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Conductance theories units

Figure 4.37. Comparison between the present theory (dashed), the Fixman theory (solid curves) and the exact numerical results by DeLacey and White (diamonds) Ka = 20, a = 200 nm, Ff /RT = 4. Left excess conductivity per unit volume fractions of the colloid right, excess dielectric loss. Figure 4.37. Comparison between the present theory (dashed), the Fixman theory (solid curves) and the exact numerical results by DeLacey and White (diamonds) Ka = 20, a = 200 nm, Ff /RT = 4. Left excess conductivity per unit volume fractions of the colloid right, excess dielectric loss.
The SCF method for molecules has been extended into the Crystal Orbital (CO) method for systems with ID- or 3D- translational periodicityiMi). The CO method is in fact the band theory method of solid state theory applied in the spirit of molecular orbital methods. It is used to obtain the band structure as a means to explain the conductivity in these materials, and we have done so in our study of polyacetylene. There are however some difficulties associated with the use of the CO method to describe impurities or defects in polymers. The periodicity assumed in the CO formalism implies that impurities have the same periodicity. Thus the unit cell on which the translational periodicity is applied must be chosen carefully in such a way that the repeating impurities do not interact. In general this requirement implies that the unit cell be very large, a feature which results in extremely demanding computations and thus hinders the use of the CO method for the study of impurities. [Pg.149]

The relationship between the diffusional flux, i.e., the molar flow rate per unit area, and concentration gradient was first postulated by Pick [116], based upon analogy to heat conduction Fourier [121] and electrical conduction (Ohm), and later extended using a number of different approaches, including irreversible thermodynamics [92] and kinetic theory [162], Pick s law states that the diffusion flux is proportional to the concentration gradient through... [Pg.562]

Grotthus chain theory phys chem An early theory used to explain the conductivity of an electrolyte. In which it was assumed that the cathode and anode attract hydrogen and oxygen respectively, and the molecules of the electrolyte are stretched out In chains between the electrodes, with decomposition occurring in molecules closest to the electrodes. grot-hus chan, the-3-re group CHEM I.Afamllyofelementswithsimilarchemical properties. 2. Acombina-tlon of bonded atoms that behave as a unit under certain conditions, for example. [Pg.171]

The Molecular Origins of Mass Diffusivity. In a manner directly analogous to the derivations of Eq. (4.6) for viscosity and Eq. (4.34) for thermal conductivity, the diffusion coefficient, or mass diffusivity, D, in units of m /s, can be derived from the kinetic theory of gases for rigid-sphere molecules. By means of summary, we present all three expressions for transport coefficients here to further illustrate their similarities. [Pg.344]

In agreement with the elementary theory of 1, the heat losses of the original mixture in the mixture heating zone in front of the flame (where a significant concentration of C02 is also attained through diffusion from the combustion zone) are numerically close to the losses through heat conduction into the products and also depend on the flame velocity, heat conduction and other parameters. We shall not consider them in detail, but instead shall double the last expression. Thus the total amount of heat lost in unit time by a unit of the flame surface is equal to... [Pg.282]

A series of extended Hiickel theory (EHT) band calculations on crystal structures 16 and 17 have been performed <2003JA14394, 2004CM1564>. They show that the dispersion curves plotted along the stacking direction arise from the SOMOs of the radicals in the cell unit, that is, the putative half-filled conduction band of the molecular metal. Clearly, none of the materials are metallic, but the dispersion curves nonetheless provide insight into the extent of the intermolecular interaction along and perpendicular to the slipped 7t-stacks. [Pg.3]

The equation of state for a perfect gas is presented and expressions arising from this for pure gases and gas mixtures are given. The kinetic theory of gases, which is a useful model of perfect gases, is introduced and two particularly useful results are emphasised. These are the mean free path (/) and the mean or thermal velocity (c). Of particular importance is Z74, which is numerically equal to the volume rate of flow per unit area and which can be used to determine quantities such as area-related pumping speeds, conductances, etc. [Pg.1]


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