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The Gibbs paradox
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Molecular collision within an ideal gas originates from an intrinsic short-range repulsive interaction. The collision reduces the average accessible physical space for a single molecule and this has a direct consequence on the entropy of the gas. The accessibility of a molecule to a spatial coordinate (x, y, z) inside the system depends on the local molecular density. By considering mechanical equilibrium between a system and a reservoir, the probability of the system in state i with volume vi is shown to be proportional to exp(-vi/v0) where v0 is the average volume per molecule. Incorporating this factor into the single particle partition function automatically leads to an N-particle entropy that is extensive without applying the N! correction factor. The exp(-vi/v0) factor plays a similar role in describing the volume distribution as the Boltzmann factor which governs the energy distribution.
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Cited by 1 Pith paper
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Solving the Gibbs Paradox by Local Free Space and Collision Potential
The paper derives a new formula for gas-mixture entropy increase that depends on molecular properties, but the derivation contains algebraic errors and predicts negative entropy for common gas pairs.
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