Strength of polymer phase boundaries with large interfacial width: Effects of interfacial profile and phase separation morphology
Author(s) -
Chang ChunJie,
Lee YiHuan,
Chiang ChiJu,
Lee YuPing,
Chien HaoChing,
Shih WenPin,
Cheng YaoYi,
Dai ChiAn,
Chang ChiaHwa
Publication year - 2010
Publication title -
journal of polymer science part b: polymer physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.65
H-Index - 145
eISSN - 1099-0488
pISSN - 0887-6266
DOI - 10.1002/polb.22057
Subject(s) - copolymer , materials science , polystyrene , annealing (glass) , polymer , polymer blend , composite material , morphology (biology) , methyl methacrylate , surface energy , volume fraction , phase (matter) , polymer chemistry , chemistry , organic chemistry , biology , genetics
In this study, we investigate the effect of random copolymer additives on the interfacial profile, the lateral phase separation morphology, and the interfacial fracture toughness ( G c ) between two immiscible polymers. The interface between polystyrene (PS)/poly(methyl methacrylate) (PMMA) was reinforced with a random copolymer mixture when two or more PS f ‐ r ‐PMMA 1‐ f random copolymers with different volume fraction, f , were blended. For short annealing time (<3 h), the random copolymer mixture exhibits a disordered and large domain structure (>1 lm) from which crazes can be extensively initiated and developed, leading to a large interfacial fracture energy. With increasing annealing time, the random copolymer mixture self‐organizes as multiple layers, with the composition that changes gradually from PS‐rich layers to PMMA‐rich layers across the interface, leading to a large interfacial width. However, within each layer, the random copolymer mixture microphase separates laterally into smaller domains (<200 nm). We found that the microphase‐separated domains with nanometer‐sized structure significantly affect the stability of craze fibrils that can be initiated and widened at the interface, leading to a decrease in the fracture energy. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 1834–1846, 2010
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