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Boltzmann energy distribution factor

The heat capacity (C ) and heat conductivity (A) of crystals depend respectively on the vibrational density of states weighted by a Boltzmann s distribution factor and the anharmonic terms in the vibrational potential energy. C has been found to be in the range 0.100 to 0,117 cal./g./°C between 100—250 °C for crystals as widely varying in lattice geometry as mercuric fulminate, silver azide and lead azide 62). This is... [Pg.41]

Statistical mechanics (cf. Chapter 13) suggests an alternative way to extract temperature-like properties from molecular energy distributions. According to the classical Boltzmann distribution law, the number N(E) of molecules having energy E is proportional under equilibrium conditions to the Boltzmann factor eE kT,... [Pg.28]

It is noted that the right-hand side is the ratio of the translational partition functions of products and reactants times the Boltzmann factor for the internal energy change. In the derivation of this expression we have only used that the translational degrees of freedom have been equilibrated at T through the use of the Maxwell-Boltzmann velocity distribution. No assumption about the internal degrees of freedom has been used, so they may or may not be equilibrated at the temperature T. The quantity K(fhl, ij) may therefore be considered as a partial equilibrium constant for reactions in which the reactants and products are in translational but not necessarily internal equilibrium. [Pg.311]

In the multicanonical ensemble [11,12], on the other hand, each state is weighted by a non-Boltzmann weight factor Wmn E) (which we refer to as the multicanonical weight factor), so that a uniform potential energy distribution Pmu E) is obtained ... [Pg.65]

Most of the last-named difficulty has been removed in a simple mathematical treatment which effectively removes a major part of the high-energy side of the electron beam (Winters et al., 1966). An experimental factor b, accounting for the lack of knowledge of electron energy distribution, has been found to be quite close to that calculated from the Maxwell-Boltzmann distribution. Recently it has been claimed that the 0 0 ionization and vibrational fine structure of acetylene had been detected (J. H. Collins et al., 1968), and this energy distribution difference (E. D. D.) method appears to be both simple and accurate. [Pg.180]

In the original treatment of Gurney/ the current was expressed as the integral of the product of electrolyte and electron energy distribution functions but with the electronic one written as a Boltzmann factor, exp( A /fcT). The symmetry factor was introduced intuitively in terms of the shift of intersection point of energy profiles in relation to change of electrode potential, i.e., of the Fermi-level energy (cf. Butler ). [Pg.136]

Figure B3.3.5. Energy distributions. The probability density is proportional to the product of the density of states and the Boltzmann factor. Figure B3.3.5. Energy distributions. The probability density is proportional to the product of the density of states and the Boltzmann factor.
The shaded area underneath the corresponding curve indicates the number of gas particles having at least the kinetic energy Wmin. As the temperature rises, the proportion of particles capable of reacting strongly increases. This is mainly due to the so-called Boltzmann factor in the energy distribution (compare... [Pg.443]

The partition function can be considered as an average excited state number-operator, since it is the probability-weighted sum of energy states, each counted with a factor of 1. It may also be viewed as the normalization factor for the Boltzmann probability distribution. [Pg.427]

Guggenheim s Boltzmann s Distribution Law treats the subject of the title in its widest aspects. The factorization of the partition function is discussed and equations are given for the partition function for some simple degrees of freedom. The results are used to outline the properties of ideal monatomic gases, and in later sections free energy, total energy. [Pg.36]

Therefore, E can easily be calculated, plotting the experimentally measured In k versus 1/T. According to the simple collision theory, an act of chemical reaction can only occur if colliding molecules have the kinetic energy which exceeds the activation barrier, The frequency factor. A, is the number of collisions of reacting molecules per unit time. The exponential term in (2.21) determines a portion of those collisions which can lead to the chemical transformation. Note that (2.21) postulates the fulfillment of the Boltzmann equilibrium distribution of molecular energies in the reaction mixture. [Pg.14]


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See also in sourсe #XX -- [ Pg.100 , Pg.132 , Pg.134 , Pg.184 , Pg.185 , Pg.235 ]




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