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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

    Saturated hydrocarbons are the basis of petroleum fuels and may be either linear or branched species. One or more of the hydrogen atoms can be replaced with other atoms, for example chlorine or another halogen: this is called a substitution reaction. An example is the conversion of methane to chloroform using a chlorination reaction ...

  9. Three-carbon molecule - Wikipedia

    en.wikipedia.org/wiki/Three-carbon_molecule

    Three-carbon molecules are based on a skeleton made from three carbon atoms. They may be in a chain, or cycles. C3 hydrocarbons are usually gases, they are inflammable, and may be harmful to humans and the environment. [1] The CAS registry number for three-carbon hydrocarbons is 68606-26-8. Hydrocarbons that include three atoms are: Propane C 3 ...