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Change of electrical conductivity with

FIGURE 2.1 Change of electrical conductivity with respect to Ni content in the Ni-YSZ cermets at 1,000°C. Two types of YSZ were used to prepare the cermets one was Toyo Soda powder with a specific surface area of 23 m2/g and an agglomerate size of -0.3 pm, and the other was Zircar powder with a specific surface area of 47 m2/g and an agglomerate size of -0.1 pm the NiO used has a specific surface area of 3.5 m2/g. (From Dees, D.W. et al., J. Electrochem. Soc., 134 2141-2146, 1987. Reproduced by permission of ECS-The Electrochemical Society.)... [Pg.77]

In our view the final verification was given to this conclusion in paper [66] in which simultaneous O2 adsorption on partially reduced ZnO and resultant change in electric conductivity was studied. It was established in this paper that the energies of activation of chemisorption and that of the change of electric conductivity fully coincide. The latter is plausible only in case when localization of free electron on SS is not linked with penetration through the surface energy barrier which is inherent to the model of the surface-adjacent depleted layer. [Pg.123]

Namely, the adsorbents of such type are polycrystalline materials with dominant type of intracrystalline contacts in the shape of open bridges enriched in superstoichiometric metal, which is the principal electron donor. Adsorption of oxygen resulting in binding of superstoichiometric metal atoms leads to the change in concentration of free electrons in bridges which results in the change of electric conductivity of the whole adsorbent. [Pg.123]

As it was mentioned in paper [48], expressions (2.44) and (2.45) perfectly describe experimental situation with kinetics of tiie change of electric conductivity of sintered and partially reduced ZnO film during adsorption and desorption of molecular oxygen. Expression (2.44) describes the kinetics of the change of a during adsorption of O2 on ZnO with the surface rich in donors due to photolytic decomposition of ZnO in vacuum fairly well [74]. [Pg.131]

The adsorption of particles of various type results in the change in electric conductivity of such bridges mainly due to local chemical interaction of adsorbed particles with electrically active defects which are electron donors and resulting, thereby, in decrease of their concentration or, on the contrary, in increase due to creation of new defects of this type. In both cases as it has been shown above there are substantially straightforward and easily verified relationships linking both the initial rates in the change of electric conductivity and the stationary values reflecting concentration of adsorbed particles in ambient volume. [Pg.163]

Fig. 6.10. The dependence of electric conductivity of the selenium film with adsorbed radicals as a function of temperature (/) at the rate of change of electric conductivity of sensor (2). Fig. 6.10. The dependence of electric conductivity of the selenium film with adsorbed radicals as a function of temperature (/) at the rate of change of electric conductivity of sensor (2).
A prerequisite for a precise and accurate titration is the reproducible identification of an end point which either coincides with the stoichiometric point of the reaction or bears a fixed and measurable relation to it. An end point may be located either by monitoring a property of the titrand which is removed when the stoichiometric point is passed, or a property which can be readily observed when a small excess of the titrant has been added. The most common processes observed in end-point detection are change of colour change of electrical cell potential change of electrical conductivity precipitation or flocculation. (Electrochemical methods are discussed in Chapter 6 precipitation indicators find only limited use.)... [Pg.193]

FIGURE 2.7 Change of electrical conductivity at 1000°C with respect to Ni volume content for Ni-YSZ cermets sintered for 2 h at 1200, 1250, 1300, and 1350°C, respectively. (From Pratihar, S.K. et al., Proceedings of the Sixth International Symposium on Solid Oxide Fuel Cells, 99(19) 513—521. Reproduced by permission of ECS-The Electrochemical Society.)... [Pg.84]

Most of the experiments were done either in the Biddulph-Plesch reaction calorimeter or in vacuum dilatomers, both types of device being fitted with electrodes so that the changes of electrical conductivity during the reactions could be followed [15]. [Pg.742]


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