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Entropy introduced

Such problems, giving more or less only partial interpretation of entropy defined in this chapter in terms of entropies introduced in the remaining chapters, are similar, apparently not incidentally, to the interpretation of statistically defined entropy, cf, e.g., [12, Sect. 11.14]. [Pg.29]

Naturally, formal symbols corresponding to the various reaction entropies can be introduced, which are more or less self-explanatory. This allows us to abbreviate the three molar entropies introduced above, and their integral counterparts, to ... [Pg.242]

The structural entropy introduced here as a localization quantity characteristic of the decay of the distribution function is related to the shape complexity as InCLMc-... [Pg.449]

Hargreaves book, which is primarily intended for Higher National Certificate and Bachelor of Science students, presents thermodynamic functions in a pictorial way. Mahan s elementary book is clearly written and gives a classical account of thermodynamic laws, with entropy introduced as a macroscopic quantity. Jancel s book, on the other hand, is highly mathematical and will probably be of interest only to those concerned with the foundations of statistical mechanics. [Pg.40]

The classical computer tomography (CT), including the medical one, has already been demonstrated its efficiency in many practical applications. At the same time, the request of the all-round survey of the object, which is usually unattainable, makes it important to find alternative approaches with less rigid restrictions to the number of projections and accessible views for observation. In the last time, it was understood that one effective way to withstand the extreme lack of data is to introduce a priori knowledge based upon classical inverse theory (including Maximum Entropy Method (MEM)) of the solution of ill-posed problems [1-6]. As shown in [6] for objects with binary structure, the necessary number of projections to get the quality of image restoration compared to that of CT using multistep reconstruction (MSR) method did not exceed seven and eould be reduced even further. [Pg.113]

In the Maximum Entropy Method (MEM) which proceeds the maximization of the conditional probability P(fl p ) (6) yielding the most probable solution, the probability P(p) introducing the a priory knowledge is issued from so called ergodic situations in many applications for image restoration [1]. That means, that the a priori probabilities of all microscopic configurations p are all the same. It yields to the well known form of the functional 5(/2 ) [9] ... [Pg.115]

As we have seen, the third law of thermodynamics is closely tied to a statistical view of entropy. It is hard to discuss its implications from the exclusively macroscopic view of classical themiodynamics, but the problems become almost trivial when the molecular view of statistical themiodynamics is introduced. Guggenlieim (1949) has noted that the usefiihiess of a molecular view is not unique to the situation of substances at low temperatures, that there are other limiting situations where molecular ideas are helpfid in interpreting general experimental results ... [Pg.374]

A second type of relaxation mechanism, the spin-spm relaxation, will cause a decay of the phase coherence of the spin motion introduced by the coherent excitation of tire spins by the MW radiation. The mechanism involves slight perturbations of the Lannor frequency by stochastically fluctuating magnetic dipoles, for example those arising from nearby magnetic nuclei. Due to the randomization of spin directions and the concomitant loss of phase coherence, the spin system approaches a state of maximum entropy. The spin-spin relaxation disturbing the phase coherence is characterized by T. ... [Pg.1552]

The most direct effect of defects on tire properties of a material usually derive from altered ionic conductivity and diffusion properties. So-called superionic conductors materials which have an ionic conductivity comparable to that of molten salts. This h conductivity is due to the presence of defects, which can be introduced thermally or the presence of impurities. Diffusion affects important processes such as corrosion z catalysis. The specific heat capacity is also affected near the melting temperature the h capacity of a defective material is higher than for the equivalent ideal crystal. This refle the fact that the creation of defects is enthalpically unfavourable but is more than comp sated for by the increase in entropy, so leading to an overall decrease in the free energy... [Pg.639]

The subject of entropy is introduced here to illustrate treatment of experimental data sets as distinct from continuous theoretical functions like Eq. (1-33). Thermodynamics and physical chemistry texts develop the equation... [Pg.24]

It is not particularly difficult to introduce thermodynamic concepts into a discussion of elasticity. We shall not explore all of the implications of this development, but shall proceed only to the point of establishing the connection between elasticity and entropy. Then we shall go from phenomenological thermodynamics to statistical thermodynamics in pursuit of a molecular model to describe the elastic response of cross-linked networks. [Pg.138]

The equations we have written until now in this section impose no restrictions on the species they describe or on the origin of the interaction energy. Volume and entropy effects associated with reaction (8.A) will be less if x is not too large. Aside from this consideration, any of the intermolecular forces listed above could be responsible for the specific value of x- The relationships for ASj in the last section are based on a specific model and are subject to whatever limitations that imposes. There is nothing in the formalism for AH that we have developed until now that is obviously inapplicable to certain specific systems. In the next section we shall introduce another approximation... [Pg.523]

Introducing the functions for standard free enthalpy and standard free entropy. [Pg.122]

We have seen that has to behave like a free energy in the MFA, and then in addition to the interaction an entropy term has to be introduced into Since the ideal entropy is a functional of the particle distributions we will assume that there is the same kind of functional in terms of fields. Thus... [Pg.809]

If the coefficients dy vanish, dy = 28y, we recover the exact Debye-Huckel limiting law and its dependence on the power 3/2 of the ionic densities. This non-analytic behavior is the result of the functional integration which introduces a sophisticated coupling between the ideal entropy and the coulomb interaction. In this case the conditions (33) and (34) are verified and the... [Pg.814]

Equation (5-43) has the practical advantage over Eq. (5-40) that the partition functions in (5-40) are difficult or impossible to evaluate, whereas the presence of the equilibrium constant in (5-43) permits us to introduce the well-developed ideas of thermodynamics into the kinetic problem. We define the quantities AG, A//, and A5 as, respectively, the standard free energy of activation, enthalpy of activation, and entropy of activation from thermodynamics we now can write... [Pg.207]

Generalized Renyi Entropies and Dimensions A hierarchy of generalized entropies and dimensions, SQ B,t), s[ B,t), S B,t),. .. - analogous to the hierarchy of fractal dimensions, Dq, Di,. .., introduced earlier in equation 4.94 for continuous systems may also be defined ... [Pg.218]

The entropies and dimensions introduced above were defined for purely spatial sequences of site values at given times as such, they can be used to characterize sets of CA configurations. An alternative behavioral characterization is of the purely temporal sequence of site-values at a given lattice site. [Pg.220]

Entropies The individual spac e and time measures introduced above may also be generalized to space-time blocks of size B x T ... [Pg.222]

The earliest hint that physics and information might be more than just casually related actually dates back at least as far as 1871 and the publication of James Clerk Maxwell s Theory of Heat, in which Maxwell introduced what has become known as the paradox of Maxwell s Demon. Maxwell postulated the existence of a hypothetical demon that positions himself by a hole separating two vessels, say A and B. While the vessels start out being at the same temperature, the demon selectively opens the hole only to either pass faster molecules from A to B or to pass slower molecules from B to A. Since this results in a systematic increase in B s temperature and a lowering of A s, it appears as though Maxwell s demon s actions violate the second law of thermodynamics the total entropy of any physical system can only increase, or, for totally reversible processes, remain the same it can never decrease. Maxwell was thus the first to recognize a connection between the thermodynamical properties of a gas (temperature, entropy, etc.) and the statistical properties of its constituent molecules. [Pg.635]

Review of Solutions in General. In the discussion of these various examples we have noticed at extreme dilution the prevalence of the term — In Xb, or alternatively — In yB. The origin of this common factor in many different types of solutions can be shown, as we might suspect, to be of a fundamental nature. For this purpose let us make the familiar comparison between a dilute solution and a gas. Since the nineteenth century it has been recognized that the behavior of any solute in extremely dilute solution is, in some ways, similar to that of a gas at low pressure. Now when a vessel of volume v contains n particles of a perfect gas at a lixed temperature, the value of the entropy depends on the number of particles per unit volume, n/v. In fact, when an additional number of particles is introduced into the vessel, the increment in the entropy, per particle added, is of the form... [Pg.87]

In the case of a sparingly soluble substance, if each of the quantities in (64) is divided by Avogadro s constant, we confirm the statement made above— namely, that, if AS at per ion pair is added to the contribution made to the entropy of the crystal by each ion pair, in this way we evaluate the contribution made by one additional ion pair to the entropy of the saturated solution and it is important to grasp that this contribution depends only on the presence of the additional pair of ions in the solution and does not depend on where they have come from. They might have been introduced into the solution from a vacuum, instead of from the surface of a solid. In (64) the quantities on the right-hand side refer to the solution of a crystal, but the quantity (S2 — Si) does not it denotes merely a change in the entropy of a solution due to the presence of additional ions, which may have come from anywhere. When Si denotes the entropy of a sufficiently large amount of solution, (S2 — Si) is the partial molal entropy of the solute in this solution. [Pg.95]


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See also in sourсe #XX -- [ Pg.300 ]




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