Gas in a box


Gas in a box

In quantum mechanics, the results of the quantum particle in a box can be used to look at the equilibrium situation for a quantum ideal gas in a box which is a box containing a large number of molecules which do not interact with each other except for instantaneous thermalizing collisions. This simple model can be used to describe the classical ideal gas as well as the various quantum ideal gases such as the ideal massive Fermi gas, the ideal massive Bose gas as well as black body radiation which may be treated as a massless Bose gas.

Using the results from either Maxwell-Boltzmann statistics, Bose-Einstein statistics or Fermi-Dirac statistics, and considering the limit of a very large box, the Thomas-Fermi approximation is used to express the degeneracy of the energy states as a differential, and summations over states as integrals. This enables thermodynamic properties of the gas to be calculated with the use of the partition function or the grand partition function. These results will be applied to both massive and massless particles. More complete calculations will be left to separate articles, but some simple examples will be given in this article.

Thomas-Fermi approximation for the degeneracy of states

For both massive and massless particles in a box, the states of a particle areenumerated by a set of quantum numbers ["n""x", "n""y", "n""z"] . The absolute value of the momentum is given by:

:p=frac{h}{2L}sqrt{n_x^2+n_y^2+n_z^2}~~~~~~~~~n_i=1,2,3,ldots ~~~~~~ for ~ i=x, y, ~or ~ z

where "h " is Planck's constant and "L " is the length of a side of the box.Each possible state of a particle can be thought of as a point on a 3-dimensionalgrid of positive integers. The distance from the origin to any point will be

:n=sqrt{n_x^2+n_y^2+n_z^2}=frac{2Lp}{h}

Suppose each set of quantum numbers specify "f " states where "f " isthe number of internal degrees of freedom of the particle that can be altered bycollision. For example, a spin 1/2 particle would have "f=2", one for each spinstate. For large values of "n ", the number of states with absolute value of momentum less than or equal to "p " from the above equation is approximately

:g=left(frac{f}{8} ight) frac{4}{3}pi n^3 = frac{4pi f}{3} left(frac{Lp}{h} ight)^3

which is just "f " times the volume of a sphere of radius "n " divided by eightsince only the octant with positive "ni " is considered. Using a continuum approximation, the number ofstates with absolute value of momentum between "p " and "p+dp " istherefore

:dg=frac{pi}{2}~f n^2,dn = frac{4pi fV}{h^3}~ p^2,dp

where "V=L3 " is the volume of the box. Notice that in using thiscontinuum approximation, the ability to characterize the low-energystates is lost, including the ground state where "ni =1". For most cases thiswill not be a problem, but when considering Bose-Einstein condensation, in which alarge portion of the gas is in or near the ground state, theability to deal with low energy states becomes important.

Without using the continuum approximation, the number of particles withenergy εi is given by

: N_i = frac{g_i}{Phi}

where:

::with β = "1/kT ", Boltzmann's constant "k", temperature "T", and chemical potential "μ". Using the continuum approximation, the number of particles "dN " with energy between"E " and "E+dE " is now written as:

:dN= frac{dg}{Phi}

The energy distribution function

Using the results derived from the previous sections of this article, some distribution functions for the "gas ina box" can now be determined. The distribution function for any variable A is PAdA andis equal to the fraction of particles which have values for "A " between"A " and "A+dA"

:P_A~dA = frac{dN}{N_T} = frac{dg}{N_TPhi}

where N_T is total number of particles.

It follows that:

:int_A P_A~dA = 1

The distribution function for the absolute value of the momentum is:

:P_p~dp = frac{Vf}{N_T}~frac{4pi}{h^3Phi}~p^2dp

and the distribution function for the energy "E " is:

:P_E~dE = P_pfrac{dp}{dE}~dE

For a particle in a box (and for a free particle as well), the relationship between energy "E " and momentum "p " is different for massive and massless particles. For massive particles,

: E=frac{p^2}{2m}

while for massless particles,

:E=pc,

where "m " is the mass of the particle and "c " is the speed of light.Using these relationships,

  • For massive particles

    :dg = left(frac{Vf}{Lambda^3} ight)frac{2}{sqrt{pi~eta^{3/2}E^{1/2}~dE

    :P_E~dE = frac{1}{N_T}left(frac{Vf}{Lambda^3} ight)frac{2}{sqrt{pi~frac{eta^{3/2}E^{1/2{Phi}~dE

    where Λ is the thermal wavelength or
    thermal de Broglie wavelengthof the gas.

    :Lambda =sqrt{frac{h^2 eta }{2pi m

    This is an important quantity, since when Λ is on the order of theinter-particle distance (V/N_T)^{1/3}, quantum effects begin todominate and the gas can no longer be considered to be a Maxwell-Boltzmann gas.See
    configuration integralfor a detailed derivation of the expression fordisplaystyle Lambda.

  • For massless particles

    :dg = left(frac{Vf}{Lambda^3} ight)frac{1}{2}~eta^3E^2~dE

    :P_E~dE = frac{1}{N_T}left(frac{Vf}{Lambda^3} ight)frac{1}{2}~frac{eta^3E^2}{Phi}~dE

    where Λ is now the thermal wavelength for massless particles.

    :Lambda = frac{cheta}{2,pi^{1/3

pecific examples

The following sections give an example of results for some specific cases.

Massive Maxwell-Boltzmann particles

For this case:

:Phi=e^{eta(E-mu)},

Integrating the energy distribution function and solving for N_T gives

:N_T= left(frac{Vf}{Lambda^3} ight),,e^{etamu}

Substituting into the original energy distribution function gives

:P_E~dE = 2 sqrt{frac{eta^3 E}{pi~e^{-eta E}~dE

which are the same results obtained classically for the
Maxwell-Boltzmann distribution. Further results can be found in the article on the
classical ideal gas.

Massive Bose-Einstein particles

For this case:

:Phi=e^{eta epsilon}/z-1,

where "z" is defined as

:z=e^{etamu},

Integrating the energy distribution function and solving for N_T gives the particle number

:N_T= left(frac{Vf}{Lambda^3} ight) extrm{Li}_{3/2}(z)

where Lis(z) is the polylogarithm function and Λ is the
thermal wavelength. The polylogarithm term must always be positiveand real, which means its value will go from 0 to ζ(3/2) as "z " goes from0 to 1. As the temperature drops towards zero, Λ will become larger and larger,until finally Λ will reach a critical value Λc where "z=1" and

:N_T = left(frac{Vf}{Lambda_c^3} ight)zeta(3/2)

The temperature at which Λ=Λc is the critical temperature. Fortemperatures below this critical temperature, the above equation for the particle numberhas no solution. The critical temperature is the temperature at which a Bose-Einsteincondensate begins to form. The problem is, as mentionedabove, that the ground state has been ignored in the continuum approximation. It turnsout, however, that the above equation for particle number expresses the number of bosons in excited statesrather well, and thus:

:N_T=frac{g_0z}{1-z}+left(frac{Vf}{Lambda^3} ight) extrm{Li}_{3/2}(z)

where the added term is the number of particles in the ground state. (The groundstate energy has been ignored.) This equation will hold down to zero temperature.Further results can be found in the article on the ideal Bose gas.

Massless Bose-Einstein particles (e.g. black body radiation)

For the case of massless particles, the massless energy distribution function must be used. It is convenient to convert this function to a frequency distribution function:

:P_ u~d u = frac{h^2}{N_T}left(frac{Vf}{Lambda^3} ight)frac{1}{2}~frac{eta^3 u^2}{e^{(h u-mu)/kT}-1}~d u

where Λ is the thermal wavelength for massless particles. The spectral energy density (energy per unit volume per unit frequency) is then

:U_ u~d u = left(frac{N_T,h u}{V} ight) P_ u~d u = frac{4pi f h u^3 }{c^3}~frac{1}{e^{(h u-mu)/kT}-1}~d u

Other thermodynamic parameters may be derived analogously to the case for massive particles. For example, integrating the frequency distribution function and solving for N_T gives the number of particles:

:N_T=frac{16,pi V}{c^3h^3eta^3},mathrm{Li}_3left(e^{mu/kT} ight)

The most common massless Bose gas is a photon gas in a black body. Taking the "box" to be a black body cavity, the photons are continually being absorbed and re-emitted by the walls. When this is the case, the number of photons is not conserved. In the derivation of Bose-Einstein statistics, when the restraint on the number of particles is removed, this is effectively the same as setting the chemical potential ("μ") to zero. Furthermore, since photons have two spin states, the value of "f" is 2. The spectral energy density is then

:U_ u~d u = frac{8pi h u^3 }{c^3}~frac{1}{e^{h u/kT}-1}~d u

which is just the spectral energy density for Planck's law of black body radiation. Note that the Wien distribution is recovered if this procedure is carried out for massless Maxwell-Boltzmann particles, which approximates a Planck's distribution for high temperatures or low densities.

In certain situations, the reactions involving photons will result in the conservation of the number of photons (e.g. light-emitting diodes, "white" cavities). In these cases, the photon distribution function will involve a non-zero chemical potential. (Hermann 2005)

Another massless Bose gas is given by the Debye model for heat capacity. This considers a gas of phonons in a box and differs from the development for photons in that the speed of the phonons is less than light speed, and there is a maximum allowed wavelength for each axis of the box. This means that the integration over phase space cannot be carried out to infinity, and instead of results being expressed in polylogarithms, they are expressed in the related Debye functions.

Massive Fermi-Dirac particles (e.g. electrons in a metal)

For this case:

:Phi=e^{eta(E-mu)}+1,

Integrating the energy distribution function gives

:N_T=left(frac{Vf}{Lambda^3} ight)left [- extrm{Li}_{3/2}(-z) ight]

Where again, Lis(z) is the polylogarithm function and Λ is the
thermal de Broglie wavelength. Further results can be found in the article on theideal Fermi gas.

References

* cite journal| last = Herrmann| first = F.| coauthors = Würfel, P.
year = 2005| month = August
title = Light with nonzero chemical potential| journal = American Journal of Physics
volume = 73| issue = 8| pages = 717–723| doi = 10.1119/1.1904623
url = http://scitation.aip.org/journals/doc/AJPIAS-ft/vol_73/iss_8/717_1.html
accessdate = 2006-11-20

* cite book |last=Huang |first=Kerson |authorlink=
title=Statistical Mechanics |year=1967 |publisher=John Wiley & Sons |location=New York

* cite book |last=Isihara |first=A.
title=Statistical Physics |year=1971 |publisher=Academic Press |location=New York

* cite book |last=Landau |first=L. D.|coauthors=E. M. Lifshitz
title=Statistical Physics |edition=3rd Edition Part 1 |year=1996
publisher=Butterworth-Heinemann |location=Oxford

* cite journal| last = Yan| first = Zijun| year = 2000
title = General thermal wavelength and its applications| journal = Eur. J. Phys.
volume = 21| pages = 625–631|doi=10.1088/0143-0807/21/6/314
url = http://www.iop.org/EJ/article/0143-0807/21/6/314/ej0614.pdf
format = PDF| accessdate = 2006-11-20


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