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Dielectric factor

Dielectric factors include the dielectric constant. This constant is the ability of a material to hold an electrical charge, as in a capacitor. The two other factors related to the dielectric constant are the "dissipation factor," which relates to the rate at which the charge is lost from the polyurethane, and the "power factor," which relates to the amount of heat generated in the storage of electricity. [Pg.132]

The total pairwise interatomic interaction energy is constructed similarly to that described in Section 3.5, except that a dielectric factor is included for all the electrostatic energy terms, including the dispersion, coulombic, induction, and hydrogen-bond shape energy terms. The procedure for calculating the dielectric constant is described in Section 5.2. [Pg.443]

The (l/e — leo) term is denoted as the dielectric factor. Figure 2 shows the dielectric factor as a function of temperature and pressure. A dielectric constant at ambient temperature and pressure is chosen as the reference state. The heavy dashed line shows the reference density isochore. At pressures from 23 to 50 MPa, where supercritical hydrothermal synthesis are mostly operated, the dielectric factor becomes significant above the critical temperature. This relation suggests that the equilibrium constant change greatly in the region around the critical point. [Pg.318]

Figure 2 Dielectric factor around the critical point. Figure 2 Dielectric factor around the critical point.
Other frequently used resonators are dielectric cavities and loop-gap resonators (also called split-ring resonators) [12]. A dielectric cavity contains a diamagnetic material that serves as a dielectric to raise the effective filling factor by concentratmg the B field over the volume of the sample. Hollow cylinders machmed from Ilised quartz or sapphire that host the sample along the cylindrical axis are conunonly used. [Pg.1560]

The dipole moments of the hydrogen halides decrease with increasing atomic number of the hydrogen, the largest difference occurring between HF and HCl, and association of molecules is not an important factor in the properties of FICl, HBr and HI. This change in dipole moment is reflected in the diminishing permittivity (dielectric constant) values from HF to HI. [Pg.327]

Also use constant dielectric Tor MM+aiul OPLS ciilciilatimis. Use the (lislance-flepeiident dielecinc for AMBER and BlO+to mimic the screening effects of solvation when no explicit solvent molecules are present. The scale factor for the dielectric permittivity, n. can vary from 1 to H(l. IlyperChem sets tt to 1. .5 for MM-r. Use 1.0 for AMBER and OPLS. and 1.0-2..5 for BlO-r. [Pg.104]

The third term in Equation (11.52) is the correction factor corresponding to the work done creating the charge distribution of the solute within the cavity in the dielectric medium. the gas-phase wavefimction. [Pg.611]

The first modification is to simply scale the dielectric permittivity of free space (8 ) by a scale factor D to mediate or dampen the long range electrostatic interactions. Its value was often set to be between 1.0 and 78.0, the macroscopic value for water. A value of D=2.5, so that 8 =2.58q, was often used in early CHARMM calculations. [Pg.180]

Tetralluoroethylene polymer has the lowest coefficient of friction of any solid. It has remarkable chemical resistance and a very low brittleness temperature ( — 100°C). Its dielectric constant and loss factor are low and stable across a broad temperature and frequency range. Its impact strength is high. [Pg.1016]

Dielectric constant (60 Hz) Dielectric constant (10 Hz) Dissipation (power) factor (60... [Pg.1034]

Dielectric strength, kV mm Electrical Volume (dc) resistivity, ohm-cm Dielectric constant (60 Hz) Dielectric constant (10 Hz) Dissipation (power) factor (60 Hz) Dissipation factor (10 Hz) Mechanical Compressive modulus, 10Mb in-2 9.8-12 24-31 16-24 1014-1016 4.5-6.0 19 335-600 14 ... [Pg.1060]

The time-temperature superpositioning principle was applied f to the maximum in dielectric loss factors measured on poly(vinyl acetate). Data collected at different temperatures were shifted to match at Tg = 28 C. The shift factors for the frequency (in hertz) at the maximum were found to obey the WLF equation in the following form log co + 6.9 = [ 19.6(T -28)]/[42 (T - 28)]. Estimate the fractional free volume at Tg and a. for the free volume from these data. Recalling from Chap. 3 that the loss factor for the mechanical properties occurs at cor = 1, estimate the relaxation time for poly(vinyl acetate) at 40 and 28.5 C. [Pg.269]

In a medium where the relative dielectric constant is e, the force between fixed chages at a definite separation is decreased by the dimensionless factor e. This is true regardless of the system of units and is incorporated into Eqs. (10.101) and (10.102) by dividing the right-hand side of each by e. ... [Pg.715]

Electrical Properties. The low polarizabiHty of perfluorinated Hquids makes them exceUent insulators. Theh dielectric strengths are about 40 kV (ASTM D877) dissipation factors are about 0.0001 at 1 MH2 dielectric constants are about 1.8 volume resistivities are about 1 x 10 ohm-cm (ASTM D257) (17). [Pg.297]

Polytetrafluoroethylene transitions occur at specific combinations of temperature and mechanical or electrical vibrations. Transitions, sometimes called dielectric relaxations, can cause wide fluctuations in the dissipation factor. [Pg.351]


See other pages where Dielectric factor is mentioned: [Pg.279]    [Pg.133]    [Pg.257]    [Pg.371]    [Pg.31]    [Pg.219]    [Pg.176]    [Pg.365]    [Pg.279]    [Pg.133]    [Pg.257]    [Pg.371]    [Pg.31]    [Pg.219]    [Pg.176]    [Pg.365]    [Pg.310]    [Pg.1170]    [Pg.2219]    [Pg.131]    [Pg.132]    [Pg.364]    [Pg.193]    [Pg.196]    [Pg.613]    [Pg.622]    [Pg.641]    [Pg.155]    [Pg.193]    [Pg.196]    [Pg.1030]    [Pg.1032]    [Pg.1038]    [Pg.1040]    [Pg.1050]    [Pg.1054]    [Pg.1056]    [Pg.400]    [Pg.400]   
See also in sourсe #XX -- [ Pg.34 , Pg.341 ]




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