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Viscosity concentrated solutions

Gum arabic has a high water solubility, up to 50% (w/v), but has a relatively low viscosity. Concentrated solutions have the consistency of a gel. [Pg.178]

Locust bean gum is not completely soluble in cold water it must be heated to 80°C and cooled to attain a stable solution that has high viscosity at low concentrations. The gum is compatible with other plant gums and the viscosity of solutions is not appreciably affected by pH or salts. [Pg.435]

Larch gum is readily soluble in water. The viscosity of these solutions is lower than that of most other natural gums and solutions of over 40% soHds are easily prepared. These highly concentrated solutions are also unusual because of their Newtonian flow properties. Larch gum reduces the surface tension of water solutions and the interfacial tension existing in water and oil mixtures, and thus is an effective emulsifying agent. As a result of these properties, larch gum has been used in foods and can serve as a gum arabic substitute. [Pg.436]

Spray Drying. Spray-dry encapsulation processes (Fig. 7) consist of spraying an intimate mixture of core and shell material into a heated chamber where rapid desolvation occurs to thereby produce microcapsules (24,25). The first step in such processes is to form a concentrated solution of the carrier or shell material in the solvent from which spray drying is to be done. Any water- or solvent-soluble film-forming shell material can, in principle, be used. Water-soluble polymers such as gum arable, modified starch, and hydrolyzed gelatin are used most often. Solutions of these shell materials at 50 wt % soHds have sufficiently low viscosities that they stiU can be atomized without difficulty. It is not unusual to blend gum arable and modified starch with maltodextrins, sucrose, or sorbitol. [Pg.321]

Viscosity—Concentration Relationship for Dilute Dispersions. The viscosities of dilute dispersions have received considerable theoretical and experimental treatment, partly because of the similarity between polymer solutions and small particle dispersions at low concentration. Nondeformable spherical particles are usually assumed in the cases of molecules and particles. The key viscosity quantity for dispersions is the relative viscosity or viscosity ratio,... [Pg.173]

In the Shoe or one-shot method (4), formamide is used to coagulate sodium silicate. The silicate solution used in the Joosten method can be diluted with water to lower its viscosity. Concentrations of sodium silicate between 10—70% are used (viscosities of 2.5—50 mPa-s). Concentrations of formamide are between 2 and 30%. Other reactants such as CaCl2 and sodium aluminate are used in concentrations between 2.4—12 g/L of silicate solution. [Pg.227]

Com symps [8029-43 ] (glucose symp, starch symp) are concentrated solutions of partially hydrolyzed starch containing dextrose, maltose, and higher molecular weight saccharides. In the United States, com symps are produced from com starch by acid and enzyme processes. Other starch sources such as wheat, rice, potato, and tapioca are used elsewhere depending on avadabiHty. Symps are generally sold in the form of viscous Hquid products and vary in physical properties, eg, viscosity, humectancy, hygroscopicity, sweetness, and fermentabiHty. [Pg.294]

The physical picture in concentrated electrolytes is more apdy described by the theory of ionic association (18,19). It was pointed out that as the solutions become more concentrated, the opportunity to form ion pairs held by electrostatic attraction increases (18). This tendency increases for ions with smaller ionic radius and in the lower dielectric constant solvents used for lithium batteries. A significant amount of ion-pairing and triple-ion formation exists in the high concentration electrolytes used in batteries. The ions are solvated, causing solvent molecules to be highly oriented and polarized. In concentrated solutions the ions are close together and the attraction between them increases ion-pairing of the electrolyte. Solvation can tie up a considerable amount of solvent and increase the viscosity of concentrated solutions. [Pg.509]

Concentrated solution viscosity higher than predicted for the intrinsic viscosity. [Pg.259]

Viscosity. Solvent viscosity of resins is influenced by the concentration of resin, the softening point, the molecular weight distribution, the chemical composition of the resin, and the type of solvent. The higher the resin concentration, the higher the viscosity. For a given concentration, solution viscosity depends on the softening point of the resin (Fig. 22). [Pg.618]

In HOPC, a concentrated solution of polymer is injected. The concentration needs to be sufficiently higher than the overlap concentration c at which congestion of polymer chains occurs. The c is approximately equal to the reciprocal of the intrinsic viscosity of the polymer. In terms of mass concentration, c is quite low. For monodisperse polystyrene, c is given as (4)... [Pg.611]

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]

In a concentrated solution, characterized by an effective medium viscosity r e "Hs, the hydrodynamic field decays much faster due to the shielding effect of the encountered polymer segments ... [Pg.91]

Fig. 2.52 Kinematic viscosity of solution vs. temperature at various Habon G concentrations. Circles (O) indicate water Habon G, boxes ( ) represent 130ppm, crosses (x) represent 260ppm, empty triangles (A) represent 530 ppm, triangles (A) represent 1,060 ppm. Reprinted from Hetsroni et al. (2001b) with permission... Fig. 2.52 Kinematic viscosity of solution vs. temperature at various Habon G concentrations. Circles (O) indicate water Habon G, boxes ( ) represent 130ppm, crosses (x) represent 260ppm, empty triangles (A) represent 530 ppm, triangles (A) represent 1,060 ppm. Reprinted from Hetsroni et al. (2001b) with permission...
The extremely low rates of solution of polymers and the high viscosities of their solutions present serious problems in the application of the delicate calorimetric methods required to measure the small heats of mixing or dilution. This method has been applied successfully only to polymers of lower molecular weight where the rate of solution is rapid and the viscosity of the concentrated solution not intolerably great.22 The second method requires very high precision in the measurement of the activity in order that the usually small temperature coefficient can be determined with sufficient accuracy. [Pg.516]

Theoretical treatment of the viscosity-concentration relationship for polyelectrolyte solutions would involve both the cumbersome statistics of highly elongated chains beyond the range of usefulness of the Gaussian approximation and the even more difficult problem of their electrostatic interactions when highly charged. There appears to be little hope for a satisfactory solution of this problem from theory. Fuoss has shown, however, that experimental data may be handled satisfactorily through the use of the empirical relation ... [Pg.636]

During drying an outward flow of Pt can exist, leading to loss of dispersion. The resulting system will depend on many factors, including impregnation time and pH value, viscosity, concentration of the impregnating solution, and the presence of other ions or solute in the solution. [Pg.82]

For concentrated solutions of polystyrene in n-butylbenzene, Graessley [40] has shown that the reduced viscosity r red Cnred=(r ( y)- rls)/(rlo rls)) can be represented on a master curve if it is plotted versus the reduced shear rate (3 ((3= y/ ycnt= y-A0). For semi-dilute solutions a perfect master curve is obtained if (3 is plotted versus a slope corrected for reduced viscosity, T corp as shown in Fig. 16. [Pg.31]


See other pages where Viscosity concentrated solutions is mentioned: [Pg.2598]    [Pg.622]    [Pg.340]    [Pg.436]    [Pg.171]    [Pg.191]    [Pg.227]    [Pg.259]    [Pg.13]    [Pg.295]    [Pg.510]    [Pg.488]    [Pg.601]    [Pg.150]    [Pg.183]    [Pg.247]    [Pg.209]    [Pg.166]    [Pg.153]    [Pg.124]    [Pg.237]    [Pg.67]    [Pg.212]    [Pg.7]    [Pg.590]    [Pg.159]    [Pg.989]    [Pg.17]    [Pg.11]    [Pg.402]    [Pg.158]    [Pg.165]   
See also in sourсe #XX -- [ Pg.275 ]




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