The thermal properties of some porous polydivinylbenzene beads, prepared fr
om commercial divinylbenzene, pure m-divinylbenzene, pure p-divinylbenzene
or their mixture, were evaluated by thermogravimetry (TG) and differential
scanning calorimetry (DSC). The results showed that two kinds of exothermal
reactions were newly found, respectively, in the range of 150-160 and 220-
280 degreesC during heating in DSC measurement of the samples while thermal
decomposition temperature in TG curves was increased with the content of d
ivinylbenzene monomers. The further study indicated that all these exotherm
al reactions were related to pendant double bonds in the porous polydivinyl
benzene beads. The first kind of exothermal reaction should be the thermal
coupling reactions of the double bonds close to each other in space. The se
cond one might be the oxidation of double bonds or the sites activated by e
thenylphenyl group. The mechanisms of two kinds of exothermal reactions wer
e proposed and the factors to affect the thermal reactions or thermal stabi
lity were discussed. As a conclusion, only those highly crosslinked polysty
renes with little or without pendant double bond, other than polymers of pu
re divinylbenzenes, would have better thermal stability chemically and/or p
hysically. (C) 2001 Elsevier Science BY. All rights reserved.