Stokes-Einstein Diffusion Calculator
Calculate diffusion coefficient or hydrodynamic radius using the Stokes-Einstein equation.
What the Equation Describes
The Stokes–Einstein relation connects two things that seem unrelated: the random thermal motion of a particle, and the viscous drag opposing it. Einstein showed that the same molecular collisions that push a particle around also resist its motion, and the balance between them fixes the diffusion coefficient.
| Term | Meaning | Value / units |
|---|---|---|
| D | Diffusion coefficient | m²/s |
| kB | Boltzmann constant | 1.381 × 10−23 J/K |
| T | Absolute temperature | K — thermal driving energy |
| η | Solvent viscosity | Pa·s — about 0.00089 for water at 25°C |
| r | Hydrodynamic radius | m — the particle plus its solvation shell |
| 6π | Stokes drag factor | For a sphere with no-slip boundary |
The inverse relationship with radius has an important consequence: D scales with 1/r, not 1/r³. A particle eight times heavier is only twice as large in radius, so it diffuses only half as slowly. Diffusion is therefore far less size-discriminating than intuition suggests, which is why size-exclusion chromatography separates poorly on diffusion alone.
Hydrodynamic Radius
The r in this equation is not the crystallographic radius. It is the effective radius of the particle together with the solvent molecules that move with it. For proteins the hydrodynamic radius is typically 10–20% larger than the radius calculated from crystal structure, and for highly charged or extended molecules the difference is larger still.
This is why the equation is used in reverse so often. Dynamic light scattering measures D directly, and rearranging gives r — the standard method for sizing nanoparticles, micelles and protein aggregates in solution rather than in a crystal.
Worked Examples
Common Mistakes
The equation requires hydrodynamic radius, which includes the bound solvation shell. Using a crystal radius systematically overestimates D, typically by 10–20% for proteins.
The 6π factor assumes a sphere. Rods, discs and unfolded polymers deviate significantly, and the calculated radius becomes an equivalent-sphere approximation rather than a real dimension.
Raising temperature increases D twice over — directly through T, and indirectly because η falls. Water’s viscosity drops roughly 2% per degree near room temperature, so the net effect is much larger than the T term alone.
The relation assumes a dilute particle in a continuous solvent. Inside cells, or in gels and concentrated solutions, anomalous diffusion applies and Stokes–Einstein substantially overestimates mobility.
Frequently Asked Questions
Formula Explorer connections
Interpretation: This formula connects concentration, time, temperature or transport to the speed of a chemical process. Assumption: The reaction order and mechanism must match the model. Temperature, catalyst, mixing and mass-transfer limitations can alter the observed rate.