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  2. Vinyl polymer - Wikipedia

    en.wikipedia.org/wiki/Vinyl_polymer

    Vinyl polymers are subject of several structural variations, which greatly expands the range of polymers and their applications. With the exception of polyethylene, vinyl polymers can arise from head-to-tail linking of monomers, head-to-head combined with tail-to-tail, or a mixture of those two patterns. Additionally the substituted carbon center in such polymers is stereogenic (a "chiral center")

  3. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    It is the ethylene (IUPAC name: ethene) molecule (H 2 C=CH 2) with one fewer hydrogen atom. The name is also used for any compound containing that group, namely R−CH=CH 2 where R is any other group of atoms. An industrially important example is vinyl chloride, precursor to PVC, [3] a plastic commonly known as vinyl. Chessboard made from ...

  4. Polyvinyl chloride - Wikipedia

    en.wikipedia.org/wiki/Polyvinyl_chloride

    The presence of chloride groups gives the polymer very different properties from the structurally related material polyethylene. [17] At 1.4 g/cm 3, PVC's density is also higher than structurally related plastics such as polyethylene (0.88–0.96 g/cm 3) and polymethylmethacrylate (1.18 g/cm 3).

  5. Repeat unit - Wikipedia

    en.wikipedia.org/wiki/Repeat_unit

    The polymer is formed by the condensation reaction of the two monomers terephthalic acid (HOOC-C 6 H 4-COOH) and ethylene glycol (HO-CH 2-CH 2-OH), or their chemical derivatives. The condensation involves loss of water, as an H is lost from each HO- group in the glycol, and an OH from each HOOC- group in the acid.

  6. Vinyl chloride - Wikipedia

    en.wikipedia.org/wiki/Vinyl_chloride

    Vinyl chloride is an organochloride with the formula H 2 C=CHCl. It is also called vinyl chloride monomer (VCM) or chloroethene. It is an important industrial chemical chiefly used to produce the polymer polyvinyl chloride (PVC). Vinyl chloride is a colourless flammable gas that has a sweet odor and is carcinogenic.

  7. Radical polymerization - Wikipedia

    en.wikipedia.org/wiki/Radical_polymerization

    Radicals can be formed by a number of different mechanisms, usually involving separate initiator molecules. Following its generation, the initiating radical adds (nonradical) monomer units, thereby growing the polymer chain. Radical polymerization is a key synthesis route for obtaining a wide variety of different polymers and materials ...

  8. Polymer - Wikipedia

    en.wikipedia.org/wiki/Polymer

    Polymer nomenclature is generally based upon the type of monomer residues comprising the polymer. A polymer which contains only a single type of repeat unit is known as a homopolymer, while a polymer containing two or more types of repeat units is known as a copolymer. [22] A terpolymer is a copolymer which contains three types of repeat units ...

  9. Acrylonitrile - Wikipedia

    en.wikipedia.org/wiki/Acrylonitrile

    Acrylonitrile is produced by catalytic ammoxidation of propylene, also known as the SOHIO process. In 2002, world production capacity was estimated at 5 million tonnes per year, [5] [8] rising to about 6 million tonnes by 2017. [9] Acetonitrile and hydrogen cyanide are significant byproducts that are recovered for sale. [5]