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The infinite volume limit

With the exception of the case of uj V, both the poly-converge as N — oo to the same limit distribution of an irreducible Markov chain on Z. This Markov chain is  [Pg.78]

As we shall see now, in all regimes P and P are exphcitly constructed. The proof of this result follows from Theorem 3.4, we give only a partial proof, which however contains the main ideas. [Pg.78]

Discussion and partial proof of Theorem 3.5. An important general fact is that we can view P in terms of [Pg.78]

One sees directly that, conditionally on t, the law of the absolute values cfclfc of the excursions under P is the same as it would be under P, in particular ek k is a (conditionally) independent sequence. The signs of the excursions instead are affected, but in a way that is easily computed and conditional independence is preserved too conditionally on t the probability that = 1 is equal to [Pg.78]

It should then be clear that in studying the convergence of P a t is sufficient to study the law of r under The rest of the process is [Pg.78]


To investigate spontaneous symmetry breaking, one ordinarily has to start at finite volume and insert a source which explicitly breaks the symmetry. The source is removed only after the infinite volume limit is taken. We stress that the source does not have to be a quark mass (it could be a higher dimension operator), so one can investigate symmetry breaking even when the quark mass is exactly zero throughout the calculation. (To be precise, a quark mass does not explicitly violate vector symmetries, so it cannot play the role of the source in the thermodynamic limit needed here.)... [Pg.186]

This is the infinite-volume limit of the corresponding sum obtained from Eq. (5.43). [Pg.115]

This can be considered as an effective Hamiltonian, which describes the evolution of the observables that are relative to the region 2 of the infinite system Z . Notice we do not have, and do not need, any such thing for 2 -> Z" the thermodynamic limit (or rather the infinite volume limit) is already taken into account in With these preliminaries, the following results of interest are immediately proven ... [Pg.361]

The uniform electron gas for rg < 30 provides a nice example of the adiabatic connection discussed in Sect. 1.3.5. As the coupling constant A turns on from 0 to 1, the ground state wavefunction evolves continuously from the Kohn-Sham determinant of plane waves to the ground state of interacting electrons in the presence of the external potential, while the density remains fixed. (One should of course regard the infinite system as the infinite-volume limit of a finite chunk of uniform background neutralized by electrons.)... [Pg.32]

Let us point out an interesting open question on the infinite volume limit measure for [3 > (3c. The two point correlation function is... [Pg.64]

The proportion of fluid elements experiencing a particular anomalous value of the Lyapunov exponent A / A°° decreases in time as exp(—G(X)t). In the infinite-time limit, in agreement with the Os-eledec theorem, they are limited to regions of zero measure that occupy zero volume (or area in two dimensions), but with a complicated geometrical structure of fractal character, to which one can associate a non-integer fractional dimension. Despite their rarity, we will see that the presence of these sets of untypical Lyapunov exponents may have consequences on measurable quantities. Thus we proceed to provide some characterization for their geometry. [Pg.56]

Here the partial molar volume is evaluated in the infinite-dilution limit with solvent-free mole fractions held fixed. [Pg.435]

The K-B theory expresses the thermodynamic quantities such as the partial molar volume and the isothermal compressibility for a solution in terms of the pair correlation functions of constituent molecular species. The expressions in terms of the site-site pair correlation functions are obtained by coupling the K-B theory with the RISM theory. When we consider a two-component system (a solute with m-sites and a solvent with n-sites) and the infinite dilution limit, the partial molar volume of the solute Vm and the isothermal compressibility kt can be expressed as, respectively. [Pg.148]

Traditional methods of determining the electrophoretic mobility in a d.c. electric field have involved particle concentrations with O g 0.001. This provides the infinite dilution limiting value, and the appropriate theoretical analysis is for an isolated particle in an infinite volume of electrolyte. [Pg.179]

The S matrix, then, would be independent of P(x ) in the zero-momentum limit in the infinite volume case, the Frohlich regime would be stable against external perturbations exciting soft (zero momentum) modes. [Pg.279]

Xhe excess apparent molar volume of electrolytes solutes in the DH model is given by Equation (2.12), referred to as the Debye-Huckel limiting law (DHLL), which becomes exact in the infinite dilution limit. Beyond the dilute region the short-range interactions among ions, neglected in the DH model, are responsible for the deviation to the DHLL. [Pg.140]

We consider both infinite volume limits and scaling limits, but in both cases we just give the basic ideas of the proofs. We will then focus on the dependence of the results on the boundary conditions. In reality, the only cases in which there is a dependence of the limit path measure on the boundary conditions is when w V ... [Pg.77]

The results of this section are taken from [Caravenna et al. (2005)] (scaling limits) and from [Caravenna et al. (2006b)] (infinite volume limits). [Pg.88]

The Debye-Htickel limiting law predicts a square-root dependence on the ionic strength/= MTLcz of the logarithm of the mean activity coefficient (log y ), tire heat of dilution (E /VI) and the excess volume it is considered to be an exact expression for the behaviour of an electrolyte at infinite dilution. Some experimental results for the activity coefficients and heats of dilution are shown in figure A2.3.11 for aqueous solutions of NaCl and ZnSO at 25°C the results are typical of the observations for 1-1 (e.g.NaCl) and 2-2 (e.g. ZnSO ) aqueous electrolyte solutions at this temperature. [Pg.488]

Here the phenomenon of capillary pore condensation comes into play. The adsorption on an infinitely extended, microporous material is described by the Type I isotherm of Fig. 5.20. Here the plateau measures the internal volume of the micropores. For mesoporous materials, one will first observe the filling of a monolayer at relatively low pressures, as in a Type II isotherm, followed by build up of multilayers until capillary condensation sets in and puts a limit to the amount of gas that can be accommodated in the material. Removal of the gas from the pores will show a hysteresis effect the gas leaves the pores at lower equilibrium pressures than at which it entered, because capillary forces have to be overcome. This Type IV isotherm. [Pg.188]

Several boundary conditions have been used to prescribe the outer limit of an individual rhizosphere, (/ = / /,). For low root densities, it has been assumed that each rhizosphere extends over an infinite volume of. soil in the model //, is. set sufficiently large that the soil concentration at r, is never altered by the activity in the rhizosphere. The majority of models assume that the outer limit is approximated by a fixed value that is calculated as a function of the maximum root density found in the simulation, under the assumption that the roots are uniformly distributed in the soil volume. Each root can then extract nutrients only from this finite. soil cylinder. Hoffland (31) recognized that the outer limit would vary as more roots were formed within the simulated soil volume and periodically recalculated / /, from the current root density. This recalculation thus resulted in existing roots having a reduced //,. New roots were assumed to be formed in soil with an initial solute concentration equal to the average concentration present in the cylindrical shells stripped away from the existing roots. The effective boundary equation for all such assumptions is the same ... [Pg.337]


See other pages where The infinite volume limit is mentioned: [Pg.38]    [Pg.51]    [Pg.323]    [Pg.38]    [Pg.238]    [Pg.246]    [Pg.273]    [Pg.164]    [Pg.165]    [Pg.56]    [Pg.78]    [Pg.38]    [Pg.51]    [Pg.323]    [Pg.38]    [Pg.238]    [Pg.246]    [Pg.273]    [Pg.164]    [Pg.165]    [Pg.56]    [Pg.78]    [Pg.85]    [Pg.369]    [Pg.40]    [Pg.269]    [Pg.125]    [Pg.40]    [Pg.97]    [Pg.18]    [Pg.125]    [Pg.103]    [Pg.332]    [Pg.91]    [Pg.91]    [Pg.163]    [Pg.223]    [Pg.2831]    [Pg.167]    [Pg.489]    [Pg.83]    [Pg.432]    [Pg.545]    [Pg.148]   


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Infinite volume

Infinite volume limit

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