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Moved page from wikipedia:en:Non-equilibrium thermodynamics (history)
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{{short description|Branch of thermodynamics}}
{{Cleanup rewrite|date=December 2018}}{{thermodynamics|cTopic=Branches}}
'''Non-equilibrium thermodynamics''' is a branch of [[thermodynamics]] that deals with physical systems that are not in [[thermodynamic equilibrium]] but can be described in terms of variables (non-equilibrium state variables) that represent an extrapolation of the variables used to specify the system in thermodynamic equilibrium. Non-equilibrium thermodynamics is concerned with [[transport phenomena|transport process]]es and with the rates of [[chemical reactions]]. It relies on what may be thought of as more or less nearness to thermodynamic equilibrium. Non-equilibrium thermodynamics is a work in progress, not an established edifice. This article will try to sketch some approaches to it and some concepts important for it.
Non-equilibrium thermodynamics is a branch of thermodynamics that deals with physical systems that are not in thermodynamic equilibrium but can be described in terms of variables (non-equilibrium state variables) that represent an extrapolation of the variables used to specify the system in thermodynamic equilibrium. Non-equilibrium thermodynamics is concerned with transport processes and with the rates of chemical reactions. It relies on what may be thought of as more or less nearness to thermodynamic equilibrium. Non-equilibrium thermodynamics is a work in progress, not an established edifice. This article will try to sketch some approaches to it and some concepts important for it.
Almost all systems found in nature are not in thermodynamic equilibrium, for they are changing or can be triggered to change over time, and are continuously and discontinuously subject to flux of matter and energy to and from other systems and to chemical reactions. Some systems and processes are, however, in a useful sense, near enough to thermodynamic equilibrium to allow description with useful accuracy by currently known non-equilibrium thermodynamics. Nevertheless, many natural systems and processes will always remain far beyond the scope of non-equilibrium thermodynamic methods due to the existence of non variational dynamics, where the concept of free energy is lost <ref>{{cite journal |last1=Bodenschatz |first1=Eberhard |last2=Cannell |first2=David S. |last3=de Bruyn |first3=John R. |last4=Ecke |first4=Robert |last5=Hu |first5=Yu-Chou |last6=Lerman |first6=Kristina |last7=Ahlers |first7=Guenter |title=Experiments on three systems with non-variational aspects |journal=Physica D: Nonlinear Phenomena |date=December 1992 |volume=61 |issue=1–4 |pages=77–93 |doi=10.1016/0167-2789(92)90150-L}}</ref>.
Almost all systems found in nature are not in thermodynamic equilibrium, for they are changing or can be triggered to change over time, and are continuously and discontinuously subject to flux of matter and energy to and from other systems and to chemical reactions. Some systems and processes are, however, in a useful sense, near enough to thermodynamic equilibrium to allow description with useful accuracy by currently known non-equilibrium thermodynamics. Nevertheless, many natural systems and processes will always remain far beyond the scope of non-equilibrium thermodynamic methods due to the existence of non variational dynamics, where the concept of free energy is lost .
The thermodynamic study of non-equilibrium systems requires more general concepts than are dealt with by [[equilibrium thermodynamics]]. One fundamental difference between equilibrium thermodynamics and non-equilibrium thermodynamics lies in the behaviour of inhomogeneous systems, which require for their study knowledge of rates of reaction which are not considered in equilibrium thermodynamics of homogeneous systems. This is discussed below. Another fundamental and very important difference is the difficulty or impossibility, in general, in defining [[entropy]] at an instant of time in macroscopic terms for systems not in thermodynamic equilibrium; it can be done, to useful approximation, only in carefully chosen special cases, namely those that are throughout in local thermodynamic equilibrium.<ref name="Grandy 2008">Grandy, W.T., Jr (2008).</ref><ref name="Lebon Jou Casas-Vázquez 2008">Lebon, G., Jou, D., Casas-Vázquez, J. (2008). ''Understanding Non-equilibrium Thermodynamics: Foundations, Applications, Frontiers'', Springer-Verlag, Berlin, e-{{ISBN|978-3-540-74252-4}}.</ref>
The thermodynamic study of non-equilibrium systems requires more general concepts than are dealt with by equilibrium thermodynamics. One fundamental difference between equilibrium thermodynamics and non-equilibrium thermodynamics lies in the behaviour of inhomogeneous systems, which require for their study knowledge of rates of reaction which are not considered in equilibrium thermodynamics of homogeneous systems. This is discussed below. Another fundamental and very important difference is the difficulty or impossibility, in general, in defining entropy at an instant of time in macroscopic terms for systems not in thermodynamic equilibrium; it can be done, to useful approximation, only in carefully chosen special cases, namely those that are throughout in local thermodynamic equilibrium.
==Scope==
==Scope==
===Difference between equilibrium and non-equilibrium thermodynamics===
===Difference between equilibrium and non-equilibrium thermodynamics===
A profound difference separates equilibrium from non-equilibrium thermodynamics. Equilibrium thermodynamics ignores the time-courses of physical processes. In contrast, non-equilibrium thermodynamics attempts to describe their time-courses in continuous detail.
A profound difference separates equilibrium from non-equilibrium thermodynamics. Equilibrium thermodynamics ignores the time-courses of physical processes. In contrast, non-equilibrium thermodynamics attempts to describe their time-courses in continuous detail.
Equilibrium thermodynamics restricts its considerations to processes that have initial and final states of thermodynamic equilibrium; the time-courses of processes are deliberately ignored. Consequently, equilibrium thermodynamics allows processes that pass through states far from thermodynamic equilibrium, that cannot be described even by the variables admitted for non-equilibrium thermodynamics,<ref name="EY 5">[[Elliott H. Lieb|Lieb, E.H.]], [[Jakob Yngvason|Yngvason, J.]] (1999), p. 5.</ref> such as time rates of change of temperature and pressure.<ref>Gyarmati, I. (1967/1970), pp. 8–12.</ref> For example, in equilibrium thermodynamics, a process is allowed to include even a violent explosion that cannot be described by non-equilibrium thermodynamics.<ref name="EY 5"/> Equilibrium thermodynamics does, however, for theoretical development, use the idealized concept of the "quasi-static process". A quasi-static process is a conceptual (timeless and physically impossible) smooth mathematical passage along a continuous path of states of thermodynamic equilibrium.<ref>[[Herbert Callen|Callen, H.B.]] (1960/1985), § 4–2.</ref> It is an exercise in differential geometry rather than a process that could occur in actuality.
Equilibrium thermodynamics restricts its considerations to processes that have initial and final states of thermodynamic equilibrium; the time-courses of processes are deliberately ignored. Consequently, equilibrium thermodynamics allows processes that pass through states far from thermodynamic equilibrium, that cannot be described even by the variables admitted for non-equilibrium thermodynamics, such as time rates of change of temperature and pressure. For example, in equilibrium thermodynamics, a process is allowed to include even a violent explosion that cannot be described by non-equilibrium thermodynamics. It is an exercise in differential geometry rather than a process that could occur in actuality.
Non-equilibrium thermodynamics, on the other hand, attempting to describe continuous time-courses, needs its [[State function|state variables]] to have a very close connection with those of equilibrium thermodynamics.<ref>Glansdorff, P., Prigogine, I. (1971), Ch. {{math|II}},§ 2.</ref> This profoundly restricts the scope of non-equilibrium thermodynamics, and places heavy demands on its conceptual framework.
Non-equilibrium thermodynamics, on the other hand, attempting to describe continuous time-courses, needs its state variables to have a very close connection with those of equilibrium thermodynamics. This profoundly restricts the scope of non-equilibrium thermodynamics, and places heavy demands on its conceptual framework.
===Non-equilibrium state variables===
===Non-equilibrium state variables===
===Non-equilibrium state variables===
The suitable relationship that defines non-equilibrium thermodynamic state variables is as follows. On occasions when the system happens to be in states that are sufficiently close to thermodynamic equilibrium, non-equilibrium state variables are such that they can be measured locally with sufficient accuracy by the same techniques as are used to measure thermodynamic state variables, or by corresponding time and space derivatives, including fluxes of matter and energy. In general, non-equilibrium thermodynamic systems are spatially and temporally non-uniform, but their non-uniformity still has a sufficient degree of smoothness to support the existence of suitable time and space derivatives of non-equilibrium state variables. Because of the spatial non-uniformity, non-equilibrium state variables that correspond to extensive thermodynamic state variables have to be defined as spatial densities of the corresponding extensive equilibrium state variables. On occasions when the system is sufficiently close to thermodynamic equilibrium, intensive non-equilibrium state variables, for example temperature and pressure, correspond closely with equilibrium state variables. It is necessary that measuring probes be small enough, and rapidly enough responding, to capture relevant non-uniformity. Further, the non-equilibrium state variables are required to be mathematically functionally related to one another in ways that suitably resemble corresponding relations between equilibrium thermodynamic state variables.<ref name="Gyarmati 1970"/> In reality, these requirements are very demanding, and it may be difficult or practically, or even theoretically, impossible to satisfy them. This is part of why non-equilibrium thermodynamics is a work in progress.
The suitable relationship that defines non-equilibrium thermodynamic state variables is as follows. On occasions when the system happens to be in states that are sufficiently close to thermodynamic equilibrium, non-equilibrium state variables are such that they can be measured locally with sufficient accuracy by the same techniques as are used to measure thermodynamic state variables, or by corresponding time and space derivatives, including fluxes of matter and energy. In general, non-equilibrium thermodynamic systems are spatially and temporally non-uniform, but their non-uniformity still has a sufficient degree of smoothness to support the existence of suitable time and space derivatives of non-equilibrium state variables. Because of the spatial non-uniformity, non-equilibrium state variables that correspond to extensive thermodynamic state variables have to be defined as spatial densities of the corresponding extensive equilibrium state variables. On occasions when the system is sufficiently close to thermodynamic equilibrium, intensive non-equilibrium state variables, for example temperature and pressure, correspond closely with equilibrium state variables. It is necessary that measuring probes be small enough, and rapidly enough responding, to capture relevant non-uniformity. Further, the non-equilibrium state variables are required to be mathematically functionally related to one another in ways that suitably resemble corresponding relations between equilibrium thermodynamic state variables. In reality, these requirements are very demanding, and it may be difficult or practically, or even theoretically, impossible to satisfy them. This is part of why non-equilibrium thermodynamics is a work in progress.
==Overview==
==Overview==
概览
Non-equilibrium thermodynamics is a work in progress, not an established edifice. This article is an attempt to sketch some approaches to it and some concepts important for it.
Non-equilibrium thermodynamics is a work in progress, not an established edifice. This article is an attempt to sketch some approaches to it and some concepts important for it.
Some concepts of particular importance for non-equilibrium thermodynamics include time rate of dissipation of energy (Rayleigh 1873,<ref name="Rayleigh 1873">{{Cite journal | last1 = Strutt | first1 = J. W. | doi = 10.1112/plms/s1-4.1.357 | title = Some General Theorems relating to Vibrations | journal = Proceedings of the London Mathematical Society | year = 1871 | volume = s1-4 | pages = 357–368 | url = https://zenodo.org/record/1447754 }}</ref> [[Lars Onsager|Onsager]] 1931,<ref name="Onsager 1931 I">{{Cite journal | doi = 10.1103/PhysRev.37.405 | last1 = Onsager | first1 = L. | year = 1931 | title = Reciprocal relations in irreversible processes, I | url = | journal = Physical Review | volume = 37 | issue = 4| pages = 405–426 |bibcode = 1931PhRv...37..405O | doi-access = free }}</ref> also<ref name="Gyarmati 1970">Gyarmati, I. (1967/1970).</ref><ref name="Lavenda 1978">Lavenda, B.H. (1978). ''Thermodynamics of Irreversible Processes'', Macmillan, London, {{ISBN|0-333-21616-4}}.</ref>), time rate of entropy production (Onsager 1931),<ref name="Onsager 1931 I"/> thermodynamic fields,<ref>Gyarmati, I. (1967/1970), pages 4-14.</ref><ref name="Ziegler 1983">Ziegler, H., (1983). ''An Introduction to Thermomechanics'', North-Holland, Amsterdam, {{ISBN|0-444-86503-9}}.</ref><ref name="Balescu">Balescu, R. (1975). ''Equilibrium and Non-equilibrium Statistical Mechanics'', Wiley-Interscience, New York, {{ISBN|0-471-04600-0}}, Section 3.2, pages 64-72.</ref> [[dissipative structure]],<ref name="G&P 1971"/> and non-linear dynamical structure.<ref name="Lavenda 1978"/>
Some concepts of particular importance for non-equilibrium thermodynamics include time rate of dissipation of energy (Rayleigh 1873, Onsager 1931, also), time rate of entropy production (Onsager 1931), dissipative structure, and non-linear dynamical structure.
One problem of interest is the thermodynamic study of non-equilibrium [[steady state]]s, in which [[entropy]] production and some [[flux|flows]] are non-zero, but there is no [[Time-variant system|time variation]] of physical variables.
One problem of interest is the thermodynamic study of non-equilibrium steady states, in which entropy production and some flows are non-zero, but there is no time variation of physical variables.
One initial approach to non-equilibrium thermodynamics is sometimes called 'classical irreversible thermodynamics'.<ref name="Lebon Jou Casas-Vázquez 2008"/> There are other approaches to non-equilibrium thermodynamics, for example [[extended irreversible thermodynamics]],<ref name="Lebon Jou Casas-Vázquez 2008"/><ref name="JCVL 1993"/> and generalized thermodynamics,<ref>Eu, B.C. (2002).</ref> but they are hardly touched on in the present article.
One initial approach to non-equilibrium thermodynamics is sometimes called 'classical irreversible thermodynamics'. but they are hardly touched on in the present article.
===Quasi-radiationless non-equilibrium thermodynamics of matter in laboratory conditions===
===Quasi-radiationless non-equilibrium thermodynamics of matter in laboratory conditions===
实验室条件下物质的准无辐射非平衡态热力学
According to Wildt<ref name="Wildt 1972">{{Cite journal |last=Wildt |first=R. |year=1972 |title=Thermodynamics of the gray atmosphere. IV. Entropy transfer and production |journal=Astrophysical Journal |volume=174 |issue= |pages=69–77 |doi=10.1086/151469 |bibcode=1972ApJ...174...69W}}</ref> (see also Essex<ref name="Essex 1984a">{{Cite journal |last=Essex |first=C. |year=1984a |title=Radiation and the irreversible thermodynamics of climate |journal=Journal of the Atmospheric Sciences |volume=41 |issue=12 |pages=1985–1991 |doi=10.1175/1520-0469(1984)041<1985:RATITO>2.0.CO;2 |bibcode = 1984JAtS...41.1985E |doi-access=free }}.</ref><ref name="Essex 1984b">{{Cite journal |last=Essex |first=C. |year=1984b |title=Minimum entropy production in the steady state and radiative transfer |journal=Astrophysical Journal |volume=285 |issue= |pages=279–293 |doi=10.1086/162504 |bibcode=1984ApJ...285..279E}}</ref><ref name="Essex 1984c">{{Cite journal |last=Essex |first=C. |year=1984c |title=Radiation and the violation of bilinearity in the irreversible thermodynamics of irreversible processes |journal=Planetary and Space Science |volume=32 |pages=1035–1043 |doi=10.1016/0032-0633(84)90060-6 |bibcode = 1984P&SS...32.1035E |issue=8 }}</ref>), current versions of non-equilibrium thermodynamics ignore radiant heat; they can do so because they refer to laboratory quantities of matter under laboratory conditions with temperatures well below those of stars. At laboratory temperatures, in laboratory quantities of matter, thermal radiation is weak and can be practically nearly ignored. But, for example, atmospheric physics is concerned with large amounts of matter, occupying cubic kilometers, that, taken as a whole, are not within the range of laboratory quantities; then thermal radiation cannot be ignored.
According to Wildt (see also Essex), current versions of non-equilibrium thermodynamics ignore radiant heat; they can do so because they refer to laboratory quantities of matter under laboratory conditions with temperatures well below those of stars. At laboratory temperatures, in laboratory quantities of matter, thermal radiation is weak and can be practically nearly ignored. But, for example, atmospheric physics is concerned with large amounts of matter, occupying cubic kilometers, that, taken as a whole, are not within the range of laboratory quantities; then thermal radiation cannot be ignored.
===Local equilibrium thermodynamics===
===Local equilibrium thermodynamics===
局域平衡热力学
The terms 'classical irreversible thermodynamics'<ref name="Lebon Jou Casas-Vázquez 2008"/> and 'local equilibrium thermodynamics' are sometimes used to refer to a version of non-equilibrium thermodynamics that demands certain simplifying assumptions, as follows. The assumptions have the effect of making each very small volume element of the system effectively homogeneous, or well-mixed, or without an effective spatial structure, and without kinetic energy of bulk flow or of diffusive flux. Even within the thought-frame of classical irreversible thermodynamics, care<ref name="Lavenda 1978"/> is needed in choosing the independent variables<ref>Prigogine, I., Defay, R. (1950/1954). ''Chemical Thermodynamics'', Longmans, Green & Co, London, page 1.</ref> for systems. In some writings, it is assumed that the intensive variables of equilibrium thermodynamics are sufficient as the independent variables for the task (such variables are considered to have no 'memory', and do not show hysteresis); in particular, local flow intensive variables are not admitted as independent variables; local flows are considered as dependent on quasi-static local intensive variables.
The terms 'classical irreversible thermodynamics' for systems. In some writings, it is assumed that the intensive variables of equilibrium thermodynamics are sufficient as the independent variables for the task (such variables are considered to have no 'memory', and do not show hysteresis); in particular, local flow intensive variables are not admitted as independent variables; local flows are considered as dependent on quasi-static local intensive variables.
Also it is assumed that the local entropy density is the same function of the other local intensive variables as in equilibrium; this is called the local thermodynamic equilibrium assumption<ref name="Gyarmati 1970"/><ref name="Lavenda 1978"/><ref name="G&P 1971">Glansdorff, P., Prigogine, I. (1971). ''Thermodynamic Theory of Structure, Stability, and Fluctuations'', Wiley-Interscience, London, 1971, {{ISBN|0-471-30280-5}}.</ref><ref name="JCVL 1993">Jou, D., Casas-Vázquez, J., Lebon, G. (1993). ''Extended Irreversible Thermodynamics'', Springer, Berlin, {{ISBN|3-540-55874-8}}, {{ISBN|0-387-55874-8}}.</ref><ref name="De Groot Mazur 1962">De Groot, S.R., Mazur, P. (1962). ''Non-equilibrium Thermodynamics'', North-Holland, Amsterdam.</ref><ref name="Balescu 1975">Balescu, R. (1975). ''Equilibrium and Non-equilibrium Statistical Mechanics'', John Wiley & Sons, New York, {{ISBN|0-471-04600-0}}.</ref><ref name="Mihalas Mihalas 1984">[http://www.filestube.com/9c5b2744807c2c3d03e9/details.html Mihalas, D., Weibel-Mihalas, B. (1984). ''Foundations of Radiation Hydrodynamics'', Oxford University Press, New York] {{ISBN|0-19-503437-6}}.</ref><ref name="Schloegl 1989">Schloegl, F. (1989). ''Probability and Heat: Fundamentals of Thermostatistics'', Freidr. Vieweg & Sohn, Braunschweig, {{ISBN|3-528-06343-2}}.</ref> (see also Keizer (1987)<ref name="Keizer 1987">Keizer, J. (1987). ''Statistical Thermodynamics of Nonequilibrium Processes'', Springer-Verlag, New York, {{ISBN|0-387-96501-7}}.</ref>). Radiation is ignored because it is transfer of energy between regions, which can be remote from one another. In the classical irreversible thermodynamic approach, there is allowed very small spatial variation, from very small volume element to adjacent very small volume element, but it is assumed that the global entropy of the system can be found by simple spatial integration of the local entropy density; this means that spatial structure cannot contribute as it properly should to the global entropy assessment for the system. This approach assumes spatial and temporal continuity and even differentiability of locally defined intensive variables such as temperature and internal energy density. All of these are very stringent demands. Consequently, this approach can deal with only a very limited range of phenomena. This approach is nevertheless valuable because it can deal well with some macroscopically observable phenomena.{{examples|date=February 2015}}
Also it is assumed that the local entropy density is the same function of the other local intensive variables as in equilibrium; this is called the local thermodynamic equilibrium assumption (see also Keizer (1987)). Radiation is ignored because it is transfer of energy between regions, which can be remote from one another. In the classical irreversible thermodynamic approach, there is allowed very small spatial variation, from very small volume element to adjacent very small volume element, but it is assumed that the global entropy of the system can be found by simple spatial integration of the local entropy density; this means that spatial structure cannot contribute as it properly should to the global entropy assessment for the system. This approach assumes spatial and temporal continuity and even differentiability of locally defined intensive variables such as temperature and internal energy density. All of these are very stringent demands. Consequently, this approach can deal with only a very limited range of phenomena. This approach is nevertheless valuable because it can deal well with some macroscopically observable phenomena.
In other writings, local flow variables are considered; these might be considered as classical by analogy with the time-invariant long-term time-averages of flows produced by endlessly repeated cyclic processes; examples with flows are in the [[thermoelectric effect|thermoelectric phenomena]] known as the Seebeck and the Peltier effects, considered by [[William Thomson, 1st Baron Kelvin|Kelvin]] in the nineteenth century and by [[Lars Onsager]] in the twentieth.<ref name="De Groot Mazur 1962"/><ref>Kondepudi, D. (2008). ''Introduction to Modern Thermodynamics'', Wiley, Chichester UK, {{ISBN|978-0-470-01598-8}}, pages 333-338.</ref> These effects occur at metal junctions, which were originally effectively treated as two-dimensional surfaces, with no spatial volume, and no spatial variation.
In other writings, local flow variables are considered; these might be considered as classical by analogy with the time-invariant long-term time-averages of flows produced by endlessly repeated cyclic processes; examples with flows are in the thermoelectric phenomena known as the Seebeck and the Peltier effects, considered by Kelvin in the nineteenth century and by Lars Onsager in the twentieth. These effects occur at metal junctions, which were originally effectively treated as two-dimensional surfaces, with no spatial volume, and no spatial variation.
====Local equilibrium thermodynamics with materials with "memory"====
====Local equilibrium thermodynamics with materials with "memory"====
具有“记忆”材料的局域平衡热力学
A further extension of local equilibrium thermodynamics is to allow that materials may have "memory", so that their [[constitutive equation]]s depend not only on present values but also on past values of local equilibrium variables. Thus time comes into the picture more deeply than for time-dependent local equilibrium thermodynamics with memoryless materials, but fluxes are not independent variables of state.<ref>{{cite journal | last1 = Coleman | first1 = B.D. | last2 = Noll | first2 = W. | year = 1963 | title = The thermodynamics of elastic materials with heat conduction and viscosity | url = | journal = Arch. Ration. Mach. Analysis | volume = 13 | issue = 1| pages = 167–178 | doi=10.1007/bf01262690| bibcode = 1963ArRMA..13..167C }}</ref>
A further extension of local equilibrium thermodynamics is to allow that materials may have "memory", so that their constitutive equations depend not only on present values but also on past values of local equilibrium variables. Thus time comes into the picture more deeply than for time-dependent local equilibrium thermodynamics with memoryless materials, but fluxes are not independent variables of state.
===Extended irreversible thermodynamics===
===Extended irreversible thermodynamics===
扩展不可逆热力学
'''Extended irreversible thermodynamics''' is a branch of non-equilibrium thermodynamics that goes outside the restriction to the local equilibrium hypothesis. The space of state variables is enlarged by including the [[flux]]es of mass, momentum and energy and eventually higher order fluxes.
Extended irreversible thermodynamics is a branch of non-equilibrium thermodynamics that goes outside the restriction to the local equilibrium hypothesis. The space of state variables is enlarged by including the fluxes of mass, momentum and energy and eventually higher order fluxes.
扩展不可逆热力学是非平衡态热力学热力学的一个分支，它超越了局部平衡假说的限制。通过包括质量、动量和能量的通量以及最终的高阶通量，状态变量的空间被扩大了。
The formalism is well-suited for describing high-frequency processes and small-length scales materials.
The formalism is well-suited for describing high-frequency processes and small-length scales materials.
==Basic concepts==
==Basic concepts==
基本概念
There are many examples of stationary non-equilibrium systems, some very simple, like a system confined between two thermostats at different temperatures or the ordinary [[Couette flow]], a fluid enclosed between two flat walls moving in opposite directions and defining non-equilibrium conditions at the walls. [[Laser]] action is also a non-equilibrium process, but it depends on departure from local thermodynamic equilibrium and is thus beyond the scope of classical irreversible thermodynamics; here a strong temperature difference is maintained between two molecular degrees of freedom (with molecular laser, vibrational and rotational molecular motion), the requirement for two component 'temperatures' in the one small region of space, precluding local thermodynamic equilibrium, which demands that only one temperature be needed. Damping of acoustic perturbations or shock waves are non-stationary non-equilibrium processes. Driven [[complex fluids]], turbulent systems and glasses are other examples of non-equilibrium systems.
There are many examples of stationary non-equilibrium systems, some very simple, like a system confined between two thermostats at different temperatures or the ordinary Couette flow, a fluid enclosed between two flat walls moving in opposite directions and defining non-equilibrium conditions at the walls. Laser action is also a non-equilibrium process, but it depends on departure from local thermodynamic equilibrium and is thus beyond the scope of classical irreversible thermodynamics; here a strong temperature difference is maintained between two molecular degrees of freedom (with molecular laser, vibrational and rotational molecular motion), the requirement for two component 'temperatures' in the one small region of space, precluding local thermodynamic equilibrium, which demands that only one temperature be needed. Damping of acoustic perturbations or shock waves are non-stationary non-equilibrium processes. Driven complex fluids, turbulent systems and glasses are other examples of non-equilibrium systems.
The mechanics of macroscopic systems depends on a number of extensive quantities. It should be stressed that all systems are permanently interacting with their surroundings, thereby causing unavoidable fluctuations of [[extensive quantity|extensive quantiti]]es. Equilibrium conditions of thermodynamic systems are related to the maximum property of the entropy. If the only extensive quantity that is allowed to fluctuate is the internal energy, all the other ones being kept strictly constant, the temperature of the system is measurable and meaningful. The system's properties are then most conveniently described using the thermodynamic potential [[Helmholtz free energy]] (''A'' = ''U'' - ''TS''), a [[Legendre transformation]] of the energy. If, next to fluctuations of the energy, the macroscopic dimensions (volume) of the system are left fluctuating, we use the [[Gibbs free energy]] (''G'' = ''U'' + ''PV'' - ''TS''), where the system's properties are determined both by the temperature and by the pressure.
The mechanics of macroscopic systems depends on a number of extensive quantities. It should be stressed that all systems are permanently interacting with their surroundings, thereby causing unavoidable fluctuations of extensive quantities. Equilibrium conditions of thermodynamic systems are related to the maximum property of the entropy. If the only extensive quantity that is allowed to fluctuate is the internal energy, all the other ones being kept strictly constant, the temperature of the system is measurable and meaningful. The system's properties are then most conveniently described using the thermodynamic potential Helmholtz free energy (A = U - TS), a Legendre transformation of the energy. If, next to fluctuations of the energy, the macroscopic dimensions (volume) of the system are left fluctuating, we use the Gibbs free energy (G = U + PV - TS), where the system's properties are determined both by the temperature and by the pressure.
Non-equilibrium systems are much more complex and they may undergo fluctuations of more extensive quantities. The boundary conditions impose on them particular intensive variables, like temperature gradients or distorted collective motions (shear motions, vortices, etc.), often called thermodynamic forces. If free energies are very useful in equilibrium thermodynamics, it must be stressed that there is no general law defining stationary non-equilibrium properties of the energy as is the second law of thermodynamics for the [[entropy]] in equilibrium thermodynamics. That is why in such cases a more generalized Legendre transformation should be considered. This is the extended Massieu potential.
Non-equilibrium systems are much more complex and they may undergo fluctuations of more extensive quantities. The boundary conditions impose on them particular intensive variables, like temperature gradients or distorted collective motions (shear motions, vortices, etc.), often called thermodynamic forces. If free energies are very useful in equilibrium thermodynamics, it must be stressed that there is no general law defining stationary non-equilibrium properties of the energy as is the second law of thermodynamics for the entropy in equilibrium thermodynamics. That is why in such cases a more generalized Legendre transformation should be considered. This is the extended Massieu potential.
非平衡系统要复杂得多，它们可能经历更广泛的量的波动。边界条件强加给它们特殊的强度变量，如温度梯度或扭曲的集体运动(剪切运动、涡旋等)。) ，通常称为热力学力。如果自由能在平衡态热力学中非常有用，那么必须强调的是，在平衡态热力学中，定义能量的稳态非平衡性质的一般定律，并不像平衡态热力学中熵的热力学第二定律定律那样。这就是为什么在这种情况下，应该考虑一个更广泛的勒壤得转换。这就是延伸的马西欧势。
By definition, the [[entropy]] (''S'') is a function of the collection of [[extensive quantity|extensive quantiti]]es <math>E_i</math>. Each extensive quantity has a conjugate intensive variable <math>I_i</math> (a restricted definition of intensive variable is used here by comparison to the definition given in this link) so that:
By definition, the entropy (S) is a function of the collection of extensive quantities <math>E_i</math>. Each extensive quantity has a conjugate intensive variable <math>I_i</math> (a restricted definition of intensive variable is used here by comparison to the definition given in this link) so that:
:<math> I_i = \frac{\partial{S}}{\partial{E_i}}.</math>
<math> I_i = \frac{\partial{S}}{\partial{E_i}}.</math>
We then define the extended [[Massieu function]] as follows:
We then define the extended Massieu function as follows:
:<math>\ k_{\rm B} M = S - \sum_i( I_i E_i),</math>
<math>\ k_{\rm B} M = S - \sum_i( I_i E_i),</math>
where <math>\ k_{\rm B}</math> is [[Boltzmann's constant]], whence
where <math>\ k_{\rm B}</math> is Boltzmann's constant, whence
:<math>\ k_{\rm B} \, dM = \sum_i (E_i \, dI_i).</math>
<math>\ k_{\rm B} \, dM = \sum_i (E_i \, dI_i).</math>
The independent variables are the intensities.
The independent variables are the intensities.
Intensities are global values, valid for the system as a whole. When boundaries impose to the system different local conditions, (e.g. temperature differences), there are intensive variables representing the average value and others representing gradients or higher moments. The latter are the thermodynamic forces driving fluxes of extensive properties through the system.
Intensities are global values, valid for the system as a whole. When boundaries impose to the system different local conditions, (e.g. temperature differences), there are intensive variables representing the average value and others representing gradients or higher moments. The latter are the thermodynamic forces driving fluxes of extensive properties through the system.
It may be shown that the Legendre transformation changes the maximum condition of the entropy (valid at equilibrium) in a minimum condition of the extended Massieu function for stationary states, no matter whether at equilibrium or not.
It may be shown that the Legendre transformation changes the maximum condition of the entropy (valid at equilibrium) in a minimum condition of the extended Massieu function for stationary states, no matter whether at equilibrium or not.
==Stationary states, fluctuations, and stability==
==Stationary states, fluctuations, and stability==
In thermodynamics one is often interested in a stationary state of a process, allowing that the stationary state include the occurrence of unpredictable and experimentally unreproducible fluctuations in the state of the system. The fluctuations are due to the system's internal sub-processes and to exchange of matter or energy with the system's surroundings that create the constraints that define the process.
In thermodynamics one is often interested in a stationary state of a process, allowing that the stationary state include the occurrence of unpredictable and experimentally unreproducible fluctuations in the state of the system. The fluctuations are due to the system's internal sub-processes and to exchange of matter or energy with the system's surroundings that create the constraints that define the process.
If the stationary state of the process is stable, then the unreproducible fluctuations involve local transient decreases of entropy. The reproducible response of the system is then to increase the entropy back to its maximum by irreversible processes: the fluctuation cannot be reproduced with a significant level of probability. Fluctuations about stable stationary states are extremely small except near critical points (Kondepudi and Prigogine 1998, page 323).<ref>Kondepudi, D., Prigogine, I, (1998). ''Modern Thermodynamics. From Heat Engines to Dissipative Structures'', Wiley, Chichester, 1998, {{ISBN|0-471-97394-7}}.</ref> The stable stationary state has a local maximum of entropy and is locally the most reproducible state of the system. There are theorems about the irreversible dissipation of fluctuations. Here 'local' means local with respect to the abstract space of thermodynamic coordinates of state of the system.
If the stationary state of the process is stable, then the unreproducible fluctuations involve local transient decreases of entropy. The reproducible response of the system is then to increase the entropy back to its maximum by irreversible processes: the fluctuation cannot be reproduced with a significant level of probability. Fluctuations about stable stationary states are extremely small except near critical points (Kondepudi and Prigogine 1998, page 323). The stable stationary state has a local maximum of entropy and is locally the most reproducible state of the system. There are theorems about the irreversible dissipation of fluctuations. Here 'local' means local with respect to the abstract space of thermodynamic coordinates of state of the system.
If the stationary state is unstable, then any fluctuation will almost surely trigger the virtually explosive departure of the system from the unstable stationary state. This can be accompanied by increased export of entropy.
If the stationary state is unstable, then any fluctuation will almost surely trigger the virtually explosive departure of the system from the unstable stationary state. This can be accompanied by increased export of entropy.
==Local thermodynamic equilibrium==
==Local thermodynamic equilibrium==
当地热力学平衡
The scope of present-day non-equilibrium thermodynamics does not cover all physical processes. A condition for the validity of many studies in non-equilibrium thermodynamics of matter is that they deal with what is known as ''local thermodynamic equilibrium''.
The scope of present-day non-equilibrium thermodynamics does not cover all physical processes. A condition for the validity of many studies in non-equilibrium thermodynamics of matter is that they deal with what is known as local thermodynamic equilibrium.
===Ponderable matter===
===Ponderable matter===
值得思考的问题
''Local thermodynamic equilibrium of matter''<ref name="Gyarmati 1970"/><ref name="G&P 1971"/><ref name="Balescu 1975"/><ref name="Mihalas Mihalas 1984"/><ref name="Schloegl 1989"/> (see also Keizer (1987)<ref name="Keizer 1987"/> means that conceptually, for study and analysis, the system can be spatially and temporally divided into 'cells' or 'micro-phases' of small (infinitesimal) size, in which classical thermodynamical equilibrium conditions for matter are fulfilled to good approximation. These conditions are unfulfilled, for example, in very rarefied gases, in which molecular collisions are infrequent; and in the boundary layers of a star, where radiation is passing energy to space; and for interacting fermions at very low temperature, where dissipative processes become ineffective. When these 'cells' are defined, one admits that matter and energy may pass freely between contiguous 'cells', slowly enough to leave the 'cells' in their respective individual local thermodynamic equilibria with respect to intensive variables.
Local thermodynamic equilibrium of matter (see also Keizer (1987) means that conceptually, for study and analysis, the system can be spatially and temporally divided into 'cells' or 'micro-phases' of small (infinitesimal) size, in which classical thermodynamical equilibrium conditions for matter are fulfilled to good approximation. These conditions are unfulfilled, for example, in very rarefied gases, in which molecular collisions are infrequent; and in the boundary layers of a star, where radiation is passing energy to space; and for interacting fermions at very low temperature, where dissipative processes become ineffective. When these 'cells' are defined, one admits that matter and energy may pass freely between contiguous 'cells', slowly enough to leave the 'cells' in their respective individual local thermodynamic equilibria with respect to intensive variables.
One can think here of two 'relaxation times' separated by order of magnitude.<ref name="Zubarev 1971/1974">[[Dmitry Zubarev|Zubarev D. N.]],(1974). ''[https://books.google.com/books?id=SQy3AAAAIAAJ&hl=ru&source=gbs_ViewAPI Nonequilibrium Statistical Thermodynamics]'', translated from the Russian by P.J. Shepherd, New York, Consultants Bureau. {{ISBN|0-306-10895-X}}; {{ISBN|978-0-306-10895-2}}.</ref> The longer relaxation time is of the order of magnitude of times taken for the macroscopic dynamical structure of the system to change. The shorter is of the order of magnitude of times taken for a single 'cell' to reach local thermodynamic equilibrium. If these two relaxation times are not well separated, then the classical non-equilibrium thermodynamical concept of local thermodynamic equilibrium loses its meaning<ref name="Zubarev 1971/1974"/> and other approaches have to be proposed, see for instance [[Extended irreversible thermodynamics]]. For example, in the atmosphere, the speed of sound is much greater than the wind speed; this favours the idea of local thermodynamic equilibrium of matter for atmospheric heat transfer studies at altitudes below about 60 km where sound propagates, but not above 100 km, where, because of the paucity of intermolecular collisions, sound does not propagate.
One can think here of two 'relaxation times' separated by order of magnitude. The longer relaxation time is of the order of magnitude of times taken for the macroscopic dynamical structure of the system to change. The shorter is of the order of magnitude of times taken for a single 'cell' to reach local thermodynamic equilibrium. If these two relaxation times are not well separated, then the classical non-equilibrium thermodynamical concept of local thermodynamic equilibrium loses its meaning and other approaches have to be proposed, see for instance Extended irreversible thermodynamics. For example, in the atmosphere, the speed of sound is much greater than the wind speed; this favours the idea of local thermodynamic equilibrium of matter for atmospheric heat transfer studies at altitudes below about 60 km where sound propagates, but not above 100 km, where, because of the paucity of intermolecular collisions, sound does not propagate.
===Milne's definition in terms of radiative equilibrium===
===Milne's definition in terms of radiative equilibrium===
米尔恩对辐射平衡的定义
[[Edward Arthur Milne|Edward A. Milne]], thinking about stars, gave a definition of 'local thermodynamic equilibrium' in terms of the [[thermal radiation]] of the [[matter]] in each small local 'cell'.<ref name="Milne 1928">{{cite journal | last1= Milne |first1= E.A. |year=1928 | title= The effect of collisions on monochromatic radiative equilibrium |journal=[[Monthly Notices of the Royal Astronomical Society]] | volume= 88|issue= 6 |pages=493–502|bibcode=1928MNRAS..88..493M | doi = 10.1093/mnras/88.6.493 |doi-access= free }}</ref> He defined 'local thermodynamic equilibrium' in a 'cell' by requiring that it macroscopically absorb and spontaneously emit radiation as if it were in radiative equilibrium in a cavity at the [[temperature]] of the matter of the 'cell'. Then it strictly obeys Kirchhoff's law of equality of radiative emissivity and absorptivity, with a black body source function. The key to local thermodynamic equilibrium here is that the rate of collisions of ponderable matter particles such as molecules should far exceed the rates of creation and annihilation of photons.
Edward A. Milne, thinking about stars, gave a definition of 'local thermodynamic equilibrium' in terms of the thermal radiation of the matter in each small local 'cell'. He defined 'local thermodynamic equilibrium' in a 'cell' by requiring that it macroscopically absorb and spontaneously emit radiation as if it were in radiative equilibrium in a cavity at the temperature of the matter of the 'cell'. Then it strictly obeys Kirchhoff's law of equality of radiative emissivity and absorptivity, with a black body source function. The key to local thermodynamic equilibrium here is that the rate of collisions of ponderable matter particles such as molecules should far exceed the rates of creation and annihilation of photons.
==Entropy in evolving systems==
==Entropy in evolving systems==
进化系统中的熵
It is pointed out by W.T. Grandy Jr,<ref>{{cite journal | doi = 10.1023/B:FOOP.0000012007.06843.ed | title = Time Evolution in Macroscopic Systems. I. Equations of Motion | year = 2004 | last1 = Grandy | first1 = W.T., Jr. | journal = Foundations of Physics | volume = 34 | issue = 1 | page = 1 |url=http://physics.uwyo.edu/~tgrandy/evolve.html |arxiv = cond-mat/0303290 |bibcode = 2004FoPh...34....1G }}</ref><ref>{{cite journal | url=http://physics.uwyo.edu/~tgrandy/entropy.html | doi=10.1023/B:FOOP.0000012008.36856.c1 | title=Time Evolution in Macroscopic Systems. II. The Entropy | year=2004 | last1=Grandy | first1=W.T., Jr. | journal=Foundations of Physics | volume=34 | issue=1 | page=21 |arxiv = cond-mat/0303291 |bibcode = 2004FoPh...34...21G }}</ref><ref>{{cite journal | url=http://physics.uwyo.edu/~tgrandy/applications.html | doi = 10.1023/B:FOOP.0000022187.45866.81 | title=Time Evolution in Macroscopic Systems. III: Selected Applications | year=2004 | last1=Grandy | first1=W. T., Jr | journal=Foundations of Physics | volume=34 | issue=5 | page=771 |bibcode = 2004FoPh...34..771G }}</ref><ref>Grandy 2004 see also [http://physics.uwyo.edu/~tgrandy/Statistical_Mechanics.html].</ref>, that entropy, though it may be defined for a non-equilibrium system is—when strictly considered—only a macroscopic quantity that refers to the whole system, and is not a dynamical variable and in general does not act as a local potential that describes local physical forces. Under special circumstances, however, one can metaphorically think as if the thermal variables behaved like local physical forces. The approximation that constitutes classical irreversible thermodynamics is built on this metaphoric thinking.
It is pointed out by W.T. Grandy Jr,, that entropy, though it may be defined for a non-equilibrium system is—when strictly considered—only a macroscopic quantity that refers to the whole system, and is not a dynamical variable and in general does not act as a local potential that describes local physical forces. Under special circumstances, however, one can metaphorically think as if the thermal variables behaved like local physical forces. The approximation that constitutes classical irreversible thermodynamics is built on this metaphoric thinking.
This point of view shares many points in common with the concept and the use of entropy in continuum thermomechanics,<ref>{{cite book| title = Rational Thermodynamics | year = 1984 | last1 = Truesdell | first1 = Clifford | publisher = Springer | edition = 2 }}</ref><ref>{{cite book| title = Continuum Thermomechanics | year = 2002 | last1 = Maugin | first1 = Gérard A. | publisher = Kluwer }}</ref><ref>{{cite book| title = The Mechanics and Thermodynamics of Continua | year = 2010 | last1 = Gurtin | first1 = Morton E. | publisher = Cambridge University Press }}</ref><ref>{{cite book| title = Thermodynamics of Materials with Memory: Theory and Applications | year = 2012| last1 = Amendola | first1 = Giovambattista | publisher = Springer }}</ref> which evolved completely independently of statistical mechanics and maximum-entropy principles.
This point of view shares many points in common with the concept and the use of entropy in continuum thermomechanics, which evolved completely independently of statistical mechanics and maximum-entropy principles.
===Entropy in non-equilibrium===
===Entropy in non-equilibrium===
To describe deviation of the thermodynamic system from equilibrium, in addition to constitutive variables <math>x_1, x_2, ..., x_n</math> that are used to fix the equilibrium state, as was described above, a set of variables <math>\xi_1, \xi_2,\ldots</math> that are called ''internal variables'' have been introduced. The equilibrium state is considered to be stable and the main property of the internal variables, as measures of [[non-equilibrium]] of the system, is their trending to disappear; the local law of disappearing can be written as relaxation equation for each internal variable
To describe deviation of the thermodynamic system from equilibrium, in addition to constitutive variables <math>x_1, x_2, ..., x_n</math> that are used to fix the equilibrium state, as was described above, a set of variables <math>\xi_1, \xi_2,\ldots</math> that are called internal variables have been introduced. The equilibrium state is considered to be stable and the main property of the internal variables, as measures of non-equilibrium of the system, is their trending to disappear; the local law of disappearing can be written as relaxation equation for each internal variable
为了描述热力学系统偏离平衡状态的情况，除了用于确定平衡状态的本构变量 math x 1，x 2，... ，xn / math 之外，还引入了一组称为内部变量的变量 math xi 1， xi 2， ldots / math。平衡态被认为是稳定的，内变量作为系统非平衡的度量，其主要性质是趋于消失，消失的局部规律可以写成每个内变量的松弛方程
{{NumBlk|:|<math>
{{NumBlk|:|<math>
{{ NumBlk | : | math
\frac{d\xi_i}{dt} = - \frac{1}{\tau_i} \, \left(\xi_i - \xi_i^{(0)} \right),\quad i =1,\,2,\ldots ,
\frac{d\xi_i}{dt} = - \frac{1}{\tau_i} \, \left(\xi_i - \xi_i^{(0)} \right),\quad i =1,\,2,\ldots ,
向左(向右) ，向左(向右) ，向右(向右) ，向左1,2,2,
</math>|{{EquationRef|1}}}}
</math>|}}
我不知道，我不知道
where <math> \tau_i= \tau_i(T, x_1, x_2, \ldots, x_n)</math> is a relaxation time of a corresponding variables. It is convenient to consider the initial value <math> \xi_i^0</math> are equal to zero. The above equation is valid for small deviations from equilibrium; The dynamics of internal variables in general case is considered by Pokrovskii.<ref> Pokrovskii V.N. (2013) A derivation of the main relations of non-equilibrium thermodynamics. Hindawi Publishing Corporation: ISRN Thermodynamics, vol. 2013, article ID 906136, 9 p. https://dx.doi.org/10.1155/2013/906136. </ref>
where <math> \tau_i= \tau_i(T, x_1, x_2, \ldots, x_n)</math> is a relaxation time of a corresponding variables. It is convenient to consider the initial value <math> \xi_i^0</math> are equal to zero. The above equation is valid for small deviations from equilibrium; The dynamics of internal variables in general case is considered by Pokrovskii.
Entropy of the system in non-equilibrium is a function of the total set of variables
Entropy of the system in non-equilibrium is a function of the total set of variables
非平衡态系统的熵是总变量集的函数
{{NumBlk|:|<math>
{{NumBlk|:|<math>
{{ NumBlk | : | math
S=S(T, x_1, x_2, , x_n; \xi_1, \xi_2, \ldots)
S=S(T, x_1, x_2, , x_n; \xi_1, \xi_2, \ldots)
S (t，x1，x2，，xn; xi 1， xi 2， ldots)
</math>|{{EquationRef|1}}}}
</math>|}}
我不知道，我不知道
The essential contribution to the thermodynamics of the [[non-equilibrium systems]] was brought by [[Prigogine]], when he and his collaborators investigated the systems of chemically reacting substances. The stationary states of such systems exists due to exchange both particles and energy with the environment. In section 8 of the third chapter of his book <ref>[[Ilya Prigogine|Prigogine, I.]] (1955/1961/1967). ''Introduction to Thermodynamics of Irreversible Processes''. 3rd edition, Wiley Interscience, New York.</ref>, Prigogine has specified three contributions to the variation of entropy of the considered system at the given volume and constant temperature <math> T</math> . The increment of [[entropy]] <math> S</math> can be calculated according to the formula
The essential contribution to the thermodynamics of the non-equilibrium systems was brought by Prigogine, when he and his collaborators investigated the systems of chemically reacting substances. The stationary states of such systems exists due to exchange both particles and energy with the environment. In section 8 of the third chapter of his book , Prigogine has specified three contributions to the variation of entropy of the considered system at the given volume and constant temperature <math> T</math> . The increment of entropy <math> S</math> can be calculated according to the formula
普里高金和他的合作者在研究化学反应物质系统时，提出了非平衡系统热力学的本质贡献。由于粒子和能量与环境的交换，这类系统的静止状态是存在的。在他的书的第三章的第8节中，普里高金详细说明了在给定体积下考虑系统的熵变化的三个贡献和恒温数学 t / math。根据这个公式可以计算出熵的增量 s / 数
{{NumBlk|:|<math>
{{NumBlk|:|<math>
{{ NumBlk | : | math
T\,dS = \Delta Q - \sum_{j} \, \Xi_{j} \,\Delta \xi_j + \sum_{\alpha =1}^k\, \mu_\alpha \, \Delta N_\alpha.
T\,dS = \Delta Q - \sum_{j} \, \Xi_{j} \,\Delta \xi_j + \sum_{\alpha =1}^k\, \mu_\alpha \, \Delta N_\alpha.
T，dS Delta q-sum { j } ， Xi { j } ， Delta Xi j + sum { alpha 1} ， mu alpha， Delta n alpha.
</math>|{{EquationRef|1}}}}
</math>|}}
我不知道，我不知道
The first term on the right hand side of the equation presents a stream of thermal energy into the system; the last term -- a stream of energy into the system coming with the stream of particles of substances <math> \Delta N_\alpha </math> that can be positive or negative, <math> \mu_\alpha</math> is [[chemical potential]] of substance <math> \alpha</math>. The middle term in (1) depicts [[energy dissipation]] ([[entropy production]]) due to the relaxation of internal variables <math> \xi_j</math>. In the case of chemically reacting substances, which was investigated by Prigogine, the internal variables appear to be measures of incompleteness of chemical reactions, that is measures of how much the considered system with chemical reactions is out of equilibrium. The theory can be generalised,<ref> Pokrovskii V.N. (2005) Extended thermodynamics in a discrete-system approach, Eur. J. Phys. vol. 26, 769-781.</ref><ref> Pokrovskii V.N. (2013) A derivation of the main relations of non-equilibrium thermodynamics. Hindawi Publishing Corporation: ISRN Thermodynamics, vol. 2013, article ID 906136, 9 p. https://dx.doi.org/10.1155/2013/906136. </ref> to consider any deviation from the equilibrium state as an internal variable, so that we consider the set of internal variables <math> \xi_j</math> in equation (1) to consist of the quantities defining not only degrees of completeness of all chemical reactions occurring in the system, but also the structure of the system, gradients of temperature, difference of concentrations of substances and so on.
The first term on the right hand side of the equation presents a stream of thermal energy into the system; the last term -- a stream of energy into the system coming with the stream of particles of substances <math> \Delta N_\alpha </math> that can be positive or negative, <math> \mu_\alpha</math> is chemical potential of substance <math> \alpha</math>. The middle term in (1) depicts energy dissipation (entropy production) due to the relaxation of internal variables <math> \xi_j</math>. In the case of chemically reacting substances, which was investigated by Prigogine, the internal variables appear to be measures of incompleteness of chemical reactions, that is measures of how much the considered system with chemical reactions is out of equilibrium. The theory can be generalised, to consider any deviation from the equilibrium state as an internal variable, so that we consider the set of internal variables <math> \xi_j</math> in equation (1) to consist of the quantities defining not only degrees of completeness of all chemical reactions occurring in the system, but also the structure of the system, gradients of temperature, difference of concentrations of substances and so on.
==Flows and forces==
==Flows and forces==
流动与力量
The fundamental relation of classical equilibrium thermodynamics <ref name="W. Greiner et. al. 1997">W. Greiner, L. Neise, and H. Stöcker (1997), ''Thermodynamics and Statistical Mechanics (Classical Theoretical Physics)'' ,Springer-Verlag, New York, '''P85, 91, 101,108,116''', {{ISBN|0-387-94299-8}}.</ref>
The fundamental relation of classical equilibrium thermodynamics
: <math>dS=\frac{1}{T}dU+\frac{p}{T}dV-\sum_{i=1}^s\frac{\mu_i}{T}dN_i</math>
<math>dS=\frac{1}{T}dU+\frac{p}{T}dV-\sum_{i=1}^s\frac{\mu_i}{T}dN_i</math>
expresses the change in [[entropy]] <math>dS</math> of a system as a function of the intensive quantities [[temperature]] <math>T</math>, [[pressure]] <math>p</math> and <math>i^{th}</math> [[chemical potential]] <math>\mu_i</math> and of the differentials of the extensive quantities [[energy]] <math>U</math>, [[Volume (thermodynamics)|volume]] <math>V</math> and <math>i^{th}</math> [[particle number]] <math>N_i</math>.
expresses the change in entropy <math>dS</math> of a system as a function of the intensive quantities temperature <math>T</math>, pressure <math>p</math> and <math>i^{th}</math> chemical potential <math>\mu_i</math> and of the differentials of the extensive quantities energy <math>U</math>, volume <math>V</math> and <math>i^{th}</math> particle number <math>N_i</math>.
Following Onsager (1931,I),<ref name="Onsager 1931 I"/> let us extend our considerations to thermodynamically non-equilibrium systems. As a basis, we need locally defined versions of the extensive macroscopic quantities <math>U</math>, <math>V</math> and <math>N_i</math> and of the intensive macroscopic quantities <math>T</math>, <math>p</math> and <math>\mu_i</math>.
Following Onsager (1931,I), let us extend our considerations to thermodynamically non-equilibrium systems. As a basis, we need locally defined versions of the extensive macroscopic quantities <math>U</math>, <math>V</math> and <math>N_i</math> and of the intensive macroscopic quantities <math>T</math>, <math>p</math> and <math>\mu_i</math>.
For classical non-equilibrium studies, we will consider some new locally defined intensive macroscopic variables. We can, under suitable conditions, derive these new variables by locally defining the gradients and flux densities of the basic locally defined macroscopic quantities.
For classical non-equilibrium studies, we will consider some new locally defined intensive macroscopic variables. We can, under suitable conditions, derive these new variables by locally defining the gradients and flux densities of the basic locally defined macroscopic quantities.
Such locally defined gradients of intensive macroscopic variables are called 'thermodynamic forces'. They 'drive' flux densities, perhaps misleadingly often called 'fluxes', which are dual to the forces. These quantities are defined in the article on [[Onsager reciprocal relations]].
Such locally defined gradients of intensive macroscopic variables are called 'thermodynamic forces'. They 'drive' flux densities, perhaps misleadingly often called 'fluxes', which are dual to the forces. These quantities are defined in the article on Onsager reciprocal relations.
Establishing the relation between such forces and flux densities is a problem in statistical mechanics. Flux densities (<math>J_i</math>) may be coupled. The article on Onsager reciprocal relations considers the stable near-steady thermodynamically non-equilibrium regime, which has dynamics linear in the forces and flux densities.
Establishing the relation between such forces and flux densities is a problem in statistical mechanics. Flux densities (<math>J_i</math>) may be coupled. The article on Onsager reciprocal relations considers the stable near-steady thermodynamically non-equilibrium regime, which has dynamics linear in the forces and flux densities.
In stationary conditions, such forces and associated flux densities are by definition time invariant, as also are the system's locally defined entropy and rate of entropy production. Notably, according to [[Ilya Prigogine]] and others, when an open system is in conditions that allow it to reach a stable stationary thermodynamically non-equilibrium state, it organizes itself so as to minimize total entropy production defined locally. This is considered further below.
In stationary conditions, such forces and associated flux densities are by definition time invariant, as also are the system's locally defined entropy and rate of entropy production. Notably, according to Ilya Prigogine and others, when an open system is in conditions that allow it to reach a stable stationary thermodynamically non-equilibrium state, it organizes itself so as to minimize total entropy production defined locally. This is considered further below.
One wants to take the analysis to the further stage of describing the behaviour of surface and volume integrals of non-stationary local quantities; these integrals are macroscopic fluxes and production rates. In general the dynamics of these integrals are not adequately described by linear equations, though in special cases they can be so described.
One wants to take the analysis to the further stage of describing the behaviour of surface and volume integrals of non-stationary local quantities; these integrals are macroscopic fluxes and production rates. In general the dynamics of these integrals are not adequately described by linear equations, though in special cases they can be so described.
===Onsager reciprocal relations===
===Onsager reciprocal relations===
{{Main article|Onsager reciprocal relations}}
Following Section III of Rayleigh (1873),<ref name="Rayleigh 1873"/> Onsager (1931, I)<ref name="Onsager 1931 I"/> showed that in the regime where both the flows (<math>J_i</math>) are small and the thermodynamic forces (<math>F_i</math>) vary slowly, the rate of creation of entropy <math>(\sigma)</math> is [[linear relation|linearly related]] to the flows:
Following Section III of Rayleigh (1873), Onsager (1931, I) showed that in the regime where both the flows (<math>J_i</math>) are small and the thermodynamic forces (<math>F_i</math>) vary slowly, the rate of creation of entropy <math>(\sigma)</math> is linearly related to the flows:
:<math>\sigma = \sum_i J_i\frac{\partial F_i}{\partial x_i} </math>
<math>\sigma = \sum_i J_i\frac{\partial F_i}{\partial x_i} </math>
and the flows are related to the gradient of the forces, parametrized by a [[matrix (mathematics)|matrix]] of coefficients conventionally denoted <math>L</math>:
and the flows are related to the gradient of the forces, parametrized by a matrix of coefficients conventionally denoted <math>L</math>:
:<math>J_i = \sum_{j} L_{ij} \frac{\partial F_j}{\partial x_j} </math>
<math>J_i = \sum_{j} L_{ij} \frac{\partial F_j}{\partial x_j} </math>
from which it follows that:
from which it follows that:
:<math>\sigma = \sum_{i,j} L_{ij} \frac{\partial F_i}{\partial x_i}\frac{\partial F_j}{\partial x_j} </math>
<math>\sigma = \sum_{i,j} L_{ij} \frac{\partial F_i}{\partial x_i}\frac{\partial F_j}{\partial x_j} </math>
The [[second law of thermodynamics]] requires that the matrix <math>L</math> be [[Positive-definite matrix|positive definite]]. [[Statistical mechanics]] considerations involving microscopic reversibility of dynamics imply that the matrix <math>L</math> is [[symmetric matrix|symmetric]]. This fact is called the ''Onsager reciprocal relations''.
The second law of thermodynamics requires that the matrix <math>L</math> be positive definite. Statistical mechanics considerations involving microscopic reversibility of dynamics imply that the matrix <math>L</math> is symmetric. This fact is called the Onsager reciprocal relations.
The generalization of the above equations for the rate of creation of entropy was given by Pokrovskii.<ref> Pokrovskii V.N. (2013) A derivation of the main relations of non-equilibrium thermodynamics. Hindawi Publishing Corporation: ISRN Thermodynamics, vol. 2013, article ID 906136, 9 p. https://dx.doi.org/10.1155/2013/906136. </ref>
The generalization of the above equations for the rate of creation of entropy was given by Pokrovskii.
==Speculated extremal principles for non-equilibrium processes==
==Speculated extremal principles for non-equilibrium processes==
{{main article|Extremal principles in non-equilibrium thermodynamics}}
Until recently, prospects for useful extremal principles in this area have seemed clouded. Nicolis (1999)<ref>{{Cite journal | doi = 10.1002/qj.49712555718 | last1 = Nicolis | first1 = C. | year = 1999 | title = Entropy production and dynamical complexity in a low-order atmospheric model | url = | journal = Quarterly Journal of the Royal Meteorological Society | volume = 125 | issue = 557| pages = 1859–1878 |bibcode = 1999QJRMS.125.1859N }}</ref> concludes that one model of atmospheric dynamics has an attractor which is not a regime of maximum or minimum dissipation; she says this seems to rule out the existence of a global organizing principle, and comments that this is to some extent disappointing; she also points to the difficulty of finding a thermodynamically consistent form of entropy production. Another top expert offers an extensive discussion of the possibilities for principles of extrema of entropy production and of dissipation of energy: Chapter 12 of Grandy (2008)<ref name="Grandy 2008"/> is very cautious, and finds difficulty in defining the 'rate of internal entropy production' in many cases, and finds that sometimes for the prediction of the course of a process, an extremum of the quantity called the rate of dissipation of energy may be more useful than that of the rate of entropy production; this quantity appeared in Onsager's 1931<ref name="Onsager 1931 I"/> origination of this subject. Other writers have also felt that prospects for general global extremal principles are clouded. Such writers include Glansdorff and Prigogine (1971), Lebon, Jou and Casas-Vásquez (2008), and Šilhavý (1997).
Until recently, prospects for useful extremal principles in this area have seemed clouded. Nicolis (1999) concludes that one model of atmospheric dynamics has an attractor which is not a regime of maximum or minimum dissipation; she says this seems to rule out the existence of a global organizing principle, and comments that this is to some extent disappointing; she also points to the difficulty of finding a thermodynamically consistent form of entropy production. Another top expert offers an extensive discussion of the possibilities for principles of extrema of entropy production and of dissipation of energy: Chapter 12 of Grandy (2008) is very cautious, and finds difficulty in defining the 'rate of internal entropy production' in many cases, and finds that sometimes for the prediction of the course of a process, an extremum of the quantity called the rate of dissipation of energy may be more useful than that of the rate of entropy production; this quantity appeared in Onsager's 1931 origination of this subject. Other writers have also felt that prospects for general global extremal principles are clouded. Such writers include Glansdorff and Prigogine (1971), Lebon, Jou and Casas-Vásquez (2008), and Šilhavý (1997).
A recent proposal may perhaps by-pass those clouded prospects.<ref name="Attard 2012">{{cite arXiv|last=Attard|first=P.|title=Optimising Principle for Non-Equilibrium Phase Transitions and Pattern Formation with Results for Heat Convection|journal=|year=2012|eprint=1208.5105|class=cond-mat.stat-mech}}</ref><ref>Attard, P. (2012). ''Non-Equilibrium Thermodynamics and Statistical Mechanics: Foundations and Applications'', Oxford University Press, Oxford UK, {{ISBN|978-0-19-966276-0}}.</ref>
A recent proposal may perhaps by-pass those clouded prospects.
==Applications==
==Applications==
申请
Non-equilibrium thermodynamics has been successfully applied to describe biological processes such as [[protein folding]]/unfolding and [[membrane transport|transport through membranes]]<ref>{{cite journal |last1=Kimizuka |first1=Hideo |last2=Kaibara |first2=Kozue |title=Nonequilibrium thermodynamics of ion transport through membranes |journal=Journal of Colloid and Interface Science |date=September 1975 |volume=52 |issue=3 |pages=516–525 |doi=10.1016/0021-9797(75)90276-3}}</ref><ref>{{cite journal |last1=Baranowski |first1=B. |title=Non-equilibrium thermodynamics as applied to membrane transport |journal=Journal of Membrane Science |date=April 1991 |volume=57 |issue=2–3 |pages=119–159 |doi=10.1016/S0376-7388(00)80675-4}}</ref>.
Non-equilibrium thermodynamics has been successfully applied to describe biological processes such as protein folding/unfolding and transport through membranes.
非平衡态热力学已成功地应用于描述诸如蛋白质折叠 / 去折叠和通过膜转运等生物学过程。
It is also used to give a description of the dynamics of nanoparticles, which can be out of equilibrium in systems where catalysis and electrochemical conversion is involved.<ref>{{cite journal |last1=Bazant |first1=Martin Z. |title=Theory of Chemical Kinetics and Charge Transfer based on Nonequilibrium Thermodynamics |journal=Accounts of Chemical Research |date=22 March 2013 |volume=46 |issue=5 |pages=1144–1160 |doi=10.1021/ar300145c|pmid=23520980 |arxiv=1208.1587 }}</ref>
It is also used to give a description of the dynamics of nanoparticles, which can be out of equilibrium in systems where catalysis and electrochemical conversion is involved.
它也被用来描述纳米颗粒的动力学，在涉及催化和电化学转化的系统中可能失去平衡。
Also, ideas from non-equilibrium thermodynamics and the informatic theory of entropy have been adapted to describe general economic systems.<ref>{{Cite book|title = Econodynamics. The Theory of Social Production.|last = Pokrovskii|first = Vladimir|publisher = Springer, Dordrecht-Heidelberg-London-New York.|year = 2011|isbn = |location = https://www.springer.com/physics/complexity/book/978-94-007-2095-4|pages = }}</ref>
Also, ideas from non-equilibrium thermodynamics and the informatic theory of entropy have been adapted to describe general economic systems.
<ref>{{Cite book|title = The Unity of Science and Economics: A New Foundation of Economic Theory|last = Chen|first = Jing|publisher = Springer|year = 2015|isbn = |location = https://www.springer.com/us/book/9781493934645|pages = }}</ref>
==See also==
==See also==
* [[Time crystal]]
* [[Dissipative system]]
* [[Entropy production]]
* [[Extremal principles in non-equilibrium thermodynamics]]
* [[Self-organization]]
* [[Autocatalytic reactions and order creation]]
* [[Self-organizing criticality]]
* [[BBGKY hierarchy|Bogoliubov-Born-Green-Kirkwood-Yvon hierarchy of equations]]
* [[Boltzmann equation]]
* [[Vlasov equation]]
* [[Maxwell's demon]]
* [[Information entropy]]
* [[Spontaneous symmetry breaking]]
* [[Autopoiesis]]
* [[Maximum power principle]]
==References==
==References==
{{Reflist|colwidth=30em}}
===Sources===
===Sources===
{{refbegin}}
*[[Herbert Callen|Callen, H.B.]] (1960/1985). ''Thermodynamics and an Introduction to Thermostatistics'', (1st edition 1960) 2nd edition 1985, Wiley, New York, {{ISBN|0-471-86256-8}}.
*Eu, B.C. (2002). ''Generalized Thermodynamics. The Thermodynamics of Irreversible Processes and Generalized Hydrodynamics'', Kluwer Academic Publishers, Dordrecht, {{ISBN|1-4020-0788-4}}.
*Glansdorff, P., [[Ilya Prigogine|Prigogine, I.]] (1971). ''Thermodynamic Theory of Structure, Stability, and Fluctuations'', Wiley-Interscience, London, 1971, {{ISBN|0-471-30280-5}}.
*Grandy, W.T., Jr (2008). ''Entropy and the Time Evolution of Macroscopic Systems''. Oxford University Press. {{ISBN|978-0-19-954617-6}}.
*Gyarmati, I. (1967/1970). ''Non-equilibrium Thermodynamics. Field Theory and Variational Principles'', translated from the Hungarian (1967) by E. Gyarmati and W.F. Heinz, Springer, Berlin.
*[[Elliott H. Lieb|Lieb, E.H.]], [[Jakob Yngvason|Yngvason, J.]] (1999). 'The physics and mathematics of the second law of thermodynamics', ''Physics Reports'', '''310''': 1–96. [https://arxiv.org/abs/cond-mat/9708200 See also this.]
{{refend}}
==Further reading==
==Further reading==
{{refbegin}}
*[[Hans Ziegler (physicist)|Ziegler, Hans]] (1977): ''An introduction to Thermomechanics''. North Holland, Amsterdam. {{ISBN|0-444-11080-1}}. Second edition (1983) {{ISBN|0-444-86503-9}}.
*Kleidon, A., Lorenz, R.D., editors (2005). ''Non-equilibrium Thermodynamics and the Production of Entropy'', Springer, Berlin. {{ISBN|3-540-22495-5}}.
*[[Ilya Prigogine|Prigogine, I.]] (1955/1961/1967). ''Introduction to Thermodynamics of Irreversible Processes''. 3rd edition, Wiley Interscience, New York.
*[[Dmitry Zubarev|Zubarev D. N.]] (1974): ''[https://books.google.com/books?id=SQy3AAAAIAAJ&hl=ru&source=gbs_ViewAPI Nonequilibrium Statistical Thermodynamics]''. New York, Consultants Bureau. {{ISBN|0-306-10895-X}}; {{ISBN|978-0-306-10895-2}}.
*Keizer, J. (1987). ''Statistical Thermodynamics of Nonequilibrium Processes'', Springer-Verlag, New York, {{ISBN|0-387-96501-7}}.
*[[Dmitry Zubarev|Zubarev D. N.]], Morozov V., Ropke G. (1996): ''Statistical Mechanics of Nonequilibrium Processes: Basic Concepts, Kinetic Theory''. John Wiley & Sons. {{ISBN|3-05-501708-0}}.
*[[Dmitry Zubarev|Zubarev D. N.]], Morozov V., Ropke G. (1997): ''Statistical Mechanics of Nonequilibrium Processes: Relaxation and Hydrodynamic Processes''. John Wiley & Sons. {{ISBN|3-527-40084-2}}.
*Tuck, Adrian F. (2008). ''Atmospheric turbulence : a molecular dynamics perspective''. Oxford University Press. {{ISBN|978-0-19-923653-4}}.
*Grandy, W.T., Jr (2008). ''Entropy and the Time Evolution of Macroscopic Systems''. Oxford University Press. {{ISBN|978-0-19-954617-6}}.
*Kondepudi, D., Prigogine, I. (1998). ''Modern Thermodynamics: From Heat Engines to Dissipative Structures''. John Wiley & Sons, Chichester. {{ISBN|0-471-97393-9}}.
*de Groot S.R., [[Peter Mazur|Mazur P.]] (1984). ''Non-Equilibrium Thermodynamics'' (Dover). {{ISBN|0-486-64741-2}}
*Ramiro Augusto Salazar La Rotta. (2011). ''The Non-Equilibrium Thermodynamics, Perpetual''
{{refend}}
==External links==
==External links==
*[https://web.archive.org/web/20110406071945/http://www-dcf.ds.mpg.de/build.php/Titel/Research_english.html?sub=1&ver=en Stephan Herminghaus' Dynamics of Complex Fluids Department at the Max Planck Institute for Dynamics and Self Organization]
* [https://web.archive.org/web/20120519172014/http://www.worldscibooks.com/physics/1622.html Non-equilibrium Statistical Thermodynamics applied to Fluid Dynamics and Laser Physics] - 1992- book by Xavier de Hemptinne.
* [https://dx.doi.org/10.1063/1.2012462 Nonequilibrium Thermodynamics of Small Systems] - PhysicsToday.org
* [https://web.archive.org/web/20050308053832/http://www.intothecool.com/energetic.php Into the Cool] - 2005 book by Dorion Sagan and Eric D. Schneider, on nonequilibrium thermodynamics and [[evolution|evolutionary theory]].
*[http://www.pnas.org/content/98/20/11081.full.pdf Thermodynamics ‘‘beyond'' local equilibrium]
{{DEFAULTSORT:Non-Equilibrium Thermodynamics}}
[[Category:Non-equilibrium thermodynamics]]
Category:Non-equilibrium thermodynamics
类别: 非平衡态热力学
[[Category:Concepts in physics]]
Category:Concepts in physics
分类: 物理概念
[[Category:Branches of thermodynamics]]
Category:Branches of thermodynamics
分类: 热力学的分支
<noinclude>
<small>This page was moved from [[wikipedia:en:Non-equilibrium thermodynamics]]. Its edit history can be viewed at [[非平衡系统/edithistory]]</small></noinclude>
[[Category:待整理页面]]
{{short description|Branch of thermodynamics}}
{{Cleanup rewrite|date=December 2018}}{{thermodynamics|cTopic=Branches}}
'''Non-equilibrium thermodynamics''' is a branch of [[thermodynamics]] that deals with physical systems that are not in [[thermodynamic equilibrium]] but can be described in terms of variables (non-equilibrium state variables) that represent an extrapolation of the variables used to specify the system in thermodynamic equilibrium. Non-equilibrium thermodynamics is concerned with [[transport phenomena|transport process]]es and with the rates of [[chemical reactions]]. It relies on what may be thought of as more or less nearness to thermodynamic equilibrium. Non-equilibrium thermodynamics is a work in progress, not an established edifice. This article will try to sketch some approaches to it and some concepts important for it.
Non-equilibrium thermodynamics is a branch of thermodynamics that deals with physical systems that are not in thermodynamic equilibrium but can be described in terms of variables (non-equilibrium state variables) that represent an extrapolation of the variables used to specify the system in thermodynamic equilibrium. Non-equilibrium thermodynamics is concerned with transport processes and with the rates of chemical reactions. It relies on what may be thought of as more or less nearness to thermodynamic equilibrium. Non-equilibrium thermodynamics is a work in progress, not an established edifice. This article will try to sketch some approaches to it and some concepts important for it.
Almost all systems found in nature are not in thermodynamic equilibrium, for they are changing or can be triggered to change over time, and are continuously and discontinuously subject to flux of matter and energy to and from other systems and to chemical reactions. Some systems and processes are, however, in a useful sense, near enough to thermodynamic equilibrium to allow description with useful accuracy by currently known non-equilibrium thermodynamics. Nevertheless, many natural systems and processes will always remain far beyond the scope of non-equilibrium thermodynamic methods due to the existence of non variational dynamics, where the concept of free energy is lost <ref>{{cite journal |last1=Bodenschatz |first1=Eberhard |last2=Cannell |first2=David S. |last3=de Bruyn |first3=John R. |last4=Ecke |first4=Robert |last5=Hu |first5=Yu-Chou |last6=Lerman |first6=Kristina |last7=Ahlers |first7=Guenter |title=Experiments on three systems with non-variational aspects |journal=Physica D: Nonlinear Phenomena |date=December 1992 |volume=61 |issue=1–4 |pages=77–93 |doi=10.1016/0167-2789(92)90150-L}}</ref>.
Almost all systems found in nature are not in thermodynamic equilibrium, for they are changing or can be triggered to change over time, and are continuously and discontinuously subject to flux of matter and energy to and from other systems and to chemical reactions. Some systems and processes are, however, in a useful sense, near enough to thermodynamic equilibrium to allow description with useful accuracy by currently known non-equilibrium thermodynamics. Nevertheless, many natural systems and processes will always remain far beyond the scope of non-equilibrium thermodynamic methods due to the existence of non variational dynamics, where the concept of free energy is lost .
The thermodynamic study of non-equilibrium systems requires more general concepts than are dealt with by [[equilibrium thermodynamics]]. One fundamental difference between equilibrium thermodynamics and non-equilibrium thermodynamics lies in the behaviour of inhomogeneous systems, which require for their study knowledge of rates of reaction which are not considered in equilibrium thermodynamics of homogeneous systems. This is discussed below. Another fundamental and very important difference is the difficulty or impossibility, in general, in defining [[entropy]] at an instant of time in macroscopic terms for systems not in thermodynamic equilibrium; it can be done, to useful approximation, only in carefully chosen special cases, namely those that are throughout in local thermodynamic equilibrium.<ref name="Grandy 2008">Grandy, W.T., Jr (2008).</ref><ref name="Lebon Jou Casas-Vázquez 2008">Lebon, G., Jou, D., Casas-Vázquez, J. (2008). ''Understanding Non-equilibrium Thermodynamics: Foundations, Applications, Frontiers'', Springer-Verlag, Berlin, e-{{ISBN|978-3-540-74252-4}}.</ref>
The thermodynamic study of non-equilibrium systems requires more general concepts than are dealt with by equilibrium thermodynamics. One fundamental difference between equilibrium thermodynamics and non-equilibrium thermodynamics lies in the behaviour of inhomogeneous systems, which require for their study knowledge of rates of reaction which are not considered in equilibrium thermodynamics of homogeneous systems. This is discussed below. Another fundamental and very important difference is the difficulty or impossibility, in general, in defining entropy at an instant of time in macroscopic terms for systems not in thermodynamic equilibrium; it can be done, to useful approximation, only in carefully chosen special cases, namely those that are throughout in local thermodynamic equilibrium.
==Scope==
==Scope==
===Difference between equilibrium and non-equilibrium thermodynamics===
===Difference between equilibrium and non-equilibrium thermodynamics===
A profound difference separates equilibrium from non-equilibrium thermodynamics. Equilibrium thermodynamics ignores the time-courses of physical processes. In contrast, non-equilibrium thermodynamics attempts to describe their time-courses in continuous detail.
A profound difference separates equilibrium from non-equilibrium thermodynamics. Equilibrium thermodynamics ignores the time-courses of physical processes. In contrast, non-equilibrium thermodynamics attempts to describe their time-courses in continuous detail.
Equilibrium thermodynamics restricts its considerations to processes that have initial and final states of thermodynamic equilibrium; the time-courses of processes are deliberately ignored. Consequently, equilibrium thermodynamics allows processes that pass through states far from thermodynamic equilibrium, that cannot be described even by the variables admitted for non-equilibrium thermodynamics,<ref name="EY 5">[[Elliott H. Lieb|Lieb, E.H.]], [[Jakob Yngvason|Yngvason, J.]] (1999), p. 5.</ref> such as time rates of change of temperature and pressure.<ref>Gyarmati, I. (1967/1970), pp. 8–12.</ref> For example, in equilibrium thermodynamics, a process is allowed to include even a violent explosion that cannot be described by non-equilibrium thermodynamics.<ref name="EY 5"/> Equilibrium thermodynamics does, however, for theoretical development, use the idealized concept of the "quasi-static process". A quasi-static process is a conceptual (timeless and physically impossible) smooth mathematical passage along a continuous path of states of thermodynamic equilibrium.<ref>[[Herbert Callen|Callen, H.B.]] (1960/1985), § 4–2.</ref> It is an exercise in differential geometry rather than a process that could occur in actuality.
Equilibrium thermodynamics restricts its considerations to processes that have initial and final states of thermodynamic equilibrium; the time-courses of processes are deliberately ignored. Consequently, equilibrium thermodynamics allows processes that pass through states far from thermodynamic equilibrium, that cannot be described even by the variables admitted for non-equilibrium thermodynamics, such as time rates of change of temperature and pressure. For example, in equilibrium thermodynamics, a process is allowed to include even a violent explosion that cannot be described by non-equilibrium thermodynamics. It is an exercise in differential geometry rather than a process that could occur in actuality.
Non-equilibrium thermodynamics, on the other hand, attempting to describe continuous time-courses, needs its [[State function|state variables]] to have a very close connection with those of equilibrium thermodynamics.<ref>Glansdorff, P., Prigogine, I. (1971), Ch. {{math|II}},§ 2.</ref> This profoundly restricts the scope of non-equilibrium thermodynamics, and places heavy demands on its conceptual framework.
Non-equilibrium thermodynamics, on the other hand, attempting to describe continuous time-courses, needs its state variables to have a very close connection with those of equilibrium thermodynamics. This profoundly restricts the scope of non-equilibrium thermodynamics, and places heavy demands on its conceptual framework.
===Non-equilibrium state variables===
===Non-equilibrium state variables===
===Non-equilibrium state variables===
The suitable relationship that defines non-equilibrium thermodynamic state variables is as follows. On occasions when the system happens to be in states that are sufficiently close to thermodynamic equilibrium, non-equilibrium state variables are such that they can be measured locally with sufficient accuracy by the same techniques as are used to measure thermodynamic state variables, or by corresponding time and space derivatives, including fluxes of matter and energy. In general, non-equilibrium thermodynamic systems are spatially and temporally non-uniform, but their non-uniformity still has a sufficient degree of smoothness to support the existence of suitable time and space derivatives of non-equilibrium state variables. Because of the spatial non-uniformity, non-equilibrium state variables that correspond to extensive thermodynamic state variables have to be defined as spatial densities of the corresponding extensive equilibrium state variables. On occasions when the system is sufficiently close to thermodynamic equilibrium, intensive non-equilibrium state variables, for example temperature and pressure, correspond closely with equilibrium state variables. It is necessary that measuring probes be small enough, and rapidly enough responding, to capture relevant non-uniformity. Further, the non-equilibrium state variables are required to be mathematically functionally related to one another in ways that suitably resemble corresponding relations between equilibrium thermodynamic state variables.<ref name="Gyarmati 1970"/> In reality, these requirements are very demanding, and it may be difficult or practically, or even theoretically, impossible to satisfy them. This is part of why non-equilibrium thermodynamics is a work in progress.
The suitable relationship that defines non-equilibrium thermodynamic state variables is as follows. On occasions when the system happens to be in states that are sufficiently close to thermodynamic equilibrium, non-equilibrium state variables are such that they can be measured locally with sufficient accuracy by the same techniques as are used to measure thermodynamic state variables, or by corresponding time and space derivatives, including fluxes of matter and energy. In general, non-equilibrium thermodynamic systems are spatially and temporally non-uniform, but their non-uniformity still has a sufficient degree of smoothness to support the existence of suitable time and space derivatives of non-equilibrium state variables. Because of the spatial non-uniformity, non-equilibrium state variables that correspond to extensive thermodynamic state variables have to be defined as spatial densities of the corresponding extensive equilibrium state variables. On occasions when the system is sufficiently close to thermodynamic equilibrium, intensive non-equilibrium state variables, for example temperature and pressure, correspond closely with equilibrium state variables. It is necessary that measuring probes be small enough, and rapidly enough responding, to capture relevant non-uniformity. Further, the non-equilibrium state variables are required to be mathematically functionally related to one another in ways that suitably resemble corresponding relations between equilibrium thermodynamic state variables. In reality, these requirements are very demanding, and it may be difficult or practically, or even theoretically, impossible to satisfy them. This is part of why non-equilibrium thermodynamics is a work in progress.
==Overview==
==Overview==
概览
Non-equilibrium thermodynamics is a work in progress, not an established edifice. This article is an attempt to sketch some approaches to it and some concepts important for it.
Non-equilibrium thermodynamics is a work in progress, not an established edifice. This article is an attempt to sketch some approaches to it and some concepts important for it.
Some concepts of particular importance for non-equilibrium thermodynamics include time rate of dissipation of energy (Rayleigh 1873,<ref name="Rayleigh 1873">{{Cite journal | last1 = Strutt | first1 = J. W. | doi = 10.1112/plms/s1-4.1.357 | title = Some General Theorems relating to Vibrations | journal = Proceedings of the London Mathematical Society | year = 1871 | volume = s1-4 | pages = 357–368 | url = https://zenodo.org/record/1447754 }}</ref> [[Lars Onsager|Onsager]] 1931,<ref name="Onsager 1931 I">{{Cite journal | doi = 10.1103/PhysRev.37.405 | last1 = Onsager | first1 = L. | year = 1931 | title = Reciprocal relations in irreversible processes, I | url = | journal = Physical Review | volume = 37 | issue = 4| pages = 405–426 |bibcode = 1931PhRv...37..405O | doi-access = free }}</ref> also<ref name="Gyarmati 1970">Gyarmati, I. (1967/1970).</ref><ref name="Lavenda 1978">Lavenda, B.H. (1978). ''Thermodynamics of Irreversible Processes'', Macmillan, London, {{ISBN|0-333-21616-4}}.</ref>), time rate of entropy production (Onsager 1931),<ref name="Onsager 1931 I"/> thermodynamic fields,<ref>Gyarmati, I. (1967/1970), pages 4-14.</ref><ref name="Ziegler 1983">Ziegler, H., (1983). ''An Introduction to Thermomechanics'', North-Holland, Amsterdam, {{ISBN|0-444-86503-9}}.</ref><ref name="Balescu">Balescu, R. (1975). ''Equilibrium and Non-equilibrium Statistical Mechanics'', Wiley-Interscience, New York, {{ISBN|0-471-04600-0}}, Section 3.2, pages 64-72.</ref> [[dissipative structure]],<ref name="G&P 1971"/> and non-linear dynamical structure.<ref name="Lavenda 1978"/>
Some concepts of particular importance for non-equilibrium thermodynamics include time rate of dissipation of energy (Rayleigh 1873, Onsager 1931, also), time rate of entropy production (Onsager 1931), dissipative structure, and non-linear dynamical structure.
One problem of interest is the thermodynamic study of non-equilibrium [[steady state]]s, in which [[entropy]] production and some [[flux|flows]] are non-zero, but there is no [[Time-variant system|time variation]] of physical variables.
One problem of interest is the thermodynamic study of non-equilibrium steady states, in which entropy production and some flows are non-zero, but there is no time variation of physical variables.
One initial approach to non-equilibrium thermodynamics is sometimes called 'classical irreversible thermodynamics'.<ref name="Lebon Jou Casas-Vázquez 2008"/> There are other approaches to non-equilibrium thermodynamics, for example [[extended irreversible thermodynamics]],<ref name="Lebon Jou Casas-Vázquez 2008"/><ref name="JCVL 1993"/> and generalized thermodynamics,<ref>Eu, B.C. (2002).</ref> but they are hardly touched on in the present article.
One initial approach to non-equilibrium thermodynamics is sometimes called 'classical irreversible thermodynamics'. but they are hardly touched on in the present article.
===Quasi-radiationless non-equilibrium thermodynamics of matter in laboratory conditions===
===Quasi-radiationless non-equilibrium thermodynamics of matter in laboratory conditions===
实验室条件下物质的准无辐射非平衡态热力学
According to Wildt<ref name="Wildt 1972">{{Cite journal |last=Wildt |first=R. |year=1972 |title=Thermodynamics of the gray atmosphere. IV. Entropy transfer and production |journal=Astrophysical Journal |volume=174 |issue= |pages=69–77 |doi=10.1086/151469 |bibcode=1972ApJ...174...69W}}</ref> (see also Essex<ref name="Essex 1984a">{{Cite journal |last=Essex |first=C. |year=1984a |title=Radiation and the irreversible thermodynamics of climate |journal=Journal of the Atmospheric Sciences |volume=41 |issue=12 |pages=1985–1991 |doi=10.1175/1520-0469(1984)041<1985:RATITO>2.0.CO;2 |bibcode = 1984JAtS...41.1985E |doi-access=free }}.</ref><ref name="Essex 1984b">{{Cite journal |last=Essex |first=C. |year=1984b |title=Minimum entropy production in the steady state and radiative transfer |journal=Astrophysical Journal |volume=285 |issue= |pages=279–293 |doi=10.1086/162504 |bibcode=1984ApJ...285..279E}}</ref><ref name="Essex 1984c">{{Cite journal |last=Essex |first=C. |year=1984c |title=Radiation and the violation of bilinearity in the irreversible thermodynamics of irreversible processes |journal=Planetary and Space Science |volume=32 |pages=1035–1043 |doi=10.1016/0032-0633(84)90060-6 |bibcode = 1984P&SS...32.1035E |issue=8 }}</ref>), current versions of non-equilibrium thermodynamics ignore radiant heat; they can do so because they refer to laboratory quantities of matter under laboratory conditions with temperatures well below those of stars. At laboratory temperatures, in laboratory quantities of matter, thermal radiation is weak and can be practically nearly ignored. But, for example, atmospheric physics is concerned with large amounts of matter, occupying cubic kilometers, that, taken as a whole, are not within the range of laboratory quantities; then thermal radiation cannot be ignored.
According to Wildt (see also Essex), current versions of non-equilibrium thermodynamics ignore radiant heat; they can do so because they refer to laboratory quantities of matter under laboratory conditions with temperatures well below those of stars. At laboratory temperatures, in laboratory quantities of matter, thermal radiation is weak and can be practically nearly ignored. But, for example, atmospheric physics is concerned with large amounts of matter, occupying cubic kilometers, that, taken as a whole, are not within the range of laboratory quantities; then thermal radiation cannot be ignored.
===Local equilibrium thermodynamics===
===Local equilibrium thermodynamics===
局域平衡热力学
The terms 'classical irreversible thermodynamics'<ref name="Lebon Jou Casas-Vázquez 2008"/> and 'local equilibrium thermodynamics' are sometimes used to refer to a version of non-equilibrium thermodynamics that demands certain simplifying assumptions, as follows. The assumptions have the effect of making each very small volume element of the system effectively homogeneous, or well-mixed, or without an effective spatial structure, and without kinetic energy of bulk flow or of diffusive flux. Even within the thought-frame of classical irreversible thermodynamics, care<ref name="Lavenda 1978"/> is needed in choosing the independent variables<ref>Prigogine, I., Defay, R. (1950/1954). ''Chemical Thermodynamics'', Longmans, Green & Co, London, page 1.</ref> for systems. In some writings, it is assumed that the intensive variables of equilibrium thermodynamics are sufficient as the independent variables for the task (such variables are considered to have no 'memory', and do not show hysteresis); in particular, local flow intensive variables are not admitted as independent variables; local flows are considered as dependent on quasi-static local intensive variables.
The terms 'classical irreversible thermodynamics' for systems. In some writings, it is assumed that the intensive variables of equilibrium thermodynamics are sufficient as the independent variables for the task (such variables are considered to have no 'memory', and do not show hysteresis); in particular, local flow intensive variables are not admitted as independent variables; local flows are considered as dependent on quasi-static local intensive variables.
Also it is assumed that the local entropy density is the same function of the other local intensive variables as in equilibrium; this is called the local thermodynamic equilibrium assumption<ref name="Gyarmati 1970"/><ref name="Lavenda 1978"/><ref name="G&P 1971">Glansdorff, P., Prigogine, I. (1971). ''Thermodynamic Theory of Structure, Stability, and Fluctuations'', Wiley-Interscience, London, 1971, {{ISBN|0-471-30280-5}}.</ref><ref name="JCVL 1993">Jou, D., Casas-Vázquez, J., Lebon, G. (1993). ''Extended Irreversible Thermodynamics'', Springer, Berlin, {{ISBN|3-540-55874-8}}, {{ISBN|0-387-55874-8}}.</ref><ref name="De Groot Mazur 1962">De Groot, S.R., Mazur, P. (1962). ''Non-equilibrium Thermodynamics'', North-Holland, Amsterdam.</ref><ref name="Balescu 1975">Balescu, R. (1975). ''Equilibrium and Non-equilibrium Statistical Mechanics'', John Wiley & Sons, New York, {{ISBN|0-471-04600-0}}.</ref><ref name="Mihalas Mihalas 1984">[http://www.filestube.com/9c5b2744807c2c3d03e9/details.html Mihalas, D., Weibel-Mihalas, B. (1984). ''Foundations of Radiation Hydrodynamics'', Oxford University Press, New York] {{ISBN|0-19-503437-6}}.</ref><ref name="Schloegl 1989">Schloegl, F. (1989). ''Probability and Heat: Fundamentals of Thermostatistics'', Freidr. Vieweg & Sohn, Braunschweig, {{ISBN|3-528-06343-2}}.</ref> (see also Keizer (1987)<ref name="Keizer 1987">Keizer, J. (1987). ''Statistical Thermodynamics of Nonequilibrium Processes'', Springer-Verlag, New York, {{ISBN|0-387-96501-7}}.</ref>). Radiation is ignored because it is transfer of energy between regions, which can be remote from one another. In the classical irreversible thermodynamic approach, there is allowed very small spatial variation, from very small volume element to adjacent very small volume element, but it is assumed that the global entropy of the system can be found by simple spatial integration of the local entropy density; this means that spatial structure cannot contribute as it properly should to the global entropy assessment for the system. This approach assumes spatial and temporal continuity and even differentiability of locally defined intensive variables such as temperature and internal energy density. All of these are very stringent demands. Consequently, this approach can deal with only a very limited range of phenomena. This approach is nevertheless valuable because it can deal well with some macroscopically observable phenomena.{{examples|date=February 2015}}
Also it is assumed that the local entropy density is the same function of the other local intensive variables as in equilibrium; this is called the local thermodynamic equilibrium assumption (see also Keizer (1987)). Radiation is ignored because it is transfer of energy between regions, which can be remote from one another. In the classical irreversible thermodynamic approach, there is allowed very small spatial variation, from very small volume element to adjacent very small volume element, but it is assumed that the global entropy of the system can be found by simple spatial integration of the local entropy density; this means that spatial structure cannot contribute as it properly should to the global entropy assessment for the system. This approach assumes spatial and temporal continuity and even differentiability of locally defined intensive variables such as temperature and internal energy density. All of these are very stringent demands. Consequently, this approach can deal with only a very limited range of phenomena. This approach is nevertheless valuable because it can deal well with some macroscopically observable phenomena.
In other writings, local flow variables are considered; these might be considered as classical by analogy with the time-invariant long-term time-averages of flows produced by endlessly repeated cyclic processes; examples with flows are in the [[thermoelectric effect|thermoelectric phenomena]] known as the Seebeck and the Peltier effects, considered by [[William Thomson, 1st Baron Kelvin|Kelvin]] in the nineteenth century and by [[Lars Onsager]] in the twentieth.<ref name="De Groot Mazur 1962"/><ref>Kondepudi, D. (2008). ''Introduction to Modern Thermodynamics'', Wiley, Chichester UK, {{ISBN|978-0-470-01598-8}}, pages 333-338.</ref> These effects occur at metal junctions, which were originally effectively treated as two-dimensional surfaces, with no spatial volume, and no spatial variation.
In other writings, local flow variables are considered; these might be considered as classical by analogy with the time-invariant long-term time-averages of flows produced by endlessly repeated cyclic processes; examples with flows are in the thermoelectric phenomena known as the Seebeck and the Peltier effects, considered by Kelvin in the nineteenth century and by Lars Onsager in the twentieth. These effects occur at metal junctions, which were originally effectively treated as two-dimensional surfaces, with no spatial volume, and no spatial variation.
====Local equilibrium thermodynamics with materials with "memory"====
====Local equilibrium thermodynamics with materials with "memory"====
具有“记忆”材料的局域平衡热力学
A further extension of local equilibrium thermodynamics is to allow that materials may have "memory", so that their [[constitutive equation]]s depend not only on present values but also on past values of local equilibrium variables. Thus time comes into the picture more deeply than for time-dependent local equilibrium thermodynamics with memoryless materials, but fluxes are not independent variables of state.<ref>{{cite journal | last1 = Coleman | first1 = B.D. | last2 = Noll | first2 = W. | year = 1963 | title = The thermodynamics of elastic materials with heat conduction and viscosity | url = | journal = Arch. Ration. Mach. Analysis | volume = 13 | issue = 1| pages = 167–178 | doi=10.1007/bf01262690| bibcode = 1963ArRMA..13..167C }}</ref>
A further extension of local equilibrium thermodynamics is to allow that materials may have "memory", so that their constitutive equations depend not only on present values but also on past values of local equilibrium variables. Thus time comes into the picture more deeply than for time-dependent local equilibrium thermodynamics with memoryless materials, but fluxes are not independent variables of state.
===Extended irreversible thermodynamics===
===Extended irreversible thermodynamics===
扩展不可逆热力学
'''Extended irreversible thermodynamics''' is a branch of non-equilibrium thermodynamics that goes outside the restriction to the local equilibrium hypothesis. The space of state variables is enlarged by including the [[flux]]es of mass, momentum and energy and eventually higher order fluxes.
Extended irreversible thermodynamics is a branch of non-equilibrium thermodynamics that goes outside the restriction to the local equilibrium hypothesis. The space of state variables is enlarged by including the fluxes of mass, momentum and energy and eventually higher order fluxes.
扩展不可逆热力学是非平衡态热力学热力学的一个分支，它超越了局部平衡假说的限制。通过包括质量、动量和能量的通量以及最终的高阶通量，状态变量的空间被扩大了。
The formalism is well-suited for describing high-frequency processes and small-length scales materials.
The formalism is well-suited for describing high-frequency processes and small-length scales materials.
==Basic concepts==
==Basic concepts==
基本概念
There are many examples of stationary non-equilibrium systems, some very simple, like a system confined between two thermostats at different temperatures or the ordinary [[Couette flow]], a fluid enclosed between two flat walls moving in opposite directions and defining non-equilibrium conditions at the walls. [[Laser]] action is also a non-equilibrium process, but it depends on departure from local thermodynamic equilibrium and is thus beyond the scope of classical irreversible thermodynamics; here a strong temperature difference is maintained between two molecular degrees of freedom (with molecular laser, vibrational and rotational molecular motion), the requirement for two component 'temperatures' in the one small region of space, precluding local thermodynamic equilibrium, which demands that only one temperature be needed. Damping of acoustic perturbations or shock waves are non-stationary non-equilibrium processes. Driven [[complex fluids]], turbulent systems and glasses are other examples of non-equilibrium systems.
There are many examples of stationary non-equilibrium systems, some very simple, like a system confined between two thermostats at different temperatures or the ordinary Couette flow, a fluid enclosed between two flat walls moving in opposite directions and defining non-equilibrium conditions at the walls. Laser action is also a non-equilibrium process, but it depends on departure from local thermodynamic equilibrium and is thus beyond the scope of classical irreversible thermodynamics; here a strong temperature difference is maintained between two molecular degrees of freedom (with molecular laser, vibrational and rotational molecular motion), the requirement for two component 'temperatures' in the one small region of space, precluding local thermodynamic equilibrium, which demands that only one temperature be needed. Damping of acoustic perturbations or shock waves are non-stationary non-equilibrium processes. Driven complex fluids, turbulent systems and glasses are other examples of non-equilibrium systems.
The mechanics of macroscopic systems depends on a number of extensive quantities. It should be stressed that all systems are permanently interacting with their surroundings, thereby causing unavoidable fluctuations of [[extensive quantity|extensive quantiti]]es. Equilibrium conditions of thermodynamic systems are related to the maximum property of the entropy. If the only extensive quantity that is allowed to fluctuate is the internal energy, all the other ones being kept strictly constant, the temperature of the system is measurable and meaningful. The system's properties are then most conveniently described using the thermodynamic potential [[Helmholtz free energy]] (''A'' = ''U'' - ''TS''), a [[Legendre transformation]] of the energy. If, next to fluctuations of the energy, the macroscopic dimensions (volume) of the system are left fluctuating, we use the [[Gibbs free energy]] (''G'' = ''U'' + ''PV'' - ''TS''), where the system's properties are determined both by the temperature and by the pressure.
The mechanics of macroscopic systems depends on a number of extensive quantities. It should be stressed that all systems are permanently interacting with their surroundings, thereby causing unavoidable fluctuations of extensive quantities. Equilibrium conditions of thermodynamic systems are related to the maximum property of the entropy. If the only extensive quantity that is allowed to fluctuate is the internal energy, all the other ones being kept strictly constant, the temperature of the system is measurable and meaningful. The system's properties are then most conveniently described using the thermodynamic potential Helmholtz free energy (A = U - TS), a Legendre transformation of the energy. If, next to fluctuations of the energy, the macroscopic dimensions (volume) of the system are left fluctuating, we use the Gibbs free energy (G = U + PV - TS), where the system's properties are determined both by the temperature and by the pressure.
Non-equilibrium systems are much more complex and they may undergo fluctuations of more extensive quantities. The boundary conditions impose on them particular intensive variables, like temperature gradients or distorted collective motions (shear motions, vortices, etc.), often called thermodynamic forces. If free energies are very useful in equilibrium thermodynamics, it must be stressed that there is no general law defining stationary non-equilibrium properties of the energy as is the second law of thermodynamics for the [[entropy]] in equilibrium thermodynamics. That is why in such cases a more generalized Legendre transformation should be considered. This is the extended Massieu potential.
Non-equilibrium systems are much more complex and they may undergo fluctuations of more extensive quantities. The boundary conditions impose on them particular intensive variables, like temperature gradients or distorted collective motions (shear motions, vortices, etc.), often called thermodynamic forces. If free energies are very useful in equilibrium thermodynamics, it must be stressed that there is no general law defining stationary non-equilibrium properties of the energy as is the second law of thermodynamics for the entropy in equilibrium thermodynamics. That is why in such cases a more generalized Legendre transformation should be considered. This is the extended Massieu potential.
非平衡系统要复杂得多，它们可能经历更广泛的量的波动。边界条件强加给它们特殊的强度变量，如温度梯度或扭曲的集体运动(剪切运动、涡旋等)。) ，通常称为热力学力。如果自由能在平衡态热力学中非常有用，那么必须强调的是，在平衡态热力学中，定义能量的稳态非平衡性质的一般定律，并不像平衡态热力学中熵的热力学第二定律定律那样。这就是为什么在这种情况下，应该考虑一个更广泛的勒壤得转换。这就是延伸的马西欧势。
By definition, the [[entropy]] (''S'') is a function of the collection of [[extensive quantity|extensive quantiti]]es <math>E_i</math>. Each extensive quantity has a conjugate intensive variable <math>I_i</math> (a restricted definition of intensive variable is used here by comparison to the definition given in this link) so that:
By definition, the entropy (S) is a function of the collection of extensive quantities <math>E_i</math>. Each extensive quantity has a conjugate intensive variable <math>I_i</math> (a restricted definition of intensive variable is used here by comparison to the definition given in this link) so that:
:<math> I_i = \frac{\partial{S}}{\partial{E_i}}.</math>
<math> I_i = \frac{\partial{S}}{\partial{E_i}}.</math>
We then define the extended [[Massieu function]] as follows:
We then define the extended Massieu function as follows:
:<math>\ k_{\rm B} M = S - \sum_i( I_i E_i),</math>
<math>\ k_{\rm B} M = S - \sum_i( I_i E_i),</math>
where <math>\ k_{\rm B}</math> is [[Boltzmann's constant]], whence
where <math>\ k_{\rm B}</math> is Boltzmann's constant, whence
:<math>\ k_{\rm B} \, dM = \sum_i (E_i \, dI_i).</math>
<math>\ k_{\rm B} \, dM = \sum_i (E_i \, dI_i).</math>
The independent variables are the intensities.
The independent variables are the intensities.
Intensities are global values, valid for the system as a whole. When boundaries impose to the system different local conditions, (e.g. temperature differences), there are intensive variables representing the average value and others representing gradients or higher moments. The latter are the thermodynamic forces driving fluxes of extensive properties through the system.
Intensities are global values, valid for the system as a whole. When boundaries impose to the system different local conditions, (e.g. temperature differences), there are intensive variables representing the average value and others representing gradients or higher moments. The latter are the thermodynamic forces driving fluxes of extensive properties through the system.
It may be shown that the Legendre transformation changes the maximum condition of the entropy (valid at equilibrium) in a minimum condition of the extended Massieu function for stationary states, no matter whether at equilibrium or not.
It may be shown that the Legendre transformation changes the maximum condition of the entropy (valid at equilibrium) in a minimum condition of the extended Massieu function for stationary states, no matter whether at equilibrium or not.
==Stationary states, fluctuations, and stability==
==Stationary states, fluctuations, and stability==
In thermodynamics one is often interested in a stationary state of a process, allowing that the stationary state include the occurrence of unpredictable and experimentally unreproducible fluctuations in the state of the system. The fluctuations are due to the system's internal sub-processes and to exchange of matter or energy with the system's surroundings that create the constraints that define the process.
In thermodynamics one is often interested in a stationary state of a process, allowing that the stationary state include the occurrence of unpredictable and experimentally unreproducible fluctuations in the state of the system. The fluctuations are due to the system's internal sub-processes and to exchange of matter or energy with the system's surroundings that create the constraints that define the process.
If the stationary state of the process is stable, then the unreproducible fluctuations involve local transient decreases of entropy. The reproducible response of the system is then to increase the entropy back to its maximum by irreversible processes: the fluctuation cannot be reproduced with a significant level of probability. Fluctuations about stable stationary states are extremely small except near critical points (Kondepudi and Prigogine 1998, page 323).<ref>Kondepudi, D., Prigogine, I, (1998). ''Modern Thermodynamics. From Heat Engines to Dissipative Structures'', Wiley, Chichester, 1998, {{ISBN|0-471-97394-7}}.</ref> The stable stationary state has a local maximum of entropy and is locally the most reproducible state of the system. There are theorems about the irreversible dissipation of fluctuations. Here 'local' means local with respect to the abstract space of thermodynamic coordinates of state of the system.
If the stationary state of the process is stable, then the unreproducible fluctuations involve local transient decreases of entropy. The reproducible response of the system is then to increase the entropy back to its maximum by irreversible processes: the fluctuation cannot be reproduced with a significant level of probability. Fluctuations about stable stationary states are extremely small except near critical points (Kondepudi and Prigogine 1998, page 323). The stable stationary state has a local maximum of entropy and is locally the most reproducible state of the system. There are theorems about the irreversible dissipation of fluctuations. Here 'local' means local with respect to the abstract space of thermodynamic coordinates of state of the system.
If the stationary state is unstable, then any fluctuation will almost surely trigger the virtually explosive departure of the system from the unstable stationary state. This can be accompanied by increased export of entropy.
If the stationary state is unstable, then any fluctuation will almost surely trigger the virtually explosive departure of the system from the unstable stationary state. This can be accompanied by increased export of entropy.
==Local thermodynamic equilibrium==
==Local thermodynamic equilibrium==
当地热力学平衡
The scope of present-day non-equilibrium thermodynamics does not cover all physical processes. A condition for the validity of many studies in non-equilibrium thermodynamics of matter is that they deal with what is known as ''local thermodynamic equilibrium''.
The scope of present-day non-equilibrium thermodynamics does not cover all physical processes. A condition for the validity of many studies in non-equilibrium thermodynamics of matter is that they deal with what is known as local thermodynamic equilibrium.
===Ponderable matter===
===Ponderable matter===
值得思考的问题
''Local thermodynamic equilibrium of matter''<ref name="Gyarmati 1970"/><ref name="G&P 1971"/><ref name="Balescu 1975"/><ref name="Mihalas Mihalas 1984"/><ref name="Schloegl 1989"/> (see also Keizer (1987)<ref name="Keizer 1987"/> means that conceptually, for study and analysis, the system can be spatially and temporally divided into 'cells' or 'micro-phases' of small (infinitesimal) size, in which classical thermodynamical equilibrium conditions for matter are fulfilled to good approximation. These conditions are unfulfilled, for example, in very rarefied gases, in which molecular collisions are infrequent; and in the boundary layers of a star, where radiation is passing energy to space; and for interacting fermions at very low temperature, where dissipative processes become ineffective. When these 'cells' are defined, one admits that matter and energy may pass freely between contiguous 'cells', slowly enough to leave the 'cells' in their respective individual local thermodynamic equilibria with respect to intensive variables.
Local thermodynamic equilibrium of matter (see also Keizer (1987) means that conceptually, for study and analysis, the system can be spatially and temporally divided into 'cells' or 'micro-phases' of small (infinitesimal) size, in which classical thermodynamical equilibrium conditions for matter are fulfilled to good approximation. These conditions are unfulfilled, for example, in very rarefied gases, in which molecular collisions are infrequent; and in the boundary layers of a star, where radiation is passing energy to space; and for interacting fermions at very low temperature, where dissipative processes become ineffective. When these 'cells' are defined, one admits that matter and energy may pass freely between contiguous 'cells', slowly enough to leave the 'cells' in their respective individual local thermodynamic equilibria with respect to intensive variables.
One can think here of two 'relaxation times' separated by order of magnitude.<ref name="Zubarev 1971/1974">[[Dmitry Zubarev|Zubarev D. N.]],(1974). ''[https://books.google.com/books?id=SQy3AAAAIAAJ&hl=ru&source=gbs_ViewAPI Nonequilibrium Statistical Thermodynamics]'', translated from the Russian by P.J. Shepherd, New York, Consultants Bureau. {{ISBN|0-306-10895-X}}; {{ISBN|978-0-306-10895-2}}.</ref> The longer relaxation time is of the order of magnitude of times taken for the macroscopic dynamical structure of the system to change. The shorter is of the order of magnitude of times taken for a single 'cell' to reach local thermodynamic equilibrium. If these two relaxation times are not well separated, then the classical non-equilibrium thermodynamical concept of local thermodynamic equilibrium loses its meaning<ref name="Zubarev 1971/1974"/> and other approaches have to be proposed, see for instance [[Extended irreversible thermodynamics]]. For example, in the atmosphere, the speed of sound is much greater than the wind speed; this favours the idea of local thermodynamic equilibrium of matter for atmospheric heat transfer studies at altitudes below about 60 km where sound propagates, but not above 100 km, where, because of the paucity of intermolecular collisions, sound does not propagate.
One can think here of two 'relaxation times' separated by order of magnitude. The longer relaxation time is of the order of magnitude of times taken for the macroscopic dynamical structure of the system to change. The shorter is of the order of magnitude of times taken for a single 'cell' to reach local thermodynamic equilibrium. If these two relaxation times are not well separated, then the classical non-equilibrium thermodynamical concept of local thermodynamic equilibrium loses its meaning and other approaches have to be proposed, see for instance Extended irreversible thermodynamics. For example, in the atmosphere, the speed of sound is much greater than the wind speed; this favours the idea of local thermodynamic equilibrium of matter for atmospheric heat transfer studies at altitudes below about 60 km where sound propagates, but not above 100 km, where, because of the paucity of intermolecular collisions, sound does not propagate.
===Milne's definition in terms of radiative equilibrium===
===Milne's definition in terms of radiative equilibrium===
米尔恩对辐射平衡的定义
[[Edward Arthur Milne|Edward A. Milne]], thinking about stars, gave a definition of 'local thermodynamic equilibrium' in terms of the [[thermal radiation]] of the [[matter]] in each small local 'cell'.<ref name="Milne 1928">{{cite journal | last1= Milne |first1= E.A. |year=1928 | title= The effect of collisions on monochromatic radiative equilibrium |journal=[[Monthly Notices of the Royal Astronomical Society]] | volume= 88|issue= 6 |pages=493–502|bibcode=1928MNRAS..88..493M | doi = 10.1093/mnras/88.6.493 |doi-access= free }}</ref> He defined 'local thermodynamic equilibrium' in a 'cell' by requiring that it macroscopically absorb and spontaneously emit radiation as if it were in radiative equilibrium in a cavity at the [[temperature]] of the matter of the 'cell'. Then it strictly obeys Kirchhoff's law of equality of radiative emissivity and absorptivity, with a black body source function. The key to local thermodynamic equilibrium here is that the rate of collisions of ponderable matter particles such as molecules should far exceed the rates of creation and annihilation of photons.
Edward A. Milne, thinking about stars, gave a definition of 'local thermodynamic equilibrium' in terms of the thermal radiation of the matter in each small local 'cell'. He defined 'local thermodynamic equilibrium' in a 'cell' by requiring that it macroscopically absorb and spontaneously emit radiation as if it were in radiative equilibrium in a cavity at the temperature of the matter of the 'cell'. Then it strictly obeys Kirchhoff's law of equality of radiative emissivity and absorptivity, with a black body source function. The key to local thermodynamic equilibrium here is that the rate of collisions of ponderable matter particles such as molecules should far exceed the rates of creation and annihilation of photons.
==Entropy in evolving systems==
==Entropy in evolving systems==
进化系统中的熵
It is pointed out by W.T. Grandy Jr,<ref>{{cite journal | doi = 10.1023/B:FOOP.0000012007.06843.ed | title = Time Evolution in Macroscopic Systems. I. Equations of Motion | year = 2004 | last1 = Grandy | first1 = W.T., Jr. | journal = Foundations of Physics | volume = 34 | issue = 1 | page = 1 |url=http://physics.uwyo.edu/~tgrandy/evolve.html |arxiv = cond-mat/0303290 |bibcode = 2004FoPh...34....1G }}</ref><ref>{{cite journal | url=http://physics.uwyo.edu/~tgrandy/entropy.html | doi=10.1023/B:FOOP.0000012008.36856.c1 | title=Time Evolution in Macroscopic Systems. II. The Entropy | year=2004 | last1=Grandy | first1=W.T., Jr. | journal=Foundations of Physics | volume=34 | issue=1 | page=21 |arxiv = cond-mat/0303291 |bibcode = 2004FoPh...34...21G }}</ref><ref>{{cite journal | url=http://physics.uwyo.edu/~tgrandy/applications.html | doi = 10.1023/B:FOOP.0000022187.45866.81 | title=Time Evolution in Macroscopic Systems. III: Selected Applications | year=2004 | last1=Grandy | first1=W. T., Jr | journal=Foundations of Physics | volume=34 | issue=5 | page=771 |bibcode = 2004FoPh...34..771G }}</ref><ref>Grandy 2004 see also [http://physics.uwyo.edu/~tgrandy/Statistical_Mechanics.html].</ref>, that entropy, though it may be defined for a non-equilibrium system is—when strictly considered—only a macroscopic quantity that refers to the whole system, and is not a dynamical variable and in general does not act as a local potential that describes local physical forces. Under special circumstances, however, one can metaphorically think as if the thermal variables behaved like local physical forces. The approximation that constitutes classical irreversible thermodynamics is built on this metaphoric thinking.
It is pointed out by W.T. Grandy Jr,, that entropy, though it may be defined for a non-equilibrium system is—when strictly considered—only a macroscopic quantity that refers to the whole system, and is not a dynamical variable and in general does not act as a local potential that describes local physical forces. Under special circumstances, however, one can metaphorically think as if the thermal variables behaved like local physical forces. The approximation that constitutes classical irreversible thermodynamics is built on this metaphoric thinking.
This point of view shares many points in common with the concept and the use of entropy in continuum thermomechanics,<ref>{{cite book| title = Rational Thermodynamics | year = 1984 | last1 = Truesdell | first1 = Clifford | publisher = Springer | edition = 2 }}</ref><ref>{{cite book| title = Continuum Thermomechanics | year = 2002 | last1 = Maugin | first1 = Gérard A. | publisher = Kluwer }}</ref><ref>{{cite book| title = The Mechanics and Thermodynamics of Continua | year = 2010 | last1 = Gurtin | first1 = Morton E. | publisher = Cambridge University Press }}</ref><ref>{{cite book| title = Thermodynamics of Materials with Memory: Theory and Applications | year = 2012| last1 = Amendola | first1 = Giovambattista | publisher = Springer }}</ref> which evolved completely independently of statistical mechanics and maximum-entropy principles.
This point of view shares many points in common with the concept and the use of entropy in continuum thermomechanics, which evolved completely independently of statistical mechanics and maximum-entropy principles.
===Entropy in non-equilibrium===
===Entropy in non-equilibrium===
To describe deviation of the thermodynamic system from equilibrium, in addition to constitutive variables <math>x_1, x_2, ..., x_n</math> that are used to fix the equilibrium state, as was described above, a set of variables <math>\xi_1, \xi_2,\ldots</math> that are called ''internal variables'' have been introduced. The equilibrium state is considered to be stable and the main property of the internal variables, as measures of [[non-equilibrium]] of the system, is their trending to disappear; the local law of disappearing can be written as relaxation equation for each internal variable
To describe deviation of the thermodynamic system from equilibrium, in addition to constitutive variables <math>x_1, x_2, ..., x_n</math> that are used to fix the equilibrium state, as was described above, a set of variables <math>\xi_1, \xi_2,\ldots</math> that are called internal variables have been introduced. The equilibrium state is considered to be stable and the main property of the internal variables, as measures of non-equilibrium of the system, is their trending to disappear; the local law of disappearing can be written as relaxation equation for each internal variable
为了描述热力学系统偏离平衡状态的情况，除了用于确定平衡状态的本构变量 math x 1，x 2，... ，xn / math 之外，还引入了一组称为内部变量的变量 math xi 1， xi 2， ldots / math。平衡态被认为是稳定的，内变量作为系统非平衡的度量，其主要性质是趋于消失，消失的局部规律可以写成每个内变量的松弛方程
{{NumBlk|:|<math>
{{NumBlk|:|<math>
{{ NumBlk | : | math
\frac{d\xi_i}{dt} = - \frac{1}{\tau_i} \, \left(\xi_i - \xi_i^{(0)} \right),\quad i =1,\,2,\ldots ,
\frac{d\xi_i}{dt} = - \frac{1}{\tau_i} \, \left(\xi_i - \xi_i^{(0)} \right),\quad i =1,\,2,\ldots ,
向左(向右) ，向左(向右) ，向右(向右) ，向左1,2,2,
</math>|{{EquationRef|1}}}}
</math>|}}
我不知道，我不知道
where <math> \tau_i= \tau_i(T, x_1, x_2, \ldots, x_n)</math> is a relaxation time of a corresponding variables. It is convenient to consider the initial value <math> \xi_i^0</math> are equal to zero. The above equation is valid for small deviations from equilibrium; The dynamics of internal variables in general case is considered by Pokrovskii.<ref> Pokrovskii V.N. (2013) A derivation of the main relations of non-equilibrium thermodynamics. Hindawi Publishing Corporation: ISRN Thermodynamics, vol. 2013, article ID 906136, 9 p. https://dx.doi.org/10.1155/2013/906136. </ref>
where <math> \tau_i= \tau_i(T, x_1, x_2, \ldots, x_n)</math> is a relaxation time of a corresponding variables. It is convenient to consider the initial value <math> \xi_i^0</math> are equal to zero. The above equation is valid for small deviations from equilibrium; The dynamics of internal variables in general case is considered by Pokrovskii.
Entropy of the system in non-equilibrium is a function of the total set of variables
Entropy of the system in non-equilibrium is a function of the total set of variables
非平衡态系统的熵是总变量集的函数
{{NumBlk|:|<math>
{{NumBlk|:|<math>
{{ NumBlk | : | math
S=S(T, x_1, x_2, , x_n; \xi_1, \xi_2, \ldots)
S=S(T, x_1, x_2, , x_n; \xi_1, \xi_2, \ldots)
S (t，x1，x2，，xn; xi 1， xi 2， ldots)
</math>|{{EquationRef|1}}}}
</math>|}}
我不知道，我不知道
The essential contribution to the thermodynamics of the [[non-equilibrium systems]] was brought by [[Prigogine]], when he and his collaborators investigated the systems of chemically reacting substances. The stationary states of such systems exists due to exchange both particles and energy with the environment. In section 8 of the third chapter of his book <ref>[[Ilya Prigogine|Prigogine, I.]] (1955/1961/1967). ''Introduction to Thermodynamics of Irreversible Processes''. 3rd edition, Wiley Interscience, New York.</ref>, Prigogine has specified three contributions to the variation of entropy of the considered system at the given volume and constant temperature <math> T</math> . The increment of [[entropy]] <math> S</math> can be calculated according to the formula
The essential contribution to the thermodynamics of the non-equilibrium systems was brought by Prigogine, when he and his collaborators investigated the systems of chemically reacting substances. The stationary states of such systems exists due to exchange both particles and energy with the environment. In section 8 of the third chapter of his book , Prigogine has specified three contributions to the variation of entropy of the considered system at the given volume and constant temperature <math> T</math> . The increment of entropy <math> S</math> can be calculated according to the formula
普里高金和他的合作者在研究化学反应物质系统时，提出了非平衡系统热力学的本质贡献。由于粒子和能量与环境的交换，这类系统的静止状态是存在的。在他的书的第三章的第8节中，普里高金详细说明了在给定体积下考虑系统的熵变化的三个贡献和恒温数学 t / math。根据这个公式可以计算出熵的增量 s / 数
{{NumBlk|:|<math>
{{NumBlk|:|<math>
{{ NumBlk | : | math
T\,dS = \Delta Q - \sum_{j} \, \Xi_{j} \,\Delta \xi_j + \sum_{\alpha =1}^k\, \mu_\alpha \, \Delta N_\alpha.
T\,dS = \Delta Q - \sum_{j} \, \Xi_{j} \,\Delta \xi_j + \sum_{\alpha =1}^k\, \mu_\alpha \, \Delta N_\alpha.
T，dS Delta q-sum { j } ， Xi { j } ， Delta Xi j + sum { alpha 1} ， mu alpha， Delta n alpha.
</math>|{{EquationRef|1}}}}
</math>|}}
我不知道，我不知道
The first term on the right hand side of the equation presents a stream of thermal energy into the system; the last term -- a stream of energy into the system coming with the stream of particles of substances <math> \Delta N_\alpha </math> that can be positive or negative, <math> \mu_\alpha</math> is [[chemical potential]] of substance <math> \alpha</math>. The middle term in (1) depicts [[energy dissipation]] ([[entropy production]]) due to the relaxation of internal variables <math> \xi_j</math>. In the case of chemically reacting substances, which was investigated by Prigogine, the internal variables appear to be measures of incompleteness of chemical reactions, that is measures of how much the considered system with chemical reactions is out of equilibrium. The theory can be generalised,<ref> Pokrovskii V.N. (2005) Extended thermodynamics in a discrete-system approach, Eur. J. Phys. vol. 26, 769-781.</ref><ref> Pokrovskii V.N. (2013) A derivation of the main relations of non-equilibrium thermodynamics. Hindawi Publishing Corporation: ISRN Thermodynamics, vol. 2013, article ID 906136, 9 p. https://dx.doi.org/10.1155/2013/906136. </ref> to consider any deviation from the equilibrium state as an internal variable, so that we consider the set of internal variables <math> \xi_j</math> in equation (1) to consist of the quantities defining not only degrees of completeness of all chemical reactions occurring in the system, but also the structure of the system, gradients of temperature, difference of concentrations of substances and so on.
The first term on the right hand side of the equation presents a stream of thermal energy into the system; the last term -- a stream of energy into the system coming with the stream of particles of substances <math> \Delta N_\alpha </math> that can be positive or negative, <math> \mu_\alpha</math> is chemical potential of substance <math> \alpha</math>. The middle term in (1) depicts energy dissipation (entropy production) due to the relaxation of internal variables <math> \xi_j</math>. In the case of chemically reacting substances, which was investigated by Prigogine, the internal variables appear to be measures of incompleteness of chemical reactions, that is measures of how much the considered system with chemical reactions is out of equilibrium. The theory can be generalised, to consider any deviation from the equilibrium state as an internal variable, so that we consider the set of internal variables <math> \xi_j</math> in equation (1) to consist of the quantities defining not only degrees of completeness of all chemical reactions occurring in the system, but also the structure of the system, gradients of temperature, difference of concentrations of substances and so on.
==Flows and forces==
==Flows and forces==
流动与力量
The fundamental relation of classical equilibrium thermodynamics <ref name="W. Greiner et. al. 1997">W. Greiner, L. Neise, and H. Stöcker (1997), ''Thermodynamics and Statistical Mechanics (Classical Theoretical Physics)'' ,Springer-Verlag, New York, '''P85, 91, 101,108,116''', {{ISBN|0-387-94299-8}}.</ref>
The fundamental relation of classical equilibrium thermodynamics
: <math>dS=\frac{1}{T}dU+\frac{p}{T}dV-\sum_{i=1}^s\frac{\mu_i}{T}dN_i</math>
<math>dS=\frac{1}{T}dU+\frac{p}{T}dV-\sum_{i=1}^s\frac{\mu_i}{T}dN_i</math>
expresses the change in [[entropy]] <math>dS</math> of a system as a function of the intensive quantities [[temperature]] <math>T</math>, [[pressure]] <math>p</math> and <math>i^{th}</math> [[chemical potential]] <math>\mu_i</math> and of the differentials of the extensive quantities [[energy]] <math>U</math>, [[Volume (thermodynamics)|volume]] <math>V</math> and <math>i^{th}</math> [[particle number]] <math>N_i</math>.
expresses the change in entropy <math>dS</math> of a system as a function of the intensive quantities temperature <math>T</math>, pressure <math>p</math> and <math>i^{th}</math> chemical potential <math>\mu_i</math> and of the differentials of the extensive quantities energy <math>U</math>, volume <math>V</math> and <math>i^{th}</math> particle number <math>N_i</math>.
Following Onsager (1931,I),<ref name="Onsager 1931 I"/> let us extend our considerations to thermodynamically non-equilibrium systems. As a basis, we need locally defined versions of the extensive macroscopic quantities <math>U</math>, <math>V</math> and <math>N_i</math> and of the intensive macroscopic quantities <math>T</math>, <math>p</math> and <math>\mu_i</math>.
Following Onsager (1931,I), let us extend our considerations to thermodynamically non-equilibrium systems. As a basis, we need locally defined versions of the extensive macroscopic quantities <math>U</math>, <math>V</math> and <math>N_i</math> and of the intensive macroscopic quantities <math>T</math>, <math>p</math> and <math>\mu_i</math>.
For classical non-equilibrium studies, we will consider some new locally defined intensive macroscopic variables. We can, under suitable conditions, derive these new variables by locally defining the gradients and flux densities of the basic locally defined macroscopic quantities.
For classical non-equilibrium studies, we will consider some new locally defined intensive macroscopic variables. We can, under suitable conditions, derive these new variables by locally defining the gradients and flux densities of the basic locally defined macroscopic quantities.
Such locally defined gradients of intensive macroscopic variables are called 'thermodynamic forces'. They 'drive' flux densities, perhaps misleadingly often called 'fluxes', which are dual to the forces. These quantities are defined in the article on [[Onsager reciprocal relations]].
Such locally defined gradients of intensive macroscopic variables are called 'thermodynamic forces'. They 'drive' flux densities, perhaps misleadingly often called 'fluxes', which are dual to the forces. These quantities are defined in the article on Onsager reciprocal relations.
Establishing the relation between such forces and flux densities is a problem in statistical mechanics. Flux densities (<math>J_i</math>) may be coupled. The article on Onsager reciprocal relations considers the stable near-steady thermodynamically non-equilibrium regime, which has dynamics linear in the forces and flux densities.
Establishing the relation between such forces and flux densities is a problem in statistical mechanics. Flux densities (<math>J_i</math>) may be coupled. The article on Onsager reciprocal relations considers the stable near-steady thermodynamically non-equilibrium regime, which has dynamics linear in the forces and flux densities.
In stationary conditions, such forces and associated flux densities are by definition time invariant, as also are the system's locally defined entropy and rate of entropy production. Notably, according to [[Ilya Prigogine]] and others, when an open system is in conditions that allow it to reach a stable stationary thermodynamically non-equilibrium state, it organizes itself so as to minimize total entropy production defined locally. This is considered further below.
In stationary conditions, such forces and associated flux densities are by definition time invariant, as also are the system's locally defined entropy and rate of entropy production. Notably, according to Ilya Prigogine and others, when an open system is in conditions that allow it to reach a stable stationary thermodynamically non-equilibrium state, it organizes itself so as to minimize total entropy production defined locally. This is considered further below.
One wants to take the analysis to the further stage of describing the behaviour of surface and volume integrals of non-stationary local quantities; these integrals are macroscopic fluxes and production rates. In general the dynamics of these integrals are not adequately described by linear equations, though in special cases they can be so described.
One wants to take the analysis to the further stage of describing the behaviour of surface and volume integrals of non-stationary local quantities; these integrals are macroscopic fluxes and production rates. In general the dynamics of these integrals are not adequately described by linear equations, though in special cases they can be so described.
===Onsager reciprocal relations===
===Onsager reciprocal relations===
{{Main article|Onsager reciprocal relations}}
Following Section III of Rayleigh (1873),<ref name="Rayleigh 1873"/> Onsager (1931, I)<ref name="Onsager 1931 I"/> showed that in the regime where both the flows (<math>J_i</math>) are small and the thermodynamic forces (<math>F_i</math>) vary slowly, the rate of creation of entropy <math>(\sigma)</math> is [[linear relation|linearly related]] to the flows:
Following Section III of Rayleigh (1873), Onsager (1931, I) showed that in the regime where both the flows (<math>J_i</math>) are small and the thermodynamic forces (<math>F_i</math>) vary slowly, the rate of creation of entropy <math>(\sigma)</math> is linearly related to the flows:
:<math>\sigma = \sum_i J_i\frac{\partial F_i}{\partial x_i} </math>
<math>\sigma = \sum_i J_i\frac{\partial F_i}{\partial x_i} </math>
and the flows are related to the gradient of the forces, parametrized by a [[matrix (mathematics)|matrix]] of coefficients conventionally denoted <math>L</math>:
and the flows are related to the gradient of the forces, parametrized by a matrix of coefficients conventionally denoted <math>L</math>:
:<math>J_i = \sum_{j} L_{ij} \frac{\partial F_j}{\partial x_j} </math>
<math>J_i = \sum_{j} L_{ij} \frac{\partial F_j}{\partial x_j} </math>
from which it follows that:
from which it follows that:
:<math>\sigma = \sum_{i,j} L_{ij} \frac{\partial F_i}{\partial x_i}\frac{\partial F_j}{\partial x_j} </math>
<math>\sigma = \sum_{i,j} L_{ij} \frac{\partial F_i}{\partial x_i}\frac{\partial F_j}{\partial x_j} </math>
The [[second law of thermodynamics]] requires that the matrix <math>L</math> be [[Positive-definite matrix|positive definite]]. [[Statistical mechanics]] considerations involving microscopic reversibility of dynamics imply that the matrix <math>L</math> is [[symmetric matrix|symmetric]]. This fact is called the ''Onsager reciprocal relations''.
The second law of thermodynamics requires that the matrix <math>L</math> be positive definite. Statistical mechanics considerations involving microscopic reversibility of dynamics imply that the matrix <math>L</math> is symmetric. This fact is called the Onsager reciprocal relations.
The generalization of the above equations for the rate of creation of entropy was given by Pokrovskii.<ref> Pokrovskii V.N. (2013) A derivation of the main relations of non-equilibrium thermodynamics. Hindawi Publishing Corporation: ISRN Thermodynamics, vol. 2013, article ID 906136, 9 p. https://dx.doi.org/10.1155/2013/906136. </ref>
The generalization of the above equations for the rate of creation of entropy was given by Pokrovskii.
==Speculated extremal principles for non-equilibrium processes==
==Speculated extremal principles for non-equilibrium processes==
{{main article|Extremal principles in non-equilibrium thermodynamics}}
Until recently, prospects for useful extremal principles in this area have seemed clouded. Nicolis (1999)<ref>{{Cite journal | doi = 10.1002/qj.49712555718 | last1 = Nicolis | first1 = C. | year = 1999 | title = Entropy production and dynamical complexity in a low-order atmospheric model | url = | journal = Quarterly Journal of the Royal Meteorological Society | volume = 125 | issue = 557| pages = 1859–1878 |bibcode = 1999QJRMS.125.1859N }}</ref> concludes that one model of atmospheric dynamics has an attractor which is not a regime of maximum or minimum dissipation; she says this seems to rule out the existence of a global organizing principle, and comments that this is to some extent disappointing; she also points to the difficulty of finding a thermodynamically consistent form of entropy production. Another top expert offers an extensive discussion of the possibilities for principles of extrema of entropy production and of dissipation of energy: Chapter 12 of Grandy (2008)<ref name="Grandy 2008"/> is very cautious, and finds difficulty in defining the 'rate of internal entropy production' in many cases, and finds that sometimes for the prediction of the course of a process, an extremum of the quantity called the rate of dissipation of energy may be more useful than that of the rate of entropy production; this quantity appeared in Onsager's 1931<ref name="Onsager 1931 I"/> origination of this subject. Other writers have also felt that prospects for general global extremal principles are clouded. Such writers include Glansdorff and Prigogine (1971), Lebon, Jou and Casas-Vásquez (2008), and Šilhavý (1997).
Until recently, prospects for useful extremal principles in this area have seemed clouded. Nicolis (1999) concludes that one model of atmospheric dynamics has an attractor which is not a regime of maximum or minimum dissipation; she says this seems to rule out the existence of a global organizing principle, and comments that this is to some extent disappointing; she also points to the difficulty of finding a thermodynamically consistent form of entropy production. Another top expert offers an extensive discussion of the possibilities for principles of extrema of entropy production and of dissipation of energy: Chapter 12 of Grandy (2008) is very cautious, and finds difficulty in defining the 'rate of internal entropy production' in many cases, and finds that sometimes for the prediction of the course of a process, an extremum of the quantity called the rate of dissipation of energy may be more useful than that of the rate of entropy production; this quantity appeared in Onsager's 1931 origination of this subject. Other writers have also felt that prospects for general global extremal principles are clouded. Such writers include Glansdorff and Prigogine (1971), Lebon, Jou and Casas-Vásquez (2008), and Šilhavý (1997).
A recent proposal may perhaps by-pass those clouded prospects.<ref name="Attard 2012">{{cite arXiv|last=Attard|first=P.|title=Optimising Principle for Non-Equilibrium Phase Transitions and Pattern Formation with Results for Heat Convection|journal=|year=2012|eprint=1208.5105|class=cond-mat.stat-mech}}</ref><ref>Attard, P. (2012). ''Non-Equilibrium Thermodynamics and Statistical Mechanics: Foundations and Applications'', Oxford University Press, Oxford UK, {{ISBN|978-0-19-966276-0}}.</ref>
A recent proposal may perhaps by-pass those clouded prospects.
==Applications==
==Applications==
申请
Non-equilibrium thermodynamics has been successfully applied to describe biological processes such as [[protein folding]]/unfolding and [[membrane transport|transport through membranes]]<ref>{{cite journal |last1=Kimizuka |first1=Hideo |last2=Kaibara |first2=Kozue |title=Nonequilibrium thermodynamics of ion transport through membranes |journal=Journal of Colloid and Interface Science |date=September 1975 |volume=52 |issue=3 |pages=516–525 |doi=10.1016/0021-9797(75)90276-3}}</ref><ref>{{cite journal |last1=Baranowski |first1=B. |title=Non-equilibrium thermodynamics as applied to membrane transport |journal=Journal of Membrane Science |date=April 1991 |volume=57 |issue=2–3 |pages=119–159 |doi=10.1016/S0376-7388(00)80675-4}}</ref>.
Non-equilibrium thermodynamics has been successfully applied to describe biological processes such as protein folding/unfolding and transport through membranes.
非平衡态热力学已成功地应用于描述诸如蛋白质折叠 / 去折叠和通过膜转运等生物学过程。
It is also used to give a description of the dynamics of nanoparticles, which can be out of equilibrium in systems where catalysis and electrochemical conversion is involved.<ref>{{cite journal |last1=Bazant |first1=Martin Z. |title=Theory of Chemical Kinetics and Charge Transfer based on Nonequilibrium Thermodynamics |journal=Accounts of Chemical Research |date=22 March 2013 |volume=46 |issue=5 |pages=1144–1160 |doi=10.1021/ar300145c|pmid=23520980 |arxiv=1208.1587 }}</ref>
It is also used to give a description of the dynamics of nanoparticles, which can be out of equilibrium in systems where catalysis and electrochemical conversion is involved.
它也被用来描述纳米颗粒的动力学，在涉及催化和电化学转化的系统中可能失去平衡。
Also, ideas from non-equilibrium thermodynamics and the informatic theory of entropy have been adapted to describe general economic systems.<ref>{{Cite book|title = Econodynamics. The Theory of Social Production.|last = Pokrovskii|first = Vladimir|publisher = Springer, Dordrecht-Heidelberg-London-New York.|year = 2011|isbn = |location = https://www.springer.com/physics/complexity/book/978-94-007-2095-4|pages = }}</ref>
Also, ideas from non-equilibrium thermodynamics and the informatic theory of entropy have been adapted to describe general economic systems.
<ref>{{Cite book|title = The Unity of Science and Economics: A New Foundation of Economic Theory|last = Chen|first = Jing|publisher = Springer|year = 2015|isbn = |location = https://www.springer.com/us/book/9781493934645|pages = }}</ref>
==See also==
==See also==
* [[Time crystal]]
* [[Dissipative system]]
* [[Entropy production]]
* [[Extremal principles in non-equilibrium thermodynamics]]
* [[Self-organization]]
* [[Autocatalytic reactions and order creation]]
* [[Self-organizing criticality]]
* [[BBGKY hierarchy|Bogoliubov-Born-Green-Kirkwood-Yvon hierarchy of equations]]
* [[Boltzmann equation]]
* [[Vlasov equation]]
* [[Maxwell's demon]]
* [[Information entropy]]
* [[Spontaneous symmetry breaking]]
* [[Autopoiesis]]
* [[Maximum power principle]]
==References==
==References==
{{Reflist|colwidth=30em}}
===Sources===
===Sources===
{{refbegin}}
*[[Herbert Callen|Callen, H.B.]] (1960/1985). ''Thermodynamics and an Introduction to Thermostatistics'', (1st edition 1960) 2nd edition 1985, Wiley, New York, {{ISBN|0-471-86256-8}}.
*Eu, B.C. (2002). ''Generalized Thermodynamics. The Thermodynamics of Irreversible Processes and Generalized Hydrodynamics'', Kluwer Academic Publishers, Dordrecht, {{ISBN|1-4020-0788-4}}.
*Glansdorff, P., [[Ilya Prigogine|Prigogine, I.]] (1971). ''Thermodynamic Theory of Structure, Stability, and Fluctuations'', Wiley-Interscience, London, 1971, {{ISBN|0-471-30280-5}}.
*Grandy, W.T., Jr (2008). ''Entropy and the Time Evolution of Macroscopic Systems''. Oxford University Press. {{ISBN|978-0-19-954617-6}}.
*Gyarmati, I. (1967/1970). ''Non-equilibrium Thermodynamics. Field Theory and Variational Principles'', translated from the Hungarian (1967) by E. Gyarmati and W.F. Heinz, Springer, Berlin.
*[[Elliott H. Lieb|Lieb, E.H.]], [[Jakob Yngvason|Yngvason, J.]] (1999). 'The physics and mathematics of the second law of thermodynamics', ''Physics Reports'', '''310''': 1–96. [https://arxiv.org/abs/cond-mat/9708200 See also this.]
{{refend}}
==Further reading==
==Further reading==
{{refbegin}}
*[[Hans Ziegler (physicist)|Ziegler, Hans]] (1977): ''An introduction to Thermomechanics''. North Holland, Amsterdam. {{ISBN|0-444-11080-1}}. Second edition (1983) {{ISBN|0-444-86503-9}}.
*Kleidon, A., Lorenz, R.D., editors (2005). ''Non-equilibrium Thermodynamics and the Production of Entropy'', Springer, Berlin. {{ISBN|3-540-22495-5}}.
*[[Ilya Prigogine|Prigogine, I.]] (1955/1961/1967). ''Introduction to Thermodynamics of Irreversible Processes''. 3rd edition, Wiley Interscience, New York.
*[[Dmitry Zubarev|Zubarev D. N.]] (1974): ''[https://books.google.com/books?id=SQy3AAAAIAAJ&hl=ru&source=gbs_ViewAPI Nonequilibrium Statistical Thermodynamics]''. New York, Consultants Bureau. {{ISBN|0-306-10895-X}}; {{ISBN|978-0-306-10895-2}}.
*Keizer, J. (1987). ''Statistical Thermodynamics of Nonequilibrium Processes'', Springer-Verlag, New York, {{ISBN|0-387-96501-7}}.
*[[Dmitry Zubarev|Zubarev D. N.]], Morozov V., Ropke G. (1996): ''Statistical Mechanics of Nonequilibrium Processes: Basic Concepts, Kinetic Theory''. John Wiley & Sons. {{ISBN|3-05-501708-0}}.
*[[Dmitry Zubarev|Zubarev D. N.]], Morozov V., Ropke G. (1997): ''Statistical Mechanics of Nonequilibrium Processes: Relaxation and Hydrodynamic Processes''. John Wiley & Sons. {{ISBN|3-527-40084-2}}.
*Tuck, Adrian F. (2008). ''Atmospheric turbulence : a molecular dynamics perspective''. Oxford University Press. {{ISBN|978-0-19-923653-4}}.
*Grandy, W.T., Jr (2008). ''Entropy and the Time Evolution of Macroscopic Systems''. Oxford University Press. {{ISBN|978-0-19-954617-6}}.
*Kondepudi, D., Prigogine, I. (1998). ''Modern Thermodynamics: From Heat Engines to Dissipative Structures''. John Wiley & Sons, Chichester. {{ISBN|0-471-97393-9}}.
*de Groot S.R., [[Peter Mazur|Mazur P.]] (1984). ''Non-Equilibrium Thermodynamics'' (Dover). {{ISBN|0-486-64741-2}}
*Ramiro Augusto Salazar La Rotta. (2011). ''The Non-Equilibrium Thermodynamics, Perpetual''
{{refend}}
==External links==
==External links==
*[https://web.archive.org/web/20110406071945/http://www-dcf.ds.mpg.de/build.php/Titel/Research_english.html?sub=1&ver=en Stephan Herminghaus' Dynamics of Complex Fluids Department at the Max Planck Institute for Dynamics and Self Organization]
* [https://web.archive.org/web/20120519172014/http://www.worldscibooks.com/physics/1622.html Non-equilibrium Statistical Thermodynamics applied to Fluid Dynamics and Laser Physics] - 1992- book by Xavier de Hemptinne.
* [https://dx.doi.org/10.1063/1.2012462 Nonequilibrium Thermodynamics of Small Systems] - PhysicsToday.org
* [https://web.archive.org/web/20050308053832/http://www.intothecool.com/energetic.php Into the Cool] - 2005 book by Dorion Sagan and Eric D. Schneider, on nonequilibrium thermodynamics and [[evolution|evolutionary theory]].
*[http://www.pnas.org/content/98/20/11081.full.pdf Thermodynamics ‘‘beyond'' local equilibrium]
{{DEFAULTSORT:Non-Equilibrium Thermodynamics}}
[[Category:Non-equilibrium thermodynamics]]
Category:Non-equilibrium thermodynamics
类别: 非平衡态热力学
[[Category:Concepts in physics]]
Category:Concepts in physics
分类: 物理概念
[[Category:Branches of thermodynamics]]
Category:Branches of thermodynamics
分类: 热力学的分支
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