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  2. 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]

  3. Propylene - Wikipedia

    en.wikipedia.org/wiki/Propylene

    Propylene, also known as propene, is an unsaturated organic compound with the chemical formula CH 3 CH=CH 2. It has one double bond, and is the second simplest member of the alkene class of hydrocarbons. It is a colorless gas with a faint petroleum-like odor. [4]

  4. Polyvinyl chloride - Wikipedia

    en.wikipedia.org/wiki/Polyvinyl_chloride

    In a fire, PVC can form hydrogen chloride fumes; the chlorine serves to scavenge free radicals, making PVC-coated wires fire retardant. While hydrogen chloride fumes can also pose a health hazard in their own right, it dissolves in moisture and breaks down onto surfaces, particularly in areas where the air is cool enough to breathe, so would ...

  5. 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")

  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. 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. Polyacrylonitrile - Wikipedia

    en.wikipedia.org/wiki/Polyacrylonitrile

    PAN is soluble in polar solvents, such as dimethylformamide, dimethylacetamide, ethylene and propylene carbonates, and in aqueous solutions of sodium thiocyanate, zinc chloride or nitric acid. [13] Solubility parameters: 26.09 MPa 1/2 (25 °C) are 25.6 to 31.5 J 1/2 cm −3/2. Dielectric constants: 5.5 (1 kHz, 25 °C), 4.2 (1 MHz, 25 °C).Can ...

  9. Polypropylene - Wikipedia

    en.wikipedia.org/wiki/Polypropylene

    In gas-phase and slurry-reactors, the polymer is formed around heterogeneous catalyst particles. The gas-phase polymerization is carried out in a fluidized bed reactor, propene is passed over a bed containing the heterogeneous (solid) catalyst and the formed polymer is separated as a fine powder and then converted into pellets. Unreacted gas is ...