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Conductivity concentration dependence

The Du Pont HaskeU Laboratory for Toxicology and Industrial Medicine has conducted a study to determine the acute inhalation toxicity of fumes evolved from Tefzel fluoropolymers when heated at elevated temperatures. Rats were exposed to decomposition products of Tefzel for 4 h at various temperatures. The approximate lethal temperature (ALT) for Tefzel resins was deterrnined to be 335—350°C. AH rats survived exposure to pyrolysis products from Tefzel heated to 300°C for this time period. At the ALT level, death was from pulmonary edema carbon monoxide poisoning was probably a contributing factor. Hydrolyzable fluoride was present in the pyrolysis products, with concentration dependent on temperature. [Pg.370]

Fig. 3. Conductivity-concentration relationship of composite depending on manufacture technique [33)... Fig. 3. Conductivity-concentration relationship of composite depending on manufacture technique [33)...
Figure 4. Concentration-dependent ion channel blockade by (R)-JV-methylanatoxinol. The patterns identified as bursts and separated by long (>8 msec) closed intervals are indicated with a bar, the figure was designed to show approximately 2 bursts per trace. The dose-related decrease in mean channel open time resulted from the blockade of the open channel by the (R)-A -methylanatoxinol. The channel amplitude is related to membrane voltage (as was given in Figure 3) by the slope conductance such that 1 pA is equivalent to 30 mV. Continued on next page. Figure 4. Concentration-dependent ion channel blockade by (R)-JV-methylanatoxinol. The patterns identified as bursts and separated by long (>8 msec) closed intervals are indicated with a bar, the figure was designed to show approximately 2 bursts per trace. The dose-related decrease in mean channel open time resulted from the blockade of the open channel by the (R)-A -methylanatoxinol. The channel amplitude is related to membrane voltage (as was given in Figure 3) by the slope conductance such that 1 pA is equivalent to 30 mV. Continued on next page.
A study of the concentration dependence of the molar conductivity, carried out by a number of authors, primarily F. W. G. Kohlrausch and W. Ostwald, revealed that these dependences are of two types (see Fig. 2.5) and thus, apparently, there are two types of electrolytes. Those that are fully dissociated so that their molecules are not present in the solution are called strong electrolytes, while those that dissociate incompletely are weak electrolytes. Ions as well as molecules are present in solution of a weak electrolyte at finite dilution. However, this distinction is not very accurate as, at higher concentration, the strong electrolytes associate forming ion pairs (see Section 1.2.4). [Pg.13]

Interionic forces are relatively less important for weak electrolytes because the concentrations of ions are relatively rather low as a result of incomplete dissociation. Thus, in agreement with the classical (Arrhenius) theory of weak electrolytes, the concentration dependence of the molar conductivity can be attributed approximately to the dependence of the degree of dissociation a on the concentration. If the degree of dissociation... [Pg.104]

Fig. 2.8 The Wien effect shown by the percentage increase of equivalent conductivity in dependence on the electric field in Li3Fe(CN)6 solutions in water. Concentrations in mmol dm-3 are indicated at each curve... [Pg.110]

The data in Figure 5 can now be considered in light of the conduction model developed above. As stated previously, conduction in reduced poly-I behaves like an activated process. There are two sources that potentially could be responsible for this behavior. The first is the Boltzmann type concentration dependence of the 1+ and 1- states discussed above. The number of charge carriers is expected to decrease approximately exponentially with T. The second is the activation barrier to self-exchange between 1+ and 0 sites and 0 and 1- sites. For low concentration of charge carriers both processes are expected to contribute to the measured resistance. [Pg.427]

The second period, from 1890 to around 1920, was characterized by the idea of ionic dissociation and the equilibrium between neutral and ionic species. This model was used by Arrhenius to account for the concentration dependence of electrical conductivity and certain other properties of aqueous electrolytes. It was reinforced by the research of Van t Hoff on the colligative properties of solutions. However, the inability of ionic dissociation to explain quantitatively the properties of electrolyte solutions was soon recognized. [Pg.467]

The activation overpotentials for both electrodes are high therefore, the electrochemical kinetics of the both electrodes can be approximated by Tafel kinetics. The concentration dependence of exchange current density was given by Costamagna and Honegger.The open-circuit potential of a SOFC is calculated via the Nernst equation.The conductivity of the electrolyte, i.e., YSZ, is a strong function of temperature and increases with temperature. The temperature dependence of the electrolyte conductivity is expressed by the Arrhenius equation. [Pg.522]

Some doubt might be expressed about the concentration dependence of the membrane conductance and the evaluation of the limiting ratio K /c in equation 24. We have found the ratio (K -K )/Cg to be aimost constant. If it is plotted against 1/c (see Figure 4) and extrapolated to 1/c =0 one obtains the... [Pg.107]

The effect of disopyramide on conduction velocity depends on extracellular K+ concentrations. Hypokalemic patients may respond poorly to the antiar-rhythmic action of disopyramide, whereas hyperkalemia may accentuate the drug s depressant actions. [Pg.174]

In addition to the similarity between the heat conduction equation and the diffusion equation, erosion is often described by an equation similar to the diffusion equation (Culling, 1960 Roering et al., 1999 Zhang, 2005a). Flow in a porous medium (Darcy s law) often leads to an equation (Turcotte and Schubert, 1982) similar to the diffusion equation with a concentration-dependent diffu-sivity. Hence, these problems can be treated similarly as mass transfer problems. [Pg.175]

It is difficult to obtain how the diffusivity depends on concentration using the bulk mass loss or gain method, although it is possible to verify specific concentration dependence by conducting experiments from small degrees of mass loss to almost complete mass loss (Wang et al., 1996). On the other hand, the shape of diffusion profiles reveals the dependence of diffusivity on concentration. [Pg.292]


See other pages where Conductivity concentration dependence is mentioned: [Pg.15]    [Pg.198]    [Pg.536]    [Pg.701]    [Pg.241]    [Pg.79]    [Pg.11]    [Pg.331]    [Pg.274]    [Pg.14]    [Pg.101]    [Pg.136]    [Pg.92]    [Pg.374]    [Pg.267]    [Pg.95]    [Pg.265]    [Pg.390]    [Pg.100]    [Pg.62]    [Pg.23]    [Pg.170]    [Pg.168]    [Pg.94]    [Pg.248]    [Pg.251]    [Pg.337]    [Pg.268]    [Pg.424]    [Pg.271]    [Pg.401]    [Pg.162]    [Pg.203]    [Pg.356]    [Pg.86]    [Pg.50]   
See also in sourсe #XX -- [ Pg.507 ]




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