Development of Internal Fine Structure in Stretched Rubber Vulcanizates

被引:5
|
作者
Tosaka, Masatoshi [1 ]
Toki, Shigeyuki [2 ]
Che, Justin [2 ]
Rong, Lixia [2 ]
Hsiao, Benjamin S. [2 ]
机构
[1] Kyoto Univ, Inst Chem Res, Kyoto 6110011, Japan
[2] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
基金
日本学术振兴会;
关键词
networks; rubber; SAXS; strain-induced crystallization; STRAIN-INDUCED CRYSTALLIZATION; SYNCHROTRON X-RAY; NATURAL-RUBBER; UNIAXIAL DEFORMATION; MOLECULAR-ORIENTATION; SYNTHETIC RUBBERS; POLYISOPRENE RUBBER; STRESS-RELAXATION; NETWORK; ELASTOMERS;
D O I
10.1002/polb.22290
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Small-angle X-ray scattering (SAXS) pattern and tensile stress during relaxation of stretched rubber vulcanizates (synthetic polyisoprene) were measured simultaneously at room temperature and at 0 degrees C. The samples were quickly stretched to the prefixed strain and then allowed to relax for 1 h. In every SAXS pattern, the intensity distribution was elongated along the equator, indicating the formation of structures elongated in the stretching direction. The so-called two-spots pattern corresponding to the long period of stacked lamellar crystals did not appear even when the critical strain to induce crystallization was exceeded. On the other hand, even below the critical strain, additional development of equatorial streaks was detected in the differential SAXS patterns. This result suggests the growth of the density fluctuation elongated in the stretching direction, which is not directly related to strain-induced crystallization. (C) 2011 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 49: 1157-1162, 2011
引用
收藏
页码:1157 / 1162
页数:6
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