- freely available
Entropy 2014, 16(4), 2362-2383; https://doi.org/10.3390/e16042362
Abstract: Like in mechanics and electrodynamics, the fundamental laws of the thermodynamics of dissipative processes can be compressed into Gyarmati’s variational principle. This variational principle both in its differential (local) and in integral (global) forms was formulated by Gyarmati in 1965. The consistent application of both the local and the global forms of Gyarmati’s principle provides all the advantages throughout explicating the theory of irreversible thermodynamics that are provided in the study of mechanics and electrodynamics by the corresponding classical variational principles, e.g., Gauss’ differential principle of least constraint or Hamilton’s integral principle.
A number of efforts have been made to formulate variational principles for dissipative processes, namely those accounted by (“classical”) irreversible thermodynamics. The results seemed, and even seem, to contradict the known result in mathematics that says the parabolic equations of heat conduction, diffusion, etc., cannot be obtained as Euler-Lagrange equations of a variational principle. The conditions of the mathematical theorem were not assumed (among which functions, the extremum was looked for), moreover, the derivation of a parabolic equation does not mean that it has to be the Euler-Lagrange equation, e.g., the variational problem may result in biparabolic Euler-Lagrange equations with transversality conditions, and the first integration of them results in the parabolic equations . Another procedure is based on some potential functions [2–4].
A brief and rather good survey can be found on Wikipedia  from the early ancestors to recent results; the works of Kelvin, Helmholtz, Rayleigh, Korteweg, Onsager, Prigogine, Casimir, Ziman, Ziegler, Gyarmati, Paltridge and others are mentioned. The survey is far from being complete; important results are missing from it; e.g., the works of Ziegler [6–12] and his influence [13–17], Biot [18,19] and Edelen [20–31] are omitted. A more skeptic website on the topics is The Azimuth Project .
In this paper, we put Gyarmati’s variational principle into the limelight. This principle was applied to several fields of irreversible processes: first of all, by his colleagues (Verhás , Böröcz , Farkas [35,36], Sándor , Vincze [38–40] and Stark [41,42]); but also by many others (Singh [43,44], Bhattacharya [45,46], Dickel [47,48], etc.).
2. The Governing Principle of Dissipative Processes (GPDP)
Gyarmati’s principle is based on the fact that the generalization of the dissipation functions that were introduced by Rayleigh and Onsager for special cases always exists locally in continua [3,4,49–52] in the linear theory with Onsager’s reciprocal relations. These functions are defined as:
The Rik coefficients (general resistivities) are the components of the inverse of the conductivity matrix, (Lik).
The most important property of the dissipation function, Ψ(X), is that it is a homogeneous quadratic function of the Xi forces in the strictly linear theory, while in the quasi-linear theory, it depends also on the state variables. In Gyarmati’s terminology, the linear laws are “strictly linear” if the conductivity coefficients do not depend on anything and are “quasi-linear” if they do not depend on the forces, Xi, or fluxes, Ji, but on anything else; say, the heat conductivity depends on temperature, but does not depend on its gradient. The other fundamental property of Ψ is that its partial derivative with respect to Xk is equal to the current, Jk.
Finally, the equality of the mixed second derivatives of Ψ with respect to the forces are equivalent to Onsager’s reciprocal relations:
Because of the above properties, the function, Ψ, is called a dissipation potential, more precisely: it is the flux potential (see Equation (3)).
The function, Φ, has similar properties. In the strictly linear theory the function, Φ, is a homogeneous quadratic function of the currents, J, while in the quasi-linear case, it depends also on the local state variables (through the coefficients). The partial derivative of the function, Φ, with respect to Jk equals Xk:
Due to this relation, the function, Φ, is also a dissipation potential, more exactly: it is the force potential.
The equality of the mixed second derivatives of Φ with respect to the Js are equivalent to the Onsager relations, now expressed in terms of the Rik resistances:
Hence, it can be seen that the necessary and sufficient condition of the existence of the dissipation potentials, Ψ and Φ, is the existence of Onsager’s reciprocal relations.
Some weighted potentials, ΨG and ΦG, can be defined, too. They show all the essential properties of Ψ and Φ, but correspond to the weighted entropy production, Gσs. (G is any always positive state function.) The dynamic laws can be formulated in different forms by the help of so-called representations and pictures, which give mathematically equivalent formulae; one of them is as good as the other from the theoretical point of view, but in particular applications, the suitable one can make life easier. We refer again to Gyarmati’s terminology. Representation means the way that the quantities accounting for the rate of processes have been chosen from the possibilities, e.g., the heat flow or the entropy flow. Picture refers to the particular weight function, G, e.g., if G = 1, we speak of the “entropy picture”, G = T gives the “energy picture”, G = T2 leads to the “Fourier picture”, etc. The general theory of the “pictures” was worked out and applied by Gyarmati  and Farkas  (see also [37,45,46,54–57]). Different pictures are obtained by multiplying both sides of the bilinear expression of the entropy production by an always positive state function, G, i.e.,
The quantity, Gσs, is evidently non-negative, taking a zero value in equilibrium only. The coefficients of the current, Jj, namely,
regarded as forces, and substituted into the original form, give the linear laws in the “G-picture”:
The coefficients obey Onsager’s reciprocal relations. By choosing various functions for G, various pictures for the description of dissipative processes are obtained [35,58,59]. Making use of Equations (8) and (9), we obtain the forms of the dissipation potentials in the general G-picture:
Finally, we note another essential property of the functions, Ψ and Φ; namely, that they are invariant scalar quantities with respect to the linear transformations of the currents and forces.
3. The Local Forms of Gyarmati’s Principle
Gyarmati’s variational principle of non-equilibrium thermodynamics can be derived from the properties in Equations (3) and (5) of the functions, Ψ and Φ. We mention that this derivation does not make use of the homogeneous quadratic forms of the functions, Ψ and Φ, given in Equations (1) and (2); thus, the variational principle is applicable to strictly non-linear phenomena that cannot be described by the linear laws, yet the currents are uniquely determined by the forces and the local variables of state. This is the situation with any phenomena the Gyarmati-Li generalization:
Notice that Equation (5) can be written in the form:
where, in executing the partial differentiation, the currents must be regarded variables independent of the forces and local state variables. This means that the constitutive relations given by Equation (5) are equivalent to the following statement: those currents correspond to a given set of forces and state variables, at which the function:
has a stationary point in the space of the currents. This form of the principle, which stands nearest to Onsager’s principle for small fluctuations around an equilibrium in an adiabatically closed discontinuous system, is called the flux representation of Gyarmati’s principle . Ziegler’s principle [7–9,11,12] is equivalent to Onsager’s one in Equation (12), but with different aspects and presentation; it was applied to several problems [13–15].
The force representation of Gyarmati’s principle is obtained by putting the relation in Equation (3) in the form:
During partial differentiation, the forces and the fluxes must be regarded again as independent variables. Thus, those forces correspond to a given set of currents and state variables at which the function:
has a stationary point in the space of the forces.
It is easily seen that the functions, J and X, in Equations (13) and (15) can be put in the same form, as the subtraction of a function, f(Xi), independent of the Js from J has no influence on Equation (12). The function, Ψ, just fits the purpose. On the other hand, Φ can be subtracted from X (due to the same reasons). Now, a universal Lagrange density of Gyarmati’s principle has been obtained:
by which the extremum properties in Equations (12) and (14) can be expressed universally. The partial forms have historical relevance. Onsager’s principle is equivalent to Equation (12). Moreover, in some practical calculations, they are easier.
It can be said, quite generally, that if a sufficient number of the currents and forces is known, that is either every force or every current, or even one part of the currents and the other part of the forces, then the remaining variables must be chosen, so that the universal Lagrangian in Equation (16) is stationary. This is a necessary and sufficient condition for the set of the currents and forces to describe a real process. In other words, the variation of the universal Lagrangian in Gyarmati’s principle is zero around the real forces and fluxes, with respect to the simultaneous variation of the currents and forces.
In the quasi-linear theory, the functions, Ψ and Φ, depend on the state variables through the conductivities, Lik, and resistivities, Rik, due to Equations (1) and (2). The matrices of the conductivities, Lik, and, resistivities Rik, are reciprocal matrices:
Let us calculate the partial derivative of the Lagrange density with respect to a local state variable denoted by Γ:
The partial derivatives ∂Rik/∂Γ, making use of Equation (17), are expressed by the coefficients, Rik, and the derivatives, ∂Lik/∂Γ, as:
Substituting this in Equation (18) and applying the reciprocal relations, the form:
is obtained. Hence, it is seen that the partial derivatives of the universal Lagrangian with respect to the local state variables, at real processes, are zero. Therefore, the parameters, Γ, can also be varied independently.
This theorem is Gyarmati’s supplementary theorem , which guarantees the validity of the universal local form of the variational principle to the quasi-linear case, too.
The universal form of the local Gyarmati principle states, consistently with the supplementary theorem, that the Lagrangian = σs − Ψ − Φ has an extremum in all points that describe a real process in the unified space of forces, currents and state variables.
In examining the type of the extremum, instead of considering second variations, we had better use another form of the Lagrangian, which is advantageous in other respects, as well. This form is:
Executing the multiplications, the form in Equation (16) of the universal Lagrange density is obtained again. This very form, however, clearly shows that the extremum for real processes is always a maximum, and the value of this maximum is zero if no constraint is maintained; in other cases, the Lagrangian is always negative, since the Riks can be replaced, without changing the whole expression, with the coefficients of a positive definite quadratic form—the elements of the symmetric part of the Rik matrix—and the variables of this quadratic form are (Ji − ∑s LisXs). This form of the local principle is considerably similar to Gauss’ principle of least constraint, so this form is often called the Gaussian form of Gyarmati’s principle. As the value of Equation (21) is zero only in the absence of local constraints, while in other cases the value of this maximum depends on the constraints, the Gauss type local principle is an excellent tool for introducing the notion of thermodynamic constraint forces; consequently, it is of great help in discussing problems with local constraints, such as ambipolar diffusion, barycentric component flows, stoichiometric restrictions, etc. (Verhás , Gyarmati , Dickel ).
The local Gyarmati principle of irreversible thermodynamics is of universal validity, yet its primary importance is that it is the ground the integral principles are built on. Before the discussion of integral principles, however, the place of the local principle in the framework of the theory should be examined. To this end, the local principle is resumed more explicitly.
The essence of the local principle is that it replaces the set of linear laws by a single scalar function. If either the function, Ψ, or the function, Φ, is known, the constitutive equations can be obtained by the variational principle. Actually, it is sufficient to know only one of the dissipation potentials, Ψ or Φ, since the matrix of the coefficients can be read from one of them, and the other potential is determined by the elements of the reciprocal matrix. This calculation can be executed via a more elegant method. Let us regard, for example, the function, Ψ, as the given one. Then, the Legendre-transformation of the function, Ψ, leads to the function, . Putting J in the place of , the function, Φ, is obtained. The function, Ψ, is gotten from Φ in the same way [60,61]. The Legendre-transformation is meant in the multidimensional sense or as the sequence with respect to all independent variables, one by one.
The advantage of the method of Legendre transformation lies in the fact that its formulation and application is independent of the linear or quasi-linear character of the theory; thus, it is applicable to dissipation potentials of an entirely different character. From the fact that the dissipation potentials, Ψ and Φ, are the Legendre transforms of each other, it is also seen that the validity of Gyarmati’s supplementary theorem is not restricted to the quasi-linear case, but holds to any strictly non-linear theory, subject to the Gyarmati-Li generalized reciprocal relations (and where the higher order coefficients also depend on the variables of state). This, at the same time, means that the Lagrangian = σs − Ψ − Φ must be stationary at every point of space in every instant of time in the case of any non-linear theory, provided that dissipation potentials exist at all.
The next question is how a dissipation potential can be constructed from the constitutive equations. The potential character of the functions, Ψ and Φ, is defined by Equations (3) and (5). The condition to the existence of such functions with potential character to a given (say, empirically proven) set of constitutive equations is that they have to obey the Gyarmati-Li generalized reciprocal relations. It is rather inconvenient that no general physical law, or exact proof based on such laws, is known that would guarantee the fulfillment of the Gyarmati-Li generalized reciprocal relations or of other equivalent conditions, for all possible constitutive equations; on the contrary, reaction kinetics in chemistry displays plenty of well-examined examples disobeying them beyond the linear approximation . If, however, the reciprocal relations in Equation (11) hold in a particular case or approximation, then the dissipation potentials can be given, and the Gyarmati principle can be applied.
The function, Ψ, can be obtained from the bilinear form of the entropy production by introducing Equations (3); we get:
for the entropy production. This expression can be regarded as a quasi-linear inhomogeneous first order partial differential equation. Its only solution subject to the condition Ψ(0) = 0 is the function:
A similar formula is obtained for Φ(J):
The knowledge of the function, Ψ or Φ, defined so, is equivalent to the knowledge of the original constitutive equations; nevertheless, to get them, it is enough to know the single function, σs(Xi) or σs(Ji), instead of the whole set of the constitutive equations.
Dissipation potentials for non-linear cases were given first (and independently) by Verhás , Edelen [20–25,29,30] and Presnov . Edelen’s works went on also to applications on non-local and non-linear mechanical problems [26–28].
3.1. The Derivation of von Mises’ Equations of Plasticity
Here, for an example, we present a very simple application of the local principle to a typical non-linear case: we derive Mises’ theory of plastic flow (Verhás ). Here, we mention that a number of variational principles and variational methods are known in the literature concerning plastic, elasto-plastic, visco-plastic or even visco-elasto-plastic flow, which works well on the field, but generalizing them to more complicated interactions is hindered by the very special presumptions, e.g., first order Euler homogeneous terms in the entropy production are assumed as core results in thermodynamic plasticity, but they are unusable if the plastic material is semitransparent and is exposed to thermal radiation or the material is a plastic material that is also electrically polarizable and is under the influence of an electromagnetic field. The theories applying “rational” methods, especially the Clausius-Duhem inequality (see, e.g., ) are questionable, because of the essential use of the the idea of temperature as well defined for equilibrium only* and being ambiguous, e.g., in the presence of dielectric relaxations, without which there is no “heat supply”. See in  how to get rid of the difficulty. The theories motivated by statistical and kinetic considerations are bearing the load of Loschmidt’s paradox having persisted for 140 years.
The existence of the function, Φ, is assumed.
Let us consider a homogeneous, isotropic, incompressible fluid continuum in local equilibrium and ignore heat conduction. The energy dissipation for this case reads:
where d̊ stands for the symmetric part of the velocity gradient and t0 for the deviatoric part of Cauchy’s stress, and T is the absolute temperature.
It is well known that the direct application of the linear laws to this expression leads to Newton’s viscosity law [59,68]. Instead, a different procedure is chosen, assuming the constitutive relation between the single thermodynamic force and non-linear flux, but still deducible from a Φ dissipation potential. This dissipation potential is a scalar and isotropic function of d̊, thus:
During isochoric motions, the trace of d̊ is zero, so:
If Φ is assumed to be a continuous function of its variables (remember that Φ = 0 at d̊ = 0 ), then, for sufficiently slow flows, we can ignore the tr d̊3 variable, too, as its value is small relative to tr d̊2. The trace of d̊3 is strictly zero for viscometric flows. Thus, the form of the potential, Φ, for viscometric flows exactly and for nearly viscometric flows approximately is:
Since Φ is regarded as a function of d̊, let us introduce (to simplify calculations) the notation: d̊
where λ is a scalar variable. The tensor, a, can be arbitrarily normed, the norm of which is now:
Thus, instead of Equation (28), we can use the function:
It is obvious that the function, g(λ), has a physical meaning, but only for the positive values of its variable; consequently, for negative λ, the function, g(λ), can be defined at will. It is plausible to assume g(λ) differentiable at λ = 0. Then, for a sufficiently small value of λ, g(λ) can be approximated by its tangent, so the function:
is obtained, from which the constitutive relation for the deviatoric part of Cauchy’s stress:
follows. Introducing the notation:
is obtained for the stress, which is well known form for the ideal plastic body in von Mises’ approximation.
From the above results, it is clear that Gyarmati’s local principle furnished with various approximations for the potential, φ, leads to the various theories of viscous flow or plasticity.
3.2. The Generalized Reciprocal Relations and the Generalization of Gyarmati’s Principle for Non-Linear Cases
The possibility of generalizing the reciprocal relations for non-linear constitutive equations has already been mentioned earlier when describing Gyarmati’s variation principle. However, the practical value of the suggestions made there is doubtful. The reason for this is that neither the macroscopic reversibility principle proposed by Meixner  nor the generalized reciprocal relations by Gyarmati [70,71] and Li [72,73] could be proved satisfactorily up to now, either theoretically or experimentally. Moreover, it is well known that the dynamic equations equivalent to the Guldberg-Waage equations for chemical reactions, which are regarded as prototypes of non-linear constitutive equations, definitely violate the general reciprocal relations of Gyarmati and Li, as well as Meixner’s macroscopic reversibility principle, at least in the case where we consider affinities as the real driving force of chemical reactions in the non-linear region far from equilibrium. We cannot deal here with this very important and persistent problem of non-linear thermodynamics, but the interested reader is referred to some papers on the subject [63,74–76].
Nevertheless, in the following, a generalization will be presented, which is proven by strict mathematics and whose validity is not restricted if we have twice continuously differentiable constitutive equations.
Start from the bilinear form of entropy production:
but let us drop our usual notation, viz. that Ji stands for “current” and Xi for “force” of the process rate. Let Xi be the independent variable from among the canonically conjugate force and current and Ji the other variable characteristic for the i-th process. The independent variables should be chosen, so that close to equilibrium, i.e., in the range of validity of the linear laws, only Onsager’s reciprocal relations should hold. We do not suppose the linearity of the constitutive equations, but they should be twice continuously differentiable with respect to Xis. The role of equilibrium state parameters is not restricted in the constitutive equations. For them, it may be written in a general way that:
where X1, X2, . . . are the independent variables selected from the expression of entropy production. For brevity, let us now call them forces; Γ1, Γ2, . . . are other local state parameters whose specification is not necessary at present. Let us then take function:
depending on λ, expand it into a Taylor series with respect to the powers of λ and stop after the linear term. On writing also the Lagrange remainder, expression:
results, which at λ = 1, gives, again, constitutive Equation (38). If the remainder is negligible, Equation (40) is identical with Onsager’s linear laws, and the derivatives included in it may be identified with the Onsager coefficients:
We note that reciprocal relations do not follow from the expression; their validity has been taken from the linear theory. Now, for brevity, we introduce coefficients:
Following from the nature of the Taylor series, derivatives should be taken at ξX1, ξX2, . . ., where ξ lies between zero and eon and whose actual value is determined by the structure of constitutive Equation (38) and the actual values of the independent variables. (If more than one ξ is possible, the smallest should be chosen.) Now, the constitutive equations may be written in form:
where coefficients lijk may also depend on X; but on the basis of Equation (42), correlations:
hold between them. Let us now introduce coefficients:
for which, on the one hand, Onsager’s reciprocal relations of the linear theory are valid and, on the other hand, as a consequence of Equation (44), generalized reciprocal relations:
hold. By using them, the constitutive equations may be written as:
Since the last term on the right-hand side is zero, Equations (43) are obtained again.
Our results can be summarized as follows. The constitutive equations, also for non-linear cases, may be written in the form:
where coefficients, Lik, may depend also on X, and between conductivity coefficients reciprocal relations:
hold if they are valid in the linear limiting case, i.e., close enough to equilibrium. Keep in mind that the so-defined Lik quantities are not uniquely determined by the constitutive equations. This form has been used by several authors, e.g., by Gurtin  or by Ván 
The selection of independent variables can be varied by a linear transformation of forces and currents, which is formally analogous to that applied in the linear theory. This means that in the equation with the changed independent variables, Casimir-type reciprocal relations also appear, similar to the linear theory. Of course, from the viewpoint of the validity of the generalized Onsager-Casimir reciprocal relations between coefficients Lik, it is of no importance what the independent variables of the coefficients are. Since the determinant of the matrix constructed from coefficients Lik is positive at equilibrium, the constitutive equations are twice continuously differentiable, and thus, the above determinant is a continuous function of the independent variables. From this, it follows that the matrix constructed from coefficients Lik can be inverted in a wider range around equilibrium than the realm of linear laws. A similar consideration is applied for the principal minors of matrix Lik; hence, the homogeneous quadratic form using coefficients Lik remains positive definite.
The above generalization of Onsager’s reciprocal relations permits the writing of the Lagrange function belonging to Gyarmati’s principle provided by Equation (21) in its usual form as:
where numbers Rik again mean the elements of the reciprocal matrix. Since the homogeneous quadratic form constructed with coefficients Lik is positive definite and, consequently, also that formed by coefficients Rik, the Lagrange function, , is always negative if constitutive equations (48) are not satisfied. If they are satisfied, is zero. This means, at the same time, that in the case of X and J, values corresponding to the real process, , were maximum, even an absolute maximum.
The Lagrange function can be reduced to its well-known simpler form by removing the parentheses:
From this expression, dissipation potentials may be determined as:
It is very important and striking that relative to the linear theory, the only change is that dissipation potential, Ψ, is not a quadratic function of Xs any more, and potential Φ also depends on Xs. However, a significant difference is that although equality:
holds also here, partial derivative:
does not give the currents, since in this non-linear theory, Ψ cannot be regarded as a potential. It should also be noted that the problem of these derivatives becomes even more complicated if Xs are not chosen as independent variables in the conduction coefficients, but this does not interfere with the validity of the variational principle.
The unchanged validity of the local form of Gyarmati’s principle in non-linear cases and the existence of an absolute maximum allows the integration of the local form with respect to time and space. Therefore, we can say that the validity of the Governing Principle of Dissipative Processes whose basis is the integrated form of Equation (51) with respect to space and time is not restricted to linear thermodynamics, but it is almost general, since the requirement of its being twice continuously differentiable is not a strong restriction from a physical point of view.
After the above results were reached, a new variational technique was proposed [2–4,49,79] that gives the transport equations as Euler-Lagrange equations for the potential functions introduced suitably. Nevertheless, this technique may be assumed as an entirely different variational principle; it is undeniably an offshoot. Nyíri [80–82] showed that a particular form of Gyarmati’s variational principle is valid even if the constitutive equations are non-linear and no symmetry relation holds even in the linear approximation.
3.3. Another Generalization for Non-Symmetric Equations
Up to now, the symmetry of the conductivity matrix was presumed. Nevertheless, the complete symmetry is frequent; it does not always hold. A magnetic field or Coriolis force in the rotating frame may result in the skew-symmetric part, even in the linear approximation. Getting rid of the skew-symmetric part is easy and always possible. Colman and Truesdell showed a good method .
If Onsager’s reciprocity does not hold, the constitutive equations have the form:
Introducing new variables for the fluxes by:
we find that the bilinear form of the entropy production remain unchanged;
as the last term in the right-hand side is zero.
The above train of thought is valid both for the linear and the non-linear approximation. This means that, even in the presence of a skew-symmetric part in the matrix of the conductivity (or the resistivity) coefficients, with changing the variables accounting on processes, the results of the previous subsection can be applied; nevertheless, the marvelous freedom of picking up the fluxes has been reduced.
4. The Governing Principle of Dissipative Processes
Though the local form of Gyarmati’s principle is indispensable for the description of local constraints, an integral form of the principle is of much greater importance in practical calculations. The integral forms are obtained by the integration of the universal Lagrange density with respect to space or space and time coordinates. The universal (global) principle, obtained so, is called the “Governing Principle of Dissipative Processes” (GPDP) .
Since the universal Lagrange density is everywhere and always stationary, it is also true that:
The Governing Principle of Dissipative Processes given by Gyarmati can be regarded as the most widely valid and the most widely applied integral principle of irreversible thermodynamics. From this principle, the parabolic transport equations of irreversible transport processes can be derived both in the linear and quasi-linear case, as well as in all those non-linear cases where dissipation potentials can be determined by Equations (23) and (24), due to the validity of the generalized reciprocal relations in Equation (11) [20,21,35,37,39,41,42,56–59,84].
The application of the governing principle can be understood through the properties of the local principle. The variational principle alone does not contain sufficient information about the system; the functional takes its absolute maximum in several points of the (Γ,X, J) space; but if the Γ and X values are given, then J can be determined. Obviously, not only the knowledge of Γ and X is suitable, but any other restrictive circumstance denoting an equivalent hypersurface in the (Γ,X, J) space. Such a restrictive condition is the ensemble of the balance equations and the definition of the forces together with the equation of state.
Hence, it follows that the variational principles in Equations (59) and (60) are to be understood with the above subsidiary conditions, and thus, the processes occurring in the system are uniquely described.
The extraordinary importance of the formula in Equation (59) arises from the fact that the Euler-Lagrange equations are identical to the parabolic transport equations. Observe that the set of functions, in which the maximum is looked for, concern a snapshot of the processes at an, otherwise arbitrary, moment; consequently, even though the Euler-Lagrange equations resemble parabolic ones, they are not, as the time is not an independent variable; they turn out to parabolic ones when the time slices are assembled into a whole. Its use has the greatest advantage in the entropy picture, since the substitution of Γ with the entropy balance gives a particular form. The corresponding Euler-Lagrange equations have a separable subsystem of differential equations (viz. independently solvable) for the Γ parameters, and neither the consideration of the balance equations as subsidiary conditions nor the determination of the J currents is necessary .
The situation with the time integrated form in Equation (60) is a bit different. The Euler-Lagrange equations do not display the set of transport equations directly. The latter can be calculated from transversality conditions and is obtained after a first integration of the Euler-Lagrange equations . The other method introduces some potential functions the Euler-Lagrange equations concern, and the customary transport equations result after eliminating them [2–4,79].
The Governing Principle of Dissipative Processes, like any other integral principle of physics, contains information on the boundary conditions, too. They have to be given, so that the absolute maximum is provided, viz. any further weakening of the proper boundary conditions may not increase the value of the maximum.
We mention that for strictly linear problems, there are two partial forms that are also valid:
The first of these is called force, and the second is called flux representation. Both representations were widely applied to the solution of several practical problems [41–43,56,57,85]. It is also well known that the force representation of Gyarmati’s governing principle is equivalent to the local potential method of Prigogine and Glansdorff , while the flux representation is the equivalent of the variational methods of Biot [18,19]. (For details, see [43,44,61,87–92].)
Here, a more or less “classical” framework of Gyarmati’s variational principle has been surveyed, but life does not stop; new fields of applications and new aspects emerge. The unification of and relating the different approaches is a permanent task. I mention only some works of Sieniutycz , Anthony , Polizzotto , Ván [96–103], Merker and Krueger , Cimmelli , Jou, Cimmelli and Sellitto , Gerasev , Triani and Cimmelli , Villaluenga and Kjelstrup  and Hutter and Svendsen  etc.
Some of them (e.g.,  and ) are loosely or not related to Gyarmati’s variational principle, but concern systems that are worth studying if they can be inserted into Gyarmati’s framework and if they can then know how to do it.
4.1. A Very Simple Illustration 
For those readers who are interested in how a parabolic equation can be derived from a variational principle, a very simple example is put forward here.
Assume one-dimensional heat conduction with constant density, specific heat and heat conductivity in, e.g., a wall with constant thickness; moreover, use such units that both the heat capacity of the unit volume and the heat conductivity are one (and dimensionless). In this model, the conservation of energy is expressed by:
Here, T is the temperature, t is the time, Jq the heat flow and x is the coordinate perpendicular to the wall. In such a simple model, the local equilibrium makes the temperature well defined.
The entropy balance reads:
In this simple case, the so-called Fourier picture is the most convenient one. The quantity:
is a comfortable starting point to write Onsager’s linear law, which reads:
Nevertheless, substituting this into Equation (63) is a straightforward way to Fourier’s equation; this time, not obtaining it is the main purpose, but it is deriving from a variational principle. The linear law is used to get the Φ and Ψ potentials only, and having got them, we pretend to have forgotten it. The mentioned potentials are:
and the Lagrangian in Equation (60) is:
The two functions looked for are correlated by the conservation of the energy in Equation (63); we have two possibilities. The first is using the Lagrangian multiplier with the auxiliary Lagrangian:
or better, introducing a potential, ϕ, with the equations:
with which the conservation of the energy automatically holds. Now, the form of the variational problem in Equation (60) takes:
The Euler-Lagrange equation reads:
The usual initial and boundary conditions prescribe the temperature; now, they prescribe the value of , i.e., the value of ϕ is free on the boundary, and at t2, consequently, the transversality conditions:
also hold. Introducing temporarily the:
auxiliary variable, the equation turns into:
with the initial (now final) and boundary conditions:
The t′= −t transformation results in the simple heat conduction problem of constant (zero) initial temperature and no heat flow on the boundary. We conclude that Equation (77) with the initial and boundary conditions is a well-posed Cauchy problem, the only solution of which is the trivial one u = 0. Now, Equation (76) turns into a parabolic equation, from which Fourier’s equation results by evaluating the partial derivative of both sides with respect to x.
This work has been supported by the Hungarian National Scientific Research Funds, OTKA(62278 and K81161).
Conflicts of Interest
The author declares no conflict of interest.
- †This is based on the paper of Verhás, J. Gyarmati’s Variational Principle of Dissipative Processes. In Proceedings of the 12th Joint European Thermodynamics Conference, JETC 2013, Brescia, Italy, 1–5 July 2013; pp. 127–132.
- Verhás, J. On the Time Integration of Gyarmati’s Variational Principle. Presented in III, Szárítási Konferencia, Budapest, Hungary; 1971. [Google Scholar]
- Gambár, K.; Márkus, F.; Nyíri, B. A Variational Principle for the Balance and Constitutive Equations in Convective Systems. J. Non-Equilib. Thermodyn 1991, 16, 217–224. [Google Scholar]
- Márkus, F.; Gambár, K. A Variational Principle in Thermodynamics. J. Non-Equilib. Thermodyn 1991, 16, 27–32. [Google Scholar]
- Márkus, F.; Gambár, K. Hamilton’s Canonical Equations and the Entropy Production. J. Non-Equilib. Thermodyn 1993, 18, 288–292. [Google Scholar]
- Extremal principles in non-equilibrium thermodynamics, Available online: http://en.wikipedia.org/wiki/Extremal_principles_in_non-equilibrium_thermodynamics accessed on 11 April 2014.
- Ziegler, H. An Attempt to Generalize Onsager’s Principle, and its Significance for Rheological Problems. J. Appl. Math. Phys 1958, 9, 748–763. [Google Scholar]
- Ziegler, H. Some extremum principles in irreversible thermodynamics with application to continuum mechanics. In Progress in Solid Mechanics; North-Holland: Amsterdam, The Netherlands, 1963; Volume Chapter 2, pp. 93–192. [Google Scholar]
- Ziegler, H. Discussion of some objections to thermomechanical orthogonality. Arch. Appl. Mech 1981, 50, 149–164. [Google Scholar]
- Ziegler, H. An Introduction to Thermomechanics; Volume 21, North-Holland series in applied mathematics and mechanics; Elsevier: Amsterdam, The Netherlands, 1983. [Google Scholar]
- Ziegler, H.J. Chemical reactions and the principle of maximal rate of entropy production. Zeitschrift für Angewandte Mathematik und Physik ZAMP 1983, 34, 832–844. [Google Scholar]
- Ziegler, H.; Wehrli, C. On a principle of maximal rate of entropy production. J. Non-Equilib. Thermodyn 1987, 12, 229–244. [Google Scholar]
- Ziegler, H.; Yu, L. Incompressible Reiner-Rivlin fluids obeying the orthogonality condition. Arch. Appl. Mech 1972, 41, 89–99. [Google Scholar]
- Collins, I.; Houlsby, G. Application of thermomechanical principles to the modelling of geotechniqueal materials. Proc. R. Soc. Lond. A 1964, 453, 1975–2001. [Google Scholar]
- Hill, R. A variational principle of maximum plastic work in classical plasticity. Quart. J. Mech. Appl. Math 1948, 1, 18–28. [Google Scholar]
- Rajagopal, K.R.; Srinivasa, A.R. A thermodynamic framework for rate type fluid models. J. Non-Newton. Fluid Mech 2000, 88, 207–227. [Google Scholar]
- Polettini, M. Fact-Checking Ziegler’s Maximum Entropy Production Principle beyond the Linear Regime and towards Steady States. Entropy 2013, 15, 2570–2584. [Google Scholar]
- Martyushev, L.M.; Seleznev, V. Maximum entropy production principle in physics, chemistry and biology. Phys. Rep 2006, 426, 1–45. [Google Scholar]
- Biot, M.A. Variational Principles in Irreversible Thermodynamics with Application to Viscoelasticity. Phys. Rev 1955, 97, 1463–1469. [Google Scholar]
- Biot, M.A. Variational Principles in Heat Transfer; Oxford University Press: London, UK, 1970. [Google Scholar]
- Edelen, D.G.B. On the Characterization of Fluxes in Nonlinear Irreversible Thermodynamics. Int. J. Eng. Sci 1974, 12, 397–411. [Google Scholar]
- Edelen, D.G.B. A Themodynamics with Internal Degrees of Freedom and Nonconservative Forces. Int. J. Eng. Sci 1976, 14, 1013–1032. [Google Scholar]
- Edelen, D.G.B. A Thermodynamic Derivation of Non-history Dependent Constitutive Relation for Elastic, Viscoelastic, Fluid and Perfectly Plastic Bodies. Arch. Mech 1974, 26, 251–261. [Google Scholar]
- Edelen, D.G.B. Generalized Onsager Fluxes and Forces: A Nonlinear Phenomenological Theory. Zeitschrift für Physikalische Chemie Neue Folge 1974, 80, 37–53. [Google Scholar]
- Edelen, D.G.B. A nonlinear Onsager theory of irreversibility. Int. J. Eng. Sci 1972, 10, 481–490. [Google Scholar]
- Edelen, D.G.B. On the existence of symmetry relations and dissipation potentials. Arch. Ration. Mech. Anal 1973, 51, 218–227. [Google Scholar]
- Edelen, D.G.B. Properties of an elementary class of fluids with nondissipative viscous stresses. Int. J. Eng. Sci 1977, 15, 727–731. [Google Scholar]
- Edelen, D.G.B.; Laws, N. On the thermodynamics of systems with nonlocality. Arch. Ration. Mech. Anal 1971, 43, 24–35. [Google Scholar]
- Edelen, D.G.B.; Green, A.E.; Laws, N. Nonlocal continuum mechanics. Arch. Ration. Mech. Anal 1971, 43, 36–44. [Google Scholar]
- Bataille, J.; Edelen, D.; Kestin, J. Nonequilibrium thermodynamics of the nonlinear equations of chemical kinetics. J. Non-Equilib. Thermodyn 1978, 3, 153–168. [Google Scholar]
- Bataille, J.; Edelen, D.; Kestin, J. On the structuring of thermodynamic fluxes: A direct implementation of the dissipation inequality. Int. J. Eng. Sci 1979, 17, 563–572. [Google Scholar]
- Goddard, J.D. Edelen’s Dissipation Potentials and the Visco-plasticity of Particulate Media. Acta Mech, 2014. preprint; Available online: http://maeresearch.ucsd.edu/goddard/ACME13.pdf accessed on 14 April 2014. [Google Scholar]
- The Azimuth Project: Extremal principles in non-equilibrium thermodynamics, Available online: http://www.azimuthproject.org/azimuth/show/Extremal+principles+in+non-equilibrium+thermodynamics accessed on 30 March 2014.
- Verhás, J. Thermodynamics and Rheology; Akadémiai Kiadó and Kluwer: Dordrecht, The Netherlands, 1997. [Google Scholar]
- Böröcz, S. An Example for Gyarmati’s Integral Principle of Thermodynamics. Zeitschrift für Physikalische Chemie—Leipzig 1967, 234, 26–32. [Google Scholar]
- Farkas, H. Reformulation of Gyarmati Principle in a Generalized Γ Picture. Zeitschrift für Physikalische Chemie—Leipzig 1968, 239, 124–132. [Google Scholar]
- Farkas, H.; Noszticzius, Z. On the Non-linear Generalization of the Gyarmati Principle and Theorem. Annalen der Physik 1971, 27, 341–348. [Google Scholar]
- Sándor, J. The Treatment of Non-isothermal Multicomponent Diffusion in Electrostatic Fields on the Basis of Gyarmati’s Variational Principle. Electrochimica Acta 1972, 17, 673–782. [Google Scholar]
- Vincze, G. Deduction of the Quasi-linear Transport Equations of Hydro-Thermodynamics from the Gyarmati Principle. Annalen der Physik 1971, 27, 225–136. [Google Scholar]
- Vincze, G. Deduction of the Reynolds Equations of Turbulence from the Gyarmati Principle. Acta Chim. Hung 1972, 75, 33–43. [Google Scholar]
- Vincze, G. On the Treatment of Thermo-Electrodynamical Processes by Gyarmati’s Principle. Annalen der Physik 1973, 30, 50–61. [Google Scholar]
- Stark, A. Approximation Methods for the Solution of Heat Conduction Problems Using Gyarmati’s Principle. Annalen der Physik 1974, 7, 53–75. [Google Scholar]
- Stark, A. Variational Properties of Irreversible Processes. Annalen der Physik 1975, 5, 481–490. [Google Scholar]
- Singh, P. An Approximate Technique to Thermodynamic Stability Problems on the Basis of the Governing Principle of Dissipative Processes. J. Non-Equilib. Thermodyn 1976, 1, 105–116. [Google Scholar]
- Singh, P.; Srivastrava, K.K. Variational Solution of Heat Convection in the Channel Flow with the Help of GPDP. Acta Physica Academiae Scientiarum Hungaricae 1978, 45, 201–211. [Google Scholar]
- Bhattacharya, D.K. The Application of Governing Principle of Dissipative Processes to Incompressible Fluid Flow and Heat Transfer. Ph.D. Thesis, University of Kharagpur, Kharagpur, India, 1978. [Google Scholar]
- Bhattacharya, D.K. A Variational Principle for Thermodynamical Wawes. Annalen der Physik 1983, 7, 325–332. [Google Scholar]
- Dickel, G. Electro-Mechanical Equilibrium in Membranes. In Topics in Bioelectrochemistry and Bioenergetics; Milazzo, G., Ed.; Wiley: New York, NY, USA, 1981; Volume 4. [Google Scholar]
- Dickel, G.; Baelz, U.; Piteza, B. Investigation of Electromechanical Equilibrium in Ion exchange Membranes. Soc. Faraday Trans 1981, 77, 451–458. [Google Scholar]
- Márkus, F.; Gambár, K. Comments “On the Relationship Between Extended Thermodynamics and the Wave Approach to Thermodynamics”. J. Non-Equilib. Thermodyn 1989, 14, 355–362. [Google Scholar]
- Onsager, L. Reciprocal Relations in Irreversible Processes. I. Phys. Rev 1931, 37, 405–426. [Google Scholar]
- Onsager, L. Reciprocal Relations in Irreversible Processes. II. Phys. Rev 1931, 38, 2265–2279. [Google Scholar]
- Onsager, L.; Maclup, S. Fluctuations and Irreversible Processes. Phys. Rev 1953, 91, 1505–1512. [Google Scholar]
- Gyarmati, I. A Termodinamika Elveiről. Ph.D. Thesis, Hungarian Acdemy of Sciences, Budapest, Hungary, 1958. (in Hungarian). [Google Scholar]
- Bhattacharya, D.K. On the Problem of Evolution Criterion for Thermodynamical Waves. Acta Mechanica 1983, 47, 87–94. [Google Scholar]
- Fekete, D. A Systematic Application of Gyarmati’s Wave Theory of Thermodynamics to Thermal Waves in Solids. Physica Status Solidi (b) 1981, 105, 161–174. [Google Scholar]
- Singh, P.; Bhattacharya, D.K. Application of G. P. D. P. to Heat Conduction Problem. Indian J. Pure Appl. Math 1978, 9, 407–416. [Google Scholar]
- Singh, P.; Bhattacharya, D.K. Application of Gyarmati Principle to Boundary Layer Flow. Acta Mechanica 1978, 30, 137–144. [Google Scholar]
- Farkas, H. On the Phenomenological Theory of Heat Conduction. Int. J. Eng. Sci 1975, 13, 1035–1053. [Google Scholar]
- Gyarmati, I. Non-Equilibrium Thermodynamics; Springer: Berlin, Germany, 1970. [Google Scholar]
- Gyarmati, I. On the Relation between Onsager’s and Prigogine’s Principles. Zeitschrift für Physikalische Chemie—Leipzig 1967, 234, 371–378. [Google Scholar]
- Gyarmati, I. On the “Governing Principle of Dissipative Processes” and its Extension to Non-Linear Problems. Annalen der Physik 1969, 23, 353–378. [Google Scholar]
- Verhás, J. Application of the Prigogine-Gyarmati Form of the Principle of Least Dissipation of Energy to Thermodynamical Constraint Problems. Proceedings of Conference on Some Aspects of Physical Chemistry, Budapest, Hungary; 1966. [Google Scholar]
- Ciancio, V.; Verhás, J. On the Non-Linear Generalizations of Onsager’s Reciprocal Relations. J. Non-Equilib. Thermodyn 1994, 19, 184–194. [Google Scholar]
- Verhás, J. The Construction of Dissipation Potentials for Non-linear Problems and the Application of Gyarmati’s Principle to Plastic Flow. Zeitschrift für Physikalische Chemie—Leipzig 1972, 249, 119–122. [Google Scholar]
- Presnov, E.V. Potencialnij kharacter kriterija evolucii termodinamiki neobratimih processov. Zh. Fiz. Himii 1973, 47, 2902–2904. (in Russian). [Google Scholar]
- Gurtin, M.E.; Williams, W.O. On the Clausius-Duhem inequality. Zeitschrift für Angewandte Mathematik und Physik ZAMP 1966, 17, 626–633. [Google Scholar]
- Gyftopoulos, E.P.; Beretta, G.P. Thermodynamics: Foundation and Application; Macmillan: New York, NY, USA, 1991. [Google Scholar]
- De Groot, S.R.; Mazur, P. Non-Equilibrium Thermodynamics; North-Holland: Amsterdam, The Netherlands, 1962. [Google Scholar]
- Meixner, J. Macroscopic and Microscopic Reversibility. Rep. Math. Phys 1975, 7, 37–57. [Google Scholar]
- Gyarmati, I. On the Phenomenological Basis of Irreversible Thermodynamics I. Chem. Eng 1961, 5, 219–243. [Google Scholar]
- Gyarmati, I. On the Phenomenological Basis of Irreversible Thermodynamics II. Chem. Eng 1961, 5, 321–339. [Google Scholar]
- Li, J.C.M. Thermodynamics for Nonisothermal Systems. The Classical Formulation. J. Chem. Phys 1958, 29, 747–754. [Google Scholar]
- Li, J.C.M. Persistency, Pseudo-Entropy and Thermokinetic Potential. Phys. Rev 1962, 127, 1784–1786. [Google Scholar]
- Hurley, J.; Garrod, C. Generalization of the Onsager Reciprocity Theorem. Phys. Rev. Lett 1982, 48, 1575–1577. [Google Scholar]
- Garrod, C.; Hurley, J. Symmetry Relations for the Conductivity Tensor. Phys. Rev. A 1983, 27, 1487–1490. [Google Scholar]
- Lengyel, S.; Gyarmati, I. On the Thermodynamics of Elementary Chemical Reactions in Homogeneous Systems. J. Chem. Phys 1981, 75, 2384–2389. [Google Scholar]
- Gurtin, M.G. Generalized Ginzburg-Landau and Cahn-Hilliard equations based on a microforce balance. Physica D 1996, 92, 178–192. [Google Scholar]
- Ván, P. Weakly nonlocal irreversible thermodynamics. Annalen der Physik 2003, 12, 142–169. [Google Scholar]
- Gambár, K.; Márkus, F. On the Global symmetry of Thermodynamics and Onsager’s Reciprocity Relations. J. Non-Equilib. Thermodyn 1993, 18, 51–57. [Google Scholar]
- Nyíri, B. A Nonlinear Extension of the Local Form of Gyarmati’s Governing Principle of Dissipative Processes. Acta Physica Academiae Scientiarum Hungaricae 1988, 63, 13–16. [Google Scholar]
- Nyíri, B. On the extension of the governing principle of dissipative processes to non-linear constitutive equations. Acta Physica Academiae Scientiarum Hungaricae 1989, 66, 19–27. [Google Scholar]
- Nyíri, B. On the Construction of Potentials and Variational Principles in Thermodynamics and Physics. J. Non-Equilib. Thermodyn 1991, 16, 39–56. [Google Scholar]
- Coleman, B.D.; Truesdell, C. On the reciprocal relations of Onsager. J. Chem. Phys 1960, 33, 28–31. [Google Scholar]
- Gyarmati, I. Generalization of the Governing Principle of Dissipative Processes to Complex Scalar Fields. Annalen der Physik 1974, 7, 18–32. [Google Scholar]
- Singh, P. Non-Equilibrium Theory of Unsteady Heat Conduction. Acta Physica Academiae Scientiarum Hungaricae 1977, 43, 59–63. [Google Scholar]
- Glansdorff, P.; Prigogine, I. Themodynamic Theory of Structure, Stability and Fluctuations; Wiley: London, UK, 1971. [Google Scholar]
- Keizer, J. Variational Principles in Nonequilibrium Thermodynamics. Biosystems 1977, 8, 219–226. [Google Scholar]
- Del Rio, J.A.; Lopez de Haro, M.; Vazquez, F. The Non-Equilibrium Thermodynamics of the Solid-Water system: a Variational Approach. J. Non-Equilib. Thermodyn 1992, 17, 67–76. [Google Scholar]
- Sieniutycz, S.; Berry, R.S. Conservation Laws from Hamilton’s Principle for Nonlocal Thermodynamic Equilibrium Fluids with Heat Flow. Phys. Rev. A 1989, 40, 348–361. [Google Scholar]
- Sieniutycz, S.; Berry, R.S. Canonical Formalism, Fundamental Equation, and Generalized Thermodynamics for Irreversible Fluids with Heat Transfer. Phys. Rev. E 1993, 47, 1765–1783. [Google Scholar]
- Sieniutycz, S.; Berry, R.S. Least-Entropy Generation: Variational Principle of Onsager’s Type for Transient, Hyperbolic Heat and Mass Transfer. Phys. Rev. A 1992, 46, 6359–6370. [Google Scholar]
- Vojta, G. Hamiltonian Formalisms in the Thermodynamic Theory of Irreversible Processes in Continuous Systems. Acta Chimica Academiae Scientarium Hungaricae 1967, 54, 55–64. [Google Scholar]
- Sieniutycz, S. Variational Approach to Extended Irreversible Thermodynamics of Heat- and Mass-Transfer. J. Non-Equilib. Thermodyn 1984, 9, 61–70. [Google Scholar]
- Anthony, K.H. Phenomenological Thermodynamics of Irreversible Processes within Lagrange Formalism. Acta Phys. Hung 1990, 67, 321–340. [Google Scholar]
- Polizzotto, C. Nonlocal elasticity and related variational principles. Int. J. Solids Struct 2001, 38, 7359–7380. [Google Scholar]
- Muschik, W.; Ván, P.; Papenfuss, C. Variational Principles in Thermodynamics. Technische Mechanik 2000, 20, 105–112. [Google Scholar]
- Ván, P.; Muschik, W. Structure of variational principles in non-equilibrium thermodynamics. Periodica Polytechnica Ser. Phys. Nucl. Sci 1994, 2, 111–121. [Google Scholar]
- Ván, P.; Muschik, W. Structure of variational principles in non-equilibrium thermodynamics. Phys. Rev. E 1995, 52, 3584–3590. [Google Scholar]
- Ván, P.; Nyíri, B. Hamilton formalism and variational principle construction. Annalen der Physik 1999, 8, 331–354. [Google Scholar]
- Ván, P. Weakly nonlocal irreversible thermodynamics—the Guyer-Krumhansl and the Cahn-Hilliard equations. Phys. Lett. A 2001, 290, 88–92. [Google Scholar]
- Ván, P.; Berezovski, A.; Engelbrecht, J. Internal variables and dynamic degrees of freedom. J. Non-Equilib. Thermodyn 2008, 33, 235–254. [Google Scholar]
- Ván, P. Weakly nonlocal non-equilibrium thermodynamics—variational principles and Second Law. In Applied Wave Mathematics: Selected Topics in Solids, Fluids, and Mathematical Methods; Quak, E., Soomere, T., Eds.; Springer: Berlin/Heidelberg, Germany, 2009; Volume Chapter III, pp. 153–186. [Google Scholar]
- Ván, P. On the structure of the Governing Principle of Dissipative Processes. J. Non-Equilib. Thermodyn 1996, 21, 17–29. [Google Scholar]
- Merker, J.; Krueger, M. On a variational principle in thermodynamics. Contin. Mech. Thermodyn 2013, 25, 779–793. [Google Scholar]
- Cimmelli, V.A. Weakly nonlocal thermodynamics of anisotropic rigid heat conductors revisited. J. Non-Equilib. Thermodyn 2011, 36, 285–309. [Google Scholar]
- Jou, D.; Cimmelli, V.A.; Sellitto, A. Dynamical temperature and renormalized flux variable in extended thermodynamics of rigid heat conductors. J. Non-Equilib. Thermodyn 2011, 36, 373–392. [Google Scholar]
- Gerasev, A.P. Variational principles in irreversible thermodynamics with application to combustion waves. J. Non-Equilib. Thermodyn 2011, 36, 55–73. [Google Scholar]
- Triani, V.; Cimmelli, V.A. Anisotropic heat transport in rigid solids. J. Non-Equilib. Thermodyn 2012, 37, 377–392. [Google Scholar]
- Villaluenga, J.P.G.; Kjelstrup, S. A non-equilibrium thermodynamics model of multicomponent mass and heat transport in pervaporation processes. J. Non-Equilib. Thermodyn 2012, 37, 353–376. [Google Scholar]
- Hutter, M.; Svendsen, B. Quasi-Linear versus Potential-Based Formulations of Force-Flux Relations and the GENERIC for Irreversible Processes: Comparisons and Examples. Contin. Mech. Thermodyn 2013, 25, 803–816. [Google Scholar]
© 2014 by the authors; licensee MDPI, Basel, Switzerland This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).