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Channel resistance equal

So far there has been no published data on inversion channel mobility in metal-HfO -SiC structures. However, even assuming extremely poor channel mobility of 0.1 cmV(V s), HfO -SiC UMOSFET can offer total specific on-resistance equal to... [Pg.160]

In addition to these pressure drop models, models to represent spreading of liquid in packed beds because of spatial variation in flow resistance are needed. In a randomly packed bed, the void fraction is not uniform. This implies that some flow channels formed within a packed bed offer less resistance to flow than other channels of equal cross-sectional area. Liquid will tend to move toward channels of lower resistance, leading to higher liquid hold-up in such channels. Thus, even if the initial liquid distribution is uniform, inherent random spatial variation of the bed leads to non-uniform liquid flow. Yin et al. (2000) assumed that the dispersion coefficient for liquid phase volume fraction is linearly proportional to the adverse gradient of... [Pg.415]

This equation facilitates understanding of how the channel dimensions (L and W) affect the relative magnitudes of the contact resistance and the channel resistance. Note that the channel resistance scales as LIW but the contact resistance scales as l/W it does not depend on L. Consider two different OFET devices on the same semiconductor/insulator/gate substrate both have the same channel width (equal W), but the length of the channel of the second device is 10 times smaller than that of the first (L2 = Ej/10), as depicted in Figure 2.4.6(a). Both devices have equal contact resistances R because W is the same. But because the channel resistance scales with L/W (the source-drain current scales with W/L), the channel resistance of the second device is 10 times smaller than that of the first device. This means that contact resistance is potentially much more important in the shorter channel device because it contributes a larger fraction of the total resistance. [Pg.145]

Equal contact resistances Device 2 has a lower channel resistance (by lOX)... [Pg.146]

Equal channel resistances Device 4 has a lower contact resistance (by 2X)... [Pg.146]

The first inhibitor of NHE, amiloride, was identified in 1982. This drug is a potassium-sparing diuretic that also inhibits the sodium-calcium exchanger and the conductive Na+ channel. Not all the NHE isoforms are inhibited equally by amiloride NHE1 and 2 are responsive, NHE5 is partially responsive and NHE3, 4 and 7 are resistant. Other weak and non-specific inhibitors are clonidine and cimetidine. [Pg.811]

Note that according to equations (1) and (2), even K+ is not really at equilibrium across the membrane AG out is small, but not zero. This is because the rate of flow of K+ out of the cell is limited by the number of K+-conducting channels and by the intrinsic resistance that these channels offer to the flow of ions. Although the overall conductivity of the resting membrane to K+ is about 100 times greater than the conductivity to Na+, it still is much lower than the conductivity of an equal thickness of water. [Pg.603]

As the potential is scanned from positive to negative, the reduction of Ox 1 takes place first. As the potential is made even more negative, Ox2 begins to be reduced, then Ox3, and so on. Thus, at the applied potential E, only Ox will be reduced, but at the more negative potential 2, simultaneous reduction of Ox and Ox2 will take place. In order to determine these two species separately, measurements at two potentials must be made. In order to do that, the two potentials have to be at least 180 mV apart. Given an electrochemical window of 2.5V, we can see that the maximum number of electroactive species that can be accommodated is not more than 13, provided that their standard potentials are equally spaced. In reality, the number of different species that can be selectively determined in a mixture by using the selection of the applied potential is 4-6 at most. Thus, the choice of applied potential offers only a very limited selectivity and is used only to complement other modes of selectivity. In the context of the equivalent electrical circuit (Fig. 7.8), this strategy would be represented by the same potential applied to all resistive channels... [Pg.215]

This vial could be placed in two positions by the inlet lift. In the lower position of the lift, EOF driven isocratic and gradient CEC was possible. The solvent was delivered by the pump to the vial through the inner channel and removed via the outer channel using a pressure of nitrogen (right panel of Fig. 2.11). The resistance of the outlet restrictor was low. The pressure in the vial equaled the external gas pressure and was the same in the outlet vial. In this way, no hydraulic flow was generated and bubble formation was suppressed. The column continuously accepted the delivered solvent from the vial by electroosmotic flow. In this position, the flow delivered by the external pump must be low to avoid solvent overflow in the vial. [Pg.78]

We assume that a moving blade creates a channel of depth d as it moves across the ice. If fj =0.5 and there is no strain recovery, the dynamic and static values of d are equal. Part of the resistance encountered by the blade is the force,, required to plough through the ice at... [Pg.498]

Cummins That is a complicated question, because it depends on where you start from. It may be very different in the cell body than it is at the terminals. I don t know what the resting potential is out in the axon and at the nerve terminal this may be where the important resting potential is. In the cell body, if I hold at very negative potentials, I will see roughly equal densities of current for T l Xsensiti ve and TTX-resistant channels. If I just look at channel densities, at the maximum channel availability the breakdown is about 50 50 in small neurons. [Pg.58]

Figures 4.3(a) and (b) are sections in the zx-plane showing the distribution of potential (( )) in the solution as cross sections of imaginary surfaces in the solution of equal potential (isopotentials) and the distribution of current as current channels with cross sections defined by traces of the surfaces. ..(n - l),n, (n + 1)... perpendicular to the isopotentials. These traces are located such that each current channel carries the same total current. Figure 4.3(a) applies to an environment of higher resistivity (e.g., water with specific resistivity of 1000 ohm-cm) and Fig. 4.3(b) to an environment of lower resistivity (e.g., salt brine, 50ohm-cm). The figures are representative of anodic and cathodic reactions, which, if uncoupled, would have equilibrium half-cell potentials of E M = -1000 mV and E x = 0 mV and would, therefore, produce a thermodynamic driving force of Ecell = E x - E M = +1000 mV. This positive Ecell indicates that corrosion will occur when the reactions are coupled. For the example of Fig. 4.3(a), the high solution resistivity allows the potential E"m at the anode to approach its equilibrium value (E M = -1000 mV) and, therefore, allows the potential in the solution at the anode interface, < )s a, to approach +1000 mV (recall that (j)s = -E"M). The first isopotential above the anode, 900 mV, approaches this value. The solution isopotentials are observed to decrease progressively and approach 0 mV at the cathode reaction site. Figures 4.3(a) and (b) are sections in the zx-plane showing the distribution of potential (( )) in the solution as cross sections of imaginary surfaces in the solution of equal potential (isopotentials) and the distribution of current as current channels with cross sections defined by traces of the surfaces. ..(n - l),n, (n + 1)... perpendicular to the isopotentials. These traces are located such that each current channel carries the same total current. Figure 4.3(a) applies to an environment of higher resistivity (e.g., water with specific resistivity of 1000 ohm-cm) and Fig. 4.3(b) to an environment of lower resistivity (e.g., salt brine, 50ohm-cm). The figures are representative of anodic and cathodic reactions, which, if uncoupled, would have equilibrium half-cell potentials of E M = -1000 mV and E x = 0 mV and would, therefore, produce a thermodynamic driving force of Ecell = E x - E M = +1000 mV. This positive Ecell indicates that corrosion will occur when the reactions are coupled. For the example of Fig. 4.3(a), the high solution resistivity allows the potential E"m at the anode to approach its equilibrium value (E M = -1000 mV) and, therefore, allows the potential in the solution at the anode interface, < )s a, to approach +1000 mV (recall that (j)s = -E"M). The first isopotential above the anode, 900 mV, approaches this value. The solution isopotentials are observed to decrease progressively and approach 0 mV at the cathode reaction site.

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See also in sourсe #XX -- [ Pg.146 ]




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