden
bottom boundary: no−flow conditions
injection well 5m above bottom boundaryT (initial) = 35°CSw (initial) = 1.0
new model domain for sensitivity analysis (20m x 20m)reservoir
Figure 4.21: Model domain for the sensitivity analysis within the reservoir.
4.5 Sensitivity Study 55
parameter unit reference value high value low value
absolute permeability K mD 75 1000 1
porosity Φ - 0.3 0.5 0.1
specific heat capacity csgJ/kg K 850 1050 650
heat conductivity λpmW/m K see figure 4.22
Van Genuchten parameter α 1/Pa 0.0028 0.01 0.0001
Table 4.3: Reference, upper and lower value for the system properties, chosen to be
analysed in the sensitivity study.
Figure 4.22: Heat conductivity as a function of water saturation. Approach of Somer-
ton, to calculate the effective heat conductivities for the fully water, and fully steam
saturated porous media. For the reference value, the method of the geometric mean is
used. The high and low value is calculated, using the method of the arithmetic mean,
respectively harmonic mean (e.g. Class (2001) [6]).
4.5 Sensitivity Study 56
4.5.1 Absolute Permeability K
For the sensitivity analysis, the absolute permeabilty K is varied within the range
given in table 4.3. Figure 4.23 indicates, that the influence of a change in K is of the
same trend for the continuous and the cyclic injection routine.
A low absolute permeability leads to a more radial distribution of the temperature
front. While a high absolute permeability results in a less radial propagation. The
reason for that is described in detail in Ochs (2006) [20]. The so-called qs/K ratio (ratio
between steam injection rate and absolute permeability) is an indication of the balance
between viscous and buoyant forces. It originates from the linear gravity number
(Grlin), derived by Van Lookeren. Based on this approach, a decrease of the absolute
permeability at a constant injection rate, results in an increasing qs/K ratio. This
increases the influence of the viscous forces, which results in a more radial spreading
and more concentrated distribution of the steam front, respectively temperature front.
A high absolute permeability, on the other hand, increases the influence of the buoyant
forces, hence causing a less radial but more linear spreading, dominated by an upward
movement of the steam, due to density differences. In figure 4.23(b) however, it is
observed, that for this example of a cyclic injection, a high K does not result in
an increased upwards growth of the temperature front. Due to condensation, the
thermal energy sinks with the hot water, resulting in a wider horizontal spreading of
the temperature front near the domain bottom.
(a) Continuous injection (b) Cyclic injection
Figure 4.23: Propagation of the temperature front (T ≥ 36 C), with varying absolute
permeability K. After 15 d for the continuous injection, and 14.5 d for the cyclic
injection.
4.5 Sensitivity Study 57
4.5.2 Porosity Φ
The influence of the Porosity Φ on the temperature front propagation is similar for a
continuous and cyclic injection process (as shown in figure 4.24). The change of poros-
ity basically has two effects relevant for the temperature front propagation. In a fully
water saturated system, a higher porosity results in more volume of water. This on the
one hand, decreases the average specific heat capacity of the system, as cw is smaller
than csg. This in turn would result in a faster temperature front propagation. On the
other hand, more volume of water simply results in the necessity of a higher energy
amount, to heat the water. Hence, with a constant energy input, the time needed to
heat a larger volume of water increases, which would result in a slower temperature
front propagation.
It is observed, that a low porosity results in a faster growth, while a high porosity
slightly slows the temperature front propagation. Thus, the latter of the effects de-
scribed above has the dominating influence.
For both cases, the general shape of the front is similar to that of the reference case.
(a) Continuous injection (b) Cyclic injection
Figure 4.24: Propagation of the temperature front (T ≥ 36 C) , with varying porosity
Φ. After 15 d for the continuous injection, and 14.5 d for the cyclic injection.
4.5 Sensitivity Study 58
4.5.3 Specific Heat Capacity of the Soil Grains csg
The specific heat capacity csg of the solid phase describes the ability of the soil grains to
store thermal energy. Consequently, a high value for csg, indicating a good heat storage
ability, results in a slow propagation of the temperature front. A low value for csg,
hence accelerates the growth of the temperature front. This is observed in figure 4.25,
which shows the influence of a varying csg on the temperature front development for a
continuous and cyclic injection. The general trend resulting from a change of csg is the
same for both injection processes.
(a) Continuous injection (b) Cyclic injection
Figure 4.25: Propagation of the temperature front (T ≥ 36 C) , with a varying specific
heat capacity csg of the solid phase. After 15 d for the continuous injection, and 14.5 d
for the cyclic injection.
4.5 Sensitivity Study 59
4.5.4 Heat Conductivity λpm
The heat conductivity λpm is a parameter, describing the average ability of the fluid
filled porous medium to transmit heat. This suggests, that an increasing λpm results in
a faster temperature front propagation and a less concentrated heat distribution. This
is also indicated by figure 4.26. The influence of λpm is rather small here, as the high
and low value has been set up accordingly to table 4.3, respectively figure 4.22.
Instead of changing the method to obtain the effective heat conductivity λpm, the
direct variation of the soil grain heat conductivity λsg may have more influence (see
section 3.3.3). λsg is set to 2.5 W/m K here, although it may be an uncertainty too. This
however is not analysed within this work.
(a) Continuous injection (b) Cyclic injection
Figure 4.26: Propagation of the temperature front (T ≥ 36 C) , with a varying heat
conductivity λ. After 15 d for the continuous injection, and 14.5 d for the cyclic injec-
tion.
4.5 Sensitivity Study 60
4.5.5 Capillary Pressure pc and Van Genuchten Parameter α
The capillary pressure pc is a function of the residual saturations Sw,r and Sg,r of
the water and steam phase, the water saturation Sw, and the two Van Genuchten
parameters n and α (see section 3.3.2). For the sensitivity study, the latter one of
the two Van Genuchten parameters is changed within the range given in table 4.3.
According to equation 3.4, an increase of α results in a decreasing pc, and vice versa.
As shown in figure 4.27, a change of α within the given range has barely any influence
on the temperature front propagation for the time period analysed. The slightly slower
propagation with an increase of α, respectively decrease of pc, can not be explained
within this work.
(a) Continuous injection (b) Cyclic injection
Figure 4.27: Propagation of the temperature front (T ≥ 36 C) , with a varying capillary
pressure. After 15 d for the continuous injection, and 14.5 d for the cyclic injection.
4.5.6 Results of the Sensitivity Study
Of the various parameters analysed within the sensitivity study, the absolute permeabil-
ity K is identified as the system property with the biggest influence on the temperature
front propagation. While a low K results in a more radial spreading of the front, a
high K leads to a more linear propagation. The reason for that is described by the
so-called qs/K ratio (see section 4.5.1).
The remaining parameters (see table 4.3) are of small or no influence.
Chapter 5
Summary
The work presented in this thesis, is inspired by the idea to increase the efficiency of
oil production from non-conventional heavy oil deposits in a way less harmful to the
environment.
Oil extraction from non-conventional reservoirs, such as the oil sand fields in Al-
berta, Canada, is increasing, as the demand for oil rises in a manner, production
from conventional deposits is soon expected to fall below. Enhanced oil recovery
technologies, often relying on steam, are usually necessary to produce oil from such
non-conventional reservoirs. The so induced increasing demand for steam, which is
produced by fossil fuel burning steam generators, presents various environmental and
economical problems.
The motivation for the presented work is thus the idea of solarthermal steam
generation plants for the steam assisted gravity drainage technology. Solarthermal
steam generation will lead to a cyclic injection process due to daily and seasonal
variations of solar radiation.
A two-dimensional, non-isothermal water steam model is used to simulate steam
injection into saturated porous media through a single injection well. The applied
model does not include oil, neither as a phase nor as a component. Hence, the
influence of a cyclic injection process on the oil production is not subject of this thesis.
The underlying mathematical model concept and the reservoir properties of the system
are described in chapter 2 and chapter 3 of this work. In chapter 4, the influence of
a cyclic injection routine on the fluid flow and transport processes is analysed and
compared to a continuous injection routine, using the described model. Furthermore,
a sensitivity study identifies the absolute permeability K as the system property,
which influences the temperature front propagation the most amongst the analysed
parameters. This is because of its influence on the balance between viscous and
buoyant forces, as described in detail in Ochs (2006) [20].
61
5.1 Conclusion 62
5.1 Conclusion
The hydrodynamical study of the two different steam injection processes, yields the
conclusion, that there is a difference between the cyclic and continuous injection
routine with respect to the steam chamber and temperature development within the
reservoir.
For the continuous injection process described in this work, the dominant transport
mechanism of thermal energy is convection. Hence, the temperature front development
basically follows the continuous steam chamber growth, as long as the steam front is
propagating.
In contrast, the temperature front development does not necessarily follow the
steam chamber growth in case of cyclic injection. In addition to convection, the
transport of thermal energy due to conduction plays an important role during
non-injection periods. As a result, the temperature propagates continuously within
the reservoir, while due to condensation, the steam chamber volume is reduced during
injection pauses.
Furthermore it is observed, that although the cumulative energy input is the same
for both injection routines, the temperature front develops differently with cyclic
injection. The thermal energy is thus differently distributed. The presented work
suggests, that the reason for the different distribution of thermal energy within the
reservoir, is the cyclic injection routine itself. This is because, based on the assumption
of the same cumulative energy input, a higher injection rate is needed in case of the
cyclic injection routine. The consequence is a higher pressure distribution within the
reservoir. This in turn results in higher temperatures where water and steam are in
equilibrium according to the curve of saturation-vapor pressure over temperature (see
figure 3.1). Hence, less steam develops within the reservoir, resulting in a decline of
buoyant transport.
In summary, two distinct influences of the cyclic injection routine on the steam
flow and energy transport in the subsurface are established in this thesis:
− Vibrant steam chamber growth with a heterogeneous steam saturation distribu-
tion
− Increased concentration of thermal energy within the central area of the reservoir.
The influence of a cyclic injection routine and its consequences on the profitability of
the bitumen and heavy oil business can not be evaluated, based on the work presented
in this thesis.
5.2 Outlook 63
5.2 Outlook
The applied 2D model represents a simplification of the situation in the reservoir and
neglects the component oil. A statement about the influence of a cyclic injection
routine on the oil production rate, respectively the adaptability of solarthermal steam
generation for SAGD, is thus not possible. Open questions remaining are:
− Would the temperature distribution within the reservoir in case of cyclic injec-
tion still differ from continuous injection, if steam and temperature fronts of
neighbouring injection wells link up?
− Would a different temperature distribution within the reservoir influnce the oil
production and if yes, in which way?
− How would the fluctuating steam chamber growth in case of cyclic injection in-
fluence the oil production rate?
Tasks for future work related to this topic may therefore be:
− Implementation of production well to complete well pair
− Model implementation of several well pairs
− Development of a non-isothermal water steam oil model.
Bibliography
[1] Bastian, P., Birken, K., Johannsen, K., Lang, S., Eckstein, K., Neuss, N., Rentz-
Reichert, H., and Wieners, C. UG - A Flexible Software Toolbox for Solving
Partial Differential Equations. Computing and Visualization in Science, 1(1), S.
27-40, 1997.
[2] BGR: Bundesanstalt fur Geowissenschaften und Rohstoffe. Energierohstoffe 2009
- Reserven, Ressourcen, Verfugbarkeit. http://www.bgr.bund.de, 2009.
[3] Birrel, G. E., Aherne, A. L., and Seleshanko, D. J. Cyclic SAGD - economic impli-
cations of manipulating steam injection rates in SAGD projects - re-examination
of the Dover project. Journal of Canadian Petroleum Technology, 44, 2005.
[4] BP. BP Statistical Review of World Energy June 2009 0. bp.com/statisticalreview,
2009.
[5] Butler, R. M. Thermal Recovery of Oil and Bitumen. Prentice Hall, 1991.
[6] Class, H. Theorie und numerische Modellierung nichtisothermer Mehrphasen-
prozesse in NAPL-kontaminierten porosen Medien. Dissertation, Institut fur
Wasserbau, Universitat Stuttgart, 2001.
[7] Corey, A. T., Kemper, W. D., and Dane, J. H. Revised Model for Molecular
Diffusion and Advection. Vadose Zone Journal, 9, 2009.
[8] Darcy, H. P. G. Les Fontaines Publiques de la Ville de Dijon. 1856.
[9] Environment Canada. National Climate Data and Information Archive.
www.climate.weatheroffice.gc.ca, 1971-2000.
[10] Faerber, A. Warmetransport in der ungesattigten Bodenzone: Entwicklung einer
thermischen In-Situ Sanierungstechnologie. Dissertation, Institut fur Wasserbau,
Universitat Stuttgart, 1997.
[11] Helmig, R., Class, H., Huber, R., Sheta, H., Ewing, R., Hinkelmann, R., Jakobs,
H., and Bastian, P. Architecture of the Modular Program System MUFTE-UG
for Simulating Multiphase Flow and Transport Processes in Heterogeneous Porous
Media. Mathematische Geologie, 2:123–131, 1998.
64
BIBLIOGRAPHY 65
[12] Helmig, R. Multiphase Flow and Transport Processes in the Subsurface. Springer,
1997.
[13] Hong, K. C. Steamflood Reservoir Management - Thermal Enhanced Oil Recovery.
Penwell Books, 1994.
[14] IEA: International Energy Agency. World Energy Outlook 2009 - Executive Sum-
mary. http://www.iea.org/ or OECD/IEA in Paris, France, 2009.
[15] IFC: International Formulation Committee. A formulation of the thermody-
namic properties of ordinary water substance. Technical report, IFC Sekretariat,
Dusseldorf, Germany, 1967.
[16] Jimenez, J. The Field Performance of SAGD Projects in Canada. International
Petroleum Technology Conference (IPTC) in Kuala Lumpur, Malaysia, 2008.
[17] Kraemer, D., Bajpayee, A., Muto, A., Berube, V., and Chiesa, M. Solar assisted
method for recovery of bitumen from oil sand. Applied Energy, 2008.
[18] Langeheinecke, K., Jany, P., and Sappert, E. Thermodynamik fur Ingenieure,
Band 4. Auflage. Vieweg Verlag, 2003.
[19] Nasr, T. N., Golbeck, H., Korpany, G., and Pierce, G. SAGD Operating Strategies.
SPE International Conference on Horizontal Well Technology in Calgary, Alberta,
Canada, 1998.
[20] Ochs, S. Steam injection into saturated porous media - process analysis including
experimental and numerical investigations. Dissertation, Institut fur Wasserbau,
Universitat Stuttgart, 2006.
[21] Panday, S., Forsyth, P. A., Falta, R. W., Wu, Y., and Huyakorn, P. S. Consider-
ations for robust compositional simulations of subsurface nonaqueous phase liquid
contamination and remediation, Band 5. Water Resources Research, 1995.
[22] Prof. Dr. Ing. Voss, A. Energiesysteme 1, Band 3. Vorlesungsskript IER, Univer-
sitat Stuttgart, Germany, 2005.