Activity coefficient

An activity coefficient is a factor used in thermodynamics to account for deviations from ideal behaviour in a mixture of chemical substances.^[1] In an ideal mixture, the microscopic interactions between each pair of chemical species are the same (or macroscopically equivalent, the enthalpy change of solution and volume variation in mixing is zero) and, as a result, properties of the mixtures can be expressed directly in terms of simple concentrations or partial pressures of the substances present e.g. Raoult's law. Deviations from ideality are accommodated by modifying the concentration by an activity coefficient. Analogously, expressions involving gases can be adjusted for non-ideality by scaling partial pressures by a fugacity coefficient.

The concept of activity coefficient is closely linked to that of activity in chemistry.

Thermodynamic definition

The chemical potential, μ_B, of a substance B in an ideal mixture of liquids or an ideal solution is given by

${\displaystyle \mu _{\mathrm {B} }=\mu _{\mathrm {B} }^{\ominus }+RT\ln x_{\mathrm {B} }\,}$

where μo
B is the chemical potential in the standard state and x_B is the mole fraction of the substance in the mixture.

This is generalised to include non-ideal behavior by writing

${\displaystyle \mu _{\mathrm {B} }=\mu _{\mathrm {B} }^{\ominus }+RT\ln a_{\mathrm {B} }\,}$

when a_B is the activity of the substance in the mixture with

${\displaystyle a_{\mathrm {B} }=x_{\mathrm {B} }\gamma _{\mathrm {B} }}$

where γ_B is the activity coefficient, which may itself depend on x_B. As γ_B approaches 1, the substance behaves as if it were ideal. For instance, if γ_B ≈ 1, then Raoult's law is accurate. For γ_B > 1 and γ_B < 1, substance B shows positive and negative deviation from Raoult's law, respectively. A positive deviation implies that substance B is more volatile.

In many cases, as x_B goes to zero, the activity coefficient of substance B approaches a constant; this relationship is Henry's law for the solvent. These relationships are related to each other through the Gibbs–Duhem equation.^[2] Note that in general activity coefficients are dimensionless.

Modifying mole fractions or concentrations by activity coefficients gives the effective activities of the components, and hence allows expressions such as Raoult's law and equilibrium constants to be applied to both ideal and non-ideal mixtures.

Knowledge of activity coefficients is particularly important in the context of electrochemistry since the behaviour of electrolyte solutions is often far from ideal, due to the effects of the ionic atmosphere. Additionally, they are particularly important in the context of soil chemistry due to the low volumes of solvent and, consequently, the high concentration of electrolytes.^[3]

Ionic solutions

For solution of substances which ionize in solution the activity coefficients of the cation and anion cannot be experimentally determined independently of each other because solution properties depend on both ions. Single ion activity coefficients must be linked to the activity coefficient of the dissolved electrolyte as if undissociated. In this case a mean stoichiometric activity coefficient of the dissolved electrolyte, γ_±, is used. It is called stoichiometric because it expresses both the deviation from the ideality of the solution and the incomplete ionic dissociation of the ionic compound which occurs especially with the increase of its concentration.

For a 1:1 electrolyte, such as NaCl it is given by the following:

$\gamma _{\pm }={\sqrt {\gamma _{+}\gamma _{-}}}$

where γ₊ and γ₋ are the activity coefficients of the cation and anion respectively.

More generally, the mean activity coefficient of a compound of formula A_pB_q is given by^[4]

${\displaystyle \gamma _{\pm }={\sqrt[{p+q}]{\gamma _{\mathrm {A} }^{p}\gamma _{\mathrm {B} }^{q}}}}$

Single-ion activity coefficients can be calculated theoretically, for example by using the Debye–Hückel equation. The theoretical equation can be tested by combining the calculated single-ion activity coefficients to give mean values which can be compared to experimental values.

The prevailing view that single ion activity coefficients are unmeasurable independently, or perhaps even physically meaningless, has its roots in the work of Guggenheim in the late 1920s.^[5] However, chemists have never been able to give up the idea of single ion activities, and by implication single ion activity coefficients. For example, pH is defined as the negative logarithm of the hydrogen ion activity. If the prevailing view on the physical meaning and measurability of single ion activities is correct then defining pH as the negative logarithm of the hydrogen ion activity places the quantity squarely in the unmeasurable category. Recognizing this logical difficulty, International Union of Pure and Applied Chemistry (IUPAC) states that the activity-based definition of pH is a notional definition only.^[6] Despite the prevailing negative view on the measurability of single ion coefficients, the concept of single ion activities continues to be discussed in the literature, and at least one author presents a definition of single ion activity in terms of purely thermodynamic quantities and proposes a method of measuring single ion activity coefficients based on purely thermodynamic processes.^[7]

Experimental determination of activity coefficients

Activity coefficients may be determined experimentally by making measurements on non-ideal mixtures. Use may be made of Raoult's law or Henry's law to provide a value for an ideal mixture against which the experimental value may be compared to obtain the activity coefficient. Other colligative properties, such as osmotic pressure may also be used.

Radiochemical methods

Activity coefficients can be determined by radiochemical methods.^[8]

Theoretical calculation of activity coefficients

UNIQUAC Regression of activity coefficients (chloroform/methanol mixture)

Activity coefficients of electrolyte solutions may be calculated theoretically, using the Debye–Hückel equation or extensions such as the Davies equation,^[9] Pitzer equations^[10] or TCPC model.^{[11][12][13][14]} Specific ion interaction theory (SIT)^[15] may also be used.

For non-electrolyte solutions correlative methods such as UNIQUAC, NRTL, MOSCED or UNIFAC may be employed, provided fitted component-specific or model parameters are available. COSMO-RS is a theoretical method which is less dependent on model parameters as required information is obtained from quantum mechanics calculations specific to each molecule (sigma profiles) combined with a statistical thermodynamics treatment of surface segments.^[16]

For uncharged species, the activity coefficient γ₀ mostly follows a salting-out model:^[17]

$\log _{{10}}(\gamma _{{0}})=bI$

This simple model predicts activities of many species (dissolved undissociated gases such as CO₂, H₂S, NH₃, undissociated acids and bases) to high ionic strengths (up to 5 mol/kg). The value of the constant b for CO₂ is 0.11 at 10 °C and 0.20 at 330 °C.^[18]

For water as solvent, the activity a_w can be calculated using:^[17]

${\displaystyle \ln(a_{\mathrm {w} })={\frac {-\nu m}{55.51}}\varphi }$

where ν is the number of ions produced from the dissociation of one molecule of the dissolved salt, m is the molality of the salt dissolved in water, φ is the osmotic coefficient of water, and the constant 55.51 represents the molality of water. In the above equation, the activity of a solvent (here water) is represented as inversely proportional to the number of particles of salt versus that of the solvent.

Link to ionic diameter

The ionic activity coefficient is connected to the ionic diameter a by the formula obtained from Debye-Huckel theory of electrolytes:

${\displaystyle \log(\gamma _{i})=-{\frac {Az_{i}^{2}{\sqrt {I}}}{1+Ba{\sqrt {I}}}}}$

where A and B are constant, z_i is the valence number of the ion, and I is ionic strength.

Dependence on state parameters

The derivative of an activity coefficient with respect to temperature is related to excess molar enthalpy by

${\displaystyle {\bar {H}}_{i}^{E}=-RT^{2}{\frac {\partial }{\partial T}}\ln(\gamma _{i})}$

Similarly, the derivative of an activity coefficient with respect to pressure can be related to excess molar volume.

${\displaystyle {\bar {V}}_{i}^{E}=RT{\frac {\partial }{\partial P}}\ln(\gamma _{i})}$

Concentrated solutions of electrolytes

For concentrated ionic solutions the activity coefficient of the electrolyte is split into electric and statistical components.

The statistical part includes hydration index number h , the number of ions from the dissociation and the ratio r between the apparent molar volume of the electrolyte and the molar volume of water and molality b.

Concentrated solution statistical part of the activity coefficient is: ${\displaystyle ln\gamma _{s}={\frac {h-\nu }{\nu }}ln(1+{\frac {br}{55.5}})-{\frac {h}{\nu }}ln(1-{\frac {br}{55.5}})+{\frac {br(r+h-\nu )}{55.5(1+{\frac {br}{55.5}})}}}$^[19]

Application to chemical equilibrium

At equilibrium, the sum of the chemical potentials of the reactants is equal to the sum of the chemical potentials of the products. The Gibbs free energy change for the reactions, Δ_rG, is equal to the difference between these sums and therefore, at equilibrium, is equal to zero. Thus, for an equilibrium such as

α A + β B ⇌ σ S + τ T

${\displaystyle \Delta _{\mathrm {r} }G=\sigma \mu _{\mathrm {S} }+\tau \mu _{\mathrm {T} }-(\alpha \mu _{\mathrm {A} }+\beta \mu _{\mathrm {B} })=0\,}$

Substitute in the expressions for the chemical potential of each reactant:

${\displaystyle \Delta _{\mathrm {r} }G=\sigma \mu _{S}^{\ominus }+\sigma RT\ln a_{\mathrm {S} }+\tau \mu _{\mathrm {T} }^{\ominus }+\tau RT\ln a_{\mathrm {T} }-(\alpha \mu _{\mathrm {A} }^{\ominus }+\alpha RT\ln a_{\mathrm {A} }+\beta \mu _{\mathrm {B} }^{\ominus }+\beta RT\ln a_{\mathrm {B} })=0}$

Upon rearrangement this expression becomes

${\displaystyle \Delta _{\mathrm {r} }G=\left(\sigma \mu _{\mathrm {S} }^{\ominus }+\tau \mu _{\mathrm {T} }^{\ominus }-\alpha \mu _{\mathrm {A} }^{\ominus }-\beta \mu _{\mathrm {B} }^{\ominus }\right)+RT\ln {\frac {a_{\mathrm {S} }^{\sigma }a_{\mathrm {T} }^{\tau }}{a_{\mathrm {A} }^{\alpha }a_{\mathrm {B} }^{\beta }}}=0}$

The sum σμo
S + τμo
T − αμo
A − βμo
B is the standard free energy change for the reaction, Δ_rG^o. Therefore,

$\Delta _{r}G^{\ominus }=-RT\ln K$

K is the equilibrium constant. Note that activities and equilibrium constants are dimensionless numbers.

This derivation serves two purposes. It shows the relationship between standard free energy change and equilibrium constant. It also shows that an equilibrium constant is defined as a quotient of activities. In practical terms this is inconvenient. When each activity is replaced by the product of a concentration and an activity coefficient, the equilibrium constant is defined as

${\displaystyle K={\frac {[\mathrm {S} ]^{\sigma }[\mathrm {T} ]^{\tau }}{[\mathrm {A} ]^{\alpha }[\mathrm {B} ]^{\beta }}}\times {\frac {\gamma _{\mathrm {S} }^{\sigma }\gamma _{\mathrm {T} }^{\tau }}{\gamma _{\mathrm {A} }^{\alpha }\gamma _{\mathrm {B} }^{\beta }}}}$

where [S] denotes the concentration of S, etc. In practice equilibrium constants are determined in a medium such that the quotient of activity coefficient is constant and can be ignored, leading to the usual expression

${\displaystyle K={\frac {[\mathrm {S} ]^{\sigma }[\mathrm {T} ]^{\tau }}{[\mathrm {A} ]^{\alpha }[\mathrm {B} ]^{\beta }}}}$

which applies under the conditions that the activity quotient has a particular (constant) value.

References

1. IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "Activity coefficient".
2. DeHoff, Robert (2006). Thermodynamics in materials science (2nd ed.). Boca Raton, Fla.: CRC Taylor & Francis. pp. 230–231. ISBN 9780849340659.
3. Ibáñez, Jorge G.; Hernández Esparza, Margarita; Doría Serrano, Carmen; Singh, Mono Mohan (2007). Environmental Chemistry: Fundamentals. Springer. ISBN 978-0-387-26061-7.
4. Atkins, Peter; dePaula, Julio (2006). "Section 5.9, The activities of ions in solution". Physical Chemisrry (8th ed.). OUP. ISBN 9780198700722.
5. Guggenheim, E. A. (1928). "The Conceptions of Electrical Potential Difference between Two Phases and the Individual Activities of Ions". The Journal of Physical Chemistry. 33 (6): 842–849. doi:10.1021/j150300a003. ISSN 0092-7325.
6. IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "pH".
7. Rockwood, Alan L. (2015). "Meaning and Measurability of Single-Ion Activities, the Thermodynamic Foundations of pH, and the Gibbs Free Energy for the Transfer of Ions between Dissimilar Materials". ChemPhysChem. 16 (9): 1978–1991. doi:10.1002/cphc.201500044. ISSN 1439-4235.
8. Betts, R. H.; MacKenzie, Agnes N. "Radiochemical Measurements of Activity Coefficients in Mixed Electrolytes". Canadian Journal of Chemistry. 30 (2): 146–162. doi:10.1139/v52-020.
9. King, E. L. (1964). "Book Review: Ion Association, C. W. Davies, Butterworth, Washington, D.C., 1962". Science. 143 (3601): 37. doi:10.1126/science.143.3601.37. ISSN 0036-8075.
10. Grenthe, I.; Wanner, H. "Guidelines for the extrapolation to zero ionic strength" (PDF).
11. Ge, Xinlei; Wang, Xidong; Zhang, Mei; Seetharaman, Seshadri (2007). "Correlation and Prediction of Activity and Osmotic Coefficients of Aqueous Electrolytes at 298.15 K by the Modified TCPC Model". Journal of Chemical & Engineering Data. 52 (2): 538–547. doi:10.1021/je060451k. ISSN 0021-9568.
12. Ge, Xinlei; Zhang, Mei; Guo, Min; Wang, Xidong (2008). "Correlation and Prediction of Thermodynamic Properties of Nonaqueous Electrolytes by the Modified TCPC Model". Journal of Chemical & Engineering Data. 53 (1): 149–159. doi:10.1021/je700446q. ISSN 0021-9568.
13. Ge, Xinlei; Zhang, Mei; Guo, Min; Wang, Xidong (2008). "Correlation and Prediction of Thermodynamic Properties of Some Complex Aqueous Electrolytes by the Modified Three-Characteristic-Parameter Correlation Model". Journal of Chemical & Engineering Data. 53 (4): 950–958. doi:10.1021/je7006499. ISSN 0021-9568.
14. Ge, Xinlei; Wang, Xidong (2009). "A Simple Two-Parameter Correlation Model for Aqueous Electrolyte Solutions across a Wide Range of Temperatures". Journal of Chemical & Engineering Data. 54 (2): 179–186. doi:10.1021/je800483q. ISSN 0021-9568.
15. "Project: Ionic Strength Corrections for Stability Constants". IUPAC. Archived from the original on 29 October 2008. Retrieved 2008-11-15.
16. Klamt, Andreas (2005). COSMO-RS from quantum chemistry to fluid phase thermodynamics and drug design (1st ed.). Amsterdam: Elsevier. ISBN 978-0-444-51994-8.
17. N. Butler, James (1998). Ionic equilibrium: solubility and pH calculations. New York, NY [u.a.]: Wiley. ISBN 9780471585268.
18. Ellis, A. J.; Golding, R. M. (1963). "The solubility of carbon dioxide above 100 degrees C in water and in sodium chloride solutions". American Journal of Science. 261 (1): 47–60. doi:10.2475/ajs.261.1.47. ISSN 0002-9599.
19. Kortüm, G. (1960). "The Structure of Electrolytic Solutions, herausgeg. von W. J. Hamer. John Wiley & Sons, Inc., New York; Chapman & Hall, Ltd., London 1959. 1. Aufl., XII, 441 S., geb. $ 18.50". Angewandte Chemie. 72 (24): 97. doi:10.1002/ange.19600722427. ISSN 0044-8249.

External links

• AIOMFAC online-model An interactive group-contribution model for the calculation of activity coefficients in organic-inorganic mixtures.
• Electrochimica Acta Single-ion activity coefficients