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Charging constant-voltage charge

Use of C is to hold the charge and provide a near constant voltage source to the Inverter... [Pg.126]

Smoothing circuit To obtain a near-constant voltage source for the inverter circuit a smoothing capacitance across the d.c. link is used to smooth the a.c. ripples present in the d.c. link after cotiversion. The capacitor retains the charge and provides a near-constant d.c. voltage output. [Pg.126]

After sjnoothing the d.c. voltage may contain moderate ripples not desirable when a constant voltage d.c. source is needed. To achieve this, a charging capacitor C is also provided across the d.c. link for all sizes of drives as show n in Figures 6.24(a) and 6.28(a). [Pg.129]

Figure 4. Discharge characteristics of RAM AA cells when cycled at 20 °C. The cells are discharged for 4 h per day at 4 Q, and charged overnight with a constant voltage charger at 1.7 V. Figure 4. Discharge characteristics of RAM AA cells when cycled at 20 °C. The cells are discharged for 4 h per day at 4 Q, and charged overnight with a constant voltage charger at 1.7 V.
For the familiar dropping mercury electrode, the electrical potential 1J1 at the metal surface relative to the bulk region of the electrolyte is controlled by an external potential source - a constant voltage source. In this case, can be set to any value (within reasonable physical limits) as the mercury/electrolyte interface does not allow charge transfer or chemical reactions to occur (at least to a good approximation for the case of NaF). Therefore, we can say that the equation of state of the mercury surface is... [Pg.100]

We saw previously that concentration polarization results in the decrease of solute concentration near the permselective interface (right at the interface in the electro-neutral version) where most of the system s resistance thus concentrates, and where the space charge develops. The system is expected to be sensitive to the minimum concentration value, and because of nonlinearity nontrivial effects, could be anticipated in response to unsteady disturbances of this value (e.g., provided by harmonic modulation superimposed upon a constant voltage applied to the system). Since it is easier to increase the minimal concentration (close to zero at the limiting current) than to decrease it, we might expect a positive rectification effect for the direct current component, counterintuitive ( anomalous ) in the present system with a convex stationary VC curve. Thus the topic of this section is the rectification effects that arise in the stationary concentration polarization in response to a harmonic voltage modulation. [Pg.185]

Figure 8.1—Principle of zone electrophoresis. Each compartment is separated by a membrane to avoid contamination of the electrolyte by secondary products formed at the electrodes. The size and the sign of the charge carried by each species depends on the chemical medium in which they are found. The experiment can be carried out at constant current, constant voltage or constant power. Figure 8.1—Principle of zone electrophoresis. Each compartment is separated by a membrane to avoid contamination of the electrolyte by secondary products formed at the electrodes. The size and the sign of the charge carried by each species depends on the chemical medium in which they are found. The experiment can be carried out at constant current, constant voltage or constant power.
After the constant voltage is applied the observed current is recorded as a function of time (Figure 6). If the dispersion contains only charged particles and counter ions then the charge Q measured at the time of observation of total plate-out represents the total charge on the particles. However, as can be seen from Figure 5 and the discussion in Section 4, there is a considerable contribution due to excess ions in the system. [Pg.324]

Suppose that some ionic species i is strongly rate-limiting and that the rapid flow of an electronic species produces a constant voltage VB across the oxide, independent of oxide thickness L. Furthermore, assume the electric field in the oxide to be due primarily to surface charge, such that space-charge effects are negligible. Then the electric field, E(x), in the oxide can be written as a constant E0... [Pg.66]


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See also in sourсe #XX -- [ Pg.48 ]




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