In this section we computed the single-particle translational partition function,Ztr, by summing over all definite-energy wave functions. An alternative approach, however, is to sum over all position and momentum vectors, as we did in Section 2.5. Because position and momentum are continuous variables, the sums are really integrals, and we need to slip a factor of 1h3to get a unitless number that actually counts the independent wavefunctions. Thus we might guess the formula

role="math" localid="1647147005946" Ztr=1h3d3rd3pe-EtrkT

where the single integral sign actually represents six integrals, three over the position components and three over the momentum components. The region of integration includes all momentum vectors, but only those position vectors that lie within a box of volume V. By evaluating the integrals explicitly, show that this expression yields the same result for the translational partition function as that obtained in the text.

Short Answer

Expert verified

The translational partition function is given byZtr=VvQ.

Step by step solution

01

Step 1. Given information

The translational partition function is given by

Ztr=1h3d3rd3pe-EtrkT...........................(1)

02

Step 2. Calculation

As the translational kinetic energy of the molecules does not depend on the position, the integrand is also independent of the position and the integral over the position variables only yields the total volume Vof the box.

The expression for the translational energy of the gas molecules is given by

Etr=px22m+py22m+pz22m..................(2)

Here, x-,y- and z- denotes the three components of the momentum.

Substitute the expression of energy into equation (1) and solve to calculate the value of the translational partition function.

role="math" localid="1647147921072" Ztr=Vh30dpxe-px22mkT0dpye-py22mkT0dpze-pz22mkT=Vh3π·2mkTπ·2mkTπ·2mkT=Vh32πmkT32........................(3)

The quantum volume of the gas molecules is given by

vQ=h22πmkT32........................(4)

Substitute the value of the quantum volume from equation (4) into equation (3) to obtain the required translational partition function.

Ztr=Vh32πmkT32=V1h22πmkT32=VvQ

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Most popular questions from this chapter

Each of the hydrogen atom states shown in Figure 6.2 is actually twofold degenerate, because the electron can be in two independent spin states, both with essentially the same energy. Repeat the calculation given in the text for the relative probability of being in a first excited state, taking spin degeneracy into account. Show that the results are unaffected.

Prove that the probability of finding an atom in any particular energy level is P(E)=(1/Z)e-F/kT, whereF=E-TS and the "'entropy" of a level is k times the logarithm of the number of degenerate states for that level.

Use the Maxwell distribution to calculate the average value of v2for the molecules of an ideal gas. Check that your answer agrees with equation 6.41.

The analysis of this section applies also to liner polyatomic molecules, for which no rotation about the axis of symmetry is possible. An example is CO2, with =0.000049eV. Estimate the rotational partition function for a CO2molecule at room temperature. (Note that the arrangement of the atoms isOCO, and the two oxygen atoms are identical.)

In the real world, most oscillators are not perfectly harmonic. For a quantum oscillator, this means that the spacing between energy levels is not exactly uniform. The vibrational levels of an H2 molecule, for example, are more accurately described by the approximate formula

Enϵ1.03n-0.03n2,n=0,1,2,

where ϵ is the spacing between the two lowest levels. Thus, the levels get closer together with increasing energy. (This formula is reasonably accurate only up to about n = 15; for slightly higher n it would say that En decreases with increasing n. In fact, the molecule dissociates and there are no more discrete levels beyond n 15.) Use a computer to calculate the partition function, average energy, and heat capacity of a system with this set of energy levels. Include all levels through n = 15, but check to see how the results change when you include fewer levels Plot the heat capacity as a function of kT/ϵ. Compare to the case of a perfectly harmonic oscillator with evenly spaced levels, and also to the vibrational portion of the graph in Figure 1.13.

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