Abstract

Block copolymers with crystalline, glassy, and rubbery blocks were synthesized by anionic polymerization of butadiene, styrene, and isoprene followed by chlorosilane coupling and hydrogenation. The performance of two pentablock copolymers, with the block sequence crystalline–glassy–rubbery–glassy–crystalline, as thermoplastic elastomers (TPEs) was evaluated against triblock copolymers having either crystalline or glassy end blocks. Judicious choices of block lengths yielded homogeneous melts for both pentablocks; consequently, the low-shear-rate viscosities of the pentablocks were more than 2 orders of magnitude lower than that of the glassy–rubbery–glassy triblock, which remained microphase-separated in the melt. In the pentablocks, physical cross-linking was achieved by crystallization of the end blocks followed by vitrification of the adjacent glassy blocks, forming composite crystalline–glassy hard domains. All of the polymers studied exhibited desirable mechanical behavior for TPEs, including low You...

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