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Aqueous systems high polymers

Now, let s look at a polymeric system. To begin with, the motion in polymer chains is hindered. The massive size of the polymer itself and the intermolecular forces within the chains create an inflexible system, especially when compared to the aqueous systems with which we are most familiar. Secondly, the entropy of mixing is not actually as great as that seen in typical solution formation. Polymers are inherently highly entropic, so the benefit of mixing them together is modest. Therefore, any two polymers that form a miscible blend depend primarily... [Pg.202]

Last but not least, catechols are highly water-soluble (the water solubility of catechol is approximately 1 g per 2.3 mL of water), which makes it difficult to directly extract them in situ from reaction media with organic, water immiscible solvents. Nevertheless, extraction of catechols from aqueous systems with hydro-phobic polymers such as the polystyrene-based resin Amberlite XAD-4 is... [Pg.289]

With the substantial interest in use of aqueous coating systems, an added burden is placed on the atomizing process. This burden results from the relatively high viscosities and surface tensions of aqueous systems. Fortunately, in applications using modified-release coatings, aqueous versions of such coating systems are typically in the form of latexes, or polymer dispersions, which have relatively low viscosities for the solids content of the coating system, and the presence of... [Pg.295]

Chain growth continues at a rate dependent on the concentrations of monomer [M] and of active sites [MJ. Monomer exponents in the range 1.3 to 1.5 or higher had been observed (110, 123, 127) especially at low [M], but first order dependence has now been established over a broad range of [M] (21). A stationary level of [M ] is reached rapidly and is typically of the order of 10-8 molar. Chains grow rapidly by successive monomer additions until the polymer chain is terminated by transfer or by reaction with another radical. The rate constant for propagation (ft2) at 60° in DMF is 1960 m-1 Is-1 (16), which is a comparatively high value [see Table 1 and ref. (76)]. On the other hand it is only about one-tenth of that found for acrylonitrile in aqueous systems (Table 6)... [Pg.404]

Aqueous systems have been studied by a very large number of investigators. Economy, safety, convenience and quality of product have combined to make this the method of choice for commercial production of copolymers. The industrial importance of such end products as elastomers and acrylic fibers has been a special incentive to related fundamental studies. Furthermore, the relatively high solubility of acrylonitrile monomer in water coupled with insolubility of the polymer make it a convenient test monomer for studies of initiation by redox systems (6, 25, 102). Large numbers of homogeneous chemical initiators and some heterogeneous initiators have been studied as well as initiation by photochemical means, by ultrasonics and by ionizing radiation. It will not be possible here to review the enormous world literature. Several publications (/, 92, 117) refer in some detail to the older papers, and we shall restrict our comments to recent interpretations that have received support from several quarters. [Pg.422]

Yuguchi, S and M. Watanabe Studies on acrylic fiber. X. Effect of agitation on polymerization of acrylonitrile in aqueous and emulsion phase initiated by persulfate-triethanolamine redox system and persulfate alone. Chem. High Polymers 17, 108—114 (1960). See also previous papers in this series. [Pg.441]

Pharmaceutical research on polymeric micelles has mainly focused on two kinds of block copolymers, namely, AB block copolymers or diblock copolymers and ABA or BAB block copolymers known as triblock copolymers (Bader et al., 1984 Yokoyama et al., 1990,1991 Kwon and Okano, 1996, 1999 Kwon, 1998, 2003 Alakahov and Kabanov, 1998). The most common hydrophilic block (A) of the block copolymers is polyethylene oxide (PEO). This polymer is highly hydrated through hydrogen bonding and sterically stabilizes surfaces of the polymeric micelles in aqueous systems. [Pg.309]

PHASE SEPARATION IN AQUEOUS SYSTEMS CONTAINING HIGH POLYMERS... [Pg.152]

Aqueous systems containing high polymers such as polyethylene glycols and dextrans may separate spontaneously into two phases (Guan et al., 1993). These... [Pg.152]

The hydrophilicity-hydrophobicity balance of the membrane polymer is another important parameter that is mainly influenced by the functional groups of the polymer. Hydrophilic polymers have high affinity to water, and therefore they are suited as a material for nonporous membranes that should have a high permeability and selectivity for water (e.g., in RO or hydrophilic PV). In addition, hydrophilic membranes have been proven to be les s prone to fouling in aqueous systems than hydrophobic materials. [Pg.23]


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See also in sourсe #XX -- [ Pg.152 ]




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Aqueous systems

Phase equilibrium, aqueous systems high polymers

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