Disk micelles from nonionic coil-coil diblock copolymers

被引:58
作者
Edmonds, William F.
Li, Zhibo
Hillmyer, Marc A.
Lodge, Timothy P.
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
关键词
BLOCK-COPOLYMERS; CONFORMATIONAL ASYMMETRY; MULTIPLE MORPHOLOGIES; MOLECULAR DIMENSIONS; TERNARY-SYSTEM; SCATTERING; CUMULANTS; CYLINDER; SOLVENT; POLYMER;
D O I
10.1021/ma060633j
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The micellization of an almost symmetric diblock copolymer, 1,2-polybutadiene-b-poly( hexafluoropropylene oxide), with block molecular weights of 6000 and 5700, respectively, was examined in the polybutadieneselective solvent bis(2-ethylhexyl) phthalate. Cryogenic transmission electron microscopy indicated that the copolymer self-assembled into thin disk micelles, with radii from 20 to 150 nm. Small-angle X-ray scattering measurements were effectively modeled by the form factor for a thin disk and gave a core thickness of approximately 10 nm. Dynamic light scattering measurements gave a distribution of hydrodynamic radii that was fully consistent with the dimensions inferred from microscopy and X-ray scattering. The unprecedented adoption of the flat disk morphology by a nonionic, coil-coil diblock copolymer is attributed to the extremely strong interfacial tension between the fluoropolymer core and the solvated hydrocarbon corona, as anticipated by superstrong segregation theory.
引用
收藏
页码:4526 / 4530
页数:5
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