Shear-induced lamellar rotation observed in a diblock copolymer by in situ small-angle X-ray scattering

被引:53
|
作者
Polis, DL
Smith, SD
Terrill, NJ
Ryan, AJ
Morse, DC
Winey, KI
机构
[1] Univ Penn, Dept Mat Sci & Engn, Res Struct Matter Lab, Philadelphia, PA 19104 USA
[2] Procter & Gamble Co, Corp Res Div, Cincinnati, OH 45239 USA
[3] SERC, Daresbury Lab, CLRC, Warrington WA4 4AD, Cheshire, England
[4] Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England
[5] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
关键词
D O I
10.1021/ma981796d
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In situ small-angle X-ray scattering (SAXS) rheology is used to st;study the dynamic process of shear alignment in a lamellar poly(styrene-b-ethylene propylene) diblock copolymer, at temperatures far below the microphase separation transition temperature. We have focused on the alignment dynamics at time scales shorter than 1 cycle of deformation. To extract this valuable information, we use prealigned specimens and follow subtle changes in the orientation during a steady shear deformation. Two notable changes in the azimuthal SAXS intensity are observed: the maximum of the main peak induced during prealignment shifts to lower azimuthal angles and a secondary peak develops and shifts to higher angles. : We effectively modeled the shift of the main peak maximum by assuming that lamellae rotate with the;. vorticity component of shear. This provides conclusive evidence for lamellar rotation in block copolymers, as opposed to a discontinuous transformation such as lamellar dissolution and reformation. Lamellar rotation also supports our previously proposed mechanism for kink band formation.
引用
收藏
页码:4668 / 4676
页数:9
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