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  2. Diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Diglycidyl_ether

    Diglycidyl ethers are chemical compounds used as a reactive diluents for epoxy resin. Other uses include treating textiles and stabilizing chlorinated organic compounds . Diglycidyl ether itself is extremely toxic, and can prove fatal or cause permanent damage if inhaled or consumed orally.

  3. Bisphenol A diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A_diglycidyl_ether

    Bisphenol A diglycidyl ether slowly hydrolyzes to 2,2-bis[4(2,3-dihydroxypropoxy)phenyl)propane (bis-HPPP). Similarly, DGEBA reacts with acrylic acid to give vinyl ester resins . The reaction results in opening of the epoxide ring, generating unsaturated esters at each terminus of the molecule.

  4. Bisphenol F - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_F

    Bisphenol F (BPF; 4,4′-dihydroxydiphenylmethane) is an organic compound with the chemical formula (HOC 6 H 4) 2 CH 2.It is structurally related to bisphenol A (BPA), a popular precursor for forming plastics, as both belong to the category of molecules known as bisphenols, which feature two phenol groups connected via a linking group.

  5. Bisphenol A - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A

    BPA diglycidyl ether (BADGE) is used as an acid scavenger, particularly in PVC dispersions, such as organosols or plastisols, [59] [60] which are used as coatings for the inside of food cans, as well as embossed clothes designs produced using heat transfer vinyl or screen printing machines. [19] Derivatives used as flame retardants

  6. Bis-GMA - Wikipedia

    en.wikipedia.org/wiki/Bis-GMA

    Bis-GMA (bisphenol A-glycidyl methacrylate) is a resin commonly used in dental composite, dental sealants. [1] [2] and dental cement. It is the diester derived from methacrylic acid and the bisphenol A diglycidyl ether. Bearing two polymerizable groups, it is prone to form a crosslinked polymer that is used in dental restorations. [3]

  7. Epoxy - Wikipedia

    en.wikipedia.org/wiki/Epoxy

    Structure of bisphenol-A diglycidyl ether epoxy resin: n denotes the number of polymerized subunits and is typically in the range from 0 to 25 Increasing the ratio of bisphenol A to epichlorohydrin during manufacture produces higher molecular weight linear polyethers with glycidyl end groups, which are semi-solid to hard crystalline materials ...

  8. Bisphenol - Wikipedia

    en.wikipedia.org/wiki/Bisphenol

    Exceptions include bisphenol S, P, and M. "Bisphenol" is a common name; the letter following denotes the variant, which depends on the additional substituents. Bisphenol A is the most popular representative of the group, with millions of metric tons produced globally in the past decade, often simply called "bisphenol".

  9. Tetrabromobisphenol A diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Tetrabromobisphenol_A...

    Tetrabromobisphenol A diglycidyl ether is an epoxy resin consisting of tetrabromobisphenol A with ether linkages to two epichlorohydrin groups. An alernative structural comparison is as brominated form of bisphenol A diglycidyl ether. It is a brominated aromatic chemical used principally for giving flame retardant properties to materials. [1]