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Conductivity changes, transfer

Wlien a temperature difference exists in or across a body, an energy transfer occurs from the high-tem-perature region to the low-temperature region. This heat transfer, q, which can occur in gases, liquids, and solids, depends on a change m temperature, AT, over a distance. Ax (i.e., AT/z)ix) and a positive constant, k, which is called the thermal conductivity of the material. In equation form, the rate of conductive heat transfer per unit area is written as... [Pg.612]

Since under normal depletion conditions, conductivity changes are dominated by majority carriers, and interfacial electron transfer can be neglected in the dark, the carrier profile can be found by solving Poisson s equation ... [Pg.508]

The sensor detection of EEPs is methodically more complicated than the detection of atoms and radicals. With atoms and radicals being adsorbed on the surface of semiconductor oxide films, their electrical conductivity varies merely due to the adsorption in the charged form. If the case is that EEPs interact with an oxide surface, at least two mechanisms of sensor electrical conductivity changes can take place. One mechanism is associated with the effects of charged adsorption and the other is connected with the excitation energy transfer to the electron... [Pg.296]

For cryptands in which the molecular cavity is larger than in the case of the [l.l.l]-species [78], proton transfer in and out of the cavity can be observed more conveniently. Proton transfer from the inside-monoprotonated cryptands [2.1.1] [79], [2.2.1] [80], and [2.2.2] [81 ] to hydroxide ion in aqueous solution has been studied by the pressure-jump technique, using the conductance change accompanying the shift in equilibrium position after a pressure jump to follow the reaction (Cox et al., 1978). The temperature-jump technique has also been used to study the reactions. If an equilibrium, such as that given in equation (80), can be coupled with the faster acid-base equilibrium of an indicator, then proton transfer from the proton cryptate to hydroxide ion... [Pg.189]

In the perpendicular direction, there may be conduction along the polar end group or by change transfer between the hydrocarbon chains. Proton conductivity is also a possibility. No gas evaluation and no increase in resistance from polarization effects were noted, however, in our preliminary experiments. Recently we have started some studies on electrolyte-lipid semiconductor structures. We observed, for example, interesting differences in the effect of divalent ions on different lipid mono-layers (55). [Pg.72]

For simplicity, it is assumed that the impact is a Hertzian collision. Thus, no kinetic energy loss occurs during the impact. The problem of conductive heat transfer due to the elastic collision of solid spheres was defined and solved by Sun and Chen (1988). In this problem, considering the heat conduction through the contact surface as shown in Fig. 4.1, the change of the contact area or radius of the circular area of contact with respect to time is given by Eq. (2.139) or by Fig. 2.16. In cylindrical coordinates, the heat conduction between the colliding solids can be written by... [Pg.133]

Heat transfer involving a change of phase is classified as convective heat transfer even though when the solid phase is involved, the overall process involves combined and interrelated convection and conduction. Heat transfer during boiling, condensation, and solidification (freezing) all, thus, involve convective heat transfer. [Pg.5]

The above derivation for LMTD involves two important assumptions (1) the fluid specific heats do not vary with temperature, and (2) the convection heat-transfer coefficients are constant throughout the heat exchanger. The second assumption is usually the more serious one because of entrance effects, fluid viscosity, and thermal-conductivity changes, etc. Numerical methods must normally be employed to correct for these effects. Section 10-8 describes one way of performing a variable-properties analysis. [Pg.538]

Conversion efficiency is definitely affected by the large void fraction, which is apparent in the results from changes in the total throughput, or space velocity (0.56 versus 1.11 sec ), shown in Fig. 7. In this comparison, the concentration of unconverted hexane increased tenfold when the flow rate was doubled. The impact of improvements in conductive heat transfer, combined with the mass transfer limitations associated with the cell size and honeycomb design, and a catalyst loading that was nearly one-half Chat of commercial pellet catalysts (average, 11.5% versus 19.2%) suggested that both carbon formation and steam/hydrocarbon reactions were better controlled with monolithic supports under the conditions employed. This comparison was made where the extent of the endothermic reaction is equal between the pellet bed and the hybrid cordierite/metal monolith bed. [Pg.188]

In an electrochemical cell, the conductivity is inversely related to the resistance in the electrolyte/test medium. The presence of certain chemical or ionic species may affect the resistance of the electrochemical cell. This change in resistance or conductivity can then be used to quantify the amount of the analyte presented. Molar and equivalent conductivities are commonly used to express the conductivity in an electrochemical cell. The conductivity measurement can be made relatively straightforward, using a DC mode or with a potential or current excitation. However, any faradaic or change transfer process occurring at the electrode surface will affect the conductivity measurement in an electrochemical cell. Furthermore, conductivity measurement in general does not provide sufficient specificity or sensitivity to quantify the analyte. This limits the use of conductivity of an electrochemical cell for sensing applications. [Pg.834]

Some of these variables can be controlled, or at least influenced, by the operator. The heating rate is clearly a variable over which the operator has control. The operator can only influence others, such as the thermal resistance of the DSC. For example, by changing the purge gas to one that has higher thermal conductivity, heat transfer is improved. [Pg.25]

Radha and Swamy (278) proposed a possible mechanism for the dehydrogenation of 2-propanol over La2MnM06 (M = Co, Ni, Cu). These authors found that admission of H2, together with the alcohol, does not have any influence on the reaction rate however, admission of acetone with 2-propanol decreases the reaction rate at all partial pressures. It can be inferred that H2 acts as a mere diluent whereas acetone has an inhibiting effect that may be due to its slow desorption. They also measured the conductivity changes of the catalyst in the presence of the reactants or products of the dehydrogenation. As a result of these studies it was concluded that the catalyst surface is covered predominantly with acetone under reaction conditions. Because acetone adsorbs by a donor-type mechanism, as shown by the decrease of the conductivity on its adsorption, its desorption involving electron transfer from the p-type semiconductor catalyst to the adsorbed species can be expected to be the slow process. [Pg.309]

The classical H-S equation is used to predict the electro-osmotic velocity of the fluid as a function of the electric field and the electrokinetic potential of the clay. Both of these parameters vary during electrokinetic transport, and result in a nonlinear process. New models have been developed that uncouple the electro-osmotic velocity from the applied field taking that surface conductivity and the resulting proportion of the current transferred over the solid-liquid interface are used as intrinsic properties of the clay to describe the velocity (Chapter 2). The pH changes affect the zeta potential, and thereby electro-osmotic conductivity. Thus, electro-osmotic conductivity changes as the dynamic changes in soil pH occur. [Pg.23]

Measurement of the electric conductivity of an electrochemical cell can be the basis for an electrochemical sensor. This differs from an electrical (physical) measurement, for the electrochemical sensor measures the conductivity change of the system in the presence of a given solute concentration. This solute is often the sensing species of interest. Electrochemical sensors may also involve measuring capacita-tive impedance resulting from the polarization of the electrodes and/or the faradaic or charge transfer processes. [Pg.85]

Thermal conductivity is a material property indicating the ease and speed with which heat can be transferred through the food item. Thermal conductivity changes with moisture content. The following equation has the widest use ... [Pg.529]


See other pages where Conductivity changes, transfer is mentioned: [Pg.508]    [Pg.92]    [Pg.128]    [Pg.118]    [Pg.171]    [Pg.213]    [Pg.86]    [Pg.7]    [Pg.260]    [Pg.288]    [Pg.300]    [Pg.32]    [Pg.223]    [Pg.199]    [Pg.321]    [Pg.116]    [Pg.499]    [Pg.2499]    [Pg.164]    [Pg.209]    [Pg.470]    [Pg.100]    [Pg.281]    [Pg.106]    [Pg.1411]    [Pg.509]    [Pg.521]    [Pg.285]    [Pg.148]    [Pg.332]    [Pg.287]    [Pg.58]    [Pg.184]    [Pg.69]   


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Transfer conduction

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