Maxwell Velocity Distribution
The Maxwell-Boltzmann distribution describes the distribution of particle speeds in an ideal gas at thermal equilibrium. Derived independently by James Clerk Maxwell (1860) and Ludwig Boltzmann (1868), it is a cornerstone of statistical mechanics and kinetic theory.
The Distribution Function
The probability that a molecule has a speed between and is:
The shape of this curve comes from two competing effects:
| Factor | Expression | Meaning |
|---|---|---|
| Phase-space factor | More ways to arrange a velocity vector at higher speeds (surface area of a sphere in velocity space) | |
| Boltzmann factor | Exponential penalty for high kinetic energy |
The peak arises where these two factors balance.
Three Characteristic Speeds
- Most probable speed — the peak of the distribution
- Mean speed — the arithmetic average, always slightly above
- RMS speed — root-mean-square speed, related to the average kinetic energy via
They always satisfy regardless of gas or temperature.
Mean Speed: 476.2 m/s
RMS Speed: 516.8 m/s
Most Probable Speed: 422.0 m/s
Things to Try
- Increase temperature from 100 K to 1000 K — watch the peak flatten and shift right. Higher temperature means molecules are faster on average, but the distribution also broadens.
- Switch between gases at the same temperature — lighter molecules (H₂, He) move much faster than heavier ones (N₂, O₂).
- Compare the three speed lines — notice they always appear in the same order: (green) < (cyan) < (yellow).
- Ghost reference — the faint dotted curve always shows the same gas at 300 K, making it easy to see how your settings differ from room temperature.
Real-World Applications
- Atmospheric escape: On small, warm bodies (like the Moon), the tail of the speed distribution for light gases exceeds escape velocity, which is why the Moon has essentially no atmosphere.
- Thermal neutrons: Nuclear reactors moderate fast neutrons to thermal energies; the resulting speed distribution is Maxwell-Boltzmann at the moderator temperature.
- Chemistry: Reaction rates depend on the fraction of molecules with kinetic energy above the activation energy — the high-speed tail of this distribution (Arrhenius equation).
- Stellar atmospheres: Spectral line broadening due to thermal Doppler shifts follows a Gaussian derived from this distribution.
Assumptions of the model — The Maxwell-Boltzmann distribution assumes an ideal gas: no intermolecular forces, elastic collisions only, and thermal equilibrium. For very dense gases, low temperatures, or quantum particles, one must use the Fermi-Dirac (fermions) or Bose-Einstein (bosons) distributions instead.