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89. "Self-Assembly and Stress Relaxation in Acrylic Triblock Copolymer Gels" Seitz, M.E.; Burghardt, W.R.; Faber, K.T.; Shull, K.R., Macromolecules, 40, 1218 (2007).
Abstract: The structure and relaxation behavior of thermoreversible gels made
with poly(methyl methacrylate)-poly(n-butyl acrylate)-poly(methyl methacrylate)
[PMMA-PnBA-PMMA] triblock copolymers in 2-ethylhexanol, a midblock selective
solvent, were studied by small-angle X-ray scattering (SAXS) and rheology.
Effects of endblock length, endblock fraction, and gel concentration on the
gel properties were investigated. A dramatic decrease in SAXS intensity was
observed over a 20 C interval where the gel transitions smoothly from elastic
to viscous behavior. SAXS patterns were fit with a Percus-Yevick disordered
hard-sphere model from which aggregation number and average domain spacing
were calculated. Aggregation number increases with increasing gel concentration
and endblock length. Increasing the endblock length from 9K to 25K increases
the relaxation time of a gel with a polymer volume fraction of 0.15 by a factor
of 106. For a given triblock endblock fraction and molecular weight, the micelle
aggregation number is strongly correlated to the gel relaxation time. Arrhenius
behavior with an effective activation energy of ~550 kJ/mol was observed for
all triblocks and concentrations. This very high effective energy barrier describes
gels relaxation behavior over a 40 C temperature range, where the relaxation
times vary by a factor of 1010.
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