Physic Labs

Classical statistical mechanics

Maxwell–Boltzmann speed distribution

Explore how temperature and molar mass change molecular speeds, compare the histogram with f(v)=4π(M/2πRT)3/2v2e−Mv2/(2RT)f(v)=4\pi(M/2\pi RT)^{3/2}v^2e^{-Mv^2/(2RT)}, and measure vrmsv_{rms}.

Undergraduate

Equipment

  • Ideal-gas sample of 6,000 molecules and a speed histogram
  • Temperature and molar-mass controls with a theoretical distribution curve

Procedure

  1. Choose a gas and temperature

    Set the molar mass and temperature. Each molecular velocity component is sampled from a thermal Gaussian distribution.

  2. Read the speed histogram

    The bars show normalized measured speeds; the smooth curve is the Maxwell–Boltzmann probability density for the selected gas and temperature.

  3. Measure the root-mean-square speed

    Compare the sample value with vrms=3RT/Mv_{rms}=\sqrt{3RT/M}. Draw a new sample and note the finite-sample variation.

Simulation

Experiment history

James Clerk Maxwell derived the distribution of molecular speeds in 1860 while developing the kinetic theory of gases. His result connected a statistical description of many molecules with measurable macroscopic properties such as temperature and pressure. Ludwig Boltzmann extended the statistical-mechanical foundations during the 1870s, clarifying how molecular probability and the distribution of energy underpin thermodynamic behavior. The modern Maxwell–Boltzmann speed law combines these classical results for a dilute ideal gas in thermal equilibrium.

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