TY - JOUR
T1 - Cure kinetics and inter-domain etherification in an amine-cured phenoxy/epoxy system
AU - Hseih, H. Kun
AU - Su, Chean C.
AU - Woo, Eamor M.
N1 - Funding Information:
The authors acknowledge with gratitude the financial support kindly provided by the National Science Council (NSC #86-2216-E006-007), which has made this study possible. Support of the SEM instrument by the Regional Analytical Instrument Center (Tainan, Taiwan), administered by the National Science Council, is also appreciated.
PY - 1998
Y1 - 1998
N2 - 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′-diaminodiphenylmethane (TGDDM) with diaminodiphenylsulfone (DDS). Similar to the case for a pure, unmodified TGDDM/DDS epoxy counterpart, an autocatalytic reaction kinetic model was found to describe the cure behaviour of the phenoxy/TGDDM/DDS mixtures up to the vitrification point. At the early stage of cure, the -OH group in the phenoxy might exert a catalytic effect for epoxide ring opening between epoxy and the amine. Subsequently, at later cure stages where phase domain boundaries were forming and the amine groups were largely depleted, the -OH groups of the phenoxy phase domain began to react with the residual epoxide groups in the epoxy domains. It is this later-stage reaction that led to interlinking chemical bonding between the phenoxy and epoxy phases at the domain boundaries.
AB - 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′-diaminodiphenylmethane (TGDDM) with diaminodiphenylsulfone (DDS). Similar to the case for a pure, unmodified TGDDM/DDS epoxy counterpart, an autocatalytic reaction kinetic model was found to describe the cure behaviour of the phenoxy/TGDDM/DDS mixtures up to the vitrification point. At the early stage of cure, the -OH group in the phenoxy might exert a catalytic effect for epoxide ring opening between epoxy and the amine. Subsequently, at later cure stages where phase domain boundaries were forming and the amine groups were largely depleted, the -OH groups of the phenoxy phase domain began to react with the residual epoxide groups in the epoxy domains. It is this later-stage reaction that led to interlinking chemical bonding between the phenoxy and epoxy phases at the domain boundaries.
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U2 - 10.1016/S0032-3861(97)00510-7
DO - 10.1016/S0032-3861(97)00510-7
M3 - Article
AN - SCOPUS:0032069961
SN - 0032-3861
VL - 39
SP - 2175
EP - 2183
JO - polymer
JF - polymer
IS - 11
ER -