Polyethylene terephthalate applications

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. 

Polyethylene terephthalate (PET) is one of the most important commercial thermoplastic polyesters, which has been on the market since 1977 and is widely used in both industrial and household applications. Under specific conditions, plastics can be converted into their primary components for use in other chemical processes by chemical recycling. PET is a thermoplastic, and so recycling by chemical methods, which converts it into primary components, can be achieved. This study examines the optimal routes of the existing chemical methods. For chemical recycling, acidic hydrolysis is used and PET is converted into terephthalic acid (TPA) and... 

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. 

Both terephthalic acid (TPA) and dimethyl terephthalate (DMT) are used exclusively for the manufacture of polyesters for textile fibers (e.g,. Dacron ), films, soft-drink bottles, and engineering resins for automotive applications. The glycol used for most TPA-based polyesters is ethylene glycol. The polyester is then known as polyethylene terephthalate, or PET. 

Many polymers are used in barrier applications, either to keep contents in or contaminants out. Food packaging is an excellent example of such usage. Plastic films and containers of many types are used to package food. Blow moldedbottles often contain numerous layers, each of which provides specific benefits. Polyethylene layers are excellent water barriers, polyvinyl alcohol is a good oxygen barrier, and polyethylene terephthalate impedes the diffusion of carbon dioxide from carbonated drinks. Other barrier applications include toothpaste tubes, diaper backsheets, tarpaulins, and geomembranes, which are used to line containment ponds and landfill pits. 

When the new product to be manufactured is the same as what it started as, for example a new bottle made from bottle scrap, the recycling is referred to as closed-loop. When the new application is different from the starting one, the process is referred to as open-loop recycling, as is the case when the polyethylene terephthalate bottle is used to produce polyester fiber for carpeting. 

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. 

Polyethylene terephthalate is most often extruded into films or fibers, or blow molded into bottles. Polybutylene terephthalate is primarily found in injection molded parts. Such parts are highly crystalline, which makes them opaque. Polybutylene terephthalate is often modified with glass fibers or impact modifiers. Table 24.1 contains applications by processing method and resin. 

Table 24.1 Applications of polyethylene terephthalate and polybutylene terephthalate by processing method...

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. 

The above-mentioned method is effective in identifying the molecules of detected ions. However, because PVDF film is not permeable to light, it is difficult to observe tissue sections. To resolve this problem, we developed a method to fix tissue sections on transparent film, and then performed MS on those sections.6 We used a conductive film because we expected the ionization efficiency would increase when the electric charge accumulation on the sample was reduced. The film used for this purpose was a polyethylene terephthalate (PET) film with a thickness of 75-125 pm, having a 5 15-nm-thick layer of evaporated oxidation indium tin (ITO) upon it (ITO film). This film is used in touch-panel displays because of its high transparency and superior conductivity. We used it to perform MS/MS for tissue sections and succeeded in identifying multiple proteins from mass spectra.6 Therefore, the further development of this method will enable the application of the mass-microscopic method to observe tissue by optical microscope and to perform tandem mass spectrometry (MSn) at the observation part, simultaneously, enabling the identification of molecules included the part. 

Franz, R., Recycled Polyethylene terephthalate) for direct food contact application, FDA submission CTS 71903, Petitioner Buhler A. G, Representative Laboratory Fraunhofer Institute for Process Engineering and Packaging, Freising, Germany, Petition to the FDA, 2000. 

Polyethylene terephthalate) (PET) has become a major synthetic polymer during the past forty years. Significant commercial markets [1] have been developed for its application in textile and industrial fibers, films, and foamed articles, containers for carbonated beverages, water and other liquids, and thermoformed applications (e.g. dual ovenable containers). 

Glass-filled, toughened polyethylene terephthalate) (PET) resins can be readily moulded into highly impact-resistant structural parts for appliances and automotive components. The PET-based compounds are also suitable for construction (e.g. as structural members), equipment housings (e.g. printer and copier parts), agricultural applications (e.g. mower and tractor engine covers), materials handling (e.g. pallets and trays), furniture (e.g. office chair bases), as well as electrical and electronic applications. 

Polyethylene terephthalate (PET) is a copolymer of ethylene glycol with either terephthalic acid or dimethyl terephthalate. PET is used in packaging applications for soft drinks and mineral water, and for the bottles that are collected by curbside or deposit systems. As it does not thermally deform below about 220° C, PET is also used for trays and dishes for microwave and conventional cooking. 

International Life Sciences Institute (2000). Report on Packaging Materials 1. Polyethylene terephthalate (PET) for food packaging applications. ILSI Europe Packaging Material Task Force, Brussels. 

Tartaric acid-glycerol polyesters were reported in 1847 by Berzelius [13] and those of ethylene glycol and succinic acid were reported by Lorenzo in 1863 [14]. Carothers and Van Natta [15] extended much of the earlier work and helped clarify the understanding of the polyesterification reaction in light of the knowledge of polymer chemistry at their time. Polyethylene terephthalate [16, 17] and the polyadipates [18] (for polyurethane resins) were the first major commercial application of polyesters. 

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

When a polymer film is used as a substrate, aqueous Ti02 paste without organic surfactants is sintered at relatively low temperatures, with approximately 150°C being sufficient to produce mechanically stable 2 films. Sommeling et al. at ECN used an ITO-coated polyethylene terephthalate) (PET) film as a substrate and prepared a plastic DSSC [164-167]. A cell performance with a 7 of 15 pA/cm2, Voc of 0.48 V, and ff of 0.67 was obtained at an illumination intensity of 250 lux. This performance is sufficient for a power supply for indoor applications such as watches and calculators. Under AM 1.5 irradiation, a Vtx of 0.7 V and /sc of 2 mA/cm2 were obtained. 

Zisman discovered that there is a critical surface tension characteristic of low-energy solids, such as plastics and waxes. Liquids ihat have a lower surface tension than the solid will spread on that solid, while liquids with a higher surface tension will not spread. Examples of critical surface tension values for plastic solids in dynes per cm are "Teflon/ 18 polyethylene, 31 polyethylene terephthalate, 43 and nylon, 42-46. As one indication of the way this information can be used in practical applications, one can consider the bonding of nylon to polyethylene. If nylon were applied as a melt to polyethylene, it would not wet the lower-energy polyethylene surface and adhesion would be poor. However, molten polyethylene would spread readily over solid nylon to provide a strong bond. 

Polystyrene itself is not used for endoprosthetic purposes and its application is accounted for only because of easy substitutions in benzene rings. The method was subsequently modified for heparinization of silicone and natural rubber, polyethylene, polypropylene, polyethylene terephthalate), and other polymers. Styrene was first grafted onto the polymers by y-radiation and then the above-described reaction was performed in the second step. All the polymers synthesized in this way contained sufficiently large amounts of immobilized heparin (2.8—15.7 ng/cm2) and displayed good thromboresistance when tested in vitro — recalcified blood was not clotted for several hours. 

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