2019
DOI: 10.1007/s00289-019-02815-x
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Acceleration of epoxy resin curing by using a combination of aliphatic and aromatic amines

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Cited by 33 publications
(24 citation statements)
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“…For instance, to obtain the best properties it is necessary an optimum curing reaction, which implies that the amount of curing reagent employed must be stoichiometric. The number of epoxy groups and reactive hydrogens of the hardener must be equal, which is the amine molecular weight divided by the number of hydrogens (amine-equivalent weight, AEW) [23]. The curing process and the chemical phenomena of cross-linking are responsible for many of the properties of the solidstate in epoxy derived materials.…”
Section: Resultsmentioning
confidence: 99%
“…For instance, to obtain the best properties it is necessary an optimum curing reaction, which implies that the amount of curing reagent employed must be stoichiometric. The number of epoxy groups and reactive hydrogens of the hardener must be equal, which is the amine molecular weight divided by the number of hydrogens (amine-equivalent weight, AEW) [23]. The curing process and the chemical phenomena of cross-linking are responsible for many of the properties of the solidstate in epoxy derived materials.…”
Section: Resultsmentioning
confidence: 99%
“…Based on the Rehm-Weller equation, the free energy changes (△G el ) for the photoelectron transfer reaction between the excited states of Y-1/Y-2 and IOPF were separately calculated. The reduction potential of IOPF is − 0.653 V [39]. The calculated values of △G el are negative for IOPF/Y-1 and IOPF/Y-2.…”
Section: Absorption Fluorescence Emission Spectra and Cyclic Voltammmentioning
confidence: 86%
“…They are resistant to alkalis and some inorganic acids, and show good resistance to water and solvents, but are not so resistant to many organic solvents. To increase the curing rate, sometimes a combination of aliphatic and aromatic amines is used [55]. Aromatic diamines are less reactive, and the curing usually stops at the formation of a linear polymer due to the large difference in the reaction of primary and secondary amines [56].…”
Section: Preparation Of Thermosets By Nucleophilic Attack To Epoxy Rementioning
confidence: 99%