Polymer dispersion

The introduction of monomers containing polar groups such as tertiary amines, imidazoles, pyrrolidones, pyridines, etc., gives the polymer dispersant properties that will be discussed in the article on dispersant additives for lubricants. 

C2.2.4.5 POLYMER DISPERSED LIQUID CRYSTAL (PDLC) DISPLAYS... 

Figure C2.2.14. Principle of operation of a polymer-dispersed liquid crystal display. The contours of the liquid...

Simoni F 1997 Nonlinear Optical Properties of Liquid Crystals and Polymer-Dispersed Liquid Crystals (Singapore World Scientific)... 

These monomers provide a means for introducing carboxyl groups into copolymers. In copolymers these acids can improve adhesion properties, improve freeze-thaw and mechanical stability of polymer dispersions, provide stability in alkalies (including ammonia), increase resistance to attack by oils, and provide reactive centers for cross-linking by divalent metal ions, diamines, or epoxides. 

Fig. 17. Polymer dispersed Hquid crystal display (PDLC). (a) U < clear state, where U) is the threshold voltage of the ceU. and rij represent the indexes of refraction for light polarized parallel and perpendicular to the director of the Hquid crystal represents the index of refraction of the isotropic...

Almost all synthetic binders are prepared by an emulsion polymerization process and are suppHed as latexes which consist of 48—52 wt % polymer dispersed in water (101). The largest-volume binder is styrene—butadiene copolymer [9003-55-8] (SBR) latex. Most SBRlatexes are carboxylated, ie, they contain copolymerized acidic monomers. Other latex binders are based on poly(vinyl acetate) [9003-20-7] and on polymers of acrylate esters. Poly(vinyl alcohol) is a water-soluble, synthetic biader which is prepared by the hydrolysis of poly(viayl acetate) (see Latex technology Vinyl polymers). 

Bicomponent technology has been used to introduce functional and novelty effects other than stretch to nylon fibers. For instance, antistatic yams are made by spinning a conductive carbon-black polymer dispersion as a core with a sheath of nylon (188) and as a side-by-side configuration (189). At 0.1—1.0% implants, these conductive filaments give durable static resistance to nylon carpets without interfering with dye coloration. Conductive materials such as carbon black or metals as a sheath around a core of nylon interfere with color, especially light shades. 

The most effective and widely used dispersants are low molecular weight anionic polymers. Dispersion technology has advanced to the point at which polymers are designed for specific classes of foulants or for a broad spectmm of materials. Acrylate-based polymers are widely used as dispersants. They have advanced from simple homopolymers of acryflc acid to more advanced copolymers and terpolymers. The performance characteristics of the acrylate polymers are a function of their molecular weight and stmcture, along with the types of monomeric units incorporated into the polymer backbone. 

All such resin solutions are based on flammable solvents and are becoming increasingly less acceptable on health and safety grounds. There is therefore increased interest in water-based polymer dispersion floor sealers, but, to date, none offer the same improvement to flooring performance that some of the resin solutions can provide. 

Polyvinyl acetate (PVA), acrylic and other polymer dispersions have been widely used as anti-dust treatments for concrete floors for many years. In general, the polymer dispersions have been similar to those used in the manufacture of emulsion paints, and until recently have tended to be based on dispersions of relatively large polymer particles (particle size 0.15-0.25 x 10 m). Dispersions are now becoming available which offer superior performance as floor sealers. The chemical and water resistance of the various polymer dispersions which have been used in the past vary considerably from the PVA types, which are rapidly softened and eventually washed out by water, to acrylic and SBR types which exhibit excellent resistance to a wide range of chemicals. Water-based sealers are gaining wider acceptance because of... 

A similar thing takes place when we consider flow curves obtained at different temperatures. As seen from Fig. 7, if we take a region of low shear rates, then due to the absence of the temperature dependence Y, the apparent activation energy vanishes. At sufficiently high shear rates, when a polymer dispersion medium flows, the activation energy becomes equal to the activation energy of the viscous flow of a polymer melt and the presence of the filler in this ratio is of little importance. 

The value for total hardness is achieved only by the use of suitable external pretreatment plants. It is essential that such plants be properly maintained. It is also recommended that a suitable polymer dispersant be used to ensure clean heat-transfer surfaces. 

Low iron levels in the feed are essential to avoid damage to the electrode from iron deposition. This is achieved only by correct condensate line corrosion treatment. Polymer dispersants should be fed direct to the feed line and boiler to ensure particulate iron is effectively removed with the BD. 

Salts of alkyl phosphates and types of other surfactants used as emulsifiers and dispersing agents in polymer dispersions are discussed with respect to the preparation of polymer dispersions for use in the manufactoring and finishing of textiles. Seven examples are presented to demonstrate the significance of surfactants on the properties, e.g., sedimentation, wetting behavior, hydrophilic characteristics, foaming behavior, metal adhesion, and viscosity, of polymer dispersions used in the textile industry [239]. 

Chitosan has been associated with other biopolymers and with synthetic polymer dispersions to produce wound dressings. Biosynthetic wound dressings composed of a spongy sheet of chitosan and collagen, laminated with a gentamicyn sulphate-impregnated polyurethane membrane, have been produced and clinically tested with good results. 

Similar behaviour has been observed by Emerson and Zannoni [112] in their simulations of polymer dispersed liquid crystal droplets where the solid... 

Fig. 20a-c. Equatorial sections through polymer dispersed Gay-Berne liquid crystal droplets of various radii at high T = 3.0) (left) and low T = 0.6) (right) scaled temperatures for droplets with scaled radii of a 7.1 b 10.0 c 20.0... 

A surface is that part of an object which is in direct contact with its environment and hence, is most affected by it. The surface properties of solid organic polymers have a strong impact on many, if not most, of their apphcations. The properties and structure of these surfaces are, therefore, of utmost importance. The chemical stmcture and thermodynamic state of polymer surfaces are important factors that determine many of their practical characteristics. Examples of properties affected by polymer surface stmcture include adhesion, wettability, friction, coatability, permeability, dyeabil-ity, gloss, corrosion, surface electrostatic charging, cellular recognition, and biocompatibility. Interfacial characteristics of polymer systems control the domain size and the stability of polymer-polymer dispersions, adhesive strength of laminates and composites, cohesive strength of polymer blends, mechanical properties of adhesive joints, etc. 

Residual monomers in polymer dispersions, alcohol and toxic substances in blood, olfactory substances in milk. 

An aqueous colloidal polymeric dispersion by definition is a two-phase system comprised of a disperse phase and a dispersion medium. The disperse phase consists of spherical polymer particles, usually with an average diameter of 200-300 nm. According to their method of preparation, aqueous colloidal polymer dispersions can be divided into two categories (true) latices and pseudolatices. True latices are prepared by controlled polymerization of emulsified monomer droplets in aqueous solutions, whereas pseudolatices are prepared starting from already polymerized macromolecules using different emulsification techniques. 

J Wang, I Ghebre-Sellassie. Aqueous polymer dispersions as film formers. In HA Lieberman, MM Rieger, GS Banker, eds. Pharmaceutical Dosage Forms Disperse Systems, Yol. 3. 2nd ed. New York Marcel Dekker, 1998, pp 129-161. 

All of these intermolecular forces influence several properties of polymers. Dispersion forces contribute to the factors that result in increased viscosity as molecular weight increases. Crystalline domains arise in polyethylene because of dispersion forces. As you will learn later in the text, there are other things that influence both viscosity and crystallization, but intermolecular forces play an important role. In polar polymers, such as polymethylmethacrylate, polyethylene terephthalate and nylon 6, the presence of the polar groups influences crystallization. The polar groups increase the intensity of the interactions, thereby increasing the rate at which crystalline domains form and their thermal stability. Polar interactions increase the viscosity of such polymers compared to polymers of similar length and molecular weight that exhibit low levels of interaction. 

Wetting polymer surfaces with ethylene glycol (92) or isopropanol (93) has also been used as a means of promoting rapid polymer dispersion prior to the onset of hydration. 

There are five prime factors that determine the properties of starches 1. starch is a polymer of glucose (dextrose) 2. the starch polymer is of two types linear and branched 3 the linear polymeric molecules can associate with each other giving insolubility in water 4. the polymeric molecules are organized and packed into granules which are insoluble in water and 5 disruption of the granule structure is required to render the starch polymer dispersible in water. The modification of starch takes into account these factors. 

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