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Water polyurethane

Applications of polyurethane are often in moist air and water. Polyurethanes are frequently used in acid or alkaline solutions even plain water is never actually neutral. Water is also present in the air and is absorbed into the polyurethane. [Pg.130]

Superabsorbents. Water-sweUable polymers are used extensively in consumer articles and for industrial appUcations. Most of these polymers are cross-linked acryUc copolymers of metal salts of acryUc acid and acrylamide or other monomers such as 2-acrylamido-2-methylpropanesulfonic acid. These hydrogel forming systems can have high gel strength as measured by the shear modulus (134). Sometimes inorganic water-insoluble powder is blended with the polymer to increase gel strength (135). Patents describe processes for making cross-linked polyurethane foams which contain superabsorbent polymers (136,137). [Pg.144]

Pentaerythritol in rosin ester form is used in hot-melt adhesive formulations, especially ethylene—vinyl acetate (EVA) copolymers, as a tackifier. Polyethers of pentaerythritol or trim ethyl ol eth an e are also used in EVA and polyurethane adhesives, which exhibit excellent bond strength and water resistance. The adhesives maybe available as EVA melts or dispersions (90,91) or as thixotropic, one-package, curable polyurethanes (92). Pentaerythritol spko ortho esters have been used in epoxy resin adhesives (93). The EVA adhesives are especially suitable for cellulose (paper, etc) bonding. [Pg.466]

Eyrol 51 is a water-soluble Hquid containing about 21% phosphoms. It is made by a multistep process from dimethyl methylphosphonate, phosphoms pentoxide, and ethylene oxide. The end groups are principally primary hydroxyl and the compound can thus be incorporated chemically into aminoplasts, phenoHc resins, and polyurethanes. Eyrol 51, or 58 if diluted with a small amount of isopropanol, is used along with amino resins to produce a flame-retardant resin finish on paper used for automotive air filters, or for backcoating of upholstery fabric to pass the British or California flammabiHty standards. [Pg.479]

Foams prepared from phenol—formaldehyde and urea—formaldehyde resins are the only commercial foams that are significantly affected by water (22). Polyurethane foams exhibit a deterioration of properties when subjected to a combination of light, moisture, and heat aging polyester-based foam shows much less hydrolytic stabUity than polyether-based foam (50,199). [Pg.415]

Commercial Construction. The same attributes desirable on residential constmction appHcations hold for commercial constmction as weU but insulation quaHty, permanence, moisture insensitivity, and resistance to free2e—thaw cycling in the presence of water are of greater significance. For this reason ceUular plastics have greater appHcation here. Both polystyrene and polyurethane foams are highly desirable roof insulations in commercial as in residential constmction. [Pg.416]

Industrially, polyurethane flexible foam manufacturers combine a version of the carbamate-forming reaction and the amine—isocyanate reaction to provide both density reduction and elastic modulus increases. The overall scheme involves the reaction of one mole of water with one mole of isocyanate to produce a carbamic acid intermediate. The carbamic acid intermediate spontaneously loses carbon dioxide to yield a primary amine which reacts with a second mole of isocyanate to yield a substituted urea. [Pg.452]

Water-Vapor Permeability. Water-vapor permeabiUty depends on the polymer used for the coating layer and its stmcture. Vinyl-coated fabrics have Httie water-vapor permeabiUty due to the coating layer. Although polyurethane polymer is water-vapor permeable, urethane-coated fabrics also have low permeabiUty values due to their soHd layer stmcture. On the other hand, man-made leathers have good permeabiUty values as high as that of leather due to their porous layer stmcture. The permeabiUty of grain-type is lower than that of suede-type, influenced by finishing method. [Pg.92]

In the wet system, manufacture proceeds as foUows (/) a 7—20% polyurethane solution of DMF is appHed onto a fabric and immersed in water containing 0—10% of DMF for coagulation (2) the coated fabric is washed and dried (4) the surface is finished by the dry system. For the substrate, a woven or knit fabric which has been bmshed on its surface is often used to improve appearance, resistance to grain break, and feel. [Pg.93]

In the second step, a papermaking method is also used for the fine fibers, less than 0.1 tex (1 den). This process is usually followed by a high pressure water jet process instead of the third step. In the fourth step, to obtain the required properties in specific appHcations, a polyurethane is selected out of the segmented polyurethanes, which comprises a polymer diol, a diisocyanate, and a chain extender (see Urethane polymers). A DMF—water bath for coagulation is also controlled to create the adequate pore stmcture in combination with fibers. [Pg.94]

Commonly used materials for cable insulation are poly(vinyl chloride) (PVC) compounds, polyamides, polyethylenes, polypropylenes, polyurethanes, and fluoropolymers. PVC compounds possess high dielectric and mechanical strength, flexibiUty, and resistance to flame, water, and abrasion. Polyethylene and polypropylene are used for high speed appHcations that require a low dielectric constant and low loss tangent. At low temperatures, these materials are stiff but bendable without breaking. They are also resistant to moisture, chemical attack, heat, and abrasion. Table 14 gives the mechanical and electrical properties of materials used for cable insulation. [Pg.534]

A hst of polyol producers is shown in Table 6. Each producer has a varied line of PPO and EOPO copolymers for polyurethane use. Polyols are usually produced in a semibatch mode in stainless steel autoclaves using basic catalysis. Autoclaves in use range from one gallon (3.785 L) size in research faciUties to 20,000 gallon (75.7 m ) commercial vessels. In semibatch operation, starter and catalyst are charged to the reactor and the water formed is removed under vacuum. Sometimes an intermediate is made and stored because a 30—100 dilution of starter with PO would require an extraordinary reactor to provide adequate stirring. PO and/or EO are added continuously until the desired OH No. is reached the reaction is stopped and the catalyst is removed. A uniform addition rate and temperature profile is required to keep unsaturation the same from batch to batch. The KOH catalyst can be removed by absorbent treatment (140), extraction into water (141), neutralization and/or crystallization of the salt (142—147), and ion exchange (148—150). [Pg.353]

R. L. Tabor, K.. Hiuze, R. D.. Priester, and R. B. Turner, "The Compatibikty of Water with Polyols," 34th Annual Polyurethane Technical Marketing Conference, New Orleans, La., Oct. 21—24,1992. [Pg.357]

The y -phenylenediamiaes are easily obtained by dinitrating, followed by catalyticaHy hydrogenating, an aromatic hydrocarbon. Thus, the toluenediamiaes are manufactured by nitrating toluene with a mixture of sulfuric acid, nitric acid, and 23% water at 330°C which first produces a mixture (60 40) of the ortho and para mononitrotoluenes. Further nitration produces the 80 20 mixture of 2,4- and 2,6-dinitrotoluene. Catalytic hydrogenation produces the commercial mixture of diamiaes which, when converted to diisocyanates, are widely used ia the production of polyurethanes (see Amines, aromatic, DIAMINOTOLUENES) (22). [Pg.255]

For other recreational surfaces, such as mnning tracks, the installation techniques are quite different. Most are poured-in-place. An interlocking tile technique may be employed for tennis courts. In all cases, adequate provision for weathering and water drainage is essential. In general, the resiHent surfaces are installed over a hard base (see Fig. 4) that contains the necessary curbs to provide the finished level. Outdoors, asphalt is the most common base, and indoors, concrete. A poured-in-place polyurethane surface (14) is mixed on-site and cast from at least two components, an isocyanate and a filled... [Pg.536]

Sucrose acrylate derivatives can be converted into polymers and hydrogels that can be used as flocculants, water adsorbents, bioimplantables, and dmg dehvery devices (42). Sucrose ethers have appHcations as surfactants and surface coatings, and as feedstocks for synthesis of polyurethane foams and... [Pg.5]


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See also in sourсe #XX -- [ Pg.28 , Pg.45 , Pg.118 ]




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Hydrophilic polyurethanes, water solubility

Polyurethane water-based

Polyurethane water-swelling

Polyurethane, water-reducible

Polyurethanes water-borne

Special Features of Water-Dispersed Polyurethane Elastomers

Water Dispersions of Polyurethane Elastomers

Water aqueous polyurethane dispersions

Water polyurethanes solubility

Water vapour permeable polyurethanes

Water, interaction with polyurethanes

Water-borne polyurethane coatings

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