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arXiv:cond-mat/9809208

Irreversibility from a Reversible Equation

Hiroshi Ezawa, Koichi Nakamura, Keiji Watanabe

Published Sep 15, 1998• 0 citations
arXivHTMLPDF

Abstract

After a discussion on the state of local equilibrium with temperature inhomogeneity, comparing mixture state reprsentation in statistical mechanics and pure state representation in thermo field dynamics, a simple model is solved to show that a reversible equation of motion with the initial condition having inhomogeneous temperature can lead to irreversible, viz. diffusive, behaviour. Yet, the solution is time symmetric exhibiting diffusion both towards future and past.

DOI
10.48550/arxiv.cond-mat/9809208

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After a discussion on the state of local equilibrium with temperature inhomogeneity, comparing mixture state reprsentation in statistical mechanics and pure state representation in thermo field dynamics, a simple model is solved to show that a reversible equation of motion with the initial condition having inhomogeneous temperature can lead to irreversible, viz. diffusive, behaviour. Yet, the solution is time symmetric exhibiting diffusion both towards future and past.
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The first question to ask about the phenomenon of relaxation is why it occurs at all. Both the Newton and the Schrödinger equations are symmetrical under time reversal: The Newton equation, dx/dt = v ; dv/dt = −∂V/∂x, implies that particles obeying this law of motion will retrace their trajectory back in time after changing the sign of both the time t and the particle velocities v. The Schrödinger equation, ∂ψ/∂t = −(i/.h) Ĥ ψ, implies that if (ψ (t) is a solution then ψ *(−t) is also one, so that observables which depend on |ψ|2 are symmetric in time. On the other hand, nature clearly evolves asymmetrically as asserted by the second law of thermodynamics. How does this asymmetry arise in a system that obeys temporal symmetry in its time evolution? Readers with background in thermodynamics and statistical mechanics have encountered the intuitive answer: Irreversibility in a system with many degrees of freedom is essentially a manifestation of the system “getting lost in phase space”:Asystem starts from a given state and evolves in time. If the number of accessible states is huge, the probability that the system will find its way back to the initial state in finite time is vanishingly small, so that an observer who monitors properties associated with the initial state will see an irreversible evolution. The question is how is this irreversible behavior manifested through the reversible equations of motion, and how does it show in the quantitative description of the time evolution. This chapter provides an introduction to this subject using the time-dependent Schrödinger equation as a starting point. Chapter 10 discusses more advanced aspects of this problem within the framework of the quantum Liouville equation and the density operator formalism.
Time-reversibility measured by the deviation of perturbed time-reversed motion from the unperturbed motion is examined for normal quantum diffusion exhibited by four classes of quantum maps with contrasting physical nature. Irrespective of the system, there exists a universal minimal quantum threshold above which the system completely loses memory of the past. The time-reversed dynamics as well as the time-reversal characteristics are asymptotically universal curves independent of the details of the systems.
What is the physical significance of entropy? What is the physical origin of irreversibility? Do entropy and irreversibility exist only for complex and macroscopic systems? The bulk of the physics community accepts and teaches that all these fundamental questions are rationalized within statistical mechanics. Indeed, for everyday laboratory physics, the mathematical formalism of statistical mechanics (canonical and grandcanonica1, Boltzmann, Bose-Einstein and Fermi-Dirac distributions) allows a successful description of the thermodynamic equilibrium properties of matter, including entropy values. But an ever growing handful of physicists (Schrodinger among the first) have realized that, even in its explanation of the meaning of entropy, statistical mechanics is impaired by ambiguities and logical inconsistencies. They have started to search for a better theory to eliminate these stumbling blocks while maintaining the mathematical formalism that has been so successful in so many applications. This handful of upstreamers must not be confused with the many schools of physicists that have thrived on the more renowned incompleteness of statistical mechanics, namely, the lack of a quantitative (and the weakness of the qualitative) explanation of the origin of irreversibility. In these studies the thrust is provided by the discovery that the macroscopic dynamics of certain complex systems may be modeled using a few-degrees-of-freedom nonlinear Hamiltonian with singularities that give rise to bifurcations and chaotic behavior. These results have generated successful ways to describe irreversible behavior, but their link to the origin of irreversibility is still only heuristic (what is the connection between the nonlinear model Hamiltonian and the true full Hamiitonian?) and does not provide yet a rigorous resolution of the century-old paradox of the conflict between the irreversibiiity of macroscopic behavior, and the reversibility of the laws of mechanics. To resolve both the problem of the meaning of entropy and that of the origin of irreversibility we have built entropy and irreversibility into the laws of mechanics. The result is a theory that we call quantum thermodynamics that has all the necessary properties to combine mechanics and thermodynamics uniting all the successful results of both theories, eliminating the logical inconsistencies of statistical mechanics and the paradox on irreversibiiity, and providing an entirely new perspective on the microscopic origin of irreversibility, nonlinearity and therefore chaotic behavior. The mathematical formalism of quantum thermodynamics differs from that of statistical mechanics mainly in the equation of motion which is nonlinear but has solutions identical to those of the Schrodinger equation for all the states for which statistical mechanics reduces to quantum mechanics. The physical meaning of the formalism of quantum thermodynamics differs more drastically from that of statistical mechanics. The significance of the state operator of quantum thermodynamics is entirely different from that of the density operator of statistical mechanics, even though the two are mathematically equivalent. Indeed they obey different equations of motion. In particular, quantum thermodynamics is concerned only with those systems for which quantum mechanics would describe the states with vectors in Hilbert space or, equivalently, projection operators. Using a well known jargon, we can say that quantum thermodynamics like quantum mechanics is concerned only with pure quantum states. However, it postulates that the set of pure quantum states of a system is much broader than contemplated by quantum mechanics. Pure quantum states must be described by operators defined by all the features of projection operators except the condition of idempotence. As a result, an operator that within statistical mechanics would describe a mixed quantum state (that is, the average state of a statistical mixture of identical systems in different pure quantum states) in quantum thermodynamics describes a pure quantum state, a state that neither quantum mechanics non statistical mechanics would contemplate. Conceptually, the increased richness of pure quantum states is a new revolutionary postulate of quantum physics. But from the point of view of the statistical mechanics practitioners the new theory is not as traumatic as it seems. Whenever one uses a nonidempotent density operator to describe a thermodynamic equilibrium state one simply has to reinterpret it as one of the new pure quantum states. One even saves the usual ad hoc arguments on thermal baths and reservoirs that are usually required in statistical mechanics to justify the use of a nonidempotent density operator to describe the state of a system. In this paper we discuss the background and formalism of quantum thermodynamics including its nonlinear equation of motion and the main general results. Our objective is to show in a not-too-technical manner that this theory provides indeed a complete and coherent resolution of the century-old dilemma on the meaning of entropy and the origin of irreversibility. As a byproduct, we discuss a long set of criteria that a theory should meet in order to afford the same claim.
Through extended consideration of two wide classes of case studies -- dilute gases and linear systems -- I explore the ways in which assumptions of probability and irreversibility occur in contemporary statistical mechanics, where the latter is understood as primarily concerned with the derivation of quantitative higher-level equations of motion, and only derivatively with underpinning the equilibrium concept in thermodynamics. I argue that at least in this wide class of examples, (i) irreversibility is introduced through a reasonably well-defined initial-state condition which does not precisely map onto those in the extant philosophical literature; (ii) probability is explicitly required both in the foundations and in the predictions of the theory. I then consider the same examples, as well as the more general context, in the light of quantum mechanics, and demonstrate that while the analysis of irreversibility is largely unaffected by quantum considerations, the notion of statistical-mechanical probability is entirely reduced to quantum-mechanical probability.