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Characterization of diaminodiphenyl sulfone (DDS) cured tetraglycidyl 4, 4'diaminodiphenyl methane (TGDDM) epoxies

Conference ·
OSTI ID:5088272
DDS and TGDDM epoxies are currently the most commonly used matrices for high performance fibrous composites. Systematic Fourier - transform infrared spectroscopy (FTIR) studies of the cure reactions of these epoxies are reported as a function of cure conditions, DDS concentration and the presence or absence of BF/sub 3/ catalyst. From these studies, the TGDDM epoxide was found to undergo homopolymerization to form either (CH/sub 2/OH)CH-CH(CH/sub 2/OH) or ether linkages in the absence of DDS. Such reactions are accelerated by epoxide impurities and a BF/sub 3/ catalyst and also occur in the presence of DDS. For TGDDM-DDS systems epoxide-amine addition reactions occur in which all primary amine and approx. 50% secondary amine groups are consumed. The BF/sub 3/ cured systems are more ductile relative to the noncatalyzed systems because they contain less network defects in the form of unreacted epoxide groups. Inhomogeneous mixing of the components together with the catalytic activity of the BF/sub 3/ catalyst in commercial TGDDM-DDS epoxies are also discussed.
Research Organization:
Lawrence Livermore National Lab., CA (USA)
DOE Contract Number:
W-7405-ENG-48
OSTI ID:
5088272
Report Number(s):
UCRL-87821; CONF-821010-2; ON: DE82019239
Country of Publication:
United States
Language:
English