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Water-soluble polymers also

A number of the water-soluble polymers also have adhesive properties which are being extensively evaluated for drug delivery (9). These polymers will adhere to the mucous coating in the gastrointestinal tract, the nose, and the mouth to delay passage and sustain drug release. Those polymers with the best adhesive properties are those with hydroxyl and carboxyl groups. Table II lists some of the bioadhesive polymers and their adhesive properties. [Pg.21]

DNA is a negatively charged polyelectrolyte and so sticks to positively charged surfaces, but not hydrophobic surfaces. Ions and water-soluble polymers also do not stick to hydrophobic surfaces. [Pg.109]

Dichromated Resists. The first compositions widely used as photoresists combine a photosensitive dichromate salt (usually ammonium dichromate) with a water-soluble polymer of biologic origin such as gelatin, egg albumin (proteins), or gum arabic (a starch). Later, synthetic polymers such as poly(vinyl alcohol) also were used (11,12). Irradiation with uv light (X in the range of 360—380 nm using, for example, a carbon arc lamp) leads to photoinitiated oxidation of the polymer and reduction of dichromate to Ct(III). The photoinduced chemistry renders exposed areas insoluble in aqueous developing solutions. The photochemical mechanism of dichromate sensitization of PVA (summarized in Fig. 3) has been studied in detail (13). [Pg.115]

Solubility. Poly(ethylene oxide) is completely soluble in water at room temperature. However, at elevated temperatures (>98° C) the solubiUty decreases. It is also soluble in several organic solvents, particularly chlorinated hydrocarbons (see Water-SOLUBLE polymers). Aromatic hydrocarbons are better solvents for poly(ethylene oxide) at elevated temperatures. SolubiUty characteristics are Hsted in Table 1. [Pg.337]

There have been numerous communications on the subject of biodegradation test methods, including aerobic compost (30), anaerobic bioreactor (31), general methodology and future directions (32—34), and a fine review article (24). ASTM (22) and MITI (35) have also set forth standard testing protocols for plastics, as shown in Table 2, whereas OECD test methods (29) are more suited to water-soluble polymers. [Pg.475]

Resin Solubilizers. In general, water-soluble resins ate amine salts of acidic polymers. Water-soluble coatings formulated with AMP-95 and DMAMP-80 exhibit superior performance (15,16) (see Water-SOLUBLE polymers). AMP-95, used in conjunction with associative thickeners (17) or hydroxy-ethylceUulose, provides for the most efficient utilization of such thickeners. It also is the neutralizer of choice for use with hair spray resins. [Pg.19]

The alkaline solutions can remove water-soluble polymers in the spinning mix and inert products such as titanium dioxide. Basic treatments can also hydroly2e a certain amount of the polyester itself. For some silk-like appHcations or for producing fine denier fabrics, this basic treatment can produce a 10—30% weight loss of polyester (190,196). Certain polyesters such as anionically modified polyester can undergo more rapid weight loss than regular polyester (189). [Pg.449]

Water-soluble polymers and polyelectrolytes (e.g., polyethylene glycol, polyethylene imine polyacrylic acid) have been used success-hilly in protein precipitations, and there has been some success in affinity precipitations wherein appropriate ligands attached to polymers can couple with the target proteins to enhance their aggregation. Protein precipitation can also be achieved using pH adjustment, since proteins generally exhibit their lowest solubility at their isoelectric point. Temperature variations at constant salt concentration allow for frac tional precipitation of proteins. [Pg.2060]

The polymers are of interest as water-soluble packaging films for a wide variety of domestic and industrial materials. (Additional advantages of the poly(ethylene oxide)s are that they remain dry to the feel at high humidities and may be heat sealed.) The materials are also of use in a number of solution application such as textile sizes and thickening agents. As a water-soluble film they are competitive with poly(vinyl alcohol) whereas in their solution applications they meet competition from many longer established natural and synthetic water-soluble polymers. [Pg.547]

Water-soluble polymers eomprise a major elass of polymerie materials and are used in a wide variety of applieations. Synthetie water-soluble polymers inelude poly(vinyl aleohol), poly(aerylamide), poly(aerylie aeid), poly(ethylene oxide), poly(vinyl pyrrolidone), eellulosies, and many eopolymers of these types. Their end uses are quite varied and their applieations depend mainly on their viseosify-ing, rheologieal, and surfaee-aetive properties (1). For example, poly (vinyl aleohol) is used in adhesives, fibers, textile and paper sizing, paekaging, as a stabilizer for emulsion polymerization, and as a preeursor for the manufaeture of poly(vinyl butyral), whieh is used in automotive windshields. Poly(vinyl aleohol) is also the world s largest volume, eommodity, water-soluble polymer. [Pg.559]

The ehemistry of water-soluble polymers ean take various forms. These polymers ean be anionie, cationie, or nonionie. Their polymer baekbone ean eontain hydrophilie and hydrophobie pendant groups. Branehing and polymer stereoregularity also play a role in the physieal behavior of these materials. [Pg.559]

The use of nonpolymeric, column supports has also been a popular way to characterize water-soluble polymers. Synchropak SEC columns from Micra... [Pg.571]

The use of bonded, silica column supports has also become a useful way to characterize cationic, water-soluble polymers. CATSEC SEC columns from Micra Scientific contain a silica support with a polymerized polyamine-bonded phase. This imparts a cationic surface charge on the packing that can be... [Pg.573]

Interest in the chemistry of water-soluble polymers (polyelectrolytes) has been continually increasing during the past 45 years. The tremendous scope of utility for water-soluble polymers has led to a vigorous search for new materials and the rapid development of polyelectrolytes into a dynamic field of industrial research. Growth in this field has been especially rapid since 1960 and today, many companies are engaged in synthesis and applications research on polyelectrolytes that are primarily used in four main marketing areas water treatment, paper, textiles, and oil recovery [1]. Polyacrylamide gel was also used as soil conditioner [2-4]. [Pg.119]

The qualitative thermodynamic explanation of the shielding effect produced by the bound neutral water-soluble polymers was summarized by Andrade et al. [2] who studied the interaction of blood with polyethylene oxide (PEO) attached to the surfaces of solids. According to their concept, one possible component of the passivity may be the low interfacial free energy (ysl) of water-soluble polymers and their gels. As estimated by Matsunaga and Ikada [3], it is 3.7 and 3.1 mJ/m2 for cellulose and polyvinylalcohol whereas 52.6 and 41.9 mJ/m2 for polyethylene and Nylon 11, respectively. Ikada et al. [4] also found that adsorption of serum albumin increases dramatically with the increase of interfacial free energy of the polymer contacting the protein solution. [Pg.137]

Various substituted styrenes have been also polymerized by NMP. These include 1 03-1 07, p-chloromethylstyrene (108), p-halostyrenes, and p-aceloxystyrene. Vinyl pyridines (e.g. 109) are amenable to NMP21 and may be quaternized post-polymerization to provide water-soluble polymers. [Pg.480]


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Soluble polymers

Water polymers

Water-soluble polyme

Water-soluble polymers

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