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Effective Medium Models

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127

Are real rocks hopelessly complex?

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Theoretical Models
During the last four decades, many theoretical models
have appeared which try to describe the elastic and
transport properties of rocks.
Some are mathematically elegant (complicated).
Most are extreme idealizations of the complexity of real
rocks

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Models with Idealized Geometries


Contact Theories

Inclusion Models

?
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Bounding Methods for Estimating Effective


Elastic Moduli
For many reasons we would like to be able to model or estimate the effective
elastic moduli of rocks in terms of the properties of the various constituent
minerals and pore fluids. To do it precisely one must incorporate
the individual elastic moduli of the constituents
the volume fractions of the constituents
geometric details of how the various constituents
are arranged
The geometric details are the most difficult to know or measure. If we ignore (or
dont know) the details of geometry, then the best we can do is estimate upper
and lower bounds on the moduli or velocities.
The bounds are powerful and robust tools. They give rigorous upper and lower
limits on the moduli, given the composition. If you find that your measurements
fall outside the bounds, then you have made a mistake - in velocity, volume
fractions, or composition!
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Voigt and Reuss Bounds


On a strictly empirical basis one can imagine defining a power law average of
the constituents

M = f1 M1 + f 2 M 2 + f 3 M 3 + ...

where

= the effective modulus of the composite


M i = the modulus of the ith constituent
f i = the volume fraction of the ith constituent
= a constant, generally between -1 and +1

Special cases are the Voigt average (an upper bound):


K V = f Q K Q + f F K F + f C K C ... + f W K W + fO K O + f G K G

V = fQ Q + f F F + fC C ... + f W W + fO O + f G G

and the Reuss average (a lower bound):


1

K R = fQ KQ1 + f F K F1 + f CKC1 ...+ fW KW1 + fO KO1 + fG KG1


1

1
1
1
1
R = f QQ1 + f F 1
+
f

...+
f

+
f

+
f

F
C C
W W
O O
G G

Since these are upper and lower bounds, an estimate of the actual value is
sometimes taken as the average of the two, known as the Voigt-Reuss-Hill
average:
MV + MR
MVRH =

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The Voigt and Reuss averages are interpreted as the ratio of average stress
and average strain within the composite.
The stress and strain are generally unknown in the composite and are expected
to be nonuniform. The upper bound (Voigt) is found assuming that the strain is
everywhere uniform. The lower bound (Reuss) is found assuming that the
stress is everywhere uniform.
Geometric interpretations:

Voigt iso-strain model


f f (E )
=
E = =
i

E = f i E i

Reuss iso-stress model

E = =

f f ( )
E

1
fi
=

Ei
E

i i

Since the Reuss average describes an isostress situation,


it applies perfectly to suspensions and fluid mixtures.

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Example: Representing a soft water-bottom sediment as a suspension.

A true suspension consists of particles suspended in a liquid. A


suspension will act like a fluid, having zero shear modulus, and a bulk
modulus given by the Reuss average. A suspension is isostress:
both liquid and particles feel the same pressure.
We often approximate a soft-water bottom as a suspension, since it is
composed of particles that are completely wet, with only slight grainto-grain contacts.

VP =

Wet sediment:

Gas-charged sediment:

4
K +
3

P-wave velocity

= (1 )solid + brine
1

K =
+

K
K
solid
brine

= (1 )solid + Sw brine + (1 Sw )gas


K = (1 )K solid + SwK brine + (1 Sw )K gas

K = 5.05GPa
= 1.99 g /cc
V = 1.59 km /s
K = 0.74 GPa
= 1.88 g /cc
V = 0.63 km /s

Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

= 0.4; Sw = 0.7; Kqtz = 37; Kw = 2.2; Kgas = 0.1 GPa; qtz = 2.65; w = 1.0; gas = 0.1 g /cc

134

Voigt

Reuss

water

Velocity-porosity relationship in clastic sediments compared with the Voigt and Reuss
bounds. Virtually all of the points indeed fall between the bounds. Furthermore, the
suspensions, which are isostress materials (points with porosity > 40%) fall very close
to the Reuss bound.
Data from Hamilton (1956), Yin et al. (1988), Han et al. (1986). Compiled by Marion, D., 1990, Ph.D.
dissertation, Stanford
Univ.
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Reuss

water
5% gas

Velocity-porosity relationship in clastic sediments compared with the Voigt and Reuss
bounds. Virtually all of the points indeed fall between the bounds. Furthermore, the
suspensions, which are isostress materials (points with porosity > 40%) fall very close
to the Reuss bound.
Data from Hamilton (1956), Yin et al. (1988), Han et al. (1986). Compiled by Marion, D., 1990, Ph.D.
dissertation, Stanford
Univ.
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Hashin-Shtrikman Bounds
The narrowest possible bounds on moduli that we can estimate for an isotropic
material, knowing only the volume fractions of the constituents, are the HashinShtrikman bounds. (The Voigt-Reuss bounds are wider.) For a mixture of 2
materials:
f2

K HS = K 1 +

(K 2 K1 )
HS = 1 +

+ f1 K 1 + 1

3
f2
2 f1 (K1 + 2 1 )
+
4

5 1 K 1 + 1

( 2 1 ) 1

where subscript 1 = shell, 2 = sphere. f1 and f2 are volume fractions.


These give upper bounds when stiff material is K1, 1 (shell) and lower bounds
when soft material is K1, 1.
Interpretation of bulk modulus:

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Hashin-Shtrikman Bounds
A more general form that applies when more than two phases are
being mixed (Berryman, 1993):
K HS + = ( max ), K HS = ( min )

HS+ = ( (Kmax,, max )), HS = ( (K min , min ))

where

(z) =

K( r) +
( z) =

1
(r) + z

(K , ) =

4
z
3

4
z
3

9K + 8

6 K + 2

indicates volume average over the spatially varying K(r), (r) of the
constituents.
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Distance between bounds depends on similarity/difference of end-member


constituents.
Here we see that a mixture of calcite and water gives widely spaced
bounds, but a mixture of calcite and dolomite gives very narrow bounds.

G13

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Wyllie Time Average


Wyllie et al. (1956, 1958, 1962) found that travel time through water saturated
consolidated rocks could be approximately described as the volume weighted
average of the travel time through the constituents:
d1

d2

d3

t=

D
V

t = t1 + t2 + t 3
D d1 d2 d3
= +
+
V V1 V2 V3
1 d1 / D d2 / D d3 / D
=
+
+
V
V1
V2
V3
1 f1 f 2 f 3
= + +
V V1 V2 V3
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Wyllies generally works best for


water-saturated rocks
consolidated rocks
high effective pressures
Limitations:

rock is isotropic
rock must be fluid-saturated
rock should be at high effective pressure
works best with primary porosity
works best at intermediate porosity
must be careful of mixed mineralogy (clay)

The time-average equation is heuristic and cannot be justified


theoretically. It is based on ray theory which requires that (1)
the wavelength is smaller than the grain and pore size, and (2)
the minerals and pores are arranged in flat layers.
Note the problem for shear waves where one of the phases is a
fluid, Vs-fluid 0!
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Modification of Wyllie's proposed by Raymer

V = (1 )2Vmineral + Vfluid

< 37%

1
2 =
2 +
2
V fluidVfluid mineralVmineral
1 0.47 1 0.37 1
=
+
V
0.10 V37
0.10 V47

> 47%

37% < < 47%

Still a strictly empirical relation.


This relation recognizes that at large porosities ( > 47%) the sediment behaves
as a suspension, with the Reuss average of the P-wave modulus, M = Vp2.

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Comparison of Wyllie's time average equationand the Raymer equations with


Marion's compilation of shaly-sand velocities from Hamilton (1956), Yin et al. (1988),
Han et al. 1986).
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Backus Average for Thinly Layered Media


Backus (1962) showed that in the long wavelength limit a stratified medium
made up of thin layers is effectively anisotropic. It becomes transversely
isotropic, with symmetry axis normal to the strata. The elastic constants (see
next page) are given by:
A B F

B A F
F F C

0 0 0
0 0 0

0 0 0

where

0
0
D

0
0
0

0
0

D
0

0
0

0
0

4 ( + )
1
A=
+
+ 2
+ 2
2
1
B=
+
+ 2
+ 2
C=

1
+ 2

F=

1
+ 2

D=

1
M = (A B)
2

+ 2

+ 2

+ 2

M=

, are the isotropic elastic constants of the individual layers. The brackets
indicate averages of the enclosed properties, weighted by their volumetric
proportions. This is often called the Backus average.

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Hookes law relating stress and strain in a linear elastic


medium can be written as

ij = S ijkl kl

ij = c ijkl kl

kl

kl

elastic stiffnesses (moduli)

elastic compliances

A standard shorthand is to write the stress and strain as


vectors:
1= 11
e 1= 11
2= 22
e 2= 22
Note the factor of 2 in the
3= 33
e 3= 33
definition of strains.
T= =
E=
4
23
e 4=2 23
5= 13
e 5=2 13
6= 12
e 6=2 12
The elastic constants are similarly written in
abreviated form, and the Backus average constants shown on the previous
page now have the meaning:

1
A B F
2
B A F
3
F F C
4 = 0 0 0
5
0 0 0
6
0 0 0

0
0
0
D
0
0

0
0
0
0
D
0

0
0
0
0
0
M

e1
e2
e3
e4
e5
e6

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Seismic Fluid Substitution


Pore fluids, pore stiffness,
and their interaction

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Typical Problem: Analyze how rock properties, logs, and seismic


change, when pore fluids change.

Example: We observe Vp, Vs, and density at a well and compute a synthetic seismic
trace, as usual. Predict how the seismic will change if the fluid changes -- either over
time at the same position, or if we move laterally away from the well and encounter
different fluids in roughly the same rocks.
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Gassmann to predict 4D changes


Can we predict signature of
saturation changes?

Initial

??

After
production

Gassmann to predict lateral variations


Well penetrates wet
sand
Can we predict
signature of oil?
??

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Effective moduli for specific pore and grain geometries


Imagine a single linear elastic body. We do two separate experiments--apply
stresses 1 and observe displacements u1, then apply stresses 2 and observe
displacements u2.
The Betti-Rayleigh reciprocity theorem states that the work done by the first set
of forces acting through the second set of displacements is equal to the work
done by the second set of forces acting through the first set of displacements.
ij(2), u(2)

ij(1), u(1)

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Estimate of Dry Compressibility

Applying the reciprocity theorem we can write:


Vbulk
Vbulk
Vpore =
K dry
K mineral

limit as

1
1 Vpore
1
=
+
K dry K mineral Vbulk
Assumptions
minerals behave elastically
friction and viscosity not important
assumes a single average mineral

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Relation of Rock Moduli to Pore Space


Compressibility -- Dry Rock
A fairly general and rigorous relation between dry rock
bulk modulus and porosity is

1
1 =
+
K dry K mineral K

where

1
1 v pore
=
K v pore

K is the pore space stiffness. This is a new concept


that quantifies the stiffness of a pore shape.

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G.4

151

What is a Dry Rock?


Many rock models incorporate the concept of a dry rock or the dry rock frame.
This includes the work by Biot, Gassmann, Kuster and Toksoz, etc, etc.
Caution: Dry rock is not the same as gas-saturated rock. The dry frame
modulus in these models refers to the incremental bulk deformation resulting from
an increment of applied confining pressure, with pore pressure held constant.
This corresponds to a drained experiment in which pore fluids can flow freely in
or out of the sample to insure constant pore pressure. Alternatively, it can
correspond to an undrained experiment in which the pore fluid has zero bulk
modulus, so that pore compressions do not induce changes in pore pressure
this is approximately the case for an air-filled sample at standard temperature and
pressure. However, at reservoir conditions (high pore pressure), gas takes on a
non-negligible bulk modulus, and should be treated as a saturating fluid.

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Relation of Rock Moduli to Pore Space


Compressibility -- Saturated Rock
A similar general relation between saturated rock bulk modulus and porosity is

1 =
1
+
K sat K mineral K

where

K = K +

K mineral K fluid
K mineral K fluid

K + K fluid

Pore space
compressibility
modified by fluids.

So we see that changing the pore fluid has the effect of changing the pore space
compressibility of the rock. The fluid modulus term is always just added to K
When we have a stiff rock with high velocity, then its value of K is large, and
changes in K fluid do not have much effect. But a soft rock with small velocity will
have a small K and changes in K fluid will have a much larger effect.
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Gassmann's Relations
Ksat
K mineral K sat

Kdry
K fluid
=
+
Kmineral Kdry (Kmineral Kfluid )
1

sat

dry

These are Transformations! Pore space geometry and stiffness are


incorporated automatically by measurements of Vp, Vs. Gassmann
(1951) derived this general relation between the dry rock moduli and
the saturated rock moduli. It is quite general and valid for all pore
geometries, but there are several important assumptions:
the rock is isotropic
the mineral moduli are homogeneous
gas
the frequency is low
Dry rock is not the same as gas saturated rock.
Be careful of high frequencies, high viscosity, clay.
Useful for Fluid Substitution problem:

water

oil

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Some Other Forms of Gassmann


K dry 2
1
K min
K sat = K dry +

1 K dry
+
2
K fluid K min K min

1
K min

1
K

fluid

1
K min

1
K dry

K sat =
1 1
1 1
+ 1
K dry K min K fluid K min K min K dry
1 = 1 +
K sat K min

K minK fluid
K +
K min K fluid

K min

+ 1 K min
K fluid
K min K sat
+
1
K fluid K min

K sat
K dry =

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Fluid Substitution Recipe


1. Begin with measured velocities and density

VP1, VS1, 1

4 2
K1 = 1VP21 VS1

2. Extract Moduli from Velocities measured with fluid 1:

2
1 = 1VS1

3. Transform the bulk modulus using Gassmann

K2
K fl 2
K1
K fl 1

K min K2 (K min K fl 2 ) K min K1 (Kmin Kfl 1 )


where K1, K2 are dynamic rock moduli with fluids 1, 2
K fl 1,K fl 2 bulk moduli of fluids 1, 2
1, 2
density of rock with fluids 1, 2
mineral modulus and porosity
K min,
density of fluids 1, 2
,
fl 1

fl 2

4. 2 = 1 shear modulus stays the same


5. Transform density

2 = (1 ) min + fl 2 = 1 + (fl 2 fl 1 )

6. Reassemble the velocities

K2 +
VP =

3 2

VS =

2
2

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Vp (km/s)

2.45
sandstone
porosity = 30%

2.4
2.35
2.3

patchy
homogeneous

2.25
2.2
2.15

0.2

0.4

0.6

0.8

Oil Saturation

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Summary of Mixing Rules

KVoigt = SwKw + SoK o + Sg Kg

K
e

K Brie = (K liquid Kg )(1 Sg ) + Kg

1 / KReuss = Sw / Kw + So / Ko + Sg / Kg
Brie, et al.SPE 30595
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Why is the shear modulus unaffected by fluids in


Gassmanns relations?

Imagine first an isotropic sample of rock with a hypothetical spherical


pore. Under pure shear loading there is no volume change of the
rock sample or the pore -- only shape changes. Since it is easy to
change the shape of a fluid, the rock stiffness is not affected by the
type of fluid in the pore.
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Why do the Gassmann relations


only work at low frequencies?
This crack decreases in
volume. Its pore pressure
locally increases if the fluid
cannot flow out of the crack.

+Pp
-Pp

This crack increases in


volume. Its pore pressure
locally decreases if the fluid
cannot flow into the crack.
Imagine an isotropic sample of rock with cracks at all orientations. Under pure shear
loading there is no volume change of the rock sample or the pore space, because
some cracks open while others close. If the frequency is too high, there is a tendency
for local pore pressures to increase in some pores and decrease in others: hence the
rock stiffness depends on the fluid compressibility.
However, if the frequency is low enough, the fluid has time to flow and adjust: there is
no net pore volume change and therefore the rock stiffness is independent of the
fluids.
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Graphical Interpretation of Gassmann's Relations


1. Plot known effective modulus K, with initial fluid.
K

K
mineral fluid Kfluid
K mineral K fluid

2. Compute change in fluid term:

3. Jump vertically up or down that number of contours.


Example: for quartz and water

Kfluid
= 0.6
K mineral

~ 3 contours.

C
C

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- Gary Mavko & Tapan Mukerji
G.6

161

Approximate Gassmann Relation


when Shear Velocity is Unknown
Normally, to apply Gassmann's relations, we need to know both Vp and Vs
so that we can extract the bulk and shear moduli:
4

K1 = VP2 VS2
3

1 = VS2

and then compute the change of bulk modulus with fluids using the usual
expression:
Kdry
Ksat
K fluid
=
+
K mineral K sat Kmineral Kdry (Kmineral Kfluid )
The problem is that we usually don't know Vs.
One approach is to guess Vs, and then proceed.
We have also found that a reasonably good approximation to Gassmann
is

Mdry
Msat
Mfluid

+
Mmineral M sat Mmineral Mdry (Mmineral Mfluid)

where M is the P-wave modulus:

M = V p2
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162

Vp-saturated,
saturated, From Approximate Gassmann

Approximate Gassmann Relation


When Shear Velocity is Unknown

Vp-saturated, From Gassmann

Predictions of saturated rock Vp from dry rock Vp are virtually the same
for the approximate and exact forms of Gassmanns relations.
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Gassmann's is a Low Frequency Relation

It is important to remember that Gassmanns relations assume low frequencies.


Measured ultrasonic Vp in saturated rocks is almost always faster than
saturated Vp predicted from dry rock Vp using Gassmann. Data here are for
shaly sandstones (Han, 1986).
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164

Water Flood Example: Pore Pressure


Increase and Change From Oil to Brine
Brine Flood into Oil
1250

(laboratory)

Pressure

depth (m)

One typical depth point

oil to water

1300
G.12

brine at
increased Pp
oil at
increased Pp
original
oil

1350

effect of pressure on frame


effect of pressure on fluids
frame+fluid: fluid substitution

2.5

Vp (km/s)

Calculated using Gassmann via dry lab data from Troll (Blangy, 1992). Virgin condition taken as low frequency,
oil saturated at Peff=30 Mpa Pressure drop to Peff=10 MPa, then fluid substitution to brine.
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165
Koil = 1., Kbrine = 2.2

Gas Flood Example: Pore Pressure


Increase and Change From Oil to Gas
Brine Flood into Oil
1250

One typical depth point

depth (m)

Pressure
oil to water

1300
G.12

brine at
increased Pp
oil at
increased Pp
original
oil

1350

effect of pressure on frame


effect of pressure on fluids
frame+fluid: fluid substitution

2.5

Vp (km/s)

Calculated using Gassmann from dry lab data from Troll (Blangy, 1992). Virgin condition taken as low
frequency, oil saturated at Peff=30 MPa. Pressure drop to Peff=10 MPa, then fluid substitution to gas.
Koil = 1., Kbrine = 2.2
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Brine Flood Example: Pore Pressure


Decrease and Change From Oil to Brine
Brine Flood with Pressure Decline

One typical depth point

depth (m)

1250

1300
brine at
decreased Pp

original
oil

frame effect
decreased Peff

oil at
decreased Pp

1350
1.8

2.4

Vp (km/s)

Calculated using Gassmann from dry lab data from Troll (Blangy, 1992). Virgin condition taken as low
frequency, oil saturated at Peff=25 MPa. Pore pressure drop to Peff=30 MPa, then fluid substitution to
brine. Koil = 1., Kbrine = 2.2
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Stiff, Turbidite Sand, Heavy Oil, Water Flood with Pp Increase

Stiff,deepwater sand, heavy oil (API20,GOR=15, T=75,Pp=18->25,


Sw=.3->.8)
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168

Fluid Substitution in Anisotropic Rocks: Brown and


Korringas Relations
(sat )
S(dry)
ijkl Sijkl

S
(
=
(S

)
)+ (

(dry)
ij

0
Sij0 (Skl(dry)
Skl )

(dry)

0
S

fl

0 )

where
)
S(dry
ijkl effective elastic compliance tensor of dry rock
)
S(sat
ijkl effective elastic compliance tensor of rock saturated with pore fluid
0
effective elastic compliance tensor of mineral
Sijkl

fl

compressibility of pore fluid

compressibility of mineral material =

porosity

This is analogous to Gassmanns relations. To apply it, one must measure


enough velocities to extract the full tensor of elastic constants. Then invert these
for the compliances, and apply the relation as shown.
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169

Challenge of Reactive Fluid Substitution


Images show changes in the rock frame after CO2 injection. Gassmanns
equations assume that the frame remains unchanged.

Noiriel, 2005

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170

Laboratory Data vs. Gassmanns Predicted Moduli


Pure Elastic Systems, Low Frequency, no rock-fluid reactions

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171

Factors Influencing Reactions in Carbonates


a) The properties of the sediment itself
- Mineralogy
- Grain size
- Texture
- Permeability
2CaCO3 + Mg2+
- Surface area

CaMg(CO3)2 + Ca2+

[Mg2+] [CaCO3]2
Kcd=
[Ca2+] [CaMg(CO3)2]

b) The properties of the pore-fluid


- salinity
- Mg/Ca ratio
- SO4-2
- HCO3-

Kcd=

[Mg2+]
[Ca2+]

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172

Factors Influencing Reactions in Carbonates


a) The properties of the sediment itself
- Mineralogy
- Grain size
- Texture
- Permeability
- Surface area
b) The properties of the pore-fluid
- salinity
- Mg/Ca ratio
- SO4-2
- HCO3Kcd= 0.67 - SPT conditions
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Factors Influencing Reactions in Carbonates


The properties of the pore-fluid
- Mg/Ca ratio
- SO4-2
- HCO3Case A
CO2 injection

Calcite dissolution

Case B
Transformation Anhydrite Gypsum
Tucker et al., 1990

Case C
Gypsum dissolution

dolomite dissolution

de-dolomitation driven by Gypsum dissolution


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Factors Influencing Reactions in Carbonates

Dissolution and mineral transformation affect the elastic moduli in a way that opposes the
high-frequency dispersion mechanisms. Thus, Gassmann fluid substitution may either
overestimate or fit high-frequency, saturated velocities, depending on the balancing of
chemical processes against dispersion mechanisms.
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175

Bounding Average Method (BAM)

Marion (1990) discovered a simple, semi-empirical way to solve the fluid substitution problem. The
Hashin-Shtrikman bounds define the range of velocities possible for a given volume mix of two
phases, either liquid or solid. The vertical position within the bounds, d/D, is a measure of the
relative geometry of the two phases. For a given rock, the bounds can be computed for any two
pore phases, 0 and 1. If we assume that d/D remains constant with a change of fluids, then a
measured velocity with one fluid will determine d/D, which can be used to predict the velocity relative
to the bounds for any other pore phase.
Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

176

An Example of the Bam Method. The wax saturated


velocities are predicted from the dry rock velocities.
Massillon Light Sandstone
4200

4000

measured parowax

P-Velocity (m/s)

3800

3600

BAM
calculated
parowax

3400

3200

3000

measured dry

2800
0

20

40

60

80

100

120

140

G.8

Temperature ( C)

Velocity in Massilon sandstone saturated with parowax. Data from Wang (1988). Wax saturated
velocities were predicted using BAM, from Wang's measured velocities in the dry rock and in wax (from
Marion, 1990)
Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

177

G.9

Velocity in dry and saturated Westerly granite. Data from Nur and Simmons (1969).
Saturated velocities were predicted using BAM, from measured velocities in the dry rock
(from Marion, 1990)
Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

178

Ellipsoidal Models for Pore Deformation


Gassmanns relation is a transformation, allowing us to predict how
measured velocities are perturbed by changing the pore fluid. Now we
discuss a different approach in which we try to model the moduli from
scratch.
Recall the general expression for the dry rock
modulus:

1
1
K dry

K mineral

Most deterministic models for effective moduli assume a specific


idealized pore geometry in order to estimate the pore space
compressibility:

1
1 v pore
=
K v pore

The usual one is a 2-dimensional or 3-dimensional ellipsoidal


inclusion or pore.
b

The quantity = b/c is called the aspect ratio.


Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

179

Estimating the Dry Rock Modulus


An externally applied compression tends to narrow the crack, with the
faces displacing toward each other.

Mathematicians have worked out in great detail the 3-D deformation field
U, of an oblate spheroid (penny-shaped crack) under applied stress. For
example, the displacement of the crack face is:
U(r) =

c
K mineral

4 1 2
3 1 2

1 cr

We can easily integrate to get the pore volume change and the dry
modulus:
16 1 2
Nc 3
1
1 =
1
+
K dry K mineral
K mineral V bulk
9 1 2
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180

Dry Rock Bulk Modulus


16(1 v 2 ) 1 Nc 3
1
1
=
+

K dry K mineral 9(1 2v ) K mineral Vbulk


2
1
1 16(1 v ) Nc 3
1 +

=
K dry K mineral 9(1 2v ) Vbulk

2
1
1 16(1 v )
1 +
=

K dry K mineral 9(1 2v )

"Crack density parameter"


=

N 3
c
Vbulk

3
4

Modulus depends directly on crack density. Crack geometry or stiffness


must be specified to get a dependence on porosity.
Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

181

Crack Density Parameter


In these and other theories we often encounter the quantity:

Nc 3
=
Vbulk
This is called the Crack Density Parameter, and has the interpretation of the
number of cracks per unit volume.
Example: 2 cracks per small cell. Each crack about 2/3 the length of a cell.

c
= 0.07
L
v = L3

2c

L
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182

Distribution of Aspect Ratios


Modulus depends on the number of cracks and their average lengths

16(1 v 2 ) Nc 3
1
1
=
+
K dry K mineral 9Kmineral (1 2v ) Vbulk
An idealized ellipsoidal crack will close when the amount of
deformation equals the original crack width:
solving gives:

U =b
close Kmineral

3 (1 2v )
4 (1 v 2 )

Kmineral
We generally model rocks as having a distribution of cracks with
different aspect ratios. As the pressure is increased, more and more
of them close, causing the rock to become stiffer.
Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

183

Kuster and Toksz (1974)


fmorulation based on longwavelength, first order scattering
theory (non self-consistent)

(K

*
KT

*
KT

Km + m
N

3
Km)
= x i (Ki K m )P mi
4 i =1
*
K KT + m

3
m )

(m + m ) =

*
KT

+ m

x (
)
i

m )Qmi

i=1

(9K + 8 )
6 (K + 2 )

Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

184

Self-Consistent Embedding Approximation

Walsh's expression for the moduli in terms of the pore compressibility is


fairly general. However attempts to estimate the actual pore
compressibility are often based on single, isolated pores.
16(1 v 2 ) Nc 3
1
1
=
+
K dry K mineral 9Kmineral (1 2v ) Vbulk

The self-consistent approach uses a single pore


in a medium with the effective modulus.
16(1 v 2 ) Nc 3
1
1
=
+
K dry K mineral 9Kdry (1 2v ) Vbulk

Solving for Kdry gives:


K dry

16(1 v 2 ) Nc 3
= K mineral 1

9
(
1
2v
)
V

bulk

Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

185

Self-Consistent Approximations
OConnell and Budiansky (1974) model for medium with randomly
oriented thin dry cracks

16 1 v *2
SC
= 1
*
K
9 1 2v SC

K *SC

*
*
*
SC
32 (1 v SC )(5 v SC )
= 1

45

(2 v *SC )

v v *SC )(2 v *SC )


45
(
=
*
*
16 (1 v *2
SC )(10v 3vv SC v SC )

K and are the bulk and shear moduli of the uncracked medium, is
the Poissons ratio, and is the crack density parameter. The
calculations are simplified by the approximation:
16
*
v SC v 1

Assumes small aspect ratios ( 0).


Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

186

Self-Consistent Approximations
Berrymans (1980) model for N-phase composites
N

x (K
i

K * )P *i = 0

* )Q*i = 0

i=1
N

x (
i

i=1

coupled equations solved by simultaneous iteration

Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

187

Comparison of Han's (1986) sandstone data with models of idealized pore


shapes. At high pressure (40-50 MPa), there seems to be some equivalent pore
shape that is more compliant than any of the convex circular or spherical models.
Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

188

Comparison of self-consistent elliptical crack models with carbonate


data. The rocks with stiffer pore shapes are fit best by spherical pore
models, while the rocks with thinner, more crack-like pores are fit
best by lower aspect ratio ellipsoids.
Data from Anselmetti and Eberli., 1997, in Carbonate Seismology, SEG.
Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

189

Differential Effective Medium


Model
The differential effective medium (DEM) theory models
two-phase composites by incrementally adding inclusions of one phase
(phase 2) to the matrix phase

d
[ K * ( y )] = ( K 2 K *) P (*2) ( y )
dy
d
(1 y ) [ * ( y )] = ( 2 *)Q (*2) ( y )
dy

(1 y )

Coupled differential equations with initial conditions K*(0) = K1 and *(0) = 1, where
K1, 1 = bulk and shear moduli of the initial host material (phase 1)
K2, 2 = bulk and shear moduli of the incrementally added inclusions (phase 2)
y = concentration of phase 2

Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

190

Differential Effective Medium


Model

The differential effective medium (DEM) theory models


two-phase composites by incrementally adding inclusions of one phase
(phase 2) to the matrix phase

Stanford Rock Physics Laboratory - Gary Mavko & Tapan Mukerji

191

Differential Effective Medium


Model
40

K (Bulk modulus, GPa)

35
30
25
20
15
10
5
0
0

0.2

0.4

0.6

0.8

porosity
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192

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