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Polymers and water

The choice of the alcohol permits manipulation of the structure of the polymer. Water and monohydric alcohols afford linear chains with carboxylic acid and ester end groups, respectively. Polyhydroxy initiators afford a route to ester end-blocked star and comb polymers (Fig. 4) (47). [Pg.79]

K., The correlation of polymer-water and octanol-water coefficients Estimation of drug solubilities in polymers, Int. J. Pharm., 45, 1-11, 1988. [Pg.116]

The polymer, water and monomer phases were heated externally and added to the reactor (previously purged with nitrogen). After thermal equilibrium (estabishment of steady state heat loss) and chemical equilibrium the reaction was initiated by a... [Pg.319]

An advantage of defining the problem in this manner is that the partition coefficient has become a central property in quantitative structure-activity relationships (QSAR) and a large data base of P values is available in the medicinal chemistry literature (22-24). In particular, if a correlation (Equation 15) between the polymer-water and octanol-water partition coefficients can be established for a series of solutes, it becomes possible to utilize log P (oc-tanol/water) value as a reference point from which to calculate the polymer-water value. [Pg.61]

This equation well describes the relation between water content of potato starch and Tg as given in Figure 16.3a the relation is less perfect for several other binary mixtures. Many low-moisture foods are mixtures of polymers, water, and several other small-molecule components. Prediction of Tg from composition then is generally uncertain in practice a (narrow) transition range rather than a sharp transition point is often observed. [Pg.675]

The introduction of polymer-water and water-water interactions are important in the modelling of the temperature-concentration behaviour of poly(ethylene oxide) [92]. This suggests that the strong and highly directional hydrogen bond formation in these systems seems to be more important than the hydrophobic interactions. It would of particular interest to know whether high pressure simulations support this hypothesis. [Pg.16]

A continuous dry spinning process has been developed where a solution of polymer, water, and salt is extruded into a gaseous medium [30]. The gaseous medium removes at least 25% weight percent of the solvent from the fiber. Then the fiber is quenched in an aqueous solution. After the fiber is conditioned, the fiber is eventually drawn. [Pg.305]

Nanocapsules consisting of the block copolymer as shell and with a liquid as core could be obtained by adding hexadecane, which is a nonsolvent for the copolymer. The block copolymer was dissolved in a mixture of chloroform and hexadecane. During evaporation of the chloroform there is a phase separation of the block copolymer and the hexadecane, and a microphase separation of the block copolymer itself. For the successful formation of nanocapsules, the interfacial tensions for the polymer/water and water/hexadecane interfaces are important. [Pg.178]

In the case that the concentration of SDS is high enough to give full coverage of the interfaces with surfactant, there are similar interfacial tensions for the polymer/ water and hexadecane/water interfaces and Janus-like particles consisting of PS-b-PMMA and liquid hexadecane are formed in the aqueous phase. After drying (and therefore complete removal of the liquid hexadecane), a half-spherical morphology is obtained as verified by electron microscopy (Fig. 54b). Please note that in this case, the copolymer is seen as one phase. [Pg.178]

The location of the rear of the oil bank at tp is determined by making a material balance on the water phase. Fig. 5.61 is a generalize saturation profile for the displacement of the oil bank by the drive water after the polymer flood front has been overtaken. The total volume of water injected (polymer water and drive water) is given by... [Pg.40]

A connate water bank forms ahead of the polymer water and the "strength Sj, of this bank is given by the intersection of the above described tangent with the normal water fractional flow curve (Fig. 3). This connate water bank front travels with velocity... [Pg.242]

IR Butyl Isobutylene, Isoprene, polymer Water and steam Petroleum solvents, coal, tar, solvents, aromatic hydrocarbons... [Pg.43]

Uses Tackiflerfor SBR, natural mbber, butyl mbber, ethylene-vinyl acetate and other polymers, water and solv.-based constmetion adhesives, pressure-sensitive, sealant, hot-melt and rubber compding. tbod-pkg. adhesives, rubber articles defoamer In food-contact paper/paperboard Regulatory FDA 21CFR 175.105,176.210,177.2600 Properties Gardner 9 flakes, solid, or soi n. sol. in aromatic, aliphatic, and chlorinated soivs. sol. > 50% in ethanol, propanol, IPA insol. in water dens. 8.8 Ib/gal vise. (Gardner) Z (75% in min. spirits) soften, pt. (R B) 80 C acid no. 140 Has Unitan-L [Universal Preserv-A-Chem]... [Pg.1201]


See other pages where Polymers and water is mentioned: [Pg.358]    [Pg.157]    [Pg.327]    [Pg.206]    [Pg.146]    [Pg.266]    [Pg.163]    [Pg.141]    [Pg.375]    [Pg.38]    [Pg.1454]    [Pg.290]    [Pg.206]    [Pg.195]    [Pg.279]    [Pg.282]    [Pg.692]    [Pg.621]    [Pg.9]    [Pg.93]    [Pg.601]    [Pg.821]    [Pg.248]    [Pg.376]    [Pg.413]    [Pg.9]   
See also in sourсe #XX -- [ Pg.772 ]




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Polymers in Water Collection and Storage

Polymers in Water Handling and Management

Polymers in water and

Some water-soluble polymers used in pharmacy and medicine

Tension Between Polymer Surface and Liquid Water

Water polymers

Water-Based Polymers and Emulsions

Water-insoluble polymers and polymer membranes

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