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  2. Tetrafluoroethylene - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroethylene

    A convenient, safe method for generating TFE is the pyrolysis of the sodium salt of pentafluoropropionic acid: [6]. C 2 F 5 CO 2 Na → C 2 F 4 + CO 2 + NaF. The depolymerization reaction – vacuum pyrolysis of PTFE at 650–700 °C (1,200–1,290 °F) in a quartz vessel – is a traditional laboratory synthesis of TFE.

  3. Fluoropolymer - Wikipedia

    en.wikipedia.org/wiki/Fluoropolymer

    A fluoropolymer is a fluorocarbon-based polymer with multiple carbon–fluorine bonds. It is characterized by a high resistance to solvents , acids , and bases . The best known fluoropolymer is polytetrafluoroethylene under the brand name "Teflon," trademarked by the DuPont Company.

  4. Polytetrafluoroethylene - Wikipedia

    en.wikipedia.org/wiki/Polytetrafluoroethylene

    Polytetrafluoroethylene (PTFE) is a synthetic fluoropolymer of tetrafluoroethylene, and has numerous applications because it is chemically inert. [3] The commonly known brand name of PTFE-based composition is Teflon by Chemours, [4] a spin-off from DuPont, which originally invented the compound in 1938. [4]

  5. Smart Watch Bands Contain 'Very High Concentrations’ of ...

    www.aol.com/lifestyle/smart-watch-bands-contain...

    Related: Cancer-Causing 'Forever Chemicals' Found in Many Kinds of Contact Lenses, Study Finds The issue, the statement says, comes from a synthetic polymer called fluoroelastomer, which is used ...

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  7. Oral-B Glide - Wikipedia

    en.wikipedia.org/wiki/Oral-B_Glide

    The origin of Glide (which is what the brand was called prior to the P&G acquisition) dates to 1971, when Bill Gore first used a Gore-Tex fiber to floss his own teeth; [1] Gore-Tex was the PTFE-based fiber he had invented as a "waterproof laminate". The company failed to market the product for more than three decades.

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  9. 2,2,2-Trifluoroethanol - Wikipedia

    en.wikipedia.org/wiki/2,2,2-Trifluoroethanol

    TFE forms complexes with Lewis bases such as THF or pyridine through hydrogen bonding, yielding 1:1 adducts. [6] It is classified as a hard Lewis acid and its acceptor properties are discussed in the ECW model yielding E A = 2.07 and C A = 1.06. TFE can be used in biochemical experiments to stabilize alpha helix.