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  2. Polytetrafluoroethylene - Wikipedia

    en.wikipedia.org/wiki/Polytetrafluoroethylene

    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.

  3. 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.

  4. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    Organofluorine chemistry describes the chemistry of organofluorine compounds, organic compounds that contain a carbon–fluorine bond. Organofluorine compounds find diverse applications ranging from oil and water repellents to pharmaceuticals, refrigerants, and reagents in catalysis. In addition to these applications, some organofluorine ...

  5. Fluorine - Wikipedia

    en.wikipedia.org/wiki/Fluorine

    Fluorine. cubic. Fluorine is a chemical element; it has symbol F and atomic number 9. It is the lightest halogen [note 1] and exists at standard conditions as pale yellow diatomic gas. Fluorine is extremely reactive as it reacts with all other elements except for the light inert gases.

  6. Hydrophobe - Wikipedia

    en.wikipedia.org/wiki/Hydrophobe

    Cutting a water droplet using a superhydrophobic knife on superhydrophobic surfaces. Water drops on the hydrophobic surface of grass. In chemistry, hydrophobicity is the physical property of a molecule that is seemingly repelled from a mass of water (known as a hydrophobe). [1] In contrast, hydrophiles are attracted to water.

  7. Fluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Fluorocarbon

    Fluorocarbons are chemical compounds with carbon-fluorine bonds. Compounds that contain many C-F bonds often have distinctive properties, e.g., enhanced [clarification needed] stability, volatility, and hydrophobicity. Several fluorocarbons and their derivatives are commercial polymers, refrigerants, drugs, and anesthetics.

  8. Phthalates - Wikipedia

    en.wikipedia.org/wiki/Phthalates

    Phthalates are produced industrially by the acid catalysed reaction of phthalic anhydride with excess alcohol.The synthesis of diethyl phthalate is illustrative of this: . The properties of the phthalate can be varied by changing the alcohol, [12] allowing for an almost limitless range of products, although only around 30 are, or have been, commercially important.

  9. Air sensitivity - Wikipedia

    en.wikipedia.org/wiki/Air_sensitivity

    Air sensitivity is a term used, particularly in chemistry, to denote the reactivity of chemical compounds with some constituent of air.Most often, reactions occur with atmospheric oxygen (O 2) or water vapor (H 2 O), [1] although reactions with the other constituents of air such as carbon monoxide (CO), carbon dioxide (CO 2), and nitrogen (N 2) are also possible.