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Transformations current

Some breakthrough was finally achieved by using Pd2(dba)3 as the Pd complex, tris(tert-butyl)phosphine as the ligand, and sodium ferf-butoxide as the base [90]. This combination of reagents proved to bring about the synthesis of unsubstituted phenazine (137) by reaction of two molecules of 2-bromoaniline (131). Remarkably, no reaction takes place under the conditions of the 133 117 transformation. Currently the scope and limitations of this new sequential inter-Zintramolecular AT-arylation for the synthesis of AT-heterocycles... [Pg.109]

The transformer primary side is powered by the battery and turns off at the same time as the HEI coil. The primary carries 5 to 10 amps, conveyed to the secondary side by its collapsing EM field. At the same time, a HV spike is emitted by the HEI coil, from the collapsing voltage in its primary. Because the transformer secondary is shorted by the HV wire, it doesn t interfere with the primary side induced current. The HV and transformer current are therefore additive, creating a much hotter spark. R = 1 M ohm. [Pg.57]

As the Laplace transformed current—potential relationship is a much simpler function than its counterpart in the time domain, it has been suggested [76, 77] that it may be advantageous to analyze experimental data in the Laplace domain. In the present case, this would require some procedure to perform Laplace transformation of current datajF(0> i.e. to calculate the integral, according to eqn. (88)... [Pg.266]

High- temperature superconduc- tors Transmission cables, transformers, current limiters, motors and generators Rolling, direct metal oxidation, tape casting Greater energy efficiency, higher critical current density... [Pg.239]

Note also that the duty cycle of such a forward converter can under no circumstances ever be allowed to exceed 50%. The reason for that is we have to unconditionally ensure that transformer reset will always occur, every cycle. Since we have no direct control on the transformer current waveforms, we have to just leave enough time for the current in the tertiary winding to ramp down to zero on its own. In other words, we have to allow voltseconds balance to occur naturally in the transformer. However, because the number of turns in the tertiary winding is equal to the primary turns, the voltage across the tertiary winding is equal to Vin when the switch is ON, and is also equal to Vin (opposite direction) when the switch is OFF. Reset will therefore occur when toFF becomes equal to toN- So, if the duty cycle exceeds 50%, toN would certainly always exceed toFF, and therefore transformer reset would never be able to occur. That would eventually destroy the switch. Therefore, just to allow toFF to be large enough, the duty cycle must always be kept to less than 50%. [Pg.155]

The transformed current data can be used directly, by (6.7.2), to obtain Cq(0, t). Under conditions where Cq(0, 0 = 0 (i e under purely diffusion-controlled conditions), 7(0 reaches its limiting or maximum value, 7/ [or, in semi-integral notation, m(0max] where... [Pg.248]

Note the similarity between this expression for the transformed current and that for the steady-state concentration in terms of the actual current, (1.4.11). Similarly for species R, assumed absent initially, the corresponding expression resulting from (6.2.9) is... [Pg.248]

These equations hold for any form of signal excitation in any electrochemical technique applied under conditions in which semi-infinite diffusion is the only form of mass transfer controlling the current. No assumptions have been made concerning the reversibility of the charge-transfer reaction or even the form of the dependence of Cq(0, t) and Cr(0, t) on E. Thus, with the application of any excitation signal that eventually drives Cq(0, t) to zero, the transformed current 7(0 will attain a limiting value, 7/, that can be used to determine Cq by equation 6.7.5 (22). [Pg.248]

Transform current MO coefficients back to original basis /... [Pg.186]

Transform current MO coefficients back to original basis / call gmprd C, Cbar, V, m, m, m) ... [Pg.565]

Fatty acid methyl esters are now the main intermediates in oleochemistry. Epox-idation can be considered as a transformation currently applied to triglycerides that is easy to perform on an industrial scale, compared with the production process for fatty alcohol. Therefore, why should epoxidized fatty acid methyl esters not become one of the commodities of the future The commercial development of these compounds requires easy, environmentally friendly (e.g., avoiding catalyst use) routes of low production cost as well as identified industrial outputs. Such considerations were taken into account in this study both rapeseed methyl esters (RME) and high-oleic sunflower methyl esters (HOSME) were used as starting materials. [Pg.142]

We recently initiated efforts within our own laboratory to synthesize terpy-based ligands that incorporate appended Lewis acid/base pairs [36]. Motivated by metal-free systems of frustrated Lewis pairs (FLPs) which bind and form adducts with small molecules, we sought to couple the reactivity of FLPs to a transition-metal fragment to afford a metal Lewis acid/base triad (LABT). The combination of both partners with a transition-metal center opens up the possibiUty to synergistically use these systems for further activation and/or redox transformations - currently a hmitation of metal-free FLP systems. [Pg.77]

The Legendre transforms currently used in thermodynamics are enthalpy, Helmholtz energy, and Gibbs energy ... [Pg.24]

Donova MV, Egorova OV (2012) Microbial steroid transformations current state and prospects. Appl Microbiol Biotechnol 94 1423-1447... [Pg.515]

This example is analogous to Example 2.13, with the exception of the periodic function, which is now the cosine. Using the Laplace transform of the cosine function the transformed current is obtained and must be separated into simple fractions ... [Pg.39]

The term in curly brackets represents the transformed current I,r(t), u in the integral is a dummy variable which vanishes after the evaluation of the integral. When c Ct) =0, 1( (0 reaches its limiting value given as... [Pg.111]

FIGURE 2.39 An auto transformer. Current directions are shown for a step-down autotransformer. [Pg.174]

Each power switch combination, that is, Q1-Q3 and Q2-Q4, is on for a maximum of half the switching frequency. Hence, each power switch combination has its own ton and toff time, see Fig. 10.55. During the time when a power switch combination is closed, the ramping transformer current and its resultant secondary current cause energy to be stored in the inductor LI. The waveform of the primary current during the on time, which is shown in Fig. 10.55(c) and Fig. 10.55(d) (see also Fig. 10.56), is described as... [Pg.1061]

The problem variables are complex numbers. Because this problem is linear, if we set the perturbed transformed current density / (co) to unity, all the transformed state variables will be so-called transfer functions of that variable with respect to current density. [Pg.319]

In three-phase three-limb transformer, DC fluxes compensate each other in the main limbs and connecting yokes. Thereby, this transformer type has the highest resiliency. Test results showed that even in case of impact of GIC equal to 50 nominal magnetization current ( 50/l), the transformer current... [Pg.1517]

Accordingly, considerable effort has been dedicated to the development of olefin metathesis catalysts exhibiting kinetic selectivity. As a result, a number of Z-selective tungsten-, molybdenum-, and ruthenium-based olefin metathesis catalysts have been recently developed (For Mo- and W-based Z-selective catalysts [24-41], For Ru-based Z-selective catalysts [42-45], For cyclometalated Ru-based Z-selective catalysts [46-58]). Many of these systems exhibit consistently high levels of activity and selectivity across a broad range of substrates. Herein, we will focus specifically on the cyclometalated ruthenium-based catalysts developed in our laboratory [46-58]. This chapter is intended to provide a comprehensive summary of the evolution of these cyclometalated ruthenium catalysts, from their initial serendipitous discovery to their recent applications in Z-selective olefin metathesis transformations. Current mechanistic hypotheses and limitations, as well as future directions, will also be discussed. [Pg.4]


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See also in sourсe #XX -- [ Pg.452 ]




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