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Initial current level

Distortion is the ratio of final current level to initial current level during transit of the stress pulse from a step-function input. [Pg.80]

The concentration of the 0.25N NaOH was selected because it has equivalent conductivity to the 3.5% NaCl solution. The initial current levels in the NaCl Versus NaOH tanks were different despite the equivalent conductivities and the equal applied potential. The difference was due to the difference in pH. The more basic solution reduced the exchange current density for the hydrogen reaction. At this potential, the principal reaction is the hydrogen reaction. [Pg.173]

The most remarkable point worthy of mention in relation to the physical aspect of the CTs of transition metal oxides and graphite is the linear relationship between the initial current level fin, and the potential step A . In these studies, the term initial current level indicates the value of current at a time of 2-10 s during the CT experiments, rather than at a moment of application of potential step [96]. [Pg.155]

The solid circles in Figure 5.13a-e denote the initial current levels Jin, at various potential steps A , calculated from the corresponding CTs. Invariably, all of the li i versus A plots show a linear relationship. It should be mentioned that even diffusion-controlled CTs can exhibit this type of linear relationship, in the case that the electrode potential curves vary linearly with lithium stoichiometry, A oc ( -c ). However, the linear relationship between and A is still valid for the electrodes (e.g., Lii + 5[Ti5/3Lii/3[O4, Lii 5CoO2, LisV2O5 and graphite) where the electrode potential versus lithium stoichiometry curves deviate strongly from the linear relationship. [Pg.155]

All the anodic CTs hold the non-Cottrell character during the entire lithium deintercalation. Moreover, it should be pointed out that, in spite of the linear increase in the magnitude of the potential jump, the initial current level increases very slowly and eventually decreases at the large potential jump (> 0.25 V). In other words, the relationship between initial current level and potential jump takes the form of a parabola (Figure 8b), rather than a monotonically increasing curve. [Pg.273]

Figure 8. (a) Logarithmic anodic current transients obtained experimentally with a Lii Ni02 electrode at potential jumps of various initial values of electrode potential to 4.00 V vs. Li/Li. (b) plot of initial current level // / against potential Jump AE obtained from Figure 8(a). Reprinted from with permission from Elsevier Science. [Pg.274]

Next, in order to determine the internal cell resistance Rceii at various electrode potentials by the CT technique, the initial current level hm is plotted against the potential drop A at various initial electrode potentials E, , (Figure 11a). Rceu is evaluated to be the reciprocal of the slope of the Im vs. A plot. Flere, the values of initial current were taken at lO s for the following reason when the potential step is applied across the electrode, faradaic and non-faradaic currents pass through the resistors and capacitors, respectively. This means that the measured current within this time range includes the non-faradaic current, which does not contribute to lithium transport through the electrode. [Pg.280]

It is readily predicted from Eq. (1) that under the dijfusion controlled lithium transport, the initial current level of CT should increase with rising potential step, i. e., with rising difference between the initial and final equilibrium lithium contents. This is not true in the case of the anodic CTs obtained with the Li. jNiOi electrode. Figure 8(a) presents on a logarithmic scale the anodic CTs measured with the Lij.jNi02 electrode by jumping the electrode potential from a value in the range 3.55 to 3.90 V vs. Li/Li to a lithium extraction potential of 4.00 V vs. Li/Lr. [Pg.273]

Figure II. (a) Plots of initial current level lim against potential drcq) DE at various initial electrode potentials, reproduced from the cathodic current transients obtained from the Lii NiOz electrode, (b) variation in current with time up to 10 s by application of a potential drop df of 0.1 V at various initial electrode potentials, calculated using the simulation program with integrated circuit emphasis (SPICE) for the electric circuit of Figure 10 b), by taking the values of resistances and capacitances determined by CNLS fitting of the impedance spectra of Figure 10(a) to the electric circuit of Figure 10(b). Figure II. (a) Plots of initial current level lim against potential drcq) DE at various initial electrode potentials, reproduced from the cathodic current transients obtained from the Lii NiOz electrode, (b) variation in current with time up to 10 s by application of a potential drop df of 0.1 V at various initial electrode potentials, calculated using the simulation program with integrated circuit emphasis (SPICE) for the electric circuit of Figure 10 b), by taking the values of resistances and capacitances determined by CNLS fitting of the impedance spectra of Figure 10(a) to the electric circuit of Figure 10(b).
These were relatively low-resolution structures, and with refinement some errors in the initial structural assignments have been detected (4-7). Since the structures were first reported the subject has been extensively reviewed in this series (8) and elsewhere 9-15). This review will focus on the structure, biosynthesis, and function of the met-allosulfur clusters found in nitrogenases. This will require a broader overview of some functional aspects, particularly the involvement of MgATP in the enzymic reaction, and also some reference will be made to the extensive literature (9, 15) on biomimetic chemistry that has helped to illuminate possible modes of nitrogenase function, although a detailed review of this chemistry will not be attempted here. This review cannot be fully comprehensive in the space available, but concentrates on recent advances and attempts to describe the current level of our understanding. [Pg.162]

From the discussion provided here, it should be apparent that the current level of theory can provide a reliable description for available experimental data that in favorable cases approaches near exact agreement. Certainly, the prediction of shape, magnitude, and importantly sign of the curves is already sufficiently good to indicate that PECD could now serve to establish absolute configuration of an enantiomer (R- or S-) where this is initially unknown. [Pg.297]

Direct current cardioversion is the process of administering a synchronized electrical shock to the chest. The purpose of DCC is to simultaneously depolarize all of the myocardial cells, resulting in interruption and termination of the multiple reentrant circuits and restoration of normal sinus rhythm. The initial energy level of the shock is 100 joules (J) if the DCC attempt is unsuccessful, successive cardioversion attempts maybe made at 200,300, and 360 J.14 Delivery of the shock is synchronized to the ECG by the cardioverter machine, such that the electrical charge is not delivered during... [Pg.117]

SAMFETs have also been used in chemical sensing. The a-substituted quincpiethiophene SAMFETs were covered with a 10-nm pinhole-riddled iron tetraphenylporphyrin chloride layer, that acts as a receptor to nitric oxide (NO), an important biomarker [74]. The threshold voltage, measured by the FET transfer characteristics with the porphyrin receptor shifts upon increased exposure to NO. Annealing the monolayer FET in vacuum restores the initial FET behavior. Also, in the single monolayer HBC assembled FETs between metallic SWCNT source and drain electrodes increased current levels were measured in /d-Fds and Aj-Fg characteristics (Fig. 9) upon exposure to solutions of the electron acceptor TCNQ [68]. While the mechanism of response is not known, TCNQ has an affinity for coronene, and likely gives rise to charge transfer between electron-deficient TCNQ... [Pg.232]

The results of a further examination of Operation Ranch Hand veterans was recently published (Burton et al. 1998). The cohort consisted of 930 exposed subjects and 1,200 comparison individuals who served in SEA during the same period but who were not involved with spraying herbicides. The authors examined the associations between serum dioxin levels and a) chloracne, b) occurrence of acne relative to the tour of duty in SEA, and c) anatomical location of acne after service in SEA. Initial dioxin levels were computed using a first-order pharmacokinetic model with a constant half-life of 8.7 years. Four exposure categories were defined 1) comparisons, with current dioxin levels of 10 ppt 2) background Operation Ranch Hand veterans, with current dioxin levels of 10 ppt 3) low category, with current dioxin levels exceeding 10... [Pg.61]

If we switch-off the current after the steady state has been reached, the voltage relaxes to the initial zero-level. The electrical behavior can be taken into account by introducing in the simple equivalent circuit (eqc) (Eq. (60)) a capacitor Cl in series to Rioa or to R,.ml (if ions or electrons are blocked) In the language of system theory the equivalent circuit of the bulk represents a PDTi-element and reads3 15 e.g., for cells 3 and 4 Par (Cx. Par (Rm , Ser ( AJrai, Cl))). [Pg.82]


See other pages where Initial current level is mentioned: [Pg.273]    [Pg.275]    [Pg.281]    [Pg.275]    [Pg.48]    [Pg.273]    [Pg.275]    [Pg.281]    [Pg.275]    [Pg.48]    [Pg.332]    [Pg.556]    [Pg.494]    [Pg.97]    [Pg.79]    [Pg.600]    [Pg.602]    [Pg.29]    [Pg.725]    [Pg.1059]    [Pg.136]    [Pg.73]    [Pg.99]    [Pg.178]    [Pg.40]    [Pg.20]    [Pg.424]    [Pg.59]    [Pg.62]    [Pg.77]    [Pg.36]    [Pg.55]    [Pg.560]    [Pg.99]    [Pg.3]    [Pg.226]   
See also in sourсe #XX -- [ Pg.273 , Pg.275 , Pg.280 ]

See also in sourсe #XX -- [ Pg.273 , Pg.275 , Pg.280 ]




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