PBT poly butylene terephthalate

The non-oxidative thermal degradation of PBT has been studied by several researchers, although the literature is not as extensive as that for PET [14,16, 26, 38, 51, 53, 56, 59, 64-71]. 

The general structures in PBT are broadly similar to those in PET and have been discussed earlier, with the exception of four methylene groups in the aliphatic portion of the polyester chain. Assuming, as is plausible, that the degradation route undergone by PET will apply to PBT, the chain scission via 3-hydrogen transfer through a six-membered cyclic intermediate will proceed as  

Via any of a number of possible reactions, the unsaturated chain end may now eliminate 3-buten-l-ol (bp = 114 °C). In this situation, a very different scenario would result than in the case of PET, i.e., the alcohol thus-formed is highly unlikely to rearrange (c/vinyl alcohol rearranging to acetaldehyde in PET) and is available for reaction with 

Ester exchange or hydrolysis to produce an alternative ester, or acid, and 1,4-butanediol. The diol may then cyclise by dehydration to form tetrahydrofuran (TFfF). 

A direct cyclisation reaction of the end group to produce an acid chain end and TFIF. 

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Chlorinated polyether Poly(butylene terephthalate) (PBT) talso called... 

Polyester sheet products may be produced from amorphous poly(ethylene terephalate) (PET) or partiaHy crystallized PET. Acid-modified (PETA) and glycol modified (PETG) resins are used to make ultraclear sheet for packaging. Poly(butylene terephthalate) (PBT) has also been used in sheet form. Liquid-crystal polyester resins are recent entries into the market for specialty sheet. They exhibit great strength, dimensional stabHity, and inertness at temperatures above 250°C (see Polyesters,thermoplastic). 

Butanediol. 1,4-Butanediol [110-63-4] made from formaldehyde and acetylene, is a significant market for formaldehyde representing 11% of its demand (115). It is used to produce tetrahydrofuran (THF), which is used for polyurethane elastomers y-butyrolactone, which is used to make various pyrroHdinone derivatives poly(butylene terephthalate) (PBT), which is an engineering plastic and polyurethanes. Formaldehyde growth in the acetylenic chemicals market is threatened by alternative processes to produce 1,4-butanediol not requiring formaldehyde as a raw material (140) (see Acetylene-derived chemicals). 

Automotive appHcations account for about 116,000 t of woddwide consumption aimuaHy, with appHcations for various components including headlamp assembHes, interior instmment panels, bumpers, etc. Many automotive appHcations use blends of polycarbonate with acrylonitrile—butadiene—styrene (ABS) or with poly(butylene terephthalate) (PBT) (see Acrylonitrile polymers). Both large and smaH appHances also account for large markets for polycarbonate. Consumption is about 54,000 t aimuaHy. Polycarbonate is attractive to use in light appHances, including houseware items and power tools, because of its heat resistance and good electrical properties, combined with superior impact resistance. 

During the eady development of polycarbonates, many bisphenols were investigated for potential useftil products. Some of these monomers and polymers are hsted in Table 3. Despite this intensive search, however, no homopolycarbonates other than that of BPA have been produced. Copolymers and blends, on the other hand, have been quite successhil. Blends of polycarbonate with ABS and with poly(butylene terephthalate) (PBT in particular have shown significant growth since the mid-1980s. 

A different approach consists of reacting dimethyl terephthalate and dimediyl adipate with 1,4-butanediol in die experimental conditions of poly(butylene terephthalate) (PBT) syndiesis. The resulting copolyester (Eastman s Eastar Bio) presents properties close to diose of odier degradable materials (Table 2.10). 

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

Another important type of condensation polymer are the linear polyesters, such as poly (ethylene terephthalate) (PET) and poly (butylene terephthalate) (PBT). Copolymers of polyesters and PA have been studied in detail, and it has been shown that random copolyesteramides have a low structural order and a low melting temperature. This is even the case for structurally similar systems such as when the group between the ester unit is the same as that between the amide unit, as in caprolactam-caprolactone copolymers (Fig. 3.10).22 Esters and amide units have different cell structures and the structures are not therefore isomorphous. If block copolymers are formed of ester and amide segments, then two melting temperatures are present. 

Poly(butylene terephthalate) (PBT) [also called polytetramethylene terephthalate (PTMT)] Poly(ethylene terephthalate) (PET)... 

Saturated complex polyesters, particularly, poly (butylene terephthalate) (PBT) are used as engineering thermoplastics possesing good thermo - and wearstability, excellent moulding. These properties also allow to use them as matrix material for polymer composites [1], One of the perspective ways of search of effective catalysts for such systems is kinetic study of the reesterification model reaction, performed in the presence of various catalysts and comparison it with the results of the similar reaction without catalyst. Clarification on the example of model system of the most effective catalysts list allows to use them for obtaining both filled and nonfilled PBT and compare catalytic activity of various catalysts. The purpose of the... 

The influence of the ratio of hydroxylic/carboxylic end groups has been studied by several research groups. In the case of PET, this varies, based on the assumed mechanism over the range of 1.5-4.5 1. For poly(butylene terephthalate) (PBT) and polyethylene naphthalate) (PEN), the optimum is indicated at 2.0 1 [19, 20]. Any deviation from this ratio affects the reaction rate. 

The above-mentioned results of the SSP of PET can be generally applied to other semicrystalline polyesters, such as poly(butylene terephthalate) (PBT), poly(tri-methylene terephthalate) PTT), polyethylene naphthalate) (PEN) or any other kind of semicrystalline co-polyester, as a result of their similar reaction behaviors. Most of the studies have been focused on PET and PBT due to their industrial importance. Meanwhile, the popularity of PEN is growing on account of the outstanding properties of this particular polymer. 

Poly(butylene terephthalate) (PBT) (1) resins are semicrystalline thermoplastics used in a wide variety of applications, most commonly in durable goods that are formed by injection molding. Applications include electronic and communications equipment, computers, televisions, kitchen and household appliances, industrial equipment, lighting systems, gardening and agricultural equipment, pumps, medical devices, food handling systems, handles, power and hand tools, bobbins and spindles, and automotive parts in both under-the-hood and exterior applications. Additionally, PBT is very widely used to form electrical connectors. PBT, through its many blended products, can be tailored to suit numerous applications. 

Poly(trimethylene terephthalate) (PTT) is a newly commercialized aromatic polyester. Although available in commercial quantities only as recently as 1998 [1], it was one of the three high-melting-point aromatic polyesters first synthesized by Whinfield and Dickson [2] nearly 60 years ago. Two of these polyesters, polyethylene terephthalate) (PET) and poly(butylene terephthalate) (PBT), have become well-established high-volume polymers. PTT has remained an obscure polymer until recent times because one of its monomers, 1,3-propanediol (PDO), was not readily available. PDO was sold as a small-volume fine chemical at more than 10/lb., and was therefore not suitable as a raw material for commercial polymers. 

It should be taken into account that all of the aspects described above are of a general nature and therefore more or less valid for any kind of industrially relevant polyester resin. Upon closer examination, the experiences gained with PET are particularly applicable to poly(butylene terephthalate) (PBT), poly(trimethylene terephthalate) (PTT) and polyethylene naphthalate) (PEN). These polymers have gained major industrial importance as a result of a number of different properties in comparison with PET. 

It should additionally be noted that a number of the paths of the schemes above have received some confirmation in a number of literature reports dealing with the photolysis and photo-oxidation of other polyesters [32-35], Because these reports investigated poly(butylene terephthalate) (PBT), poly(ethylene naphthalate) and poly(butylene naphthalate), however, they may not have direct application to understanding of the processes involved in PET and PECT and so have not been discussed in this present chapter. All do contain support for the formation of radicals leading to CO and C02 evolution, as well as the hydrogen abstraction at glycolic carbons to form hydroperoxides which then decompose to form alkoxy radicals and the hydroxyl radical. These species then were postulated to undergo further reaction consistent with what we have proposed above. 

Poly(butylene terephthalate) (PBT) is a semicrystalline, thermoplastic polyester which is completely analogous to PET except that it has a longer, more flexible butylene chain linkage which imparts a rapid crystallization rate, thus making PBT well suited to injection moulding processes. This polyester is used widely for electrical and electronic components due to its high temperature resistance and good electrical properties (Chapter 8). 

Poly(butylene terephthalate) (PBT), because of the addition of two methylene units in the diol-derived portion, has a lower melting point than PET with a Eg of about 170°C (structure 4.49). Moldability of aryl polyesters has been improved through the use of PBT instead of PET or by use of blends of PET and PBT. These aryl polyesters are used for bicycle wheels, springs, and blow-molded containers. 

Poly(trimethylene terephthalate). Poly(trimethylene terephthal-ate) (PIT) is a crystalline polymer that is used for fibers, films, and engineering plastics. The polymer has an outstanding tensile elastic recovery, good chemical resistance, a relative low melting temperature, and a rapid crystallization rate. It combines some of the advantages of poly(ethylene terephthalate) (PET) and poly(butylene terephthalate) (PBT). Disadvantageous are the low heat distortion temperature, low melt viscosity, poor optical properties, and pronounced brittleness low temperatures. 

The structure and mechanical properties of ASA and blends of ASA and poly(butylene terephthalate) (PBT) have been studied. 40/60 and 60/40 blends of ASA/PBT are composed of two phases, thus are dispersed, while a 50/50 blend shows a cocontinuous structure. With increasing processing temperature, the mechanical properties decrease, probably due to the degradation of PBT in the course of processing. The mechanical properties do not as much decrease for blends with a continuous structure (24). 

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