Dacron terephthalate

The ethylene glycol liberated by reaction (5.L) is removed by lowering the pressure or purging with an inert gas. Because the ethylene glycol produced by reaction (5.L) is removed, proper stoichiometry is assured by proceeding via the intermediate, bis(2-hydroxyethyl) terephthalate otherwise the excess glycol used initially would have a deleterious effect on the degree of polymerization. Poly(ethylene terephthalate) is more familiar by some of its trade names Mylar as a film and Dacron, Kodel, or Terylene as fibers it is also known by the acronym PET. 

Poly(ethylene terephthalate), the predominant commercial polyester, has been sold under trademark names including Dacron (Du Pont), Terylene (ICI), Eortrel (Wellman), Trevira (Hoechst-Celanese), and others (17). Other commercially produced homopolyester textile fiber compositions iaclude p oly (1,4-cyc1 oh exa n e- dim ethyl en e terephthalate) [24936-69-4] (Kodel II, Eastman), poly(butylene terephthalate) [26062-94-2] (PBT) (Trevira, Hoechst-Celanese), and poly(ethylene 4-oxyben2oate) [25248-22-0] (A-Tell, Unitika). Other polyester homopolymer fibers available for specialty uses iaclude polyglycoHde [26124-68-5] polypivalolactone [24937-51-7] and polylactide [26100-51-6],... 

The successful development of polyfethylene terephthalate) fibres such as Dacron and Terylene stimulated extensive research into other polymers containing p-phenylene groups in the main chain. This led to not only the now well-established polycarbonates (see Chapter 20) but also to a wide range of other materials. These include the aromatic polyamides (already considered in Chapter 18), the polyphenylene ethers, the polyphenylene sulphides, the polysulphones and a range of linear aromatic polyesters. 

Linear polyesters were studied by Carothers during his classieal researches into the development of the nylons but it was left to Whinfield and Dickson to discover polyfethylene terephthalate) (BP 578079), now of great importance in the manufacture of fibres (e.g. Terylene, Dacron) and films (e.g. Melinex, Mylar). The fibres were first announced in 1941. 

Paraxylene is used to make terephthalic acid, the raw material for manufacturing polyester fibers, such as Dacron, Kodel, Fortrel and Terylene. 

The most generally useful polyester is that made by reaction between dimethyl terephthalate (dimethyl 1,4-benzenedicarboxylate) and ethylene glycol (1,2-ethanediol). The product is used under the trade name Dacron to make clothing fiber and tire cord and under the name Mylar to make recording tape. The tensile strength of polyethylene terephthalate) film is nearly equal to that of steel. 

Perhaps the most important polyester is polyethylene terephthalate), commonly known as PET (or PETE 1 on plastic beverage bottles). The annual production of PET in the United States is of the order of 108 kg (105 metric tons). Much of this is converted into fabric (trade name, Dacron) or magnetically coated film (Mylar). 

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. 

In analogy to the transesterification of diethyl terephthalate used in the preparation of commercially important polyester fibers such as Dacron (24), a transesterification reaction waus successfully employed for the preparation of poly(N-acylhydroxyproline esters) (Scheme 1). 

That fall, Carothers assistant Edgar W. Spanagel discovered polyethylene terephthalate, the polyester that Du Pont later manufactured under license as Dacron fiber and Mylar film. Carothers had made most of the polyesters, but he and others in his group assumed that Spanagel s polyester, like their earlier ones, melted at too low a temperature to be practical. As a result, Carothers did not have this one tested for spinnability. British scientists later used it to make Terylene. When Du Pont executives had to buy a license from the British to make Spanagel s fiber, their faces were bright red with embarrassment. 

Some other example of condensation polymers are Dacron (a polymer of ethylene glycol), polyester (a polymer of p-terephthalic acid), Bakelite (a polymer of phenol and formaldehyde). 

Mixed xylenes are used as an octane improver in gasoline and for commercial solvents, particularly in industrial cleaning operations. By far, most of the commercial activity is with the individual isomers. Para-xylene, the most important, is principally used in the manufacture of terephthalic acid and dimethyl terephthalate en route to polyester plastics and fibers (Dacron, films such as Mylar, and fabricated products such as PET plastic bottles). Ortho-xylene is used to make phthalic anhydride, which in turn is used to make polyester, alkyd resins, and PVC plasticizers. Meta-xylene is used to a limited extent to make isophthahc acid, a monomer used in making thermally stable polyimide, polyester, and alkyd resins. 

The sole use for para-xylene is to make terephthalic acid (TPA) and its derivative, dimethyl terephthalate (DMT). When DMT is copolymerized with ethylene glycol, chemists call it polyethylene terephthalate. On Seventh Avenue in New York, they call it polyester. On the labels, it is sometimes called Dacron. 

Uses Preparation of terephthalic acid for polyester resins and fibers (Dacron, Mylar, Terylene), vitamins, pharmaceuticals, and insecticides. Major constituent in gasoline. 

How Is dacron obtained from ethylene glycol and terephthalic acid ... 

The formation of teiylene or dacron by the interaction of ethylene glycol and terephthalic acid Is an example of this type of polymerisation. 

Poly(ethylene terephthalate), known by the trade names Mylar, Dacron, and Terylene, is a very high volume polymer—the United States production of PET fiber and plastic was over... 

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

Problem 16.56 Indicate the reactions involved and show the structures of the following condensation polymers obtained from the indicated reactants (a) Nylon 66 from adipic acid and hexamethylene diamine (b) Nylon 6 from e-caprolactam (c) Dacron from methyl terephthalate and ethylene glycol (d) Glyptal from glycerol and terephthalic acid (e) polyurethane from diisocyanates and ethylene glycol. ... 

Chemically, Dacron and Mylar are polymers made from a ring structure called dimethyl terephthalate and ethylene glycol (HO-CH2CH2-OH). The polymer unit is called polyethylene terephthalate, or PET. Dacron fiber is used in tires and fabrics, and is even used to repair blood vessels. Mylar is used in magnetic recording tape. In the 1960s, it was used in huge balloons that were sent into orbit around Earth. Plastic soda containers are made of PET. 

The first really successful artificial material used in the manufacture of synthetic blood vessels was Dacron , a polyester fiber made from polyethylene terephthalate (PET). The material is woven or knitted into thin tubes with dimensions similar to those of a natural blood vessel. The tubes are then treated with coagulated blood or with albumin, an important blood protein, to block the tiny holes in the fabric of which they are made. Over time, cells migrate into the blood or albumin trapped within the Dacron matrix and deposit collagen. As the blood or albumin degrades, it is replaced by the collagen, producing a vessel with some properties similar to those of natural blood vessels. 

Polyesters Right now, you are probably using at least five things that are made from polyesters. Your clothes probably have some Dacron polyester fiber in them, and they are almost certainly sewn with Dacron thread. Ancient computers used floppy disks made of Mylar , and the optical film in your DVD is made of Mylar . Some of the electronics in your cell phone are probably potted (covered and insulated from shock) in Glyptal polyester resin. The soft drink in your hand probably came in a plastic bottle that was blow-molded from polyethylene terephthalate) resin, better known as PET. 

Dacron fiber is used to make fabric and tire cord, and Mylar film is used to make magnetic recording tape. Mylar film is strong, flexible, and resistant to ultraviolet degradation. Aluminized Mylar was used to make the Echo satellites, huge balloons that were put into orbit around the Earth as giant reflectors in the early 1960s. Polyethylene terephthalate) is also blow-molded to make plastic soft-drink bottles that are sold by the billions each year. 

Polyester. Polyester is made by the polymerization reaction of a diol and a diester. The main commercial polymer is formed by a condensation reaction using ethylene glycol and terephthalic acid. Fibers are formed by meltspinning. Commercially introduced in 1953 by the DuPont Company as Dacron, polyester fibers have high strength, and very low moisture absorbance. The fiber is usually spun with a round cross section. Polyester is the most-used synthetic fiber around the world. 

Polyethylene terephthalate) in short PET is a polyester. It is mainly used in the garment industry with or without natural cotton and has trade names such as Terylene , Dacron , etc. As the name indicates, it is a polymer between terephthalic acid (PT) and ethylene glycol. Both terephthalic acid and dimethyl terephthalate (DMT) can be used to make the polymer. A majority of the modem plants tend to use PT as the starting material because of the availability of high-purity PT on a large scale. Both PT and DMT are first converted to bis(hydroxy ethyl) terephthalate 8.17 (see reaction 8.26). For PT this is effected by a straightforward esterification reaction. For DMT a transesterification reaction catalyzed by zinc and manganese acetate is used. 

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