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Properties polyethylene terephthalate

In this review recent theoretical developments which enable quantitative measures of molecular orientation in polymers to be obtained from infra-red and Raman spectroscopy and nuclear magnetic resonance have been discussed in some detail. Although this is clearly a subject of some complexity, it has been possible to show that the systematic application of these techniques to polyethylene terephthalate and polytetramethylene terephthalate can provide unique information of considerable value. This information can be used on the one hand to gain an understanding of the mechanisms of deformation, and on the other to provide a structural understanding of physical properties, especially mechanical properties. [Pg.114]

TABLE 2.11 Typical Properties of Unfilled Polyethylene terephthalate) (PET), Poly(trimethylene terephthalate) (PTT), and Poly(butylene terephthalate (PBT) Solid-State Polyester Resins... [Pg.46]

The effect of incorporating p-hydroxybenzoic acid (I) into the structures of various unsaturated polyesters synthesised from polyethylene terephthalate (PET) waste depolymerised by glycolysis at three different diethylene glycol (DEG) ratios with Mn acetate as transesterification catalyst, was studied. Copolyesters of PET modified using various I mole ratios showed excellent mechanical and chemical properties because of their liquid crystalline behaviour. The oligoesters obtained from the twelve modified unsaturated polyesters (MUP) were reacted with I and maleic anhydride, with variation of the I ratio with a view to determining the effect on mechanical... [Pg.31]

The performance properties of PEN present opportunities for replacement of rayon or polyamide in carcass construction. The use of PEN cord in these applications is currently being evaluated in both Asia and Europe. PEN has demonstrated acceptable flexural fatigue equivalent to polyethylene terephthalate (PET) and rayon. It has equivalent toughness to rayon, which is important for sidewall impact resistance. PEN s superior mechanical properties also afford opportunities to use less fiber in carcass construction enabling production of lighter-weight, more fuel-efficient tires. [Pg.924]

All of these intermolecular forces influence several properties of polymers. Dispersion forces contribute to the factors that result in increased viscosity as molecular weight increases. Crystalline domains arise in polyethylene because of dispersion forces. As you will learn later in the text, there are other things that influence both viscosity and crystallization, but intermolecular forces play an important role. In polar polymers, such as polymethylmethacrylate, polyethylene terephthalate and nylon 6, the presence of the polar groups influences crystallization. The polar groups increase the intensity of the interactions, thereby increasing the rate at which crystalline domains form and their thermal stability. Polar interactions increase the viscosity of such polymers compared to polymers of similar length and molecular weight that exhibit low levels of interaction. [Pg.76]

Polyesters, which are a class of engineering thermoplastics, are found in a wide variety of applications including carbonated drink bottles, fibers for synthetic fabrics, thin films for photographic films and food packaging, injection molded automotive parts, and housings for small appliances. In this chapter, we svill explore the synthesis of this class of polymers. We will also look at the typical properties and end uses for the most common of these resins, polyethylene terephthalate and polybutylene terephthalate, which are commonly known as PET and PBT, respectively. [Pg.371]

In addition to the desired polymerization reaction, the dialcohol reactants can participate in deleterious side reactions. Ethylene glycol, used in the manufacture of polyethylene terephthalate, can react with itself to form a dialcohol ether and water as shown in Fig. 24.4a). This dialcohol ether can incorporate into the growing polymer chain because it contains terminal alcohol units. Unfortunately, this incorporation lowers the crystallinity of the polyester on cooling which alters the polymer s physical properties. 1,4 butanediol, the dialcohol used to manufacture polybutylene terephthalate, can form tetrahydrofuran and water as shown in Fig. 24.4b). Both the tetrahydrofuran and water can be easily removed from the melt but this reaction reduces the efficiency of the process since reactants are lost. [Pg.374]

Because polyethylene terephthalate crystallizes slowly, it can readily be produced in its amorphous state. This is especially true when it is used in packaging materials, such as thin films and carbonated drink bottles. The final products exhibit high clarity and directionally balanced properties because they lack crystalline regions. [Pg.377]

Polyesters exhibit excellent high temperature strength and electrical properties making them a good choice for many demanding applications. They also are physiologically inert allowing them to be used in food contact applications. The two common polyesters, polyethylene terephthalate and polybutylene terephthalate, are both used in injection molded products. Polyethylene terephthalate is often used in both extrusion and blow molded processes also. [Pg.381]

How do polyethylene terephthalate and polybutylene terephthalate differ from one another chemically How do these differences affect their properties ... [Pg.381]

Polyethylene terephthalate is often used to produce films for food packaging. What properties of this material are critical when designing food packaging ... [Pg.382]

Polyethylene terephthalate is unsuitable for carpets because it crystallizes slowly and the fibers therefore break with time and wear. However, if EG is replaced by 1,3-propanediol, the fibers do not crystallize and wear resistance is greatly improved. The 1,2-diol has properties similar to EG. There are several routes to prepare this diol with reasonable selectivity from propane. [Pg.472]

Polyethylene terephthalate-g-cholesterol) has been reported in the patent literature as having similar properties as those in the current application. [Pg.85]

TPX does not mix with other thermoplastic resins, e.g., as polyethylene terephthalate) (PET) or PP. It can be used to impart mi-croporous properties in films made from PET and PP. [Pg.119]

Condensation monomers having the benzimidazolin-2-one ring system have found utility as modifiers in polyester synthesis. In particular, halogenated diols (73) and dicarboxylic acids (74) may be incorporated (78MI11100) into polyethylene terephthalate) or poly(butyl-ene terephthalate) at fairly low levels to impart flame retardancy. This can be accomplished without adverse effects upon other polymer properties. [Pg.281]


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Mechanical Properties of Polyethylene Terephthalate

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