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  2. Polystyrene - Wikipedia

    en.wikipedia.org/wiki/Polystyrene

    Polystyrene (PS) / ˌ p ɒ l i ˈ s t aɪ r iː n / is a synthetic polymer made from monomers of the aromatic hydrocarbon styrene. [5] Polystyrene can be solid or foamed. General-purpose polystyrene is clear, hard, and brittle. It is an inexpensive resin per unit weight. It is a poor barrier to air and water vapor and has a relatively low ...

  3. Styrene - Wikipedia

    en.wikipedia.org/wiki/Styrene

    Styrene is an organic compound with the chemical formula C 6 H 5 CH=CH 2.Its structure consists of a vinyl group as substituent on benzene.Styrene is a colorless, oily liquid, although aged samples can appear yellowish.

  4. Pendant group - Wikipedia

    en.wikipedia.org/wiki/Pendant_group

    In IUPAC nomenclature of chemistry, a pendant group (sometimes spelled pendent) or side group is a group of atoms attached to a backbone chain of a long molecule, usually a polymer. Pendant groups are different from pendant chains, as they are neither oligomeric nor polymeric. [2] For example, the phenyl groups are the pendant groups on a ...

  5. Polymer backbone - Wikipedia

    en.wikipedia.org/wiki/Polymer_backbone

    Formation of polystyrene, a polymer with an organic backbone. Common synthetic polymers have main chains composed of carbon, i.e. C-C-C-C.... Examples include polyolefins such as polyethylene ((CH 2 CH 2 ) n ) and many substituted derivative ((CH 2 CH(R)) n ) such as polystyrene (R = C 6 H 5 ), polypropylene (R = CH 3 ), and acrylates (R = CO 2 ...

  6. Polymer - Wikipedia

    en.wikipedia.org/wiki/Polymer

    The degradation of polyethylene occurs by random scission—a random breakage of the bonds that hold the atoms of the polymer together. When heated above 450 °C, polyethylene degrades to form a mixture of hydrocarbons. In the case of chain-end scission, monomers are released and this process is referred to as unzipping or depolymerization ...

  7. Ethylbenzene - Wikipedia

    en.wikipedia.org/wiki/Ethylbenzene

    Ethylbenzene is an organic compound with the formula C 6 H 5 CH 2 CH 3.It is a highly flammable, colorless liquid with an odor similar to that of gasoline.This monocyclic aromatic hydrocarbon is important in the petrochemical industry as a reaction intermediate in the production of styrene, the precursor to polystyrene, a common plastic material.

  8. Hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon

    [1]: 623 The most general form of saturated hydrocarbons, (whether linear or branched species, and whether with or without one or more rings) is C n H 2n+2(1-r), where r is the number of rings. Those with exactly one ring are the cycloalkanes. Saturated hydrocarbons are the basis of petroleum fuels and may be either linear or branched species ...

  9. Polycyclic aromatic hydrocarbon - Wikipedia

    en.wikipedia.org/.../Polycyclic_aromatic_hydrocarbon

    A Polycyclic aromatic hydrocarbon (PAH) is a class of organic compounds that is composed of multiple aromatic rings.Most are produced by the incomplete combustion of organic matter— by engine exhaust fumes, tobacco, incinerators, in roasted meats and cereals, [1] or when biomass burns at lower temperatures as in forest fires.