Several new epoxy monomers were synthesized from glycidylation of functional aromatic amines containing hydroxyl or thiol groups. The epoxy monomers were triglycidyl-2-aminophenol, triglycidyl-2-aminothiophenol, tetraglycidyl-1,2-phenylenediamine and tetraglycidyl-4-methyl-1,2-phenylenediamine. The characterization of the epoxy monomers was carried out by FTIR and ¹H NMR spectroscopy. Rheological properties of solutions of the epoxy monomers in ethanol were evaluated using an advanced rheometer. The effect of solution concentration and temperature on the viscosity of the epoxy solution was evaluated. The shear rheology study at various temperatures of the epoxy resins solutions in ethanol was carried out on solutions with concentrations ranges form 0.5 to 5 wt% and temperatures (20–70 °C). The results revealed that the tetra-functional epoxy resins behave as Newtonian liquids and its viscosity is independent on the shear rate. However, the solutions of tri-functional epoxy resins are non-Newtonian liquids, and their viscosities are shear rate dependent. The activation energy of the epoxy monomers was calculated from the Arrhenius equation using solution with concentrations ranges of 0.5–5 wt%. © 2018, Springer-Verlag GmbH Germany, part of Springer Nature.

العنوان

Polymer Bulletin

الناشر

Springer Verlag

بلد الناشر

ألمانيا

Indexing

Thomson Reuters

معامل التأثير

1,589

نوع المنشور

مطبوع فقط

المجلد

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السنة

2018

الصفحات

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