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Electrical conductivity variation with temperature

Fig. 26. Electric conductivity variation with temperature for StCeo YbdojOj., in hydrogen atmosphere (Iwahara et al. 1986). (Reprinted by permission of the publisher, Elsevier Science Publishers B.V.)... Fig. 26. Electric conductivity variation with temperature for StCeo YbdojOj., in hydrogen atmosphere (Iwahara et al. 1986). (Reprinted by permission of the publisher, Elsevier Science Publishers B.V.)...
To a good approximation, thermal conductivity at room temperature is linearly related to electrical conductivity through the Wiedemann-Eran2 rule. This relationship is dependent on temperature, however, because the temperature variations of the thermal and the electrical conductivities are not the same. At temperatures above room temperature, thermal conductivity of pure copper decreases more slowly than does electrical conductivity. Eor many copper alloys the thermal conductivity increases, whereas electrical conductivity decreases with temperature above ambient. The relationship at room temperature between thermal and electrical conductivity for moderate to high conductivity alloys is illustrated in Eigure 5. [Pg.222]

The non-stoichiometric Ca2LaFe308+x ferrite was also studied by measuring the electrical conductivity variation with oxygen partial pressure, p02, at various temperatures (Fig. 18). In each curve, three ranges of variation are observable as represented for the imaginary temperature tp... [Pg.20]

FIGURE 30.4 Conductivity variations with temperature for the different classes of electrical conductor. The shading indicates the range of values at room temperature. [Pg.533]

Electrical Conductivity This is often a convenient and accurate measurement of salinity or chlorinity. Here, too, there is considerable variation with temperature, so that simultaneous observation of temperature is essential. Figure 2.16 shows the relationship between conductivity and chlorinity at various temperatures. [Pg.366]

The only new chemistry concerns electrochemical oxidation of the tetrathiafulvene derivative 41 to the radical cation perchlorate 42 (Equation 1) <2005MCL575>. The salt 42 was formed electrochemically as a dense thin film on the electrode surface and shown to be a conducting cation-radical salt that behaves like an organic metal. The electrical conductivity shows an interesting variation with temperature which may be related to a phase transition at 102K <2005MCL575>. [Pg.708]

For the composite polymer electrolytes, the conductive carbonaceous filler must be below the electrical percolation threshold, due to the need to obtain an electronically insulating material with suitable ionic conductivity. These fillers are also used to improve the thermal stabilization and serve as mechanical reinforcement to improve the electrolyte/ electrode compatibility. CNT/P(VDF-TrFE) composites showed higher porosity and electrolyte uptake compared to the pristine polymer. CNT also contributed to increase ionic conductivity (2.6 xlO S cm , 0.1 wt.% CNT) and diminished its variations with temperature. [Pg.131]

Conclusive additional evidence for the metallic nature of PAni and its blends with PMMA is provided by electron spin resonance (ESR) studies with the observation of a Dysonian line shape [104]. In both cases, the asymmetry ratio (A/B) decreases with decreasing temperature. The observed changes in the line shape from Dysonian to Lorentzian are thus seen to be a manifestation of the variation with temperature of the electrical conductivity (Figure 1.46). The g value is calculated as 2.00191 + 0.00005. The g value, which is close to the fi-ee spin value, confirms that the spins are indeed polarons. [Pg.1099]

Figure 8.20a shows the temperature variation of the dielectric permittivity of undoped BNT samples (curves a-c), as well as of BNT doped with 1 at% La (curve d) and 2at% La (curve e), aU sintered at 1000 C. For this, the measurement frequency was lOkHz. The dielectric permittivihes of the undoped samples varied approximately Hnearly with temperature, and hence followed the Curie-Weiss law. The low values of dielectric permittivity, and their near-linear variation with temperature, could be assigned to the deviation from the ferroelectric perovskite composihon, and the increasing presence of paraelectric contributions from the decomposition products that cause an increase in electrical conductivity. On the other hand, in concurrence with the diffuse OD phase transition from the antiferroelectric to the paraelectric phase at Tq, the dielectric permittivity of the La-doped samples reached a maximum at 350 °C. The dielectric permittivity of BNT doped with lanthanum was more than twice that of undoped BNT, and was larger for lat% La (-2300) than for 2at% La (-2000). The lower value at a higher La concentration was presumed to be related to the superposition of an increasing deformation of the rhombohedral lattice of BNT towards a (pseudo)... [Pg.280]

This chapter discusses the electrolytic-solution properties of low-di-electric-constant nematic solvents. Dissolved substances, if electrolytes, can contribute only a fraction of their ions to the conductance because of equilibrium between the free ions and ion pairs. If the solute forms ions through intermediate charge-transfer reactions, additional equilibria must be considered. For nematics, the solvent fluidity is anisotropic, and the conductance depends on the direction of current flow with respect to the orientation of the fluid. The variation of the conductance with temperature is directly related to the variation with temperature of both the ionic equilibrium and the fluidity. [Pg.319]

The Contact between Solvent and Solute Particles Molecules and Molecular Ions in Solution. Incomplete Dissociation into Free Ions. Proton Transfers in Solution. Stokes s Law. The Variation of Electrical Conductivity with Temperature. Correlation between Mobility and Its Temperature Coefficient. Electrical Conductivity in Non-aqueous Solvents. Electrical Conduction by Proton Jumps. Mobility of Ions in D20. [Pg.58]

The room temperature electrical conductivity of single crystals of M03S7 (dmit)3 along the c axis is 25 S cm, which is very high for a neutral molecular crystal. The variation of the magnetic susceptility (/) with the temperature does not follow a Curie-Weis law with a continuous decrease of /T vs. Tupon cooling... [Pg.116]

Fig. 4.20. Variation of electric conductivity of ZnO film under bombardment with silver atoms (to the left from the dashed line) and after termination of the atomic beam (to the right from the dashed line). The film temperature is equal to 1 - 94 C 2 - 193°C Ta = 780 C... Fig. 4.20. Variation of electric conductivity of ZnO film under bombardment with silver atoms (to the left from the dashed line) and after termination of the atomic beam (to the right from the dashed line). The film temperature is equal to 1 - 94 C 2 - 193°C Ta = 780 C...
The influence of other active components, such as 1, OH, H on a semiconductor sensor, with other conditions being the same, is comparable with the influence of atomic oxygen [50]. Contribution of N and OH is proportional to their relative contents (compared to that of atomic oxygen) in the atmosphere and may become essential at altitudes lower than 60 - 70 km. The use of selective detectors excludes the influence of atomic hydrogen. Studies of adsorption of water vapours on ZnO films [50] show that their influence is negligibly small at the film temperatures below 100°C. Variations of electric conductivity of the films under the influence of water vapours and of an atomic oxygen are comparable at the ratio of their concentrations [H20]/[0] = 10" . [Pg.257]

Fig. 4.27. Variation of electric conductivity of ZnO film under the influence of adsorption of CH3 radicals at room temperature for various pressures of acetone vapours 1,2 - 200 Torr 5-1 Torr 1, 2 - before and after immersion of the film in liquid acetone 4 - the film covered with a liquid layer. Fig. 4.27. Variation of electric conductivity of ZnO film under the influence of adsorption of CH3 radicals at room temperature for various pressures of acetone vapours 1,2 - 200 Torr 5-1 Torr 1, 2 - before and after immersion of the film in liquid acetone 4 - the film covered with a liquid layer.
The results obtained in above experiments confirm the removal of chemisorbed particles in the process of immersion of the film with preliminary chemisorbed radicals in a liquid acetone. Note that at low pressures of acetone, the CHa-radicals absorbed on ZnO film could be removed only by heating the film to the temperature of 200 - 250°C. Moreover, if the film with adsorbed radicals is immersed in a nonpolar liquid (hexane, benzene, dioxane), or vapours of such a liquid are condensed on the surface of the film, then the effect of removal of chemisorbed radicals does not take place, as is seen from the absence of variation of electric conductivity of the ZnO film after it is immersed in liquid and methyl radicals are adsorbed anew onto its surface. We explain the null effect in this case by suggesting that the radicals adsorbed on the surface of the ZnO film in the first experiment remained intact after immersion in a nonpolar liquid and blocked all surface activity of the adsorbent (zinc oxide). [Pg.266]

High electrical conductivity is also attained in oxides with very narrow, partially filled conduction bands the best known example is Ru02. This material has a conductivity of about 2-3 104S/cm at the room temperature, and metal-like variations with the temperature. Some authors consider Ru02 and similar oxides as true metallic conductors, but others describe them rather as n-type semiconductors. [Pg.323]

In the system Mo,Fe3 x04, there is a regular variation with x, from Fe304 to MoFe204, in the lattice parameter (ao), the magnetization (Ms), the Curie temperature (Tc) and the electrical conductivity (a, AH ) apparently substitution of Fe by Mo leads to a mixed iron valence on both sites for 0 < x < 1. It is worth noting that AH varies smoothly with x from a AH < kT for x = 0 in the temperature interval 300 < T < 600 K to 0.027 eV for x = 1.0, where the narrow minority-spin band is maximally perturbed and filled by the introduction of substitutional Mo ... [Pg.41]

Experimentally, as illustrated in Figure 6.34, the electrical conductivity of CU2O is found to be proportional to Pq, which is in reasonable agreement with the prediction of Eq. (6.54). The variation of another oxide semiconductor, CdO, with temperature is also shown in Figure 6.34 for comparison. [Pg.583]

In 1908, Kamerlingh Onnes succeeded in liquefying helium, and this paved the way for many new experiments to be performed on the behaviour of materials at low temperatures. For a long time, it had been known from conductivity experiments that the electrical resistance of a metal decreased with temperature. In 1911, Onnes was measuring the variation of the electrical resistance of mercury with temperature when he was amazed to find that at 4.2 K, the resistance suddenly dropped to zero. He called this effect superconductivity and the temperature at which it occurs is known as the (superconducting) critical temperature, Tc. This effect is illustrated for tin in Figure 10.1. One effect of the zero resistance is that no power loss occurs in an electrical circuit made from a superconductor. Once an electrical current is established, it demonstrates no discernible decay for as long as experimenters have been able to watch ... [Pg.395]

As is to be expected the equilibrium between the two above-mentioned forms of liquid sulphur affects other properties in addition to the colour and the viscosity. Thus, the electrical conductivity 5 and the surface tension6 of molten sulphur exhibit abnormal variation with alteration in temperature also the solubility curves for A-sulphur and p-sulphur in high-boiling solvents such as triphenylmethane are quite distinct, the solubility of the former increasing and that of the latter decreasing with rise of temperature the respective coefficients of expansion are also quite independent.7 The reactivities of the two forms towards rubber arc practically equal.8... [Pg.19]


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See also in sourсe #XX -- [ Pg.158 ]

See also in sourсe #XX -- [ Pg.183 ]




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