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1987 J. Phys. D: Appl. Phys. 20 1637
(http://iopscience.iop.org/0022-3727/20/12/015)
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1. Introduction
= af/a,.
(1)
F = T/q
(2)
E Guyon et a/
k = q3/S;TI.
(5)
CC
qm'.
10-2
10"
Porosity
(6)
In the recent work of WKT, they analyse their experimental data of formation factor and permeability on
monosize sintered spheres using an idealised medium
made of interconnected tubes, which can be replaced
by a random resistor network model havingvariable
resistances Ri. The effect of sintering is modelled by
shrinkingtheradius
of the resistors (i.e.,tubes)at
random. The local electrical conductance of a bond,
R;l, scales as rt where ri would be the radius of an
equivalent
hydraulic
circuit
filled with conducting
brine. The local flow resistance, however, should vary
as r! as is expected from the Poiseuille flow in a cylindrical tube of radius ri anda fixed length. Using
this description, they find numerically that m and m'
of (3) and (6) are related as
m' = 2m
(7)
wherethefactor
2 is associated with thedifferent
exponents of ri in the two problems.
The WKT results coupled with the fact that the tortuousgeometry
plays asomewhatsimilarrolefor
both k and a, suggests a simple relation, independent
of the degree of compaction, between k and F such
as
k = CF-2L2
(8)
where L is a characteristic length scale necessary for
thenormalisation
of therelation.
By making the
appropriate choice of theconstant C , L canbeset
equal to a.
2.2. Experiments
Theexperimentalresults
of WKT onthe monosize
sintered samples support this description. In figure 1,
1638
theformationfactor
is plottedasafunction
of cp
(open circles) forsintered glass samples of different
sphere diameters (a = 50, 100, 200 pm). The result is
unique
a
curve
independent
of thediameter,
as
expected. The linear fit corresponds to Archie's law
with m = 8 (Maxwell 1881). Thebroken curve is a
theoretical
prediction
of Roberts
and
Schwartz
(1985). In their analysis, the formation factor is calculated using aperiodicarray
of spheres in contact
which they
subsequently
grow uniformly
without
changing thedistancebetweenspherecentres(not
allowing sphere overlap) to simulate the reduction
in
porosity due
sintering.
to
There
is general
a
agreementbetweentheoryandexperimentbetween
Q, = 0.40 (nearthe
limit of denserandom packing
withoutsintering) toaround Q, = 0.10. The agreement between quite different models and the experimental
data
suggests that (3) is reasonably
independent of geometry details.
of F
Below Q, = 0.10, there is afasterincrease
with decreasing Q, which comesfromthe
successive
closing of pores. In the Roberts and Schwartz model,
the closing takes place at the same time at all throats
at a concentration that depends on the particular lattice. Quite generally, we expect that this closing takes
place in a more or less random fashion in disordered
materials
and
that
percolation
a
threshold
type
description could apply. We are presently studying, in
some detail, the formation factor in this low porosity
limit. The crucial problem, in this
case,
is
to define thecorrect porositysincealargefraction
of theremainingporosity
is closed(asalso
seen
of BourbieandZinszner
(1985) on
in thework
Fontainebleau sandstones). In our work, as
in WKT'S
\.
J
\
I
10
IO2
lo3
- 36
c32
x
(rnlrn
g 28
24
N
Figure 3. The
of porosity ~u for unconsolidated
binary
packings
with
ratio
a
diameters
of
R = D, /D2 as a
function of the volume fraction of small spheres N. The
unsintered porosity for the particular diameter ratio 4 of the
particles used in Our experiments was not known
accurately enough to be included in this figure or in table
The non~monotonicvariation with a
porosity
around N = 0.3hasbeendocumented in DreviouS
experimental and theoretical
analyses.
E Guyon et a/
ticular set of variables, we also define a particular distribution of pore sizes. Therefore, we have the procedures
at hand to fabricate a set of samples with a wide distribution of pore sizes. For example, we can see in figure
4 two distributionsof pore sizes obtained fora ratio 1:4
with the same porosity (91 = 0.30)but with the two
different volume fractions of small particles N = 0.05
and 0.80. Thcse pore size distributions are calculated
based on a model of Doddst (1980).
Small p a r t l c l e s i 2 1
"
f)
Translatlon
f
0
0.3
/
Series o f s l e v e s
0.2
"
0 . 0 . 0 . 0 . 0 . 1 . 1 . 1 . 1 . 1 . 1 . 2
22 39 71 55
87 03 19 35 51 68 8 4
0.3 1
0.
0.
22
(bl
0 . 0 . 0.
39 7155
87
1 . 1 .
0 3 19
1 . 1 . 1 .
35 51 6 8
1.
84
Rotatlon
Slze
All of thedataaboutthesamplesas
well asthe
measurements of cps, k , and F are contained in table 1.
Name
qs
k(mD)
L2
L1
4.28
4.2T
4.1T
4.18
12.1T
1.2T
12.1C
12.18
6.1T
6.18
3.1T
1.3C
3.1 B
13.1T
1.28
2.18
11.1C
13.1C
13.1 B
11.1T
7,18
8.1T
8.18
7.1T
0.124
0.126
0.1 29
0.130
0.164
0.183
0.185
0.195
0.216
0.219
0.222
0.235
0.248
0.260
0.277
0.280
0.297
0.299
0.301
0.311
0.314
0.328
0.334
0.344
29.87
35.09
30.67
27.48
23.88
14.1 2
17.35
16.40
14.02
26.84
10.62
10.1 8
10.04
7.43
7.26
6.89
7.43
5.64
6.32
6.63
4.46
5.84
5.97
5.88
500.0
400.0
486.8
585.1
1149.5
3691.6
2542.1
2916.5
5250.0
1304.0
3504.0
6247.4
4366.1
5171.1
15933.1
8595.3
2647.0
12265.0
9537.0
3553.0
5309.0
42698.0
41 816.0
461 2.0
177.85
186.91
180.22
177.02
215.58
228.46
232.99
235.87
270.55
258.12
167.34
214.33
176.73
142.37
243.95
170.02
101.83
166.37
164.40
105.31
86.50
321.20
325.19
106.39
N
195.56
195.56
195.56
195.56
227.32
214.52
227.32
227.32
257.64
257.64
182.55
214.52
182.55
189.09
214.52
188.57
96.50
189.09
189.09
96.50
102.26
325.50
325.50
102.26
0.28
0.28
0.28
0.28
0.18
0.21
0.18
0.18
0.11
0.11
0.33
0.21
0.33
0.30
0.21
0.30
1.0
0.30
0.30
1.0
0.92
0
0
0.92
~~
1641
E Guyon et a/
We performed measurements on twenty samples covering a porosity range from 0.35 to 0.10. The volume
fraction N of small beads mixed with large ones range
from 0 to 1.
The first results to be discussed are the measurements of the formation factor. In figure 1, we show the
measured formation factor versus porosity for all the
binary samples. We see that thebinary data (full circles)
are consistent with the monosize data (open circles)
and depend only on the total porosity and not on any
characteristic pore or grain size.
300
*/
100
2 00
L , I@)
300
100
2 00
L ! (pm1
100
3 00
k u - q3
(TSZ) P2'F
where the hydraulic radius p = q / S , is the ratio of the
surface to volume of the pores. Note that this relation
which establishes a proportionality between k and F'
ko = AA2/F
(11)
F"
d r P(r)r*
results of mercury porosimetry experiments.In particular, the critical bonds correspond to the inflection point
in the porosimetry curves
which determines theweakest
bonds needed to insure breakthrough of the invading
fluid.
We
are
presently
testing the
correspondence
betweenporosimetryresultsandthetransportproperties of our multiple poresize systems. As seen above,
we do not expect majordifferences between the various
length parameters involved in (10) or (11) in well connected porous systems. On the other hand, we would
expect more marked changes in a weakly poorly connectedsamplesuchasaporousmedianexttothe
percolation threshold of the pore space (where A does
not include the effect of dead arms). We also should
not expect the empirical relation (8) with L defined by
(9) to apply.
5. Conclusion
Wehavebeenabletopreparehomogeneous
synthetic porous samples yielding a large distribution of
pore sizes. The comparison of the formation factor and
permeability for various mixtures and sintering rates
leads to thedefinition of a characteristic transport property length scale L that is a simple average of volume
over surface of the unconsolidated grains. The present
extension of thework is twofold. On one hand, we
know how to prepare materials with much larger heterogeneitiesthatcanseparatethedifferent
length
scales. On the other hand, the study suggests that the
formation factor and permeability are not sensitive tools
to study the distribution of current in the porous media
due to the distribution of pore sizes. Tracer dispersion
in which a dye is injected in a porous media penetrated
by a flowing fluid appears to bea more sensitive tool to
study these heterogeneities. Recent experimental work
alongtheselineshavebeendone
by Lemaitre et a1
(1986) on unconsolidatedbinarypackings of spheres
similar to ours and by Charlaix et a1 (1986) on sintered
monosize glass spheres.
Acknowledgments
and
k
d r P(r)r4
where n is the number of pores per unit area. If one shrinks all the
pores by a constant factor, one recovers the WKT results obtained
on a lattice k F-' (equation (8)). On the other hand, if one
changes the porosity b changing the density of pores, n , then
k F'(equation (l0)Y. The presentexperiments suggest that
sintering decreases the pores in proportion to their radius.
References
Ambegaokar V, Halperin B I and Langer J S 1971 Phys.
Rev. B 4 2612-20
Ben Aim R and Le Goff P 1967 Powder Technol. 1 281-90
Bourbie T and Zinszner B 1985 J. Geophys. Res. B 90
11524-32
1643
D12
E Guyon et a/
1644