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Linear polyethylene terephthalate

A polyester fiber is any long-chain synthetic polymer composed of at least 85 wt% of an ester of a dihydric alcohol (HOROH) and terephthalic acid (TA) (p-HOOCCgH4COOH). The most widely used polyester fiber is made from linear polyethylene terephthalate (PET). [Pg.952]

Example PET. Let us consider polyethylene terephthalate) (PET, C oHK(h n, Ppet=1-35 g/cm3) of tpET =2 mm thickness and an X-radiation wavelength X= 0.15418 nm (CuKa). We set up a table with one row for each chemical element and sum both the masses and the mass absorption coefficients multiplied by the masses. After normalization to the molecular mass of the PET monomer, 192.17 amu, we find (p/p)pet = 1291.97/192.17 cm2/g a value 6.72 cm2/g. Considering the density ppet we find for the linear absorption coefficient Ppet =... [Pg.98]

Peebles, L. H., Huffmann, M. W. and Ablett, C. T Isolation and identification of the linear and cyclic oligomers of polyethylene terephthalate... [Pg.107]

Linear polyesters, such as polyethylene terephthalate (PET, Dacron, Mylar), are heteropolymers with carbon and oxygen atoms in the polymer chain ... [Pg.13]

The largest commercial use of ethylene glycol is its reaction with dicarboxylic acids to form linear polyesters. Polyethylene terephthalate) [25038-59-9] (PET) is produced by esterification of terephthalic acid [100-21 -0] (1) to form bishydroxyethyl terephthalate [959-26-2] (BHET) (2). BHET polymerizes in a transesterification reaction catalyzed by antimony oxide to form PET (3). [Pg.357]

Manufacture. The manufacture of 1,4-cyclohexanedimethanol can be accomplished by the catalytic reduction under pressure of dimethyl terephthalate in 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. Polyethylene terephthalate) may be hydrogenated in the presence of methanol under pressure and heat to give good yields of the glycol (see Polyesters) (66,67). [Pg.374]

Eq. (5) in conjunction with Eqs. (8) and (9) have, so far, provided adequate representation of experimental isotherms6 32, which are characterized by an initial con vex-upward portion but tend to become linear at high pressures. Values of K, K2 and s0 have been deduced by appropriate curve-fitting procedures for a wide variety of polymer-gas systems. Among the polymers involved in recent studies of this kind, one may cite polyethylene terephthalate (PET) l2 I4), polycarbonate (PC) 19 22,27), a polyimide l6,17), polymethyl and polyethyl methacrylates (PMMA and PEMA)l8), polyacrylonitrile (PAN)15), a copolyester 26), a polysulphone 23), polyphenylene oxide (PPO)25), polystyrene (PS) 27 28), polyvinyl acetate 29) and chloride 32) (PVAc and PVC), ethyl cellulose 24) (EC) and cellulose acetate (CA) 30,3I>. A considerable number of gases have been used as penetrants, notably He, Ar, N2, C02, S02 and light hydrocarbons. [Pg.97]

High speed stirring has be claimed by Nozaki for giving block copolymers from polymer-monomer mixtures (775). Among the polymers which have been subjected to such a degradation are addition polymers (polyvinyl chloride, polystyrene, polyacrylamide) as well as cellulose derivatives, phenol-formaldehyde linear condensation products and polyethylene terephthalate. [Pg.194]

ABA ABS ABS-PC ABS-PVC ACM ACS AES AMMA AN APET APP ASA BR BS CA CAB CAP CN CP CPE CPET CPP CPVC CR CTA DAM DAP DMT ECTFE EEA EMA EMAA EMAC EMPP EnBA EP EPM ESI EVA(C) EVOH FEP HDI HDPE HIPS HMDI IPI LDPE LLDPE MBS Acrylonitrile-butadiene-acrylate Acrylonitrile-butadiene-styrene copolymer Acrylonitrile-butadiene-styrene-polycarbonate alloy Acrylonitrile-butadiene-styrene-poly(vinyl chloride) alloy Acrylic acid ester rubber Acrylonitrile-chlorinated pe-styrene Acrylonitrile-ethylene-propylene-styrene Acrylonitrile-methyl methacrylate Acrylonitrile Amorphous polyethylene terephthalate Atactic polypropylene Acrylic-styrene-acrylonitrile Butadiene rubber Butadiene styrene rubber Cellulose acetate Cellulose acetate-butyrate Cellulose acetate-propionate Cellulose nitrate Cellulose propionate Chlorinated polyethylene Crystalline polyethylene terephthalate Cast polypropylene Chlorinated polyvinyl chloride Chloroprene rubber Cellulose triacetate Diallyl maleate Diallyl phthalate Terephthalic acid, dimethyl ester Ethylene-chlorotrifluoroethylene copolymer Ethylene-ethyl acrylate Ethylene-methyl acrylate Ethylene methacrylic acid Ethylene-methyl acrylate copolymer Elastomer modified polypropylene Ethylene normal butyl acrylate Epoxy resin, also ethylene-propylene Ethylene-propylene rubber Ethylene-styrene copolymers Polyethylene-vinyl acetate Polyethylene-vinyl alcohol copolymers Fluorinated ethylene-propylene copolymers Hexamethylene diisocyanate High-density polyethylene High-impact polystyrene Diisocyanato dicyclohexylmethane Isophorone diisocyanate Low-density polyethylene Linear low-density polyethylene Methacrylate-butadiene-styrene... [Pg.958]

Polyethylene terephthalate cannot be solvent-cemented or heat-welded. Adhesives are the prime way of joining PET to itself and to other substrates. Only solvent cleaning of PET surfaces is recommended as a surface treatment. The linear film of polyethylene terephthalate (Mylar) provides a surface that can be pretreated by alkaline etching or plasma for maximum adhesion, but often a special treatment such as this is not necessary. An adhesive for linear polyester has been developed from a partially amidized acid from a secondary amine, reacted at less than stoichiometric with a DGEB A epoxy resin, and cured with a dihydrazide.72... [Pg.375]

Within the family of polyolefins there are many individual families that include low density polyethylenes, linear low density polyethylenes, very low polyethylenes, ultra low polyethylenes, high molecular weight polyethylenes, ultra high molecular weight polyethylenes, polyethylene terephthalates, ethylene-vinyl acetate polyethylenes, chlorinated polyethylenes, crosslinked polyethylenes, polypropylenes, polybutylenes, polyisobutylene, ionomers, polymethylpentene, thermoplastic polyolefin elastomers (polyolefin elastomers, TP), and many others. [Pg.45]

LDPE, Low density polyethylene LLDPE, Linear low density polyethylene HDPE, High density polyethylene PP, Polypropylene PVC, Polyvinyl chloride GPS, General purpose polystyrene HIPS, High impact polystyrene SAN, Styrene acrylonitrile ABS, Acrylonitrile butadiene styrene PC, Polycarbonate PA, Polyamide PET, Polyethylene terephthalate. [Pg.151]

The butyrate or octanoate copolymer and butyrate or hexanoate or decanoate terpolymer have properties similar to those of higher-grade LLDPE (linear low-density polyethylene) and higher-grade PET (polyethylene terephthalate). They can be molded or converted into films, fibers, and nonwoven fabrics. The biopolymer is produced by low-cost fermentation or from wastestream substrates. [Pg.322]

Another motivation for measurement of the microhardness of materials is the correlation of microhardness with other mechanical properties. For example, the microhardness value for a pyramid indenter producing plastic flow is approximately three times the yield stress, i.e. // 3T (Tabor, 1951). This is the basic relation between indentation microhardness and bulk properties. It is, however, only applicable to an ideally plastic solid showing no elastic strains. The correlation between H and Y is given in Fig. 1.1 for linear polyethylene (PE) and poly(ethylene terephthalate) (PET) samples with different morphologies. The lower hardness values of 30-45 MPa obtained for melt-crystallized PE materials fall below the /// T cu 3 value, which may be related to a lower stiff-compliant ratio for these lamellar structures (BaM Calleja, 1985b). PE annealed at ca 130 °C... [Pg.9]

Experimental data for v can often be correlated quite well by using Equation 6.44, which was originally developed by Mandelkern et al [190]. Another general expression for v, Equation 6.45, was suggested by vail Antwerpen and van Krevelen [191] who found it to be more useful in correlating their extensive set of data for the linear growth rate in polyethylene terephthalate). In these equations, b, b, b", c, c and c" denote the model fitting parameters. [Pg.289]

A variety of linear polymers—polyethylene (86), numerous polyamides with three or more CH2 units between amide links (30, 86) a polyurethane (86), a polyurea (30), and various polyesters of terephthalic acid (10, 21)— exhibit a loss maximum at about 170°K. ( 103 c.p.s.), the so-called y process. Ti minima, believed to correspond to the mechanical phenomenon, are found for linear polyethylene (20), 66 nylon (35), and 6-10 nylon... [Pg.309]


See other pages where Linear polyethylene terephthalate is mentioned: [Pg.611]    [Pg.611]    [Pg.30]    [Pg.15]    [Pg.69]    [Pg.401]    [Pg.251]    [Pg.286]    [Pg.22]    [Pg.268]    [Pg.252]    [Pg.141]    [Pg.264]    [Pg.223]    [Pg.260]    [Pg.471]    [Pg.388]    [Pg.54]    [Pg.21]    [Pg.114]    [Pg.33]    [Pg.103]    [Pg.458]    [Pg.78]    [Pg.143]    [Pg.23]    [Pg.602]    [Pg.415]    [Pg.415]    [Pg.395]    [Pg.42]   


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Polyethylene terephthalate)

Polyethylene terephthalates)

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