Study of cure kinetics of DGEBA with optically active curing agents
3-Deoxy-D- erythro -hexos-2-ulose bis (thiosemicarbazone) ( I ) readily obtained from d -glucose reacts with copper acetate hydrate to give the corresponding chelate ( II ). The complex ( II ) was acetylated to give the corresponding tri- O -acetyl derivative ( III ). The ( I ), ( II ), and ( III )...
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Veröffentlicht in: | Journal of thermal analysis and calorimetry 2010-09, Vol.101 (3), p.1011-1017 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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Zusammenfassung: | 3-Deoxy-D-
erythro
-hexos-2-ulose bis (thiosemicarbazone) (
I
) readily obtained from
d
-glucose reacts with copper acetate hydrate to give the corresponding chelate (
II
). The complex (
II
) was acetylated to give the corresponding tri-
O
-acetyl derivative (
III
). The (
I
), (
II
), and (
III
) were used as optically active curing agents for diglycidyl ether of bisphenol A (DGEBA)-based epoxy resin, and the cure reaction was studied by the non-isothermal DSC method. The maximum exothermic temperature (
T
p
) of curing of DGEBA-(
III
) system shifted about 313 K toward lower temperature in comparison with the
T
p
of DGEBA/(
II
) system. The average
E
a
values obtained by using Kissinger–Akahira–Sunose (KAS), Flynn–Wall–Ozawa (FWO), and isoconversional methods for non-isothermal curing of DGEBA-(
I
), DGEBA-(
II
), and DGEBA-(
III
) systems are 95.8, 135.5, and 85.8 kJ mol
−1
, respectively. The higher reactivity of (
III
) toward epoxide groups can be due to better solubility of the (
III
) in DGEBA as a result of acetylation of hydroxyl groups. |
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ISSN: | 1388-6150 1588-2926 1572-8943 |
DOI: | 10.1007/s10973-010-0812-y |