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Poly manufacture

Four other groups of synthetic adhesives find uses in secondary processing, ie, overlaying, assembly gluing, etc, and in furniture and cabinet manufacture. Poly(vinyl acetate) (PVA) adhesives are widely used in appHcation of veneers and other overlays to panel substrates and in some unit-assembly operations. PVA adhesives are an emulsion of polyvinyl acetate in water and cure by loss of water. The PVA adhesives are somewhat... [Pg.378]

Vinyl Fluoride. Vinyl fluoride [75-02-5] C2H2F, the monomer for poly(vinyl fluoride), is manufactured by addition of hydrogen fluoride to acetylene (see Fluorine COMPOUNDS, ORGANIC, POLY(viNYL FLUORIDE)). [Pg.102]

Uses. The largest uses of butanediol are internal consumption in manufacture of tetrahydrofuran and butyrolactone (145). The largest merchant uses are for poly(butylene terephthalate) resins (see Polyesters,thermoplastic) and in polyurethanes, both as a chain extender and as an ingredient in a hydroxyl-terminated polyester used as a macroglycol. Butanediol is also used as a solvent, as a monomer for vadous condensation polymers, and as an intermediate in the manufacture of other chemicals. [Pg.109]

The major use of vinylpyrrohdinone is as a monomer in manufacture of poly(vinylpyrrohdinone) (PVP) homopolymer and in various copolymers, where it frequendy imparts hydrophilic properties. When PVP was first produced, its principal use was as a blood plasma substitute and extender, a use no longer sanctioned. These polymers are used in pharmaceutical and cosmetic appHcations, soft contact lenses, and viscosity index improvers. The monomer serves as a component in radiation-cured polymer compositions, serving as a reactive diluent that reduces viscosity and increases cross-linking rates (see... [Pg.114]

Table 6 shows the sales estimates for principal film and sheet products for the year 1990 (14). Low density polyethylene films dominate the market in volume, followed by polystyrene and the vinyls. High density polyethylene, poly(ethylene terephthalate), and polypropylene are close in market share and complete the primary products. A number of specialty resins are used to produce 25,000—100,000 t of film or sheet, and then there are a large number of high priced, high performance materials that serve niche markets. The original clear film product, ceUophane, has faUen to about 25,000 t in the United States, with only one domestic producer. Table 7 Hsts some of the principal film and sheet material manufacturers in the United States. Table 6 shows the sales estimates for principal film and sheet products for the year 1990 (14). Low density polyethylene films dominate the market in volume, followed by polystyrene and the vinyls. High density polyethylene, poly(ethylene terephthalate), and polypropylene are close in market share and complete the primary products. A number of specialty resins are used to produce 25,000—100,000 t of film or sheet, and then there are a large number of high priced, high performance materials that serve niche markets. The original clear film product, ceUophane, has faUen to about 25,000 t in the United States, with only one domestic producer. Table 7 Hsts some of the principal film and sheet material manufacturers in the United States.
Mixed Metal Antimony Synergists Worldwide scarcities of antimony have prompted manufacturers to develop synergists that contain less antimony. Other metals have been found to work in concert with antimony to form a synergist that is as effective as antimony alone. Thermoguard CPA from Elf Atochem NA, which contains zinc in addition to antimony, can be used instead of antimony oxide in flexible poly(vinyl chloride) (PVC) as well as some polyolefin appHcations. The Oncor and AZ products which contain siUcon, zinc, and phosphoms from Anzon Inc. can be used in a similar manner. The mixed metal synergists are 10 to 20% less expensive than antimony trioxide. [Pg.455]

Poly etrafluoroethylene is manufactured and sold in three forms granular, fine powder, and aqueous dispersion each requires a different fabrication technique. Granular resins are manufactured in a wide variety of grades to obtain a different balance between powder flows and end use properties (Pig. 1). Pine powders that are made by coagulating aqueous dispersions also are available in various grades. Differences in fine powder grades correspond to their usefulness in specific appHcations and to the ease of fabrication. Aqueous dispersions are sold in latex form and are available in different grades. A variety of formulation techniques are used to tailor these dispersions for specific appHcations. [Pg.349]

Physical Stabilization Process. Cellulai polystyrene [9003-53-6] the outstanding example poly(vinyl chloride) [9002-86-2] copolymers of styrene and acrylonitrile (SAN copolymers [9003-54-7]) and polyethylene [9002-88-4] can be manufactured by this process. [Pg.405]

Physical Stabilization Process. CeUular polystyrene, ceUulose acetate, polyolefins, and poly(vinyl chloride) can be manufactured by this... [Pg.406]

Manufacture. The manufacture of 1,4-cyclohexanedimethanol can be accompHshed by the catalytic reduction under pressure of dimethyl terephthalate ia a methanol solution (47,65). This glycol also may be prepared by the depolymerization and catalytic reduction of linear polyesters that have alkylene terephthalates as primary constituents. Poly(ethylene terephthalate) may be hydrogenated ia the presence of methanol under pressure and heat to give good yields of the glycol (see Polyesters) (66,67). [Pg.374]

Vinyl fluoride (fluoroethene), is manufactured from the cataly2ed addition of hydrogen fluoride to acetylene. It is used to prepare poly(vinyl fluoride) which has found use in highly weather-resistant films (Tedlar film, Du Pont). Poly(vinyhdene fluoride) also is used in weather-resistant coatings (see Eluorine compounds, organic). The monomer can be prepared from acetylene, hydrogen fluoride, and chlorine but other nonacetylenic routes are available. [Pg.393]

Applications. Among the P—O- and P—N-substituted polymers, the fluoroalkoxy- and aryloxy-substituted polymers have so far shown the greatest commercial promise (14—16). Both poly[bis(2,2,2-trifluoroethoxy)phosphazene] [27290-40-0] and poly(diphenoxyphosphazene) [28212-48-8] are microcrystalline, thermoplastic polymers. However, when the substituent symmetry is dismpted with a randomly placed second substituent of different length, the polymers become amorphous and serve as good elastomers. Following initial development of the fluorophosphazene elastomers by the Firestone Tire and Rubber Co., both the fluoroalkoxy (EYPEL-F) and aryloxy (EYPEL-A) elastomers were manufactured by the Ethyl Corp. in the United States from the mid-1980s until 1993 (see ELASTOLffiRS,SYNTHETic-PHOSPHAZENEs). [Pg.257]

Three generations of latices as characterized by the type of surfactant used in manufacture have been defined (53). The first generation includes latices made with conventional (/) anionic surfactants like fatty acid soaps, alkyl carboxylates, alkyl sulfates, and alkyl sulfonates (54) (2) nonionic surfactants like poly(ethylene oxide) or poly(vinyl alcohol) used to improve freeze—thaw and shear stabiUty and (J) cationic surfactants like amines, nitriles, and other nitrogen bases, rarely used because of incompatibiUty problems. Portiand cement latex modifiers are one example where cationic surfactants are used. Anionic surfactants yield smaller particles than nonionic surfactants (55). Often a combination of anionic surfactants or anionic and nonionic surfactants are used to provide improved stabiUty. The stabilizing abiUty of anionic fatty acid soaps diminishes at lower pH as the soaps revert to their acids. First-generation latices also suffer from the presence of soap on the polymer particles at the end of the polymerization. Steam and vacuum stripping methods are often used to remove the soap and unreacted monomer from the final product (56). [Pg.25]

Lead sesquioxide is used as an oxidation catalyst for carbon monoxide ia exhaust gases (44,45) (see Exhaust control), as a catalyst for the preparation of lactams (46) (see Antibiotics, P-lactams), ia the manufacture of high purity diamonds (47) (see Carbon, diamond-natural), ia fireproofing compositions for poly(ethylene terephthalate) plastics (48), ia radiation detectors for x-rays and nuclear particles (49), and ia vulcanization accelerators for neoprene mbber (50). [Pg.69]

About 35% of total U.S. LPG consumption is as chemical feedstock for petrochemicals and polymer iatermediates. The manufacture of polyethylene, polypropylene, and poly(vinyl chloride) requires huge volumes of ethylene (qv) and propylene which, ia the United States, are produced by thermal cracking/dehydrogenation of propane, butane, and ethane (see Olefin polymers Vinyl polymers). [Pg.187]

Although synthetic lubrication oil production amounts to only about 2% of the total market, volume has been increasing rapidly (67). Growth rates of the order of 20% per year for poly( a-olefin)s, 10% for polybutenes, and 8% for esters (28) reflect increasing automotive use and these increases would accelerate if synthetics were adopted for factory fill of engines by automotive manufacturers. The estimated production of poly( a-olefin)s for lubricants appears to be approximately 100,000 m /yr, esters 75,000, poly(alkylene glycol)s 42,000, polybutenes 38,000, phosphates 20,000, and dialkyl benzene 18,000 (28,67). The higher costs reflected in Table 18 (18,28) have restricted the volume of siUcones, chlorotrifluoroethylene, perfluoroalkylpolyethers, and polyphenyl ethers. [Pg.255]

Catalysts. Mercury is or has been used in the catalysis (qv) of various plastics, including polyurethane [26778-67-6] poly(vinyl chloride) [9002-86-2] and poly(vinyl acetate) [9003-20-7]. Most poly(vinyl chloride) and poly(vinyl acetate) is manufactured by processes that do not use mercury (3). [Pg.110]


See other pages where Poly manufacture is mentioned: [Pg.259]    [Pg.389]    [Pg.2762]    [Pg.118]    [Pg.317]    [Pg.172]    [Pg.443]    [Pg.373]    [Pg.377]    [Pg.378]    [Pg.378]    [Pg.270]    [Pg.283]    [Pg.452]    [Pg.361]    [Pg.362]    [Pg.363]    [Pg.366]    [Pg.374]    [Pg.549]    [Pg.67]    [Pg.72]    [Pg.72]    [Pg.73]    [Pg.153]    [Pg.323]    [Pg.525]    [Pg.526]    [Pg.71]    [Pg.245]    [Pg.42]    [Pg.63]    [Pg.254]    [Pg.261]   
See also in sourсe #XX -- [ Pg.774 ]




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