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Capacitance, vacuum

The pressure range for DR measurements is normally one decade below the above data, and this has to be considered in the specification of the plant. All measurements discussed above have to be carried out by capacitance vacuum gauge, because these instruments measure pressure independently of the type of gas. All vacuum gauges based on the change of heat conductivity as a function of pressure show a result which depends... [Pg.88]

To insure an undisturbed water vapor transport (see Section 1.2.4) the leak rate of a freeze-drying plant must allow BTM with sufficient accuracy. This applies for vapor pressures with ice temperatures ranging between -50 and -10 °C corresponding to 0.04—2.5 mbar. The pressure range for DR measurements is normally one decade below the above data and this has to be considered in the specification of the plant. All measurements discussed above have to be carried out with a capacitance vacuum gauge, because these instruments measure pressure independently of the type of gas. All vacuum gauges based on the change of heat conductivity as a function of pressure show a result which depends not only on the pressure of the gas mixture but also on the type of gas. Leybold AG [1.67] indicate that for instruments based on heat con-... [Pg.114]

It has been shown in Figures 1.73.2, 1.73.3, 1.85.2, 1.85.3 and 1.85.4 how DR data not document only the desorption process, but also reflect the product structure after freezing and during MD. Furthermore, the limits of DR measurements by the reproducibility of the capacitive vacuum gauge (CA) were discussed with those figures. [Pg.278]

The origin of this kind of behavior is fundamental to the understanding of the difference of capacitance response to a modulating signal when the capacitance is developed in a porous-electrode matrix in comparison with that at a sohd, plane electrode of the same (e.g. carbon) material for which a circuit of type 1(b) apphes. It can be understood in terms of the hierarchy of equivalent circuits (illustrated in Figure 4.5.22), representing the electrical behavior of a pure capacitance (vacuum... [Pg.470]

C = Q/V. In a vacuum, the charge density on the surfaces of the conductors is affected by the permittivity of free space, q. When a dielectric material is placed between the conductors, the capacitance increases because of the higher permittivity, e, of the material. The ratio of e and q gives the dielectric constant, K, of the material, k = e/eg The dielectric constant of siHca glass is 3.8. [Pg.333]

The influence of a particular dielectric on the capacitance of a condenser is conveniently assessed by the dielectric constant, also known as the relative permittivity or rarely specific inductive capacity. This is defined as the ratio of the relative condenser capacity, using the given material as a dielectric, to the capacity of the same condenser, without dielectric, in a vacuum (or for all practical intents and purposes, air). [Pg.112]

Capacitance is related to the area of the plates (yi), the distance between the plates (d), and the dielectric constant (e) of the material between the plates (Figure 2, equation I). The dielectric constant or permittivity of a material is the increased capacitance observed compared to the condition if a vacuum was present between the plates. Common dielectric materials are polystyrene (e = 2.5), mylar (e = 3), mica (e = 6), aluminum oxide (e = 7), tantalum oxide (e = 25), and titania (e = 100). In the Leyden jar the dielectric is silica. [Pg.212]

According to the method developed by Izumi [593], magnesium chloride is added to the reactor as a diluent, along with K2TaF7 and NaCl, prior to the reduction process. The powder obtained by the above method is washed and treated thermally at 1200°C in vacuum. The final product has a specific capacitance of 12,000 p.C/g, contains 1800 ppm of oxygen, and its Mg content is as low as 20 ppm. [Pg.334]

We measure the capacitive properties of a polymer in a capacitor that is constructed so that we can compare the properties of the test material relative to a vacuum. [Pg.184]

The first term tends to make the capacitance greater for increasing qM. For the interface in vacuum, this term is outweighed by the other, so that the calculated capacitance decreases with qM, reflecting the fact that it is easier to spill more electrons out into the vacuum than to push them back into the metal againtst the repulsive forces. In the metal-solution interface, however, it is surmised92... [Pg.69]

Moreover, despite the many advances in electrochemical measurement and modeling, our understanding of SOFC cathode mechanisms remains largely circumstantial today. Our understanding often relies on having limited explanations for an observed phenomenon (e.g., chemical capacitance as evidence for bulk transport) rather than direct independent measures of the mechanism (e.g., spectroscopic evidence of oxidation/reduction of the electrode material). At various points in this review we saw that high-vacuum techniques commonly employed in electrocatalysis can be used in some limited cases for SOFC materials and conditions (PEEM, for example). New in-situ analytical techniques are needed, particularly which can be applied at ambient pressures, that can probe what is happening in an electrode as a function of temperature, P02, polarization, local position, and time. [Pg.599]


See other pages where Capacitance, vacuum is mentioned: [Pg.267]    [Pg.267]    [Pg.232]    [Pg.291]    [Pg.385]    [Pg.331]    [Pg.488]    [Pg.502]    [Pg.513]    [Pg.267]    [Pg.267]    [Pg.232]    [Pg.291]    [Pg.385]    [Pg.331]    [Pg.488]    [Pg.502]    [Pg.513]    [Pg.314]    [Pg.206]    [Pg.26]    [Pg.434]    [Pg.328]    [Pg.137]    [Pg.281]    [Pg.554]    [Pg.70]    [Pg.110]    [Pg.15]    [Pg.4]    [Pg.46]    [Pg.374]    [Pg.82]    [Pg.131]    [Pg.284]    [Pg.259]    [Pg.184]    [Pg.48]    [Pg.80]    [Pg.175]    [Pg.90]    [Pg.448]    [Pg.456]    [Pg.139]    [Pg.195]   
See also in sourсe #XX -- [ Pg.27 ]




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