reservorios
DESCRIPTION
Esta presentacion nos da un base teorica para el curso de reservorios de petroleo. Se estudia las propiedades, caractersiticasy calculos de dichos reservorios.TRANSCRIPT
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PP 324
Professor: Luis Alberto Colán García
Senior Reservoir Engineering Pluspetrol Norte S.A.
(Operating Company fields Jungle
Block 1AB & Block 8)
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DK
- 4
-
Parameter Symbol Dimensions cgs SI Darcy Field
Length L L cm metre cm ft
Mass m M gm kg gm lb
Time t T sec Sec sec hr
Velocity u L/T cm/sec metre/sec cm/sec ft/sec
stb/d
(liquid)
Rate q L3 /T cc/sec metre3 /sec cc/Sec
Mscf/d
(gas)
Pressure p (ML/T2 )/L2 dyne/cm2 Newton/metre2
(Pascal)
atm psia
Density M/L3 gm/cc kg/metre3 gm/cc lb/cu.ft
Viscosity M/LT gm/cm.sec
(Poise)
kg/metre.sec cp cp
Permeability k L2 cm2 metre2 Darcy mD
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DK
- 5
-
1 ft = 0.3048 m 1 acre = 4047 m2 = 43560 ft2
1 bbl = 0.159 m3 1 acre-ft = 1233 m3
1 dyne = 10-5 N 1 atm = 101.3 kPa
1 psi = 6.9 kPa 1 cal = 4.817 J
1 Btu = 1055 J 1 HP = 746 W
1 cp = 0.001 Pa s 1 md = 10-15 m2
1 lb = 0.454 kg 1 bar = 100 kPa
•1 acre-ft = 43560 ft3 •1 acre-ft = 7758 barrels •1 barrel = 5.61458 ft3 Temperature Farenheit Pressure Psia Thickness ft. Gravity oil API • 1 atm = 14.7 Psia
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LECTURE 1
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How is petroleum formed?
Petroleum is result of the deposition of plant or animal matter in areas
which are slowly subsiding.These areas are usually in the sea or along its
margins in coastal lagoons or marshes, occasionally in lakes or inland
swamps. Sediments are deposited along with that at least part of the
organic matter is preserved by burial before being destroyed by decay. As
time goes on and the areas continue to sink slowly, the organic material is
buried deeper an hence is exposed to higher temperatures and
pressures.Eventually chemical changes result in the generation of
petroleum,a complex,highly variable mixture lf hydrocarbons.
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Objectives are to be able to:
Discuss basic elements of Petroleum Systems
Describe plate tectonics and sedimentary basins
Recognize names of major sedimentary rock types
Describe importance of sedimentary environments to petroleum industry
Describe the origin of petroleum
Identify hydrocarbon trap types
Define and describe the important geologic controls on reservoir properties, porosity and permeability
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Petroleum Systems approach
Geologic Principles and geologic time
Hydrocarbon Generation, Migration, and Accumulation
Rock and minerals, rock cycle, reservoir properties
Hydrocarbon origin, migration and accumulation
Sedimentary environments and facies; stratigraphic traps
Plate tectonics, basin development, structural geology
Structural traps
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Petroleum System - A Definition
•A Petroleum System is a dynamic hydrocarbon
system that functions in a restricted geologic
space and time scale.
•A Petroleum System requires timely
convergence of geologic events essential to
the formation of petroleum deposits.
These Include:
Mature source rock Hydrocarbon expulsion Hydrocarbon migration Hydrocarbon accumulation Hydrocarbon retention
(modified from Demaison and Huizinga, 1994)
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Cross Section Of A Petroleum System
Overburden Rock
Seal Rock
Reservoir Rock
Source Rock
Underburden Rock
Basement Rock
Top Oil Window
Top Gas Window
Geographic Extent of Petroleum System
Petroleum Reservoir (O)
Fold-and-Thrust Belt
(arrows indicate relative fault motion)
Essential
Elements
of
Petroleum
System
(Foreland Basin Example)
(modified from Magoon and Dow, 1994)
O O
Sed
imen
tary
Basin
Fil
l
O
Stratigraphic
Extent of
Petroleum
System
Pod of Active
Source Rock
Extent of Prospect/Field
Extent of Play
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Uniformitarianism
Original Horizontality
Superposition
Cross-Cutting Relationships
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Angular Unconformity
A
B
C
D
E
F
G
H I J
K
Igneous
Dike
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Disconformity ◦ An unconformity in which the beds above and
below are parallel
Angular Unconformity ◦ An unconformity in which the older bed intersect
the younger beds at an angle
Nonconformity ◦ An unconformity in which younger sedimentary
rocks overlie older metamorphic or intrusive igneous rocks
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Establishes the age equivalence of rock layers in different areas
Methods: ◦ Similar lithology
◦ Similar stratigraphic section
◦ Index fossils
◦ Fossil assemblages
◦ Radioactive age dating
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Geologic Cycle The cooling and movements of earth inner
molten rocks caused warping and movements of the crust resulting in the formation of mountains and valleys.
Erosion /weathering (wind, water and temp) is the process of earth breakdown into rock grains.
Rock grains are transported by water and deposited in the sedimentary basins (valleys or the sea) in horizontal beds.
Sedimentary beds are uplifted by structural movements and the cycle is repeated.
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Geologic Time
Oldest beds are deposited in the bottom
Due to erosion and /or non-deposition , no single sequence is a complete record of geologic time (table 1)
Paleontology (study of fossils) is used to define geologic períods.
Natural radioactivity of minerals (Uranium & Thorium) determines absoluter rock age.
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Geologic Time Chart
0
50
100
150
200
250
300
350
400
450
500
550
600
0
10
20
30
40
50
60
Cry
pto
zo
ic
(Pre
cam
bri
an
)
Phanerozoic
Quaternary
Tertiary
Cretaceous
Jurassic
Triassic
Permian
Pennsylvanian
Mississippian
Devonian
Silurian
Ordovician
Cambrian
Millio
ns
of
ye
ars
ag
o
Millio
ns
of
ye
ars
ag
o
Bil
lio
ns
of
ye
ars
ag
o 0
1
2
3
4
4.6
Paleocene
Eocene
Oligocene
Miocene
Pliocene
Pleistocene Recent
Qu
ate
rnary
peri
od
Tert
iary
peri
od
Eon Era Period Epoch
Pale
ozoic
M
esozoic
Ce
no
zo
ic E
ra
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LECTURE 2
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SEDIMENTARY
Ro
ck-f
orm
ing
pro
cess
So
urc
e o
f
mate
rial
IGNEOUS METAMORPHIC
Molten materials in
deep crust and
upper mantle
Crystallization
(Solidification of melt)
Weathering and
erosion of rocks
exposed at surface
Sedimentation, burial
and lithification
Rocks under high
temperatures
and pressures in
deep crust
Recrystallization due to
heat, pressure, or
chemically active fluids
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The Rock Cycle
Magma
Metamorphic Rock
Sedimentary Rock
Igneous Rock
Sediment
Heat and Pressure
Weathering, Transportation and Deposition
a
n
i
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Sedimentary rocks
• Are formed by sediments that have settled into layers. The layers are squeezed together until they harden into rock.
• Formed by the cementation of sediment grains/particles on or near surface at ordinary temperature .
• Sandstone
• Limestone (CaCO3)
• Dolomite (CaMg(CO3)2
Igneous Rocks • An igneous rock is a rock that had molted
(derritió) but it later cooled and hardened
(endureció).
• Formed by solidification of molten
minerals/materials:
• Beneath surface (magma):Granite
• At surface (lava): Basalt
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Metamorphic Rocks
• Is an igneous or sedimentary rock that has been changed (alterada) by heat and pressure.
• Formed within earth’s crust by transformation of other rocks at high pressure and temperature (marble,slate)
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Siltstone, mud
and shale
~75%
• Relative abundance Sandstone
and conglomerate
~11%
Limestone and
dolomite
~13%
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Quartz Crystals
Naturally Occurring Solid
Generally Formed by Inorganic Processes
Ordered Internal Arrangement of Atoms (Crystal Structure)
Chemical Composition and Physical Properties Fixed or Vary Within A Definite Range
Minerals - Definition
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Mineral Composition Shale (%) Sandstone (%)
Clay Minerals
Quartz
Feldspar
Rock Fragments
Carbonate
Organic Matter, Hematite, and Other Minerals
60
30
4
<5
3
<3
5
65
10-15
15
<1
<1
(modified from Blatt, 1982)
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Quartz
Feldspar
Calcite
Mechanically and Chemically Stable
Can Survive Transport and Burial
Nearly as Hard as Quartz, but
Cleavage Lessens Mechanical Stability
May be Chemically Unstable in Some
Climates and During Burial
Mechanically Unstable During Transport
Chemically Unstable in Humid Climates
Because of Low Hardness, Cleavage, and
Reactivity With Weak Acid
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Some Common Minerals
Silicates
Oxides Sulfides Carbonates Sulfates Halides
Non-Ferromagnesian (Common in Sedimentary Rocks)
Anhydrite Gypsum
Halite Sylvite
Aragonite Calcite Dolomite Fe-Dolomite Ankerite
Pyrite Galena Sphalerite
Ferromagnesian (not common in sedimentary rocks)
Hematite Magnetite
Quartz Muscovite (mica) Feldspars Potassium feldspar (K-spar) Orthoclase Microcline, etc . Plagioclase Albite (Na-rich - common) through Anorthite (Ca-rich - not common)
Olivine Pyroxene Augite Amphibole Hornblende Biotite (mica)
Red = Sedimentary Rock- Forming Minerals
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Framework ◦ Sand (and Silt) Size Detrital Grains
Matrix ◦ Clay Size Detrital Material
Cement ◦ Material precipitated post-depositionally, during
burial. Cements fill pores and replace framework grains
Pores ◦ Voids between above components
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Norphlet Sandstone, Offshore Alabama, USA
Grains are About =< 0.25 mm in Diameter/Length
PRF KF
P
KF = Potassium Feldspar
PRF = Plutonic Rock Fragment
P = Pore
Potassium Feldspar is Stained Yellow With a Chemical Dye
Pores are Impregnated With Blue-Dyed Epoxy
CEMENT
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Scanning Electron Micrograph
Norphlet Formation, Offshore Alabama, USA
Pores Provide the
Volume to Contain
Hydrocarbon Fluids
Pore Throats Restrict
Fluid Flow
Pore
Throat
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Secondary Electron Micrograph
Jurassic Norphlet Sandstone Hatters Pond Field, Alabama, USA (Photograph by R.L. Kugler)
Illite
Significant Permeability Reduction
Negligible Porosity Reduction
Migration of Fines Problem
High Irreducible Water Saturation
Clay Minerals in Sandstone Reservoirs
Fibrous Authigenic Illite
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Secondary Electron Micrograph
Jurassic Norphlet Sandstone Offshore Alabama, USA (Photograph by R.L. Kugler)
Occurs as Thin Coats on Detrital Grain Surfaces
Occurs in Several Deeply Buried Sandstones With High Reservoir Quality
Iron-Rich Varieties React With Acid
~ 10 m
Clay Minerals in Sandstone Reservoirs
Authigenic Chlorite
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Secondary Electron Micrograph
Carter Sandstone North Blowhorn Creek Oil Unit Black Warrior Basin, Alabama, USA
Significant Permeability Reduction
High Irreducible Water Saturation
Migration of Fines Problem
(Photograph by R.L. Kugler)
Clay Minerals in Sandstone Reservoirs
Authigenic Kaolinite
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100
10
1
0.1
0.01 0.01
0.1
1
10
100
1000
2 6 10 14 2 6 10 14 18
Pe
rme
ab
ilit
y (
md
)
Porosity (%)
Authigenic Illite Authigenic Chlorite
(modified from Kugler and McHugh, 1990)
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Dispersed Clay
Clay Lamination
Structural Clay (Rock Fragments,
Rip-Up Clasts, Clay-Replaced Grains)
f e
f e
f e
Clay Minerals
Detrital Quartz Grains
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Precipitation
Subsidence
CH 4 ,CO 2 ,H 2 S
Petroleum
Fluids
Meteoric
Water
Meteoric Water
COMPACTIONAL
WATER
Evapotranspiration Evaporation
Infiltration
Water Table
Zone of abnormal pressure
Isotherms
(modified from from Galloway and Hobday, 1983)
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Thin Section Micrograph - Plane Polarized Light
Avile Sandstone, Neuquen Basin, Argentina
Dissolution of
Framework Grains
(Feldspar, for
Example) and
Cement may
Enhance the
Interconnected
Pore System
This is Called
Secondary Porosity
Pore
Quartz Detrital
Grain
Partially
Dissolved
Feldspar
(Photomicrograph by R.L. Kugler)
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LECTURE 3
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Organic Matter in Sedimentary Rocks
Reflected-Light Micrograph of Coal
Vitrinite
Kerogen Disseminated Organic Matter in Sedimentary Rocks That is Insoluble in Oxidizing Acids, Bases, and Organic Solvents.
Vitrinite A nonfluorescent type of organic material in petroleum source rocks derived primarily from woody material.
The reflectivity of vitrinite is one of the best indicators of coal rank and thermal maturity of petroleum source rock.
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Hydrocarbon Generation Potential
TOC in Shale (wt. %)
TOC in Carbonates (wt. %)
Poor
Fair
Good
Very Good
Excellent
0.0-0.5
0.5-1.0
1.0-2.0
2.0-5.0
>5.0
0.0-0.2
0.2-0.5
0.5-1.0
1.0-2.0
>2.0
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Schematic Representation of the
Mechanism
of Petroleum Generation and Destruction
(modified from Tissot and Welte, 1984)
Organic Debris
Kerogen
Carbon
Initial Bitumen
Oil and Gas
Methane
Oil Reservoir
Migration Thermal Degradation
Cracking
Diagenesis
Catagenesis
Metagenesis
Pro
gre
ssiv
e B
uri
al an
d H
eati
ng
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Incipient Oil Generation
Max. Oil Generated
Oil Floor
Wet Gas Floor
Dry Gas Floor
Max. Dry Gas Generated
(modified from Foster and Beaumont, 1991, after Dow and O’Conner, 1982)
Vit
rin
ite R
efl
ecta
nce (
Ro)
%
We
igh
t %
Carb
on
in
Kero
gen
Sp
ore
Co
lora
tio
n In
de
x (
SC
I)
Pyro
lysis
T
(C)
max
0.2
0.3
0.4
0.5
4.0
3.0
2.0
1.3
1
2
3
4
5 6
7 8 9
10
430
450
465
65
70
75
80
85
90
95
0.6 0.7 0.8 0.9 1.0 1.2
OIL
Wet Gas
Dry Gas
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Reservoir rock
Seal
Migration route
Oil/water contact (OWC)
Hydrocarbon accumulation
in the reservoir rock
Top of maturity
Source rock
Fault (impermeable)
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Cross Section Of A Petroleum System
Overburden Rock
Seal Rock
Reservoir Rock
Source Rock
Underburden Rock
Basement Rock
Top Oil Window
Top Gas Window
Geographic Extent of Petroleum System
Petroleum Reservoir (O)
Fold-and-Thrust Belt
(arrows indicate relative fault motion)
Essential
Elements
of
Petroleum
System
(Foreland Basin Example)
(modified from Magoon and Dow, 1994)
O O
Sed
imen
tary
Basin
Fil
l
O
Stratigraphic
Extent of
Petroleum
System
Pod of Active
Source Rock
Extent of Prospect/Field
Extent of Play
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what is “trap” ?
The term “trap” was first applied to a hydrocarbon accumulation
by Orton: “…stocks of oil and gas might be reapped in the
summits of folds or arches found along their wat to higher
ground .”A detailed historical account of the subsequent
evolution of the concept and etymology of the term trap is found
in Dott and Reynolds(1969).
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Structural traps
Stratigraphic traps
Combination traps
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Structural Hydrocarbon Traps
(modified from Bjorlykke, 1989)
Oil/Wat
er
Contact
Gas Oil/Gas
Contact
Oil
Closure
Fold Trap
Oil Shale Trap
Fracture Basement
Oil Salt
Diapir Salt
Dom
e
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Oil
Sandstone Shale
Hydrocarbon Traps - Dome
Gas
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Fault Trap
Oil / Gas
Normal Faults
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Oil/Gas
Oil/Gas
Oil/Gas
Stratigraphic Hydrocarbon Traps
Uncomformity
Channel Pinch Out
(modified from Bjorlykke, 1989)
Unconformity Pinch out
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Asphalt Trap
Water
Meteoric
Water
Biodegraded
Oil/Asphalt
Partly
Biodegraded Oil
Hydrodynamic Trap
Shale
Oil
Water
Hydrostatic
Head
(modified from Bjorlykke, 1989)
Other Traps
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where can we find petroleum ?
Hydrocarbons—crude oil and natural gas—are found in
certain layers of rock that are usually buride deep beneath
the surface of the earth.
Salt
Dome
Faul
t
Unconfor
mity
Pincho
ut
Anticli
ne
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LECTURE 4
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• Source Rock - A rock with abundant hydrocarbon-prone organic matter
• Reservoir Rock - A rock in which oil and gas accumulates:
• Porosity - space between rock grains in which oil accumulates
• Permeability - passage-ways between pores through which oil and gas moves
• Seal Rock - A rock through which oil and gas cannot move effectively (such as mudstone and claystone)
•Trap - The structural and stratigraphic configuration that focuses oil and gas into an accumulation
•Migration Route - Avenues in rock through which oil and gas moves from source rock to trap
Petroleum System Elements
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DK
-
58
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1. Source Rock
2. Reservoir Rock
3. Timing / Burial History
4. Maturation
5. Migration
6. Cap Rock
7. Trap HIGH PRESSURE
10 km
1000
0
2000
3000
4000
5000
6000
7000
8000
9000
10000
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DK
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59
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Reservoir Components
Reservoir Rock
Cap Rock Reservoir Trap Fluids
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LECTURE 5
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For rock to contain petroleum and later allow
petroleum to flow,it must have certain physical
characteristics. Obvilusly, there must be some spaces
in the rock in which the petroleum can be stored.
If rock has openings, voids, and spaces in which
liquid and gas may be stored, it is said to be porous .
For a given volume of rock, the ratio of the open
space to the total volume of the rock is called porosity,
the porosity may be expressed a decimal fraction but
is most often expressed as a percentage. For
example,if 100 cubic feet of rock contains many tiny
pores and spaces which together have a volume of 10
cubic feet, the porosity of the rock is 10%.
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Structure contour maps of structure or zone tops
Data is obtained from open hole logs or seismic interpretations.
Net pay map using specific cut-off values to gross pay thickness
Hydro-carbon pore volume map (HCPV)
Cross-section
Structural: Open hole logs are illstrated, as such, “hanging the wells” is based on a selected datum depth
Stratigraphic: Open hole logs are illustrated, as such, “hanging the wells” is based on a selected strato or zone.
Geologic Subsurface Maps
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POROSITY The porosity of a rock is a measure of the storage capacity (pore
volume)that is capable of holding fluids. Quantitatively, the
porosity is the ratio of the pore volume to the total volume (bulk
volume). This important rock property is determined
mathematically by the following generalized
relationship:
where f=porosity
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As the sediments were deposited and the rocks were being formed during past geological times, some void spaces that developed became isolated from the other void spaces by excessive cementation. Thus, many of the void spaces are interconnected while some of the pore spaces arecompletely isolated. This leads to two distinct types of porosity, namely:
• Absolute porosity
• Effective porosity
POROSITY
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Absolute porosity
The absolute porosity is defined as the ratio of the total pore space in
the rock to that of the bulk volume. A rock may have considerable
absolute porosity and yet have no conductivity to fluid for lack of pore
interconnection. The absolute porosity is generally expressed
mathematically by the following relationships:
or
where fa =absolute porosity.
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Effective porosity
The effective porosity is the percentage of interconnected
pore space with respect to the bulk volume, or
where f=effective porosity.
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One important application of the effective porosity is its use in determining the original hydrocarbon volume in place. Consider a reservoir with an areal extent of A acres and an average thickness of h feet. The total bulk volume of the reservoir can be determined from the following expressions:
Bulk volume =43,560 Ah, ft3
or
Bulk volume =7,758 Ah, bbl
where A =areal extent, acres
h =average thickness
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When porosity was developed?
Primary porosity.- Rock porosity developed during the initial rock deposition.
Secondary porosity.- Rock porosity due to a chemical reaction between the reservoir fluids and the rock, wich could occur for instance if some of the rock minerals are dissolved by the formation water (leaching) This phenomena is called “Diagenesis”
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Factors affecting porosity values
• Sorting
• Arragement
• Cementation
How is porosity determined?
• Open hole logs
• Core samples
• Core plugs vs. Full core diameter (plug selection, fractures, vuggs)
• Overburden pressure correction (for permeability rocks)
• Core cleaning (humidity oven)
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Porosity
i. Define: Porosity = Total pore volume in the rock sample Total rock sample volume (solid+pore)
ii. Mathematically:
iii. Range of porosity: 0.1 to 0.3
iv. Use reservoir core to measure porosity
v. Limitations
a. Rock sample must be large enough to obtain many sand grains and many pores to be representative
b. Features sample has a different type of pore space from sandstone
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Porosity Determination from Logs Porosity Determination from Logs
Most log interpretation techniques in use today use a bulk volume rock approach
Quantitative rock data must be input into equations to derive values of phi and Sw. For example:
Db = Φ x Df + (1 - Φ) Dm
Porosity is then derived:
Φ = (Dma - Db)/(Dma - Df)
Values of matrix density are normally assumed:
Dma = 2.65 for clean sand
= 2.68 for limy sands or sandy limes
= 2.71 for limestone
= 2.87 for dolomite
Fluid density is that of the mud filtrate:
Df = 1.0 (fresh)
= 1.0 = 0.73N (salt)
Where: N = NaCl concentration, ppm x 10-6
Accurate knowledge of grain density is essential
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Porosity at Net Overburden (NOB)
Increase in NOB can reduce porosity. Generally
the reduction is <10% of total porosity.
Less severe in consolidated rocks, more severe
in unconsolidated rocks
Grain Density
Measure the bulk volume of the sample. Weigh
the sample. GD = Dry weight/Grain volume
Most rocks are mixtures of minerals. The grain
density of any rock is variable and is dependent
on the mineralogy:
1.25gm/cc -- volcanic ash, some coals
2.65gm/cc -- clean, quartz sandstone
2.68gm/cc -- shaly sandstone with some carbonate
2.71gm/cc -- clean limestone
2.87 - >3.0gm/cc – dolomite
2.32gm/cc -- gypsum
2.96gm/cc -- anhydrite
3.89gm/cc -- siderite
Accurate values of grain density are important
because grain density is used to correct wireline
logs for potential sources of error
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Example
One of the most important determinations for an oil accumulation is the volume of oil in place. Suppose that in geological evidence is known that the area extent of an oil reservoir is 2 million sqft and that the thickness of the bay zone is 30 ft. If the sand porosity and water saturation are 0.2 and 0.3, respectively, how much oil is present?
Solution:
Volume of bay = 2,000,000 ft3 x 30 ft = 6x107ft3
Total pore volume = 0.2 x 6x107 = 12x106 ft3
Then Sw+So=1; So = 1 - 0.3 = 0.7
Total oil volume = 0.7 x 12x106 = 8.4x106 ft3
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LECTURE 6
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PERMEABILITY
Permeability is a property of the porous medium that measures the
capacity and ability of the formation to transmit fluids. The rock
permeability, k, is a very important rock property because it
controls the directional movement and the flow rate of the reservoir
fluids in the formation. This rock characterization was first defined
mathematically by Henry Darcy in 1856. In fact, the equation that
defines permeability in terms of measurable quantities is called
Darcy’s Law.
Darcy developed a fluid flow equation that has since become one of
the standard mathematical tools of the petroleum engineer. If a
horizontal linear flow of an incompressible fluid is established
through a core sample of length L and a cross-section of area A,
then the governing fluidflow equation is defined as
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where n=apparent fluid flowing velocity, cm/sec
k =proportionality constant, or permeability, Darcys
=viscosity of the flowing fluid, cp
dp/dL =pressure drop per unit length, atm/cm
The apparent velocity determined by dividing the flow rate by the cross-sectional area across which fluid is flowing. Substituting the relationship, q/A, in place of nin Equation 3-21 and solving for q results in
where q =flow rate through the porous medium, cm3/sec
A =cross-sectional area across which flow occurs, cm2
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One Darcy is a relatively high permeability as the permeabilities of
most reservoir rocks are less than one Darcy. In order to avoid the use of fractions in describing permeabilities, the term millidarcy is used. As the term indicates, one millidarcy, i.e., 1 md, is equal to one-thousandth of one Darcy or,
1 Darcy =1000 md
The negative sign in Equation is necessary as the pressure increases in one direction while the length increases in the opposite direction.
Integrate the above equation
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Linear flow model
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where L =length of core, cm
A =cross-sectional area, cm2
The following conditions must exist during the
measurement of permeability:
• Laminar (viscous) flow
• No reaction between fluid and rock
• Only single phase present at 100% pore space
saturation
This measured permeability at 100% saturation of a
single phase is called the absolute permeability of the
rock.
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For a radial flow, Darcy’s equation in a differential form can be
written as:
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Intergrating Darcy’s equation gives:
The term dL has been replaced by dr as the length term has now become a radius term.
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Rock Permeability
i. Measurement of the fluid ability to flow through the connected pores of the reservoir.
ii. A function of a degree of interconnection between pores in the rock
iii. The concept was introduced by Darcy in a classical experimental work from both petroleum engineering and ground water hydrology. Is expressed in milidarcies or Darcies.
iv. The flow rate can be measured against pressure (head) for different porous media
v. The flow rate of fluid thru specific porous medium is linearly proportional top head difference betwen the inlet and outlet and characteristic property of the medium, thus u = kDP
Where k = permeability and is a characteristic property of the porous medium
vi. The rock permeability is measured from core samples (plugs or whoke core) in the laboratory or it could also be calculated from well testing
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a. Suppose a cylindrical sample (core) of a porous rock is fully saturated with liquid of viscosity .
b. Experimentally for a particular rock sample the expression
Darcy Equation
where k is constant
c. Q will increase a k increases, the higher the value of k the more readily will liquid flow through the core
l
A Q
P1 P2
)( 21 PPA
lQk
=
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d. If in flow rate contain two fluid (oil and water), free gas is not present then,
d. If Q (cm3/s), (cp), l (cm) A (cm2), and P1 and P2 (atm), the value of k in Darcy is
1 Darcy = 10-8 cm2
)( 21 PPA
lQk oo
o
=
)( 21 PPA
lQk ww
w
=
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LECTURE 7
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SATURATION
Saturation is defined as that fraction, or percent, of the pore volume
occupied by a particular fluid (oil, gas, or water). This property is
expressed mathematically by the following relationship:
Applying the above mathematical concept of saturation to each reservoir
fluid gives
where
So =oil saturation
Sg =gas saturation
Sw =water saturation
Sg +So +Sw =1.0
Fluid Saturations from Cores
Through knowledge of porosity,
permeability and residual fluid saturations
(oil, water and gas), it is possible to predict
with a high degree of accuracy the probable
type of fluid
which will be produced from a given interval.
Review of the core fluorescence can also
be an indicator of oil gravity and should be
factored when type of production is
predicted.
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Critical oil saturation, Soc
For the oil phase to flow, the saturation of the oil must exceed a
certain value which is termed critical oil saturation. At this particular
saturation, the oil remains in the pores and, for all practical
purposes, will not flow.
Fluid Saturation
i. Water saturation, Sw = Volume filled by water/ Total pore volume
Oil saturation, So = Volume filled by oil/ Total pore volume
ii. If oil and water is the only fluid present, Sw + So = 1
iii. In most oil fields Sw tends to increase as porosity decrease
iv. Typical value of Sw – 0.1 to 0.5
v. Free gas also present in oil pools,
Free gas saturation, Sg = Volume filled by free gas/total pore volume
vi. 3 factors should always be remembered conceiving fluid saturation
a. It vary from place to place in reservoir rock; Sw higher in less
porous sections due to gravity segregation of the gas, oil and water
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Residual oil saturation, Sor
During the displacing process of the crude oil system
from the porous media by water or gas injection (or
encroachment) there will be some remaining oil left that
is quantitatively characterized by a saturation value that
is larger than the critical oil saturation. This saturation
value is called the residual oil saturation, Sor. The term
residual saturation is usually associated with the
nonwetting phase when it is being displaced by a
wetting phase.
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Movable oil saturation, Som
Movable oil saturation Som is another saturation of
interest and is defined as the fraction of pore
volume occupied by movable oil as expressed by
the following equation:
Som =1 Swc Soc
where
Swc =connate water saturation
Soc =critical oil saturation
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Critical gas saturation, Sgc
As the reservoir pressure declines below the bubble-point pressure,
gas evolves from the oil phase and consequently the saturation
of the gas increases as the reservoir pressure declines. The gas
phase remains immobile until its saturation exceeds a certain
saturation, called critical gas saturation, above which gas begins
to move.
Critical water saturation, Swc
The critical water saturation, connate water saturation, and
irreducible water saturation are extensively used interchangeably
to define the maximum water saturation at which the water
phase will remain immobile.
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LECTURE 8
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Capillary pressure If a glass capillary tube is placed in a large open vessel containing
water, the combination of surface tension and wettability of tube to
water will cause water to rise in the tube above the water level
in the container outside the tube as shown in Figure 3.
The water will rise in the tube until the total force acting to pull the
liquid upward is balanced by the weight of the column of liquid
being supported in the tube.
Figure 3
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CAPILLARY PRESSURE
The capillary forces in a petroleum reservoir are the result of the combined effect of the surface and interfacial tensions of the rock and fluids, the pore size and geometry, and the wetting characteristics of the system.
Any curved surface between two immiscible fluids has the tendency to
contract into the smallest possible area per unit volume. This is true
whether the fluids are oil and water, water and gas (even air), or oil and gas. When two immiscible fluids are in contact, a discontinuity in pressure exists between the two fluids, which depends upon the curvature of the interface separating the fluids. We call this pressure difference the capillary pressure and it is referred to by pc.
Capillary pressure =(pressure of the nonwetting phase) (pressure of
the wetting phase)
pc =pnw pw
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Figure4
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Transition Zone
The figure indicates that the saturations are gradually
changing from 100% water in the water zone to irreducible
water saturation some vertical distance above the water
zone. This vertical area is referred to as the transition zone,
which must exist in any reservoir where there is a bottom
water table. The transition zone is then defined as the
vertical thickness over which the water saturation ranges
from 100% saturation to irreducible water saturation Swc.
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Water Oil Contact
The WOC is defined as the “uppermost depth in the
reservoir where a 100% water saturation exists.”
Gas Oil Contact
The GOC is defined as the “minimum depth at which a
100% liquid, i.e., oil +water, saturation exists in the
reservoir.”
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Figure 5
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It should be noted that there is a difference between
the free water level (FWL) and the depth at which 100%
water saturation exists. From a reservoir engineering
standpoint, the free water level is defined by zero
capillary pressure. Obviously, if the largest pore is so
large that there is no capillary rise in this size pore, then
the free water level and 100% water saturation level,
i.e., WOC, will be the same.
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Capillary Pressure
Capillary pressure in reservoirs can be defined
as the difference between the force acting
downwards (hydrostatic head, related to density
contrasts) and the force acting upwards
(buoyancy, related to pore throat size, interfacial
tension and contact angle)
Capillary pressure is measured in the laboratory
generally using plug samples or rotary sidewall
cores. Occasionally cuttings samples are used
In the most common type of test, a non-wetting
phase fluid (e.g. mercury) is injected into the
rock at slowly increasing values of pressure. The
amount of fluid injected at each increment of
pressure is recorded and is presented as a
capillary curve
Capillary Pressure (1)
Capillary pressure exists in a hydrocarbon
reservoir fundamentally because of
differences in the density of various fluids
that affect the pressure gradients:
Pressure gradient of water = 0.44 psi/ft
(density = 1gm/cc)
Pressure gradient of oil = 0.33 psi/ft
(density = 0.8gm/cc)*
Pressure gradient of gas = 0.09 psi/ft
(density = 0.2gm/cc)**
* 30°API
** 5000psi
As hydrocarbons accumulate in a trap, the
difference in density between the fluids
results in a vertical segregation of the
fluids: gas on oil, oil on water For
example, at 10,000ft, oil pressure = 3300
psi and water pressure = 4400 psi
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Capillary Pressure and
Water Saturation (2)
Reservoir Sw decreases with increasing height above the free water level (the level at
which the reservoir produces only water) .
Zones that are at irreducible water saturation (Swirr) produce only hydrocarbons. Swirr
occurs where sufficient closure and hydrocarbon column exist the transition zone occurs
between the free water level and the Swirr level. Formations in this zone produce water
and hydrocarbons. The magnitude of the Swirr and the thickness of the transition zone
are a function of the pore size distribution Small pore throats = low permeability = high
Swirr
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Initial Reservoir Fluid Distribution
The amount of Sw at any height in the reservoir is a function of:
Pore throat size, wettability, interfacial tension, saturation history and differences
in fluid densities.
These variables control capillary pressure, therefore there is a relationship
between Sw, h, Pc and pore throat size.
Laboratory measurements of capillary pressure are used to relate Sw to height
above the free water level as long as appropriate values of laboratory and
reservoir interfacial tension and contact angle are used Laboratory tests can be
made with different fluids oil, brine, mercury
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Capillary Pressure:
Static Measurement
Static Method – Mercury injection
Widely used, rapid, economic and simple. Mercury is the non-wetting phase and is injected into
a cleaned and evacuated core plug at successively increasing pressures from 0 to 60,000psi.
The core plug cannot be used for further testing because of residual Hg saturation Hg capillary
pressure data must be scaled to reservoir conditions using the following formula:
. Conversion factor = Mercury Pc = Sm Cos è m
Water-Air Pc Sw Cos è w
Where:
Sm = surface tension of mercury
Sw = surface tension of water
è m = contact angle of mercury against a solid (140 degrees)
è w = contact angle of water against a solid (0 degrees)
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Capillary Pressure:
Dynamic Measurement
Dynamic Method -- Centrifuge
Generally uses oil-brine fluid system but
actual reservoir fluids can also be used
Rapid, more complicated and more expensive
than mercury Pc measurements
Requires preserved or restored-state core
plugs Large (2 inch) plugs are required. These
can be used for further analysis Brine
saturated samples are centrifuged at ever
increasing speeds under oil to obtain a
relationship between capillary pressure and
saturation
Capillary Pressure: Rock Controls
Pore geometry is a fundamental control on
capillary pressure, in particular the size of the pore
throats: the capillary pressure characteristics
change with changes in Rock
Type (pore geometry) In heterogeneous reservoirs,
it is essential to collect capillary pressure data for
each Rock Type that is present in the reservoir All
other factors being equal, the lower the
permeability the smaller the pore throats the higher
the Pce and the higher the Swirr.
Capillary pressure data is used to determine the
height above free water (column height) for each
Rock Type and to improve the prediction of the type
of fluid produced (hydrocarbon/water)
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Use of Pc in Reservoir Simulation and Reservoir
Characterization
For purposes of simulation and characterization, it is
necessary to know the Free Water Level (FWL)
When FWL is known it is possible to predict Sw at any
height in the reservoir even in areas that lack well
Penetrations.
This is particularly important in the following cases:
Areas with long transition zones and no obvious FWL
Areas with misidentified or unknown FWL
Areas with unknown or incorrect Rw
Areas where a, m and/or n are incorrect or unknown
Areas with multiple Rock Types (where a, m,n and Sw
vary as a function of Rock Type)
In these situations, it is possible to solve for Sw using
either the Pc curves or the Leverett J Function.
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LECTURE 9
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WETTABILITY
Wettability is defined as the tendency of one fluid to spread
on or adhere to a solid surface in the presence of other
immiscible fluids. The concept of wettability is illustrated in
Figure1. Small drops of three liquids-mercury, oil, and
water—are placed on a clean glass plate.
![Page 111: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/111.jpg)
The three droplets are then observed from one side as
illustrated in Figure 3-1. It is noted that the mercury retains a
spherical shape, the oil droplet develops an approximately
hemispherical shape, but the water tends to spread over the
glass surface.
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The tendency of a liquid to spread over the surface of a
solid is an indication of the wetting characteristics of
the liquid for the solid. This spreading tendency can be
expressed more conveniently by measuring the angle
of contact at the liquid-solid surface. This angle, which
is always measured through the liquid to the solid, is
called the contact angle q.
The contact angle q has achieved significance as a
measure of wettability.
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As shown in Figure 1, as the contact angle decreases, the wetting characteristics of the
liquid increase. Complete wettability would be evidenced by a zero contact angle, and
complete nonwetting would be evidenced by a contact angle of 80°. There have been
various definitions of intermediate wettability but, in much of the published literature,
contact angles of 60° to 90° will tend to repel the liquid.
The wettability of reservoir rocks to the fluids is important in that the distribution of the
fluids in the porous media is a function of wettability.
Because of the attractive forces, the wetting phase tends to occupy the smaller pores of
the rock and the nonwetting phase occupies the more open channels.
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LECTURE 10
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UNIT PUMPING
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UNIT PUMPING
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UNIT PUMPING
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SYSTEM PRODUCTION
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INJECTION GAS
PRODUCED FLUID
PRESSURE (PSI)
DE
PT
H (
FT
TV
D)
1000
2000
3000
4000
5000
6000
7000
0
1000 2000 0
OPERATING GAS LIFT VALVE
CASING PRESSURE WHEN
WELL IS BEING GAS LIFTED
FBHP
SIB
HP
CONSTANT FLOW GAS LIFT WELL
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DISSOLVED GAS DRIVEDISSOLVED GAS DRIVE
GAS CAP DRIVEGAS CAP DRIVE
WATER DRIVE
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Sistema cerrado (un pozo)
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Field Production 1.Primary Recovery (Natural Methods)
i. 1st method of producing oil from a well
ii. Solution gas drive
a. pressure inside reservoir relieved when well punctures and gas trapped in oil forms bubbles
b. Bubbles grow, exert pressure push oil to well and up to surface (20-30%)
iii. Gas cap drive
a. If contain gas cap, drill well directly into oil layer – gas cap expand
b. Expanding gas pushes oil into well (40%)
iv. Water drive scenario
a. Water layer press against oil layer
b. Water pushes oil towards surface and replace it within the pores of the reservoir rock
c. Highest recovery: up to 75%
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2.Secondary Recovery
i. Used to enhance or replace primary techniques
ii. Water flooding
a. Additional injection well is drilled into the reservoir
b. Pressure water injected
c. Water displaces the oil in reservoir
iii. Mechanical Lift
a. Reciprocating or plunger pumping called “horsehead”
b. Pump barrel lowered into well on 6 inch string steel rod (sucker rods)
c. Up and down movement force oil up to tubing
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3. Tertiary Recovery
i. When 2nd recovery no longer effective
ii. Thermal Process
a. Steam Flooding – steam injected, heats oil to flow readily
b. in-situ combustion (fire flooding) – air injected, a portion if oil ignited , combustion front moves away from air injection well toward production well
iii. CO2 injection
a. CO2 injected, mix with oil – reduces forces that hold oil to pores, allows easily displace by injected water
iv. Chemical recovery
i. Inject polymer into water phase of reservoir trap, large molecule add bulk to water, water thicken, wash oil from pores
ii. Sometimes surfactant added to reduce force water to solid
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4. Improvement of formation characteristic
i. To aid 3rd recovery because production drop
ii. Acidizing
a. Injecting acid into a soluble formation (exp: carbonate) to dissolve rocks
b. Enlarge the existing voids and increase permeability
iii. Hydraulic Fracturing
a. Inject a fluid into formation under significant pressure to enlarge existing fracture and create new fracture
b. This fracture extend outward from well bore into formation therefore increase permeability
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Petroleum Production System
1. Petroleum hydrocarbon production involve 2 districts
i. Reservoir – a porous medium with a unique storage and flow characteristic
ii. Artificial structures includes well, bottom hole, surface gathering, separation and storage facilities
2. Production Engineering - attempts to maximize production in a cost effective way
3. Appropriate production technology and method related directly with other major area of petroleum engineering such as formulation evaluation, drilling and reservoir engineering
4. Petroleum Hydrocarbon
i. Mixture of many compounds – petroleum and natural gas
ii. Mixture depending on its composition and conditions of P and T occur as liquid or gas or mixture of 2 phase
![Page 128: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/128.jpg)
4. Oil Gravity
i. Commonly expressed in degree API
ii. The terms heavy, medium and light crude cover approximately the ranges 10 to 20o, 20 to 30o and over 30o API, respectively
5. Instantaneous Water/Oil Ratio (WOR)
i. Homogeneous formation produce only oil and water (no free gas) then
ii. The pressure drop in oil may differ slightly from that in the water owing to effect of capillary forces, so dividing the equations above, results in
5.1315.141
60
=
F
o
oSGAPI
dl
dPkq
o
oo =
dl
dPkq
w
ww
=
wo
ow
o
w
k
k
q
q
=
![Page 129: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/129.jpg)
iii. At the surface
iv. Or from above equation
(surface)
Where Bo is oil formation volume factor:
v. Bo is defined as ratio of the volume of oil (plus the gas in solution) at reservoir T and P to the volume of oil at standard conditions (so-called stock-tank oil)
o
wo
oo
w
q
qB
Bq
q=
wo
owo
k
kBWOR
=
![Page 130: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/130.jpg)
6. Instantaneous Gas/Oil Ratio (GOR)
i. Homogeneous formation producing only oil and gas (no water production, although water may be present in the formation)
ii. Where the pressure drop across the distance dl is the same for both fluid, if capillary forces are neglected. Dividing
iii. Stock-tank oil rate will be qo/Bo, and surface free gas rate qg/Bg. In addition to free gas produced from the formation, each barrel of stock-tank oil will release a volume Rs of gas, then the total surface gas/oil ratio is
dl
dPkq
o
oo =
dl
dPkq
g
g
g =
go
og
o
g
k
k
q
q
=
![Page 131: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/131.jpg)
iv. At the surface
v. Therefore
(surface)
7. Productivity Index
i. Bottom hole flowing pressure - producing pressure (Pwf) at the bottom of the well
ii. The difference bettwen this and the well static pressure (Ps) is
og
os
oo
gg
sqB
qgBR
Bq
BqR +=+
gog
ogo
skB
kBRGOR
+=
wfs PPDrawdown =
![Page 132: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/132.jpg)
iii. Ratio of producing rate of the well to its draw down is called Producing Index.
iv. If the rate q (bbl/day) of stock-tank liquid and draw down (psi), the productivity index (J) is defined as
(bbl/day/psi)
iii. Productivity index is based on the gross liquid rate (oil rate + water rate)
iv. Specific productivity index, Js is the number of barrel (gross) of stock-tank liquid produced/day/psi/ft net thickness
wfs PP
qJ
=
)( wfs
sPPh
q
h
JJ
==
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LECTURE 11
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LECTURE 12
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Petroleum reservoirs are broadly classified as oil or gas reservoirs.
These broad classifications are further subdivided depending on:
The composition of the reservoir hydrocarbon mixture
Initial reservoir pressure and temperature
Pressure and temperature of the surface production
The conditions under which these phases exist are a matter of
considerablepractical importance. The experimental or the
mathematical determinations of these conditions are conveniently
expressed in different types of diagrams commonly called phase
diagrams. One such diagram is called the pressure-
temperature diagram.
![Page 140: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/140.jpg)
Figure 1-1 shows a typical pressure-temperature diagram of a
multicomponent system with a specific overall composition.
Although a different hydrocarbon system would have a
different phase diagram, the general configuration is similar.
These multicomponent pressure-temperature diagrams are
essentially
used to:
• Classify reservoirs
• Classify the naturally occurring hydrocarbon systems
• Describe the phase behavior of the reservoir fluid
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LECTURE 13
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Petroleum reservoirs are broadly classified as oil or
gas reservoirs.
The composition of the reservoir hydrocarbon
mixture
Initial reservoir pressure and temperature
pressure-temperature diagram
![Page 152: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/152.jpg)
![Page 153: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/153.jpg)
Figure 1-1 shows a typical pressure-temperature diagram of a
multicomponent system with a specific overall composition.
Although a different hydrocarbon system would have a different
phase diagram, the general configuration is similar.
These multicomponent pressure-temperature diagrams are essentially
used to:
• Classify reservoirs
• Classify the naturally occurring hydrocarbon systems
• Describe the phase behavior of the reservoir fluid
![Page 154: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/154.jpg)
Critical point—The critical point for a multicomponent mixture is
referred to as the state of pressure and temperature at which all
intensive properties of the gas and liquid phases are equal (point C).
At the critical point, the corresponding pressure and temperature are
called the critical pressure pc and critical temperature Tc of the
mixture.
![Page 155: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/155.jpg)
Bubble-point curve—The bubble-point curve (line BC) is
defined as the line separating the liquid-phase region from the
two-phase region.
Dew-point curve—The dew-point curve (line AC) is defined as
the line separating the vapor-phase region from the two-phase
region.
![Page 156: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/156.jpg)
Oil reservoirs—If the reservoir temperature T is less
than the critical temperature Tc of the reservoir fluid,
the reservoir is classified as an oil reservoir.
Gas reservoirs—If the reservoir temperature is greater
than the critical temperature of the hydrocarbon fluid,
the reservoir is considered a gas reservoir.
![Page 157: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/157.jpg)
Low-shrinkage oil
• Oil formation volume factor
less than 1.2 bbl/STB
• Gas-oil ratio less than 200
scf/STB
• Oil gravity less than 35° API
• Black or deeply colored
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In general, if the reservoir temperature is above the
critical temperature of the hydrocarbon system, the
reservoir is classified as a natural gas reservoir. On
the basis of their phase diagrams and the prevailing
reservoir conditions, natural gases can be classified
into 3 categories:
Retrograde gas-condensate
Wet gas
Dry gas
![Page 161: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/161.jpg)
If the reservoir temperature T lies
between the critical temperature Tc
and cricondentherm Tct of the
reservoir fluid, the reservoir is
classified as a retrograde gas-
condensate reservoir.
• the gas-oil ratio for a condensate
system increases with time due to the
liquid dropout and the loss of heavy
components in the liquid.
• Condensate gravity above 50° API
• Stock-tank liquid is usually water-white
or slightly colored.
Retrograde gas-condensate reservoir
![Page 162: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/162.jpg)
Temperature of wet-gas reservoir
is above the cricondentherm of
the hydrocarbon mixture. Because
the reservoir temperature exceeds
the cricondentherm of the
hydrocarbon system, the reservoir
fluid will always remain in the
vapor phase region as the
reservoir is depleted isothermally,
along the vertical line A-B.
Wet-gas reservoir
![Page 163: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/163.jpg)
Wet-gas reservoirs are characterized by the following
properties:
• Gas oil ratios between 60,000 to 100,000 scf/STB
• Stock-tank oil gravity above 60° API
• Liquid is water-white in color
• Separator conditions, i.e., separator pressure and
temperature, lie within the two-phase region
Wet-gas reservoir
![Page 164: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/164.jpg)
The hydrocarbon mixture
exists as a gas both in the
reservoir and in the
surface facilities.
Usually a system having a
gas-oil ratio greater than
100,000 scf/STB is
considered to be a dry gas.
Dry-gas reservoir
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Temperature of Test = Reservoir Temperature
V t1
V t2
V t3
= V
b
V t5 V
t4
oil oil oil oil
oil
gas gas
Hg Hg Hg Hg
Hg
P 1 >> P
b P
2 > P
b P
3 = P
b P
4 < P
b P
5 < P
4
1 2 3 4 5
Properties determined ◦ Pb ◦ Co
![Page 178: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/178.jpg)
gas
oil
oil oil oil
oil
gas
Hg
Hg
Hg Hg
Hg
P 1 = P b P 2 < P b P 2 < P b P 2 < P b P 3 < P 2 < P b
1 2 3 4 5
gas oil
Gas off
Temperature of Test = Reservoir Temperature
![Page 179: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/179.jpg)
Properties Determined ◦ Oil formation volume factor at the Bubble Point
pressure Bodb and below the bubble point pressure Bod
◦ Solution gas-oil ratio at the Bubble Point pressure Rsdb and below the bubble point pressure Rsd
◦ Isothermal compressibility (derived property)
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LECTURE 14
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The Water-Drive Mechanism Many reservoirs are bounded on a portion or all of their peripheries
by water bearing rocks called aquifers. The aquifers may be so
large compared to the reservoir they adjoin as to appear infinite for
all practical purposes, and they may range down to those so small
as to be negligible in their effects on the reservoir performance.
Reservoir have
a water drive
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Characteristics Trend
Reservoir pressure Declines very slowly (remains
very high)
Gas oil ratio Little change during the life of
the reservoir (remains low)
Water production Early excess water production
Well behavior Flow until water production gets
excessive.
Oil recovery 35 to 75 %
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Rock and Liquid Expansion
When an oil reservoir initially exists at a pressure higher than
its bubble-point pressure, the reservoir is called an
undersaturated oil reservoir.
At pressures above the bubble-point pressure, crude oil,
connate water, and rock are the only materials present. As the
reservoir pressure declines, the rock and fluids expand due to
their individual compressibilities.
The reservoir rock compressibility is the result of two factors:
• Expansion of the individual rock grains
• Formation compaction
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Both of the above two factors are the results of a
decrease of fluid pressure within the pore spaces,
and both tend to reduce the pore volume through
the reduction of the porosity.
This driving mechanism is considered the least
efficient driving force and usually results in the
recovery of only a small percentage of the total
oil in place.
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LECTURE 15
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The Depletion Drive Mechanism This driving form may also be referred to by the following various
terms:
• Solution gas drive
• Dissolved gas drive
• Internal gas drive
In this type of reservoir, the principal source of energy is a result of gas
liberation from the crude oil and the subsequent expansion of the
solution gas as the reservoir pressure is reduced. As pressure falls
below the bubble-point pressure, gas bubbles are liberated within
the microscopic pore spaces. These bubbles expand and force the
crude oil out of the pore space as shown conceptually in Figure 1
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Figure 1 Solution gas drive reservoir
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Gas Cap Drive
Gas-cap-drive reservoirs can be identified by the presence of
a gas cap with little or no water drive as shown in Figure 2.
Due to the ability of the gas cap to expand, these reservoirs
are
characterized by a slow decline in the reservoir pressure.
The natural energy available to produce the crude oil
comes from the following two sources:
• Expansion of the gas-cap gas
• Expansion of the solution gas as it is liberated
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Figure 2 Gas-cap drive reservoir
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The Gravity-Drainage-Drive Mechanism
The mechanism of gravity drainage occurs in petroleum
reservoirs as a result of differences in densities of the
reservoir fluids. The effects of gravitational forces can be
simply illustrated by placing a quantity of crude oil and a
quantity of water in a jar and agitating the contents. After
agitation, the jar is placed at rest, and the more denser
fluid (normally water) will settle to the bottom of the jar,
while the less dense fluid (normally oil) will rest on top of
the denser fluid. The fluids have separated as a result of
the gravitational forces acting on them.
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Characteristics Trend
Reservoir pressure Variable rates of pressure
decline, depending principally
upon the amount of gas
conservation.
Gas oil ratio Low gas-oil ratio
Water production Little or no water production.
Well behavior
Oil recovery Near to 80 %
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The principle of natural water drive is that an aquifer provides the energy for
hydrocarbon production. Both water expansion, as a result of pressure
reduction, and inflow are involved.
Natural water drive is associated with high recovery rates; oil from
35-75% OIIP; gas from 60-80% GIIP.
It is not uncommon for flow from the
surface to supply the energy for
natural water drive.
When a pressure drop occurs, both
the oil and water liquid phases
expand resulting in production.
Additionally, water inflow radially and
vertically displaces the oil towards
the producers.
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Cross-section view
Plane view
Water
Hydrocarbon
The Upper Devonian Leduc pools are driven by inflow from the Cooking Lake
Aquifer.
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Oil producing well
Water Water
Cross Section
Oil Zone
Both bottom water drive, where the water leg underlies the entire reservoir, and
edge water drive, where only part of the areal extent is contacted by water, are
recognized.
Oil producing well
Cross Section
Oil Zone
Water
Edge Water Drive Bottom Water Drive
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NATURAL WATER
DRIVE HISTORY watercut
GOR (R)
pressure
time
Rsi
OIL PRODUCTON
• Pressure remains high; small drop.
• R (producing gas oil ratio) remains low.
• Water influx starts early and increases to appreciable levels.
• Residual oil may be trapped behind the advancing water.
• Wells flow freely until water production (watercut) becomes excessive.
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The Combination-Drive Mechanism
The driving mechanism most commonly encountered is one in
which both water and free gas are available in some degree to
displace the oil toward the producing wells. The most common
type of drive encountered,
therefore, is a combination-drive mechanism as illustrated in Figure
4. Two combinations of driving forces can be present in
combinationdrive reservoirs. These are (1) depletion drive and a
weak water drive and; (2) depletion drive with a small gas cap
and a weak water drive.
Then, of course, gravity segregation can play an important role in
any of the aforementioned drives.
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Figure 4 Combination drive reservoir
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RESERVOIR PERFORMANCE DATA (1)
Pressure trends in reservoirs under various drive mechanisms are distinctive.
100
0 10 20 30 40 50
% OIIP Produced
P
%
WATER DRIVE
GAS CAP DRIVE SOLUTION
GAS DRIVE
80
60
40
20
0
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RESERVOIR PERFORMANCE DATA (2)
Producing GOR is also strongly diagnostic of drive mechanism.
0 10 20 30 40 50
%OIIP Produced
GOR
%
SOLUTION
GAS DRIVE
GAS CAP DRIVE
WATER DRIVE
100
80
60
40
20
0
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Average Oil RecoveryFactors,
% of OOIPDrive Mechanism
Range Average
Solution-gas drive 5 - 30 15
Gas-cap drive 15 - 50 30
Water drive 30 - 60 40
Gravity-drainagedrive
16 - 85 50
Recovery factor is defined as the fraction (or percentage) of the volume of
hydrocarbon produced (recovered) from the amount of volume initially in place.
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Average Gas RecoveryFactors,
% of OGIPDrive Mechanism
Range Average
Volumetric reservoir(Gas expansion drive)
70 - 90 80
Water drive 35 - 65 50
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Solution-gas drive - API study
Water drive - API study
Water drive - Guthrie-Greenberger study
( (
=
1741.0
3722.0
0979.01611.0
18.41
a
bwi
obob
wiR
p
pS
k
B
SE
f
( (
=
2159.0
1903.0
0770.00422.0
19.54
a
iwi
oi
w
oi
wiR
p
pS
k
B
SE
f
114.00003.0538.1log136.0256.0log272.0 1010 ++= hSkE owiR f
![Page 210: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/210.jpg)
These correlations work best for sandstone reservoirs.
Nomenclature
ER = Oil recovery efficiency (recovery factor), [% (for API
study); fraction (for G-G study)]
f = Reservoir porosity, fraction
Swi = Interstitial water saturation, fraction
Bob = Formation volume factor of oil at bubblepoint, RB/STB
k = Reservoir permeability, [darcy (for API study);
md (For G-G study)]
ob = Oil viscosity at bubblepoint pressure, cp
pb = Bubblepoint pressure of oil, psig
pa = Abandonment reservoir pressure, psig
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Solution-gas drive oil reservoirs Low oil density Low oil viscosity High oil bubblepoint pressure
Gas-cap drive oil reservoirs Favorable oil properties Relatively large ratio of gas cap to
oil zone High reservoir dip angle Thick oil column
Water drive oil reservoirs
– Large aquifer
– Low oil viscosity
– High relative oil permeability
– Little reservoir heterogeneity
and stratification
Gravity drainage oil reservoirs
– High reservoir dip angle
– Favorable permeability distribution
– Large fluid density difference
– Large segregation area
– Low withdrawal
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Volumetric gas reservoir (gas expansion drive)
◦ Low abandonment pressure
Water-drive gas reservoir
– Small aquifer
– Small degree of reservoir heterogeneity and stratification
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LECTURE 16
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When an oil and gas reservoir is trapped with wells, oil and gas, and frequently some water, are produced, thereby reducing the reservoir pressure and causing the remaining oil and gas to expand to fill the space vavated by the fluids removed. When the oil-and gas-bearing strata are hydraulically connected with water-bearing strata, or aquifers, water encroaches into the reservoir as the pressure drops owing to production .This water encroachment decreases the extent to which the remaining oil and gas expand and accordingly retards the decline in reservoir pressure.
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In as much as the temperature in oil and gas reservoir remains substantially constant during the course of production, the degree to which the remaining oil and gas expand depends only on the pressure .By taking bottom-hole samples of the reservoir fluids under pressure and measuring their relative volumes in the laboratory at reservoir temperature and under various pressures ,it is possible to predict how these fluids behave in the reservoir as reservoir pressure declines.
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The general material balance equation is simply a volumetric balance, Which states that since the volume of a reservoir (as defined by its initial limits)is a constant , the algebraic sum of the volume changes of the oil , free gas , water , and rock volumes in the reservoir volumes decreases , the sum of these two decreases must be balanced by changes of equal magnitude in the water and rock volumes .
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If the assumption is made that complete equilibrium is attained at all times in the reservoir between the oil and its solution gas , it is possible to write a generalized material balance expression relating the quantities of oil , gas and water produced , the average reservoir pressure , the quantity of water that may have encroached from the aquifer , and finally the initial oil and gas content of the reservoir.
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LECTURE 17
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Reserves are natural resources that have already been discovered and can be exploited for profit today
Resources are deposits that we know of (or believe to exist), but are not exploitable today
Example: oil reserves ~1.2 trillion barrels, oil resources ~2 trillion barrels
Types: Oil, Gas, Natural Gas, Condensated gas, GNL and other fluids(CO2,N2,H2S)
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Based :
Interpretation of Data Engineering and / or Geology available to date. Economic conditions such as prices, costs and market.
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NATURAL ENERGY (PRIMARY RECOVERY)
ENHANCED RECOVERY METHODS
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Analogies Volumetric Methods Material balance Decline Curve Analysis Reservoir Simulation Probalistic (Monte Carlo)
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•Contour map of the productive
zone (net productive sand).
•Two methods are used for determining the gross volume:
•Trapezoidal V = h*( 0.5*A0 + A1+A2+A3+0.5*A4)
•Pyramidal V = h (A0 + 4*A1+2*A2+4*A3+A4)
3
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For calculating insitu oil:
N = 7758*V*f*(1-Swi) / Boi STB
For the remaining oil:
Nf = 7758*V*f*(1-Swg) / Bo
Nf = 7758*V*f*(1-Sw -Sg) / Bo
The recovery factor F.R. :
F.R. = Np/N = 1 - Nf/N
V = Gross volume in Acres*ft
f = Porosity in fraction
Swi = Initial water saturation Fraction
Boi = Formation volume factor initial oil
Bo = formation volume factor of the final oil
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Gas for calculating insitu: G = 43560*V*f*(1-Swi) / Bgi SCF
Para el gas remanente:
Ga = 43560*V*f*(Sgr) / Bga
The recovery factor F.R. :
F.R. = Gp/G =(Bga-Bgi)/Bgi
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Méthod
o = 141.5 / (131.5 + API)
Mo= 6084/(API-5.9)
mw = R g 28.97 + 350 o
379
nw = R + 350 o
379 Mo
Mw = 0.07636 Rg + 350 o
0.002636 R + 350 o
Mo
w = Mw/28.97=Rg + 4584 o
R + 132800o
Mo
We found the Tr and Pr and
then the value of Z then
determine:
Gw = 379 PV/ ZRT
V = 43560 AH f(1-Swi)
R = 10.73 Psia-ft3 / lb-mol °R
Gas fraction:
fg = R /(R + 132800o/Mo
Amount of gas:
G = Gw* fg
Amount of liquids
N = Gw fg/R
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Method 2.
avg gas prod. = gt ;
gt = qps ps + qst st
qps + qst Knowing STB cond. / MMSCF
and developed by using a
graph Standing can determine
a ratio (R)= u/ gt and by
empirical correlation can be
developed by finding Bo
Standing for condensate
reservoir.
There is a graph of Bo
function:
R SCF/STB, gt , st ,
Temperature reserv.
P reservoir,
relations at high gas / oil.
Amount of liquids
N = 7758Ah f (1-Swi)/ Bo
Amount of gas:
G = Rsi* N
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Exponential Decline Conversions (where b = 0)
Hyperbolic Decline Conversions (where 0 < b < 1)
Harmonic Decline Conversions (where b = 1)
Lineal (where b = 1)
( ( b
i
i
tbD
qtq
11+
=
( tD
i
ie
qtq =
( ( tD
qtq
i
i
+=
1
( )*1(* tDqtq ii =
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Exponential Decline Conversions (where b = 0)
Hyperbolic Decline Conversions (where 0 < b < 1)
Harmonic Decline Conversions (where b = 1)
Lineal (where b = 1)
)/()(* 11
ii
bb
iip bDDqqbqN =
iip DqqN /)( =
iiip DqqqN /)/ln(=
2/)( 21 qqNp =
![Page 238: Reservorios](https://reader033.vdocuments.net/reader033/viewer/2022042721/577cbfe11a28aba7118e5b93/html5/thumbnails/238.jpg)
Applications Mechanism PLOT
Hyperbolic • Solution Gas log (Np) vs log (q)
Exponential • Solution Gas Np vs q
• Water drive
wc = 0Np vs q
2
Lineal
• Water drive
wc <> 0Np vs cut (oil/water)
Exponential • Water drive with
fluid production cte. Np vs q
Harmonic • Water drive edge Np vs q
Lineal
• Gas cap
with slow GOR,
Solution gas = 0
Np vs 1/p
Hyperbolic
• Gas cap drive
with slow GOR
with solution gas slow
log (Np) vs log (q) b = 2,0
• Gas cap drive
after GOC break through
well producres.
Np vs GOR
Np vs Depth GOC
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Para el cálculo tenemos: masa inicial- masa final final = masa removida
ni - nf = n producido del reservorio
PiVi/ziRT - PfVf/zfRT = PscGp/RTsc
Vf = Vi - We + WpBw
GBgi -(G -Gp) Bgf = We + WpBw
Reservorio volumétrico, no hay intrusión de
agua entonces Vi=Vf
Pf/zf = Pi/zi - Psc TGp/Tsc = b - m Gp
P/z
Gp MMM SCF
Gi
Pi/zi
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Reservorios No saturado, producción
cerca al punto de Burbuja no hay intrusión
de agua, Compresibilidad de la formación
y agua=0
Vi = Vf ; Vi = N Boi ;
Vf = Nf Bof = (N - Np) Bof
Luego: N Boi = (N - Np) Bof
N = Np Bof / (Bof - Boi )
F.R. = (Bof - Boi )/ Bof
PETROLEO PETROLEO
AGUA AGUA
Pi Pb
Reservorios No saturado, producción
cerca al punto de Burbuja no hay intrusión agua , si
efectos compresibilidades
Cf +w = Cf +CwSwi/ (1-Swi)
N = Np Bof / (Bof - Boi (1- Cw+f DP))
F.R. = Bof - Boi (1- Cw+f DP)/ Bof
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Reservorios No saturado, producción
debajo al punto de Burbuja no hay
intrusión de agua
Vi = Vf = Vo + Vg;
N Boi = (N - Np) Bof + Gf Bgf
Gf = Nrsi - (N-Np)Rs - NpRp siendo Rp = Gp/Np
N = Np [Bof + Bg (Rp- Rs)]/ [Bof - Boi + Bg(Rsi-Rs)]
F.R.= [Bof - Boi + Bg(Rsi-Rs)]/ [ Bof + Bg (Rp- Rs)]
Si hay intrusión de agua:
Vi = Vf = Vo + Vg+ Vw
Vw = We-BwWp
N ={ Np [Bof + Bg (Rp- Rs)]- (We-BwWp)}
[Bof - Boi + Bg(Rsi-Rs)]
PETROLEO PETROLEO
AGUA AGUA
Pi Pf
GAS
Pb
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Reservorios No saturado, producción
debajo al punto de Burbuja no hay
intrusión de agua, considerando la
expansión del volumen poroso
N = Np [Bof + Bg (Rp- Rs)]
[Bof - Boi + Bg(Rsi-Rs) + Cf+w Boi DP]
F.R.= [Bof - Boi + Bg(Rsi-Rs) + Cf+w Boi DP ]
[ Bof + Bg (Rp- Rs)]
PETROLEO PETROLEO
AGUA AGUA
Pi Pf
GAS
Pb
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Reservorios saturado, producción
debajo al punto de Burbuja , intrusión
de agua, considerando la
expansión del volumen poroso
m= Vgli/Voi
Vi = Vf = Vo + Vgd + Vgl + Vw;
Vgl = m N Boi [Bg - Bgi] / Bgi
N = Np [Bof + Bg (Rp- Rs) - (We-BwWp) ]
[Bof - Boi + Bg(Rsi-Rs) + m Boi [Bg - Bgi] / Bgi]
PETROLEO PETROLEO
AGUA AGUA
Pi Pf
GAS
Pb
Intrusión de agua.
GAS
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LECTURE 17
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The area of concern in this lecture includes:
• Types of fluids in the reservoir
• Flow regimes
• Reservoir geometry
• Number of flowing fluids in the reservoir
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TYPES OF FLUIDS
In general, reservoir fluids are classified into three
groups:
• Incompressible fluids
• Slightly compressible fluids
• Compressible fluids
Incompressible fluids
An incompressible fluid is defined as the fluid whose
volume (or density) does not change with pressure.
Incompressible fluids do not exist; this behavior,
however, may be assumed in some cases to simplify
the derivation and the final form of many flow
equations.
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Slightly compressible fluids
These “slightly” compressible fluids exhibit small changes in
volumeor density, with changes in pressure.
It should be pointed out that crude oil and water systems fit into
this category.
Compressible Fluids
These are fluids that experience large changes in volume as a
function of pressure. All gases are considered compressible
fluids.
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FLOW REGIMES
There are three flow regimes:
• Steady-state flow
• Unsteady-state flow
• Pseudosteady-state flow
Steady-State Flow
The flow regime is identified as a steady-state flow if
the pressure at every location in the reservoir
remains constant, i.e., does not change with time.
Mathematically, this condition is expressed as:
(4-1)
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The above equation states that the rate of change of pressure p
with respect to time t at any location i is zero. In reservoirs, the
steady-state flow condition can only occur when the reservoir is
completely recharged and supported by strong aquifer or
pressure maintenance operations.
Unsteady-State Flow
The unsteady-state flow (frequently called transient flow) is
defined as the fluid flowing condition at which the rate of change
of pressure with respect to time at any position in the reservoir
is not zero or constant.
This definition suggests that the pressure derivative with respect
to time is essentially a function of both position i and time t, thus
(4-2)
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Pseudosteady-State Flow
When the pressure at different locations in the reservoir is
declining
linearly as a function of time, i.e., at a constant declining rate, the
flowing condition is characterized as the pseudosteady-state
flow. Mathematically, this definition states that the rate of
change of pressure with respect to time at every position is
constant, or
(4-3)
It should be pointed out that the pseudosteady-state flow is
commonly referred to as semisteady-state flow and
quasisteady-state flow.
Figure shows a schematic comparison of the pressure declines as
a function of time of the three flow regimes.
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RESERVOIR GEOMETRY
For many engineering purposes, however, the actual flow geometry
may be represented by one of the following flow geometries:
• Radial flow
• Linear flow
• Spherical and hemispherical flow
Because fluids move toward the well from all directions and
coverage at the wellbore, the term radial flow is given to
characterize the flow of fluid
into the wellbore. Figure 4-1 shows idealized flow lines and iso-
potential lines for a radial flow system.
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Figure 4-1 Ideal radial flow into a wellbore
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Linear Flow
Linear flow occurs when flow paths are parallel and the fluid flows
in a
single direction. In addition, the cross sectional area to flow must
be
constant. Figure 4-2 shows an idealized linear flow system.
Figure 4-2 Ideal linear flow
into vertical fracture
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Spherical and Hemispherical Flow Depending upon the type of wellbore completion configuration,
it is possible to have a spherical or hemispherical flow near
the wellbore. A well with a limited perforated interval could
result in spherical flow in the vicinity of the perforations as
illustrated in Figure 4-3. A well that only partially penetrates
the pay zone, as shown in Figure 4-4, could result in
hemispherical flow. The condition could arise where coning
of bottom water is important.
Figure 4-3 Spherical flow due to limited entry
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Figure 4-4 Hemispherical flow in a partially penetrating well
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NUMBER OF FLOWING FLUIDS IN THE RESERVOIR
There are generally three cases of flowing systems:
• Single-phase flow (oil, water, or gas)
• Two-phase flow (oil-water, oil-gas, or gas-water)
• Three-phase flow (oil, water, and gas)
The description of fluid flow and subsequent analysis of pressure
data becomes more difficult as the number of mobile fluids increases.
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LECTURE 18
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Since 1980, horizontal wells began capturing an ever-increasing
share of hydrocarbon production. Horizontal wells offer the
following advantages over those of vertical wells:
• Large volume of the reservoir can be drained by each horizontal
well.
• Higher productions from thin pay zones.
• Horizontal wells minimize water and gas zoning problems.
• In high permeability reservoirs, where near-wellbore gas velocities
are high in vertical wells, horizontal wells can be used to reduce
near-wellbore velocities and turbulence.
• In secondary and enhanced oil recovery applications, long
horizontal injection wells provide higher injectivity rates.
• The length of the horizontal well can provide contact with multiple
fractures and greatly improve productivity.
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The actual production mechanism and reservoir flow regimes around
the horizontal well are considered more complicated than those for
the vertical well, especially if the horizontal section of the well is of
a considerable length. Some combination of both linear and radial
flow actually exists, and the well may behave in a manner similar
to that of a well that has been extensively fractured.
Assuming that each end of the horizontal well is represented by a
vertical well that drains an area of a half circle with a radius of b,
Joshi (1991) proposed the following two methods for calculating
the drainage area of a horizontal well.
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Method I
Joshi proposed that the drainage area is represented by two half
circles of radius b (equivalent to a radius of a vertical well rev) at
each end and a rectangle, of dimensions L(2b), in the center.
The drainage area of the
horizontal well is given then by:
Figure 5-1
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(5-1)
where
A =drainage area, acres
L =length of the horizontal well, ft
b =half minor axis of an ellipse, ft
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Method II
Joshi assumed that the horizontal well drainage area is an ellipse
and given by:
(5-2)
with
(5-3)
where a is the half major axis of an ellipse.
Joshi noted that the two methods give different values for the
drainage area A and suggested assigning the average value for
the drainage of the horizontal well. Most of the production rate
equations require the value of the drainage radius of the
horizontal well, which is given by:
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(5-4)
Where
reh =drainage radius of the horizontal well, ft
A =drainage area of the horizontal well, acres
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LECTURE 19
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A thorough understanding of the flowing well is necessary prior to placing it on artificial lift . There are two surface conditions under which a flowing well is produced , that is , it may be produced with a choke at the surface or it may be produced with no choke at the surface. The majority of all flowing wells utilize surface chokes . Some of the reasons for this are safety ; to maintain production allowable ; to maintain an upper flow rate limit to prevent sand entry ; to produce the reservoir at the most efficient rate ; to prevent water or gas coning ; and others.
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In particular , flowing wells utilize a choke in their early stages of production . As time progresses , the choke size may have to be increased and eventually removed completely in order to try to optimize production .
The second condition that we are concerned with is producing the flowing well with no restrictions at the surface except normal Christmas tree turn , bends, etc . Even these may be streamlined in order to obtain the maximum flowing rate possible .
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In order to analyze the performance of a conventionally completed flowing well , in is necessary to recognize that there are three distinct phases , which have to be studied separately and then finally linked together before an overall picture of a flowing well’s behavior can be obtained . These phase are the inflow performance , the vertical lift performance , and the choke (or bean )performance.
The inflow performance , that is , the flow of oil , water , and gas from the formation into the bottom of the well , is typified , as far as gross liquid production is concerned , by the PI of well or , more generally , by the IPR .
The vertical lift performance involves a study of the pressure losses in vertical pipes carrying two-phase mixtures(gas and liquid).
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LECTURE 20
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Oil well pumping methods can be divided into two main groups:
Rod systems.Those in which the motion of the subsurface pumping equipment originates at the surface and is transmitted to the pump by means of a rod string.
Rod less systems.Those in which the pumping motion of the subsurface pump is produced by means other than sucker rods.
Of these teo groups,the first is represented by the beam pumping system and the second is represented by hydraulic and centrifugal pumping systems.
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The beam pumping system consists essentially of five parts:
The subsurface sucker rod—friven pump. The sucker rod string which transmits the
surface pumping motion and power to the subsurface pump.Also included is the necessary string of tubing and/or casing within which the sucker rods operate and which conducts the pumped fluid from the pumpto the surface.
The surface pumping eauipment which changes the rotating motion of the prime mover into oscillatinf linear pumping motion .
The power transmiddion unit or speed reducer. The prime mover which furnishes the necessary
power to the system.
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LECTURE 22
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Skin Factor
It is not unusual for materials such as mud
filtrate, cement slurry, or clay particles to
enter the formation during drilling,
completion or workover operations and
reduce the permeability around the wellbore.
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This effect is commonly referred to as a wellbore damage and
the region of altered permeability is called the skin zone. This
zone can extend from a few inches to several feet from the
wellbore. Many other wells are stimulated by acidizing or
fracturing which in effect increase the permeability near the
wellbore. Thus, the permeability near the wellbore is always
different from the permeability away from the well where the
formation has not been affected by drilling or stimulation. A
schematic illustration of the skin zone is shown in Figure 4-5.
Skin Factor
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Those factors that cause damage to the formation can produce
additional localized pressure drop during flow. This additional
pressure drop is commonly referred to as Dpskin. On the other
hand, well stimulation techniques will normally enhance the
properties of the formation and increase the permeability around
the wellbore, so that a decrease in pressure drop is observed.
Figure 4-5
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• Positive Skin Factor, s > 0
When a damaged zone near the wellbore exists, k-skin is less
than k and hence s is a positive number. The magnitude of the
skin factor increases as k-skin decreases and as the depth of
the damage r skin increases.
• Negative Skin Factor, s < 0
When the permeability around the well k-skin is higher than that of
the formation k, a negative skin factor exists. This negative
factor indicates an improved wellbore condition.
• Zero Skin Factor, s = 0
Zero skin factor occurs when no alternation in the permeability
around the wellbore is observed, i.e., k-skin =k.
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LECTURE 23;24
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LECTURE 25
FINAL TEST