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This timeline of events related to per- and polyfluoroalkyl substances (PFASs) includes events related to the discovery, development, manufacture, marketing, uses, concerns, litigation, regulation, and legislation, involving the human-made PFASs. The timeline focuses on some perfluorinated compounds, particularly perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS)[1] and on the companies that manufactured and marketed them, mainly DuPont and 3M.[2] An example of PFAS is the fluorinated polymer polytetrafluoroethylene (PTFE), which has been produced and marketed by DuPont under its trademark Teflon. GenX chemicals and perfluorobutanesulfonic acid (PFBS) are organofluorine chemicals used as a replacement for PFOA and PFOS.[3]
The examples and perspective in this deal primarily with the United States and do not represent a worldwide view of the subject. (September 2022) |
PFAS compounds and their derivatives are widely used in many products from water resistant textiles to fire-fighting foam.[4][1] PFAS are commonly found in every American household in products as diverse as non-stick cookware, stain resistant furniture and carpets, wrinkle free and water repellent clothing, cosmetics, lubricants, paint, pizza boxes, popcorn bags and many other everyday products.[5]
"PFOS was measured in the tissues of wildlife, including, fish, birds, and marine mammals. Some of the species studied include bald eagles, polar bears, albatrosses, and various species of seals. Samples were collected from urbanized areas in North America, especially the Great Lakes region and coastal marine areas and rivers, and Europe. Samples were also collected from a number of more remote, less urbanized locations such as the Arctic and the North Pacific Oceans. ... Concentrations of PFOS in animals from relatively more populated and industrialized regions, such as the North American Great Lakes, Baltic Sea, and Mediterranean Sea, were greater than those in animals from remote marine locations. Fish-eating, predatory animals such as mink and bald eagles contained concentrations of PFOS that were greater than the concentrations in their diets."
— John P. Giesy and Kurunthachalam Kannan. 2001.
Compound | Chemical formula | Structural model | 3D image | Other names | Notes |
---|---|---|---|---|---|
Tetrafluoroethylene (TFE) | C2F4 | Tetrafluoroethene, Perfluoroethylene, Perfluoroethene | Precursor to PTFE (Teflon) | ||
Perfluorooctanoic acid (PFOA) | C8HF15O2 | perfluorooctanoic acid, PFOA, C8, perfluorooctanoate, perfluorocaprylic acid, FC-143, F-n-octanoic acid, PFO | |||
Perfluorononanoic acid (PFNA) | C9HF17O2 | As ion: perfluorononanoate | Here the health effects of PFNA, one of the ten most common PFAS, has been more widely studied.[82] Some of the "highest levels" of PFNA "ever found anywhere" are present in the Superfund Coakley landfill site in North Hampton, New Hampshire, and Greenland, New Hampshire.[98] | ||
Perfluorooctanesulfonic acid (PFOS) | C8HF17O3S | As ion: perfluorooctanesulfonate | |||
Polytetrafluoroethylene (PTFE) | (C2F4)n | Syncolon, Fluon, Poly(tetrafluroethene), Poly(difluoromethylene), Poly(tetrafluoroethylene), Teflon | |||
Perfluorohexanesulfonic acid (PFHxS) | C6HF13O3S | Perfluorohexane-1-sulphonic acid | |||
Perfluorohexanoic acid (PFHxA) | C6HF11O | Perfluoro-1-pentanecarboxylic acid | |||
GenX | C6H4F11NO3 | GenX, FRD-902, Ammonium 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propanoate | Replacement for PFOA developed by DuPont. GenX is created by combining two HFPO molecules to form HFPO-DA fluoride which is then converted to HFPO-DA. GenX is the ammonium salt of HFPO-DA. When GenX contacts water it releases HFPO-DA.
This ammonium salt is the chemical compound trademarked by Chemours as GenX, though many other compounds related to the GenX process are informally referred to as GenX.[124] | ||
Hexafluoropropylene oxide (HFPO) | C3F6O | 2,2,3-Trifluoro-3-(trifluoromethyl)oxirane | Precursor to GenX | ||
Hexafluoropropylene oxide dimer acid fluoride (HFPO-DA fluoride) | C6F12O2 | 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propionyl fluoride | Precursor to GenX | ||
Hexafluoropropylene oxide dimer acid (HFPO-DA) | C6HF11O3 | FRD-903, 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propanoic acid | Chemical used in the GenX process. GenX hydrolyzes in the presence of water to form HFPO-DA.[124] | ||
Perfluorobutanesulfonic acid (PFBS) | C4HF9O3S |
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