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Polyester Polybutylene-terephthalate

Aromatic polyester (TS) Thermoplastic polyester Polybutylene terephthalate (PBT) Polyethylene terephthalate (PET)... [Pg.25]

Polyester Polybutylene terephthalate (PBT) thermoplastic polyester is less often used. It has good stability and temperature resistance especially glass-filled grades. [Pg.57]

BDO is a pivotal starting material for the production of several bulk chemicals, such as tetrahydrofuran (THF) and y-butyrolactone. It is also used as a cross-linking agent in polymers (polyurethanes) and as an alcohol component in polyesters (polybutylene terephthalate (PBT)) [16]. [Pg.419]

Johns ManviUe has proprietary technology for the production of both glass and spunbond nonwovens, and is currently introducing hybrid products comprising glass mat and polyester/polybutylene terephthalate (PBT) bicomponent spunbond fibres in one nonwoven product. [Pg.268]

PBT (Polyester, polybutylene terephthalate) PET (Polyester, polyethylene terephthalate) PBT (Glass reinforced)... [Pg.103]

Polybutylene terephthalate (PBT) is another thermoplastic polyester produced by the condensation reaction of terephthalic acid and 1,4-butanediol ... [Pg.337]

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]

Polyesters form via a condensation reaction between a dicarboxylic acid and a dialcohol to create an ester linkage, as shown in Fig. 24.1. By far, the two most common polyesters are polyethylene terephthalate and polybutylene terephthalate, the chemical structures of which are shown in Fig. 24.2. These two polymers differ from one another by the length... [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]

Typically, polyester resins are used for high-end applications that require excellent electrical and thermal resistance. When dimensional stability under load is more critical, glass fibers are incorporated to increase the heat distortion temperature and the stiffness of the part. Examples of glass fiber reinforced parts include electrical housings, electrical adapters, computer components, telephone housings, and light bulb sockets. When impact modified, polybutylene terephthalate can be injection molded to make car bumpers. [Pg.380]

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]

We previously reported that brominated aromatic phosphate esters are highly effective flame retardants for polymers containing oxygen such as polycarbonates and polyesters (9). Data were reported for use of this phosphate ester in polycarbonates, polyesters and blends. In some polymer systems, antimony oxide or sodium antimonate could be deleted. This paper is a continuation of that work and expands into polycarbonate alloys with polybutylene terephthalate (PBT), polyethylene terephthalate (PET) and acrylonitrile-butadiene-styrene (ABS). [Pg.255]

Rigid segments can be, for example, a semicrystalline polybutylene terephthalate, and flexible sequences can be polyesters or polyethers - polyetherglycol, for example. [Pg.701]

PBDEs are used in different resins, polymers, and substrates at levels ranging from 5 to 30% by weight (EU 2001). Plastic materials that utilize PBDEs as flame retardants include ABS polyacrylonitrile (PAN) polyamide(PA) polybutylene terephthalate (PBT) polyethylene (PE) cross-linked polyethylene (XPE) polyethylene terephthalate (PET) polypropylene (PP) polystyrene (PS) high-impact polystyrene (HIPS) polyvinyl chloride (PVC) polyurethane (PUR) and unsaturated polyester (UPE). These polymers and examples of their final products are summarized inTable 5-2 (Hardy 2002 WHO 1994a). [Pg.310]

For conventional technical applications aromatic polyesters such as polyethylene terephthalate (PET) and polybutylene terephthalate (PBT) are widely used. But these polymers are biologically inert and thus not directly applicable as biodegradable plastics. Combining both the excellent material properties of aromatic polyesters and the potential biodegradability of aliphatic polyesters has led to the development of a number of commercially available aliphatic-aromatic co-polyesters over the last decade or so. [Pg.24]

Aliphatic polyesters like polycaprolactone (PCL) or polybutylene adipate (PBA) are readily biodegradable, but because of their melting points of 60 °C are unsuitable for many applications. On the other hand, aromatic polyesters like polyethylene terephthalate (PET) or polybutylene terephthalate (PBT) have high melting points above 200 °C and very good material properties, but are not biodegradable. [Pg.87]

Typical polyesters characterized by GPC include polyethylene terephthalate (PET), polybutylene terephthalate (PBT), and polycylohexylenedimethyl-ene terephthalate (PCT). Polyphthalamides (PPA) and polyamides are also commonly analyzed. [Pg.1225]

Polybutylene Terephthalate (PBT) Solvents recommended by General Electric for their VALOX thermoplastic polyester are (11) ... [Pg.271]

Apart from ZHS and ZS, little work has generally been undertaken on tin-based Are retardants in nonhalogen polymer systems. However, certain tin(II) compounds have shown excellent flame-retardant and smoke-suppressant properties when incorporated at levels of 20-30% into aromatic polyesters, specifically polybutylene terephthalate (PBT). Hence, tin(ll) oxide, tin(II) oxalate, and tin(II) phosphate have been shown to markedly increase flame retardancy in PBT, whereas, interestingly, tin(IV) oxide is almost totally ineffective in the same polymeric substrate. [Pg.343]


See other pages where Polyester Polybutylene-terephthalate is mentioned: [Pg.124]    [Pg.223]    [Pg.227]    [Pg.29]    [Pg.255]    [Pg.52]    [Pg.421]    [Pg.11]    [Pg.124]    [Pg.223]    [Pg.227]    [Pg.29]    [Pg.255]    [Pg.52]    [Pg.421]    [Pg.11]    [Pg.162]    [Pg.945]    [Pg.15]    [Pg.325]    [Pg.341]    [Pg.377]    [Pg.378]    [Pg.269]    [Pg.368]    [Pg.242]    [Pg.1335]    [Pg.105]    [Pg.153]    [Pg.643]    [Pg.162]    [Pg.374]    [Pg.85]    [Pg.1008]    [Pg.930]   


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