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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. Reactivity (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Reactivity_(chemistry)

    Reactivity is a somewhat vague concept in chemistry. It appears to embody both thermodynamic factors and kinetic factors (i.e., whether or not a substance reacts, and how fast it reacts). Both factors are actually distinct, and both commonly depend on temperature. For example, it is commonly asserted that the reactivity of alkali metals (Na, K ...

  5. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    Fluorine compounds. Fluorine forms a great variety of chemical compounds, within which it always adopts an oxidation state of −1. With other atoms, fluorine forms either polar covalent bonds or ionic bonds. Most frequently, covalent bonds involving fluorine atoms are single bonds, although at least two examples of a higher order bond exist. [2]

  6. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    As a result, the physical and chemical properties of organofluorines can be distinctive in comparison to other organohalogens. The carbon–fluorine bond is one of the strongest in organic chemistry (an average bond energy around 480 kJ/mol [ 1 ]). This is significantly stronger than the bonds of carbon with other halogens (an average bond ...

  7. 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.

  8. Surface energy - Wikipedia

    en.wikipedia.org/wiki/Surface_energy

    The surface energy of a liquid may be measured by stretching a liquid membrane (which increases the surface area and hence the surface energy). In that case, in order to increase the surface area of a mass of liquid by an amount, δA, a quantity of work, γ δA, is needed (where γ is the surface energy density of the liquid).

  9. Relative permittivity - Wikipedia

    en.wikipedia.org/wiki/Relative_permittivity

    Permittivity is a material's property that affects the Coulomb force between two point charges in the material. Relative permittivity is the factor by which the electric field between the charges is decreased relative to vacuum. Likewise, relative permittivity is the ratio of the capacitance of a capacitor using that material as a dielectric ...