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Polymeric liquids solubility

Pure polyvinyl chloride alone It a rigid plastic of high volume resistivity. Addition of monomeric liquid plasticizer makes It flexible but lowers volume resistivity seriously. This loss of volume resistivity was not prevented by pre-purification of commercial resin and plasticizer, though It could be worsened by addition of Ionic soluble Impurities. Volume resistivity was surprisingly Increased by heat aging. It was not improved by use of polymeric liquid plasticizers, nor even, surprisingly, by use of nitrile rubber as plasticizer. Flexlblllzatlon without serious loss of volume resistivity was best achieved by internal plasticization by copolymerization with 2-ethylhexyl acrylate. Further studies are needed to explain these observations and to optimize the use of Internal plasticization In this way. [Pg.148]

Properties Colorless or pale-yellow liquid. Bp 90.6C, d 1.265 (25/25C), refr index 1.432 (20C), flash p 16F (-8.89C). Readily hydrolyzed with liberation of hydrogen chloride polymerizes easily soluble in most organic solvents reacts with alcohol. [Pg.1320]

Membrane separations involve the selective solubility in a thin polymeric membrane of a component in a mixture and/or the selective diffusion of that component through the membrane. In reverse osmosis (3) applications, which entail recovery of a solvent from dissolved solutes such as in desalination of brackish or polluted water, pressures sufficient to overcome both osmotic pressure and pressure drop through the membrane must be applied. In permeation (4), osmotic pressure effects are negligible and the upstream side of the membrane can be a gas or liquid mixture. Sometimes a phase transition is involved as in the process for dehydration of isopropanol shown in Fig. 1.8. In addition, polymeric liquid surfactant and immobilized-solvent membranes have been used. [Pg.405]

Unlike reagents bound to crosslinked polymeric supports, soluble macromolecules are able to interact with reactive groups attached to insoluble polymers. This fact was demonstrated by Frank and Hagenmaier, who developed an alternating liquid-solid phase peptide synthesis procedure. Amino acids attached to crosslinked polystyrene via a carbamate linker were condensed with a peptide ester of polyethyleneglycol monostearylether (Scheme 1.6.12). [Pg.52]

A thermodynamic model meeting all the above requirements is presented in the next section. It is based on the Lattice-Fluid theory of Sanchez and Lacombe(7) as modified recently by the author (8-12).So far the model has been applied to solvent-homopolymer and homopolymer-homopolymer(both monodisperse) mixtures (1 0), to the gas solubility in polymeric liquids... [Pg.106]

A group of colorants that falls outside of the classical definition of dyes and pigments consists of polymeric colorants. In this group, the chromogen (i.e., the molecular moiety responsible for color) is attached to a polymer backbone. The polymer is chosen to change or enhance the colorant properties such as liquidity, solubility, compatibility, or fugitivity. An example of a polymeric, water-soluble colorant is shown in scheme 3 in Fig. 3 [32,33]. [Pg.726]

In suspension polymerization, liquid vinyl fluoride was suspended in water with the help of a dispersion stabilizer. Polymerization was initiated by an organic peroxide such as diisopropyl peroxydicarbonate below the critical temperature of vinyl fluoride.bo lb ] The reaction could also be initiated by ultraviolet light and ionizing radiation.VF dispersions were usually stabilized by water-soluble polymers such as cellulose derivatives like cellulose ester and sodium car-boxymethylcellulose, andpoly(vinyl alcohol). Inorganic salts such as magnesium carbonate, barium sulfate, and alkylsulfoacids were also used. [Pg.103]

Among the factors that affect column efficiency and selectivity are the structure of the mesogen (in relation to the solutes of interest), the phase type(s) and degree of ordering, temperature, column loading and coverage, concentration (solubility) effects, and the surface structure and specialized treatment of the support. The column surface can dramatically affect the orientation of the liquid crystalline molecules (especially for monomeric mesogens) and thus alter separation efficiency. For polymeric liquid... [Pg.890]

In mass polymerization bulk monomer is converted to polymers. In solution polymerization the reaction is completed in the presence of a solvent. In suspension, dispersed mass, pearl or granular polymerization the monomer, containing dissolved initiator, is polymerized while dispersed in the form of fine droplets in a second non-reactive liquid (usually water). In emulsion polymerization an aqueous emulsion of the monomer in the presence of a water-soluble initiator Is converted to a polymer latex (colloidal dispersion of polymer in water). [Pg.321]

Methacrylic acid 77 CH2 C(CH3)C00H 158 Colourless, water soluble liquid Polymerizes readily unless inhibited or stored <15°C Irritant... [Pg.251]

Vinyl acetate -8 CH3C00CH CH2 427 2.6-13.4 1.1 3.0 72 Colourless, partially water soluble liquid Faint odour Polymerizes with heat or organic peroxides... [Pg.251]

The main purpose of pesticide formulation is to manufacture a product that has optimum biological efficiency, is convenient to use, and minimizes environmental impacts. The active ingredients are mixed with solvents, adjuvants (boosters), and fillers as necessary to achieve the desired formulation. The types of formulations include wettable powders, soluble concentrates, emulsion concentrates, oil-in-water emulsions, suspension concentrates, suspoemulsions, water-dispersible granules, dry granules, and controlled release, in which the active ingredient is released into the environment from a polymeric carrier, binder, absorbent, or encapsulant at a slow and effective rate. The formulation steps may generate air emissions, liquid effluents, and solid wastes. [Pg.70]

The solubilities of the various gases in [BMIM][PFg] suggests that this IL should be an excellent candidate for a wide variety of industrially important gas separations. There is also the possibility of performing higher-temperature gas separations, thanks to the high thermal stability of the ILs. For supported liquid membranes this would require the use of ceramic or metallic membranes rather than polymeric ones. Both water vapor and CO2 should be removed easily from natural gas since the ratios of Henry s law constants at 25 °C are -9950 and 32, respectively. It should be possible to scrub CO2 from stack gases composed of N2 and O2. Since we know of no measurements of H2S, SO, or NO solubility in [BMIM][PFg], we do not loiow if it would be possible to remove these contaminants as well. Nonetheless, there appears to be ample opportunity for use of ILs for gas separations on the basis of the widely varying gas solubilities measured thus far. [Pg.91]

The effects of increasing the concentration of initiator (i.e., increased conversion, decreased M , and broader PDi) and of reducing the reaction temperature (i.e., decreased conversion, increased M , and narrower PDi) for the polymerizations in ambient-temperature ionic liquids are the same as observed in conventional solvents. May et al. have reported similar results and in addition used NMR to investigate the stereochemistry of the PMMA produced in [BMIM][PFgj. They found that the stereochemistry was almost identical to that for PMMA produced by free radical polymerization in conventional solvents [43]. The homopolymerization and copolymerization of several other monomers were also reported. Similarly to the findings of Noda and Watanabe, the polymer was in many cases not soluble in the ionic liquid and thus phase-separated [43, 44]. [Pg.326]


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See also in sourсe #XX -- [ Pg.474 , Pg.477 ]




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