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Kuster-Toksoz Original Paper
Kuster-Toksoz Original Paper
, 3 TABLES
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The velocity and attenuation of ultrasonic different models. The closest agreement is ob-
waves are measured in suspensions of solid tained for the dynamic interaction model given
spherical particles in fluid matrices as a function in Part I by Kuster and Toksiiz (1974) and for
of the concentration of inclusions. Polystyrene the Reuss model.
and glass beads were used as inclusions and they The theoretical formulas ior the attenuation in
were suspended in pure water, oil, or acetylene composite media are given. The observed at-
tetrabromide. Velocities were measured by a pulse tenuation agrees reasonably. well with th, theo-
propagation technique. Attenuation in mixtures retical values computed by including geometrical
was measured relative to attenuation in pure scattering, viscous absorption in the fluid matrix,
matrix fluid. The observed velocities were com- and the anelasticity of the solid inclusions.
pared to theoretical values calculated using six
607
608 Kuster and Toks6z
SUSPENSIONS USED IN THE EXPERIMENTS Nujol. Its density and viscosity were measured
The choice of suitable solid particles to be sus- in the laboratory at 20°C. We mixed benzene and
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pended in a fluid matrix is limited by a number acetylene tetrabromide in order to obtain a mix-
of constraints if one wants to make accurate and ture whose density is slightly lower than that
precise measurements and compare them with of glass. Since benzene evaporates faster than
theoretical results. These include (a) the inclu- acetylene tetrabromide, the matrix composition
sions should be spherical and of small diameter changed slowly with time For this reason, the
compared to the wavelength to minimize the ap- experiment was carried out in a few hours, and
proximations made in theoretical formulations; no attenuation measurements were performed
(b) the properties of the inclusion material should since these require a longer time The size dis-
be either known or measurable (the latter condi- tribution of the polystyrene spheres (Figure 1)
tion implies that it must also be available as a was obtained by sieving a sample through 16
bulk material and not only as a powder); (c) the sieves ranging from 707 to 53 microns. It can be
densities of the matrix and inclusions must be approximated by a Gaussian distributior) with
close so that the inclusions remain in suspension mean of 140~ and standard deviation of 30~. The
for a period sufficiently long for the measure- glass beads used were smaller than 50~ in radius,
ments; and (d) both materials must be miscible and their size distribution was not determined.
yet chemically nonreacting. We used the follow-
ing three combinations of materials for our lab-
oratory measurements: polystyrene beads in
water (WE’S), polystyrene beads in oil (OPS),
and glass beads in a mixture of benzene and
acetylene tetrabromide (ATBG). The physical
constants of the constituents are given in Table 1.
They are used in calculating the theoretical
values.
The polystyrene spheres were provided by Sin-
clair-Koppers Co.; soda-lime glass beads were
obtained from Potters Brothers, Inc. The densi-
ties of both materials were measured in the lab-
oratory. For soda-lime glasswe adopted the elastic
velocities tabulated by Press (1966). For poly-
styrene WC measured the velocities on a disc of
polystyrene provided by the manufacturer. To
obtain the Q values we measured attenuation in
lucite and used these as representative for poly- FIG. I. Distribution of the radiusa (in microns) of the
styrene. The trademark of the oil we used is polystyrene beads used in the experiments.
EXPERIMENTAL PROCEDURE
Bs\I\I-
---Jt
4P=
1 1 1
I the ATBG suspension because all measurements
were made in a few hours under a hood.
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fl ttenuation meusuvemzenls
where I’ is the wave velocity. Combining (2) and spherical. In the formulas given below, b is the
(3), we obtain ratio of the bulk modulus of the inclusion to that
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WATER -POLYSTYRENE
?
a
IO 20 30 40 50 60 70
CONCENTRATION (%)
FIG. 5. Normalized effectivevelocityversusvolumeconcentrationof inclusionsfor a water-polystyrenesuspension.
Normalized velocity is the ratio of the observedvelocity to the velocityof pure matrix material (water in this case).
Experimentaldata are shownby solid circles.The numbersnext to the theoreticalcurvesindicatethe model number
given in the text (e.g. “I” is Mal and Knopoff, “2” is Kuster and ToksGz).Model 3.IScloseto model 2 and not shown
separately.
612 Kuster and Toksijz
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OIL-POLYSTYRENE
:
i 1.20 _
I-
3
0’
d I.15
>
i -
1.10
7
a
r
E
z Ii05
IO 20 60 70
CC?N’CENT%T ION ‘;:o,
FIG. 6. Normalized effective velocity versusconcentrationfor an oil-polystyrenesuspension.
All other parameters same as those in Figure 5.
2b+c(l--c)(l--b)* 112 I
(
I I I I
---__ -_- ___ 5
cyN= [lf(r-l)c][2c(l-b)+2b] > . (9)
theoretical grounds (see Part I), however, we centration of 50 percent, this uncertainty on the
favor model (2) over model 13). It is not clear theoretical values is about 0.5 percent. From
whether experimental data which would allow Figures 5, 6, and 7, it is clear that models (4),
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such a discrimination could actually be obtained, (S), and (6) do not fit the data. Model (1) also
since suspensions with a large density ratio be- appears unsatisfactory especially at large con-
tween inclusion and matrix are difficult to main- centrations. Model (2), and thus model (3), fall
tain. [Urick (1947) reports velocity measure- closest to the data for all three suspensions, but
ments in a water-kaolin suspension with a nom- they are consistently above the measured values.
inal density ratio of 2.60. However, kaolinite ab- The discrepancy increases with concentration and
sorbs water and the solution becomes a viscous is undoubtedly significant since it is larger than
model rather than the elastic spheres in an ideal the combined uncertainties on the measured and
fluid treated theoretically.] computed values.
In all models given above, it is assumed that The observed systematic difference between the
the matrix is nonviscous. Of course, this does not measured and computed values is most likely due
correspond to the reality of our experiments. to some theoretical limitations and the assump-
Ament (1953) showed that matrix viscosity has a tions involved in- die derivation of model (2).
negligible effect on the effective P-wave velocity There are two possible causes. One is the effects
when the wavelength of the S-waves in the fluid of multiple scattering and interaction between
is much smaller than the radius of the inclusion. inclusions. The other is the dispersion in a two-
This is the case in our experiments, and we may phase medium where the velocity may be depen-
safely use the velocity models derived with the dent on frequency. Both of these subjects were in-
nonviscous matrix assumption. However, the vestigated theoretically by Kuster (1072). Both
matrix viscosity plays an important role in the mechanisms would tend to decrease the theoret-
attenuation of seismic waves in suspensions, as ical velocities and improve the fit between ob-
will be shown later. served and theoretical values in Figures 5, 6, and
The uncertainty on our velocity data is about 7. A calculation with higher order terms is com-
0.2 percent. There is also some uncertainty on the plicated and was carried out for only one case.
theoretical values since they are computed from The results arc demonstrated semiquantitatively
parameters measured in the laboratory. At a con- in Figure 8. The velocity curve at very long wave-
1
\
\
\
\
\
x/o
FIG. 8. Effective P-wave velocity versuswavelength( x ) to inclusionsize ratio
for the WPS (water-polystyrene)suspensionat a concentrationof 50 percent.Long
wavelength and short wavelength hmits are computed with models (2) and (6),
respectively.
Kuster and ToksSs
OPS OPS
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c = 5 % c = 20 %
-2
L 1 I I I I I I I I I
OPS OPS
4- c = 40 % 4 c = 50 %
2- 2
.;?\
.
O- . 0
. \ .
-2- . -2
-4
I I I I I
WPS
4 c = 68 %
-2
-4
1 I I I I I I I I I I
.I .2 .3 4 .5 .I .2 .3 .4 .5
f, MHz f, MHz
FIG. 10.Natural logarithm of the ratio of amplitudesmeasuredin a suspension
and in the pure matrix fluid versus
frequencyfor oil-polystyrene(OPS) and water-polystyrene(WPS) mixtures. Observedpoints and linear fits (solid
line) to these are shown for different concentrations,
616 Kuster and Toks6z
Table 2. Observed and calculated Q in water-polystyrene (WPS) and oil-polystyrene (OPS) suspensions
Volume concentration
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(percent) Qcalcu
Ned Qobserved Frequency band (khz)
-___ -__
OPS 40 200 230 24&440
OPS 50 147 150 200-440
OPS 2; 111 80 160-440
WPS 119 160 200-440
1 c is the volume concentration of inclusions. 0 is related to the total attenuation factory hy Q=r/vr, where I’
is the wave velocity.
[IP ,
;\nniversary Vol., p. 162-188.
1 1 li?
Epstein, P. S., and Carhart, R. R., 1953, The absorp-
tion of sound in suspensions and emulsions: I. \Vater
fog in air: J. Acous. Sot. Am., v. 25, p. 553-565.
Hamilton, E. L., 1972, Compressional-wave attenua-
P
- = p”? Real ~
l/2
(A41)
tion in marine sediments: Geophysics, v. 37, p. 620- 7r 1
646.
Hill, R., 1952, The elastic behavior of a crystalline
aggregate: Proc. Phys. Sot. London, ser. A, v. 65,
76 = _-
Q3P
= - 2,~“~ Imag
[I
~
!J
,
(with solid anelastic matrix and solid anelastic where d is the thickness of the inclusion.
inclusions) we must set In a two-phase medium there are other sources
of attenuation besides anelasticity of the constit-
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K = KR + iKr, P = PR + +I
uent phases, The attenuation coefficient due to
and geometrical scattering was computed by Yama-
kawa (1962). For a P-wave in a solid-solid, two-
K’ = K’, +iK:, /A’ = /.lz +ip:. phase medium
(A@
The effective bulk and shear moduli are complex
2B: + $(l + 2v3)B;
and can be found from
K* - K K’-K 1
-_= c------- - Tiijj
3K* + 4p 3K’ + 4p 3
P* - P where
(A7)
6r*(K + 2~) + p(9K + 8~)
K - K’
B. =---,
= $f4z [Tijij - +Tiijj], 3K’ + 4~
P
where T;ijj and Tij;j are scalars depending on the
B
1
_‘-”
3P
matrix and inclusion properties and on the shape
of the inclusion (see Part I, Kuster and ToksGz, crG’ - cr)
& ~20
this issue).
3 W(K + 2~) + d9K + 8~)
To determine the effective anelastic properties
(Q values) of the two-phase medium, we use the v = a/P, and
real and imaginary parts of the effective moduli f = frequency.
K* and p* and equations (A3) and (A4).
Because of the algebraic complexity of (A7), In a suspension where the matrix is a Newtonian
it is difficult to derive analytic expressions for Q fluid with viscosity TJ,part of the attenuation of
values. However, the effective velocities and Q the wave train stems from the absorption of the
values can be calculated by a computer using com- scattered S-waves in the very neighborhood of
plex algebra routines. This procedure was fol- each inclusion. The attenuation coefficient for
lowed in this paper. P-waves was derived for this case by Epstein
The particular cases of viscous fluid inclusions (1941)
or matrix can be treated as shown above by
letting the shear modulus become purely imagin-
ary
y = c _”(p - p’)
a (All)
/.l = iwn, (A@ i + b. - ib;/3
where
-
UP 57
d
J a<< 1, (L49) ba = (1 +i)a __
9
.