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Conductivity variational model

So from electrical data, it is possible to get information on partial thermodynamic functions of the salt and then develop thermodynamic models for quantitative interpretation of the conductivity variation with composition. These models are not very different from those already developed for molten salt mixtures or metallic alloys. [Pg.87]

There is a striking similarity between the experimentally observed and the theoretically calculated profiles, and all four characteristic features occur in both. The calculated location of the minimum, which mainly depends on the vacancy mobility, is close to the location observed in the experiment. The computed temperature dependence of the depth of the minimum corresponds with the results of the measurement. Obviously, the stoichiometry polarization model of resistance degradation correctly predicts the conductivity variations. In particular the almost quantitative agreement of the very characteristic shape of the conductivity distribution proves the validity of the existing model described above. It should be noted that in the calculations only the hole mobility is chosen such that the theoretically and the experimentally observed depth of the minimum is similar, but all other parameters used in the simulation are taken from literature [77, 336, 338],... [Pg.61]

Fig. 5.9. Electrical conductivity variation versus weight fraction of SWNTs in the blend (filled circles). The percolation threshold is found to be 11%. The solid line is the fit of the percolation model [132]. Fig. 5.9. Electrical conductivity variation versus weight fraction of SWNTs in the blend (filled circles). The percolation threshold is found to be 11%. The solid line is the fit of the percolation model [132].
Note that the differential sensitivities are vector functions, because they characterize the sensitivity of the vector electric and magnetic fields to the conductivity variation. From the last formulae we see that Green s electromagnetic tensors provide the sensitivity estimation of the electromagnetic field to the model conductivity. [Pg.242]

The argument in the expressions for the Prechet differentials, FE,H b,Aa), consists of two parts. The first part, at, is the background conductivity distribution, for which we calculate the forward modeling operator variation the second part, Aa, is the anomalous conductivity, which plays the role of the background conductivity variation. We will use below the following simplified notations for the Fr6chet differentials... [Pg.291]

Additional experiments on the same Pt(NH3)4 and PtCb " solutions demonstrated that certain solutions consistently gave crystals of higher conductivity, which suggests that differences in the composition of these solutions were responsible for the observed conductivity variations. On the basis of these findings and the previously mentioned arguments against the intrinsic band model, it was suggested that the conductivity in MGS was impurity dominated (24, 31). [Pg.10]

Found values of a and other observed regularities of electrical conductivity variations for the OIL coincide mainly with the studied earlier for simple REO, including doped oxides. These results can be explained within the framework of theoretical model of equilibrium between electronic and ionic defects in crystals, which application for the analysis of defect structure of REO is reviewed in [1]. [Pg.263]

Electrical conductivity (or its mathematical inverse, resistivity) of a soil solution is strongly correlated with total salt content. Therefore, laboratory methods involving solution or saturated paste conductivity are often used to assess soil salinity. Electrical conductivity measurements of bulk soil (designated as ECa for apparent electrical conductivity) were also first used to assess salinity. Resistivity and conductivity measurements are also useful for estimating other soil properties, as reviewed by and. Factors that influence ECa include soil salinity, clay content and cation exchange capacity (CEC), clay mineralogy, soil pore size and distribution, soil moisture content, and temperature. ° For saline soils, most of the variation in ECa can be related to salt concentration. In non-saline soils, conductivity variations are primarily a function of soil texture, moisture content, bulk density, and CEC. The theoretical basis for the relationship between ECa and soil physical properties has been described by a model where ECa was a function of soil water content (both the mobile and immobile fractions), the electrical conductivity of the soil water, soil bulk density, and the electrical conductivity of the soil solid phase.Later, this model was used to predict the expected correlation structure between ECa data and multiple soil properties. ... [Pg.39]

Early models used a value for that remained constant throughout the day. However, measurements show that the deposition velocity increases during the day as surface heating increases atmospheric turbulence and hence diffusion, and plant stomatal activity increases (50—52). More recent models take this variation of into account. In one approach, the first step is to estimate the upper limit for in terms of the transport processes alone. This value is then modified to account for surface interaction, because the earth s surface is not a perfect sink for all pollutants. This method has led to what is referred to as the resistance model (52,53) that represents as the analogue of an electrical conductance... [Pg.382]

If structural information of the protein target is available, e.g., a crystal structure, in silico screening of huge virtual compound libraries can be conducted by the use of docking simulations. Based on identified primary hits, structural variations of the ligand can be evaluated by computational modeling of the ligand-protein complex. [Pg.384]

Figure 5.7. Schematic representation of the definitions of work function O, chemical potential of electrons i, electrochemical potential of electrons or Fermi level p = EF, surface potential %, Galvani (or inner) potential Figure 5.7. Schematic representation of the definitions of work function O, chemical potential of electrons i, electrochemical potential of electrons or Fermi level p = EF, surface potential %, Galvani (or inner) potential <p, Volta (or outer) potential F, Fermi energy p, and of the variation in the mean effective potential energy EP of electrons in the vicinity of a metal-vacuum interface according to the jellium model. Ec is the bottom of the conduction band and dl denotes the double layer at the metal/vacuum interface.

See other pages where Conductivity variational model is mentioned: [Pg.171]    [Pg.57]    [Pg.171]    [Pg.1721]    [Pg.301]    [Pg.478]    [Pg.330]    [Pg.102]    [Pg.103]    [Pg.252]    [Pg.887]    [Pg.321]    [Pg.62]    [Pg.1156]    [Pg.311]    [Pg.3]    [Pg.450]    [Pg.37]    [Pg.99]    [Pg.214]    [Pg.265]    [Pg.519]    [Pg.508]    [Pg.424]    [Pg.46]    [Pg.474]    [Pg.129]    [Pg.136]    [Pg.162]    [Pg.322]    [Pg.157]    [Pg.13]    [Pg.14]    [Pg.458]    [Pg.479]    [Pg.242]    [Pg.312]   
See also in sourсe #XX -- [ Pg.164 ]

See also in sourсe #XX -- [ Pg.164 ]




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