Polytetrafluoroethylene Explained

Polytetrafluoroethylene (PTFE) is a synthetic fluoropolymer of tetrafluoroethylene, and has numerous applications because it is chemically inert. The commonly known brand name of PTFE-based composition is Teflon by Chemours,[1] a spin-off from DuPont, which originally discovered the compound in 1938.

Polytetrafluoroethylene is a fluorocarbon solid, as it is a high-molecular-weight polymer consisting wholly of carbon and fluorine. PTFE is hydrophobic: neither water nor water-containing substances wet PTFE, as fluorocarbons exhibit only small London dispersion forces due to the low electric polarizability of fluorine. PTFE has one of the lowest coefficients of friction of any solid.

Polytetrafluoroethylene is used as a non-stick coating for pans and other cookware. It is non-reactive, partly because of the strength of carbon–fluorine bonds, so it is often used in containers and pipework for reactive and corrosive chemicals. Where used as a lubricant, PTFE reduces friction, wear, and energy consumption of machinery. It is used as a graft material in surgery and as a coating on catheters.

PTFE and chemicals used in its production are some of the best-known and widely applied PFAS, which are persistent organic pollutants. For decades, DuPont used perfluorooctanoic acid (PFOA, or C8) during production of PTFE, later discontinuing its use due to legal actions over ecotoxicological and health issues. Dupont's spin-off Chemours today manufactures PTFE using an alternative chemical it calls GenX, another PFAS.

History

Polytetrafluoroethylene (PTFE) was accidentally discovered in 1938 by Roy J. Plunkett while he was working in New Jersey for DuPont. As Plunkett attempted to make a new chlorofluorocarbon refrigerant, the tetrafluoroethylene gas in its pressure bottle stopped flowing before the bottle's weight had dropped to the point signaling "empty". Since Plunkett was measuring the amount of gas used by weighing the bottle, he became curious as to the source of the weight, and finally resorted to sawing the bottle apart. He found the bottle's interior coated with a waxy white material that was oddly slippery. Analysis showed that it was polymerized perfluoroethylene, with the iron from the inside of the container having acted as a catalyst at high pressure.[2] Kinetic Chemicals patented the new fluorinated plastic (analogous to the already known polyethylene) in 1941,[3] and registered the Teflon trademark in 1945.[4] [5]

By 1948, DuPont, which founded Kinetic Chemicals in partnership with General Motors, was producing over 2000000lb of Teflon-brand polytetrafluoroethylene per year in Parkersburg, West Virginia.[6] An early use was in the Manhattan Project as a material to coat valves and seals in the pipes holding highly reactive uranium hexafluoride at the vast K-25 uranium enrichment plant in Oak Ridge, Tennessee.[7]

In 1954, Colette Grégoire urged her husband, the French engineer Marc Grégoire, to try the material he had been using on fishing tackle on her cooking pans. He subsequently created the first PTFE-coated, non-stick pans under the brand name Tefal (combining "Tef" from "Teflon" and "al" from aluminium).[8] In the United States, Marion A. Trozzolo, who had been using the substance on scientific utensils, marketed the first US-made PTFE-coated pan, "The Happy Pan", in 1961.[9] Non-stick cookware has since become a common household product, now offered by hundreds of manufacturers across the world.

The brand name Zepel was used for promoting its stain-resistance and water-resistance when applied to fabrics.[10]

In the 1990s, it was found that PTFE could be radiation cross-linked above its melting point in an oxygen-free environment.[11] Electron beam processing is one example of radiation processing. Cross-linked PTFE has improved high-temperature mechanical properties and radiation stability. That was significant because, for many years, irradiation at ambient conditions has been used to break down PTFE for recycling.[12] This radiation-induced chain scission allows it to be more easily reground and reused.

Corona discharge treatment of the surface to increase the energy and improve adhesion has been reported.[13]

Production

PTFE is produced by free-radical polymerization of tetrafluoroethylene.[14] The net equation is

n F2C=CF2 → −(F2C−CF2)n−Because tetrafluoroethylene can explosively decompose to tetrafluoromethane (CF4) and carbon, a special apparatus is required for the polymerization to prevent hot spots that might initiate this dangerous side reaction. The process is typically initiated with persulfate, which homolyzes to generate sulfate radicals:

[O<sub>3</sub>SO−OSO<sub>3</sub>]2− ⇌ 2 The resulting polymer is terminated with sulfate ester groups, which can be hydrolyzed to give OH end-groups.[15]

Granular PTFE is produced via suspension polymerization, where PTFE is suspended in an aqueous medium primarily via agitation and sometimes with the use of a surfactant. PTFE is also synthesized via emulsion polymerization, where a surfactant is the primary means of keeping PTFE in an aqueous medium.[16] Surfactants in the past have included toxic perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS). More recently, Perfluoro 3,6 dioxaoctanoic acid (PFO2OA) and FRD-903 (GenX) are being used as an alternative surfactants.[17]

Properties

PTFE is a thermoplastic polymer, which is a white solid at room temperature, with a density of about 2200 kg/m3 and a melting point of .[18] It maintains high strength, toughness and self-lubrication at low temperatures down to 5K, and good flexibility at temperatures above 194K.[19] PTFE gains its properties from the aggregate effect of carbon-fluorine bonds, as do all fluorocarbons. The only chemicals known to affect these carbon-fluorine bonds are highly reactive metals like the alkali metals, at higher temperatures such metals as aluminium and magnesium, and fluorinating agents such as xenon difluoride and cobalt(III) fluoride.[20] At temperatures above 650– PTFE undergoes depolymerization.[21] However, it begins to decompose at about through, and pyrolysis occurs at temperatures above 400C.

PropertyValue
Glass temperature114.85C[22]
Thermal expansion112–125×10−6 K−1[23]
Thermal diffusivity0.124 mm/s[24]
Young's modulus0.5 GPa
Yield strength23 MPa
Coefficient of friction0.05–0.10
Dielectric constant,
Dielectric constant (60 Hz),
Dielectric strength (1 MHz)60 MV/m
Magnetic susceptibility (SI, 22 °C)−10.28×10−6[25]

The coefficient of friction of plastics is usually measured against polished steel.[26] PTFE's coefficient of friction is 0.05 to 0.10,[18] which is the third-lowest of any known solid material (aluminium magnesium boride (BAM) being the first, with a coefficient of friction of 0.02; diamond-like carbon being second-lowest at 0.05). PTFE's resistance to van der Waals forces means that it is the only known surface to which a gecko cannot stick.[27] In addition, PTFE can be used to prevent insects from climbing up surfaces painted with the material. For example, PTFE is used to prevent ants from climbing out of formicaria. There are surface treatments for PTFE that alter the surface to allow adhesion to other materials.

Because of its chemical and thermal properties, PTFE is often used as a gasket material within industries that require resistance to aggressive chemicals such as pharmaceuticals or chemical processing.[28] However, until the 1990s,[11] PTFE was not known to crosslink like an elastomer, due to its chemical inertness. Therefore, it has no "memory" and is subject to creep. Because of the propensity to creep, the long-term performance of such seals is worse than for elastomers that exhibit zero, or near-zero, levels of creep. In critical applications, Belleville washers are often used to apply continuous force to PTFE gaskets, thereby ensuring a minimal loss of performance over the lifetime of the gasket.[29]

PTFE is an ultraviolet (UV) transparent polymer. However, when exposed to an excimer laser beam it severely degrades due to heterogeneous photothermal effect.[30]

Processing

Processing PTFE can be difficult and expensive, because the high melting temperature,, is above the decomposition temperature. Even when molten, PTFE does not flow due to its exceedingly high melt-viscosity.[31] [32] The viscosity and melting point can be decreased by inclusion of small amount of comonomers such as perfluoro (propylvinyl ether) and hexafluoropropylene (HFP). These cause the otherwise perfectly linear PTFE chain to become branched, reducing its crystallinity.[33]

Some PTFE parts are made by cold-moulding, a form of compression molding.[34] Here, fine powdered PTFE is forced into a mould under high pressure (10–100 MPa). After a settling period, lasting from minutes to days, the mould is heated at, allowing the fine particles to fuse (sinter) into a single mass.[35]

Applications and uses

Wire insulation, electronics

The major application of PTFE, consuming about 50% of production,[36] is for the insulation of wiring in aerospace and computer applications (e.g. hookup wire, coaxial cables).[37] This application exploits the fact that PTFE has excellent dielectric properties, specifically low group velocity dispersion,[38] especially at high radio frequencies, making it suitable for use as an excellent insulator in connector assemblies and cables, and in printed circuit boards used at microwave frequencies. Combined with its high melting temperature, this makes it the material of choice as a high-performance substitute for the weaker, higher dispersion and lower-melting-point polyethylene commonly used in low-cost applications.

Bearings seals

In industrial applications, owing to its low friction, PTFE is used for plain bearings, gears, slide plates, seals, gaskets, bushings,[39] and more applications with sliding action of parts, where it outperforms acetal and nylon.[40]

Electrets

Its extremely high bulk resistivity makes it an ideal material for fabricating long-life electrets, the electrostatic analogues of permanent magnets.

Composites

PTFE film is also widely used in the production of carbon fiber composites as well as fiberglass composites, notably in the aerospace industry. PTFE film is used as a barrier between the carbon or fiberglass part being built, and breather and bagging materials used to incapsulate the bondment when debulking (vacuum removal of air from between layers of laid-up plies of material) and when curing the composite, usually in an autoclave. The PTFE, used here as a film, prevents the non-production materials from sticking to the part being built, which is sticky due to the carbon-graphite or fiberglass plies being pre-pregnated with bismaleimide resin. Non-production materials such as Teflon, Airweave Breather and the bag itself would be considered F.O.D. (foreign object debris/damage) if left in layup.

Gore-Tex is a brand of expanded PTFE (ePTFE), a material incorporating a fluoropolymer membrane with micropores. The roof of the Hubert H. Humphrey Metrodome in Minneapolis, US, was one of the largest applications of PTFE coatings. 20acres of the material was used in the creation of the white double-layered PTFE-coated fiberglass dome.

Chemically inert liners

Because of its extreme non-reactivity and high temperature rating, PTFE is often used as the liner in hose assemblies, expansion joints, and in industrial pipe lines, particularly in applications using acids, alkalis, or other chemicals. Its frictionless qualities allow improved flow of highly viscous liquids, and for uses in applications such as brake hoses.

Tensioned membrane structures

PTFE architectural membranes are created by coating a woven glass-fibre base cloth with PTFE, forming one of the strongest and most durable materials used in tensile structures.[41] Some notable structures featuring PTFE-tensioned membranes include The O2 Arena in London, Moses Mabhida Stadium in South Africa, Metropolitano Stadium in Spain and the Sydney Football Stadium Roof in Australia.[42]

Musical instruments

PTFE is often found in musical instrument lubrication products; most commonly, valve oil.

Lubricants

PTFE is used in some aerosol lubricant sprays, including in micronized and polarized form. It is notable for its extremely low coefficient of friction, its hydrophobia (which serves to inhibit rust), and for the dry film it forms after application, which allows it to resist collecting particles that might otherwise form an abrasive paste.[43] Brands include GT85.[44]

Kitchen ware

PTFE is best known for its use in coating non-stick frying pans and other cookware, as it is hydrophobic and possesses fairly high heat resistance.

The sole plates of some clothes irons are coated with PTFE.[45]

Others

Other niche applications include:

Safety

While PTFE is stable at lower temperatures, it begins to deteriorate at temperatures of about, it decomposes above, and pyrolysis occurs at temperatures above 400C.[60] The main decomposition products are fluorocarbon gases and a sublimate, including tetrafluoroethylene (TFE) and difluorocarbene radicals (RCF2).

An animal study conducted in 1955 concluded that it is unlikely that these products would be generated in amounts significant to health at temperatures below .[61] Above those temperatures the degradation by-products can be lethal to birds,[62] and can cause flu-like symptoms in humans (polymer fume fever),[63] although in humans those symptoms disappear within a day or two of being moved to fresh air.

Most cases of polymer fume fever in humans occur due to smoking PTFE-contaminated tobacco, although cases have occurred in people who have welded near PTFE components. PTFE-coated cookware is unlikely to reach dangerous temperatures with normal use, as meat is usually fried between, and most cooking oils (except refined safflower and avocado oils) start to smoke before a temperature of 260C is reached. A 1973 study by DuPont's Haskell Laboratory found that a 4-hour exposure to the fumes emitted by PTFE cookware heated to was lethal for parakeets, although that was a higher temperature than the 260C required for fumes from pyrolyzed butter to be lethal to the birds.[64]

Perfluorooctanoic acid (PFOA), a chemical formerly used in the manufacture of PTFE products such as non-stick coated cookware, can be carcinogenic for people who are exposed to it (see Ecotoxicity).[65] Concerning levels of PFOA have been found in the blood of people who work in or live near factories where the chemical is used, and in people regularly exposed to PFOA-containing products such as some ski waxes and stain-resistant fabric coatings, but non-stick cookware was not found to be a major source of exposure, as the PFOA is burned off during the manufacturing process and not present in the finished product. Non-stick coated cookware has not been manufactured using PFOA since 2013,[66] and PFOA is no longer being made in the United States.

Ecotoxicity

Trifluoroacetate

Sodium trifluoroacetate and the similar compound sodium chlorodifluoroacetate can both be generated when PTFE undergoes thermolysis, as well as producing longer chain polyfluoro- and/or polychlorofluoro- (C3-C14) carboxylic acids which may be equally persistent. These products can accumulate in evaporative wetlands and have been found in the roots and seeds of wetland plant species, but has not been observed to have an adverse impact on plant health or germination success.[67]

PFOA

See main article: Perfluorooctanoic acid. Perfluorooctanoic acid (PFOA, or C8) has been used as a surfactant in the emulsion polymerization of PTFE, although several manufacturers have entirely discontinued its use.

PFOA persists indefinitely in the environment.[68] PFOA has been detected in the blood of many individuals of the general US population in the low and sub-parts per billion range, and levels are higher in chemical plant employees and surrounding subpopulations. PFOA and perfluorooctanesulfonic acid (PFOS) have been estimated to be in every American person's blood stream in the parts per billion range, though those concentrations have decreased by 70% for PFOA and 84% for PFOS between 1999 and 2014, which coincides with the end of the production and phase out of PFOA and PFOS in the US.[69] The general population has been exposed to PFOA through massive dumping of C8 waste into the ocean and near the Ohio River Valley.[70] [71] [72] PFOA has been detected in industrial waste, stain-resistant carpets, carpet cleaning liquids, house dust, microwave popcorn bags, water, food and PTFE cookware.

As a result of a class-action lawsuit and community settlement with DuPont, three epidemiologists conducted studies on the population of Parkersburg, WV surrounding the (former DuPont) Chemours Washington Works chemical plant that was exposed to PFOA at levels greater than in the general population. The studies concluded that there was an association between PFOA exposure and six health outcomes: kidney cancer, testicular cancer, ulcerative colitis, thyroid disease, hypercholesterolemia (high cholesterol), and pregnancy-induced hypertension.[73]

Overall, PTFE cookware is considered a minor exposure pathway to PFOA.[74]

GenX

See main article: GenX. As a result of the lawsuits concerning the PFOA class-action lawsuit, DuPont began to use GenX, a similarly fluorinated compound, as a replacement for perfluorooctanoic acid in the manufacture of fluoropolymers, such as Teflon-brand PTFE.[75] [76] However, in lab tests on rats, GenX has been shown to cause many of the same health problems as PFOA.[77] [78]

The chemicals are manufactured by Chemours, a corporate spin-off of DuPont, in Fayetteville, North Carolina.[79] Fayetteville Works was the site where DuPont began manufacture of PFOA after the lawsuit in Parkersburg WV halted their production there. When EPA asked companies to voluntarily phase out PFOA production, it was replaced by GenX in Fayetteville Works. In June of 2017, The Wilmington Star-News broke the story[80] that GenX was found in the Cape Fear River – the drinking water supply for 500,000 people. The source of the pollution was determined to be the Fayetteville Works site, which had been run by DuPont since its founding in 1971 and then managed by DuPont spinoff, The Chemours Company, since 2015. The water utility confirmed they had no ability to filter these chemicals from the drinking water. NC Dpt of Environmental Quality records[81] indicate that DuPont started release PFAS into the area beginning in 1976 with the production of Nafion, and that PFAS including GenX had been released as a byproduct of the production of Vinyl Ethers since 1980, exposing the Cape Fear Basin for decades. A small nonprofit called Cape Fear River Watch sued the NC Dept. of Environmental Quality (DEQ) for not taking swifter and stronger action, and sued the polluter, Chemours for violations of the Clean Water Act and the Toxic Substances Control Act. The result was a Consent Order,[82] signed February 25, 2019 by Cape Fear River Watch, NC Department of Environmental Quality, and Chemours.[83] The order has required Chemours to stop wastewater discharge, air emissions, groundwater discharge, sampling and filtration options to well users, and required sampling that proved there were upwards of 300 distinct PFAS being released from Fayetteville Works.[84]

Similar polymers

The Teflon trade name is also used for other polymers with similar compositions:

These retain the useful PTFE properties of low friction and nonreactivity, but are also more easily formable. For example, FEP is softer than PTFE and melts at ; it is also highly transparent and resistant to sunlight.[85]

See also

Further reading

External links

Notes and References

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