Polytetrafluoroethylene (PTFE) is a synthetic fluoropolymer of tetrafluoroethylene and is a PFAS that has numerous applications. 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.[1]

Polytetrafluoroethylene
Names
IUPAC name
Poly(1,1,2,2-tetrafluoroethylene)[2]
Other names
Fluon, Poly(tetrafluoroethene), Poly(difluoromethylene), Poly(tetrafluoroethylene), teflon
Identifiers
Abbreviations PTFE
ChEBI
ChemSpider
  • None
ECHA InfoCard 100.120.367 Edit this at Wikidata
KEGG
UNII
Properties
(C2F4)n
Density 2200 kg/m3
Melting point 327 °C
Electrical resistivity 1018 Ω·cm[a]
Thermal conductivity 0.25 W/(m·K)
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazard OX: Oxidizer. E.g. potassium perchlorate
1
0
0
OX
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

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 is one of the best-known and widely applied PFAS commonly described as persistent organic pollutants or "forever chemicals". Only since the start of the 21st century has the environmental impact and toxicity to human and mammalian life been studied in depth. For decades, DuPont used perfluorooctanoic acid (PFOA, or C8) during production of PTFE, later discontinuing its use due to ecotoxicological and health issues that led to legal actions. Dupont's spin-off Chemours today manufactures PTFE using an alternative chemical it calls GenX, another PFAS.

History

Advertisement of the Happy Pan, a Teflon-coated pan from the 1960s
Advertisement for Zepel, the trade name used to market Teflon as a fabric treatment
PTFE thermal cover showing impact craters, from NASA's Ultra Heavy Cosmic Ray Experiment (UHCRE) on the Long Duration Exposure Facility (LDEF)
Logo of Teflon, the commonly known brand name of PTFE-based compositions manufactured by Chemours

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.[4] Kinetic Chemicals patented the new fluorinated plastic (analogous to the already known polyethylene) in 1941,[5] and registered the Teflon trademark in 1945.[6][7]

By 1948, DuPont, which founded Kinetic Chemicals in partnership with General Motors, was producing over 2,000,000 pounds (910,000 kg) of Teflon-brand polytetrafluoroethylene per year in Parkersburg, West Virginia.[8] 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.[9]

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).[10] 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.[11] 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.[12]

In the 1990s, it was found that PTFE could be radiation cross-linked above its melting point in an oxygen-free environment.[13] 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.[14] 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.[15]

Production

PTFE is produced by free-radical polymerization of tetrafluoroethylene.[16] The net equation is

n F2C=CF2 → −(F2C−CF2)n−

Because tetrafluoroethylene can explosively decompose to tetrafluoromethane (CF4) and carbon, 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:

[O3SO−OSO3]2− ⇌ 2 SO•−
4

The resulting polymer is terminated with sulfate ester groups, which can be hydrolyzed to give OH end-groups.[17]

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.[18] 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.[19]

Properties

PTFE is often used to coat non-stick pans as it is hydrophobic and possesses fairly high heat resistance.

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 600 K (327 °C; 620 °F).[20] It maintains high strength, toughness and self-lubrication at low temperatures down to 5 K (−268.15 °C; −450.67 °F), and good flexibility at temperatures above 194 K (−79 °C; −110 °F).[21] 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, and at higher temperatures also such metals as aluminium and magnesium, and fluorinating agents such as xenon difluoride and cobalt(III) fluoride.[22] At temperatures above 650–700 °C (1,200–1,290 °F) PTFE undergoes depolymerization.[23]

Property Value
Glass temperature 114.85 °C (238.73 °F; 388.00 K)[24]
Thermal expansion 112–125×10−6 K−1[25]
Thermal diffusivity 0.124 mm2/s[26]
Young's modulus 0.5 GPa
Yield strength 23 MPa
Coefficient of friction 0.05–0.10
Dielectric constant ε = 2.1, tan(δ) < 5×10−2
Dielectric constant (60 Hz) ε = 2.1, tan(δ) < 2×10−2
Dielectric strength (1 MHz) 60 MV/m
Magnetic susceptibility (SI, 22 °C) −10.28×10−6[27]

The coefficient of friction of plastics is usually measured against polished steel.[28] PTFE's coefficient of friction is 0.05 to 0.10,[20] 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.[29] In fact, PTFE can be used to prevent insects from climbing up surfaces painted with the material. PTFE is so slippery that insects cannot get a grip and tend to fall off. For example, PTFE is used to prevent ants from climbing out of formicaria.

Because of its superior 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.[30] However, until the 1990s,[13] 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.[31]

PTFE is an ultraviolet (UV) transparent polymer. However, when exposed to an excimer laser beam it severely degrades due to heterogeneous photothermal effect.[32]

Processing

Processing PTFE can be difficult and expensive, because the high melting temperature, 327 °C (621 °F), is above the initial decomposition temperature, 200 °C (392 °F).[33] Even when molten, PTFE does not flow due to its exceedingly high melt-viscosity.[34][35] 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.[36]

Some PTFE parts are made by cold-moulding, a form of compression molding.[37] Here, fine powdered PTFE is forced into a mould under high pressure (10–100 MPa).[37] After a settling period, lasting from minutes to days, the mould is heated at 360 to 380 °C (680 to 716 °F),[37] allowing the fine particles to fuse (sinter) into a single mass.[38]

Applications and uses

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PTFE-jacketed (white) shielded twisted-pair cables

Wire insulation, electronics

The major application of PTFE, consuming about 50% of production,[citation needed] is for the insulation of wiring in aerospace and computer applications (e.g. hookup wire, coaxial cables). This application exploits the fact that PTFE has excellent dielectric properties, specifically low group velocity dispersion,[39] especially at high radio frequencies,[39] 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,[40] and more applications with sliding action of parts, where it outperforms acetal and nylon.[41]

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. 20 acres (81,000 m2) 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.[42] 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.

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]

Two teflon jars
Two PTFE jars[clarification needed]

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

This section contains a list of miscellaneous information. Please relocate any relevant information into other sections or articles. (August 2023)
PTFE tapes with pressure-sensitive adhesive backing

Other niche applications include:

Safety

While PTFE is stable at lower temperatures, it begins to deteriorate at temperatures of about 260 °C (500 °F), it decomposes above 350 °C (662 °F), and pyrolysis occurs at temperatures above 400 °C (752 °F).[60] The main decomposition products are fluorocarbon gases and a sublimate, including tetrafluoroethylene (TFE) and difluorocarbene radicals (RCF2).[60]

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 250 °C (482 °F).[33] Above those temperatures the degradation by-products can be lethal to birds,[61] and can cause flu-like symptoms in humans (polymer fume fever),[62] although in humans those symptoms disappear within a day or two of being moved to fresh air.[63]

Most cases of polymer fume fever in humans occur due to smoking PTFE-contaminated tobacco,[63] although cases have occurred in people who have welded near PTFE components.[63] PTFE-coated cookware is unlikely to reach dangerous temperatures with normal use, as meat is usually fried between 204 and 232 °C (399 and 450 °F), and most cooking oils (except refined safflower and avocado oils) start to smoke before a temperature of 260 °C (500 °F) 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 280 °C (536 °F) was lethal for parakeets, although that was a higher temperature than the 260 °C (500 °F) 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.[63] Non-stick coated cookware has not been manufactured using PFOA since 2013,[66] and PFOA is no longer being made in the United States.[65]

Ecotoxicity

Trifluoroacetate

Sodium trifluoroacetate and the similar compound 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.[63]

PFOA

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.[67] 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.[68] The general population has been exposed to PFOA through massive dumping of C8 waste into the ocean and near the Ohio River Valley.[69][70][71] 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 surrounding a 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.[72]

Overall, PTFE cookware is considered a minor exposure pathway to PFOA.[73]

GenX

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.[74][75] However, in lab tests on rats, GenX has been shown to cause many of the same health problems as PFOA.[76][77]

The chemicals are manufactured by Chemours, a corporate spin-off of DuPont, in Fayetteville, North Carolina.[78] While PFOA was phased out by 2014, Chemours was found to be discharging GenX into the Cape Fear River in 2017, with the North Carolina Department of Environmental Quality (NCDEQ) ordering Chemours to halt discharges of all fluorinated compounds on September 5, 2017.[citation needed]

Similar polymers

Teflon is also used as the trade name for a polymer with similar properties, perfluoroalkoxy polymer resin (PFA).

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 533 K (260 °C; 500 °F); it is also highly transparent and resistant to sunlight.[79]

See also

Notes

  1. ^ Dielectric. Bulk resistivity.[3]

References

  1. ^ a b "The History of Teflon Fluoropolymers". Teflon.com. Retrieved 3 February 2021.
  2. ^ "poly(tetrafluoroethylene) (CHEBI:53251)". ebi.ac.uk. Retrieved 12 July 2012.
  3. ^ "PTFE". Microwaves101. Archived from the original on 16 July 2014. Retrieved 16 February 2012.
  4. ^ "Roy J. Plunkett". Science History Institute. June 2016. Retrieved 10 February 2020.
  5. ^ US 2230654, Plunkett, Roy J, "Tetrafluoroethylene polymers", issued 4 February 1941 
  6. ^ "History Timeline 1930: The Fluorocarbon Boom". DuPont. Retrieved 10 June 2009.
  7. ^ "Roy Plunkett: 1938". Archived from the original on 17 February 2012. Retrieved 10 June 2009.
  8. ^ American Heritage of Invention & Technology, Fall 2010, vol. 25, no. 3, p. 42
  9. ^ Rhodes, Richard (1986). The Making of the Atomic Bomb. New York: Simon and Schuster. p. 494. ISBN 0-671-65719-4. Retrieved 31 October 2010.
  10. ^ "Teflon". Useless Information. home.nycap.rr.com. Archived from the original on 14 February 2008.
  11. ^ Robbins, William (21 December 1986) "Teflon Maker: Out Of Frying Pan Into Fame ", New York Times, Retrieved 21 December 1986 (Subscription)
  12. ^ Fenton, Lois (2 January 1992). "GO, SPOT, GO Teflon enters fashion world as a protective coating". Baltimore Sun. Archived from the original on 20 June 2021.
  13. ^ a b Sun, J.Z.; et al. (1994). "Modification of polytetrafluoroethylene by radiation—1. Improvement in high temperature properties and radiation stability". Radiat. Phys. Chem. 44 (6): 655–679. Bibcode:1994RaPC...44..655S. doi:10.1016/0969-806X(94)90226-7.
  14. ^ Electron Beam Processing of PTFE Archived 6 September 2013 at the Wayback Machine E-BEAM Services website. Accessed 21 May 2013
  15. ^ "Corona Discharge Treatment - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 28 April 2022.
  16. ^ Puts, Gerard J.; Crouse, Philip; Ameduri, Bruno M. (28 January 2019). "Polytetrafluoroethylene: Synthesis and Characterization of the Original Extreme Polymer". Chemical Reviews. 119 (3): 1763–1805. doi:10.1021/acs.chemrev.8b00458. hdl:2263/68582. PMID 30689365. S2CID 59338589.
  17. ^ Carlson, D. Peter and Schmiegel, Walter (2000) "Fluoropolymers, Organic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim. doi:10.1002/14356007.a11_393
  18. ^ "Manufacturing Polytetrafluoroethylene". Introduction to Fluoropolymers. William Andrew. 2013. pp. 91–124. doi:10.1016/B978-1-4557-7442-5.00007-3. ISBN 9781455774425.
  19. ^ Pierozan, Paula; Cattani, Daiane; Karlsson, Oskar (February 2022). "Tumorigenic activity of alternative per- and polyfluoroalkyl substances (PFAS): Mechanistic in vitro studies". Science of the Total Environment. 808: 151945. Bibcode:2022ScTEn.808o1945P. doi:10.1016/j.scitotenv.2021.151945. PMID 34843762. S2CID 244730906.
  20. ^ a b "Fluoroplastic Comparison - Typical Properties". Chemours. Archived from the original on 3 February 2016.
  21. ^ Teflon PTFE Properties Handbook. Retrieved 11 October 2012.
  22. ^ "Chemours Teflon™ Coating Applications". plastechcoatings.com.
  23. ^ R. J. Hunadi; K. Baum (1982). "Tetrafluoroethylene: A Convenient Laboratory Preparation". Synthesis. 39 (6): 454. doi:10.1055/s-1982-29830. S2CID 96276938.
  24. ^ Nicholson, John W. (2011). The Chemistry of Polymers (4, Revised ed.). Royal Society of Chemistry. p. 50. ISBN 9781849733915.
  25. ^ "Reference Tables – Thermal Expansion Coefficients – Plastics". engineershandbook.com. Archived from the original on 3 January 2012. Retrieved 2 January 2012.
  26. ^ Blumm, J.; Lindemann, A.; Meyer, M.; Strasser, C. (2011). "Characterization of PTFE Using Advanced Thermal Analysis Technique". International Journal of Thermophysics. 40 (3–4): 311. Bibcode:2010IJT....31.1919B. doi:10.1007/s10765-008-0512-z. S2CID 122020437.
  27. ^ Wapler, M. C.; Leupold, J.; Dragonu, I.; von Elverfeldt, D.; Zaitsev, M.; Wallrabe, U. (2014). "Magnetic properties of materials for MR engineering, micro-MR and beyond". JMR. 242: 233–242. arXiv:1403.4760. Bibcode:2014JMagR.242..233W. doi:10.1016/j.jmr.2014.02.005. PMID 24705364. S2CID 11545416.
  28. ^ Coefficient of Friction (COF) Testing of Plastics. MatWeb Material Property Data. Retrieved 1 January 2007.
  29. ^ "Research into Gecko Adhesion", Berkeley, 2007-10-14. Retrieved 8 April 2010.
  30. ^ "PTFE Sheet". Gasket Resources Inc. Retrieved 16 August 2017.
  31. ^ Davet, George P. "Using Belleville Springs To Maintain Bolt Preload" (PDF). Solon Mfg. Co. Archived from the original (PDF) on 18 May 2014. Retrieved 18 May 2014.
  32. ^ Ferry, Laurent; Gérard, Vigier; Bessede, Jean Luc (June 1996). "Effect of ultraviolet radiation on polytetrafluoroethylene: Morphology influence". Polymers for Advanced Technologies. 7 (5–6): 493–500. doi:10.1002/(SICI)1099-1581(199605)7:5/6<493::AID-PAT536>3.0.CO;2-D – via Wiley.
  33. ^ a b Zapp JA, Limperos G, Brinker KC (26 April 1955). "Toxicity of pyrolysis products of 'Teflon' tetrafluoroethylene resin". Proceedings of the American Industrial Hygiene Association Annual Meeting.
  34. ^ "COWIE TECHNOLOGY - PTFE: High Thermal Stability". Cowie.com. Retrieved 16 August 2017.
  35. ^ "Free Flow Granular PTFE" (PDF). Inoflon Fluoropolymers. 16 August 2017.
  36. ^ Sina Ebnesajjad (21 September 2016). Expanded PTFE Applications Handbook: Technology, Manufacturing and Applications. William Andrew. pp. 31–32. ISBN 978-1-4377-7856-4.
  37. ^ a b c "Polyflon PTFE Molding Powder" (PDF). Daikin Chemical. 16 August 2017.
  38. ^ "Unraveling Polymers: PTFE". Poly Fouoro Ltd. 26 April 2011. Retrieved 23 April 2017.
  39. ^ a b Mishra, Munmaya; Yagci, Yusuf (208). Handbook of Vinyl Polymers: Radical Polymerization, Process, and Technology, Second Edition (2nd, illustrated, revised ed.). CRC Press. p. 574. ISBN 978-0-8247-2595-2. Extract of page 574
  40. ^ "Teflon Machining & Fabrication". Espemfg.com. Retrieved 28 August 2018.
  41. ^ Mishra & Yagci, p 573
  42. ^ "PTFE". MakMax Australia.
  43. ^ "What is MicPol?". Interflonusa.com. Archived from the original on 3 October 2018. Retrieved 3 October 2018.
  44. ^ "GT85 General Lubricant with PTFE - 400ml". Baysidemarine.co.uk. Retrieved 5 March 2022.
  45. ^ Fers à repasser semelle teflon - Fiche pratique - Le Parisien. Pratique.leparisien.fr. Retrieved on 2016-11-17.
  46. ^ "A Motorcyclist's Guide To Gore-Tex". Infinity Motorcycles. Archived from the original on 5 July 2015. Retrieved 17 January 2019.
  47. ^ "Advantages and Disadvantages of Teflon-coated Covert Cloth". The Cutter and Tailor. Archived from the original on 3 July 2015. Retrieved 22 May 2015.
  48. ^ "PTFE & Industrial Non-Stick Fluoropolymer Coating Services | Delta Coatings & Linings, Inc". Deltacoatingsandliningsbr.com. Retrieved 5 March 2022.
  49. ^ "Film Interface Patch". American Academy of Orthotists & Prosthetists.
  50. ^ Park, Junghyun; Rittiphairoj, Thanitsara; Wang, Xue; E, Jian-Yu; Bicket, Amanda K. (13 March 2023). "Device-modified trabeculectomy for glaucoma". The Cochrane Database of Systematic Reviews. 2023 (3): CD010472. doi:10.1002/14651858.CD010472.pub3. ISSN 1469-493X. PMC 10010250. PMID 36912740.
  51. ^ Koch, E.-C. (2002). "Metal-Fluorocarbon Pyrolants:III. Development and Application of Magnesium/Teflon/Viton". Propellants, Explosives, Pyrotechnics. 27 (5): 262–266. doi:10.1002/1521-4087(200211)27:5<262::AID-PREP262>3.0.CO;2-8.
  52. ^ "Lubicle 1". TheCubicle.us. Retrieved 20 May 2017.
  53. ^ "Interview with an inventor of the KTW bullet". NRAction Newsletter. 4 (5). May 1990.
  54. ^ Pomeroy, Ross (24 August 2013). "The World's Strongest Acids: Like Fire and Ice". Retrieved 9 April 2016.
  55. ^ "Industrial Air Permits - New Clean Air Regulations And Baghouses". Baghouse.com. 28 May 2012.
  56. ^ Brown, DDS, Dennis E. (January 2002). "Using Plumber's Teflon Tape to Enhance Bonding Procedures". Dentistry Today. 21 (1): 76–8, 80–1. PMID 11824121.
  57. ^ Dunn, WJ; et al. (2004). "Polytetrafluoroethylene (PTFE) tape as a matrix in operative dentistry". Operative Dentistry. 29 (4): 470–2. PMID 15279489.
  58. ^ Rosenthal, Ed (21 October 2014). Beyond Buds (Revised ed.). Quick American Archives. ISBN 978-1936807239.
  59. ^ a b "Fluoropolymer PTFE coating services from Surface Technology UK". Surface Technology. Retrieved 26 February 2018.
  60. ^ a b Sajid, Muhammad; Ilyas, Muhammad (October 2017). "PTFE-coated non-stick cookware and toxicity concerns: a perspective". Environmental Science and Pollution Research. 24 (30): 23436–23440. Bibcode:2017ESPR...2423436S. doi:10.1007/s11356-017-0095-y. ISSN 0944-1344. PMID 28913736. S2CID 10437300.
  61. ^ "Key Safety Questions About Teflon Nonstick Coatings". DuPont. Archived from the original on 2 May 2013. Retrieved 28 November 2014.
  62. ^ "Key Safety Questions about the Safety of Nonstick Cookware". DuPont. Archived from the original on 2 May 2013. Retrieved 28 November 2014.
  63. ^ a b c d e "Hazardous Substances Data Bank (HSDB) : 833". pubchem.ncbi.nlm.nih.gov. National Center for Biotechnology Information National Library of Medicine. Retrieved 4 April 2022.
  64. ^ Griffith, Franklin D.; Stephens, Susan S.; Tayfun, Figen O. (April 1973). "Exposure of Japanese Quail and Parakeets to the Pyrolysis Products of Fry Pans Coated with Teflon® and Common Cooking Oils". American Industrial Hygiene Association Journal. 34 (4): 176–178. doi:10.1080/0002889738506828. PMID 4723395.
  65. ^ a b "Perfluorooctanoic Acid (PFOA), Teflon, and Related Chemicals". www.cancer.org. Retrieved 4 April 2022.
  66. ^ "The truth about teflon: are non-stick pans safe?". Better Homes and Gardens. 2 October 2019. Retrieved 11 June 2020.
  67. ^ Emerging Contaminants Fact Sheet – Perfluorooctane Sulfonate (PFOS) and Perfluorooctanoic Acid (PFOA). National Service Center for Environmental Publications (Report). United States Environmental Protection Agency. March 2014. p. 1. 505-F-14-001. Retrieved 10 February 2019.
  68. ^ "PFAs Factsheet" (PDF). Casaweb.org. Retrieved 5 March 2022.
  69. ^ RIch, Nathaniel (6 January 2016). "The Lawyer Who Became Dupont's Worst Nightmare". The New York Times. Retrieved 7 January 2016.
  70. ^ Blake, Mariah. "Welcome to Beautiful Parkersburg, West Virginia Home to one of the most brazen, deadly corporate gambits in U.S. history". HuffPost. Retrieved 31 August 2015.
  71. ^ Fellner, Carrie (16 June 2018). "Toxic Secrets: Professor 'bragged about burying bad science' on 3M chemicals". The Sydney Morning Herald. Retrieved 25 June 2018.
  72. ^ Nicole, W. (2013). "PFOA and Cancer in a Highly Exposed Community: New Findings from the C8 Science Panel". Environmental Health Perspectives. 121 (11–12): A340. doi:10.1289/ehp.121-A340. PMC 3855507. PMID 24284021.
  73. ^ Trudel D, Horowitz L, Wormuth M, Scheringer M, Cousins IT, Hungerbühler K (April 2008). "Estimating consumer exposure to PFOS and PFOA". Risk Anal. 28 (2): 251–69. Bibcode:2008RiskA..28..251T. doi:10.1111/j.1539-6924.2008.01017.x. PMID 18419647. S2CID 10777081.
  74. ^ Beekman, M.; et al. (12 December 2016). "Evaluation of substances used in the GenX technology by Chemours, Dordrecht". National Institute for Public Health and the Environment (RIVM, The Netherlands). Retrieved 23 July 2017.
  75. ^ "What is the difference between PFOA, PFOS and GenX and other replacement PFAS?". PFOA, PFOS and Other PFASs. EPA. 18 February 2018.
  76. ^ Caverly Rae, JM; Craig, Lisa; Stone, Theodore W.; Frame, Steven R.; Buxton, L. William; Kennedy, Gerald L. (2015). "Evaluation of chronic toxicity and carcinogenicity of ammonium 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)-propanoate in Sprague–Dawley rats". Toxicology Reports. 2: 939–949. doi:10.1016/j.toxrep.2015.06.001. PMC 5598527. PMID 28962433.
  77. ^ Lerner, Sharon (3 March 2016). "New Teflon Toxin Causes Cancer in Lab Animals". The Intercept. Retrieved 14 December 2018.
  78. ^ "GenX Frequently Asked Questions" (PDF). GenX Investigation. Raleigh, NC: North Carolina Department of Environmental Quality (NCDEQ). 15 February 2018.
  79. ^ FEP Detailed Properties, Parker-TexLoc, 13 April 2006. Retrieved 10 September 2006.

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