posted on 2016-12-19, 13:20authored byMadalyn
R. Radlauer, Christophe Sinturel, Yusuke Asai, Akash Arora, Frank S. Bates, Kevin D. Dorfman, Marc A. Hillmyer
Three poly(styrene)-block-poly(isoprene)-block-poly(lactide)
(PS-b-PI-b-PLA, SIL) triblock terpolymers
were synthesized and characterized
in the bulk and as thin films. The pronounced incompatibility of the
covalently connected PI and PLA led to significant frustration and
the tendency to minimize their intermaterial dividing surface area.
This resulted in the formation of a core–shell cylinder morphology
with exaggerated nonconstant mean curvature from triblock polymers
with equal block volume fractions rather than the more typical lamellar
morphology. The effect of frustration was magnified in thin films
by both confinement and interfacial interactions such that the PI
domains became discontinuous. Self-consistent field theory (SCFT)
calculations emphasize that the marked difference in the PS/PI and
PI/PLA interaction parameters promotes the formation of nonlamellar
morphologies. However, SCFT predicts that lamellar morphology is more
stable than the observed cylindrical morphology, demonstrating a limitation
that arises from the underlying assumptions.