scholarly journals Dielectric loss due to polar molecules in solid paraffin wax

According to most theories of dielectric loss the maximum rate of change of dielectric constant and the maximum value of the specific energy loss per unit volume occur at an angular frequency ω (= 2 πv ) which is the inverse of a quantity r known as the relaxation time of the dielectric. The relaxation time is the time required for the polarization of the dielectric to revert to 1/ ϵ of its value after the removal of the applied electric field: and this is a quantity which can be determined experimentally. According to Debye’s theory of polar molecules, part of the dielectric polarization is due to the orientation of the dipoles in line with the applied field and the relaxation time is related closely to the time taken for the molecules to revert to their random positions after removal of the field.

1984 ◽  
Vol 52 (01) ◽  
pp. 015-018 ◽  
Author(s):  
A Girolami ◽  
A Sticchi ◽  
R Melizzi ◽  
L Saggin ◽  
G Ruzza

SummaryLaser nephelometry is a technique which allows the evaluation of the concentration of several serum proteins and clotting factors. By means of this technique it is also possible to study the kinetics of the reaction between antigen and antibody. We studied the kinetics of the reaction between prothrombin and an antiprothrombin antiserum using several prothrombins namely: Prothrombin Padua, prothrombin Molise, which are two congenital dysprothrombinemias, cirrhotic, coumarin or normal prothrombins. Different behaviors in the kinetics of the reactions were shown even when the concentration of prothrombins was about the same in all plasma tested. These differences were analyzed by means of a computer (Apple II 48 RAM) programmed to solve four unknown equations (Rodbard’s equation). From the data so obtained one can see that when voltages at the beginning and at the end of the reaction are in all cases about the same, a clear difference in the time required to reach half the maximum value of the voltage can still be demonstrated. This parameter, which is expressed in minutes, is longer in coumarin and prothrombin Molise than in controls. On the contrary it is shorter in prothrombin Padua and has about the same value of controls in the cirrhotic patient. Moreover the time at which the maximum rate is obtained is longer in coumarin and prothrombin Molise than in controls and shorter in liver cirrhosis and prothrombin Padua. In conclusion data obtained show that coumarin prothrombin behaves in a different way from cirrhotic prothrombin and also that there is a different behaviour between the two congenital dysprothrombinemias.


2000 ◽  
Vol 11 (07) ◽  
pp. 1357-1369 ◽  
Author(s):  
SITANGSHU BIKAS SANTRA ◽  
WILLIAM A. SEITZ

Diffusion on 2D site percolation clusters at p = 0.7, 0.8, and 0.9 above pc on the square lattice in the presence of two crossed bias fields, a local bias B and a global bias E, has been investigated. The global bias E is applied in a fixed global direction whereas the local bias B imposes a rotational constraint on the motion of the diffusing particle. The rms displacement Rt ~ tk in the presence of both biases is studied. Depending on the strength of E and B, the behavior of the random walker changes from diffusion to drift to no-drift or trapping. There is always diffusion for finite B with no global bias. A crossover from drift to no-drift at a critical global bias Ec is observed in the presence of local bias B for all disordered lattices. At the crossover, value of the rms exponent changes from k = 1 to k < 1, the drift velocity vt changes from constant in time t to decreasing power law nature, and the "relaxation" time τ has a maximum rate of change with respect to the global bias E. The value of critical bias Ec depends on the disorder p as well as on the strength of local bias B. Phase diagrams for diffusion, drift, and no-drift are obtained as a function of bias fields E and B for these systems.


Considerable attention has been devoted of recent years to the development of synthetic insulating material devoid of the uncertainties and limitation of naturally occurring dielectrics and their modifications (such as cellulose, rubber, oil, and wax compound). Into this category falls a range of non-inflammable chlorinated diphenyl compounds known in this country as Permitol. The members of this range consist of a double benzene ring as basis with which chlorine atoms have been combined. By controlling the degree of chlorination, it is possible to produce compounds ranging at room temperatures from crystalline solids to liquids of relatively low viscosity. The present paper deals with a study of the dielectric behaviour over the frequency range 50 to 10 7 cycles per second and at temperatures extending from — 20 to + 80° C of a sample of chlorinated diphenyl classed as suitable for condenser impregnation. Its viscosity at 60° C is that of a light transformer oil, but with temperature decrease the viscosity increases very rapidly until the material becomes a glassy 8olid about — 10° C. One of the most desirable characteristics of a material to be used for this purpose is a high dielectric constant (permittivity) allied to freedom from dielectric loss. A high permittivity is usuallv associated, however, with the presence of polar molecules in the material, and these, according to the Debye theory of dielectric absorption, must be responsible for dielectric loss in alternating electric fields under suitable conditions of temperature and frequency. For a dilute solution of polar molecules in a non-polar solvent, the power factor passes through a maximum at a frequency given by f = k t/8π 2 a 3 η, where k is Boltzmann's constant, T is the absolute temperature, a is the radius of an equivalent sphere representing the dipole molecule or group, and η is the viscosity opposing molecular orientation. The power factor becomes zero at both zero and infinite frequency. At sufficiently low frequency the polar molecules orient freely in sympathy with the electric field variations ; the power factor is therefore low and the dielectric con­stant high; but at high frequencies the sympathetic orientation of the polar molecules is prevented by their viscous environment, their contribution to the total dielectric polarization becomes negligible, and the power factor and dielectric constant are together low. similar power factor and permit­tivity changes result on variation of the temperature, and with it the viscosity at con8tant frequency. It is evident that maximum dielectric constant and low dielectric loss for a given polar material can exist simultaneously by a suitable choice of the operating conditions of tempera­ture and frequency.


1986 ◽  
Vol 250 (1) ◽  
pp. F86-F91
Author(s):  
R. V. Pinnick ◽  
V. J. Savin

We measured glomerular ultrafiltration coefficient (Kf) of isolated superficial (S) and deep (D) glomeruli of normovolemic and volume-depleted rats. Filtration was induced in vitro, and Kf was calculated from the maximum rate of change in glomerular size. Basement membrane area (A) for each glomerulus was estimated from morphometric analyses, and glomerular capillary hydraulic conductivity (Lp) was calculated by the formula Lp = Kf/A. Kf of S and D glomeruli of normovolemic rats were 2.98 +/- 0.98 and 4.25 +/- 0.07 nl . min-1 . mmHg-1, respectively. In hypovolemic rats, Kf of S glomeruli fell by approximately 50% to 1.52 +/- 0.14 nl . min-1 . mmHg-1 (P less than 0.001), whereas Kf of D glomeruli remained unchanged at 4.28 +/- 0.10 nl . min-1 . mmHg-1. Lp, calculated using the peripheral capillary area, averaged 1.98 +/- 0.09 and 1.98 +/- 0.06 microliter . min-1 . mmHg-1 . cm-2 in S and D glomeruli of normovolemic rats and 1.89 +/- 0.11 microliter . min-1 . mmHg-1 . cm-2 in D glomeruli of hypovolemic rats. Lp of S glomeruli of volume-depleted rats (0.90 +/- 0.03 microliter . min-1 . mmHg-1 . cm-2) was lower than in any of the other three samples. Mild hypovolemia causes the Kf of S glomeruli to decline, whereas Kf of D glomeruli remains constant. The decrease in Kf occurs without an alteration in capillary area and is most likely due to a decrease in Lp.


Author(s):  
М.С. Воробьёв ◽  
П.В. Москвин ◽  
В.И. Шин ◽  
Н.Н. Коваль ◽  
К.Т. Ашурова ◽  
...  

The paper describes a method for a controlled change in the power of an electron beam during a pulse of submillisecond duration, using a source "SOLO" with a plasma cathode. The beam power is controlled by changing the amplitude of the beam current with a corresponding change in the concentration of the emission plasma. This control method allows generating submillisecond beams of variable power (up to 10 MW at a maximum rate of change of no more than 0.5 MW/µs), which can be used for processing various metallic materials in order to change the functional properties of their surface with the ability to control the rate of input of beam energy into the surface of these materials.


1970 ◽  
Vol 25 (11) ◽  
pp. 1685-1687
Author(s):  
F. F. Hanna ◽  
K. N. Abd-El-Nour

Abstract The dielectric constant (ε′) and dielectric loss (ε′′) of 3,5 dimethyl 3-hexanol in heptane have been measured for dilute and concentrated solutions at five wavelengths between 25 cm and 2 mm and at 20°, 40° and 60 °C. The data have been analysed and two relaxation times are obtained. The long relaxation time is attributed to the rotation of the whole molecule and the short relaxation time to the relaxation of the OH-group. For the range of concentrations used, the results show that associates are hardly detectable.


1965 ◽  
Vol 208 (4) ◽  
pp. 720-723 ◽  
Author(s):  
Gordon M. Schoepfle ◽  
Eliska Atkins ◽  
Larry A. Schafer

Under conditions of continuous fluid exchange at a pH 7.55, a 10-min exposure of Xenopus sciatic single nerve fibers to iodoacetate results in eventual decline in the maximum rate of change of membrane potential, even after a delay of an hour or more during which no changes are apparent. This delayed effect is obtained over an iodoacetate concentration range of 0.1–20.0 mm sodium iodoacetate. Neither the resting membrane potential nor the maximal limiting response obtained during hyperpolarization are affected at a time when iodoacetate has appreciably depressed the spike in the nonpolarized fiber. These findings are taken to indicate that iodoacetate blocks a chain of reactions at a link remote from the process directly concerned with maintenance of the resting level of the sodium conductance. Neither lactate nor pyruvate can be relied on to bring about recovery from the iodoacetate depression.


1977 ◽  
Vol 23 (8) ◽  
pp. 1456-1464 ◽  
Author(s):  
J C Sternberg

Abstract A kinetic nephelometric method and instrument have been developed for the rapid determination of specific serum proteins by means of immunoprecipitin reactions. The maximum rate of change of scattered light intensity in an antigen-antibody reaction can be made to occur within 60 s after initiation of the reaction and provides a measure of the antigen concentration under antibody excess conditions. A mathematical relationship has been found for the conversion of the nonlinear maximum rate data directly into a linear concentration read-out, making possible the use of single-point calibration. Instrument operating parameters and computations are programmed for a particular analysis by means of machine-readable cards. Antigen-excess samples are detected rapidly by injection of calibrator into the reaction mixture after the rate signal has dropped to a pre-selected level. The method correlates well with both radial immunodiffusion and end-point nephelometric methods.


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