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Characteristics polyethylene terephthalate

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. [Pg.1582]

Most of the polymer s characteristics stem from its molecular structure, which like POE, promotes solubility in a variety of solvents in addition to water. It exhibits Newtonian rheology and is mechanically stable relative to other thermoplastics. It also forms miscible blends with a variety of other polymers. The water solubility and hot meltable characteristics promote adhesion in a number of applications. PEOX has been observed to promote adhesion comparable with PVP and PVA on aluminum foil, cellophane, nylon, poly(methyl methacrylate), and polyethylene terephthalate), and in composite systems improved tensile strength and Izod impact properties have been noted. [Pg.320]

Vinylidene Chloride Copolymer Latex. Vinylidene chloride polymers are often made in emulsion, but usually are isolated, dried, and used as conventional resins. Stable latices have been prepared and can be used diiecdy for coatings (171—176). The principal applications for these materials are as barrier coatings on paper products and, more recently, on plastic films. The heat-seal characteristics of VDC copolymer coatings are equally valuable in many applications. They are also used as binders for paints and nonwoven fabrics (177). The use of special VDC copolymer latices for barrier laminating adhesives is growing, and the use of vinylidene chloride copolymers in flame-resistant carpet backing is well known (178—181). VDC latices can also be used to coat polyethylene terephthalate) (PET) bottles to retain carbon dioxide (182). [Pg.442]

Condensation polymerizations are equilibrium reactions, which means they eventually stop reacting when small molecular weight reaction products like water are no longer removed from the system. These characteristics of the condensation polymerization reaction also have an effect on the chemical properties of such plastics. In the presence of water, particularly at high temperatures, polyethylene terephthalate begins to hydrolyze and low molecular weight oligomers are produced which can be transferred into a food in contact with the plastic. [Pg.14]

PLA compares well with petrochemical-based plastics used for packaging. It is clear and naturally glossy like polystyrene, it is resistant to moisture and grease, it has flavour and odour barrier characteristics similar to polyethylene terephthalate (PET). The tensile strength and modulus of elasticity of PLA is also comparable to PET. [Pg.20]

Plasticization proves to be true by measurements of electro physical characteristics at modified polyethylene terephthalate (figure 4). [Pg.50]

Hahgenated polymers, both brominated and chlorinated, have been developed to yield better polymer compatibility, improve physical properties, and long-term-aging characteristics in many thermoplastic resins, particularly the high-performance engineering thermoplastics, such as nylon, polybutylene terephthalate (PBT) and polyethylene terephthalate (PET). These materials still use antimony oxide as a synergist to achieve the desired flame resistance (31). [Pg.298]

Table VI compares the key properties of these two types of thermotropic polymers category by category. The samples compared had the same melting ranges, but were very different in reduced viscosities and solubility characteristics. The data compared were those processed under the most favorable conditions. Interestingly enough, the as-spun fibers from the polyester-carbonate can be heat-treated more efficiently than those fibers (of same tenacity) spun from the polyester. Both of them gave fiber properties far superior to those of nylons and polyethylene terephthalate. These two classes of polymers also had comparative properties (such as tensile strength, tensile modulus, flex modulus, notched Izod impact strength) as plastics and their properties were far superior to most plastics without any reinforcement. Table VI compares the key properties of these two types of thermotropic polymers category by category. The samples compared had the same melting ranges, but were very different in reduced viscosities and solubility characteristics. The data compared were those processed under the most favorable conditions. Interestingly enough, the as-spun fibers from the polyester-carbonate can be heat-treated more efficiently than those fibers (of same tenacity) spun from the polyester. Both of them gave fiber properties far superior to those of nylons and polyethylene terephthalate. These two classes of polymers also had comparative properties (such as tensile strength, tensile modulus, flex modulus, notched Izod impact strength) as plastics and their properties were far superior to most plastics without any reinforcement.
Doshi and Reneker have experimented with the spinning of PEO fibers from aqueous solutions and studied the relationship between process and solution parameters on fiber characteristics (Doshi and Reneker 1995). Electrospun fibers were about 0.05 to 5 pm in diameter Reneker and Chun demonstrated the spinning of polyethylene terephthalate fibers of 300 nm in diameter with cylindrical structures (Reneker and Chun 1996). [Pg.214]

When polyester fibres (polyethylene terephthalate, PET) are heated in 15% alcoholic potassium hydroxide (KOH) on a microscope slide with a cover slip, typical needles are formed from the potassium salt of terephthalic acid. This characteristic reaction for polyester is simpler and less problematical than the staining of fibre ends with Oil Red in m-crcsol as described by Stratmann. ... [Pg.153]

Table 28. Thermal characteristics of used hexaazocyclanes and initial polyethylene terephthalate... Table 28. Thermal characteristics of used hexaazocyclanes and initial polyethylene terephthalate...
In dishwashing, one must consider soil and surfactant adsorption to both polar and nonpolar surfaces. Metals (aluminum, stainless steel, carbon steel, cast iron, silver, and tin), siliceous surfaces (china, glass, and pottery), and organics (polyethylene, polypropylene, polyethylene terephthalate (PET), polytetrafluoroethylene (PTFE), and wood) present a wide variety of surface characteristics. They span the range of high interfacial free energy (metals and many ceramics) to low interfacial free energy (hydrocarbon polymers) surfaces [27,28],... [Pg.180]

Flame treatment is a commercial process to render polyolefins and polyethylene terephthalate adherable. The polymer article (e.g., film) is passed over an oxidizing flame formed by of an oxygen-rich (relative to stoichiometry) mixture of hydrocarbon gas. Variables affecting the extent of oxidation include the flame characteristics (e.g., excess oxygen) and the speed of the article movement. Gas flame... [Pg.261]

Chiu (116) used the apparatus previously described to study the thermal decomposition of selected polymers such as polyethylene terephthalate), po y(vinyl fluoride), po y(vinylidene fluoride), and others. The dielectric constant curves of a group of fluorocarbon polymers are shown in Figure 11.33. As illustrated, the more polar polymers such as poly(vinylidinefiuoride) (PVDF) and poly(vinyl fluoride) (PVF) show characteristic dielectric loss peaks that are distinguishable from the relatively featureless and low-loss curves of the other polymers. For PVF, the low-temperature process is due... [Pg.724]

Ion-track etching is a unique technique for the production of polymer membranes with statistically distributed nanopores. The size, shape, and density of these pores can be varied in a controllable manner by achieving the required transport and retention membrane characteristics (Apel 2001). The widely used polymer materials for ion-track membranes production are polyethylene terephthalate (PET) and polycarbonate (PC) thin films. The commercially available polymer membranes contain... [Pg.424]

Ski boots use a wide variety of plastics adapted for low temperatures. Thermoplastic polyurethane/ABS blends and plyamides are used for the outer shell of ski boots and modified polyethylene terephthalate for the binding. Polyurethane (PU) foam is often used to line the boots. Microsphere fillers may be incorporated into foam-lined boots to add further thermal insulation to the wax binder. The antivibrational characteristics of PU foams have also led to their use in ski fittings. A sandwich construction of polyurethane elastomer and aluminum alloy has been fitted between the ski and the binding to reduce shock and vibration. [Pg.796]

Solubility tests permit at least a tentative identification of the components also in polymer blends. Blends of ABS and polycarbonate are soluble in most polar solvents. Solubility in tetrahydrofuran and methyl ethyl ketone demonstrates the absence of polyolefins in such blends and the presence of aromatic polyesters or of polyamides can also be excluded. On the other hand, generally they may contain such highly soluble polymers as polystyrene, PVC, ABS, or polymethacrylates. However, blends that contain polybutylene terephthalate or polyethylene terephthalate do not dissolve in the usual solvents, but require m-cresol, which can he a clear indication that aromatic polyesters are present. Polyolefins dissolve at high temperatures, at least 110 °C, in toluene and p-xylene, and this behavior is characteristic of blends that contain polyethylene or polypropylene. [Pg.76]


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