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Phase separation, high temperature

Finally, the current status of the inorganic membrane technology is summarized for an overall perspective. The future is speculated based on that perspective to provide a framework for future developments in the synthesis, fabrication and assembly of inorganic membranes and their uses for traditional liquid-phase separation, high-temperature gas separation and membrane reactor applications. [Pg.581]

Immobilized ionic liquid-based stationary phases for high-temperature separations... [Pg.158]

When the minimum against temperature of the interfacial tension between the two phases separated by a planar surface has a positive value (Fig. 3), their mixing will lead to an emulsion whose stability depends upon the magnitude of the surface excess. When the surfactant is sufficiently hydrophilic, it will be mostly distributed in water at low temperatures, and the surface excess will be small because of the high compatibility of the surfactant with the water phase. At high temperatures, the surfactant will be mostly distributed in the oil phase and the surface excess will be small because of the high compatibility between the surfactant and oil. At the moderate temperature T0 at which the concentrations in the two phases become equal, the surface excess is again small. [Pg.188]

As will be introduced in the next chapter, a new class of reactors called membrane reactors combines two unit operations (membrane separation and catalytic reaction) into one compact operation. Many of the membrane reactors of potential interest use inorganic membranes and are operated in gas/vapor phases at high temperatures involving gas separation. Thus membrane separation of gases is often a critical part of a membrane reactor and the aforementioned material and engineering considerations apply. Therefore, discussions on these and other additional considerations will be treated in detail later in Chapters 9 through 11. [Pg.284]

One way to conceptualize this phenomenon is to view the ponytails as short pieces of Teflon, which does not dissolve in any common solvent. As the ponytails become longer, some physical properties of the molecule approach those of Teflon. However, just as the miscibilities of fluorous liquid phases and organic liquid phases are highly temperature dependent, so are the solubilities of fluorous solids in fluorous or non-fluorous liquid phases. Hence, much higher solubilities can be achieved at elevated temperatures. This phenomenon can be used to conduct homogeneous reactions at elevated temperatures, with catalyst or reagent recovery by solid/liquid phase separation at lower temperatures. ... [Pg.68]

Usually, cream containing stearic acid could be prepared easily by melting method as reference recording, which can be sketched as melting oily phase and aqueous phase at high temperature separately and then mixing the phases. In detail, the preparation process, as recorded in Richard Lobo et al. s study, usually contains three steps [41]. [Pg.71]

Oshima, T., Yoon, H.-S. and Koizumi, C. (1989) Application of selective ion monitoring to the analysis of molecular species of vegetable oil triacylglycerols separated by open-tubular column GLC on a methylphenylsilicone phase at high temperature. Lipids, 24, 535 4. [Pg.246]

As found in previous observations [8], polyisocyanurate networks display two transitions with respect to their composition the first is low-temperature transition associated with devitrification of the rubbery phase, and high-temperature related to devitrification of the glassy phase. Hence, both transitions are temperature-shifted towards one another, and the progress of such shift depends on the microphase composition. Therefore, Figure lb presents separately thermomechanical curves of polyurethane isoeyanurate samples related to the low-temperature area. [Pg.137]

An excess of solubilizate is shaken up with the surfactant solution until equilibrium is attained and the two phases separated. High-speed centrifugation has been used, particularly for liquid solubilizates or if one phase is liquid crystalline [20, 21]. Filtration through filters of 0.4-1.5/im pore size has been used when the solubilizate is solid [22,23]. Supersaturation is a potential source of trouble, especially as surfactants tend to inhibit crystallization, but can be minimized by adequate temperature control. [Pg.231]

The lighter lanthanides (La Eu) have a high-temperature form (above 1000°C) with hexagonal glaserite structure, while the sodium phosphates of the heavier lanthanides have a medium-temperature phase and a separate high-temperature phase. The medium-temperature phase (850-1000°C) found for... [Pg.123]

Phase separation in this way is most effective if the light key component is significantly above its critical temperature. If a component is above its critical temperature, it does not truly condense. Some, however, dissolves in the liquid phase. This means that it is bound to have an extremely high K value. [Pg.108]

The previous seetion showed how the van der Waals equation was extended to binary mixtures. However, imieh of the early theoretieal treatment of binary mixtures ignored equation-of-state eflfeets (i.e. the eontributions of the expansion beyond the volume of a elose-paeked liquid) and implieitly avoided the distinetion between eonstant pressure and eonstant volume by putting the moleeules, assumed to be equal in size, into a kind of pseudo-lattiee. Figure A2.5.14 shows sohematieally an equimolar mixture of A and B, at a high temperature where the distribution is essentially random, and at a low temperature where the mixture has separated mto two virtually one-eomponent phases. [Pg.626]

Figure A2.5.14. Quasi-lattice representation of an equimolar binary mixture of A and B (a) randomly mixed at high temperature, and (b) phase separated at low temperature. Figure A2.5.14. Quasi-lattice representation of an equimolar binary mixture of A and B (a) randomly mixed at high temperature, and (b) phase separated at low temperature.
Elastomeric Modified Adhesives. The major characteristic of the resins discussed above is that after cure, or after polymerization, they are extremely brittie. Thus, the utility of unmodified common resins as stmctural adhesives would be very limited. Eor highly cross-linked resin systems to be usehil stmctural adhesives, they have to be modified to ensure fracture resistance. Modification can be effected by the addition of an elastomer which is soluble within the cross-linked resin. Modification of a cross-linked resin in this fashion generally decreases the glass-transition temperature but increases the resin dexibiUty, and thus increases the fracture resistance of the cured adhesive. Recendy, stmctural adhesives have been modified by elastomers which are soluble within the uncured stmctural adhesive, but then phase separate during the cure to form a two-phase system. The matrix properties are mosdy retained the glass-transition temperature is only moderately affected by the presence of the elastomer, yet the fracture resistance is substantially improved. [Pg.233]

The physical properties of polyurethane adhesives result from a special form of phase separation which occurs in the cross-linked polyurethane stmcture. The urethane portions of polyurethanes tend to separate from the polyol portion of the resin, providing good shear strength, good low temperature flexibiUty, and high peel strength. Catalysts such as dibutyltin dilaurate [77-58-7], stannous octoate [1912-83-0], l,4-diazabicyclo[2.2.2]octane... [Pg.233]

The question of whether adsorption should be done ia the gas or Hquid phase is an interesting one. Often the choice is clear. Eor example, ia the separation of nitrogen from oxygen, Hquid-phase separation is not practical because of low temperature requirements. In C q—olefin separation, a gas-phase operation is not feasible because of reactivity of feed components at high temperatures. Also, ia the case of substituted aromatics separation, such as xylene from other Cg aromatics, the inherent selectivities of iadividual components are so close to one another that a simulated moving-bed operation ia hquid phase is the only practical choice. [Pg.303]

Formex pro-cess, Snam-progetti /V-formyl-morph o-line (FM) water is added to the FM to increase its se-lectivity and also to avoid high reboiler temperatures during solvent recovery by distillation 40 perforated-tray ex-tractor, FM density at 1.15 aids phase separation low corrosion allows use of carbon steel equipment... [Pg.78]


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