Professional Documents
Culture Documents
Petroleum
University Of Mehdi
Technology Imanian
Najafabadi
Course Notes
M
for
Authors:
Im
1980 — Von Gonten, W.D.
1986 — McCain, W.D., Jr.
1990 — Wu, C.H.
an
ian
Na
ja fa
ba
di
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Petroleum
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M
eh
RESERVOIR PETROPHYSICS
Im
Instructor/Author:
Ching H. Wu
Na
ja fa
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TABLE OF CONTENTS
ii
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I) Introduction VII-1
II) Frequency Distributions VII-2
III) Histogram VII-3
M
IV) Cumulative Frequency Distributions VII-6
V) Normal Distribution VII-8
VI) Log Normal Distribution VII-9
eh
VII) Measures of Central Tendency VII-10
VIII) Measures of Variability (dispersion) VII-11
IX) Normal Distribution VII-12
X) Log Normal Distribution VII-16
di
Im
an
ian
Na
jafa
ba
di
iii
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I. ROCK POROSITY
I) Definition
M
A measure of the pore space available for the storage of fluids in
rock
eh
In general form:
Vp Vb - Vm
Porosity = φ = =
di
Vb Vb
where:
φ is expressed in fraction
Im
Vb = Vp + Vm
Vb = bulk volume of reservoir rock, (L3)
Vp = pore volume, (L3)
an
II) Classification
B. Secondary Porosity
C. Total Porosity
Vb Vb
D. Effective Porosity
ba
1. Clean sandstones: φe = φt
2. Carbonate, cemented sandstones: φe < φt
I-1
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M
eh
di
Im
an
ian
Na
jaf
ab
ad
i
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A. Factors:
1. Particle shape
M
2. Particle arrangement
3. Particle size distribution
4. Cementation
eh
5. Vugs and fractures
B. Particle shape
50
ian
40
SANDSTONES
Na
30
POROSITY, %
ja
20
fa
SHALES
10
ba
0
0 1000 2000 3000 4000 5000 6000
di
DEPTH OF BURIAL, ft
I-3
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Im
INTERSTITIAL MATERIALS
AND MUD FRAGMENTS
an
0
1.0 0.1 0.01 0.001
ian
GRAIN SIZE DIAMETER, MM
F. Vugs, Fractures
I-4
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V) Measurement of porosity
Vb - Vm Vp
φ= =
Vb Vb
M
Table of matrix densities
ρ m (g/cm3)
eh
Lithology
___________ ___________
Quartz 2.65
di
Limestone 2.71
Dolomite 2.87
Im
A. Laboratory measurement
1) bulk volume, Vb
2) matrix volume, Vm
ian
3) pore volume, Vp
b. bulk volume
I-5
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c. matrix volume
dry weight
M
Vm =
matrix density
2) displacement method
eh
Reduce sample to particle size, then
a) volumetric
di
b) gravimetric
P(1)
an
V(1)
ian
VALVE CLOSED
c) Open valve
P(2)
ja
CORE
fa
VALVE OPEN
ba
4) Vm =V T - V2
I-6
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d. pore volume
1) gravimetric
VALVE CLOSED
an
c) Open valve
P(2)
Na
V(1) CORE
VALVE OPEN
ja fa
3) Vp = V2 - V1
di
I-7
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a. intergranular porosity
(sandstone, some carbonates)
M
1) use representative plugs from whole core in
laboratory measurements
eh
2) don't use sidewall cores
b. secondary porosity
(most carbonates)
di
1) use whole core in laboratory measurements
I-8
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Example I-1
A core sample coated with paraffin was immersed in a Russell tube. The dry sample weighed 20.0
gm. The dry sample coated with paraffin weighed 20.9 gm. The paraffin coated sample displaced
10.9 cc of liquid. Assume the density of solid paraffin is 0.9 gm/cc. What is the bulk volume of
M
the sample?
eh
Solution:
The core sample of problem I-1 was stripped of the paraffin coat, crushed to grain size, and
immersed in a Russell tube. The volume of the grains was 7.7 cc. What was the porosity of the
sample? Is this effective or total porosity.
ian
Solution:
Vb 9.9 cc
fa
It is total porosity.
ba
di
I-9
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Example I-3
Calculate the porosity of a core sample when the following information is available:
Solution:
Im
21.3 cm3
ian
Vp =
Vb = 448.6 gm - 269.6 gm
Na
1 gm/cm3
Vb = 179.0 cm3
ja
Vp
φ = = 21.3 cm3 = .119
Vb 179.0 cm3
fa
φ = 11.9%
ba
di
I - 10
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Vm = Vb - Vp
M
Vm = 179.0 cm3 - 21.3 cm3 = 157.7 cm 3
eh
ρm = wt. of dry sample = 427.3 gm = 2.71 gm/(cm3)
matrix vol. 157.7 cm3
di
The lithology is limestone.
I - 11
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Example I-4
A carbonate whole core (3 inches by 6 inches, 695 cc) is placed in cell two of a Boyles
Law device. Each of the cells has a volume of 1,000 cc. Cell one is pressured to 50.0 psig. Cell
M
two is evacuated. The cells are connected and the resulting pressure is 28.1 psig. Calculate the
porosity of the core.
eh
Solution:
di
P V = P V
1 1 2 2
V = 1,000 cc
1
Im
P = 50 psig + 14.7 psia = 64.7 psia
1
V = 1,512 cc
2
V = VT - V2
m
VT - Vm 695 cc - 488 cc
φ = = = .298 = 29.8%
VT 695 cc
ja fa
ba
di
I - 12
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1. Density log:
M
ρ -ρ
φd = m L
ρm - ρf
eh
2. Sonic log:
∆tL - ∆tm
di
φs =
∆tf - ∆tm
3. Neutron log:
Im
e-kφ = CNf
an
Table of Matrix Properties
(Schlumberger, Log Interpretation Principles, Volume I)
Lithology
I - 13
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B. Density Log
FORM ATION
di
GAM M A RAY
SOURCE
Im
SHORT SPACE
DETECTOR
an
LONG SPACE
DETECTOR
ian
Na
2. Gamma rays are stopped by electrons - the denser the rock the fewer gamma
ja
3. Equation
fa
ρL = ρm 1 - φ + ρf φ
ba
ρ -ρ
φd = m L
ρm - ρf
di
I - 14
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ρ, gm/cc
M
GR, API depth, ft
4100
eh
4120
di
4140
Im
4160
an
4180
ian
4200
Na
4220
ja
4240
0 40 80 120 160 200 2.0 2.2 2.4 2.6 2.8 3.0
fa
ba
di
I - 15
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Example I-5
Use the density log to calculate the porosity for the following intervals assuming ρ matrix = 2.68
M
gm/cc and ρ fluid = 1.0 gm/cc.
eh
Interval, ft ρ φd ,%
L, gm/cc
__________ _________ ______
4143-4157 2.375 18
di
4170-4178 2.350 20
4178-4185 2.430 15
4185-4190 2.400 17
4197-4205 2.680 0
Im
4210-4217 2.450 14
an
Example:
ρ = 2.375 gm/cc
L
I - 16
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C. Sonic Log
B
Im
C
R1
D
an
E
R2
ian
Na
2. Sound travels more slowly in fluids than in solids. Pore space is filled with
fluids. Travel time increases as porosity increases.
3. Equation
ja
I - 17
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SONIC LOG
4160
an
4180
ian
4200
Na
4220
4240
ja
I - 18
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Example I-6
Use the Sonic log and assume sandstone lithology to calculate the porosity for the following
intervals.
M
φs ,%
Interval ∆tL
eh
(ft) µ second/ft
4,144-4,150 86.5 25
di
4,150-4,157 84.0 24
4,171-4,177 84.5 24
Im
4,177-4,187 81.0 21
4,199-4,204 53.5 1
an
4,208-4,213 75.0 17
Example:
ian
I - 19
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D. Neutron Log
ian
103 1
O
FOR COLLISION
102 10-1
Si H
10 10-2
O
H
Si
1 10-3
Na
3. If the log is not calibrated, it is not very reliable for determining porosity.
Run density log to evaluate porosity, lithology, and gas content.
ba
di
I - 20
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4140
Im
4160
an
4180
ian
4200
Na
4220
ja
4240
0 200 30 -10
fa
ba
di
I - 21
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Example I-7
Use the neutron log to determine porosity for the following intervals.
M
Solution:
eh
Interval φ
n
(ft) (%) .
di
4,143-4,149 23
4,149-4,160 20
Im
4,170-4,184 21
4,198-4,204 9
an
4,208-4,214 19
ian
Na
ja fa
ba
di
I - 22
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Example I-8
Calculate the porosity and lithology of the Polar No. 1 drilled in Lake Maracaibo. The depth of
interest is 13,743 feet. A density log and a sonic log were run in the well in addition to the
standard Induction Electric Survey (IES) survey.
M
The readings at 13,743 feet are:
eh
bulk density = 2.522 gm/cc
travel time = 62.73 µ-sec/ft
di
Solution:
ρ m = 2.65 gm/cc
an
ρ -ρ
ian
2.65 gm/cc - 2.522 gm/cc
φd = m L = = 7.76%
ρm - ρf 2.65 gm/cc - 1.0 gm/cc
Assume limestone:
ρm = 2.71 gm/cc
ja
I - 23
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Assume dolomite:
ρm = 2.87 gm/cc
M
∆tm = 43.5 µ-sec/ft
eh
ρ -ρ 2.87 gm/cc - 2.522 gm/cc
φd = m L= = 18.619%
ρm - ρf 2.87 gm/cc - 1.0 gm/cc
di
∆tL - ∆tm 62.73 µ sec/ft - 43.5 µ sec/ft
φs = = = 13.22%
∆tf - ∆tm 189.0 µ sec/ft - 43.5 µ sec/ft
Im
φlimestone = 11%
Since both logs "read" nearly the same porosity when a limestone lithology was
assumed then the hypothesis that the lithology is limestone is accepted.
an
The density log measures total compressibility because is "sees" the entire rock
ian
volume,including all pores. The sonic log tends to measure the velocity of
compressional waves that travel through interconnected pore structures as well as the
rock matrix. The general consensus is that the sonic log measures effective porosity
when we use the Wyllie "time-average" equation.
It is expected that the effective porosity is always less than ,or equal to,the total
porosity.
Na
ja fa
ba
di
I - 24
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∆V
M
∂V V T
c=- 1 ≅ -
V ∂P T ∆P
eh
A. Normally pressured reservoirs
Fo
Im
an
Fm Ff
ian
2. Thus,
Fo = Fm + Ff
Na
it follows that
Po = pm + pf
ja
3. Po ≅ 1.0 psi/ft
fa
Pf ≅ 0.465 psi/ft
ba
di
I - 25
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1. Matrix Compressibility, cm
di
cm ≅ 0
2. Bulk Compressibility cb
Im
used in subsidence studies
4) by definition
∂Vp
cf = - 1
Na
Vp ∂pm
dPm = - dP f
ja fa
ba
di
I - 26
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1) Thus,
∂Vp
cf = - 1
Vp ∂pm
M
2) where the subscript of f on cf means
"formation" and the subscript of f on Pf
eh
means "fluid"
3) procedure
di
(a) measure volume of liquid expelled as a
function of "external" pressure
dPo = dP m
an
∂Vp
cf = - 1
Vp ∂pm
Na
it follows that
∆ Vp expelled
cf = + 1
ja
Vp ∆Po
fa
ba
di
I - 27
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(f) plot
M
eh
VOLUME EXPELLED
di
PORE VOLUME
CUMULATIVE
Im
an
slope = cf.
ja fa
ba
di
I - 28
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C. Measurement of compressibility
Internal
di
Pressure
Gauge
Im
Hydraulic
Pump
an
Overburden
Pressure
Gauge
Na
Hydraulic
Pump
ja
Copper - Jacketed
Core
fa
ba
I - 29
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Example I-9
Given the following lab data, calculate the pore volume compressibility for a sandstone sample at
4,000 and 6,000 psi.
M
pore volume = 50.0 cc
eh
pressure, psi vol. fluid expelled, cc
1000 0.244
2000 0.324
3000 0.392
di
4000 0.448
5000 0.500
6000 0.546
7000 0.596
Im
8000 0.630
Solution:
an
from graph
@ 4,000 psi:
Slope = 0.009
ian
4000 psi
cf = 2.25 X 10-6 1
psi
@ 6000 psi:
Na
Slope = 0.011
6000 psi
= 1.83 X 10-6 1
ja
cf
psi
fa
ba
di
I - 30
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0.015
M
VOLUME EXPELLED, cc
PORE VOLUME, cc
0.010
eh
di
0.005
Im
0.000
an
0 2000 4000 6000 8000 10000
I - 31
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PORE-VOLUME COMPRESSIBILITY AT 75 %
LITHOSTATIC PRESSURE VS INITIAL SAMPLE
POROSITY FOR CONSOLIDATED SANDSTONES.
PORE-VOLUME COMPRESSIBILITY AT 75 %
LITHOSTATIC PRESSURE VS INITIAL SAMPLE
POROSITY FOR UNCONSOLIDATED SANDSTONES.
PORE VOLUME COMPRESSIBILITY X 10-6 psi-1
100
Na
UNCONSOLIDATED SANDSTONES
ja
10
fa
HALL'S CORRELATION
ba
1
0 5 10 15 20 25 30
di
I - 32
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"abnormal pressure": fluid pressures greater than or less than the hydrostatic fluid
pressure expected from an assumed linear pressure gradient
M
PRESSURE
eh
di
NORMAL LINEAR
Im
an
DEPTH
SUBNORMAL
(LOWER)
ian
Na
SURNORMAL
(GREATER)
ja fa
ba
di
I - 33
Page 37 / 224
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A limestone sample weighs 241.0 gm. The limestone sample coated with paraffin was found to
weigh 249.5 gm. The coated sample when immersed in a partially filled graduated cylinder
displaced 125.0 cc of water. The density of the paraffin is 0.90 gm/cc.
M
What is the porosity of the rock? Does the process measure total or effective porosity?
eh
Solution:
di
wt. dry 241.0 gm
Vm = = = 88.9 cc
ρ ls 2.71 gm/cc
Im
Vp = Vb - Vm
Vp 26.7 cc
φ = = = 0.231
Vb 115.6 cc
ja
I - 34
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You are furnished with the results of a sieve analysis of a core from Pete well #1. Previous
laboratory work indicates there is a correlation between grain size and porosity displayed by those
particular particles. The correlation is seen below:
M
gravel - 25% porosity
eh
coarse sand - 38% porosity
remaining remaining
pore matrix
component volume porosity volume
ian
I - 35
Page 39 / 224
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A sandstone reservoir has an average thickness of 85 feet and a total volume of 7,650 acre-feet.
Density log readings through the fresh water portion of the reservoir indicate a density of 2.40
gm/cc.
M
The Highgrade #1 Well was drilled and cored through the reservoir. A rock sample was sent to the
laboratory and the following tests were run.
eh
pressure cum. pore vol. change
(psig) (-cc)_________
1,000 0.122
2,000 0.162
di
3,000 0.196
4,000 0.224
5,000 0.250
6,000 0.273
Im
7,000 0.298
8,000 0.315
The dry weight of the core sample was found to be 140 gm while the sample dimensions were
an
1.575 inches long and 1.960 inches in diameter.
Assuming the compressibility at 4,500 psi is the average compressibility in the reservoir, how
much subsidence occurs when the reservoir pressure declines from 5,500 psi to 3,500 psi?
ian
Calculate:
A. Reservoir Porosity
Solution:
A. Reservoir Porosity
fa
ρ -ρ
φ = m L = 2.65 - 2.40 = 15.22%
ρ m - ρ f 2.65 - 1.00
ba
di
I - 36
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Vp = 25.7 cc
Im
Vp = 25.7 cc
an
D. Subsidence
ian
∆H = H cp φ ∆P
∆H = 0.026 ft
Na
∆H = 0.32 inches
Note: the pore volume (formation) compressibility is somewhat smaller than usually
ja
encountered. An experienced engineer would be wary of this small number. Also it was
assumed that the formation compressibility was exactly the same as the bulk volume
compressibility. Experience shows that this is not the case.
fa
ba
di
I - 37
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0.0100
Im
0.0080
an
0.0060
ian
0.0040
0 2000 4000 6000 8000
PRESSURE, psig
Na
ja fa
ba
di
I - 38
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Compressibility Problem
A 160-acre and 100 ft thick reservoir has a porosity of 11%. The pore compressibility is 5.0 x 10-
M
6 (1/psi). If the pressure decreases 3,000 psi, what is the subsidence (ft)? Assume Cf = Cb
eh
Solution:
dVp
Cp = - 1
Vp dp
an
dVp
5 x 10-6 (1/psi) = -1
76,665,600 ft3 3,000 psi
ian
I - 39
Page 43 / 224
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h1
an
Z
h2
ian
WATER
Na
SAND
ja
DARCY'S FOUNTAIN.
kA(h1 - h2)
fa
q=
µL
Length of sand pack,L = Z
ba
2. Darcy's work confined to sand packs that were 100% saturated with water
II - 1
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kA(h1 - h2)
q=
µL
M
B. Generalized form of Darcy's equation
eh
1. Equation
ρg
vs = -k dP - dz
µ ds 1.0133 x 10 6 ds
di
+Z
Im
s
Θ
+X
ian
-Z
-1
+Y θ
Na
2. Nomenclature
µ = viscosity - centipoise
k = permeability - darcies
II - 2
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3. Conversion factors
L = length
Im
m = mass
t = time
vs = L/t
an
µ = m/Lt
ρ = m/L3
ian
p = m/Lt2
g = L/t2
Na
dp ρg
vs = - k - dz
µ ds 1.0133 x 10 6 ds
t m/Lt L L
k = L2 = cross-sectional area
fa
ba
di
II - 3
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c. definition of darcy
di
A porous medium has a permeability of one darcy when a single-phase fluid of one
centipoise that completely fills the voids of the medium will flow through it under conditions of
viscous flow at a rate of one cubic centimeter per second per square centimeter cross-sectional area
under a pressure or equivalent hydraulic gradient of one atmosphere per centimeter.
Im
k A P1 - P2
q =
µL
an
ian
Na
ja fa
ba
di
II - 4
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A
q q
di
P1 P2
Im
L
an
a. Conditions
ian
dz
1) horizontal system, ds = 0
7) constant temperature, µ, q
fa
ba
di
II - 5
Page 48 / 224
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ρg
vs = - k dP - dz
µ ds 1.0133 x 10 6 ds
M
q
vs = - k dP =
µ ds A
eh
L p2
q ds = - kA dP
µ p
0 1
di
qL-0 = - kA P2 - P1
µ
Im
q = kA P2 - P1
Lµ
Note: P1 acts at L = 0
an
P2 acts at L = L
q is + if flow is from L = 0 to L = L
ian
Na
ja fa
ba
di
II - 6
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Example II-1
What is the flow rate of a horizontal rectangular system when the conditions are as follows:
M
permeability = k = 1 darcy
area = A = 6 ft2
eh
viscosity = µ = 1.0 cp
length = L = 6 ft
di
inlet pressure = P1 = 5.0 atm
Solution:
an
We must insure all the variables are in the correct units.
k = 1 darcy
ian
P1 = 5.0 atm
Na
P2 = 2.0 atm
q = kA P2 - P1
Lµ
ja
q = 91.42 cm 3/sec
ba
di
II - 7
Page 50 / 224
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P1
ian
a. Conditions
dz = sinθ
1) non-horizontal system, ds = constant
7) constant temperature µ, q
ba
di
II - 8
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b. derivation of equation
ρg
vs = - k dP - dz
µ ds 1.0133 x 10 6 ds
M
q k ρg sin θ
vs = - = - k dP +
A µ ds µ 1.0133 x 10 6
eh
L P2 L
kA ρg sin θ
q ds = - kA dp + ds
µ µ 1.0133 x 10 6
0 P1 0
di
ρgLsinθ
Im
q = - kA P1 - P2 +
µL 1.0133 x 10 6
an
ian
Na
ja fa
ba
di
II - 9
Page 52 / 224
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a. Conditions
dz
Na
8) constant temperature, µ
di
II - 10
Page 53 / 224
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k dP - ρg dz
vs =
µ
M
ds 1.0133 x 10 6 ds
q ρg
vs = = - k dP +
µ
eh
A ds 1.0133 x 10 6
kA P1 - P2 ρg
q = -
µ L 1.0133 x 10 6
di
ρg (h + x + L)
P1 = -
1.0133 x 10 6
ρg x
Im
P2 =
1.0133 x 10 6
P1 - P2 ρg h ρg
= +
an
L 1.0133 x 10 6 L 1.0133 x 10 6
ρg h ρg ρg
ian
q = kA + -
µ 1.0133 x 10 6 L 1.0133 x 10 6 1.0133 x 10 6
ρg h
q = kA
µL 1.0133 x 10 6
Na
ja fa
ba
di
II - 11
Page 54 / 224
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h
ian
a. Conditions
dz
1) horizontal system, ds = 0
Na
8) constant temperature, µ, q
di
II - 12
Page 55 / 224
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ρg
vs = - k dP - dz
µ ds 1.0133 x 10 6 ds
M
q q
vs = + k dP = =
µ dr A 2πrh
eh
re pe
q dr = k dp
2πh r µ
rw pw
di
q
1n(re) - 1n( rw) = k Pe - Pw
2πh µ
Im
q = 2πhk P - Pw
µ 1n (re/rw) e
A
q q
P1 P2
Na
L
ja
a. Conditions
dz
fa
1) horizontal system, ds = 0
7) constant temperature
II - 13
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b. Assumptions
1) µ, Z = constant
M
2) Z(and µ ) can be determined at mean pressure
but
Im
Psc qscz T
q =
PTsc
an
thus
L p2
Psc T qsc PdP
ds = - k
Tsc A µz
ian
o p1
qsc = kA Tsc
µL Tz Psc 2
Pq = ZnRT
n = mass flow/time
thus,
Pq
ba
= ZnRT
Pscqsc n R Tsc
Psc qscz T 1
q =
Tsc P
di
Z is determined at P, T
II - 14
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but
eh
P q Tsc Tsc P12 - P22
qsc = = k A
Z Psc T µL T z Psc 2
di
q = k A 1 P12 - P22
µL P 2
P12 - P22
Im
q = k A 2
µL P1 + P 2 2
q = k A P - P
µL 1 2
an
This equation is identical to the equation for horizontal, linear flow of incompressible liquid
ian
thus
if gas flow rate is determined at mean pressure, P, the equation for incompressible liquid
can be used for compressible gas!
Pq = ZnRT
thus
=
Pq znRT
fa
where
P1 + P 2
P =
ba
2
P = volumetric flow rate at P, T
z is determined at P, T
di
P q Tsc
qsc =
z Psc T
II - 15
Page 58 / 224
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h
ian
a. Conditions
dz
1) horizontal system ds = 0
Na
8) constant temperature
di
II - 16
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b. Assumptions
µz = constant
M
z (and µ ) can be determined at mean pressure
but
Im
P q zT
q = sc sc
PTsc
an
and
A = 2πrh and ds = - dr
thus
ian
re Pe
Psc T qsc dr = k ρdP
2Tsc π h r µz
rw Pw
Na
=
µ 1n re/rw Psc zT 2
fa
ba
di
II - 17
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Petroleum
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but
eh
P q Tsc
q =
z Psc T
di
thus
q = 2 π h k 1 (P2e - P2w)
µ 1n re/rw P 2
an
q = 2πhk P - Pw
µ 1n re/rw e
Note: Equation for real gas is identical to equation for incompressible liquid when
volumetric flow rate of gas, q, is measured at mean pressure.
Na
ja fa
ba
di
II - 18
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Example:
Im
hkA P1 - P2
q=
µL in Darcy's units
an
cc = q bbl 5.615 cu ft 1,728 cu in 16.39 cc d hr
q sec
d bbl cu ft cu in 24hr 3,600 sec
cc = 1.841 q bbl
q sec
d
ian
darcy
k darcy = k md 1,000md
k darcy = 0.001 k md
Na
929.0 sq cm
A sq cm = A sq ft
sq ft
A sq cm = 929.0 A sq ft
ja
L cm = L ft 30.48 cm
ft
ba
meter = 100 cm
µ 30.48 L
0.01127 k A P1 - P2
q = in oilfield units
µL
II - 19
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D. Table of Equations
1. Darcy Units
M
System Fluid Equation
eh
Horizontal, Incompressible q = kA P1 - P2
Linear Liquid µL
di
Dipping, Incompressible ρ g L sin θ
Linear Liquid q = kA P1 - P2 +
µL 1.0133 x 10 6
Im
Horizontal, Incompressible q = 2 π kh Pe - Pw
Radial Liquid µ ln (re/rw)
an
q = kA P1 - P2
µL
q = 2 π kh Pe - Pw
µ ln (re/rw)
ja fa
ba
di
II - 20
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2. Oilfield Units
M
System Fluid Equation
q = res bbl/d
di
Dipping, Incompressible q = 0.001127 kA P1 - P2
Linear Liquid µL
Im
ρg L sinθ
+
1.0133 x 10 6
an
Horizontal, Incompressible q = .007082 kh Pe - Pw
Radial Liquid µ ln (re/rw)
ian
qsc = scf/d
Na
q = .001127 kA P1 - P2
µL
ja
q = res bbl/d
fa
q = .007082 kh Pe - Pw
µ ln (re/rw)
di
II - 21
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Example II-2
What is the flow rate of a horizontal rectangular system when the conditions are as follows:
permeability = k = 1 darcy
M
area = A = 6 ft2
viscosity = µ = 1.0 cp
eh
length = L = 6 ft
inlet pressure = P1 = 5.0 atm.
outlet pressure = P2 = 2.0 atm.
di
Solutions:
Im
We must insure that all the variables are in the correct units.
k = 1 darcy = 1,000 md
A = 6 ft2
an
L = 6 ft
P1 = (5.0 atm) (14.7 psi/atm) = 73.5 psi
P2 = (2.0 atm) (14.7 psi/atm) = 29.4 psi
ian
q = 1.1271 x 10-3 kA P1 - P2
µL
1,000 6
q = 1.1271 x 10-3 73.5 - 29.4
1 6
Na
II - 22
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Example II-3
Determine the oil flow rate in a radial system with the following set of conditions:
M
K = 300 md re = 330 ft
h = 20 ft rw = 0.5 ft
eh
Pe =2,500 psia re/rw = 660
7.082 x 10 -3 kH Pe - Pw
q=
µ ln Re / Rw
ian
7.082 x 1--3 300 20 2,500 - 1,740
q=
1.3 6.492
II - 23
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E. Layered Systems
q q
A
Im
B
C
an
W
L
ian
qt = qA + qB + qC
h = hA + hB + hC
Na
then
ja
k wh P1 - P2
qt =
µL
fa
and
then
k h = kA hA + kB hB + kC hC
di
n kj hj
k = ∑
j=1 h
II - 24
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Pe
di
hB qB
ht
Im
hC qC
Pw
an
again
ian
qt = qA + qB + qC
h = hA + hB + hC
qt = 2πk h Pe - Pw
µ ln (re/rw)
Na
and
2 π kA hA 2 π kB hB
ja
qt = Pe - Pw + Pe - Pw
µ ln (re/rw) µ ln (re/rw)
fa
2 π kc hc
+ Pe - Pw
µ ln (re/rw)
then
ba
k h = kA hA + kB hB + kC hC
and again
di
n kj hj
k = ∑
j=1 h
II - 25
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A B C
M
P1 P2
eh
q q
kA kB kC
∆P A ∆P B ∆P C
h
LA LB LC
di
W
Im
L
an
qt = qA = qB = qC
L = LA + LB + LC
k wh P1 - P2
qt =
µL
Na
since qt = qA = qB = qC
ba
L = LA + LB + LC
k kA kB kC
di
thus
K = L
n Lj
∑
j = 1 kj
II - 26
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h
an
rw
rA
rB
rC
ian
qt = qA = qB = qC
2 π k h Pe - Pw
q =
µ ln (re/rw)
ja
qt µ ln (re/rw) qA µ ln (rA/rw)
Pe - Pw = =
2π k h 2 π kAh
fa
qB µ ln (rB/rA) q µ ln (rC/re)
+ + C
2 π kB h 2 π kC h
ba
then
ln re/rw
k =
di
n ln(rj/rj-1)
∑
j=1 kj
II - 27
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Example II-4
Solution:
di
ln (re/rw)
k =
n ln (rj/rj-1 )
∑
Im
j=1 kj
ln 300
an
k = 0.25
ln 2/0.25 ln 300/2
+
10 200
ian
k = 30.4 md
The permeability of the damaged zone near the wellbore influences the average permeability more
Na
II - 28
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πr4
Im
q= P1 - P2
8µL
A = π r2, therefore
an
q= Ar2 P1 - P2
8µL
ian
q = kA P1 - P2
µL
Na
Ar2 P1 - P2 = kA P1 - P2
8µL µL
ja fa
thus
2
k = r2 = d
ba
8 32
where d = inches, k = 20 x 10 9 d2 md
di
II - 29
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Example II-4
B. If only 25 percent of the rock is pore channels (f = 0.25), what will the
eh
permeability be?
di
Solution:
Im
A. k = 20 x 109 d2
k = 50 md
Na
ja fa
ba
di
II - 30
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b
di
Im
q h2
v= = (P 1-P 2)
A 12 µ L
an
2
q = b A (P1 -P2)
12 µ L
ian
b2 A P1 - P2 = kA P1 - P2
12 µ L µL
Na
2
k = b in darcy units, or
12
ja
k = 54 x 109 b2
where b = inches
fa
k = md
ba
di
II - 31
Page 74 / 224
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Example II-6
Consider a rock of very low matrix permeability, 0.01 md, which contains on the average a
fracture 0.005 inches wide and one foot in lateral extent per square foot of rock.
M
Assuming the fracture is in the direction of flow, determine the average permeability using the
equation for parallel flow.
eh
Solution:
di
∑ kj Aj
k = , similar to horizontal, linear flow parallel to fracture
A
Im
matrix k matrix area + fracture k fracture area
k =
total area
12 in 2 + 12 in
an
0.01 0.005 in
k = +
144 in2
144 in2
1.439 + 81,000
k =
144
k = 563 md
Na
ja fa
ba
di
II - 32
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A. Procedure
TURBULENCE
qsc P sc
an
A SLOPE = k / m
ian
P 12 - P 22
2L
Na
kA P12 - P22
qsc = horizontal, linear, real gas flow with
ja
2 µ L Psc
T = Tsc and Z = 1.0
fa
k = ( slope ) m
di
II - 33
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Petroleum
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b. mount core in special holders and flow fluid through core as in perm
M
plug method
eh
VERTICAL FLOW
LOW AIR
PRESSURE
(FLOW)
di
Im
CORE
RUBBER
TUBING
an
HIGH AIR
PRESSURE
PIPE
ian
TO FLOWMETER
Na
c. the horizontal flow data must be adjusted due to complex flow path
II - 34
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measurement.
ba
di
II - 35
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H2
M
N2
eh
k CALCULATED
CO2
di
Im
0
1
P
an
(1/p => 0)
ja fa
kMEASURED
ba
di
0
1
P
II - 36
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Example II-7
Another core taken at 8815 feet from the Brazos County well was found to be very shaly. There
was some question about what the true liquid permeability was, since nitrogen was used in the
permeameter.
M
Calculate the equivalent liquid permeability from the following data.
eh
Mean Measured
Pressure Permeability
( atm ) ( md )
1.192 3.76
2.517 3.04
di
4.571 2.76
9.484 2.54
Solution:
Im
Plot kmeasured vs. 1/pressure
an
Intercept is equivalent to liquid permeability
From graph:
ian
kliq = 2.38 md
5
Na
GAS PERMEABILITY, md
3
ja
2
fa
0
0.0 0.2 0.4 0.6 0.8 1.0
di
II - 37
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3. Reactive fluids
100
an
ian
10
Water concentration
20,000 - 25,000 ppm Cl ion.
Na
1
1 10 100 1000 10000
AIR PERMEABILITY, md
ja fa
b. Injection water may,if its salinity is less than that of the formation water,
reduce the permeability due to clay swelling.
ba
di
II - 38
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M
Effect of Water Salinity on Permeability of Natural Cores
(Grains per gallon of chloride ion as shown).
eh
Field Zone Ka K1000 K500 K300 K200 K100 Kw
Ka means permeability to air; K500 means permeability to 500 grains per gallon chloride solution;
Kw means permeability to fresh water
Na
a. The removal of the core from the formation will likely result in a change in
pore volume.This is likely to result in a change in permeability (+ or -).
ja
II - 39
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I) Boundary tension, σ
M
A. at the boundary between two phases there is an imbalance of molecular forces
SURFACE
ian
LIQUID
Na
ja fa
ba
di
III- 1
Page 83 / 224
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1. Forces
fa
2. Liquid-Gas Boundary
3. Solid-Liquid Boundary
III- 2
Page 84 / 224
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4. Liquid-Liquid Boundary
some of each
M
II) Wettability
eh
A. forces at boundary of two liquids and a solid (or gas-liquid-solid)
σow
di
Im
OIL OIL
an
WATER
Θ
ian
σos σw s
SOLID
B. Adhesion Tension, AT
σws ≥ σos
fa
AT = +
ba
cos θ = +
0° ≤ θ ≤ 90°
di
if θ = 0° - strongly water-wet
III- 3
Page 85 / 224
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σos ≥ σws
M
AT = -
cos θ = -
eh
90° ≤ θ ≤ 180°
θ = 1580
Im
θ= 300 θ= 830 θ = 350
(A)
an
(B)
Na
ja
III- 4
Page 86 / 224
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1. liquid will rise in the tube until total force up equals total force down
= 2πr AT
= πr2 hgρ w
d. units
dyne gm
cm cm = cm2 cm cm
sec2 cm3
ba
gm cm
dyne =
sec2
dyne = force unit
di
e. adhesion tension
dyne
AT = 1 r hgρ w cm
2
III- 5
Page 87 / 224
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2. liquid will rise in the tube until the vertical component of surface tension
equals the total force down
= πr2 hgρ w
di
c. thus when the column of water comes to equilibrium
d. units
an
dyne gm
cm cm = cm2 cm cm
sec cm3
2
gm
cm dyne = cm
cm sec2
ian
2 σaw cos θ
h=
rg ρw
Na
ja fa
ba
di
III- 6
Page 88 / 224
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Pa
B'
M
Pw B
h Θ
Pa
eh
AIR
A' A
di
WATER
Im
an
pressure relations in capillary tubes
Pa' = Pa
ian
pw = pa - ρ wgh
Na
dyne dyne gm ⋅ cm
units: = - cm
cm2 cm2 cm3 ⋅ sec2
pa - pw = pa - (pa - ρ wgh)
fa
pa - pw = ρ wgh
ba
e. remember
di
2 σgw cos θ
h=
rg ρ w
III- 7
Page 89 / 224
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f. thus
2 σgw cos θ
M
Pc = r
WATER
ian
1. liquid will rise in the tube until the vertical component of surface tension
equals the total force down
between oil and water multiplied by the cosine of the contact angle
acting along the circumference of the water-oil-solid interface
c. thus, total force down equals the weight of the column of water
minus the weight of an equivalent column of oil converted to force
ba
= ρw h
di
= ρo h
III- 8
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= ρ wh - ρ oh = h(ρ w - ρ o)
M
4) total force down
eh
= πr2 gh (ρ w - ρ o)
2 σow cos θ
h=
rg (ρ w - ρo)
an
Po
ian
B'
Pw B
h Θ
Po OIL
A
Na
WATER
ja fa
Poa = Pwa
ba
c. pressure at B' equal to the pressure at A' minus the head of oil
between A' and B'
III- 9
Page 91 / 224
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2 σow cos θ
h=
rg (ρ w - ρo)
an
f. thus
2 σow cos θ
Pc =
ian
r
4. same expression as for the air-solid system except for the boundary
tension term
Pc = 2 σ cos θ
r
Na
AT = σow cosθ,
ja
and
2 σow cos θ
fa
Pc = r
thus
ba
III- 10
Page 92 / 224
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ADHESION TENSION
M
AIR AIR AIR
eh
WATER Hg
WATER
di
1/radius of tube
2. thus, the pressure on the concave side of a curved surface is greater than
the pressure on the convex side
an
Pc = σ 1 + 1
R1 R2
R1 and R2 are the principal radii of curvature for a liquid adhering to two spheres in
contact with each other.
ja
1 + 1 = 2 cos θ
fa
R1 R2 r
where Pc = 2 σ cos θ
ba
r
call it Rm(mean radius), i.e.
di
1 = 2 cos θ = (∆ρ)gh
Rm rm σ
III- 11
Page 93 / 224
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F. wettability-consolidated sand
(A) (B)
Na
III- 12
Page 94 / 224
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1. adhesion
M
2. fluid density
3. variation of tube diameter with height
eh
B. consider an experiment in which liquid is allowed to rise in a tube of varying
diameter under atmospheric pressure. Pressure in the gas phase is increased
forcing the interface to a new equilibrium position.
ATMOSPHERIC HIGHER
di
PRESSURE PRESSURE
R
Im
R
an
ian
Na
interface.
2. This illustrates:
fa
curvature which means that the wetting phase will occupy smaller
pores in reservoir rock
III- 13
Page 95 / 224
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1. tube is filled with a wetting fluid and allowed to drain until the interface
M
between wetting fluid and non-wetting fluid reaches equilibrium
(drainage)
eh
2. tube is filled with non-wetting fluid and immersed in wetting fluid
allowing wetting fluid to imbibe until the interface reaches equilibrium
(imbibition)
di
LOW PC HIGHER P C HIGHER P C LOW PC
Θ
Θ
Im
R
Θ Θ
SATURATION = 100% SATURATION = 80% SATURATION = 0% SATURATION = 10%
an
PC = LOW VALUE CAPILLARY PRESSURE = P C P C = HIGH VALUE CAPILLARY PRESSURE = P C
(A) (B)
ian
III- 14
Page 96 / 224
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Φ Φ Sand II
di
1.0
∆ρgh
Φ
0.8
Im
σ
0.6 Drainage
Φ
an
0.4
0.2
Imbibition
ian
0.0
0 20 40 60 80 100
WATER SATURATION, Sw %
Na
2. in general terms,
III- 15
Page 97 / 224
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M
eh
di
DRAINAGE
PC
Im
an
IMBIBITION
ian
Na
0 100
WATER SATURATION, S W
ja fa
ba
di
III- 16
Page 98 / 224
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Water Oil
M
eh
ρw h ρoh
P w = Po/w - P w2 P o2 P o = Po/w -
144 144
di
Im
Oil and Water
P o1 = P w1
100% Water
an
Pc = P o - Pw = h ρ w - ρo
ian
144
Where: Po = pressure in oil phase, psia
Pw = pressure in water phase, psia
h = distance above 100% water level, ft
Po/w = pressure at oil-water contact, psia
Na
III- 17
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M
eh
di
ρoH
PC P O = PO/W -
144
Im
HEIGHT
an
ABOVE
O-W-C
ian
ρ H
P w = PO/W - w
144
Na
ja
PRESSURE
fa
ba
di
III- 18
A. Methods
1. porous diaphragm
M
2. mercury injection
eh
3. centrifuge
4. dynamic method
B. Porous diaphragm
di
1. Start with core saturated with wetting fluid.
3. The pressure difference between the pressure in the non-wetting fluid and
the pressure in the wetting fluid is equal to Pc.
an
5. Measure Sw periodically.
ian
6. Results
7. Advantages
a. very accurate
Na
8. Disadvantages
III- 19
4. Advantages
a. fast-minutes
di
b. reasonably accurate
5. Disadvantages
Im
a. ruins core
b. difficult to relate data to oil-water systems
an
D. Centrifuge Method
TUBE BODY
ja
4. Advantages
di
a. fast
b. reasonably accurate
c. use reservoir fluids
III- 20
E. Dynamic Method
∆P g Pc
eh
di
CORE
Im
an
TO ATMOSPHERE OIL INLET
OIL BURETTE
ian
4. advantages
fa
5. Disadvantages
a. very tedious
di
III- 21
F. Comparison of methods
III- 22
Example VIII-1
Comparison of Mercury Injection Capillary Pressure Data with Porous Diaphragm Data
M
A. Calculate capillary pressure ratio,
eh
PcAH
g
, for the following data:
PcAW
di
σAHg = 480 Dynes/cm σAW = 72 Dynes/cm
Im
θ AH = 140°
g θ AW = 0°
B. Pore geometry is very complex. The curvature of the interface and pore radius are
not necessarily functions of contact angles. Calculate the ratio using the
an
relationship.
g σAHg
PcAH
ian
=
PcAW σAW
Solution:
PcAH
g = 5.1
PcAW
fa
PcAH
(B) σAHg
ba
g @
= 480
PcAW σAW 70
di
PcAH
g = 6.9
PcAW
III- 23
Discussion:
A. Best way to determine the relationship between mercury and air-water data
is to generate capillary pressure curves for each set of data and compare
M
directly.
eh
III- 24
= 2σLcos θ L
PcL
M
r
= 2σRcos θ R
PcR
eh
r
setting r = r
2σLcos θ L 2σRcos θ R
di
r= =
PcL PcR
σcos θ R
∴ PcR = PcL
Im
σcos θ L
where
an
Pc = reservoir capillary pressure, psi
R
θR
Na
III- 25
Example III-2
σAW = 0o
di
Solution:
an
σcos θ R
= PcL
PcR σcos θ L
ian
24 cos20°
= P cL
PcR 72 cos0°
=
Na
III- 26
B. calculate capillary pressure in reservoir for various heights above height at which
M
capillary pressure is zero
(∆ρ)gh
eh
Pc =
144 gc
in English units
di
∆ρ = ρ w - ρ O, lb/cu ft
g = 32 ft/sec2
Im
gc = 32 lbm ft
lbf sec2
h = ft
an
thus
ian
III- 27
Example III-3
P CL 10
8.3
an
ian
0
0 50 100
SW
Na
Solution:
ρw − ρ o h
PcR =
144
ja
PcR
PcL =
0.313
ba
move to the right horizontally from PcL = 8.3 psi to the capillary pressure curve. Drop vertically
di
Sw = 50%
III- 28
A. effect of permeability
200 md
100 md
10 md
Im
180
Height above zero capillary pressure, ft
24 160 72
Oil - Water Capillary Pressure, psi
(laboratory data)
18 120 54
100
ian
12 80 36
60
6 40 18
Na
20
0 0 0
0 10 20 30 40 50 60 70 80 90 100
ja
Sw %
fa
ba
di
III -29
30 225.0
M
25 187.5
10 75.0
5 37.5
Im
0 0
0 20 40 60 80 100
Water
an
100 80 60 40 20 0
Hg
60 348
ian
50 290
Water/nitrogen capillary pressure, psi
30 174
20 116
Limestone Core
Porosity = 23.0%
Permeability = 3.36 md
ja
10 Factor = 5.8 58
0
fa
0
0 20 40 60 80 100
Water
100 80 60 40 20 0
ba
Hg
di
1. majority of grains same size, so most pores are same size - curve (a) (well
sorted)
2. large range in grain and pore sizes - curve (b) (poorly sorted)
III -30
J-function
Pc k 1/2
M
J Sw =
σcos θ φ
eh
attempt to convert all capillary pressure data to a universal curve
where
Im
Pc = dyne/(sq cm)
σ = dyne/cm
k = (sq cm)
φ = fraction
an
III -31
1.4
1.3 EL ROBLE
di
1.2
1.1 KINSELLA
1.0
0.9
0.8
Im
0.7
0.6
0.5 HAWKINS
0.4
an
0.3
0.2
0.1
0.0
ian
0 10 20 30 40 50 60 70 80 90 100
WATER SATURATION, Sw
Reservoir Formation
Na
Hawkins Woodbine
El Roble Moreno
Kinsella Viking
Katie Deese
Leduc Devonian
ja
Alundum (consolidated)
Leverett (unconsolidated)
fa
ba
di
III -32
1. A glass tube is placed vertically in a beaker of water. The interfacial tension between the
air and water is 72 dynes/cm and the contact angle is 0 degree.
M
Calculate:
a. the capillary rise of water in the tube if the radius of the tube is 0.01
eh
centimeters.
b. what is the difference in pressure in psi across the air-water interface in the
tube.
di
2. The displacement pressure for a water saturated porcelain plate is 55 psi of air. What is
the diameter in inches of the largest pore in the porcelain plate? Assume 72 dynes/cm
and 0 degrees.
Im
Solution:
g = 980 dynes/gm
ian
θ = 0o
2σAWcos θ 2 72 cos0°
h= =
rρg .01 1.0 980
Na
h = 14.69 cm
= 14.696 psi
Pc 0.0142 atm
atm
ba
Pc = 0.209 psi
di
III -33
(2) 2σAWcos θ
Pc =
r
Pc = 55 psi
M
Pc atm 1.0133 x 10 6 dynes/cm2
= 55 psi
14.696 psi atm
eh
= 3.792 x 106 dynes/cm2
r = 2σAW cos θ
di
Pc
r = 2 72 cos0° in
= 3.797 x 10 -5 cm
6 2.54 cm
Im
3.792 x 10
r = 1.495 x 10-5 in
d = 2.99 x 10-5 in
an
ian
Na
ja fa
ba
di
III -34
Given the information below and graph of PcL vs. wetting phase saturation Sw , construct the
M
curves for PcR, h in reservoir, and J-function vs. Sw. Water is the wetting phase in both the
laboratory and the reservoir.
eh
lab res
di
fluids air-water oil-water
θ 0° 25°
Im
σ 60 dyne/cm 20 dyne/cm
k 37 md variable
ian
φ 16% variable
Pc k/φ 1/2
Na
J=
σ cos θ
ja fa
ba
di
III -35
35.0
32.5
M
30.0
27.5
eh
25.0
22.5
PCL, psi
20.0
di
17.5
15.0
12.5
Im
10.0
7.5
5.0
an
2.5
0.0
0 10 20 30 40 50 60 70 80 90 100
ian
Sw %
Solution:
Na
(1) = σR cosθ R
Pc
PcR σL cosθ L L
ja
= 20 cos25
P
60 cos0 cL
fa
=
PcR 0.302 P cL
ba
di
III -36
hR ρw - ρo
(2) P =
cR 144
PcL k 1/2
Im
=
σAW cosθ L φ L
PcL
= 37 1/2
an
60 cos0° .16
J = .253 P cL
ian
Sw PcL PcR hR J
% psi psi ft assorted
III -37
10
8
M
6
R
Pc
4
eh
2
0
di
0 20 40 60 80 100
Sw %
100
Im
80
60
R
an
h
40
20
ian
0
0 20 40 60 80 100
Sw %
10
8
Na
6
J
4
ja
2
fa
0
0 20 40 60 80 100
Sw %
ba
di
III -38
IV - 1
sat at surface
eh
flushing by bit trip to surface compared to res
Sw ↑ ↓ ? probably ↑
di
So ↓ ↓ ↓
Sg - ↑ ↑
Im
Gas zone at minimum interstitial water saturation:
sat at surface
an
flushing by bit trip to surface compared to res
Sw ↑ ↓ ?
ian
So - - -
Sg ↓ ↑ ?
Na
Water zone:
sat at surface
flushing by bit trip to surface compared to res
ja
Sw - ↓ ↓
fa
So - - -
Sg - ↑ ↑
ba
di
IV - 2
So - ↓ ↓
di
Sg - ↑ ↑
Im
Gas zone at minimum interstitial water saturation:
sat at surface
flushing by bit trip to surface compared to res
an
Sw - - -
So ↑ ↓ ↑
ian
Sg ↓ ↑ ↓
Water zone:
Na
sat at surface
flushing by bit trip to surface compared to res
Sw ↓ ↓ ↓
ja
So ↑ ↓ ↑
↑ ↑
fa
Sg -
ba
di
IV - 3
HEATING ELEMENT
ian
CORE
Na
COOLING WATER IN
CONDENSER
COOLING WATER OUT
ja fa
ba
di
IV - 4
1) process
1.4
Im
1.3
an
1.2
Multiplying Factor
ian
1.1
Na
1.0
0.9
ja
15 20 25 30 35 40 45 50 55 60 65
IV - 5
e) determine saturations
V V
Sw = w So = o
Vp Vp
M
Sg = 1 - S o - Sw
eh
where
WATER
Na
RECOVERED
PORE WATER
0
ja
0
TIME
fa
IV - 6
WATER OUT
di
WATER IN
Im
GRADUATED TUBE
CORE
an
ian
SOLVENT
Na
HEATER
ja fa
1) process
IV - 7
Wi - Wdry - Vw ρ w
eh
Vo =
ρo
where:
di
Wi = weight of core sample
after leaching
Im
Wdry = weight of core sample
after leaching
V V
Sw = w So = o
an
Vp Vp
2) disadvantages of leaching
ian
a) process is slow
3) advantages of leaching
Na
IV - 8
OIL
ian
WATER
Na
So ≅ 0 in gas zone
ja
IV - 9
3) oil/water contact
eh
B. Capillary pressure measurements (discussed in Chapter VIII)
di
C. Electric logs
Im
an
ian
Na
ja fa
ba
di
IV - 10
Example IV-1
You want to analyze a core sample containing oil, water and gas.
M
Vb bulk volume = 95 cm3
eh
Wt initial = 216.7 gm
the sample was evacuated and the gas space was saturated with water ρ w = 1 gm/cm3
di
Wt new = 219.7 gm
Wt dry = 199.5 gm
an
calculate:
ian
(1) porosity
(6) lithology
ja
Solution:
fa
water vol. = 13 - 3 ; Vw = 10 cc
ba
IV - 11
Vp = 8.49 + 3 + 10 = 21.47 cc
eh
φ = 21.47/95 = 22.6%
Sw = 10/21.47 = 46.57%
di
So = 8.49/21.47 = 39.46%
Sg = 3/21.47 = 13.97%
Im
ρm = 199.5/(95-21.47) = 2.71 gm/cc
lithology = limestone
an
ian
Na
jafa
ba
di
IV - 12
Example IV-2
M
A core sample was brought into the laboratory for analysis. 70 gm of the core sample were placed
in a mercury pump and found to have 0.71 cc of gas volume. 80 gm of the core sample was
eh
placed in a retort and found to contain 4.5 cc of oil and 2.8 cc of water. A piece of the original
sample weighing 105 gm was placed in a pycnometer and found to have a bulk volume of 45.7 cc.
di
(Assume ρ w = 1.0 gm/cc and 35o API oil)
calculate:
Im
(1) porosity
(5) lithology
Solution:
70 gm
80 gm
105 gm
ba
φ = 10.14/43.52 = 23.31%
IV - 13
Sw = 3.50/10.14 = 34.5%
So = 5.63/10.14 = 55.5%
M
Sg = 1.014/10.14 = 10%
eh
ρm = (91.71/33.38) = 2.75
di
Im
an
ian
Na
ja fa
ba
di
IV - 14
Calculate porosity, water, oil, and gas saturations, and lithology from the following core analysis
M
data.
How should the calculated saturations compare with the fluid saturations in the reservoir?
eh
Oil well core with water base mud
di
initial weight of saturated core = 86.4 gm
after gas space was saturated with water, weight of core = 87.95 gm
Im
weight of core immersed in water = 48.95 gm
Solution: γo = 141.5
131.5 + °API
γo
Na
= 141.5 = 0.825
131.5 + 40°
ρo = 0.825 gm/cc
ja
Vp
(1) φ = Vb
fa
Vp = Vw + Vo + Vg
ba
Wo = 1.66 gm
IV - 15
Vo = Wo
ρo
1.66 gm
M
Vo = = 2.01 cc
0.825 gm/cc
Vw = Vwrec - Wsat - Wi / ρ w
eh
= 7.12 - (87.95 - 86.4)/(1.0)
Vw = 5.57 cc
di
Vg = 1.55 cc
Vp = 9.13 cc
Wsat - Wimm
an
Vb =
ρw
Vb = (87.95 - 48.95) gm
= 39.0 cc
1 gm/cc
ian
φ = 9.13 = 23.4%
39.0
Vw
Vp
Na
(2) Sw =
Sw = 5.57 cc = 61.0%
9.13 cc
ja
So = Vo
Vp
fa
So = 2.01 cc = 22.0%
9.13 cc
ba
Vg
Sg =
Vp
di
Sg = 1.55 cc = 17.0%
9.13 cc
(3) Vm = Vb - Vp
IV - 16
Vm = 39 - 9.13 = 29.87 cc
Wdry
M
=
ρm Vm
=
eh
gm
ρm 79.17 gm/29.87 cc = 2.65 cc
. . lithology is sandstone
di
(4) water saturation at surface will probably be greater than reservoir water
saturation
IV - 17
Calculate porosity, water saturation, oil saturation, gas saturation, and lithology from the following
M
core analysis data.
How should the saturations you have calculated compare with the fluid saturations in the reservoir?
eh
Oil well core cut with an oil base mud
di
Sample 1 weighed 130 gm and was found to have a bulk volume of 51.72 cc
Sample 2 weighed 86.71 gm, and from the retort method was found to contain 1.90 cc of water
and 0.87 cc of oil
Im
Sample 3 weighed 50 gm and contained 0.40 cc of gas space
141.5
ian
γo = 141.5 = 0.825
131.5 + 40°
Na
ρo = 0.825 gm/cc
Vp
(1) φ = Vb
ja
Vp = Vo + Vw +Vg
fa
50 gm 100 gm
IV - 18
Vp = 3.99 cc/100 gm
Vo
x 100
Vp
an
(3) So =
= 1.0 cc x 100
3.99 cc
ian
So = 25.1%
Vg
x 100
Vp
(4) Sg =
Na
= 0.80 cc x 100
3.99 cc
Sg = 20.1%
ja
(5) Vm = Vb - Vp
fa
= 39.78 - 3.99
Vm = 35.79 cc/100 gm
ba
86.71
Wm = 97 gm/100 gm
IV - 19
ρm = Wm
Vm
ρm
M
= 97 gm/100 gm
35.79 cc/100 gm
ρm
eh
= 2.71 gm/cc
.. lithology - limestone
di
IV - 20
given a box of length (L) and cross-sectional area (A) completely filled with
brine of resistivity (Rw)
Na
the resistance of the brine in the box to current flow may be expressed as
r = Rw L
A
ja
r = resistance - ohm
L = length - meters
ba
A = area - (meters)2
di
V-1
B. Nonconductors of electricity
1. oil
2. gas
M
3. pure water
eh
4. minerals
5. rock fragments
di
C. Conductors of electricity
AP
A
ian
ELECTRICAL
CURRENT FLOW
Na
L
ja
Ap < A
ba
Lp > L
di
V-2
3. Since
Ap
≅ porosity, φ
fa
A
and
ba
Lp
≅
L tortuosity, a measure of rock cementation.
then
di
RwALp
Ro =
ApL
V-3
becomes
Ro = f Rw, φ, tortuosity
M
E. Electrical formation resistivity factor, F
Ro = f Rw, φ, tortuosity
di
2. can be written as
Ro = F R w
Im
where F is the electrical formation resistivity factor
Ro
F=
Rw
an
3. cementation factor, m
F = C φ-m
where C is a constant
m is the cementation factor
Na
b. thus
V-4
100
M
F 10
eh
di
1
0.01 0.1 1.0
Im
φ
when intercept = C
an
slope = -m, the cementation factor
a. Archie's Equation
F = φ-m
b. Humble Equation
Na
F = 0.62 φ-2.15
Lithology m values
Very slightly cemented (Gulf Coast type of sand, except Wilcox) 1.4-1.5
Slightly cemented (most sands with 20% porosity or more) 1.6-1.7
Moderately cemented (highly consolidated sands of 15% porosity or less) 1.8-1.9
Highly cemented (low-porosity sands, quartzite, limestone,dolomite) 2.0-2.2
di
V-5
Example V-1
Determine the porosity for a sandstone using Archie's and Humble equation .
The formation water's resisitivity was 0.5 ohm-meters. The formation rock 100% saturated with
M
this water was 21.05 ohm-meters.
Which of the two equations will give the most reasonable answer?
eh
Solution:
F =21.05/0.5 = 42.1
di
Archie's: F = φ-m
φ= 1
an
42.1
φ = 15.41%
ian
Humble: F = 0.62/φ2.15
φ2.15 = 0.62/F
Na
φ = 2.15 0.62
42.1
φ = 14.06%
ja
V-6
Rt
M
I=
Ro
-1 R -1
Sw = I n = t n
Ro
an
3. rearrange
Rt
Sw-n =
Ro
Na
Rt
-n log Sw = log
Ro
ja fa
ba
di
V-7
100
M
Rt
10
eh
Ro
di
1
.1 1.0
Im
Sw
an
slope = -n, when n is the saturation exponent
ian
NOTE:
log y1 - log y2
slope =
log x1 - log x2
Na
II) Use of Electrical Formation Resistivity Factor, Cementation Factor, and Saturation
Exponent
A.
-m
B. F=Cφ (usually use Archie or Humble equation)
fa
D. Ro = F R w
Ro 1n
Sw =
Rt
V-8
A. Apparatus
M
AC SOURCE
eh
di
CORE
an
ian
VOLTMETER
Na
B. Calculations
1. resistance of core
ja
E = Ir
fa
I = current, amperes
r = resistance, ohms
di
∴ rcore = E
I
V-9
2. resistivity of core
r A
Rcore = core
M
L
substituting r = E into the equation
I
eh
Rcore = EA
IL
di
C. Procedure
100%, R core = Ro
where
(irreducible), fraction
ohm-m
Rt = resistivity index = I
Ro
di
V - 10
Rt
2. Plot log vs log Sw or log I vs log Sw
Ro
ian
100
Na
Rt
I= 10
Ro
ja fa
1
.1 1.0
ba
Sw
V - 11
Example V-2
Given the following data, calculate the electrical formation resistivity factor and saturation exponent
of the core.
M
Rw = 55 ohm-cm
eh
I = 0.01 amp
D = 2.54 cm
di
L = 3.2 cm
E
Im
Sw Voltage across
Water Saturation, % Core, volts
100.0 7.64
86.0 10.50
an
74.0 14.34
63.0 20.16
54.0 27.52
49.0 = Swir 34.67
ian
Solution:
F = Ro
Na
Rw
F = Ro 1210
= = 22
Rw 55
ba
di
V - 12
saturation exponent
Rt
-n log Sw = log
M
Ro
rA Rt
Sw rt = E Rt = t Ro
eh
I L
% (ohm) (ohm-cm)
1.00 1.000
.86 1050 1663 1.374
di
.74 1434 2271 1.877
.63 2016 3192 2.638
.54 2452 4358 3.601
.49 3467 5490 4.537
Im
(.334,10)
an
10
ian
Na
Rt/Ro
ja fa
1 (1.0,1.0)
ba
.1 1
Sw
di
V - 13
-n = 1-0
M
-.4763 - 0
n = 2.10 = saturation exponent
eh
NOTE:
di
Rt Et
=
Ro Eo
V - 14
Ro
F=
c. Rw
di
2. plot data according to form of equation for electrical formation
resistivity factor
Im
F = C φ-m
an
log F = log C - mlog φ
ian
100
Na
F 10
ja fa
1
0.01 0.1 1.0
φ
ba
V - 15
Example V-3
The laboratory test of Example IV-2 has been repeated for several core samples from the reservoir.
Data is given below. Calculate the cementation factor and intercept for the formation resistivity
factor equation.
M
Porosity Formation Resistivity Factor
eh
φ F
0.152 40
0.168 32
di
0.184 26
0.199 22
0.213 19
0.224 17
Im
Solution:
F = C φ-m
an
100
Na
10
ja
F
fa
ba
1
.1 1
di
V - 16
-m = slope = -2.21
M
eh
m = 2.21 = cementation factor
di
intercept
log C = -.2082
an
C = 062 = intercept
ian
Na
ja fa
ba
di
V - 17
CLAY
Im
1 = 1 + 1
RoA Rclay Ro
an
1 = 1 + 1
ja
RoA Rclay F Rw
fa
V - 18
3. plot
M
eh
di
1
ROA
(OHM - M) -1
Im
an
1 -1
RW (OHM - M)
ian
1 = 1 + 1 1
RoA Rclay F Rw
Na
where
ja
1 = intercept
Rclay
fa
1 = slope
F
ba
di
V - 19
D. effect of clay
RoA
M
FA =
1. define Rw , clays reduced the apparent formation resistivity
factor
eh
CLEAN SAND
di
F
SHALY SAND
FA
Im
an
RW
ian
100
Na
CLEAN SAND
F 10
ja
SHALY SAND
fa
1
0.1 φ 1.0
ba
di
V - 20
CLEAN SAND
Rt
Swn-1 = I
di
I= 10
Ro SHALY SAND n =?
Im
CLEAN SAND HIGH R w
n=1
1
.1 1.0
an
Sw
ian
Na
ja fa
ba
di
V - 21
I) Effective permeability
M
A. Permeability, k, previously discussed applies only to flow when pores are
100% saturated with one fluid - sometimes called absolute permeability
eh
kA∆ρ
q=
µL
di
B. When pore space contains more than one fluid, the above equation becomes
k A∆Pο
qo = o
µoL
Im
k A∆Pw
qw = w
µw L
an
kgA∆Pg
qg =
µgL
ian
3. fluid saturations
VI - 1
k A P1 - P2
qo = 1.1271 x 10-3 o
µoL
M
k A P1 - P2 w
qw = 1.1271 x 10-3 w
µw L
eh
kg A P1 - P2 g
qg = 1.1271 x 10-3
µgL
di
when k = md
A = ft2
Im
P = psia
L = ft
q = res bbl/day
an
k
kro = o
Na
k
k
krw = w
k
kg
ja
krg =
k
B. It is normally assumed that the effective permeability at 100% saturation is
fa
the same for all fluid in a particular rock. (not necessarily true in shaly sand)
ba
VI - 2
1
1
M
NON-WETTING PHASE
eh
di
Kr
Im
2
an
WETTING PHASE
ian
3
4
0
0
Na
SWP, % 100
MINIMUM INTERSTITIAL S WP EQUILIBRIUM S NWP
ja
krwp
1. = 1, only at S wp = 100%
fa
k
2. rapid decrease in rwp as Swp decreases
krwp
ba
krnwp
4. = 0, at equilibrium Snwp
di
VI - 3
VI - 4
1
M
eh
Krnwp
DRAINAGE
di
Im
Kr
an
IMBIBITION
ian
Krwp
Na
0
0 SWP, % 100
ja
VI - 5
3. the word "hysteresis" describes the process in which the results (kr)
are different when measurements are made in different directions
5. wetting preference for reservoir rocks is usually water first, then oil,
di
finally gas
Im
Fluids Present Wetting Phase
VI - 6
VI - 7
1%
di
5
Im
10
20
an
40
60
ian
VI - 8
40%
ian
60%
80%
VI - 9
100% GAS
M
eh
50%
40
30
di
20
5
Im
1
an
k
a. curves above indicate that rg is a function of saturations of
other phases present.
k
b. other research shows that rg is a unique function of gas
saturation
Na
c. the other phases, oil and water, occupy the smaller pore
openings and wet the surface of the rock
k
therefore, rg should be dependent only on the total
ja
d.
saturation of the other two phases (i.e. 1-Sg) and
independent of how much of that total is composed of either
fa
phase
k
e. thus rg can be plotted on Cartesian coordinates against So +
ba
Sw
di
VI - 10
1.0
M
0.8
eh
0.6
krg
di
0.4
Im
0.2
an
0.0
0 20 40 60 80 100
So + Sw
ian
a. water
Na
b. gas
k
2) therefore rg is a function of Sg only
k
thus plot rg against Sg (or So + Sw) on rectangular
di
3)
coordinate
VI - 11
c. oil
1.0
an
0.8
ian
0.6
kro
0.4
Na
0.2
ja
0.0
fa
0 20 40 60 80 100
So, %
ba
Minimum Interstitial
Water Saturation
di
VI - 12
5% oil
an
5% gas
ian
5% water
Region of three-phase flow in reservoir centers around 20% gas, 30% oil,
50% water
ja fa
ba
di
VI - 13
kg krg
permeability ratio = =
Im
ko kro
an
2. When the permeability to gas is zero (no gas or gas below "critical
gas saturation") it is sometimes convenient to use permeability ratio
to represent the flow conductance of the rock to oil and water as a
ratio
ian
k kr
permeability ratio = o = o
kw krw
A. Methods
B. Laboratory Methods
ba
VI - 14
q µ L
di
ko = o o
A∆p
q µ L
Im
kw = w w
A∆p
1
ian
Na
kr kro krw
ja fa
ba
di
0
0 Sw, % 100
VI - 15
1) resistivity
Ro 1n Eo 1n
M
Sw = =
Rt Et
eh
where: Ro = resistivity of core 100% saturated with
wetting-phase, ohm-m
2) volumetric balance
an
Wf = Wt - Wd
ian
Wf = ρ oVo + ρ wVw
and
ja
Vf = Vo + Vw
fa
V = volume, cc
ba
Sw = Vw/Vf
thus
VI - 16
Wf/Vf - ρ o
Sw = ρw - ρo
M
i. same procedure can be used starting with 100% saturation of
non-wetting phase
eh
1) injection ratio start with high ratio of non-wetting
phase
essentially equal
Pnwp = P wp
fa
VI - 17
100 100
Oil Saturation, %
M
60 60
20 20
di
0 0
0 5 10 15 20 25 0 5 10 15 20 25
Thermometer Inlet
Copper
Packing Nut Orifice
Electrodes
Plate
Na
Differential
Pressure Taps
ba
VI - 18
Example VI-1
The relative permeability apparatus shown above was used in a steady-state flow process to obtain
the data given below at a temperature of 70oF. See figure on previous page.
M
eh
di
The Core The Fluids
Oil Flow Water Flow Inlet Pressure Outlet Pressure Voltage Drop Electrical Current
cc/sec cc/sec psig psig volts amps
ian
Solution:
ja
1. Calculate absolute permeability using data with core 100% saturated with water
fa
qwµwL
k =
ba
A∆p
k = 0.482 darcy
VI - 19
qoµoL
M
ko = A∆P
ko = 0.0134 darcy
di
qwµwL
kw = A∆P
Im
0.8898 1.07 2.30
kw = 2.688 67.5 - 13.5 / 14.696
kw = 0.2217 darcy
an
k
kro = o = .0134 = 0.028
ian
k .482
k
krw = w = .2217 = 0.460
k .482
4. Calculate water saturations
Na
Sw = Eo 1/2
Et
2.10
5. Results
fa
VI - 20
1.0
M
0.8
eh
Relative Permeability
0.6
Kro
Krw
di
0.4
Im
0.2
0.0
an
0 20 40 60 80 100
1
Na
ja
.1
fa
.01
ba
0 20 40 60 80 100
Sw, % of pore space
di
VI - 21
0.62 φ-2.15
M
F =
F = Ro
eh
Rw
F = 140 = 11.7
Im
12
Φ = 1 1
.62 2.15 = .62 2.15
F 11.7
an
Φ = .255
ian
Na
ja fa
ba
di
VI - 22
2. Displacement (unsteady-state)(Welge)
c. conditions
an
1) pressure drop across core high enough to make end
effects negligible,but not enough to cause turbulent
(non-darcy) flow.
ian
P + Po
Pm = i
2
3) flow is horizontal and core is short so that effects of
Na
d. calculations
Gipi
fa
Gipv =
LAφ pm
ba
volume
VI - 23
pm = pi + po
, psi
2
LA φ = pore volume, cc
M
2) calculate average gas saturation, Sgav
eh
Np
=
Sgav LAφ
Sgav
GAS BREAKTHROUGH
ja fa
ba
0
0 Gipv
di
VI - 24
d Sgav
M
fo =
d Gipv
ko/µo
an
fo =
ko/µo + kg/µg
kg 1 - fo
=
ko fo µo/µg
ian
kg
where = permeability ratio of gas to oil
ko
face of core
Gipv
ba
= cumulative gas
injected, pore volumes
VI - 25
e. advantages
2) rapid
M
f. disadvantages
eh
k
1) results in kg/ko, not kro and rg
VI - 26
Example VI-2
The data from an unsteady-state displacement of oil by gas in a 2 inch diameter by 5 5/8 inch long
sandstone core are given below.
M
eh
Cumulative Gas Injection, Gi, cc Cumulative Oil Produced, Np, cc
14.0 14.6
50.2 19.5
di
112.6 22.5
202.3 25.5
401.4 28.6
546.9 30.4
Im
769.9 32.2
1226.5 33.4
3068.9 35.3
5946.6 35.9
an
Other data
ian
G
Prepare to determine kg/ko by calculating Sgav and ipv.
ja
Solution:
1. Calculate Sgav
fa
Np
Sgav =
LAφ
ba
Sgav = 14.6 cc
14.3 cm 20.27 cm2 .210
di
Sgav = 0.24
G
2. Calculate ipv
VI - 27
Gipi
Gipv =
LAφ pm
M
14.0 cc 19.7 psia
Gipv =
14.3 cm 20.27 cm2 .210 19.7 psia + 14.7 psia /2
eh
Gipv = 0.264 pv
3. Results
di
Sgav Gipv pv
Im
0.24 0.264
0.32 0.945
0.37 2.12
0.42 3.81
an
0.47 7.56
0.50 10.3
0.53 14.5
0.55 23.1
0.58 57.8
ian
0.59 112.0
Na
ja fa
ba
di
VI - 28
Example VI-3
A core sample initially saturated with oil is flooded with gas. The following data was obtained:
Gipv pv
M
Sgav
0.24 0.264
0.32 0.945
eh
0.37 2.12
0.42 3.81
0.47 7.56
0.50 10.3
di
0.53 14.5
0.55 23.1
0.58 57.8
0.59 112.0
Im
µo = 2.25 cp
µg = 0.0185 cp
an
S
Calculate and construct a fg verses Sgo plot. Convert gavg to Sgo. Determine kg/ko for each of
the given saturations. Construct a graph of kg/ko versus S go.
ian
Solution:
1 - fo
kg/ko =
µ
fo o
µo
ja
VI - 29
0.6
M
0.5
eh
Sgav 0.4
fraction
di
0.3
Im
0.2
an
0 20 40 60 80 100 120
Gipv, pv
ian
100
10
Na
kg/ko 1
ja fa
.1
ba
.01
0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0
di
Sg, %
VI - 30
1. equations
M
kg A ∆p
qg µgL
eh
qo = k A ∆p
o
µoL
thus,
kg qg µg
an
=
ko qo µo
qg Bg Rp - Rs
qo = 5.615 B o
thus
kg µgBg Rp - Rs
fa
=
ko µo 5.615 Bo
2. procedure
ba
VI - 31
Example VI-4
Discovery pressure for your well was 4250 psia, temperature is 200oF, and initial producing gas-
M
oil ratio was 740 SCF/STB. Stock tank oil gravity is 30oAPI and surface gas gravity is 0.7.
Production history and correlations indicate the bubble point at 3500 psia. Reservoir pressure is
eh
now 3000 psia. Producing gas-oil ratio is 18,100 SCF/STB. What is kg/ko in the reservoir at this
time.
Solution:
di
Correlations covered in the fluid properties portion of this course yield the following value
of the physical properties of the gas and oil at 3000 psia and 200o F.
Im
Rs = 560 SCF/STB
z = 0.86
µg = 0.0192 cp
µo = 0.75 cp
ja
kg = µgBg Rp - Rs
ko µo 5.615 Bo
fa
kg = 0.325
ko
di
VI - 32
Log Response
0 Diagram
0 Sw, % 100
ian
SP Log RT Log
Na
h, ft
100% Water Production
ja fa
ba
100 % Sw
0
0 Sw, % 100
di
VI - 33
1
M
eh
kr
di
Im
an
0 Log Response
0 Sw, % 100 Diagram
SP Log RT Log
ian
h, ft
ja fa
100 % Sw
0
0 Sw, % 100
ba
di
VI - 34
1
M
eh
kr Low K
di
High K
Im
an
0
0 Sw, % 100
h = height of zone
ian
of interest
Na
h, ft
Low K
ja
High K
fa
0
0 Sw, % 100
ba
di
VI - 35
kw A ∆ P
M
q q µw L
fw = q w = q +wq = = 1
tot o w ko A ∆ P kw A ∆ P ko µw
+
eh
1+
µo L µo L kw µo
1
di
Im
fw
100
an
0
0 Sw 100
ian
100
Na
0
0 1
fw
h
ja fa
0
0 Sw 100
ba
di
VI - 36
160
10 md
140
M
120
Height above free water level, ft
eh
100
80
50 md
di
60
40
Im
100 md
20
200 md
0
an
0 20 40 60 80 100
This figure indicates that lower permeabilities result in longer transition zones
1
Na
Oil
Water
kr
ja fa
0
0 100
ba
Sw
Residual Oil
Saturation
VI - 37
1
di
4
fw
Im
an
2 3
0
ian
0 Sw 100
1. fw at water breakthrough
Na
VI - 38
1 3
M
eh
2
di
Water input
fw Pore vols.
Im
1
an
ian
0 0
0 100
Oil Rec - % Oil in Place
Na
ja fa
ba
di
VI - 39
I) Introduction
M
Usually we can not examine an entire "population" (i.e. we can not dig up an entire
eh
reservoir, cut it into plugs, and measure the porosity of every plug). We can only
"sample" the population and use the properties of the sample to represent the
calculations.
Im
an
If the sample is representative of the population, we have a statistical basis for
The classification of data for a large number of samples will often provide
VII - 1
class mark.
an
Rules for forming frequency distributions
ian
B. Divide the range of numbers into a convenient number of equal sized class
intervals. The number of class intervals depends on the data but is usually
Na
C. The number of observations for each class interval is the class frequency.
ja
D. The relative frequency of a class is the frequency of the class divided by the
fa
VII - 2
III) Histogram
Frequency of Occurence
Mean
di
Im
Magnitude of Variable
8
an
6
# of Samples
ian
2
Na
0
12 16 20 24
Porosity, %
8
ja
6
# of Samples
fa
2
ba
0
20 60 100 140
Permeability, md
di
VII - 3
Net pay thickness data from 20 wells summarized as relative frequency data
M
Frequency Relative Frequency
Range of (No. of wells (No. of wells having thickness Relative
eh
thickness, having thickness values in each range, Frequency
ft. values in the range) fraction of total wells) as percentage.
di
50-80 4 0.20 20%
81-110 7 0.35 35%
111-140 5 0.25 25%
141-170 3 0.15 15%
171-200 1 0.05 5%
Im
20 1.00 100%
an
ian
10
8
Frequency
Na
4
ja
0
fa
VII - 4
.3
an
.2
ian
.1
0
0 50 80 110 140 170 200
Na
VII - 5
Relative frequencies are summed and plotted at the higher ends of the class intervals
M
to create a "cumulative frequency less than or equal to" distribution
eh
di
Cumulative frequency less than for equal to
1.0 100%
Im
.8 80%
an
.6 60%
.4 40%
ian
.2 20%
0 0
0 50 80 110 140 170 200
Na
VII - 6
plotted. Relative frequencies are summed from the highest class interval and plotted
1.0
Cumulative % greater than or equal to
100%
Im
.8 80%
an
.6 60%
.4 40%
ian
.2 20%
0 0
0 50 80 110 140 170 200
Na
Probability graph paper has been constructed so that data from certain probability
fa
distributions plot as a straight line. Different probability paper is used for data with
ba
different distributions
di
VII - 7
V) Normal Distribution
f(x)
an
Inflection point
of curve
a a
ian
µ −a µ +a
Random variable x
Na
This distribution is completely and uniquely defined by two values - the mean, m,
ja
VII - 8
an exponential distribution.
eh
di
Im
Mode
an
f(x)
Median (geometric mean)
ian
Mean (arithmetic mean)
Na
Random variable x
ja
This distribution can also be completely and uniquely defined by the mean, m, and
the standard deviation, σ.
fa
If random variable xi are log normally distributed then the variables log xi are
ba
normally distributed.
di
VII - 9
center of these data. These averages are called measure of central tendency.
eh
mean - the arithmetic average value of the samples
di
n
Σ xi
µ = i =1n
Im
where xi = values of the variable of interest for each sample
nµ = number of samples
an
median - the value equalled or exceeded by exactly one-half of the samples.
n 1/n
Na
µg = π xi
i=1
VII - 10
n
Σ xi - µ 2
Im
σ =
2 i=1
n-1
n
Σ xi - µ
MD = i=1 n
Na
Σ fi xi - µ 2
j
σ2 =
ja
Σ fi
j
fa
xj = class mark
ba
or
σ2 = Σ frj xj - µ 2
di
f
where rj = relative frequency for each class
VII - 11
Σ fj xj
an
j
µ=
Σ fj
j
ian
where j refers to each class interval
fj is the frequency of the class
or
Na
µ = Σ frj xj
j
f
ja
VII - 12
.999 .999
M
Cumulative Frequency
Cumulative Frequency
eh
di
.001 .001
Im
Random variable x Random variable x
.999 .999
µ+a
distributed normally
distributed normally
Random variable x,
Random variable x,
σ
ja
µ µ
fa
.001 .001
ba
VII - 13
Σ fi xi
µ= = 745.0 = 17.7%
Σ fi 42
Σ fi xi - µ 2
j
σ2 = = 376.18 = 8.96
Na
Σ fi 42
j
σ = 8.96 = 2.99%
ja fa
ba
di
VII - 14
Cumulative
Frequency Cumulative
M
Than or Equal to Frequency
Porosity Upper Limit of Expressed as
eh
Interval, % Frequency Interval Percentage
7.0<x<10.0 1 1 2.4%
di
10.0<x<12.0 0 1 2.4%
12.0<x<14.0 1 2 4.8%
14.0<x<16.0 10 12 28.6%
Im
16.0<x<18.0 12 24 57.1%
18.0<x<20.0 8 32 76.2%
20.0<x<22.0 7 39 92.9%
an
22.0<x<25.0 3 42 100.0%
42
ian
26
24
22
20
Na
Core porosity, %
18
16
ja
14
12
fa
10
ba
8
2 10 20 30 40 50 60 70 80 90 96
σ = 20.7 - 17.7 = 3%
VII - 15
n 1/n
µ = π xi
i=1
ian
or
n
log (m) = 1 Σ log xi
Na
n i=1
ja fa
ba
di
VII - 16
Cumulative
Frequency Less Cumulative
Permeability Than or Equal to Frequency
Interval Upper Limit of Expressed As
M
(millidarcies) Frequency Interval Percentage
0-50 2 2 4.8%
eh
51-100 2 4 9.5%
101-150 4 8 19.0%
151-200 4 12 28.6%
201-250 4 16 38.1%
di
251-300 8 24 57.1%
301-350 4 28 66.7%
351-400 2 30 71.4%
401-450 4 34 81.0%
451-500 1 35 83.3%
Im
501-700 5 40 95.2%
701-1000 2 42 100.0%
42
an
1000
ian
Core permeability, md
Na
100
ja fa
ba
10
2 10 20 30 40 50 60 70 80 90 96
di
VII - 17
P c = 2 σ cosθ
Im
r
π r4
i ∆p
qi =
8µL
ian
3. Darcy's equation,
qt = kA ∆p
µL
Na
P c = dynes
cm2 k = cm2
ja
σ = dynes
cm A = cm2
fa
r = cm L = cm
ba
q = cm
2 µ = poise = dynes-sec
sec cm2
di
∆p = dyne
cm2
2
Let V i = πr i L,
M
then the flow rate in a capillary is
eh
2
qi = Vr i ∆p, V = cm3
2
8µL
di
Since
r i = 2σ cosθ
Im
Pci
σ cosθ 2 Vi
qi = ∆p
an
Pci 2 2 µ L 2
i = n σ cosθ 2 ∆p i=n V
qt = Σ Σ i
i=1 2µL 2
i=1 Pci 2
Na
Since,
qt = k A ∆p
µL
ja
i=n
σ cosθ 2
fa
k = Σ Vi 2
2 A L i=n Pci
ba
di
φ = VT , φ = fraction
di
AL
i=n
σ cosθ 2
k= φ Σ Si
Im
2 i=1 Pci 2
i=n
σ cosθ 2
k= φλ Σ Si
ian
2 i=1 Pci 2
In integral form,
S=1
Na
σ cosθ 2
k= φλ dS
2 2
S=0 Pc
ja
fa
ba
di
Purcell approach:
di
The absolute permeability may be expressed as
Im
S=1
σ cosθ 2
k= φλ dS
2 2
S=0 Pc
an
S=Swt
σ cosθ 2
kwt = φλ dS
2 P2c
S=0
Na
The relative permeability of the wetting phase is the ratio of the wetting
phase effective permeability to the absolute permeability
S=Swt
ja
dS
P2c
S=0
krwt = kwt =
fa
k S=1
dS
ba
2
S=0 Pc
di
S=1
M
σ cosθ 2
knwt = φλ dS
2 2
S=Swt Pc
eh
The relative permeability of the nonwetting phase is the ratio of the
nonwetting phase effective permeability to the absolute permeability
di
S=1
dS
Im
2
S=Swt Pc
krnwt = knwt =
k S=1
an
dS
2
S=0 Pc
ian
Na
ja fa
ba
di
Burdine Approach:
λrwti = λi
eh
λwti
The relative permeability of the wetting phase is the ratio of the wetting
di
phase effective permeability to the absolute permeability
S=Swt
Im
dS
P2c
S=0
krwt = kwt = λrwt 2
k S=1
an
dS
2
S=0 Pc
ian
λrwt = Swt - S m
Na
1 - Sm
ja fa
ba
di
λrnwt = Snwt - S e
1 - Sm - Se
ian
Na
ja fa
ba
di
4
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