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  2. Epoxy - Wikipedia

    en.wikipedia.org/wiki/Epoxy

    Epoxy is the family of basic components or cured end products of epoxy resins. Epoxy resins, also known as polyepoxides, are a class of reactive prepolymers and polymers which contain epoxide groups. The epoxide functional group is also collectively called epoxy. [1] The IUPAC name for an epoxide group is an oxirane.

  3. Epoxy molding compounds - Wikipedia

    en.wikipedia.org/wiki/Epoxy_Molding_Compounds

    Epoxy resins can be categorized into three distinct types based on the chemical structure of their resin backbone: aliphatic, cycloaliphatic, and aromatic epoxy resins. [4] An increase in the molecular length between reactive epoxy groups results in a reduction of crosslink density and resin modulus, while simultaneously enhancing the failure ...

  4. Bisphenol S - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_S

    Bisphenol S (BPS, dioxydiphenylsulfone) is an organic compound with the formula (HOC 6 H 4) 2 SO 2. It has two phenol functional groups on either side of a sulfonyl group. It is commonly used in curing fast-drying epoxy resin adhesives. It is classified as a bisphenol, and a close molecular analog of bisphenol A (BPA).

  5. Epoxy resins - Wikipedia

    en.wikipedia.org/?title=Epoxy_resins&redirect=no

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  6. C12–C14 alcohol glycidyl ether - Wikipedia

    en.wikipedia.org/wiki/C12–C14_alcohol_glycidyl...

    As an epoxy modifier it is classed as an epoxy reactive diluent. [8] It is one of a family of glycidyl ethers available used for viscosity reduction of epoxy resins. [9] These are then further formulated into coatings, sealants, adhesives, and elastomers. [10] [11] Resins with this diluent tend to show improved workability. [12]

  7. Pentaerythritol tetraacrylate - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol_tetraacrylate

    PETA is part of a family of acrylates used in epoxy resin chemistry and ultraviolet cure of coatings. Similar monomers used are 1,6-hexanediol diacrylate and trimethylol propane triacrylate . It is a derivative of pentaerythritol [ 2 ] One of the key uses of the material is in polymeric synthesis where it can form micelles and block copolymers.

  8. Sharpless epoxidation - Wikipedia

    en.wikipedia.org/wiki/Sharpless_epoxidation

    The Sharpless epoxidation is viable with a large range of primary and secondary alkenic alcohols. Furthermore, with the exception noted above, a given dialkyl tartrate will preferentially add to the same face independent of the substitution on the alkene.To demonstrate the synthetic utility of the Sharpless epoxidation, the Sharpless group created synthetic intermediates of various natural ...

  9. Epoxide - Wikipedia

    en.wikipedia.org/wiki/Epoxide

    A generic epoxide. In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen.This triangular structure has substantial ring strain, making epoxides highly reactive, more so than other ethers.