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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. 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.

  4. 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 ...

  5. 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 ...

  6. 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 .

  7. 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")

  8. 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.

  9. Addition polymer - Wikipedia

    en.wikipedia.org/wiki/Addition_polymer

    Addition polymers form high molecular weight chains rapidly, with much monomer remaining. Since addition polymerization has rapidly growing chains and free monomer as its reactants, and condensation polymerization occurs in step-wise fashion between monomers, dimers, and other smaller growing chains, the effect of a polymer molecule's current ...