Thermal analysis provides very useful tools for the characterization a
nd identification of both, elastomer compound and finished product. Th
is investigation focuses on the use of different thermal techniques fo
r compositional analysis, characterization of thermal, oxidative stabi
lity and glass-transition temperature (T-g) of different components pr
esent in the elastomeric systems. Thermogravimetry (TG) is critical fo
r identification of composition. TG analysis of three compositions (S-
1, S-2 and S-3) shows S-1 and S-2 are soft-oil extended compounds and
S-3 is a hard compound, all comprising ethylene propylene diene rubber
(EPDM). Energy dispersive X-ray analysis (EDAX) of the residues from
TGA reveals the presence of mineral filler clay in sample (S-3) beside
s carbon black. The use of high-resolution TG has been found to give b
etter resolution between overlapping weight loss steps leading to bett
er quantification of various components compared to conventional TG. T
he coefficient of expansion of the rubber compound (from thermo-mechan
ical analysis - TMA) above T-g is correlated to the hardness of the sa
mples. The use of differential scanning calorimetry (DSC) to determine
oxidative stability identifies also the presence of similar antioxida
nts, Dynamic mechanical analysis (DMA) is found to be very sensitive f
or characterization of glass-transition temperature, visco-elastic pro
perties and, in particular, the adhesion between the elastomer compoun
d and coating. (C) 1998 Elsevier Science B.V.