Asymmetric Double Tetragonal Domain Packing from ABC Triblock Terpolymer Blends with Chain Length Difference

被引:22
|
作者
Asai, Yusuke [1 ]
Takano, Atsushi [1 ]
Matsushita, Yushu [1 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648603, Japan
关键词
PHASE-BEHAVIOR; DIBLOCK COPOLYMERS; BLOCK-COPOLYMERS; DOUBLE-DIAMOND; MORPHOLOGY; POLYMERS; LAMELLAR; MELTS; SUPERLATTICES; HOMOPOLYMER;
D O I
10.1021/acs.macromol.6b01670
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A specific phase structure was observed for binary blends of poly(isoprene)-block-poly(styrene)-block-poly(2-vinylpyridine) (ISP) triblock terpolymers with asymmetric chain lengths of two end-blocks. Tetragonal-packed cylinders were obtained from various binary blends on a wide range of volume fractions, although the sizes of I and P cylinders were highly asymmetric. Those structures have never been found for monodisperse ABC triblock terpolymers, and the three specific features have been confirmed: (1) I cylinders were metamorphosed into rod domains, and their interfaces have nonconstant mean curvatures; (2) the cross-sectional area ratio of I/P domain is qualitatively changed with the volume fraction of each component; and (3) spherical and cylindrical domains of P component coexist. The molecular design adopted in the present work, that is, I and P blocks in two parent terpolymers have both fairly large chain length difference, must lead to these new morphologies.
引用
收藏
页码:6940 / 6946
页数:7
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