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5 Relative Permeability

Relative permeability is a ratio that describes how the permeability of a rock to a particular fluid is affected by the presence of other fluids. It is determined through steady-state laboratory experiments where fluids are injected into a core sample at different saturation levels until steady flow is achieved. This provides data points that define the relative permeability curves and determine important saturation levels like irreducible water saturation and residual oil saturation. Special techniques are required to minimize errors from capillary end effects and ensure measurements represent the bulk rock properties. Correlations can also be used to estimate relative permeability based on rock and fluid properties when direct measurement is not possible.

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0% found this document useful (0 votes)
323 views

5 Relative Permeability

Relative permeability is a ratio that describes how the permeability of a rock to a particular fluid is affected by the presence of other fluids. It is determined through steady-state laboratory experiments where fluids are injected into a core sample at different saturation levels until steady flow is achieved. This provides data points that define the relative permeability curves and determine important saturation levels like irreducible water saturation and residual oil saturation. Special techniques are required to minimize errors from capillary end effects and ensure measurements represent the bulk rock properties. Correlations can also be used to estimate relative permeability based on rock and fluid properties when direct measurement is not possible.

Uploaded by

ikhwanu huda
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Relative Permeability

Definitions
• Absolute permeability – ability of the porous
media to transmit fluids
• Effective permeability – permeability of a
given phase when more than one phase is
present
• Relative permeability is the ratio of the
effective permeability for a particular fluid to
a reference or base permeability of the rock.
Applications of relative permeability
data:
• to model a particular process, for example,
fractional flow, fluid distributions, recovery
and predictions
• Determination of the free water surface;
i.e., the level of zero capillary pressure or
the level below which fluid production is
100% water.
• Determination of residual fluid saturations
Relative Permeability Curve
Hysteresis Effect on Rel. Perm.
100 Non-wetting Wetting
phase phase
Relative Permeability, %

80

Imbibition krnw krw


60 krnw Drainage

40

20 Irreducible wetting Residual non-wetting


phase saturation phase saturation
0
0 20 40 60 80 100

Wetting Phase Saturation, %PV


Hysteresis Effect on Rel. Perm.
• During drainage, the wetting phase ceases to flow at the
irreducible wetting phase saturation
– This determines the maximum possible non-wetting
phase saturation
– Common Examples:
• Petroleum accumulation (secondary migration)
• Formation of secondary gas cap
• During imbibition, the non-wetting phase becomes
discontinuous and ceases to flow when the non-wetting
phase saturation reaches the residual non-wetting phase
saturation
– This determines the minimum possible non-wetting
phase saturation displacement by the wetting phase
– Common Example: waterflooding water wet reservoir
Review: Effective Permeability
Steady state, 1D, linear flow
ko A  o equation (Darcy units):
• Oil qo 
o L qn = volumetric flow rate for a
specific phase, n

k w A  w
• Water qw  A = flow area
w L n = flow potential drop for
phase, n (including pressure,
gravity and capillary pressure
k g A  g terms)
• Gas qg 
g L n = fluid viscosity for phase n

L = flow length

Modified from NExT, 1999; Amyx, Bass, and Whiting, 1960; PETE 311 NOTES
Rel. Perm. - Steady State
• Purpose: determination of
– two phase relative permeability functions
– irreducible wetting phase saturation (drainage)
– residual non-wetting phase saturation (imbibition)
Rel. Perm. - Steady State
• Process (oil/water, water wet case):
– simultaneously inject constant rates of oil and
water until steady state behavior is observed
• production will be constant at same oil and
water rates as injection
• pressure drop for each phase will be constant
– determine saturation of core sample
• usually by resistivity or weighing
• this is typically not the same as the injection
ratio
– change injection ratio and repeat
Rel. Perm. - Steady State
• Imbibition Relative Permeability
Functions
– Stage 1: Preparation for
drainage
• core saturated with
wetting phase
• steady state injection of
wetting phase used to
determine absolute
permeability
– Stage 2: Irreducible wetting
phase
• inject non-wetting phase
until steady state,
measure saturation
– no wetting phase will
be produced at steady
state
Rel. Perm. - Steady State
• Imbibition Relative Permeability
Functions (continued)
– Stage 3 (A-C): determination
of points on imbibition
relative permeability function
• steady state injection at
constant rates of wetting
and non-wetting phase
– Initially ratio qw/qnw is
small
• measure saturation and
phase pressure drops at
steady state
– saturation ratio will in
general, not be the
same as injection ratio
• repeat with increasing rate
ratio, qw/qnw
Rel. Perm. - Steady State
• Imbibition Relative Permeability
Functions (continued)
– Stage 4: determination of
residual non-wetting phase
saturation
• inject wetting phase until
steady state behavior
observed
• measure saturation and
pressure drop
Capillary End Effect
• During immiscible displacement
– In the bulk of the core plug
• Pc= f (Swet)
– At the outflow face
• Pc= 0  Swet=1
– There must be a gradient of saturation from the the
bulk of the core to the outflow face
• This saturation gradient is the “Capillary End
Effect”
Capillary End Effect
• Comparison for low
flow rate
– Theoretical gradient
(dashed line)
– Experimental data
(circles)
– Saturation gradient
extends over half of
the length of the
core plug
Capillary End Effect
• Comparison for higher
flow rate
– Theoretical gradient
(dashed line)
– Experimental data
(circles)
– At higher flow rate,
saturation gradient
extends over only 1/5
of the length of the
core plug
Capillary End Effect
• Eliminating errors due to end effect in measurement of
relative permeability functions
– Measure saturation far enough away from outflow face
(e.g. Penn State Method)
– Use high flow rates to make error in measured
saturation negligible
Relative Permeability Stady-State
Measurment

Dispersed
Hafford
Method
Penn-State

Single
Simple Hassler
Dynamic
STEADY-STATE RELATIVE
PERMEABILITY TEST EQUIPMENT
(HASSLER METHOD)
• Baik untuk
kondisi batuan
yang memiliki
kebasahan yang
tinggi dengan
salah satu fluida
• Sudah jarang
digunakan
PENN STATE METHOD FOR
MEASURING STEADY-STATE RELATIVE
PERMEABILITY
• Untuk
menghindari
capillary end
effect
HAFFORD’S METHOD FOR MEASURING
STEADY-STATE RELATIVE
PERMEABILITY
Gas

Gas
pressure
Porous end plate gauge

Oil
pressure

Oil pressure pad


Gas meter Oil

Oil burette
DISPERSED FEED METHOD FOR
MEASURING STEADY-STATE RELATIVE
PERMEABILITY
Gas meter Gas-pressure
gauge Gas
Lucite

Core
material

Dispersing
Lucite-mounted section
core
Oil
Oil burette
Dispersing
section face
Relative Permeability Unstady-
State Measurment
• Waktu yang dibutuhkan lebih cepat
• Hal yang perlu diperhatikan:
– Gradien tekanan harus tinggi
menghindari capillary-pressure end
effect
– Beda tekanan di dalam core kecil
dibandingkan dengan tekanannya
– Core sebaiknya homogeny
– Sifat fluida diusahakan konstan
Saturation by Weighing
(Review)
• Determine mass of fluid
• Solve from Mass Balance
mfluid = moil + mwater
= Vp(1 - Sw)ro + VpSwrw
PENENTUAN PERMEABILITAS RELATIF MENGGUNAKAN KORELASI

Permeabilitas relatif sistem minyak-gas (psoses drainage):


a. Unconsolidated Sand, well sorted

kro  (S *)3 krg  (1  S *)3

b.Unconsolidated Sand, poorly sorted


kro  (S *)3.5 krg  (1  S *)2 (1  S *1.5 )

c. Cemented Sandstones, oolitic


limestones, rocks with vugular porosity

kro  (S *)4 krg  (1  S *)2 (1  S *2 )

Dimana:

S*  So /(1  S wi )
Penentuan Permeabilitas Relatif Menggunakan
Korelasi

Permeabilitas relatif sistem minyak-gas (proses drainage):


a. Unconsolidated Sand, well sorted

kro  (S *)3 krg  (1  S *)3

b. Unconsolidated Sand, poorly sorted

kro  (S *)3.5 krg  (1  S *)2 (1  S *1.5 )

c. Cemented Sandstones, oolitic limestones, rocks with vugular porosity

kro  (S *)4 krg  (1  S *)2 (1  S *2 )

Dimana:

S*  So /(1  Swi )
Normalisasi Permeabilitas Relatif

1 1

0.8 0.8

0.6 0.6

0.4 0.4

0.2 0.2

0 0
0 0.1 0.2 0.3 0.4 0 0.05 0.1 0.15 0.2 0.25 0.3 0.35

0.8

0.6

0.4

0.2

0
0 0.05 0.1 0.15 0.2 0.25 0.3 0.35
Normalisasi Permeabilitas Relatif (Lanjutan)

Sistem Air – Minyak

S w  S wc k ro @ S w k rw @ S w
Sw*  k ro *  k rw * 
1  S wc  S or k ro @ S wc k rw @ S or

Sistem Gas – Minyak


krg @ S L
krg * 
krg @ Sor

S L  S wc k ro @ S L
SL *  k ro * 
1  S wc  S or k ro @ S wc

Sistem Gas – Air

S w  S wc k rg @ S w k rw @ S w
Sw*  k rg *  k rw * 
1  S wc  S gr k rg @ S wc k rw @ S gr
Perhitungan Kurva Permeabilitas Relatif Tiga Fasa

 Kondisi fluida tiga fasa (minyak, gas dan air) dalam reservoir
bukanlah hal yang jarang terjadi selama proses produksi.

 Pengukuran secara langsung permeabilitas relatif tiga fasa di


laboratorium tidaklah mudah dan memerlukan jumlah
percobaan yang berlipat dibandingkan dengan mengukur
permeabilitas relatif dua fasa.

 Dua metode yang digunakan untuk menghitung permeabilitas


relatif tiga fasa adalah Normalized Stone’s Method I dan
Normalized Stone’s Method II.

 Metode ini mensyaratkan tersedianya dua set data


permeabilitas relatif air-minyak dan minyak-gas. Sistem
dianggap water-wet (akan tetapi dapat juga dipakai untuk oil-
wet), minyak dianggap sebagai intermediate wetting phase, dan
gas dianggap sebagai least wetting phase.
Perhitungan Kurva Permeabilitas Relatif Tiga Fasa

 Pemilihan kurva relatif dua fasa yang digunakan


dalam perhitungan kurva permeabilitas tiga fasa
adalah: jika saturasi minyak berkurang, gunakan kurva
imbibisi untuk air-minyak dan kurva drainage untuk
minyak-gas. Sedangkan jika saturasi air berkurang,
gunakan kurva drainage untuk air-minyak dan minyak-
gas.

 Berdasarkan asumsi di atas, maka permeabilitas


relatif air dan permeabilitas relatif gas tiga fasa sama
dengan pada kondisi dua fasa, yaitu:

k rw ( S w , S g )  k rw ( S w )

k rg ( S w , S g )  k rg ( S g )
Sedangkan permeabilitas relatif minyak pada kondisi
tiga fasa adalah:
Normalized Stone’s Method I

S o*k rowk rog


k ro ( S w , S g ) 
(1  S w* )(1  S g* )
S o  S om
S o* 
1  S wc  S om

S w  S wc
S w* 
1  S wc  S om

Sg
S g* 
1  S wc  S om

S om  S orw  (1   ) S org

Sg
  1
1  S wc  S org

Normalized Stone’s Method II


 k  k rog
k ro ( S w , S g )  k rocw  row  k rw 


 k rg   k rw  k rg 
 k rocw  k rocw  
Contoh Soal
Dari hasil pengukuran permeabilitas relatif sistem air-minyak dan minyak-
gas diperoleh data berikut ini. Hitung permeabilitas relatif minyak sistem
tiga fasa jika Sw = 0.4 dan Sg = 0.2 menggunakan metode Stone I dan
Stone II. S k k S k k
w row rw g rog rg

0.3 1 0 0.00E+00 1.00E+00 0.00E+00


0.33 0.85845 0.01139 3.50E-02 7.64E-01 5.90E-06
0.36 0.7318 0.02138 7.00E-02 5.76E-01 7.04E-04
0.39 0.61916 0.03037 1.05E-01 4.29E-01 3.46E-03
0.42 0.51967 0.03873 1.40E-01 3.15E-01 9.26E-03
0.45 0.43243 0.04685 1.75E-01 2.28E-01 1.87E-02
0.48 0.35657 0.05512 2.10E-01 1.62E-01 3.23E-02
0.51 0.29122 0.06391 2.45E-01 1.13E-01 5.02E-02
0.54 0.23549 0.07362 2.80E-01 7.67E-02 7.24E-02
0.57 0.1885 0.08462 3.15E-01 5.10E-02 9.89E-02
0.6 0.14938 0.0973 3.50E-01 3.29E-02 1.30E-01
0.63 0.11725 0.11204 3.85E-01 2.06E-02 1.64E-01
0.66 0.09123 0.12923 4.20E-01 1.24E-02 2.02E-01
0.69 0.07044 0.14925 4.55E-01 7.15E-03 2.44E-01
0.72 0.054 0.17248 4.90E-01 3.91E-03 2.90E-01
0.75 0.04103 0.19931 5.25E-01 2.01E-03 3.38E-01
0.78 0.03066 0.23013 5.60E-01 9.51E-04 3.90E-01
0.81 0.02201 0.26531 5.95E-01 4.08E-04 4.45E-01
0.84 0.01419 0.30524 6.30E-01 1.54E-04 5.03E-01
0.87 0.00633 0.3503 6.65E-01 4.85E-05 5.64E-01
0.9 0 0.40088 7.00E-01 0 6.28E-01
Jawab
Metode Stone I

Sg 0.2
  1  1  0.714286
1  Swc  Sorg 1  0.3  0

Som  Sorw  (1   ) Sorg


 0.714286(0.1)  (1 - 0.714286)(0)
 0.0714286
So  Som 0.4  0.0714286
So*    0.522727
1  S wc  Som 1  0.3  0.0714286

S w  S wc 0.4  0.3
S w*    0.159091
1  S wc  Som 1  0.3  0.0714286

Sg 0.2
S g*    0.318182
1  S wc  Som 1  0.3  0.0714286

So*k rowk rog


k ro ( S w , S g ) 
(1  S w* )(1  S g* )
0.522727(0.585999)(0.180571)

(1  0.159091)(1  0.318182)
 0.096472
Metode Stone II

krocw  1

krog ( S g  0.2)  0.180571


krow (Sw  0.4)  0.585999
krw (Sw  0.4)  0.033153

krg ( S g  0.2)  0.028453


 k  k rog
k ro ( S w , S g )  k rocw  row  k rw 


 k rg   k rw  k rg 
 k rocw  k rocw  
 0.585999  0.180571 
    
 1 
0.033153 0.028453
 1  1 
 0.033153  0.028453 
 0.067812

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