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Consider a gas of hard spheres with the 2-body interaction $$ \begin{aligned} V\left(\left|\mathbf{r}_i-\mathbf{r}_j\right|\right) & =0, & & \left|\mathbf{r}_i-\mathbf{r}_j\right|>a, \\ & =\infty, & & \left|\mathbf{r}_i-\mathbf{r}_j\right|<a . \end{aligned} $$ Using the classical partition function, calculate the average energy at a given temperature and density (thermodynamics: the internal energy). On the basis of simple physical arguments, would you expect this same simple answer to also result from a calculation with the quantum mechanical partition function?

   Consider a gas of hard spheres with the 2-body interaction
$$
\begin{aligned}
V\left(\left|\mathbf{r}_i-\mathbf{r}_j\right|\right) & =0, & & \left|\mathbf{r}_i-\mathbf{r}_j\right|>a, \\
& =\infty, & & \left|\mathbf{r}_i-\mathbf{r}_j\right|<a .
\end{aligned}
$$

Using the classical partition function, calculate the average energy at a given temperature and density (thermodynamics: the internal energy).

On the basis of simple physical arguments, would you expect this same simple answer to also result from a calculation with the quantum mechanical partition function?
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Problems and Solutions on Thermodynamics and Statistical Mechanics
Problems and Solutions on Thermodynamics and Statistical Mechanics
U.S.T. of China… 1st Edition
Chapter 2, Problem 144 ↓

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e., their centers are less than a distance \(a\) apart). The potential energy \(V\) is zero when the spheres are apart and infinite when they overlap. This means that the particles cannot occupy the same space, leading to a hard-core repulsion.  Show more…

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Consider a gas of hard spheres with the 2-body interaction $$ \begin{aligned} V\left(\left|\mathbf{r}_i-\mathbf{r}_j\right|\right) & =0, & & \left|\mathbf{r}_i-\mathbf{r}_j\right|>a, \\ & =\infty, & & \left|\mathbf{r}_i-\mathbf{r}_j\right|<a . \end{aligned} $$ Using the classical partition function, calculate the average energy at a given temperature and density (thermodynamics: the internal energy). On the basis of simple physical arguments, would you expect this same simple answer to also result from a calculation with the quantum mechanical partition function?
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Key Concepts

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Quantum Partition Function
The quantum partition function extends the classical approach to systems where quantum effects are non-negligible. It takes into account quantum statistics and the proper counting of states (such as symmetrization or antisymmetrization for bosons and fermions, respectively). Although in the high temperature and low density limit the quantum calculations tend to recover the classical results, deviations may appear at lower temperatures or higher densities due to quantum effects.
Internal Energy Calculation
Calculating the internal energy involves using the partition function to compute the average energy of the system. In the case of a classical gas of hard spheres, the interaction potential merely restricts the spatial configurations, leading to the internal energy corresponding solely to the kinetic energy of the particles, typically given by (3/2)Nk_BT in three dimensions according to the equipartition theorem.
Hard Sphere Interaction
This concept refers to a simplified model in which particles are represented as spheres that interact via a potential that is infinite when the spheres overlap and zero otherwise. This model is used to capture the idea of excluded volume and is fundamental for understanding non-ideal gas behavior in both classical and quantum statistical mechanics.
Classical Partition Function
The classical partition function is a central concept in statistical mechanics. It is a sum (or integral) over all possible microstates of the system, weighted by the Boltzmann factor. For a gas of hard spheres, it incorporates the effects of the hard-core potential by excluding configurations where particles overlap. From this function, key thermodynamic quantities like internal energy can be derived using relationships such as the equipartition theorem.

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1.4. In a classical gas of hard spheres (of diameter D), the spatial distribution of the particles is no longer uncorrelated. Roughly speaking, the presence of n particles in the system leaves only a volume (V - nv₀) available for the (n + 1)th particle; clearly, v₀ would be proportional to D³. Assuming that Nv₀ ≪ V, determine the dependence of Ω(N, V, E) on V (compare to equation (1.4.1)) and show that, as a result of this, V in the ideal-gas law (1.4.3) gets replaced by (V - b), where b is four times the actual volume occupied by the particles. 1.5. Read Appendix A and establish formulae (1.4.15) and (1.4.16). Estimate the importance of the linear term in these formulae, relative to the main term (π/6)ε*^(3/2), for an oxygen molecule confined to a cube of side 10 cm; take ε = 0.05 eV.

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