Microdomain orientation in chelate-doped block copolymers by a high magnetic field

被引:2
|
作者
Yasui, Akifumi [1 ]
Kimura, Fumiko
Kiyoshi, Tsukasa
Kimura, Tsunehisa
Yeonhwan, Jeong
Sakurai, Shinichi
机构
[1] Kyoto Inst Technol, Grad Sch Engn, Sakyo Ku, Kyoto 6068585, Japan
[2] Tokyo Metropolitan Univ, Dept Appl Chem, Hachioji, Tokyo 1920397, Japan
[3] Natl Inst Mat Sci, Tsukuba, Ibaraki 3050003, Japan
关键词
block copolymer; chelate doping; high magnetic field; microdomain; orientation; cylinder; symmetry breaking; mode selection; interfacial undulation;
D O I
10.1295/koron.64.317
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Magnetic orientation of microdomain structures has been examined for block copolymers consisting of non-crystalline block chains. In order to enhance the effect of the magnetic field, the difference in magnetic susceptibility between the microdomain (dispersed phase) and the matrix phase was increased by doping a metal chelate selectively in the microdomain. A polystyrene-block-poly (ethylene-co-but-1-ene)-block-polystyrene triblock copolymer (SEBS), which forms polystyrene (PS) cylinders in the poly (ethylene-co-but-l-ene) (PEB) matrix, was employed. By solution casting using dichloromethane, a good solvent selectively for PS, non-equilibrium lamellar microdomains were formed and frozen in the as-cast film. The SEBS sample, cast on aluminum foil in the presence of a high magnetic field of 12 T, was then annealed at 190 degrees C for 3 h. The orientation of PS cylinders was examined by small angle X-ray scattering at room temperature. It was found that the lamellar microdomains were oriented parallel to the magnetic field. After annealing, 6-folded pattern appeared, which was ascribed to well-ordered cylinders aligned parallel to the applied magnetic field.
引用
收藏
页码:317 / 323
页数:7
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