Ordering kinetics of cylindrical and spherical microdomains in an SIS block copolymer by synchrotron SAXS and rheology

被引:2
|
作者
Kim, JK [1 ]
Lee, HH
Ree, M
Lee, KB
Park, Y
机构
[1] Pohang Univ Sci & Technol, Dept Chem Engn, Pohang 790784, Kyungbuk, South Korea
[2] Pohang Univ Sci & Technol, Polymer Res Inst, Pohang 790784, Kyungbuk, South Korea
[3] Pohang Univ Sci & Technol, Dept Chem, Pohang 790784, Kyungbuk, South Korea
[4] Pohang Univ Sci & Technol, Dept Phys, Pohang 790784, Kyungbuk, South Korea
[5] Pohang Univ Sci & Technol, Pohang Accelerator Lab, Pohang 790784, Kyungbuk, South Korea
关键词
D O I
10.1002/(SICI)1521-3935(19980401)199:4<641::AID-MACP641>3.3.CO;2-4
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 ordering kinetics of cylindrical and spherical microdomains in a polystyrene-block-poly-isoprene-block-polystyrene (SIS) copolymer were studied using synchrotron small-angle X-ray scattering (SAXS) and rheology upon quenching the sample from a disordered state to an ordered state having either spherical or cylindrical microdomains. The SIS exhibits an order to order transition at approximate to 181 degrees C, a lattice disordering transition at approximate to 210 degrees C and becomes disordered at higher temperatures. Higher order peaks in the SAXS profiles corresponding to hexagonally packed cylindrical (HEX) microdomains appeared after less than Ih when the sample was quenched from 235 degrees C to 170 degrees C. When quenched from 235 degrees C to 200 degrees C, a broad higher order peak at approximate to 1.65 q(m), corresponding to spheres with liquid-like short-range order, was persistent up to 4 h before higher order peaks corresponding to body-centered cubic (BCC) microdomains appeared. We repeated this experiment by changing temperature from one ordered state with BCC microdomains to another with HEX microdomains, and vice versa. The BCC microdomains were attained within 1 h when heating from 170 degrees C to 200 degrees C. The transition between HEX and BCC is thermoreversible. The time evolution of dynamic storage modulus G' is in good agreement with that of SAXS intensity.
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页码:641 / 653
页数:13
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