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Viscosity electrolytes and

Increasing the temperature will have the main effect to reduce the electrolyte viscosity and to improve the accessibility of the surface for the ions. The ions, thanks to their higher mobility in the warm solvent, will be able to reach deeper carbon area in a shorter time. The increased accessible surface area results in a reduced DLC series resistance and in an increased capacitance with the temperature. Figures 11.5 and 11.6 show the measured and simulated frequency spectra of the BCAP0010 DLC capacitance and series resistance for different temperatures. [Pg.439]

FIGURE 2.70 Cyclic voltammograms for [EMIMllBFJ at 5 mV s" . (Sillars, F. B. et al. 2012. Variation of electrochemical capacitor performance with room temperature ionic liquid electrolyte viscosity and ion size. Physical Chemistry Chemical Physics 14 6094-6100. Reproduced by permission of The Royal Society of Chemistry.)... [Pg.152]

Latex Types. Latexes are differentiated both by the nature of the coUoidal system and by the type of polymer present. Nearly aU of the coUoidal systems are similar to those used in the manufacture of dry types. That is, they are anionic and contain either a sodium or potassium salt of a rosin acid or derivative. In addition, they may also contain a strong acid soap to provide additional stabUity. Those having polymer soUds around 60% contain a very finely tuned soap system to avoid excessive emulsion viscosity during polymeri2ation (162—164). Du Pont also offers a carboxylated nonionic latex stabili2ed with poly(vinyl alcohol). This latex type is especiaUy resistant to flocculation by electrolytes, heat, and mechanical shear, surviving conditions which would easUy flocculate ionic latexes. The differences between anionic and nonionic latexes are outlined in Table 11. [Pg.547]

Viscosities and specific weights of complexes and the corresponding aqueous phases, with the aim of simulating realistic battery conditions with MEP MEM ratio of 1 1, 3 1 and 6 1 in the electrolyte at 50, 75 and 100% states of charge, were studied in a temperature range between 10 and 50 °C [83], Kinematic viscosities between 5 10 6 and 30 -10 6 m2s of the complex phases were found. MEP-rich ones. [Pg.187]

In the tradition of previous reviews [1-22], this section addresses various aspects of nonaqueous electrolytes, including intrinsic properties, such as local structures caused by ion-ion and ion-solvent interactions and bulk properties, such as ionic conductivity, viscosity, and electrochemical stability (voltage window), and their relationships to intrinsic properties. [Pg.457]

The intrinsic properties of an electrolyte evaluated at low concentrations of the salt and from the viscosity and permittivity of the solvent also determine the conductivity of concentrated solutions. Various systems were studied to check this approach. The investigated parameters and effects were ... [Pg.486]

The results of an investigation performed upon various salts in PC [207] or MeOH [15] can be summarized as follows. Both the maximum conductivity and the appertaining concentration 41 are determined by the viscosity and ionic radii (nonsolvated ions) or Stokes radii (solvated ions), meaning that electrolytes show a Stokes-Walden behavior, entailing... [Pg.487]

Filter aids are widely used in die fermentation industry to improve the efficiency of filtration. It is a pre-coated filter medium to prevent blockage or blinding of the filter by solids, which would otherwise wedge diemselves into the pores of the cloth. Filter aid can be added to the fermentation broth to increase the porosity of the cake as it formed. This is only recommended when fermentation product is extracellular. Filter aid adds to the cost of filtration. The minimum quantity needed to achieve the desired result must be established experimentally. Fermentation broths can be pretreated to improve filtration characteristics. Heating to denature proteins enhances the filterability of mycelial broths such as in penicillin production. Alternatively, electrolytes may be added to promote coagulation of colloids into larger, denser particles, which are easier to filter. The filtration process is affected by the viscosity and composition of the broth, and the cell cake.5... [Pg.173]

Furthermore a good electrolyte stability and temperature stability are necessary, and they must not show phase inversion over the temperature range which exists in the reservoir because of the increase in viscosity. [Pg.343]

The addition of salts modifies the composition of the layer of charges at the micellar interface of ionic surfactants, reducing the static dielectric constant of the system [129,130]. Moreover, addition of an electrolyte (NaCl or CaCli) to water-containing AOT-reversed micelles leads to a marked decrease in the maximal solubihty of water, in the viscosity, and in the electrical birefringence relaxation time [131],... [Pg.485]

Electrophoretic separations occur in electrolytes. The type, composition, pH, concentration, viscosity, and temperature of the electrolytes are all crucial parameters for separation optimization. The composition of the electrolyte determines its conductivity, buffer capacity, and ion mobility and also affects the physical nature of a fused silica surface. The general requirements for good electrolytes are listed in Table 1. Due to the complex effects of the type, concentration, and pH of the separation media buffer, conditions should be optimized for each particular separation problem. [Pg.390]

McCormick, C.L., et al. "Development of Laboratory Screening Tests to Predict Polymer Performance in Enhanced Oil Recovery (I). Shear Degradation, Viscosity, and Electrolyte Studies," prepared for DOE under contract No. EF-77-S-05-5603, 1977. [Pg.668]

Figure 12.4 Equilibrium absorption isotherms at 34 °C and rate of dyeing curves at 40 °C for Cl Direct Blue 1 on viscose in the presence of electrolytes singly and in binary mixtures [70]... Figure 12.4 Equilibrium absorption isotherms at 34 °C and rate of dyeing curves at 40 °C for Cl Direct Blue 1 on viscose in the presence of electrolytes singly and in binary mixtures [70]...
PVA and TaM -for the 88%-hydrolyzed PVA. The same dependence was found for the adsorbed layer thickness measured by viscosity and photon correlation spectroscopy. Extension of the adsorption isotherms to higher concentrations gave a second rise in surface concentration, which was attributed to multilayer adsorption and incipient phase separation at the interface. The latex particle size had no effect on the adsorption density however, the thickness of the adsorbed layer increased with increasing particle size, which was attributed to changes in the configuration of the adsorbed polymer molecules. The electrolyte stability of the bare and PVA-covered particles showed that the bare particles coagulated in the primary minimum and the PVA-covered particles flocculated in the secondary minimum and the larger particles were less stable than the smaller particles. [Pg.77]

No attempt will be made here to extend our results beyond the simple lowest-order limiting laws the often ad hoc modifications of these laws to higher concentrations are discussed in many excellent books,8 11 14 but we shall not try to justify them here. As a matter of fact, for equilibrium as well as for nonequilibrium properties, the rigorous extension of the microscopic calculation beyond the first term seems outside the present power of statistical mechanics, because of the rather formidable mathematical difficulties which arise. The main interests of a microscopic theory lie both in the justification qf the assumptions which are involved in the phenomenological approach and in the possibility of extending the mathematical techniques to other problems where a microscopic approach seems necessary in the particular case of the limiting laws, obvious extensions are in the direction of other transport coefficients of electrolytes (viscosity, thermal conductivity, questions involving polyelectrolytes) and of plasma physics, as well as of quantum phenomena where similar effects may be expected (conductivity of metals and semi-... [Pg.161]

The instrument constant B can be determined by measuring the t in two fluids of known density. Air and water are used by most workers (22). In our laboratory we used seawater of known conductivity and pure water to calibrate our vibrating flow systems (53). The system gives accurate densities in dilute solutions, however, care must be taken when using the system in concentrated solutions or in solutions with large viscosities. The development of commercial flow densimeters has caused a rapid increase in the output of density measurements of solutions. Desnoyers, Jolicoeur and coworkers (54-69) have used this system to measure the densities of numerous electrolyte solutions. We have used the system to study the densities of electrolyte mixtures and natural waters (53,70-81). We routinely take our system to sea on oceanographic cruises (79) and find the system to perform very well on a rocking ship. [Pg.587]

Wagner s solution See Wagner s reagent. vag narz sa.Iu shan 1 Walden s rule phys chem A rule which states that the product of the viscosity and the equivalent ionic conductance at infinite dilution In electrolytic solutions is a constant, independent of the solvent It Is only approximately correct. wol-danz, rul ... [Pg.401]


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See also in sourсe #XX -- [ Pg.19 , Pg.20 ]




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Electrolyte Effects on Viscosity and Stability

Viscosity electrolyte

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