Imide formation from -CONH and -COOH functional groups of 2-carboxyphe
nylmethacrylamide (2-CPM), 4-carboxyphenylmethacrylamide (4-CPM), 4-ca
rboxyphenyl methacrylamide/methylmethacrylate (4-CPM/MMA) and 4-carbox
yphenylmethacrylamide/N-phenylmaleimide (4-CPM/NPMI) electropolymerize
d matrices was investigated. It was found that 2-CPM polymers undergo
intramolecular imidization and anhydride formation, which result in a
small amount of crosslinked network. On the other hand, the thermally
cured 4-CPM polymer demonstrates a significant increase in gel fractio
n. T(g) and dynamic storage modulus, owing to crosslinked network form
ation. T(g)s of 4-CPM/MMA and 4-CPM/NPMI composites measured by thermo
mechanical analysis after thermal heating were increased and were corr
elated very well with the preheating time. The 4-CPM/MMA composites wi
th a particle crosslinking (T(g) increased to 245-degrees-C) maintaine
d a higher Izod impact strength than a typical epoxy composite (200 kJ
/m2 VS. 100 kJ/m2). Upon heating to promote crosslinking, a lower shea
r strength (65 MPa) of a 4-CPM/MMA composite increased to a strength o
f 78 MPa, close to the 80 MPa of an epoxy composite at 67% fiber volum
e fraction. A lower water absorption of around 1% was associated with
the increased crosslinking. The mechanical properties of the 4-CPM/NPM
I composites showed a similar trend upon preheating.