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  2. Ethylene-vinyl acetate - Wikipedia

    en.wikipedia.org/wiki/Ethylene-vinyl_acetate

    The weight percent of vinyl acetate usually varies from 10 to 50%, with the remainder being ethylene. There are three different types of EVA copolymer, which differ in the vinyl acetate (VA) content and the way the materials are used. The EVA copolymer which is based on a low proportion of VA (approximately up to 4%) may be referred to as vinyl ...

  3. Vinyl acetate - Wikipedia

    en.wikipedia.org/wiki/Vinyl_acetate

    Vinyl acetate is the acetate ester of vinyl alcohol. Since vinyl alcohol is highly unstable (with respect to acetaldehyde), the preparation of vinyl acetate is more complex than the synthesis of other acetate esters. The major industrial route involves the reaction of ethylene and acetic acid with oxygen in the presence of a palladium catalyst. [6]

  4. Polyethylene - Wikipedia

    en.wikipedia.org/wiki/Polyethylene

    In addition to copolymerization with alpha-olefins, ethylene can be copolymerized with a wide range of other monomers and ionic composition that creates ionized free radicals. Common examples include vinyl acetate (the resulting product is ethylene-vinyl acetate copolymer, or EVA, widely used in athletic-shoe sole foams) and a variety of acrylates.

  5. Polyvinyl acetate - Wikipedia

    en.wikipedia.org/wiki/Polyvinyl_acetate

    Polyvinyl acetate was discovered in Germany in 1912 by Fritz Klatte. [3] The monomer, vinyl acetate, was first produced on an industrial scale by the addition of acetic acid to acetylene with a mercury(I) salt, [4] but it is now primarily made by palladium-catalyzed oxidative addition of acetic acid to ethylene.

  6. Vinyltriethoxysilane - Wikipedia

    en.wikipedia.org/wiki/Vinyltriethoxysilane

    Vinyltriethoxysilane and the related vinyltrimethoxysilane are used as monomers and comonomer for polymers such as ethylene-vinyltrimethoxysilane and ethylene-vinyl acetate-vinyltrimethoxysilane. Vinyltrialkoxysilanes are also used as cross-linking agents during the manufacture of cross-linked polyethylene (PEX).

  7. Polyvinyl butyral - Wikipedia

    en.wikipedia.org/wiki/Polyvinyl_butyral

    CAS Number. 63148-65-2 915977 ... used in the solar industry is ethylene-vinyl acetate ... tend to adhere to the interlayer rather than falling free and potentially ...

  8. 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.

  9. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    Chemical structure of the vinyl functional group. In organic chemistry , a vinyl group (abbr. Vi ; [ 1 ] IUPAC name : ethenyl group [ 2 ] ) is a functional group with the formula −CH=CH 2 . It is the ethylene (IUPAC name: ethene) molecule ( H 2 C=CH 2 ) with one fewer hydrogen atom.