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Solute dispersion

The McMillan-Mayer theory allows us to develop a fomialism similar to that of a dilute interacting fluid for solute dispersed in the solvent provided that a sensible description of W can be given. At the Ihnit of dilution, when intersolute interactions can be neglected, we know that the chemical potential of a can be written as = W (a s) + IcT In where W(a s) is the potential of mean force for the interaction of a solute... [Pg.565]

Photomultipliers are used to measure the intensity of the scattered light. The output is compared to that of a second photocell located in the light trap which measures the intensity of the incident beam. In this way the ratio [J q is measured directly with built-in compensation for any variations in the source. When filters are used for measuring depolarization, their effect on the sensitivity of the photomultiplier and its output must also be considered. Instrument calibration can be accomplished using well-characterized polymer solutions, dispersions of colloidal silica, or opalescent glass as standards. [Pg.692]

Over the years, the term gums has been used to denote a wide range of compounds including polysaccharides, terpenes, proteins, and synthetic polymers. In the 1990s, the term more specifically denotes a group of industrially useful polysaccharides or their derivatives that hydrate in hot or cold water to form viscous solutions, dispersions, or gels (1). [Pg.430]

There are more than 100 commercially available organic peroxides ia well over 300 formulations, eg, neat Hquids and soflds, and pastes, powders, solutions, dispersions, and emulsions, that have utihty ia many commercial appHcations (13,14,16,21,22,24—26,44,98,99,208,209,291—305). Many of the commercially available peroxides are Hsted ia Table 17 along with 10-h HLTs. [Pg.133]

Mixing of latex compounds is accompHshed by stirring ingredients into the latex in the form of water solutions, dispersions, or emulsions. Although the mbber softeners needed to process dry mbber are not necessary for latex, use of emulsified softeners or polymeric plasticizers in natural or synthetic latex compounds provides lower modulus in the finished products. This reduces hand fatigue and increases touch sensitivity in dipped mbber gloves. Mineral oils are also used as an economy. [Pg.253]

There are two fundamental chromatography theories that deal with solute retention and solute dispersion and these are the Plate Theory and the Rate Theory, respectively. It is essential to be familiar with both these theories in order to understand the chromatographic process, the function of the column, and column design. The first effective theory to be developed was the plate theory, which revealed those factors that controlled chromatographic retention and allowed the... [Pg.4]

The suspension polymerization of 65% acrylamide aqueous solution dispersed in n-hexane (aqueous phase -hexane = 1 5) in the presence of a stabilizer (sorbitan monostearate, 1.4% with respect to -hexane) and an initiator (2,2 -azo-bis-A/, A/ -dimethyleneisobutylamide chloride) carried out at 65°C for 3 h, with subsequent holding at 110°C, yields a powdered product with the granule size of 0.5 mm, while the addition of Na2S04... [Pg.67]

It is seen that when operating at the optimum velocity that provides the minimum value of (H) and thus, the maximum efficiency, solute diffusivity has no effect on solute dispersion and consequently, the column efficiency is independent of temperature. [Pg.147]

A. Padron, L. Castro, and G. Zamora. Transportable and stable hydrocarbons in buffer solution dispersions. In Proceedings Volume, volume 2, pages 587-596. 6th Unitar et al Heavy Crude Tar Sands Int Conf (Houston, TX, 2/12-2/17), 1995. [Pg.444]

Liquid raw materials such as polymer emulsions, defoamers, pigment dispersions, dye solutions, dispersing aids and emulsifiers are all products that can themselves become infected with micro-organisms if not produced from non-contaminated ingredients, under good manufacturing conditions and with an effective preservative. [Pg.71]

As implied above, the principal interaction mechanism for polar solutes seems to be the reaction field effect. Specific interactions, notably hydrogen bonding, are also common. For non-polar solutes dispersion interactions seem to predominate. None of the investigations reported to date have developed completely satisfactory solutions to the interaction question, but it appears from the most recent studies that all interaction mechanisms are present in all systems. Most authors have simply reported the dominant effect for the particular case with which they were concerned. Particularly intriguing is the indication that dispersion interactions and reaction field effects produce the opposite affect on coupling constants. [Pg.184]

The main sources of broadening are the solute dispersion in the connecting tubes, the effective working volume of the detector and the dynamics of the sensor, of the electronic circuitry and of the recording device. [Pg.117]

In the first flow regime, the velocity is small and Peclet number is of order one or smaller. Molecular diffusion plays the dominant role in solute dispersion. This case is well-understood even for reactive flows (see e.g. Conca et al., 2004, 2003 van Duijn and Knabner, 1997 van Duijn and Pop, 2004 van Duijn et al., 1998 Hornung and Jager, 1991 Knabner et al., 1995 Mikelic and Primicerio, 2006 and references therein). [Pg.2]

Pikal, M., and Lukes, A. L. (1976), Kundsen vapor pressure measurements on pure materials and solutions dispersed in porous media Molded nitroglycerin tablets, /. Pharm. Sci., 65,1269. [Pg.680]

In addition to the considerations mentioned above, it is rather important to keep in mind that a common aspect in determining the overall thermodynamic behaviour of a biopolymer solution/dispersion is the necessity of taking into account all of the component interactions. This includes the interactions of the biopolymer(s) with the water molecules, including both hydration (attraction) and dehydration (release), as well as the interactions amongst the water molecules themselves. [Pg.129]

Brusseau, M. L., The influence of solute size, pore water velocity, and intraparticle porosity on solute dispersion and transport in soil , Water Resour. Res., 29,1071-1080 (1993). [Pg.1218]

FIGURE 8.28 If dissolution is endothermic, it will occur only if the disorder caused by the solute dispersing is great enough to produce an overall increase in entropy. [Pg.519]

The sample diluent affects the solute dispersion. If we consider the effects of three different diluents (hexane, chloroform, and acetone) on the chromatographic behavior of a TG mixture on RP columns using, for example, acetonitrile and ethanol as the mobile phase, we can see that the TGs dissolved in hexane provided only a minute chromatographic trace, whereas dissolution in chloroform yielded excellent detection and resolution. These results can best be explained by invoking the solvophobic theory of Horvath and Melander (85). [Pg.211]

The starting mass is a smelt, solution, dispersion, emulsion or sol. [Pg.291]

Fluorescent brighteners soaps and detergents, all fibers, oils, paints, and plastics from solution, dispersion or suspension in a mass stilbene, pyrazoles, coumarin, and naphthalimides... [Pg.4]

Dye Fixation. On the dried fabric, the dye is only deposited on the fiber surface. It must penetrate into the fiber during a fixation step and be incorporated in the fiber by chemical reaction (reactive dyes), aggregation (vat, sulfur dyes), ion-pair formation (acid, cationic dyes), or in the form of a solid solution (disperse dyes). [Pg.344]

Rao, P. S. C. (1974). Pore-geometry effects on solute dispersion in aggregated soils and evaluation of a predictive model. Ph.D, Dissertation, University of Hawaii, Honolulu. [Pg.202]

Table A.5 is the output file for salts in the 4.5- to 5.0-km layer, where the system pressure is 484.5 bars (102 bars km-1 x 4.75 km). The temperature of 268.28 K is the freezing point depression for this particular composition and pressure at 268.27 K, ice forms. The pH of this system is 8.02. The number of independent components is seven. This example deals with lithostatic pressures on solutions dispersed in a regolith, which is fundamentally different from the previous examples (Tables A.2-A.4) that dealt with seawaters. Table A.5 is the output file for salts in the 4.5- to 5.0-km layer, where the system pressure is 484.5 bars (102 bars km-1 x 4.75 km). The temperature of 268.28 K is the freezing point depression for this particular composition and pressure at 268.27 K, ice forms. The pH of this system is 8.02. The number of independent components is seven. This example deals with lithostatic pressures on solutions dispersed in a regolith, which is fundamentally different from the previous examples (Tables A.2-A.4) that dealt with seawaters.

See other pages where Solute dispersion is mentioned: [Pg.228]    [Pg.230]    [Pg.258]    [Pg.486]    [Pg.270]    [Pg.6]    [Pg.62]    [Pg.312]    [Pg.352]    [Pg.474]    [Pg.225]    [Pg.334]    [Pg.41]    [Pg.45]    [Pg.160]    [Pg.258]    [Pg.74]    [Pg.45]    [Pg.45]    [Pg.486]    [Pg.144]    [Pg.247]    [Pg.297]    [Pg.139]    [Pg.19]   
See also in sourсe #XX -- [ Pg.534 ]

See also in sourсe #XX -- [ Pg.366 ]




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Advection-dispersion equation numerical solution

Aqueous solutions dispersion-derivative measurement

Colloidal Solutions and Dispersions

Dispersed Medium Model of Micellar Solution

Dispersed plug flow model solutions

Dispersion from NAPL to Solution

Dispersion interactions, solute-solvent

Dispersion of solutes

Dispersion solutions

Dispersion solutions

Dispersion systems aqueous solution medium

Equilibrium-dispersive model numerical solution

Ionic dispersion, aqueous electrolyte solutions

Nonlinear Tubular Reactor with Dispersion Quasilinearization Solution

Numerical Solutions of the Equilibrium-Dispersive Model

On the Dispersion of a Solute by Diffusion, Convection, and Exchange between Phases

Polymer dispersal in solution

Polymer solution, dispersion

SEDS (Solution Enhanced Dispersion with Supercritical

Solute The dispersed phase

Solute diffusion-dispersion

Solute diffusion-dispersion study

Solute dispersed phase

Solution enhanced dispersion

Solution enhanced dispersion supercritical fluid process

Solution enhanced dispersion supercritical fluids

Solution of the Dispersion Equation

Solution-enhanced dispersion by supercritical

Solution-enhanced dispersion by supercritical fluids

Solution/dispersion method

Solutions RCAs dispersed

Structure of Ice, Solutions and Dispersions

The Relationship between Dispersion in a Packed Column to Solute Molecular Weight

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