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Polyester poly

L. Rozes, Synthese de poly(polyester-bloc-polyether)s thermotropes. Approche des proprietes thermiques, viscoelastiques et rheologiques, These, de l Universite P. et M. Curie, Paris, 1996. [Pg.133]

Poly with friction nylon with butyral and butyral with Poly- Polyester ceramic-... [Pg.859]

Nylon Butyral Butyral widi Poly- Polyester Ceramic-... [Pg.788]

Poly- Polyester ceramic imide polyimide silicon... [Pg.372]

Rozes L (1996) Synthesis of thermotropic poly(polyester-61ocA -polyether)s, Thesis, University of Paris. [Pg.69]

Rozes L, Tessier M and Marechal E (1996) Synthesis and characterization of thermotropic poly (polyesters-block-polyethers, Proc Int Symp Poly condensation 96, Paris, p. 334. [Pg.111]

Organic polyesters, obtained either from a diacid and a mono-alcohoi, or from poly-alcohols and a monoacid, or from di-alcohols and a diacid. This class represented 29% of the synthetic base market in France in 1992. [Pg.279]

A great many polymers appear to form films having a flat molecular configuration. Thus various polyesters [7] gave extrapolated areas of about 2.5 m /mg corresponding to about the calculated 60-70 area per segment, or mono-layer Sickness of 3-5 A. A similar behavior was noted for poly(vinyl acetate)... [Pg.539]

ETHYLENE We discussed ethylene production in an earlier boxed essay (Section 5 1) where it was pointed out that the output of the U S petrochemi cal industry exceeds 5 x 10 ° Ib/year Approximately 90% of this material is used for the preparation of four compounds (polyethylene ethylene oxide vinyl chloride and styrene) with polymerization to poly ethylene accounting for half the total Both vinyl chloride and styrene are polymerized to give poly(vinyl chloride) and polystyrene respectively (see Table 6 5) Ethylene oxide is a starting material for the preparation of ethylene glycol for use as an an tifreeze in automobile radiators and in the produc tion of polyester fibers (see the boxed essay Condensation Polymers Polyamides and Polyesters in Chapter 20)... [Pg.269]

The production of polyester fibers leads that of all other types Annual United States production of poly ester fibers is 1 6 million tons versus 1 4 million tons for cotton and 1 0 million tons for nylon Wool and silk trail far behind at 0 04 and 0 01 million tons re spectively... [Pg.869]

Commonly used isocyanates are toluene dhsocyanate, methylene diphenyl isocyanate, and polymeric isocyanates. Polyols used are macroglycols based on either polyester or polyether. The former [poly(ethylene phthalate) or poly(ethylene 1,6-hexanedioate)] have hydroxyl groups that are free to react with the isocyanate. Most flexible foam is made from 80/20 toluene dhsocyanate (which refers to the ratio of 2,4-toluene dhsocyanate to 2,6-toluene dhsocyanate). High-resilience foam contains about 80% 80/20 toluene dhsocyanate and 20% poly(methylene diphenyl isocyanate), while semi-flexible foam is almost always 100% poly(methylene diphenyl isocyanate). Much of the latter reacts by trimerization to form isocyanurate rings. [Pg.1022]

Properties Poly(aryl ether), unfilled Polycarbonate Thermoplastic polyester ... [Pg.1044]

Polyolefin Polyester Block copolymers of styrene and butadiene or styrene and isoprene Block copolymers of styrene and ethylene or styrene and butylene Poly(vinyl chloride) and poly(vinyl acetate) ... [Pg.1058]

Those polymers which are the condensation product of two different monomers are named by applying the preceding rules to the repeat unit. For example, the polyester formed by the condensation of ethylene glycol and terephthalic acid is called poly(oxyethylene oxyterphthaloyl) according to the lUPAC system, as well as poly (ethylene terephthalate) or polyethylene terephthalate. [Pg.22]

Other examples of materials that respond smartly to changes in temperature are the poly(ethylene glycol)s-modifted cottons, polyesters, and... [Pg.250]

Acrylics. Acetone is converted via the intermediate acetone cyanohydrin to the monomer methyl methacrylate (MMA) [80-62-6]. The MMA is polymerized to poly(methyl methacrylate) (PMMA) to make the familiar clear acryUc sheet. PMMA is also used in mol ding and extmsion powders. Hydrolysis of acetone cyanohydrin gives methacrylic acid (MAA), a monomer which goes direcdy into acryUc latexes, carboxylated styrene—butadiene polymers, or ethylene—MAA ionomers. As part of the methacrylic stmcture, acetone is found in the following major end use products acryUc sheet mol ding resins, impact modifiers and processing aids, acryUc film, ABS and polyester resin modifiers, surface coatings, acryUc lacquers, emulsion polymers, petroleum chemicals, and various copolymers (see METHACRYLIC ACID AND DERIVATIVES METHACRYLIC POLYMERS). [Pg.99]

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]

Dry chlorine has a great affinity for absorbing moisture, and wet chlorine is extremely corrosive, attacking most common materials except HasteUoy C, titanium, and tantalum. These metals are protected from attack by the acids formed by chlorine hydrolysis because of surface oxide films on the metal. Tantalum is the preferred constmction material for service with wet and dry chlorine. Wet chlorine gas is handled under pressure using fiberglass-reinforced plastics. Rubber-lined steel is suitable for wet chlorine gas handling up to 100°C. At low pressures and low temperatures PVC, chlorinated PVC, and reinforced polyester resins are also used. Polytetrafluoroethylene (PTFE), poly(vinyhdene fluoride) (PVDE), and... [Pg.510]

However, because of the low melting poiats and poor hydrolytic stabiUty of polyesters from available iatermediates, Carothers shifted his attention to linear ahphatic polyamides and created nylon as the first commercial synthetic fiber. It was nearly 10 years before. R. Whinfield and J. T. Dickson were to discover the merits of poly(ethylene terephthalate) [25038-59-9] (PET) made from aromatic terephthaUc acid [100-21-0] (TA) and ethylene glycol [107-21-1] (2G). [Pg.325]

Poly(ethylene terephthalate), the predominant commercial polyester, has been sold under trademark names including Dacron (Du Pont), Terylene (ICI), Eortrel (Wellman), Trevira (Hoechst-Celanese), and others (17). Other commercially produced homopolyester textile fiber compositions iaclude p oly (1,4-cyc1 oh exa n e- dim ethyl en e terephthalate) [24936-69-4] (Kodel II, Eastman), poly(butylene terephthalate) [26062-94-2] (PBT) (Trevira, Hoechst-Celanese), and poly(ethylene 4-oxyben2oate) [25248-22-0] (A-Tell, Unitika). Other polyester homopolymer fibers available for specialty uses iaclude polyglycoHde [26124-68-5] polypivalolactone [24937-51-7] and polylactide [26100-51-6],... [Pg.325]

Polyester sheet products may be produced from amorphous poly(ethylene terephalate) (PET) or partiaHy crystallized PET. Acid-modified (PETA) and glycol modified (PETG) resins are used to make ultraclear sheet for packaging. Poly(butylene terephthalate) (PBT) has also been used in sheet form. Liquid-crystal polyester resins are recent entries into the market for specialty sheet. They exhibit great strength, dimensional stabHity, and inertness at temperatures above 250°C (see Polyesters,thermoplastic). [Pg.377]

Quenched sheet is pulled horizontally from the stack and is then either wound on roUs or sheared into sheets of the required dimension. Among the polymers made into sheet this way are the polyolefins, poly(vinyl chloride), amorphous polyester, polycarbonate, and polyarjiate. [Pg.379]

Molybdenum Oxides. Molybdenum was one of the first elements used to retard the flames of ceUulosics (2). Mote recently it has been used to impart flame resistance and smoke suppression to plastics (26). Molybdic oxide, ammonium octamolybdate, and zinc molybdate ate the most widely used molybdenum flame retardants. Properties ate given in Table 5. These materials ate recommended almost exclusively for poly(vinyl chloride), its alloys, and unsaturated polyesters (qv). [Pg.458]

Polyester Fibers Containing Phosphorus. Numerous patents describe poly(ethylene terephthalate) (PET) flame-retarded with phosphoms-containing diftmctional reactants. At least two of these appear to be commercial. [Pg.480]

This phosphinic anhydride [15171 -48-9] C H O P, is then reacted with glycol and other precursors of poly(ethylene terephthalate), to produce a flame-retardant polyester [82690-14-0] having phosphinate units of the stmcture —0P(0)(CH2)CH2CH2C00—. Trevira 271 is useflil for children s sleepwear, work clothing, and home flirnishings. A phosphoms content as low as 0.6% is reported to be sufficient for draperies and upholstery tests if melt-drip is not retarded by print pigments or the presence of nonthermoplastic fibers (28). [Pg.480]

Alternative technology for modifying a poly(aLkylene terephthalate) by incorporation of a phosphinate stmcture has been developed by Enichem. Phosphinate units of the stmcture —P(CgH5) (0)CH20— are introduced into a polyester such as PET or PBT by transesterification with an oligomer comprised of the aforementioned units (136). [Pg.480]

THPC—Amide—PoIy(vinyI bromide) Finish. A flame retardant based on THPC—amide plus poly(vinyl bromide) [25951-54-6] (143) has been reported suitable for use on 35/65, and perhaps on 50/50, polyester—cotton blends. It is appUed by the pad-dry-cure process, with curing at 150°C for about 3 min. A typical formulation contains 20% THPC, 3% disodium hydrogen phosphate, 6% urea, 3% trimethylolglycouril [496-46-8] and 12% poly(vinyl bromide) soUds. Approximately 20% add-on is required to impart flame retardancy to a 168 g/m 35/65 polyester—cotton fabric. Treated fabrics passed the FF 3-71 test. However, as far as can be determined, poly(vinyl bromide) is no longer commercially available. [Pg.491]

Polyester. Poly(ethylene terephthalate) [25038-59-9] (PET) polyester film has intermediate gas- and water- vapor barrier properties, very high tensile and impact strengths, and high temperature resistance (see Polyesters, thermoplastic). AppHcations include use as an outer web in laminations to protect aluminum foil. It is coated with PVDC to function as the flat or sealing web for vacuum/gas flush packaged processed meat, cheese, or fresh pasta. [Pg.452]

Poly(vinylidene chloride). Poly(viayHdene chloride) [9002-85-1] (PVDC), most of which is produced by Dow Chemical, is best known in its saran or PVC-copolymerized form (see Vinylidene chloride and poly(VINYLIDENE chloride)). As solvent or emulsion coating, PVDC imparts high oxygen, fat, aroma, and water-vapor resistance to substrates such as ceUophane, oriented polypropylene, polyester, and nylon. [Pg.452]

The white cell adsorption filter layer is typically of a nonwoven fiber design. The biomaterials of the fiber media are surface modified to obtain an optimal avidity and selectivity for the different blood cells. Materials used include polyesters, eg, poly(ethylene terephthalate) and poly(butylene terephthalate), cellulose acetate, methacrylate, polyamides, and polyacrylonitrile. Filter materials are not cell specific and do not provide for specific filtration of lymphocytes out of the blood product rather than all leukocytes. [Pg.523]

The largest commercial use of ethylene glycol is its reaction with dicarboxyUc acids to form linear polyesters. Poly(ethylene terephthalate)... [Pg.357]

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]


See other pages where Polyester poly is mentioned: [Pg.322]    [Pg.1010]    [Pg.139]    [Pg.400]    [Pg.450]    [Pg.264]    [Pg.307]    [Pg.341]    [Pg.373]    [Pg.377]    [Pg.377]    [Pg.378]    [Pg.426]    [Pg.469]    [Pg.281]    [Pg.361]    [Pg.363]   
See also in sourсe #XX -- [ Pg.4 ]




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