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In the present work the Stochastic generalization of the quantum hydrodynamic analogy (SQHA) is used to obtain the far-from-equilibrium kinetics for a real gas and its fluid phase. In gases and their liquids, interacting by Lennard-Jones potentials whose mean distance is bigger than the quantum correlation distance and the molecular interaction distance r0, it is possible to define a Fokker-Plank type equation of motion as a function of the mean phase space molecular volume that far-from-equilibrium shows maximizing the dissipation of a part of the generalized SQHA-free energy. In the case of a real gas with no chemical reactions with small temperature gradients, the principle disembogues into the maximum free energy dissipation confirming the experimental outputs of electro-convective instability. In this case, the model shows that the transition to stationary states with higher free energy can happen and that in incompressible fluids, the increase of free energy is almost given by a decrease of entropy leading to the appearance of self-ordered structures. The output of the theory showing that the generation of order via energy dissipation, is more efficient in fluids than in gases, because of their incompressibility, which leads to the reconciliation between physics and biology furnishing the explanation why the life was born in water. The theoretical output also suggests that the search for life out of the earth must consider the possibility to find it in presence of liquid phases different from water.

The missing bridge between the physics and life disciplines constitutes one of the greatest problems of science nowadays. The situation is similar to that exists between physics and chemistry at the beginning of the past century. Every scientist was intimately convinced that once the physical laws of particles belonging to the atoms were established, the chemical properties of elements should possibly be derived and explained.

With the advent of quantum mechanics, this view came to realization and the quantum physics is at the base of modern chemistry.

A similar state of fact exists between the physics and biology. The unavailability of a physical theory capable of explaining the order generation at the base of the evolution of biological system is the major obstacle to give the physical basis to biology.

One of the most known and experimentally verified laws of the physics is the second law of thermodynamics that expresses the tendency of any physical system toward the maximum possible disorder. Even verified only near the thermodynamic equilibrium, this law has lead many thinkers to a “pessimistic” view of the world and to the so-called “obscurantism” in many fields of human science.

Starting by the thirties of the last century, mainly due to the work of Prigogine, it was born in the physicists and chemists the idea that the tendency to the entropy production was a bounded process and that generation of order was possible out of the neighborhoods of thermodynamic equilibrium [1-8]. Various principles have been proposed for the self-organized regimes governed by classical linear and non-linear non-equilibrium thermodynamic laws, with stable stationary configurations being particularly investigated.

Nevertheless, an organic understanding for a long time has been unavailable. In 1945, Prigogine [1,2] proposed the “Theorem of Minimum Entropy Production” which applies only to near-equilibrium stationary state. The proof offered by Prigogine is open to serious criticism [

Sawada postulated the principle of largest amount of entropy production [

Sawada and Suzuki showed that the maximum entropy production leads electro-convective phenomena to the maximum rate of energy dissipation. This principle was confirmed, both by numerical simulations and by experiments [

The rate of dissipation of energy appeared for the first time in Onsager’s work [

Nowadays, the debate about the principle of maximum free energy dissipation (MFED) and the Prigogine’s one comes to a possible solution. The author has shown that in the frame of the quantum stochastic approach of hydrodynamic analogy [10-13], it is possible to define a phase space Wigner-type distribution functions. In (classical) phases, the mean of inter-particle distance is bigger than the distance over which the quantum correlations take place. It can lead to the definition of an energy function (named stochastic free energy) whose dissipation is at maximum during the out of equilibrium relaxation process.

Following the tendency to reach the highest rate stochastic free energy dissipation (SFED), a system relaxing to equilibrium goes through states with higher order so that the matter self-organization becomes possible.

Moreover, near equilibrium the maximum of SFED is shown to lead to the Prigogine’s principle of minimum entropy production, while far-from-equilibrium, in quasi-isothermal states and in the case of elastic molecular collisions and in absence of chemical reactions, the maximum SFED reduces to the maximum free energy dissipation.

The Prigogine’s principle of minimum entropy production near-equilibrium and the far-from-equilibrium Sawada’s principle of maximum energy dissipation consists of two complementary principia of a more general theory that do not contradict each other. The availability of a clear general model applying to the irreversible processes far from equilibrium is a great tool to investigate the generation of order and matter self-assembling in presence of large gradients of thermodynamic forces.

In the present paper the author shows that in quasiisothermal far from equilibrium states with no chemical reactions, the principle of maximum SFED, that can generally lead to transition to a state with an increase of free energy, in the case of incompressible phase (e.g., fluid one) this increase of free energy is basically almost given by an increase of order since the energy variation of the system associated to the external work is quite null.

For the first time it comes out from a physical theory the information about how and why a fluid phase is necessary to the development of matter self-assembling process that is at the base of the emerging of life.

The physical model is not devoid of new information signaling that ordering processes (and life) can also happen in fluids different from water, an interesting chance in searching for life in the universe out of the earth.

The quantum hydrodynamic analogy (QHA) equations are based on the fact that the Schrödinger equation, applied to a wave function, is equivalent to the motion of a fluid owing the particle density with a velocitygoverned by the equations [10-14]

where, , is the Hamiltonian of the system and is the quantum pseudo-potential that reads

For the phase space analysis, it is useful to observe that Equations (1)-(3) can be derived by the following phase-space equations [

where and where

where

and where

The Madelung approach, as well as the Schrödinger one, are non-local and are not able to give rise to local limit.

When fluctuations are added to the QHA equation of motion, the resulting stochastic-QHA (SQHA) dynamics shows that is possible to obtain local dynamics on large scale, preserving the quantum behavior on a microscopic one. In a preceding paper [

where the phase space distribution

is a Wigner-like distribution obeying, in the limit of null noise, to the property

where is a measure of the vacuum noise amplitude (VNA) and

is the VNA variance, where the quantum correlation length reads [

where

where

where is obtained from the zero order of approximation Equation (1).

Given the physical length of the system, the macroscopic local dynamics is achieved for those problems that satisfy the condition

.

From the condition it follows that [

and the SPDE of motion acquires the form [

where dp is a small fluctuation of momentum and

Being also, represents a small energy fluctuation due to the quantum potential [

As derived in reference [

With, where is the mean-field Hamiltonian, and where obeys to the equation [

For a (classical) gas phase made up of structureless point-like particles interacting by central symmetric potential that do not undergo to chemical reactions (particles do not have bounded states (e.g., Lennard-Jones potential with small well, compared to the mean energy of particles) so that molecules with internal structure are not created) can be further simplified by excluding the cross-correlations concerning different co-ordinates components, namely

Equation (28) is basically the Fokker-Plank form of the Maxwell equation.

In order to obtain from (28) a closed kinetic equation, the standard approach is to introduce additional information about the diffusion coefficient. Under the local equilibrium condition this is usually achieved by the semiempirical assumption of linear relation between flows and fluxes.

In order to obtain an evolutionary principle far from equilibrium, here we use (28) without the assumption of linear relation between flows and thermodynamic forces.

In order to grasp information from (28) we observe that (for gasses and mean-field fluids) the SQHA approach shows two competitive dynamics: 1) the enlargements of the molecular DF [

As consequence of free expansions and collapses, the pseudo-Gaussian molecular DF in the phase space cell will occupy the mean volume that we pose

where reads:

where.

In the case of sufficiently weak radiative coupling between vacuum fluctuations and thermal ones [

where in the synthetic notation of the right side

is a 2 × 2 matrix that applies to the 2-element vector representing phase space gradient

that introduced into the FPE (27)

leads to the kinetic equation for stationary states [

Even if the -function is well defined far from equilibrium, without the explicit form of the diffusion coefficient and the initial and boundary conditions of an assigned problem, the kinetic Equations (27) and (28) are just symbolic equations.

Nevertheless, the existence of the -function far from equilibrium allows the definition of a formal criterion of evolution.

In fact from Equation (33) it is possible to derive an evolutionary principle along the relaxation pathway that can be formulated in terms of dissipation of the -function (named here normalized hydrodynamic free energy (NHFE) since at equilibrium it converges to the free energy normalized to kT [

Given that, the total differential of the normalized hydrodynamic free-energy can be written as a sum of two terms, such as:

where we name

as “dynamic differential” and

as “stochastic differential”.

Under the range of validity of Equation (35) (i.e., structureless punt-like particles, interacting by L-J central symmetric potential that do not undergo to chemical reactions) the stochastic velocity vector evolves through a pathway that follows the -function negative gradient so that

is minimum with respect the choice of (38)

With since and are anti-parallel to and, respectively.

Sometime, some authors speak in term of energy dissipation, so that in this case the criterion (38) reads

In order to elucidate the significance of the criterion given by (39), we analyze the spatial kinetics far from equilibrium.

By using a well known method [

Given a quantity per particle

its spatial density:

and its first moment

by using the motion Equation (34) it is possible to obtain the spatial differential equation:

that by choosing

where T is the “mechanical” temperature defined as

where is defined at thermodynamic equilibrium, in quasi-isothermal condition and elastic molecular collisions (i.e., absence of chemical reactions) leads to the maximal condition respect to [

Equation (46) has been proven to be experimentally verified by Sawada in the electro-convective instability [8,17].

From general point of view the SQHA system of differential equations is unmanageable as well as the far-from equilibrium kinetics.

In order to gain information about (46) let’s analyze it in the simple case of quasi-isothermal stationary states far from equilibrium (chemically and mechanically speaking). This case is still sufficiently general to be interesting since the matter self-assembling phenomena concerning the life generation happen in quasi-isothermal condition.

As a figurative example we take in mind the case of the electro-convective instabilities [

In the case of quasi-isothermal system with no chemical reaction taking place, it has been assumed that each infinitesimal volume of fluid is at quasi-thermal equilibrium. On this base, in Equation (46) equals the free energy F, as well as Ss the thermodynamic entropy S.

In the following we are going to show that the transitions to states with a higher amount of free energy are possible in far from equilibrium kinetics.

To this end, let’s consider the overall system with the energetic reservoirs that works reversibly onto the system so that we have

where is the energy of reservoir that for our purpose can be assumed to work in reversible manner onto the system, and the heat generated into the system is exchanged with the environment reversibly so that

and

then, for the overall system it follows that

This has been proven in electro-convective instability very far from equilibrium and confirmed by numerical simulation by Sawada et al. [

Let’s consider the case that, far from equilibrium in subcritical conditions, the system makes a transition (at time t = 0) from a metastable state 1) to another metastable one 2) so that for t < 0^{-} and t > 0^{+} we have the sub-system in a stationary state for which it holds

so that by (50) for (t ¹ 0) we have

Given (50), in principle, the following cases are possible when the system makes the transition between states 1 and 2. Case “a”:

Case “b”:

Hence, given that for the inverse transition 2®1 it would result Case “a”

Case “b”:

since transition between metastable happens in both directions, it follows that one of the two following cases must happen

or

and since, considering the whole back and forth transition cycle, at least in one of the two directions, we have that

Generally speaking, the increase of free energy does not also mean that the entropy of the system decreases. This depends by how much is the energy change in the transition.

Nevertheless due to the incompressibility of the fluid phase that makes null energy variations due to the volume change, from the general point of view, in isothermal transitions in fluids (as the electro-convective ones) the free energy increase is almost due by the entropy decrease.

In fact given that

Since in isothermal transitions in fluids the temperature as well as the fluid density is practically constant, for van der Waals type fluids where the internal energy depends only by the temperature, it follows that and hence that

Moreover, given that in transition between metastable state the macroscopic kinetic energy of the molecules may not appreciably increases (as showed by Sawada and Suzuki [

From (62) we can see that the ability of a system to make back and forth transitions between metastable states as the consequence both of the presence of fluctuations and the tendency to the maximum stochastic free energy dissipation, allows the spontaneous increase of order in far from equilibrium stationary states in incompressible fluid phase.

Finally it is worth mentioning that the possibility of having matter self-assembling in fluids different from water, in principle, allows the possibility to find organized structures and even living ones in presence of liquid phase such the methane ocean of the Saturn’s moon Titan as hypothesized by the NASA [18,19].

Actually, Equation (37) has not been directly used to obtain (65). Nevertheless, it enters in the mechanism that allows the system to make transitions between metastable states.

Even if a large fluctuation would displace the system from a metastable stationary state, this fact will not be enough to bring the system toward a different stationary state.

It is the tendency to the (local) maximum stochastic free energy dissipation that makes it possible.

As shown by Sawada and Suzuki in electro-convective instabilities [8,17], the tendency to maximize the free energy is the real force that attracts the system toward the new stationary condition. In fact, they showed that: 1) The stationary state with the higher free energy dissipation is the most stable (i.e., it owns a longer living time before the transition to another metastable state takes place); 2) Approaching the fully stationary condition, the free energy dissipation of the system increases and reaches the top at the establishing of final stationary configuration.

Therefore, we can depict the following mechanism: the maximum free energy dissipation generates a basin of attraction (see the appendix) (possibly larger, higher is the dissipation rate of the metastable state) for each metastable state and the fluctuations make the system to jump between them.

This process allows having transition to a state with higher free energy, but this still does not warrant the generation of order.

It is the incompressibility of fluids that transforms the free energy increase into an increase of system order.

This step is just the first step toward the generation of life since many subsequent steps are needed.

It is matter of evidence that living systems own four common elements: 1) The matter substrate, 2) Energy, 3) Organization, and 4) Water (fluid). Even this is well accepted, the relationship between these characteristics has to be fully disclosed.

As shown by Katchalsky and Perelson [20-22] the physical approach to biological systems puts its foundations on the postulate that it is possible to have spontaneous order generation and that the physical law of entropy increase can break itself down far from equilibrium. Although the Prigogine’s principle brought new perspectives, it is limited to the existence of local equilibrium and a coherent general understanding is not available.

On the other hand, it is possible to model the generation of organic molecules at the base of living structures [23,24] and in some cases the far from equilibrium evolution can be described by reaction-kinetics equations, but a general criterion is not available.

The present paper shows that organization is promoted by energy dissipation and that the fluid is the phase that allows the generation of order. This picture satisfactorily explains why the four basic characteristics of living system appear always together.

Given this mechanism, the development of life follows a well-defined pathway.

The need of (fluid) water-type chemical process and reactions with the advantages of owing a rheological organized structure has brought to development of the biphasic structure in living system.

The wide spread bi-phasic structure of living systems (a solid matrix whose interstitial pores are filled by a fluid [

Energy is necessary for both macroscopic movements and microscopic ones (such as: tissue plasticity, selfrepairing, brain plasticity, fluxes of matter and energy at the base of information storing and thinking) and it is at the base of the development, transformation and functioning of any “living” system.

The matter is just the substrate. Thence being the energy the fundamental element of life, the evolution of living systems follows the way of finding better and better synergies.

The system that is more efficient has higher probability of adaptation (to develop functionalities that improve its existence) and surviving, so that life is not only complexity of structure but also (and mainly) complexity of functions.

The present work aims to bring to the light the general criterion able to get insight into life expression and evolution eliminating the non-communicability between the physics and the life science.

In the present work the SQHA is used as a model to obtain the non-equilibrium kinetics of a real gas of L-J interacting particles and its fluid phase.

In the case of particles whose mean distance is bigger than the quantum potential range of interaction. For L-J interaction potential is of order of the molecular interaction distance (so that particles can be described by the classic rigid sphere approximation), it is possible to describe the SQHA evolution by means of a Fokker-Plank equation holding even far from the local thermodynamic equilibrium.

In gasses and Marcovian liquids, close to stationary states, it is possible to define the kinetic equation of motion as a function of the mean phase space molecular volume that shows maximizing the dissipation of the stochastic part of the SQHA-free energy.

In the case of a real gas with no chemical reactions and at quasi-isothermal conditions, the principle disembogues into the maximum free energy dissipation confirming the experimental outputs of electro-convective instability.

In this case, the model shows that the transition to states with higher free energy can happen and that the increase of free energy in incompressible fluids is almost given by a decrease of entropy leading to order increase and hence to matter self-organization.

The output of the theory showing that the generation of order, via energy dissipation, is more efficient in fluids than in gases, because of their incompressibility, which leads to the re-conciliation between physics and biology furnishing the explanation why the life was born in water.

The theoretical output also suggests that the life searching, out of the earth, must consider the possibility to find organized structures in presence of liquid phases different from water.

If we instantaneously perturb the stationary state at time t = 0 (i.e., by generating a force input

) so that the total -derivative

(37) reads

for t > 0, it follows that the system begins a transient maximizing the stochastic free energy dissipation by aligning and along each other. If the process ends in a stationary state, the final kinetic equation reads

Depending by the boundary conditions and by the physical constants of the system, assigned a perturbation (or a fluctuation) leading to a response

, the final stationary value is assigned.

During the relaxation process and are coupled each other. Approaching the stationary state, the vector draws closer to the vector with complying with the maximum SFED given by the right side of (A.2).

The maximal condition of right side of (A.2) is just a local property holding for sufficiently small variation. The basin of attraction of such maximum is the complex core of the problem once the system is assigned. It depends by the specific kinetic behavior of the system that defines the coupling between and.

If we apply a large perturbation the final stationary state (configuration) may differ from the initial one.

If the fluctuation or perturbation is large enough to generate a response able to sensibly modify the free energy gradient field, the system falls into the basin of convergence of a different local maximum so that the maximum SFED brings the system to a new stationary state [