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Normalisation current

The data in the first frame are the (normalised) current, representing the electron flux. In the second frame, the overall mass flux (transfer of charge-compensating ions as well as neutral species) is shown. The third frame corresponds to the difference between the first two. The quantity defined by equation [3] with tm = 99.5 g mol"1 and Z = -1, represents the flux of all species other than perchlorate. In the case of the dilute (concentrated) electrolyte, this corresponds to the mass flux of water (water+salt). [Pg.162]

The normalised current, that is the gradient G, is given by using matrix V and (9.87). The operation returns gradients at all collocation points, and one just takes the first of these, which refers to X = 0. Alternatively, one can multiply just the top row of V with the concentration vector C, which gives dC/dX X = 0) directly. Note that this is not our usual G yet, because of the way X is normalised here. Regarding (9.77), clearly,... [Pg.180]

Fig. 8.6. Components of the current response of a n-type semiconductor electrode to an illumination step. ch is the charging current, is the current due to interfacial electron transfer and rc,. is the current due to electrons recombining with holes via surface states. The total current, given by the sum of and j , is equal to qg - /rec, where g is the flux of minority carriers given by the Gartner equation. The dimensionless normalised time axis is ( lr + k,c<.)t. The dimensionless normalised current axis is jlqg. Fig. 8.6. Components of the current response of a n-type semiconductor electrode to an illumination step. ch is the charging current, is the current due to interfacial electron transfer and rc,. is the current due to electrons recombining with holes via surface states. The total current, given by the sum of and j , is equal to qg - /rec, where g is the flux of minority carriers given by the Gartner equation. The dimensionless normalised time axis is ( lr + k,c<.)t. The dimensionless normalised current axis is jlqg.
Figure 4.7 Step input for a terminal voltage lower than the critical voltage (a) bubble coverage fraction 0 step input (b) normalised current J step input. Figure 4.7 Step input for a terminal voltage lower than the critical voltage (a) bubble coverage fraction 0 step input (b) normalised current J step input.
For each value of Rd thus generated ARd, 2ARd, , MARd), simulate a domain of that radius and record the normalised current response,... [Pg.214]

Fig. 6.10 shows theoretical cyclic voltammograms for the ce system under various conditions. The data are presented as a normalised current plotted as a function of potential for various values of where X is defined by... [Pg.192]

The physical significance of K is that each normalised current/voltage plot in the form of f/fiim vs 6 (= P/RT(E — ) where E is the potential) is a function only... [Pg.176]

Normalised current-voltage characteristics of melt-spun PP fibres containing 10 and 15 vol% of carbon nanofibres drawn to different draw ratios (DR). Reproduced from Ref. 213. [Pg.220]

To verify the modelling of the data eolleetion process, calculations of SAT 4, in the entrance window of the XRII was compared to measurements of RNR p oj in stored data as function of tube potential. The images object was a steel cylinder 5-mm) with a glass rod 1-mm) as defect. X-ray spectra were filtered with 0.6-mm copper. Tube current and exposure time were varied so that the signal beside the object. So, was kept constant for all tube potentials. Figure 8 shows measured and simulated SNR oproj, where both point out 100 kV as the tube potential that gives a maximum. Due to overestimation of the noise in calculations the maximum in the simulated values are normalised to the maximum in the measured values. Once the model was verified it was used to calculate optimal choice of filter materials and tube potentials, see figure 9. [Pg.212]

The electrolyser has been operated over a range of current densities. Figure 18.8 shows the performance of the electrolyser normalised to an operational current density of 5 kA m-2 (the data are broken down in Table 18.1). Furthermore, ICI ETB s operating personnel confirm that one Nestpak can be changed in less than 4 h (power off to power back on). [Pg.249]

A micro computer system allowed voltage and current measurements to be synchronised plus data logging and averaging of measurements. Alongside each "measurement" foil was a "control" foil, coated with paint plus a protective epoxy coating, which did not corrode and allowed resistance measurements to be normalised. [Pg.21]

It follows from the above discussion that the effect of a chemical follow-up reaction in which the primary intermediate R is consumed is that the current ratio, — z x/z fed> is smaller than the no-reaction-value, 0.2929. The faster the reaction of R, the smaller the ratio, and in the limit where R reacts so rapidly that the oxidation back to O cannot be observed, the ratio is, of course, zero. It is convenient to normalise the current ratio by the no-reaction-value by introduction of the parameter Ri defined in Equation 6.34 clearly, Ri may vary from 1 (no reaction) to 0 (complete reaction). [Pg.145]

The reference time scale r depends on the system to be simulated, as will be seen in the next section, where some model systems are described. There, the characteristic distance 6 will also be defined as used in this book (Sect. 2.4.1). Other variables that are normalised are the current and electrode potential. Current i is proportional to the concentration gradient, by Fick s first equation (2.2), as expressed in (2.9). We introduce the dimensionless gradient or flux, defined as... [Pg.14]

These attempts to express deviations of the current at a UMDE from the Cottrell current are somewhat fruitless because the expressions do not hold for other than rather small t values or rather, dimensionless values of the normalised time, Dt/a2. General solutions were - and are - needed. There have been no analytical solutions holding for all times, but some limiting expressions, and an approximate one, have been derived. [Pg.203]

The steady-state value is the normalising quantity for the current as a function of time in most studies except those where the Cottrell current is used as the reference value. Saito also derived the concentration profile at steady state. It was printed incorrectly in the paper [490], but Crank and Furzeland [184] present the correct equation ... [Pg.204]

There is, however, a much better pair of solutions, recently obtained by Mahon and Oldham [377]. They used what they call the Cope-Tallman method, involving the Green function, to find a much improved short-time and long-time solutions for the current at a disk electrode. Their formulae express currents at T values as defined above (12.13) (previously designated by r), and normalised by 7rnFDac, rather than the steady-state value. Here... [Pg.206]


See other pages where Normalisation current is mentioned: [Pg.256]    [Pg.184]    [Pg.65]    [Pg.79]    [Pg.79]    [Pg.171]    [Pg.219]    [Pg.261]    [Pg.285]    [Pg.286]    [Pg.220]    [Pg.118]    [Pg.256]    [Pg.184]    [Pg.65]    [Pg.79]    [Pg.79]    [Pg.171]    [Pg.219]    [Pg.261]    [Pg.285]    [Pg.286]    [Pg.220]    [Pg.118]    [Pg.923]    [Pg.504]    [Pg.1043]    [Pg.64]    [Pg.72]    [Pg.291]    [Pg.288]    [Pg.202]    [Pg.267]    [Pg.29]    [Pg.267]    [Pg.435]    [Pg.636]    [Pg.74]    [Pg.174]    [Pg.204]    [Pg.244]    [Pg.499]   
See also in sourсe #XX -- [ Pg.41 ]




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