The simplified Helgeson-Kirkham-Flowers (HKF) model
The equation to calculate the activity coefficient,
γi, of an ion i with
electric charge Zi is:
| |
log γi = |
−Aγ Zi2
(√I /
(1 + åBγ √I
))
− log(1+0.018 ∑mk)
+ bγ,MX I
|
where I is the ionic strength,
Aγ and Bγ are
Debye-Hückel parameters
which are temperature- and pressure dependent
(see Table),
å is the effective ionic radius (discussed below), and
bγ,MX is a solute-specific parameter.
The sum (∑mk) is made over all solute species k in the aqeuous solution, both
charged and neutral. The model is further described in
Helgeson, Kirkham and Flowers (1981) (eqs. 121, 165-167, 297, 298),
Oelkers and Helgeson (1990) (eqs. 22 & 23) and in
Oelkers and Helgeson (1991) (eqs. 3 & 9).
In SPANA (and SED/PREDOM)
the HKF model is simplified by using the NaCl parameters:
- the parameter å
is the effective ionic distance for NaCl: å
= (1.91+1.81) Å = 3.72 Å; see Table 9 in
Shock et al. (1992) and Table 3 in
Helgeson et al. (1981).
This results in åBγ = 1.22
(mol/kg)−½ at 25°C.
This effective ionic distance changes at high temperature or pressure as
described in Shock et al. (1992) (eqs. 4-5, 24-26, Table 3).
- bγ,MX for NaCl solutions
is used, see Table.
bγ,NaCl= 0.064 kg/mol at 25°C.
- the calculated ionic strength (I) is used instead of
∑mk. This avoids problems when making
diagrams where the redox potential, Eh, is outside
the stability range of H2O. Convergence problems
in the calculations occur if large amounts of either O2(aq)
or H2(aq) are calculated when Eh is
too high or too low, respectively, because then
∑mk becomes unrealistically large.
The activity of water (H2O) is given by
| |
log aH2O = |
− Φ ∑mk /
(ln(10) 55.508)
|
where Φ is the osmotic coefficient,
calculated using the HKF model as follows:
| |
Φ = |
ln(1+0.018 ∑mk)/(0.018 ∑mk)
− (2 AΦ (1/∑mk) I3/2
σ(åBγ√I))
+ (1/∑mk)
(1/2) ln(10) bγ,NaCl I
|
where AΦ = (1/3) ln(10) Aγ, and
| |
σ(x) = |
(3/x3) ((1+x) − 1/(1+x) − 2 ln(1+x))
|
In SPANA (and SED/PREDOM)
these equations are simplified by using the ionic strength value (I)
instead of ∑mk. This avoids the
convergence problems explained above in diagrams where the redox potential,
Eh, is outside the stability range of H2O.
References
-
H.C. Helgeson, D.H. Kirkham and G.C. Flowers, Amer. Jour. Sci., 281 (1981)
1249-1516. doi: 10.2475/ajs.281.10.1249
-
E.H. Oelkers and H.C. Helgeson, Geochim. Cosmochim. Acta, 54 (1990)
727-738. doi: 10.1016/0016-7037(90)90368-U
-
E.H. Oelkers and H.C. Helgeson, Geochim. Cosmochim. Acta, 55 (1991) 1235–1251.
doi: 10.1016/0016-7037(91)90303-M
-
E.L. Shock, E.H.Oelkers, J.W. Johnson, D.A. Sverjensky, H.C.Helgeson
J. Chem. Soc. Faraday Trans., 88 (1992) 803-826.
doi: 10.1039/FT9928800803
Models for activity coefficients
Comparison between experimental data and models