Buffer Capacity Calculator
Calculate buffer capacity beta using the Van Slyke equation from pKa, concentration, and pH.
What Buffer Capacity Measures
A buffer resists pH change, but not equally at every pH. Buffer capacity β quantifies that resistance: how many moles of strong acid or base must be added per litre to shift the pH by one unit. Higher β means a more resilient buffer.
The expression peaks sharply when [H+] equals Ka — that is, when pH = pKa. At that point the weak acid and its conjugate base are present in equal amounts, so the system can absorb added acid or base with equal facility. The maximum simplifies neatly:
That gives a useful rule of thumb: a 0.1 M buffer at its pKa has a capacity of about 0.058 mol/L per pH unit, regardless of which acid it is. Capacity scales linearly with concentration, so doubling the buffer concentration doubles β.
The Useful Range
| pH relative to pKa | Ratio base:acid | β as % of βmax |
|---|---|---|
| pKa | 1:1 | 100% |
| pKa ± 0.5 | ~3:1 | ~80% |
| pKa ± 1 | 10:1 | ~33% |
| pKa ± 2 | 100:1 | ~4% |
This is the basis of the familiar “pKa ± 1” rule. Beyond one unit either side, capacity has fallen to about a third of maximum and continues dropping steeply — at two units away the buffer is doing almost nothing. Choosing a buffer whose pKa is close to the target pH matters far more than choosing a high concentration.
Worked Examples
Common Mistakes
The only question that matters is how close the pKa is to your working pH. A phosphate buffer is excellent at pH 7.2 and nearly useless at pH 5.0, where acetate would be far better.
Capacity scales linearly with concentration but falls steeply with distance from pKa. Two pH units away you would need roughly 25 times the concentration to match a well-chosen buffer.
pKa values shift with ionic strength and temperature. Tris is notorious — its pKa changes by about −0.03 per °C, so a buffer set at room temperature drifts noticeably at 37°C.
Diluting a buffer leaves pH nearly unchanged, since the acid-to-base ratio is preserved. But capacity falls proportionally, so the diluted buffer is far more easily overwhelmed.
Frequently Asked Questions
Formula Explorer connections
Interpretation: This relationship connects hydrogen-ion activity, dissociation, conjugate ratios or titration stoichiometry to acid–base behavior. Assumption: Concentration approximates activity mainly in dilute solutions. Temperature, ionic strength, acid strength and equilibrium approximations affect accuracy.