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Lecture Presentation
PGE368Fall 2001 Semester
December 5 and 7
Fundamentals of Nuclear Magnetic Resonance
Logging
Carlos Torres-Verdn, Ph.D. Assistant Professor
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Bedding scale Well logs
Stratum scale
Core plug scalePore scale
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SPIN MAGNETIZATION
N
S Proton
H
Hydrogen
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PRECESSION
B
Parallel
Antiparallel
100,006
100,000
oBo
Larmor Precession
freq. = 4258 HGauss
z B o
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ELEMENTAL NMR RESPONSE
Nucleus[most common
applications in log &core analysis]
2ss
Naturalabundance
(%)
Relativesensitivity I (Hz/Gau )
4257.591H[core and log]
2
H[aqueous phase]13 C
[need high freq.]19
F[nonwetting phase]
1/2 99.99 1.000
653.57 1 0.015 0.0097
1070.5 1/2 1.10 0.0159
4005.5 1/2 100.00 0.83323 Na
[salinity]11.26 3/2 100.00 0.0925
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TRANSVERSAL TIPPING
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TRANSVERSAL TIPPING and PROTON PRECESSION
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BASIC NMR INSTRUMENTATION COMPONENTS
B1
B0N
S
A time-constant magneticfield used to polarize thespins
A time-varying RFmagnetic field to excitethe spins
A magnetic receptor tomeasured the spinresponse
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COMMERCIAL NMR WIRELINE TOOLS
MRIL CMR
B 0
Magnet
B1
vs. Homogeneous B 0Gradient field
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LONGITUDINAL AND TRANSVERSE RELAXATION
TW
T2 T1
TETw= wait timeTE= inter-echo timeT1= Longitudinal magnetization build upT2= Transverse magnetization decay
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T1 BUILD-UP OF OILS
T1 Buildup
0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
0.9
1
0 0
. 5 1 1
. 5 2 2
. 5 3 3
. 5 4 4
. 5 5 5
. 5 6 6
. 5 7 7
. 5 8 8
. 5 9 9
. 5 1 0
1 0
. 5 1 1
1 1
. 5 1 2
1 2
. 5 1 3
1 3
. 5 1 4
1 4
. 5 1 5
Time (sec.)
% P
o l a r i z a
t i o n
0.2 cP
0.4 cP0.6 cP
0.8 cP
1 cP
2 cP
4 cP
Water (512 m)
Water (256 ms)
Water (64 ms)
Water (16 ms)
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TRANSVERSE RELAXATIONAmplitude Decay Explanation
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Gradient Field and DiffusionGradient Field and Diffusion
TT11
TT22
BB 00 BB 00 BB 00 BB 00BB 00
f f f f f f f f --f f Diffusion during the pulse sequence causes a reductionDiffusion during the pulse sequence causes a reduction
in signal amplitude with time and decreases T2.in signal amplitude with time and decreases T2.
MM
TimeTime
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Elements of T2 DecayElements of T2 Decay
(Wetting Phase Saturation = 100%)(Wetting Phase Saturation = 100%)
1
2T
= + + 1T 2D
S
V
1T 2b
Bulk Fluid Relaxivity
Surface Relaxivity Pore Surface Area to Volume RatioPore Surface Area to Volume Ratio
Diffusion DecayDiffusion Decay
lP i C l T2 D
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Primary Controls on T2 DecayPrimary Controls on T2 Decay
(Wetting Phase Saturation = 100%)(Wetting Phase Saturation = 100%)
1122
T T == ++ ++S S
V V 11
T T 2b2b
Pore Fluid Viscosity
Pore Fluid Diffusivity
Magnetic Field GradientInter-Echo Spacing (TE)
11T T 2D2D
Pore Size & Geometry
M a g n e t i c
s
Pore Mineralogy
Wettability
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TT22 Decay and Pore SizeDecay and Pore Size(Wetting Phase Saturation = 100%)(Wetting Phase Saturation = 100%)
0
20
40
60
80
100
0 50 100 150 200 250 300 350 400 450 500
Time (ms)
E c h
o A m p
l i t u d e
( p u
) Small Pore Size = Rapid Decay RateLarge Pore Size = Slow Decay Rate
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M ltiM lti ti l Dti l D
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MultiMulti --exponential Decayexponential Decay
== por por .. ee -- t / Tt / T 22
16 64 25616 64 256
TT22 (ms)(ms)
I n c r e m e n
t a l
I n c r e m e n
t a l
( ( p u p u
) )
1010
151564 ms64 ms
16 ms16 ms
256256
msms
55
= 30p.u.= 30p.u.
tt
y = 5y = 5 .. ee --t/t/ 1616 + 10+ 10 .. ee --t/t/ 6464 + 15+ 15 .. ee --t/t/ 256256
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T2 RELAXATION AND PORE SIZE
0.5 100101.0 1,000
T2 ms
Clay Silt Fine Coarse
Clay Domain
2 = 1 m/sSand Domain
2 = 5 m/s
d b k
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Water-Wet Hydrocarbon-Bearing Rock Formation
Clay
Wilcox SandOklahoma City
1 cm
Close-Up
Effect of Pore Size on T2 SpectraEffect of Pore Size on T2 Spectra
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Effect of Pore Size on T2 SpectraEffect of Pore Size on T2 Spectra
I n c r e m e n
t a l P o r o s
i t y
[ p u
]
T2 [msec]
0.00
0.50
1.00
1.50
2.00
0.1 1. 10. 100. 1000. 10000.
T2 Spectra @ Sw = 1.0
Formation AFormation B
T2 Cut-off
Small Pores Large PoresMicro-Pores
NMR = 25 pu
Formation B (high-k)
Formation A (Low-k)
BVI = 10 pu BVM = 15 pu
BVI = 6 pu BVM = 19 pu
(Wetting Phase Saturation = 100%)(Wetting Phase Saturation = 100%)
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SurfaceSurface RelaxivityRelaxivity and Tand T 22 DecayDecay
Controls on SurfaceControls on Surface Relaxivity Relaxivity
Pore surface mineralogyPara, ferri, and ferro-magnetic ions (e.g., Fe 3+ , Mn 2+)
Wettability
Effects ofEffects of VariationsVariations (Wetting Phase Only)(Wetting Phase Only)
Higher results in faster T 2 Decay
Lower results in slower T 2 Decay
SurfaceSurface RelaxivityRelaxivity and Tand T DecayDecay
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SurfaceSurface RelaxivityRelaxivity and Tand T 22 DecayDecay
(Wetting Phase Saturation = 100%)(Wetting Phase Saturation = 100%)
Low (Carbonates)High (Clastics)
E c
h o
A m p
l i t u d e
[ p u
]
I n c r e m e n t a
l P o r o s
i t y
[ p u
]
T2 [ms]
0.00
0.50
1.00
1.50
2.00
0.1 1.0 10. 100. 1000. 10000.
NMR porosity
Time [ms]
SurfaceSurface RelaxivityRelaxivity and Tand T 22 DecayDecay
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SurfaceSurface RelaxivityRelaxivity and Tand T 22 DecayDecay
Low (Carbonates)High (Clastics)
22 --phase Fluid System, Wetting Phasephase Fluid System, Wetting Phase@ Irreducible Saturation@ Irreducible Saturation
E c
h o
A m p
l i t u d e
[ p u
]
I n c r e m e n t a
l P o r o s
i t y [ p u
]
T2 [ms]
0.00
0.50
1.00
1.50
2.00
0.1 1.0 10. 100. 1000. 10000.
NMR porosity
Time [ms]
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Effect of Magnetic Ions on TEffect of Magnetic Ions on T 22 DecayDecay
The presence of Para, ferri, and ferro-magnetic ions (e.g., Fe 3+ , Mn 2+
will increase and produce internal magnetic field gradients which
attenuate echo amplitudes due to accelerated diffusion decay (T 2D).Mineral Constituents with Low Magnetic SusceptibilitMineral Constituents with Low Magnetic Susceptibilit
Mineral Constituents with High Magnetic SusceptibilitMineral Constituents with High Magnetic Susceptibilit
NMR porosity
Time [ms]
E c
h o
A m p
l i t u d e
[ p u ]
I n c r .
P o r o s
i t y
[ p u
]
T2 [ms]0.00
0.50
1.00
1.50
2.00
0.1 1. 10. 100. 1000. 10000.
Basic NMR Field DeliverableBasic NMR Field Deliverable
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Basic NMR Field DeliverableBasic NMR Field Deliverable
GR T 2 Spectra Resistivity &Permeability Pore Volumetrics
Formation Tester Data and NMR Data
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Formation Tester Data and NMR Data
Patagonia Example
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g p
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Patagonia
Example
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PatagoniaExample
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China Example
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VenezuelaExample
Petrophysical Applications of NMR DataPetrophysical Applications of NMR Data
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Mineralogically-Independent Porosities ( Total & Effective )
Clay-Bound Water Volume
Capillary-Bound Water & Free Fluid Volumes
Pore Size Distribution ( Single Phase Fluid Saturation )
Permeability ( With calibration to core or test data )Shale Volume & Distribution
Flushed Zone Fluid Saturations ( DTW analysis )
Hydrocarbon Viscosity ( DTE analysis )
Electrical Properties & Water Saturation ( Integrated Products )
Basic MRIL Field DeliverableBasic MRIL Field Deliverable
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Basic MRIL Field Deliverable
GR T 2 Spectra Resistivity &Permeability Pore Volumetrics
Basic NMR DataBasic NMR Data
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Basic NMR DataBasic NMR Data
NMR measurements provideNMR measurements provide ::Echo Amplitudes
Echo Decay RatesCalibrated transforms provide:
Mineralogically Independent Porosities.
Clay Bound Water
Capillary Bound Water & Free Fluid Volumes
Permeability
Echo Train Inversion ProcessingEcho Train Inversion Processing
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C u m u
l a t i v e
P o r o s i t y
[ p u
]
I n c r e m e n
t a l P o r o s i t y
[ p u
]
T2 [msec]
0.00
0.50
1.00
1.50
2.00
0.1 1. 10. 100. 1000. 10000.
0.0
2.0
4.0
6.0
8.0
10.0
12.0
14.0
16.0
multi-exponential fit
to spin-echo amplitudes
NMR porosity
Time [msec]
E c
h o A m p
l i t u d e
[ p u
]
Acquisition Time Domain T2 Relaxation Time DomainInversion
Processing
NMR Porosity DefinitionsNMR Porosity Definitions
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yy
Effective - Pore volume excluding clay bound water.
Total - Pore volume including clay bound water.CBW - Clay bound water, which represents anion-freewater adsorbed within clay inter-layers.
BVI - Bulk volume irreducible water which includeswater retained by capillary forces in small pores, andwater wetting pore surfaces.
BVM - Free-fluid volume which is available forhydrocarbon storage and fluid flow.
MRIL PorosityMRIL Porosity -- Test Pit VerificationTest Pit Verification
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Echo Spacing of 1.75 ms
E c
h o
A m
p l i t u d e
1500 15 1351201059075604530
BVM = 20.30 puMRIL = 26.25 pu
BVI = 5.95 pu
Time ( ms )
25
20
15
10
5
Limestone Block
core = 25.5%
E c
h o
A m p
l i t u d e
0 15 1501351201059075604530
MRIL = 19.82 pu
BVM = 15.61 pu
BVI = 4.21 puEcho Spacing of 1.5 ms
Time (ms)
20
15
10
5
Berea Sandstone Block
core = 20.3%
BVM Fit ResultsEcho Amplitude Complete Echo Fit Results
MineralogyMineralogy --Independent PorosityIndependent Porosity
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Gulf of Mexico SandstoneGulf of Mexico Sandstone Middle East CarbonateMiddle East Carbonate
20
Core Porosity (%)
M R I L P o r o s
i t y
( % )
0
2
4
6
8
10
12
14
16
18
20
0 2 4 6 8 10 12 14 16 180
0.05
0.1
0.15
0.2
0.25
0.3
0 0.05 0.1 0.15 0.2 0.25 0.3
Core Porosity (frac.)
M R I L P o r o s i t y
( f r a c . )
Porosity ConsiderationsPorosity Considerations
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y
Although NMR porosity isAlthough NMR porosity is mineralogicallymineralogicallyIndependent, it is not fluid independent.Independent, it is not fluid independent.
NMR porosity can be too low whenNMR porosity can be too low when :: Hydrogen Index of reservoir fluids < 1.0Hydrogen Index of reservoir fluids < 1.0 Reservoir fluids with long T1 are only partiallyReservoir fluids with long T1 are only partially
polarized due to insufficient acquisition wait time (TW)polarized due to insufficient acquisition wait time (TW) Solid hydrocarbons (tar) are present with relaxationSolid hydrocarbons (tar) are present with relaxation
rates faster than the measurement time windowrates faster than the measurement time window
Internal gradients caused from magnetic mineralsInternal gradients caused from magnetic mineralsaccelerate NMR echo decay to below measurementaccelerate NMR echo decay to below measurementtime windowtime window
T2 Decay and Pore SizeT2 Decay and Pore Size
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y
(Wetting Phase Saturation = 100%)(Wetting Phase Saturation = 100%)
Pore Volumetric DistributionPore Volumetric Distribution
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E c h o
A m p
l i t u
d e
0 15 1501351201059075604530
Time (ms)
20
15
10
5
0.00
1.00
2.00
3.00
4.00
0.1 1 10 100 1000 10000
BVI BVM
4.00
0.00
1.00
2.00
3.00
I n c r e m e n
t a l P o r o s
i t y
( p u )
CBW
MatrixMatrix DryDryClayClay
Clay-Clay-BoundBoundWater Water
MobileMobileWater Water
CapillaryCapillaryBoundBoundWater Water
HydrocarbonHydrocarbon
T2 Decay
NMR Porosity
T2 Decay (ms)
T2 Cutoffs
Transform
BulkBulk VolumetricsVolumetrics -- Light HCLight HC
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Matrix DryClay
Clay-BoundWater
MobileWater
MobileHC
Capillary-BoundWater
Res.HC
MBVM
MPHS
MPHE
MBVIMCBW
Effect of Oil Saturation & TEffect of Oil Saturation & T 22 SpectraSpectra
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Adapted fromAdapted from StraleyStraley et al, Log Analyst (Jan. 1995)et al, Log Analyst (Jan. 1995)
OilOil
Water Water
SwSw = 100%= 100%
SwSw = 76%= 76%
SwSw = 57%= 57%
SwSw = 34%= 34%
SwSw = 0%= 0%
Bulk OilBulk Oil
TT22
T2 Decay in a 2T2 Decay in a 2 --Phase SystemPhase System
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Wetting Phase Relaxivity
++ 11T T 2D2D water water
11T T 2b2b water water
11T T
== ++ S S V V 2b2b water water
((SwSw ))S S V V
Non-Wetting Phase Relaxivity
11
22hchcT T
== ++ 11T T 2D2D hchc
11T T 2b2b hchc
T2 Spectra for Various Fluid TypesT2 Spectra for Various Fluid Types
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Water Water
OilOil
GasGas
Effect of Pore Size on T2 SpectraEffect of Pore Size on T2 Spectra
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Small Pores Large PoresMicro-Pores
NMR = 25 pu
Formation B (high-k)
Formation A (Low-k)
BVI = 10 pu BVM = 15 pu
BVI = 6 pu BVM = 19 pu
I n c r e m e n
t a l P o
r o s
i t y
[ p u ]
T2 [msec]
0.00
0.50
1.00
1.50
2.00
0.1 1. 10. 100. 1000. 10000.
T2 Spectra @ Sw = Swir
Formation AFormation B
T2 Cut-off
(2(2 --Phases with Wetting Phase Saturation @ Irreducible)Phases with Wetting Phase Saturation @ Irreducible)
Default TDefault T 22 CutCut --off Valuesoff Values
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T 2 [msec]
Carbonates : 92 msecSandstones : 33 msec
0.00
1.00
2.00
3.00
4.00
0.1 1 10 100 1000 10000
BVI BVM
4.00
0.00
1.00
2.00
3.00T2 Cut-off
I n c r e m e n
t a l P o r o s
i t y
( p u
)
CBW
CoreCore -- Calibration ProcessCalibration Process
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Capillary Pressure DataCore NMR Data
Calibrate BVI Model
Core Perm DataCalibrate Permeability Model
TT22 CutCut --off from Core NMRoff from Core NMR
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-- Obtain two core NMR measurements at:Obtain two core NMR measurements at:
SwSw = 1.0= 1.0SwSw == Swir Swir (obtained with centrifuging)(obtained with centrifuging)
-- Determine TDetermine T 22 cutcut --off where the terminaloff where the terminalcumulative porosity @cumulative porosity @ SwSw == SwirSwir is equalis equalto the cumulative porosity @to the cumulative porosity @ SwSw = 1.0.= 1.0.
T2 Cut-offs from Core NMR
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T2 (ms)10 10 100 2 4
0
5
10
15
C
u m u
l a t i v e
( p u )
T2 cut-off (Sxo = Swi)
S w = 1.0
S w (air-brine) = S wir
BVI
T2 cut-off(Sxo = 1.0)
S w (oil-brine) = S wir
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TT22 CutCut --off from Pc & Log NMR Dataoff from Pc & Log NMR Data
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0 100
Sw (%)
Pc
T2 cutoff Capillary Pressure Data
Swir core
BVIcore
NMR Post-Processing
Cumulative LogNMR Porosity
10 0 10 3T2 (ms)
4 8 16 32 64 128 256 512
T2 (ms)
BVI BVM
Integrated Petrophysical Analysis ResultsIntegrated Petrophysical Analysis Results
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Resistivity &Permeability
RockVolume
FluidSaturation
PoreVolume
T2Spectra
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Permeability from NMRPermeability from NMR
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k k
aa
S S wir wir
11 -- S S wir wir
C C
bb
=
Generalized CoatesGeneralized Coates --Timur Timur Model:Model:
This model is designed to compute the effective (nonThis model is designed to compute the effective (non --wettingwettingphase) permeability model based on the lower permeabilityphase) permeability model based on the lower permeabilityboundary condition which is controlled by the ratio of nonboundary condition which is controlled by the ratio of non --wetting phase (1wetting phase (1 --Swir Swir ) to wetting phase () to wetting phase ( Swir Swir ) saturation .) saturation .
Permeability from NMRPermeability from NMR
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Coates-Timur Model ( NMR version ):
NMR NMR
BVI BVI
BVM BVM
C C k k
bb
= aa
Where default parameters are: C =10 , a = 4 & b = 2
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BVI Dependence on CapillaryBVI Dependence on CapillaryPressure/Height above FWLPressure/Height above FWL
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0
2
4
6
8
10
12
14
16
18
0 50 100 150 200 250 300 350 400 450
Capillary Pressure (psi)
N M R P r e d
i c t e d B V I ( % )
Calibration Pc
BVI at calibration Pc
Capillary Drainage Curve
CoatesCoates --Timur Timur Permeability vs. Column HeightPermeability vs. Column Height
24
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Coates-Timur Permeability
k = (20 / 10) 4 (15.7 / 4.3) 2 = 213 md
NMR = 20 pu
2
k
= BVI
BVI NMR 4
10
NMR
P c
( p s
i )
1 10 100 10000 20 40 60 80 100
Sw (%)
0
250
100
150
200
50
T2 (ms)
T2 Cut-off @ Reference Pc
Capillary Pressure T2 Spectra
BVI = 4 pu
BVI = 4.3 pu
BVI = 6 pu
BVI = 5 pu
k = (20 / 10) 4 (16 / 4)2 = 256 md
k = (20 / 10) 4 (15 / 5)2 = 144 md
k = (20 /10) 4 (14 /6)2 = 87 md
k absolute = 256 md
Limitations of CoatesLimitations of Coates --TimurTimurPermeability ModelPermeability Model
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Application of the model is predicated on assumption thatApplication of the model is predicated on assumption that
the porosity is all interconnected, and that pore throatthe porosity is all interconnected, and that pore throatdiameterdiameter sytematicallysytematically increases proportional to an increaseincreases proportional to an increasein the magnitude of the bulk free fluid volume (BVM).in the magnitude of the bulk free fluid volume (BVM).
Computed permeability may systematically increase as afunction of increasing height above free water level. Thiseffect is most likely to occur for lower quality reservoirs withhighly sloped capillary pressure curves, but should not bean issue for very high permeability reservoirs wherecapillary presure curves are near-asymptotic.
Model Losses sensitivity at very high permeabilities whereirreducible water saturation is on the asymptote of thecapillary pressure curve, and porosity doesnt increaserelative to increased pore size and/or pore throat size.
Calibration of Coates-Timur Permeability Model
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Local calibration of model fitting parameters (C, a & b) arenecessary to account for variations in the complexity andconnectivity of the pore system, which control thepermeability and its correlation to the bulk pore volumetric
elements of which model is strictly comprised.
Multi-linear regression can be employed to solve for the theformation-specific fitting parameters (C, m & n) whenreference permeability data from core or formation tests areavailable.
Minimum error analysis can also be employed to solve foran optimum value of the porosity denominator C whileholding parameters a and b constant at default values.
Multiple Water SaturationMultiple Water Saturation ModelsModels
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ShaleShale --Free Conductance ModelFree Conductance Model
ArchieArchie
Laminated Shale Conductance ModelLaminated Shale Conductance Model
PouponPoupon --LeveauxLeveaux (Indonesian)(Indonesian)
DoubleDouble --Layer Dispersed Clay Conductance ModelsLayer Dispersed Clay Conductance Models
WaxmanWaxman --SmitsSmits
DualDual --WaterWater
Mixed DispersedMixed Dispersed --Clay / Laminar Clay / Laminar --Shale Conductance ModelShale Conductance Model
PatchettPatchett --HerrickHerrick
WaxmanWaxman -- SmitsSmits Water Saturation ModelWater Saturation Model
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C t C w
F* S wn* =
F* S w
B Q v
WaxmanWaxman --SmitsSmits Model:Model:
Where, F* is the Total Formation ResistivityFactor, and Q v = Total Q v
PatchettPatchett --Herrick Water Saturation ModelHerrick Water Saturation Model
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PatchettPatchett --Herrick Model:Herrick Model:
C t = (1 - V sh ) C w
F* S wn*
F* S w
B Q v (V sh C sh )
Where, V sh = Laminar Shale Volume, F* is theFormation Resistivity Factor of the Sand layers,and Q v = Q v of Dispersed Shale in Sand Layers
CoreCore --Calibrated Analyses ResultsCalibrated Analyses Results
Permeability & T2Rock Fluid Porosity
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Permeability &
Resistivity
T2
Spectra
Rock
Volumetrics
Fluid
Saturations
Porosity
Volumetrics
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