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These cure reactions of the 'ene' molecule can initiate intra- or inter-molecularly and, hence, the cure path sequence is dependent on viscosity-time-temperature cure conditions.
measurements is less sensitive to the dehydration reaction because of a lower heat of reaction compared to the double CC bond cure reactions.
This study presents a perspective on using this capability to monitor polymer chemistry with an emphasis on the study of polymer cure reactions.
Cure reactions of the stoichiometric mixtures of diglycidyl ether of bisphenol A (DGEBA) and two very low molecular weight aliphatic polyether diamines (PED) were studied by using fluorescence and mid- and near-IR spectroscopic techniques.
With the E constant method, E variable method and heating FTIR spectra used together, we can have a comprehensive and profound understanding of the cure reactions of the LEPL MA system.
The aim of this study was to examine possible effects of the hydroxyl group (−OH) in phenoxy-type polymers on the cure reactions and network morphology of a crosslinking epoxy system, tetraglycidyl-4,4′-diamino-diphenylmethane (TGDDM) with diaminodiphenylsulfone (DDS).
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The cure reaction was described by an autocatalytic reaction mechanism.
But initially, the die needs to be heated in order to start the cure reaction.
The activation energy for cure reaction was lower in epoxy/HBP system.
CTBN modifies the cure reaction and the relaxation process of the epoxy resin.
The existence of SBS increased the initial viscosity of the epoxy asphalt during cure reaction.
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