聚苯乙烯
共聚物
线性低密度聚乙烯
材料科学
高分子科学
聚乙烯
高分子化学
块(置换群论)
复合材料
聚合物混合物
增容
化学工程
聚合物
数学
几何学
工程类
作者
T. Li,Vasily A. Topolkaraev,Ann Hiltner,E. Baer,X. Z. Ji,Roderic P. Quirk
标识
DOI:10.1002/polb.1995.090330416
摘要
Abstract Compatibilization of blends of linear low‐density polyethylene (LLDPE) and polystyrene (PS) with block copolymers of styrene (S) and butadiene (B) or hydrogenated butadiene (EB) has been studied. The morphology of the LLDPE/PS (50/50) composition typically with 5% copolymer was characterized primarily by scanning electron microscopy (SEM). The SEB and SEBS copolymers were effective in reducing the PS domain size, while the SB and SBS copolymers were less effective. The noncrystalline copolymers lowered the tensile modulus of the blend by as much as 50%. Modulus calculations based on a coreshell model, with the rubbery copolymer coating the PS particle, predicted that 50% of the rubbery SEBS copolymer was located at the interface compared to only 5–15% of the SB and SBS copolymers. The modulus of blends compatibilized with crystalline, nonrubbery SEB and SEBS copolymers approached Hashin's upper modulus bound. An interconnected interface model was proposed in which the blocks selectively penetrated the LLDPE and PS phases to provide good adhesion and improved stress and strain transfer between the phases. © 1995 John Wiley & Sons, Inc.
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