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Current Regime

The majority of contaminated land analyses depend upon site-specific requirements. Only when the history of the use of individual sites has been determined can the analytical requirements be seriously considered. Since no two sites are exactly the same, and because all have individual aspects that need individual considerations, it is unlikely that analytical requirements will be identical. In addition, the matrix of samples taken from a particular site may be different for different samples, as well as for different sites. This variety in the nature of matrices and analytical requirements makes the imposition of either prescribed standardised suites of analyses or the specification of methodology somewhat meaningless as in many cases, these would not be appropriate. [Pg.25]

Current laboratory practices revolve around the use of accredited methods, and indeed, these practices need to be supported and complimented. However, the use of an accredited method in itself is not a guarantee of the generation of good quality data. Methods, whether accredited or not, need to be used in correct circumstances, especially in their applicability to specific or defined matrices. [Pg.25]


For the same the single layer devices based on Alq3, Peyghambarian et al. [83] found that the 1/V characteristics can also be described by an SCL current flow in the low cu ire lit regime. However, in the low current regime the 1/V characteristics can be qualitatively modeled by the Fowler-Nordheim equation (even if, quantitatively, the real device current differs from the calculated by seven orders of magnitude) [83] and thermionic emission ]78]. [Pg.474]

The basic theory of mass transfer to a RHSE is similar to that of a RDE. In laminar flow, the limiting current densities on both electrodes are proportional to the square-root of rotational speed they differ only in the numerical values of a proportional constant in the mass transfer equations. Thus, the methods of application of a RHSE for electrochemical studies are identical to those of the RDE. The basic procedure involves a potential sweep measurement to determine a series of current density vs. electrode potential curves at various rotational speeds. The portion of the curves in the limiting current regime where the current is independent of the potential, may be used to determine the diffusivity or concentration of a diffusing ion in the electrolyte. The current-potential curves below the limiting current potentials are used for evaluating kinetic information of the electrode reaction. [Pg.192]

The current regime in EPA seems to need no reminding about the second lesson. In an effort partially motivated by the desire to reduce the amount of incoming information it has sharply narrowed the purposes for which information will be... [Pg.217]

For a constant-potential regime, if the electrode potential is set negative enough (for a reduction, positive enough for an oxidation), (Ca) c=0 = 0. For a constant-current regime,... [Pg.425]

Here N(sQ is the electron density of states on the Fermi surface for one direction of spin, is the effective volume of phonon generation, is the point contact form factor, averaged over the Fermi surface. It should be noted that point contacts of sizes d > l, d l can work also in diffusive or thermal current regimes [5] and are used for the study of EPI, phase transitions, superconductivity and other interesting physical phenomena. [Pg.291]

Here, the key point is that free allocation under the current regime effectively grants a windfall benefit to recipients of allowances, which is not related to the environmental gains that the EU ETS aims to secure this is a good basis for an argument that such aid may be disproportionate. [Pg.124]

The merit of this package deal would be to provide reassurance to operators under the current regime, while permitting the design of a transition from the old allocation arrangements to the new system as introduced under the new Directive. [Pg.132]

Low current regime the time between tunneling electrons should be much larger than the vibrational lifetime. The theory only assumes one excitation at a time. [Pg.229]

Titov VB (1989) Characterization of coastal current regime off northern Caucasus coast. SB IO RAS, Gelendjic (in Russian)... [Pg.192]

Figure 4 The transition from the emission-limited (dashed lines) to space-charge-limited current regimes (solid lines). Figure 4 The transition from the emission-limited (dashed lines) to space-charge-limited current regimes (solid lines).
In the second part, theories of catalyst layers are presented. They account for the transport of feed gas, protons and electrons and rationalize the distribution of the rate of electrochemical reaction. A theoretically derived phase diagram suggests an optimum thickness of the layer, subject to the basic parameters and the target current regime. [Pg.450]

Any model of PEFC must cover at least the three basic processes (1) transport of reactants to/from the catalyst sites, (2) charged particles production or consumption at these sites, and (3) transport of charged particles (electron and proton currents). The simplest realistic model of PEFC must take into account these processes. (More sophisticated models, particularly important for high current regimes, ought to take into account on the same footing the production of water at the cathode side and dynamic liquid-vapor phase balance.)... [Pg.507]

At Kriegers Flak in the open Arkona Sea, the weak mean speeds and the small stability factors are caused by alternations of the current regime during the 7 months observation period. Compared to sites B, C, and D further south, in agnitudes are weak owing to the nearby shoal of Kriegers Flak, which hinders the free propagation of the currents. [Pg.140]


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Analytical high-current regime

Concentration-Time Dependence at Constant Current (Galvanostatic Regime)

Current-Time Dependence at Constant Potential (Potentiostatic Regime)

Heat flux current regime

High-current regime

Periodically changing currents regimes

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