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Stochastic thermodynamics

Stochastic thermodynamics describe small systems like biomolecules in contact with a well-defined heat bath at constant temperature and driven out of equilibrium. Based on an individual trajectory, stochastic thermodynamics formulates the first law and identifies entropy production (Seifert, 2012). Macromolecules of biological systems like proteins, enzymes, and molecular motors are embedded in an... [Pg.664]

Stratonovich, R. L. (1985). Nonlinear nonequilibrium stochastic thermodynamics. Nauka, Moscow (in Russian). [Pg.246]

By far the most common methods of studying aqueous interfaces by simulations are the Metropolis Monte Carlo (MC) technique and the classical molecular dynamics (MD) techniques. They will not be described here in detail, because several excellent textbooks and proceedings volumes (e.g., [2-8]) on the subject are available. In brief, the stochastic MC technique generates microscopic configurations of the system in the canonical (NYT) ensemble the deterministic MD method solves Newton s equations of motion and generates a time-correlated sequence of configurations in the microcanonical (NVE) ensemble. Structural and thermodynamic properties are accessible by both methods the MD method provides additional information about the microscopic dynamics of the system. [Pg.349]

A general theory of the equilibrium polycondensation of an arbitrary mixture of monomers, described by the FSSE model, has been developed [75]. Proceeding from rigorous thermodynamic considerations a branching process has been indicated which describes the chemical structure of condensation polymers and expressions have been derived which relate the probability parameters of this stochastic process to the thermodynamic parameters of the FSSE model. [Pg.198]

Nonequilibrium statistical mechanics Green-Kubo theory, 43-44 microstate transitions, 44-51 adiabatic evolution, 44—46 forward and reverse transitions, 47-51 stationary steady-state probability, 47 stochastic transition, 464-7 steady-state probability distribution, 39—43 Nonequilibrium thermodynamics second law of basic principles, 2-3 future research issues, 81-84 heat flow ... [Pg.284]

TNC.35. I. Prigogine et R. Lefever, Aspect thermodynamique et stochastique de revolution (Thermodynamic and stochastic aspects of evolution), Ecole de Roscoff, 1974, pp. 95-103. [Pg.47]

G. N. Bochkov and Y. E. Kuzovlev, Non-linear fluctuation relations and stochastic models in nonequilibrium thermodynamics. 1. Generalized fluctuation-dissipation theorem. Physica A 106, 443-J79 (1981). [Pg.116]

An interesting, but probably incorrect, application of the probabilistic master equation is the description of chemical kinetics in a dilute gas.5 Instead of using the classical deterministic theory, several investigators have introduced single time functions of the form P(n1,n2,t) where P(nu n2, t) is the probability that there are nl particles of type 1 and n2 particles of type 2 in the system at time t. They use the transition rate A(nt, n2 n2, n2, t) from the state with particles of type 1 and n2 particles of type 2 to the state with nt and n2 particles of types 1 and 2, respectively, at time t. The rates that are used are obtained by assuming that only uncorrelated binary collisions occur in the system. These rates, however, are only correct in the thermodynamic limit for a low density system. In this limit, the Boltzmann equation is valid from which the deterministic theory follows. Thus, there is no reason to attach any physical significance to the differences between the results of the stochastic theory and the deterministic theory.6... [Pg.8]

Similar methods have been used to integrate thermodynamic properties of harmonic lattice vibrations over the spectral density of lattice vibration frequencies.21,34 Very accurate error bounds are obtained for properties like the heat capacity,34 using just the moments of the lattice vibrational frequency spectrum.35 These moments are known35 in terms of the force constants and masses and lattice type, so that one need not actually solve the lattice equations of motion to obtain thermodynamic properties of the lattice. In this way, one can avoid the usual stochastic method36 in lattice dynamics, which solves a random sample of the (factored) secular determinants for the lattice vibration frequencies. Figure 3 gives a typical set of error bounds to the heat capacity of a lattice, derived from moments of the spectrum of lattice vibrations.34 Useful error bounds are obtained... [Pg.93]


See other pages where Stochastic thermodynamics is mentioned: [Pg.664]    [Pg.665]    [Pg.667]    [Pg.669]    [Pg.671]    [Pg.680]    [Pg.681]    [Pg.763]    [Pg.93]    [Pg.664]    [Pg.665]    [Pg.667]    [Pg.669]    [Pg.671]    [Pg.680]    [Pg.681]    [Pg.763]    [Pg.93]    [Pg.187]    [Pg.227]    [Pg.228]    [Pg.298]    [Pg.469]    [Pg.391]    [Pg.5]    [Pg.5]    [Pg.279]    [Pg.287]    [Pg.288]    [Pg.180]    [Pg.13]    [Pg.33]    [Pg.34]    [Pg.85]    [Pg.95]    [Pg.124]    [Pg.199]    [Pg.212]    [Pg.564]    [Pg.150]   
See also in sourсe #XX -- [ Pg.664 , Pg.665 , Pg.666 , Pg.667 , Pg.668 , Pg.669 , Pg.670 , Pg.671 ]

See also in sourсe #XX -- [ Pg.93 ]




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