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  2. 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]

  3. A No-Regrets Guide to Picking the Right Vinyl Siding Color

    www.aol.com/lifestyle/no-regrets-guide-picking...

    Granite Gray. For a stately look against an open sky, try a medium-toned gray. It feels grounded, but not too dark. On this two-story home, blue accent siding on the peaks adds some color variation.

  4. 2-Acrylamido-2-methylpropane sulfonic acid - Wikipedia

    en.wikipedia.org/wiki/2-Acrylamido-2-methyl...

    AMPS is made by the Ritter reaction of acrylonitrile and isobutylene in the presence of sulfuric acid and water. [2] The recent patent literature [3] describes batch and continuous processes that produce AMPS in high purity (to 99.7%) and improved yield (up to 89%, based on isobutene) with the addition of liquid isobutene to an acrylonitrile / sulfuric acid / phosphoric acid mixture at 40°C.

  5. Vinyl siding - Wikipedia

    en.wikipedia.org/wiki/Vinyl_siding

    Thicker grades of vinyl siding may, according to some, exhibit more resistance to the most common complaint about vinyl siding – its tendency to crack in very cold weather when it is struck or bumped by a hard object while others feel that a thinner product may allow more 'flex before cracking' and is a subject of debate. However, at "This ...

  6. Vinylation - Wikipedia

    en.wikipedia.org/wiki/Vinylation

    In organic chemistry, vinylation is the process of attaching a vinyl group (CH 2 =CH−) to a substrate. Many organic compounds contain vinyl groups, so the process has attracted significant interest, especially since the reaction scope includes substituted vinyl groups. The reactions can be classified according to the source of the vinyl group.

  7. Chromism - Wikipedia

    en.wikipedia.org/wiki/Chromism

    In chemistry, chromism is a process that induces a change, often reversible, in the colors of compounds.In most cases, chromism is based on a change in the electron states of molecules, especially the π- or d-electron state, so this phenomenon is induced by various external stimuli which can alter the electron density of substances.

  8. Acrylamide - Wikipedia

    en.wikipedia.org/wiki/Acrylamide

    Acrylamide (or acrylic amide) is an organic compound with the chemical formula CH 2 =CHC(O)NH 2.It is a white odorless solid, soluble in water and several organic solvents. From the chemistry perspective, acrylamide is a vinyl-substituted primary amide (CONH 2).

  9. Vinyl sulfone dyes - Wikipedia

    en.wikipedia.org/wiki/Vinyl_sulfone_dyes

    The vinyl sulfone parabase ester can be used as a diazo component in the preparation of azo dyes. [1] A further possibility is the condensation reaction of parabase ester with a chlorine or fluorotriazine residue, which in turn can be linked to any chromophore via a further amino group. Vinyl sulfone parabase ester