Activity coefficient calculator explained
This calculator lets you quickly estimate ionic activity coefficients using the Debye-Huckel limiting law. Enter the solvent constant , the ion charge number {charge}, and the ionic strength {ionic_strength}; the tool computes and the corresponding activity coefficient {coefficient} so you can benchmark lab measurements or design electrolyte solutions.
Use it when you need to know how strongly non-ideal behavior suppresses thermodynamic activities in dilute solutions, especially for comparing mono- and multivalent ions during speciation studies or electrochemical design work.
How the conversion works
For dilute electrolytes the limiting law states:
where depends on temperature and solvent dielectric constant (0.509 for water at 25 deg C), is the ionic charge number, and is the ionic strength in mol/L. Solving for is therefore:
The calculator keeps the logarithm base consistent and handles very small numbers without rounding errors.
Units and conversions
| Quantity | Symbol | Units | Notes |
|---|---|---|---|
| Solvent constant | dimensionless | 0.509 for water at 25 deg C, 0.491 at 18 deg C. | |
| Charge number | unitless integer | Use the algebraic value (+2 for Ca, -1 for Cl). | |
| Ionic strength | mol/L | . | |
| Activity coefficient | dimensionless | Applies to mean ionic activity for electrolytes. |
Worked examples
- Monovalent electrolyte check
, , mol/L.
so . Activities are therefore 11% lower than concentrations.
- Calcium ion in moderately ionic water
, , mol/L.
giving . The calculator reports this instantly and highlights how divalent ions depart from ideality sharply.
Tips and pitfalls
- Debye-Huckel limiting law holds reliably only for mol/L; switch to extended models for higher ionic strength.
- Always specify whether you need individual ionic coefficients or the mean ionic coefficient for salts.
- Update if temperature deviates significantly from 25 deg C or if the solvent is not water.
- Use measured ionic strength from conductivity or detailed composition instead of guessing to avoid compounding errors.