C. Wang et Ci. Chang, FRACTURE ENERGIES OF STYRENE-BUTADIENE-STYRENE BLOCK-COPOLYMERS .2. STRENGTH AT HIGH-TEMPERATURES, Journal of polymer science. Part B, Polymer physics, 35(13), 1997, pp. 2017-2027
It has been found that SBS block copolymers possess excellent tear str
ength at room temperature. However, tear strength is virtually zero at
temperatures higher than the glass transition temperature of PS phase
, ca. 95 degrees C. Tear strength at high temperatures can be improved
by slight crosslinking of PB chains of SBS molecules with a small amo
unt of dicumyl peroxides (DCP). The present work describes results of
measurements of strength at high temperatures carried out on the DCP-c
ured SBS block copolymers. Fracture energies of DCP-cured specimens we
re determined using both a conventional tear test and a recently devel
oped cutting test. The effect of crosslink density on fracture energy
was investigated and correlated with microstructure. It has been found
that specimens crosslinked with 0.01 phr DCP still possess relatively
large tear strength at room temperature, about 10 kJ/m(2), when compa
red with uncrosslinked SBS specimens. Tear strength at high temperatur
es has been effectively enhanced to be about 100 to 1000 J/m(2), depen
ding on the tearing rate. Specimens crosslinked with a higher level of
DCP, however, showed a pronounced reduction of tear strength at room
temperature, with tear strength of SBS specimens crosslinked with 1 ph
r DCP about one-tenth of that of neat SBS. The threshold fracture ener
gy of crosslinked SBS copolymers is found to be proportional to the sq
uare root of the molecular weight between chemical crosslinks in the P
B phase, which is in accord with the theory of Lake and Thomas. Moreov
er, from the results of cutting test, it is found that the majority, a
bout 70%, of the fracture energy of neat SBS specimens comes from the
rupture of the long PB chains of SBS molecules. The rest is the contri
bution from the energy associated with the PB/PS interface. (C) 1997 J
ohn Wiley & Sons, Inc.