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  2. 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 ...

  3. 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.

  4. Tetraethylenepentamine - Wikipedia

    en.wikipedia.org/wiki/Tetraethylenepentamine

    It is primarily used as a curing agent or hardener in epoxy chemistry. This can be on its own or reacted with tall oil fatty acid (TOFA) and its dimer to make an amidoamine. [2] This amidoamine is then used as the curing agent for epoxy resin systems. TEPA is a pentadentate ligand in coordination chemistry.

  5. Epoxy resins - Wikipedia

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

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  6. Johnson–Corey–Chaykovsky reaction - Wikipedia

    en.wikipedia.org/wiki/Johnson–Corey...

    The vast majority of reagents are monosubstituted at the ylide carbon (either R 1 or R 2 as hydrogen). Disubstituted reagents are much rarer but have been described: [1] If the ylide carbon is substituted with an electron-withdrawing group (EWG), the reagent is referred to as a stabilized ylide. These, similarly to sulfoxonium reagents, react ...

  7. 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.

  8. C12–C14 alcohol glycidyl ether - Wikipedia

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

    C12-C14 alcohol glycidyl ether (AGE) is an organic chemical in the glycidyl ether family. [2] It is a mixture of mainly 12 and 14 carbon chain alcohols, also called fatty alcohols that have been glycidated.

  9. Bisphenol S - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_S

    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). BPS differentiates from BPA by possessing a sulfone group (SO 2 ) as the central linker of the molecule instead of a dimethylmethylene group (C(CH 3 ) 2 ) , which is the case of bisphenol A.