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  2. Ethylene vinyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Ethylene_vinyl_alcohol

    Ethylene vinyl alcohol (EVOH) is a formal copolymer of ethylene and vinyl alcohol. Because the latter monomer mainly exists as its tautomer acetaldehyde , the copolymer is prepared by polymerization of ethylene and vinyl acetate to give the ethylene vinyl acetate (EVA) copolymer followed by hydrolysis.

  3. Polyethylene - Wikipedia

    en.wikipedia.org/wiki/Polyethylene

    The less the polymer chains are branched, and the lower the molecular weight, the higher the crystallinity of polyethylene. Crystallinity ranges from 35% (PE-LD/PE-LLD) to 80% (PE-HD). Polyethylene has a density of 1.0 g/cm 3 in crystalline regions and 0.86 g/cm 3 in amorphous regions. An almost linear relationship exists between density and ...

  4. Monomer - Wikipedia

    en.wikipedia.org/wiki/Monomer

    Ethylene gas (H 2 C=CH 2) is the monomer for polyethylene. Other modified ethylene derivatives include: tetrafluoroethylene (F 2 C=CF 2) which leads to Teflon; vinyl chloride (H 2 C=CHCl) which leads to PVC; styrene (C 6 H 5 CH=CH 2) which leads to polystyrene; Epoxide monomers may be cross linked with themselves, or with the addition of a co ...

  5. Anionic addition polymerization - Wikipedia

    en.wikipedia.org/wiki/Anionic_addition...

    Two broad classes of monomers are susceptible to anionic polymerization. [3] Vinyl monomers have the formula CH 2 =CHR, the most important are styrene (R = C 6 H 5), butadiene (R = CH=CH 2), and isoprene (R = C(Me)=CH 2). A second major class of monomers are acrylate esters, such as acrylonitrile, methacrylate, cyanoacrylate, and acrolein.

  6. Ring-opening polymerization - Wikipedia

    en.wikipedia.org/wiki/Ring-opening_polymerization

    A polymerization in which a cyclic monomer yields a monomeric unit which is acyclic or contains fewer cycles than the monomer. Note: If monomer is polycyclic, the opening of a single ring is sufficient to classify the reaction as ring-opening polymerization. Modified from the earlier definition. [1] [2]

  7. Polyolefin - Wikipedia

    en.wikipedia.org/wiki/Polyolefin

    Alpha-olefins such as 1-hexene may be used as co-monomers to give an alkyl branched polymer (see chemical structure below), although 1-decene is most commonly used for lubricant base stocks. [8] 1-hexene, an example of an alpha-olefin. Many poly-alpha-olefins have flexible alkyl branching groups on every other carbon of their polymer backbone ...

  8. Emulsion polymerization - Wikipedia

    en.wikipedia.org/wiki/Emulsion_polymerization

    In polymer chemistry, emulsion polymerization is a type of radical polymerization that usually starts with an emulsion incorporating water, monomers, and surfactants.The most common type of emulsion polymerization is an oil-in-water emulsion, in which droplets of monomer (the oil) are emulsified (with surfactants) in a continuous phase of water.

  9. Repeat unit - Wikipedia

    en.wikipedia.org/wiki/Repeat_unit

    For example, in polyethylene terephthalate (PET or "polyester"), the repeat unit is -CO-C 6 H 4-CO-O-CH 2-CH 2-O-. 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 ...