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Resistivity poly acetals

Poly acetals are highly crystalline polymers. The number of repeating units ranges from 500 to 3,000. They are characterized by high impact resistance, strength, and a low friction coefficient. [Pg.341]

Sulfone-hased polymers show a very good resistance to prolonged chlorine exposure at elevated temperatures. The weight change after an exposure of 6 months to static chlorinated water at 60°C at chlorine levels of up to 30 ppm is essentially zero for Udel , whereas e.g., poly(acetal) exhibits a weight loss of ca. 5% at 30 ppm chlorine in water after 6 months. This property suggests applications in water delivery systems. [Pg.257]

Under conditions of extreme acidity or alkalinity, acryhc ester polymers can be made to hydroly2e to poly(acryhc acid) or an acid salt and the corresponding alcohol. However, acryhc polymers and copolymers have a greater resistance to both acidic and alkaline hydrolysis than competitive poly(vinyl acetate) and vinyl acetate copolymers. Even poly(methyl acrylate), the most readily hydroly2ed polymer of the series, is more resistant to alkah than poly(vinyl acetate) (57). Butyl acrylate copolymers are more hydrolytically stable than ethyl acrylate copolymers (58). [Pg.164]

Tetraethylene glycol may be used direcdy as a plasticizer or modified by esterification with fatty acids to produce plasticizers (qv). Tetraethylene glycol is used directly to plasticize separation membranes, such as siHcone mbber, poly(vinyl acetate), and ceUulose triacetate. Ceramic materials utilize tetraethylene glycol as plasticizing agents in resistant refractory plastics and molded ceramics. It is also employed to improve the physical properties of cyanoacrylate and polyacrylonitrile adhesives, and is chemically modified to form polyisocyanate, polymethacrylate, and to contain siHcone compounds used for adhesives. [Pg.363]

Other Polymers. Besides polycarbonates, poly(methyl methacrylate)s, cycfic polyolefins, and uv-curable cross-linked polymers, a host of other polymers have been examined for their suitabiUty as substrate materials for optical data storage, preferably compact disks, in the last years. These polymers have not gained commercial importance polystyrene (PS), poly(vinyl chloride) (PVC), cellulose acetobutyrate (CAB), bis(diallylpolycarbonate) (BDPC), poly(ethylene terephthalate) (PET), styrene—acrylonitrile copolymers (SAN), poly(vinyl acetate) (PVAC), and for substrates with high resistance to heat softening, polysulfones (PSU) and polyimides (PI). [Pg.162]

The web materials used to form dmms and cans can be customized to each packaging apphcation. The materials are selected based on the package properties of moisture and humidity resistance, nonstick resistance, or barrier properties required. The adhesives used to bond the phes together include sihcates, poly(vinyl alcohol), and poly(vinyl acetate) (10). Sihcate adhesives are most commonly used in the manufacture of dmm packages. [Pg.519]

Small amounts of TAIC together with DAP have been used to cure unsaturated polyesters in glass-reinforced thermo sets (131). It has been used with polyfunctional methacrylate esters in anaerobic adhesives (132). TAIC and vinyl acetate are copolymerized in aqueous suspension, and vinyl alcohol copolymer gels are made from the products (133). Electron cure of poly(ethylene terephthalate) moldings containing TAIC improves heat resistance and transparency (134). [Pg.88]

Vinyl Acetate—Ethylene Copolymers. In these random copolymers, the ratio of ethylene to vinyl acetate (EVA) is varied from 30—60%. As the vinyl acetate content increases, the oil and heat resistance increases. With higher ethylene content the physical strength, tensile, and tear increases. The polymers are cured with peroxide. The main properties of these elastomers include heat resistance, moderate oil and solvent resistance, low compression set, good weather resistance, high damping, exceUent o2one resistance, and they can be easily colored (see Vinyl polymers, poly(VINYL acetate)). [Pg.234]

Poly(ethyl methacrylate) (PEMA) yields truly compatible blends with poly(vinyl acetate) up to 20% PEMA concentration (133). Synergistic improvement in material properties was observed. Poly(ethylene oxide) forms compatible homogeneous blends with poly(vinyl acetate) (134). The T of the blends and the crystaUizabiUty of the PEO depend on the composition. The miscibility window of poly(vinyl acetate) and its copolymers with alkyl acrylates can be broadened through the incorporation of acryUc acid as a third component (135). A description of compatible and incompatible blends of poly(vinyl acetate) and other copolymers has been compiled (136). Blends of poly(vinyl acetate) copolymers with urethanes can provide improved heat resistance to the product providing reduced creep rates in adhesives used for vinyl laminating (137). [Pg.467]

Poly(vinyl acetate) emulsions are excellent bases for water-resistant paper adhesives destined for use in manufacturing bags, tubes, and cartons. Glue-lap adhesives, which require moderate-to-high resistance to water, exemplify this type. When routine water resistance is required, a homopolymer vinyl acetate emulsion containing a ceUulosic protective coUoid is effective for most purposes. Next effective are emulsions containing fuUy hydrolyzed poly(vinyl alcohol) as a protective coUoid, foUowed by those containing partiaUy hydrolyzed poly(vinyl acetate). [Pg.469]

In contrast to other polymers the resistance to water permeation is low due to the hydrolysis of the poly(vinyl acetate) (163,164). Ethylene copolymers have been developed which have improved water resistance and waterproofness. The polymer can be used in the latex form or in a spray-dried form which can be preblended in with the cement (qv) in the proper proportion. The compressive and tensile strength of concrete is improved by addition of PVAc emulsions to the water before mixing. A polymer-soHds-to-total-soHds ratio of ca 10 90 is best. The emulsions also aid adhesion between new and old concrete when patching or resurfacing. [Pg.471]


See other pages where Resistivity poly acetals is mentioned: [Pg.502]    [Pg.504]    [Pg.442]    [Pg.88]    [Pg.94]    [Pg.132]    [Pg.95]    [Pg.198]    [Pg.233]    [Pg.378]    [Pg.378]    [Pg.487]    [Pg.523]    [Pg.546]    [Pg.262]    [Pg.10]    [Pg.230]    [Pg.164]    [Pg.449]    [Pg.450]    [Pg.454]    [Pg.463]    [Pg.463]    [Pg.463]    [Pg.468]    [Pg.469]    [Pg.470]    [Pg.470]    [Pg.470]    [Pg.471]    [Pg.471]    [Pg.477]    [Pg.488]    [Pg.489]    [Pg.433]    [Pg.296]    [Pg.331]    [Pg.102]   
See also in sourсe #XX -- [ Pg.91 ]




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