共聚物
增容
高分子化学
材料科学
高分子科学
化学工程
聚合物混合物
化学
聚合物
复合材料
工程类
作者
Daun Jeong,Shuquan Cui,Nusrat Jahan,Christopher J. Ellison,Frank S. Bates
标识
DOI:10.1021/acs.macromol.5c01877
摘要
Mechanical recycling of plastics benefits from block copolymer compatibilizers, yet a limited understanding of optimal polymer design hinders widespread applications. In this study, we synthesized poly(styrene)-block-poly(ethylene-ran-ethylethylene) (SX) diblock and SXS triblock copolymers via sequential anionic polymerization followed by catalytic hydrogenation and investigated their effectiveness in compatibilizing semicrystalline isotactic polypropylene (iPP) blended with glassy polystyrene (PS). By tuning the S block molecular weight (10–80 kDa) and block architecture (diblock vs. triblock), we probed the underlying compatibilization mechanisms. Our findings corroborate the recently proposed "threading-the-needle" mechanism of engagement between the X block and iPP. A new mechanism for creating ductility in the semicrystalline iPP matrix without stress transfer across the phase-separated interface with PS is demonstrated with SX diblock copolymer. Remarkably, incorporating just 0.1 wt % SX diblock enhances ductility in blends containing 20% PS (strain at break εb > 400%) through dissipating strain energy thereby suppressing void formation upon deformation. This study provides fresh insights into the design of block copolymers for blend compatibilization and toughening.
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