Jh. Laurer et al., THERMOPLASTIC ELASTOMER GELS - I - EFFECTS OF COMPOSITION AND PROCESSING ON MORPHOLOGY AND GEL BEHAVIOR, Journal of polymer science. Part B, Polymer physics, 36(13), 1998, pp. 2379-2391
Thermoplastic elastomer gels (TPEGs) composed of a poly[styrene-b-(eth
ylene-co-butylene)-b-styrene] triblock copolymer and a low-volatility,
midblock-compatible mineral oil have been investigated at different o
il concentrations to ascertain the effect of composition on TPEG morph
ology and mechanical properties. The impact of thermal processing is a
lso examined by comparing gels thermally quenched to 0 degrees C or sl
owly cooled to ambient temperature. Transmission electron micrographs
reveal that gels with 70 to 90 wt % oil exhibit styrenic micelles meas
uring ca. 24 nm in diameter. Variation in composition or cooling rate
does not have any perceivable effect on micelle size or shape, whereas
the rate at which the gels are cooled influences the extent of micros
tructural order and the time to rupture (t(R)) at constant strain. Dyn
amic rheological testing confirms the presence of a physically crossli
nked network at TPEG compositions ranging from 70 to 90 wt % oil, inde
pendent of cooling rate. Results presented here suggest that the dynam
ic elastic shear modulus (G') scales as t(R)(alpha), where a varies fr
om 0.41 to 0.59, depending on cooling rate. (C) 1998 John Wiley & Sons
, Inc.