Maxwell-Boltzmann distribution for three different temperatures
. Experimental verification of the Maxwell-Boltzmann distribution by
Ciro Santilli 37 Updated 2025-07-16
Most applications of the Maxwell-Boltzmann distribution confirm the theory, but don't give a very direct proof of its curve.
Here we will try to gather some that do.
Measured particle speeds with a rotation barrel! OMG, pre electromagnetism equipment?
- bingweb.binghamton.edu/~suzuki/GeneralPhysNote_PDF/LN19v7.pdf
- chem.libretexts.org/Bookshelves/Physical_and_Theoretical_Chemistry_Textbook_Maps/Book%3A_Thermodynamics_and_Chemical_Equilibrium_(Ellgen)/04%3A_The_Distribution_of_Gas_Velocities/4.07%3A_Experimental_Test_of_the_Maxwell-Boltzmann_Probability_Density
edisciplinas.usp.br/pluginfile.php/48089/course/section/16461/qsp_chapter7-boltzman.pdf mentions
- sedimentation
- reaction rate as it calculates how likely it is for particles to overcome the activation energy
Bibliography:
This is not a truly "fundamental" constant of nature like say the speed of light or the Planck constant.
Rather, it is just a definition of our Kelvin temperature scale, linking average microscopic energy to our macroscopic temperature scale.
The way to think about that link is, at 1 Kelvin, each particle has average energy:per degree of freedom.
For an ideal monatomic gas, say helium, there are 3 degrees of freedom. so each helium atom has average energy:
Another conclusion is that this defines temperature as being proportional to the total energy. E.g. if we had 1 helium atom at 2 K then we would have about energy, 3 K and so on.
This energy is of course just an average: some particles have more, and others less, following the Maxwell-Boltzmann distribution.
chemistry.stackexchange.com/questions/7696/how-do-i-distinguish-between-internal-energy-and-enthalpy/7700#7700 has a good insight:
To summarize, internal energy and enthalpy are used to estimate the thermodynamic potential of the system. There are other such estimates, like the Gibbs free energy G. Which one you choose is determined by the conditions and how easy it is to determine pressure and volume changes.
Adds up chemical energy and kinetic energy.
The sum is of interest when thinking about reactions because chemical reactions can change the number of molecules involved, and therefore the pressure.
To predict if a reaction is spontaneous or not, negative enthalpy is not enough, we must also consider entropy via Gibbs free energy.
At least from the formula we see that:
- the more exothermic, the more likely it is to occur
- if the entropy increases, the higher the temperature, the more likely it is to occur
- otherwise, the lower the temperature the more likely it is to occur
A prototypical example of reaction that is exothermic but does not happen at any temperature is combustion.
Lab 7 - Gibbs Free Energy by MJ Billman (2020)
Source. Shows the shift of equilibrium due to temperature change with a color change in a HCl CoCl reaction. Unfortunately there are no conclusions because its student's homework.I think these are the ones where , i.e. enthalpy and entropy push the reaction in different directions. And so we can use temperature to move the Chemical equilibrium back and forward.
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