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American Journal of Physics

Another look at the quantum mechanical entropy of mixing

Dennis Dieks, Vincent van Dijk

Published May 1, 1988• 18 citations
Publisher

Abstract

It is often stated that the Gibbs ‘‘paradox’’ is resolved or at least alleviated in quantum mechanics because the value of the quantum mechanical entropy of mixing continuously approaches zero if the difference between the particles that are being mixed is made to vanish (i.e., if the value of the inproduct of the respective quantum states goes to one). In this article, the justification of that claim is discussed. It is pointed out that, strictly speaking, an entropy of mixing is not defined if the quantum states of the particles are no longer orthogonal. It seems, therefore, that from a fundamental point of view the Gibbs ‘‘paradox’’ is there no less in quantum mechanics than in classical statistical mechanics.

DOI
10.1119/1.15571

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It is often stated that the Gibbs ‘‘paradox’’ is resolved or at least alleviated in quantum mechanics because the value of the quantum mechanical entropy of mixing continuously approaches zero if the difference between the particles that are being mixed is made to vanish (i.e., if the value of the inproduct of the respective quantum states goes to one). In this article, the justification of that claim is discussed. It is pointed out that, strictly speaking, an entropy of mixing is not defined if the quantum states of the particles are no longer orthogonal. It seems, therefore, that from a fundamental point of view the Gibbs ‘‘paradox’’ is there no less in quantum mechanics than in classical statistical mechanics.
The issue of the Gibbs paradox is that when considering the mixing of two gases within classical thermodynamics, the entropy of mixing is a discontinuous function of the difference between the gases: it is finite for no matter how small difference, but vanishes for identical gases. The resolution offered in literature with help of quantum mixing entropy was later on shown to be unsatisfactory precisely where it sought to resolve the paradox. Within quantum thermodynamics entropy looses its dominant place. It is argued that the target of the paradox is shifted to the decrease of the available work upon mixing (mixing work), which in contrast to entropy is an unambiguous quantity. For almost identical gases the mixing work continuously goes to zero, thus resolving the paradox. In this approach the concept of ``difference between the gases'' attains a clear operational meaning related to possibilities of controlling the involved quantum states. The difficulties which prevent the resolution of the paradox in its entropic formulation do not arise here. The mixing work can increase when less precise operations are allowed. In contrast to the classical situation, in the quantum case the amount of mixing work can also increase when decreasing the degree of mixing between the gases, or when decreasing their distinguishability. These points go against a direct quantitative association of physical irreversibility with lack of information.
A consensus seems to have developed that the Gibbs paradox in classical thermodynamics (the discontinuous drop in the entropy of mixing when the mixed gases become equal to each other) is unmysterious: in any actual situation, two gases can be separated or not, and the associated harmless discontinuity from “yes” to “no” is responsible for the discontinuity. By contrast, the Gibbs paradox in statistical physics continues to attract attention. Here, the problem is that standard calculations in statistical mechanics predict a non-vanishing value of the entropy of mixing even when two gases of the same kind are mixed, in conflict with thermodynamic predictions. This version of the Gibbs paradox is often seen as a sign that there is something fundamentally wrong with either the traditional expression S=klnW or with the way W is calculated. It is the aim of this article to review the situation from the orthodox (as opposed to information theoretic) standpoint. We demonstrate how the standard formalism is not only fully capable of dealing with the paradox, but also provides an intuitively clear picture of the relevant physical mechanisms. In particular, we pay attention to the explanatory relevance of the existence of particle trajectories in the classical context. We also discuss how the paradox survives the transition to quantum mechanics, in spite of the symmetrization postulates.
The issue of the Gibbs paradox is that when considering mixing of two gases within classical thermodynamics, the entropy of mixing appears to be a discontinuous function of the difference between the gases: it is finite for whatever small difference, but vanishes for identical gases. The resolution offered in the literature, with help of quantum mixing entropy, was later shown to be unsatisfactory precisely where it sought to resolve the paradox. Macroscopic thermodynamics, classical or quantum, is unsuitable for explaining the paradox, since it does not deal explicitly with the difference between the gases. The proper approach employs quantum thermodynamics, which deals with finite quantum systems coupled to a large bath and a macroscopic work source. Within quantum thermodynamics, entropy generally loses its dominant place and the target of the paradox is naturally shifted to a decrease of the maximally available work before and after mixing (mixing ergotropy). In contrast to entropy this is an unambiguous quantity. For almost identical gases the mixing ergotropy continuously goes to zero, thus resolving the paradox. In this approach the concept of "difference between the gases" gets a clear operational meaning related to the possibilities of controlling the involved quantum states. Difficulties which prevent resolutions of the paradox in its entropic formulation do not arise here. The mixing ergotropy has several counterintuitive features. It can increase when less precise operations are allowed. In the quantum situation (in contrast to the classical one) the mixing ergotropy can also increase when decreasing the degree of mixing between the gases or when decreasing their distinguishability. These points go against a direct association of physical irreversibility with lack of information.
The Gibbs paradox in statistical mechanics is often taken to indicate that already in the classical domain particles should be treated as fundamentally indistinguishable. This paper shows, on the contrary, how one can recover the thermodynamical account of the entropy of mixing, while treating states that only differ by permutations of similar particles as distinct. By reference to the orthodox theory of thermodynamics, it is argued that entropy differences are only meaningful if they are related to reversible processes connecting the initial and final state. For mixing processes, this means that processes should be considered in which particle number is allowed to vary. Within the context of statistical mechanics, the Gibbsian grandcanonical ensemble is a suitable device for describing such processes. It is shown how the grandcanonical entropy relates in the appropriate way to changes of other thermodynamical quantities in reversible processes, and how the thermodynamical account of the entropy of mixing is recovered even when treating the particles as distinguishable.
Gibbs paradox in the context of statistical mechanics addresses the issue of additivity of entropy of mixing gases. The usual discussion attributes the paradoxical situation to classical distinguishability of identical particles and credits quantum theory for enabling indistinguishability of identical particles to solve the problem. We argue that indistinguishability of identical particles is already a feature in classical mechanics and this is clearly brought out when the problem is treated in the language of information and associated entropy. We pinpoint the physical criteria for indistinguishability that is crucial for the treatment of the Gibbs’ problem and the consistency of its solution with conventional thermodynamics. Quantum mechanics provides a quantitative criterion, not possible in the classical picture, for the degree of indistinguishability in terms of visibility of quantum interference, or overlap of the states as pointed out by von Neumann, thereby endowing the entropy expression with mathematical continuity and physical reasonableness.
The “Gibbs Paradox” refers to several related questions concerning entropy in thermodynamics and statistical mechanics: whether it is an extensive quantity or not, how it changes when identical particles are mixed, and the proper way to count states in systems of identical particles. Several authors have recognized that the paradox is resolved once it is realized that there is no such thing as the entropy of a system, that there are many entropies, and that the choice between treating particles as being distinguishable or not depends on the resolution of the experiment. The purpose of this note is essentially pedagogical; we add to their analysis by examining the paradox from the point of view of information theory. Our argument is based on that ‘grouping’ property of entropy that Shannon recognized, by including it among his axioms, as an essential requirement on any measure of information. Not only does it provide the right connection between different entropies but, in addition, it draws our attention to the obvious fact that addressing issues of distinguishability and of counting states requires a clear idea about what precisely do we mean by a state.