Polyester is a category of that contain the ester functional group in their main chain. As a specific material, it most commonly refers to a type called polyethylene terephthalate (PET). Polyesters include naturally occurring chemicals, such as in the cutin of , as well as synthetics such as polybutyrate. Natural polyesters and a few synthetic ones are biodegradable, but most synthetic polyesters are not. The material is used extensively in clothing.
Polyester fibers are sometimes spun together with natural fibers to produce a cloth with blended properties. Cotton-polyester blends can be strong, wrinkle- and tear-resistant, and reduce shrinking. using polyester have high water, wind and environmental resistance compared to plant-derived fibers. They are less Fireproofing and can melt when ignited.
Polyester blends have been renamed so as to suggest their similarity or even superiority to natural fibers (for example, some varieties of China silk, which is an essentially deceptive term in the textiles industry for a synthetic fiber woven to resemble the sheen and durability of insect-derived silk, are 100% polyester or a polyester-rayon blend.)
Liquid crystalline polyesters are among the first industrially used liquid crystal polymers. They are used for their mechanical properties and heat-resistance. These traits are also important in their application as an abradable seal in jet engines.
Natural polyesters could have played a significant role in the origins of life. Long heterogeneous polyester chains and membraneless structures are known to easily form in a one-pot reaction without catalyst under simple prebiotic conditions.
Depending on the chemical structure, polyester can be a thermoplastic
. There are also
cured by hardeners; however, the most common polyesters are thermoplastics.
Examples of thermoset polyesters include some of the Desmophen brand from Bayer. The OH group is reacted with an Isocyanate
functional compound in a 2 component system producing coatings which may optionally be pigmented. Polyesters as thermoplastics may change shape after the application of heat. While combustible at high temperatures, polyesters tend to shrink away from flames and self-extinguish upon ignition. Polyester fibers have high tenacity and E-modulus as well as low water absorption and minimal shrinkage in comparison with other industrial fibers.
Polyester resin (UPR) are thermosetting . They are used in the liquid state as casting materials, in sheet molding compounds, as fiberglass laminating resins and in non-metallic auto-body fillers. They are also used as the thermoset polymer matrix in . Fiberglass-reinforced unsaturated polyesters find wide application in bodies of yachts and as body parts of cars.
According to the composition of their main chain, polyesters can be:
|Aliphatic||Homopolymer||Polycondensation of glycolic acid|
|Ring-opening polymerization of lactide|
|Ring-opening polymerization of caprolactone|
|Polycondensation of succinic acid with 1,4-butanediol|
|Copolymerization of 3-hydroxybutanoic acid and 3-hydroxypentanoic acid,|
butyrolactone, and valerolactone (oligomeric aluminoxane as a catalyst)
|Semi-aromatic||Copolymer||Polycondensation of terephthalic acid with ethylene glycol|
|Polycondensation of terephthalic acid with 1,4-butanediol|
|Polycondensation of terephthalic acid with 1,3-propanediol|
|Polycondensation of at least one naphthalene dicarboxylic acid with ethylene glycol|
|Polycondensation of 4-hydroxybenzoic acid and 6-hydroxynaphthalene-2-carboxylic acid|
Increasing the aromatic parts of polyesters increases their glass transition temperature, melting temperature, thermostability, chemical stability...
Polyesters can also be telechelic like the polycaprolactone diol (PCL) and the polyethylene adipate diol (PEA). They are then used as .
Uses and applications
woven or knitted from polyester thread or yarn are used extensively in apparel and home furnishings, from shirts and pants to jackets and hats, bed sheets, blankets, upholstered furniture and computer mouse mats. Industrial polyester fibers, yarns and ropes are used in car tire reinforcements, fabrics for conveyor belts, safety belts, coated fabrics and plastic reinforcements with high-energy absorption. Polyester fiber is used as cushioning and insulating material in pillows, comforters and upholstery padding. Polyester fabrics are highly stain-resistant—in fact, the only class of dyes which can
be used to alter the color of polyester fabric are what are known as
Polyesters are also used to make bottles, films, tarpaulin, canoes, liquid crystal displays, , filters, dielectric film for , film insulation for wire and . Polyesters are widely used as a finish on high-quality wood products such as , and vehicle/yacht interiors. Thixotropic properties of spray-applicable polyesters make them ideal for use on open-grain timbers, as they can quickly fill wood grain, with a high-build film thickness per coat. Cured polyesters can be sanded and polished to a high-gloss, durable finish.
Polyester is a synthetic polymer made of purified terephthalic acid (PTA) or its dimethyl ester dimethyl terephthalate (DMT) and monoethylene glycol (MEG). With 18% market share of all plastic materials produced, it ranges third after polyethylene
(33.5%) and polypropylene
The main raw materials are described as follows:
- Purified terephthalic acid (PTA) CAS-No. 100-21-0
- Dimethylterephthalate (DMT) CAS-No. 120-61-6
- Mono-ethylene glycol (MEG) CAS No. 107-21-1
To make a polymer of high molecular weight a catalyst is needed. The most common catalyst is antimony trioxide (or antimony tri-acetate):
- Antimony trioxide (ATO) CAS-No. 1309-64-4
- mol. weight
In 2008, about 10,000 tonnes Sb2O3 were used to produce around 49 million tonnes polyethylene terephthalate.
Polyester is described as follows:
- Polyethylene terephthalate CAS-No. 25038-59-9
There are several reasons for the importance of polyester:
The relatively easy accessible raw materials PTA or DMT and MEG
The very well understood and described simple chemical process of polyester synthesis
The low toxicity level of all raw materials and side products during polyester production and processing
The possibility to produce PET in a closed loop at low emissions to the environment
The outstanding mechanical and chemical properties of polyester
The wide variety of intermediate and final products made of polyester.
In the following table, the estimated world polyester production is shown. Main applications are textile polyester, bottle polyester resin, film polyester mainly for packaging and specialty polyesters for engineering plastics. According to this table, the world's total polyester production might exceed 50 million tons per annum before the year 2010.
|+ World polyester production by year
! Product type
! 2002 (million tonnes/year)
! 2008 (million tonnes/year)|
Raw material producer
The raw materials PTA, DMT, and MEG are mainly produced by large chemical companies which are sometimes integrated down to the crude oil refinery where P-Xylene
is the base material to produce PTA and liquefied petroleum gas (LPG) is the base material to produce MEG.
After the first stage of polymer production in the melt phase, the product stream divides into two different application areas which are mainly textile applications and packaging applications. In the following table, the main applications of textile and packaging of polyester are listed.
|+ Textile and packaging polyester application list (melt or pellet)
|Staple fiber (PSF)||Bottles for CSD, water, beer, juice, detergents, etc.|
|Filaments POY, DTY, FDY||A-PET film|
|Technical yarn and tire cord||Thermoforming|
|Non-woven and spunbond||biaxial-oriented film (BO-PET)|
- Polyester-staple fiber;
- Partially oriented yarn;
- Drawn textured yarn;
- Fully drawn yarn;
- Carbonated soft drink;
- Amorphous polyester film;
- Biaxial-oriented polyester film;
A comparable small market segment (much less than 1 million tonnes/year) of polyester is used to produce engineering plastics and masterbatch.
In order to produce the polyester melt with a high efficiency, high-output processing steps like staple fiber (50–300 tonnes/day per spinning line) or POY /FDY (up to 600 tonnes/day split into about 10 spinning machines) are meanwhile more and more vertically integrated direct processes. This means the polymer melt is directly converted into the textile fibers or filaments without the common step of pelletizing. We are talking about full vertical integration when polyester is produced at one site starting from crude oil or distillation products in the chain oil → benzene → PX → PTA → PET melt → fiber/filament or bottle-grade resin. Such integrated processes are meanwhile established in more or less interrupted processes at one production site. Eastman Chemicals were the first to introduce the idea of closing the chain from PX to PET resin with their so-called INTEGREX process. The capacity of such vertically integrated production sites is >1000 tonnes/day and can easily reach 2500 tonnes/day.
Besides the above-mentioned large processing units to produce staple fiber or yarns, there are ten thousands of small and very small processing plants, so that one can estimate that polyester is processed and recycled in more than 10 000 plants around the globe. This is without counting all the companies involved in the supply industry, beginning with engineering and processing machines and ending with special additives, stabilizers and colors. This is a gigantic industry complex and it is still growing by 4–8% per year, depending on the world region.
Synthesis of polyesters is generally achieved by a polycondensation reaction. See "condensation reactions in polymer chemistry".
The general equation for the reaction of a diol with a diacid is :
- (n+1) R(OH)2 + n R´(COOH)2 → HOROOCR´COOnROH + 2n H2O
In this classical method, an alcohol
and a carboxylic acid
react to form a carboxylic ester.
To assemble a polymer, the water formed by the reaction must be continually removed by azeotrope
Acylation (HCl method)
The acid begins as an acid chloride, and thus the polycondensation proceeds with emission of hydrochloric acid (HCl) instead of water. This method can be carried out in solution or as an vitreous enamel
- Silyl method
- In this variant of the HCl method, the carboxylic acid chloride is converted with the trimethyl silyl ether of the alcohol component and production of trimethyl silyl chloride is obtained
Acetate method (esterification)
- Silyl acetate method
polyesters can be assembled from
under very mild conditions, catalyzed
A number of catalytic methods for the copolymerization of epoxides with cyclic anhydrides have also recently been shown to provide a wide array of functionalized polyesters, both saturated and unsaturated.
In 1926, United States-based DuPont
began research on large molecules and synthetic fibers. This early research, headed by W.H. Carothers, centered on what became nylon
, which was the first synthetic fiber.
Carothers was working for duPont at the time. Carother’s research was incomplete and had not advanced to investigating the polyester formed from mixing ethylene glycol and terephthalic acid. The project was revived by British scientists Whinfield and Dickson, who patented polyethylene terephthalate (PET) or PETE in 1941. Polyethylene terephthalate forms the basis for synthetic fibers like Dacron
, Terylene and polyester. In 1946, duPont bought all legal rights from Imperial Chemical Industries (ICI).
house was made of fibreglass-reinforced polyester plastic; polyester-polyurethane, and poly(methylmethacrylate) one of them was found to be degrading by Cyanobacteria
Unsaturated polyesters are thermosetting resins. They are generally copolymers prepared by polymerizing one or more diol
with saturated and unsaturated dicarboxylic acids (maleic acid
, fumaric acid
...) or their
. The double bond of unsaturated polyesters reacts with a vinyl group
monomer, usually styrene
, resulting in a 3-D cross-linked structure. This structure acts as a thermoset. The exothermic
reaction is initiated through a catalyst
, usually an organic peroxide
such as methyl ethyl ketone peroxide or benzoyl peroxide
Pollution of freshwater and seawater habitats
A team at Plymouth University in the UK spent 12 months analysing what happened when a number of synthetic materials were washed at different temperatures in domestic washing machines, using different combinations of detergents, to quantify the microfibres shed. They found that an average washing load of 6 kg could release an estimated 137,951 fibres from polyester-cotton blend fabric, 496,030 fibres from polyester and 728,789 from acrylic. Those fibers add to the general microplastics
[O'Connor, Mary Catherine (27 October 2014) Inside the lonely fight against the biggest environmental problem you've never heard of. The Guardian]
Polyester is a synthetic petroleum-based fibre, and is therefore a non-renewable carbon-intensive resource.
Nearly 70 million barrels of oil are used each year to make polyester around the world, which is now the most commonly used fiber in making clothes. But it takes more than 200 years to decompose.
Textiles, by Sara Kadolph and Anna Langford. 8th Edition, 1998.