Strain induced nanocavitation and crystallization in natural rubber probed by real time small and wide angle X-ray scattering

被引:37
|
作者
Zhang, Huan [1 ]
Scholz, Arthur K. [2 ,3 ]
Merckel, Yannick [4 ]
Brieu, Mathias [4 ]
Berghezan, Daniel [5 ]
Kramer, Edward J. [2 ,3 ,6 ]
Creton, Costantino [1 ]
机构
[1] Univ Paris 06, ESPCI Paristech, CNRS, Lab Sci & Ingn Matiere Molle, F-75005 Paris, France
[2] Univ Calif Santa Barbara, Mat Res Lab, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
[4] Ecole Cent Lille, LML, F-59650 Villeneuve Dascq, France
[5] Michelin, CERL Ladoux, F-63040 Clermont Ferrand, France
[6] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 83106 USA
关键词
cavitation; crystallization; elastomers; natural rubber; nanocomposite; SAXS; WAXS; STRESS-INDUCED CRYSTALLIZATION; UNIAXIAL DEFORMATION; CRYSTAL-STRUCTURE; ORIENTATION; REINFORCEMENT; MECHANISM; EVOLUTION; INSIGHTS; NETWORK; FILLER;
D O I
10.1002/polb.23313
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 concomitant appearance of crystallites and nanocavities under uniaxial strain is investigated by X-ray scattering in a model natural rubber system. The nanocavities appear after crystallization and only when the true stress is above a critical cavitation stress sigma Cav. The presence of crystallites alone does not influence the calculation of the void volume fraction phi void. The nanocavities formed are 20-50 nm in size with a constant aspect ratio. The presence of filler shifts the critical crystallization extension ratio Cry, Cav, and sigma Cav to lower values. The clear correlation between sigma Cav and the crystallinity at the onset of cavitation C(Cav) implies that the crystallites take most of the mechanical loading thus delaying the cavitation in the amorphous phase. Under cyclic loading, nanocavitation is significant only in the first loading and in the successive loadings if the extension ratio is above its maximum historical value. (c) 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013, 51, 1125-1138
引用
收藏
页码:1125 / 1138
页数:14
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