Summary
Above a concentration c* close to 0.3 wt%, blends of 12-hydroxystearic acid (HSA) with diglycidyl ether of bisphenol A (DGEBA) prepolymer mixed at 80°C give thermally reversible physical gels (organogels) on cooling.
According with the literature, the turbidity of the gels indicates fibres of rectangular cross-sectional shapes. The slope of the linear melting heats versus concentration is equal to the melting heat of the pure HSA (-182 ± 4 J.g-1).
The blends are gels as the elastic modulus G’ is about ten times larger than the loss one G” and G’ is practically independent of the frequency at a given concentration.
The sharp variation of the temperature of the endothermic peak T peak , of the time to reach the rubbery plateau t r , of the exponent Δ (G’∝ωΔ) and of the limiting strain γ l of the linear viscoelastic domain below 2.5 wt%, is attributed to smaller crystallites in the blend.
At a given frequency, G’ follows a scaling law with the concentration (\(G^{\prime}\propto{c}^{\beta_1}\)), the scaling exponent β1 being equal to 3.87 ± 0.02 at 1 rad.s-1. This indicates that the gel structure is independent of the concentration.
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Eloundou, J., Girard-Reydet, E., Gérard, JF. et al. Calorimetric and rheological studies of 12-hydroxystearic acid / digycidyl ether of bisphenol A blends. Polym. Bull. 53, 367–375 (2005). https://doi.org/10.1007/s00289-005-0345-x
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DOI: https://doi.org/10.1007/s00289-005-0345-x