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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 neodecanoate - Wikipedia

    en.wikipedia.org/wiki/Vinyl_neodecanoate

    Vinyl neodecanoate (trade name VeoVa 10) is a vinylic monomer that is virtually always used in combination with other monomers to create latices or emulsion polymers. [3] The trade name is an acronym of Vinyl ester of Versatic Acid with the number 10 meaning 10 carbons in the molecule. It has a medium to low glass transition temperature of -3 °C.

  4. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_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.

  5. Calender - Wikipedia

    en.wikipedia.org/wiki/Calender

    Polymers such as vinyl and ABS polymer sheets, and to a lesser extent HDPE, polypropylene and polystyrene, are calendered. The calender is also an important processing machine in the rubber industries, especially in the manufacture of tires, where it is used for the inner layer and fabric layer.

  6. N-Vinylpyrrolidone - Wikipedia

    en.wikipedia.org/wiki/N-Vinylpyrrolidone

    N-Vinylpyrrolidone (NVP) is an organic compound consisting of a 5-membered lactam ring linked to a (2 carbon) vinyl group. It is a colorless liquid although commercial samples can appear yellowish. It is produced industrially by vinylation of 2-pyrrolidone, i.e. the base-catalyzed reaction with acetylene. [2]

  7. 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).

  8. 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.

  9. N-Vinylacetamide - Wikipedia

    en.wikipedia.org/wiki/N-Vinylacetamide

    N-Vinylacetamide (NVA) is a non-ionic monomer. Copolymers made of NVA and other monomers can exhibit practical characteristics in addition to those common with the existing hydrophilic polymers. History