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  2. Dibromo neopentyl glycol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Dibromo_neopentyl_glycol...

    A key use of the material is reducing the viscosity of epoxy resins. As an epoxy modifier it is classed as a reactive diluent, which may then be formulated into CASE applications (coatings, adhesives, sealants, and elastomers and composite materials). [2]

  3. File:1963 Preventing Dermatitis If You Work with Epoxy Resins.pdf

    en.wikipedia.org/wiki/File:1963_Preventing...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Donate; Pages for logged out editors learn more

  4. Poly(propylene glycol) diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Poly(propylene_glycol...

    The molecule has 2 oxirane functionalities, and so a key use is modifying and reducing the viscosity of epoxy resins. [9] [10] These reactive diluent modified epoxy resins may then be further formulated into CASE applications: coatings, [11] adhesives, sealants, and elastomers. It produces epoxy coatings with high impact resistance. [12]

  5. Epoxy - Wikipedia

    en.wikipedia.org/wiki/Epoxy

    Epoxy resin formulations are important in the electronics industry, and are employed in motors, generators, transformers, switchgear, bushings, insulators, printed wiring boards (PWB), and semiconductor encapsulants. Epoxy resins are excellent electrical insulators and protect electrical components from short circuiting, dust and moisture.

  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. Neopentyl glycol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_glycol...

    A key use is modifying the viscosity and properties of epoxy resins. As an Epoxy modifier it is classed as an epoxy reactive diluent. [8] which may then be formulated into CASE applications: Coatings, [9] Adhesives, [10] Sealants and Elastomers and composite materials. These uses include cationic polymerization reactions. [11] [12] The use of ...

  8. Epoxide - Wikipedia

    en.wikipedia.org/wiki/Epoxide

    It is a precursor in the production of epoxy resins. [19] Halohydrins react with base to give epoxides. [20] The reaction is spontaneous because the energetic cost of introducing the ring strain (13 kcal/mol) is offset by the larger bond enthalpy of the newly introduced C-O bond (when compared to that of the cleaved C-halogen bond).

  9. n-Butyl glycidyl ether - Wikipedia

    en.wikipedia.org/wiki/N-Butyl_glycidyl_ether

    As an Epoxy modifier it is classed as an epoxy reactive diluent. [8] It is also used to synthesize other molecules. [9] The use of the diluent does effect mechanical properties and microstructure of epoxy resins. [10] [11] It has been used to simultaneously increase cryogenic strength, ductility and impact resistance of epoxy resins. [12]