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Electrostatic saturation

It is known that the dielectric constant of the solution close to the surface of a charged colloidal particle is lower than that in the bulk because of the electrostatic saturation effect [26]. Therefore, the hydration energy is also lower, and ions tend to leave this region and move to a region with a higher dielectric constant [27]. [Pg.599]

FIG. 6 Influence of electrostatic saturation on the pH dependencies of (a) surface charge density and (b) surface potential for different degrees of overlapping of the... [Pg.601]

In relation to general interactions, the solvent is assumed to be a dielectric continuum. The earliest models for this type of interaction were developed by Kirkwood and Onsager, and were later modified with corrections for the effect of electrostatic saturation. " The intrinsic difficulty of these models in accurately determining the dimensions of the cybotactic region (viz. the solvent region where solvent molecules are directly per-tmbed by the presence of solute molecule) that surrounds each solute molecule in the solvent bulk, have usually raised a need for empirical approximations to the determination of a parameter encompassing solvent polarity and polarizability. An alternative approach to... [Pg.581]

As with SCRF-PCM only macroscopic electrostatic contribntions to the Gibbs free energy of solvation are taken into account, short-range effects which are limited predominantly to the first solvation shell have to be considered by adding additional tenns. These correct for the neglect of effects caused by solnte-solvent electron correlation inclnding dispersion forces, hydrophobic interactions, dielectric saturation in the case of... [Pg.838]

Excluding the phenomenon of hyperconjugation, the only other means by which electronic effects can be transmitted within saturated molecules, or exerted by inductive substituents in aromatic molecules, is by direct electrostatic interaction, the direct field effect. In early discussions of substitution this was usually neglected for qualitative purposes since it would operate in the same direction (though it would be expected to diminish in the order ortho > meta > para) as the cr-inductive effect and assessment of the relative importance of each is difficult however, the field effect was recognised as having quantitative significance. ... [Pg.126]

The gaseous ammonia is passed through electrostatic precipitators for particulate removal and mixed with the cooled gas stream. The combined stream flows to the ammonia absorber where the ammonia is recovered by reaction with a dilute solution of sulfuric acid to form ammonium sulfate. Ammonium sulfate precipitates as small crystals after the solution becomes saturated and is withdrawn as a slurry. The slurry is further processed in centrifuge faciHties for recovery. Crystal size can be increased by employing one of two processes (99), either low differential controUed crystallization or mechanical size enlargement by continuous compacting and granulation. [Pg.359]

FIG. 17-75 Schematic circuits for silicon rectifier sets with saturable reactor control, a) Full-wave silicon rectifier, (h) Half-wave silicon rectifier. Industrial Electrostatic Vreci])itation, Addison-Wesley, Read-... [Pg.1617]

RooBng plants (asphalt saturators) Felt or paper saturators spray section, asphalt tank, wet looper Crushed rock or other minerals handling Asphalt vapors and particulates (liquid) Particulates (dust) Exhaust system with high inlet velocity at hoods (3658 m/s [>200 ft/min]) with either scrubbers, baghouses, or two-stage low-voltage electrostatic precipitators Local exhaust system, cyclone or multiple cyclones... [Pg.2177]

The electrostatic behavior of intrinsically nonconductive substances, such as most pure thermoplastics and saturated hydrocarbons, is generally governed by chemical species regarded as trace contaminants. These are components that are not deliberately added and which may be present at less than detectable concentrations. Since charge separation occurs at interfaces, both the magnitude and polarity of charge transfer can be determined by contaminants that are surface active. This is particularly important for nonconductive liquids, where the electrostatic behavior can be governed by contaminants present at much less than 1 ppm (2-1.3). [Pg.9]

According to this approximation, the drift velocity is proportional to the square of the electric field. This is a clear indication of the importance of the electric field inside an electrostatic precipitator. Equation (13.60) is a valid approximation for large particles [dp > 0.5 m), provided that particle charge is close to the saturation level. In the case of small particles, the effect of diffusion charging must be taken into account. [Pg.1226]

Electrostatic fields applied slightly above the onset of the saturation region had little effect on product distribution (37). This presumably indicates that homogeneous ion-electron recombination is the same as neutralization at the electrodes, or that one is simply not observing the products of neutralization in either case. [Pg.253]

The modification by method 2 is more acceptable. Although several types of modifications have been reported, Abraham and Liszi [15] proposed one of the simplest and well-known modifications. Figure 2(b) shows the proposed one-layer model. In this model, an ion of radius r and charge ze is surrounded by a local solvent layer of thickness b — r) and dielectric constant ej, immersed in the bulk solvent of dielectric constant ),. The thickness (b — r) of the solvent layer is taken as the solvent radius, and its dielectric constant ej is supposed to become considerably lower than that of the bulk solvent owing to dielectric saturation. The electrostatic term of the ion solvation energy is then given by... [Pg.41]

Chipot C, Angyan JG, Ferenczy GG, Scheraga HA (1993) Transferable net atomic charges from a distributed multipole analysis for the description of electrostatic properties — a case-study of saturated-hydrocarbons. J Phys Chem 97(25) 6628—6636... [Pg.249]

Figure 5. The critical absolute permeability necessary to sustain the stability of a static foam as a function of liquid saturation. Calculations are for the constant-charge electrostatic model. Figure 5. The critical absolute permeability necessary to sustain the stability of a static foam as a function of liquid saturation. Calculations are for the constant-charge electrostatic model.

See other pages where Electrostatic saturation is mentioned: [Pg.55]    [Pg.584]    [Pg.599]    [Pg.601]    [Pg.601]    [Pg.584]    [Pg.55]    [Pg.100]    [Pg.315]    [Pg.55]    [Pg.584]    [Pg.599]    [Pg.601]    [Pg.601]    [Pg.584]    [Pg.55]    [Pg.100]    [Pg.315]    [Pg.395]    [Pg.127]    [Pg.411]    [Pg.502]    [Pg.372]    [Pg.374]    [Pg.218]    [Pg.270]    [Pg.453]    [Pg.467]    [Pg.146]    [Pg.947]    [Pg.294]    [Pg.161]    [Pg.122]    [Pg.688]    [Pg.62]    [Pg.757]    [Pg.262]    [Pg.281]    [Pg.508]    [Pg.99]    [Pg.282]    [Pg.3]    [Pg.158]    [Pg.285]    [Pg.287]    [Pg.466]   
See also in sourсe #XX -- [ Pg.581 ]




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