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Currents associated charge

Hays measured the current associated with electrically charged 99 p.m diameter particles of styrene divinylbenzene particles as these particles traversed gaps of 520 and 137 p.m separating two parallel electrodes. Based on these results. Hays [81 ] argued for the existence of locally charged patches on the particles. [Pg.167]

The power factor cos 6 is always a positive fraction between 0 and 1 (as long as 161 < 90°). The smaller the power factor, the greater the current that must be supplied to the circuit for a given active (useful) power output requirement. The increase in current associated with low power factors causes greater line losses or requires an increase in the capacity of the transmission equipment (wire size, transformers, etc.). As a result, for industrial applications there is often a power factor charge in the rate structure for supplying electricity. The usual situation is for loads to be inductive, and the industrial consumer may add capacitance to their circuits to correct the lagging power factor. [Pg.286]

As already indicated, quantitative conventional d.c. polarography is limited at best to solutions with electrolytes at concentrations greater than 10-5M, and two different ions can only be investigated when their half-wave potentials differ by at least 0.2 V. These limitations are largely due to the condenser current associated with the charging of each mercury drop as it forms, and various procedures have been devised to overcome this problem. These include ... [Pg.611]

The distribution of charges on an adsorbate is important in several respects It indicates the nature of the adsorption bond, whether it is mainly ionic or covalent, and it affects the dipole potential at the interface. Therefore, a fundamental problem of classical electrochemistry is What does the current associated with an adsorption reaction tell us about the charge distribution in the adsorption bond In this chapter we will elaborate this problem, which we have already touched upon in Chapter 4. However, ultimately the answer is a little disappointing All the quantities that can be measured do not refer to an individual adsorption bond, but involve also the reorientation of solvent molecules and the distribution of the electrostatic potential at the interface. This is not surprising after all, the current is a macroscopic quantity, which is determined by all rearrangement processes at the interface. An interpretation in terms of microscopic quantities can only be based on a specific model. [Pg.249]

In electrochemistry, the electrode current is conventionaUy classified into the faradaic current and the nonfaradaic current. The former is the electric current associated with charge transfer reactions at nonpolarizable electrodes and the latter is the current that is required to establish the electrostatic equilibrium at the interfacial double layer on both polarizable and nonpolarizable electrodes. The nonfaradaic ciurent, sometimes called a transient current, flows also in the course of establishing the adsorption of ions on electrodes. [Pg.90]

In photoexcited n-type semiconductor electrodes, photoexcited electron-hole pairs recombine in the electrodes in addition to the transfer of holes or electrons across the electrode interface. The recombination of photoexcited holes with electrons in the space charge layer requires a cathodic electron flow from the electrode interior towards the electrode interface. The current associated with the recombination of cathodic holes, im, in n-type electrodes, at which the interfadal reaction is in equilibrium, has already been given by Eqn. 8-70. Assuming that Eqn. 8-70 applies not only to equilibrium but also to non-equilibrium transfer reactions involving interfadal holes, we obtain Eqn. 10-43 ... [Pg.352]

There is one caveat that should be mentioned. Note that both the anodic and cathodic peaks in Figure 13.2 sit on top of flat (ideally) background currents. These are the capacitive currents associated with double charging (see Chaps. 3 and 12). We do not want to include these capacitive currents in our determination of rFc. We want to integrate only the current associated with the oxidation of Fc, that is, the Faradaic current. We have delineated the area of the curve associated with the Faradaic current by extrapolating the background current (dashed line underneath the peak). The area we will use to determine TFc is the area under the peak but above this dashed line. [Pg.420]

Residual currents, also referred to as background currents, are the sum of faradaic and nonfaradaic currents that arise from the solvent/electrolyte blank. Faradaic processes from impurities may be practically eliminated by the careful experimentalist, but the nonfaradaic currents associated with charging of the electrode double layer (Chap. 2) are inherent to the nature of a potential sweep experiment. Equation 23.5 describes the relationship between this charging current icc, the double-layer capacitance Cdl, the electrode area A, and the scan rate v ... [Pg.687]

The dimensional constant ke has units of charge per unit energy. Hence, I, Xi are proportional to energy flow along the u axis, and flow of energy into (from) our 3D world from (resp. into) the u axis. In this sense, electric current and charge density are simple auxiliary 3D concepts associated with the 4D energy-momentum source f = (Sj, S). This result is reminiscent of some opinion of Warburton [34], who claims that the displacement current is not a fundamental concept. [Pg.363]

Nonfaradaic current — A current where the chemical entity associated to the charge does not change the current appears as if it made an electric condenser charged (or discharged) thus we often denote the nonfaradaic currents as -> charging currents. Currents of adsorption and of double-layer charging belong to the class of nonfaradaic currents. From an electrical point of view, the impedance element associated to the nonfaradaic current is a capacitor. [Pg.130]

Precise quantitative measurements are sometimes difficult in CV, especially when the solution resistance is high (causing perturbation of the measured peak potentials because of the uncompensated iR drop), the nonfaradaic current associated with charging the double... [Pg.201]

The current associated with the imposition of the potential pulse and the appropriate charging of the electrical double layer. This component always exists and can be described as... [Pg.108]


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See also in sourсe #XX -- [ Pg.31 , Pg.465 ]




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Current charged

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