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Inverse swollen

Polymer-based, synthetic ion-exchangers known as resins are available commercially in gel type or truly porous forms. Gel-type resins are not porous in the usual sense of the word, since their structure depends upon swelhng in the solvent in which they are immersed. Removal of the solvent usually results in a collapse of the three-dimensional structure, and no significant surface area or pore diameter can be defined by the ordinaiy techniques available for truly porous materials. In their swollen state, gel-type resins approximate a true molecular-scale solution. Thus, we can identify an internal porosity p only in terms of the equilibrium uptake of water or other liquid. When crosslinked polymers are used as the support matrix, the internal porosity so defined varies in inverse proportion to the degree of crosslinkiug, with swelhng and therefore porosity typically being more... [Pg.1500]

Suspension polymerization of water-insoluble monomers (e.g., styrene and divinylbenzene) involves the formation of an oil droplet suspension of the monomer in water with direct conversions of individual monomer droplets into the corresponding polymer beads. Preparation of beaded polymers from water-soluble monomers (e.g., acrylamide) is similar, except that an aqueous solution of monomers is dispersed in oil to form a water-in-oil (w/o) droplet suspension. Subsequent polymerization of the monomer droplets produces the corresponding swollen hydrophilic polyacrylamide beads. These processes are often referred to as inverse suspension polymerization. [Pg.4]

By performing in situ the polymerization of acrylamide in water/AOT/toluene microemulsions, clear and stable inverse latexes of water-swollen polyacrylamide particles stabilized by AOT and dispersed in toluene have been found [192-194], It was shown that the final dispersions consist of two species of particles in equilibrium, surfactant-coated polymer particles (size about 400 A) with narrow size distribution and small AOT micelles (size about 30 A). [Pg.490]

As for direct emulsions, the presence of excess surfactant induces depletion interaction followed by phase separation. Such a mechanism was proposed by Binks et al. [ 12] to explain the flocculation of inverse emulsion droplets in the presence of microemulsion-swollen micelles. The microscopic origin of the interaction driven by the presence of the bad solvent is more speculative. From empirical considerations, it can be deduced that surfactant chains mix more easily with alkanes than with vegetable, silicone, and some functionalized oils. The size dependence of such a mechanism, reflected by the shifts in the phase transition thresholds, is... [Pg.113]

Although planar structures for 111 and 112 were not attained, it is still likely that these novel diazabiaryls can serve as chiral ligands with C2 symmetry. In support of this likelihood, the resolution of 112 was accomplished recently on swollen, microcrystalline triacetylcellulose by Jan Sandstrom. The free energy barrier to ring inversion of 112 was found to be about 101 kJ/mol, through a thermal racemization process using chiral 112. ... [Pg.133]

It is well known that swelling of resins increases the particle radius. When resin beads are immersed in the solution, water uptake takes place almost immediately, resulting in a new swollen radius. The swollen radius is inversely proportional to the initial solution concentration (Hellferich, 1962). This effect has not been taken into account in the original model of Levenspiel (1972). However, the actual swollen radius of the resin should be used in the model equations, and so measurements should be performed in order to estimate this radius. [Pg.284]

The volume swelling ratios (Vr) are inversely proportional to the equilibrium volume fraction of the rubber in the corresponding swollen systems (filled and gum, represented by subscripts f and 0, respectively), such that ... [Pg.66]

Fig 4. Polymer-solvent interaction parameter % calculated from Eq. (10) using the experimental swelling ratio as a function of inverse absolute temperature. Dashed lines represent fits to straight lines which should be obeyed in a highly swollen state. NIPA/water, O NIPA/ethanol, NIPA/n-propanol. (Reproduced with permission from Ref. 19)... [Pg.11]

Nafion is a novel and unique family of polymers which consist of a perfluorinated backbone and short pendant chains terminated by sulfonic groups. When swollen in water, the structure of Nafion is believed to resemble that of an inverse micelle (Fig. 3) [16-18], The hydrated SOf head groups are clustered together in a... [Pg.321]

The azo-modified, elastin-like polypeptide XIV illustrated in Scheme 9 exhibits a so-called inverse temperature transition" that is, the compound gives cross-linked gels that remain swollen in water at temperature below 25 °C but deswell and contract upon a rise of temperature. The trans-cis photoisomerization of the azo units, obtained through alternating irradiation at 350 and 450 nm, permits photomodulation of the inverse temperature transition.[S9] The result indicates that attachment of a small proportion of azobenzene chromophores is sufficient to render inverse temperature transition of elastin-like polypeptides photoresponsive, and provides a route to protein-based polymeric materials capable of photomechanical transduction. [Pg.418]

An aggregate of surfactant molecules or ions in solution. Such aggregates form spontaneously at sufficiently high surfactant concentration, above the critical micelle concentration. The micelles typically contain tens to hundreds of molecules and are of colloidal dimensions. If more than one kind of surfactant forms the micelles, they are referred to as mixed micelles . If a micelle becomes larger than usual as a result of either the incorporation of solubilized molecules or the formation of a mixed micelle, then the term swollen micelle is applied. See also Inverse Micelle. [Pg.382]

Fig. 4. Example of electron micrograph of the inverse hexagonal structure. Copolymer poly-butadiene-poly(vinyl-2-naphthalene) BVN.ll containing 62% polybutadiene, swollen with 36% MMA, and post-polymerized87. Main figure section along the plane perpendicular to the direction of the axis of the poly(vinylnaphthalene) cylinders swollen with the solvent insert section by a plane parallel to the axis of the cylinders. Poly butadiene stained by osmium tetroxide in dark... Fig. 4. Example of electron micrograph of the inverse hexagonal structure. Copolymer poly-butadiene-poly(vinyl-2-naphthalene) BVN.ll containing 62% polybutadiene, swollen with 36% MMA, and post-polymerized87. Main figure section along the plane perpendicular to the direction of the axis of the poly(vinylnaphthalene) cylinders swollen with the solvent insert section by a plane parallel to the axis of the cylinders. Poly butadiene stained by osmium tetroxide in dark...
Corpart and Candau [68, 69] described the formulation of polyampholytes containing both positive and negative charges in inverse microemulsions. The copolymers can show very different behaviors in the aqueous solution, ranging from insoluble, water-swollen hydrogels to water-soluble compounds, depending on the monomer composition. For polyampholytes with balanced stoichiometry, the polymer behavior is controlled by attractive electrostatic forces. The compound is usually insoluble in water, but becomes soluble upon the addition of salt. [Pg.49]

The main fact of the book so far is that the clay particles sit at about 7 Debye lengths from each other when the clay is in its swollen gel state. The interplate separation in the gel state is therefore inversely proportional to the square root of the electrolyte concentration, a fact noted by Walker in 1960 [1], Such a separation of 7 Debye lengths is no special feature of clay science associated with the large... [Pg.159]


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See also in sourсe #XX -- [ Pg.165 ]




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