Both viscoelastic and plastic properties were investigated on random c
opolymers of methylmethacrylate (MMA) and N-methyl-glutarimide (GIM) i
n the range 0-76 mol%. All the measurements were performed on samples
quenched from the melt in order to break free from physical aging effe
cts. Dynamic mechanical experiments were performed at very low deforma
tion and temperatures ranging from - 150 degrees C up to the glass tra
nsition temperature (T-g) region. Increase in GIM amount improves the
thermomechanical stability of the copolymers, as revealed by the incre
ase of both T-g and alpha relaxation temperature. In the beta relaxati
on region, the E '' loss peak first decreases in amplitude with increa
sing GIM content and then broadens further and finally spreads out til
l the onset of the alpha peak at the largest GIM amounts. A quantitati
ve analysis of the beta relaxation phenomena was performed by consider
ing the loss compliance J '' instead of the loss modulus E ''. It turn
s out that in the low temperature range (-80 degrees C-0 degrees C) th
e mechanical damping associated with the MMA motions is stronger for M
MA-GIM than for MMA-MMA linkages; in addition, the mechanical damping
associated with the motions of the GIM units is very low. By contrast,
in the high temperature range (30 degrees C to about 100 degrees C),
the mechanical damping associated with the MMA motions drops with incr
easing GIM amount, whereas a significant damping coming from the GIM u
nits is observed. These results suggest that the beta relaxation would
mainly consist of MMA isolated motions at low temperature and of coop
erative motions at higher temperature, involving the MMA units at GIM
amounts lower or equal to 58 mol% and the GIM units at higher GIM cont
ent. The stress-strain curves were determined at low strain rate (2 X
10(-3) s(-1)) and temperatures ranging from -120 degrees C to T-g. Ana
lysis of the plastic deformation region shows that the yield stress de
creases with increasing GIM amount at low temperatures. The opposite t
rend shows up on the high temperature side of the beta relaxation, whe
re strain softening peaks at intermediate GIM amounts. As a plausible
explanation, the cooperative beta motions, whenever they exist, are su
spected to be responsible for the decrease of both yield stress and st
rain softening. These conclusions agree well with those of a previous
study on methylmethacrylate-co-maleimide copolymers. They are also con
sistent with our earlier identification of the microdeformation mechan
isms involved in the stretching of methylmethacrylate-co-N-methylgluta
rimide thin films. (C) 1998 Elsevier Science Ltd. All rights reserved.