
Note that here and in the following we use shaley sand equations F ¼ af
–m
and not
s
w
/s. The cation exchange capacity is a measure of the excess charges and Q
v
is the
charge per unit pore volume. Clays often have an excess negative electrical charge
within the sheet-like particles. This is compensated by positive counterions clinging
to the outside surface of the dry clay sheets. The resulting positive surface charge is a
property of the dry clay mineral and is called the cation exchange capacity (Clavier
et al., 1984). In the presence of an electrolytic solution such as brine, the electrical
forces holding the positive counterions at the clay surface are reduced. The counter-
ions can move along the surface contributing to the electrical conductivity. The
average mobility of the ions is described by B. The parameter B is a source of
uncertainty, and several expressions for it have been developed since the original
paper. Juha
´
sz (1981) gives the following expressions for B:
B ¼
5:41 þ 0:133T 1:253 10
4
T
2
1 þ R
1:23
w
ð0:025T 1:07Þ
where T is the temperature in degrees Fahrenheit or
B ¼
1:28 þ 0:225T 4:059 10
4
T
2
1 þ R
1:23
w
ð0:045T 0:27Þ
for temperature in degrees Celsius. Application of the Waxman–Smits equation
requires calibration with core CEC measurements, which are not always available.
The normalized Waxman–Smits or Waxman–Smits–Juha
´
sz model (Juha
´
sz, 1981)
does not require CEC data because it uses V
sh
derived from logs to estimate Q
v
by
normalizing it to the shale response. In this model
BQ
v
¼ Q
vn
ð
wsh
w
Þ
Q
vn
¼
Q
v
Q
vsh
¼
V
sh
sh
where f is the total porosity (density porosity), f
sh
is the total shale porosity, and
s
wsh
is the shale water conductivity obtained from s
wsh
¼ Fs
sh
, where s
sh
is the
conductivity of 100% brine-saturated shale. The normalized Q
v
ranges from 0 in
clean sands to 1 in shales. Brine saturation S
w
can be obtained from these models by
solving (Bilodeaux, 1997)
S
w
¼
FR
w
R
t
1 þ R
w
BQ
v
=S
w
ðÞ
1=n
427 9.4 Electrical conductivity in porous rocks