Uniaxial deformation of an elastomer nanocomposite containing modified carbon nanofibers by in situ synchrotron X-ray diffraction

被引:42
作者
Kelarakis, A [1 ]
Yoon, KW [1 ]
Sics, I [1 ]
Somani, RH [1 ]
Hsiao, BS [1 ]
Chu, B [1 ]
机构
[1] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
基金
美国国家科学基金会;
关键词
ethylene-propylene elastomer; carbon nanofiber; nanocomposite;
D O I
10.1016/j.polymer.2005.04.057
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Structure and property of a nanocomposite consisting of modified carbon nanofibers (MCNFs), homogenously dispersed in an elastomeric ethylene/propylene (EP) random copolymer (84.3 wt% P) matrix, were studied by in situ synchrotron X-ray diffraction during uniaxial deformation. The MCNF acted as a nucleating agent for crystallization of the alpha-form of isotactic polypropylene (W) in the matrix. During deformation at room temperature, strain-induced crystallization took place, while the transformation from the gamma phase to alpha phase also occurred for both unfilled and 10 wt% MCNF-filled samples. The tensile strength of the filled material was consistently higher than that of pure copolymer. However. when compared with pure copolymer, the highly stretched nanocomposite exhibited a higher amount of unoriented crystals. a lower degree of crystal orientation and a higher amount of gamma crystals. This behavior indicated that polymer crystals in the filled nanocomposite experienced a reduced load, suggesting an effective load transfer from the matrix to MCNFs. At elevated temperatures. the presence of MCNFs resulted in a thermally stable physically cross-linked network, which facilitated strain-induced crystallization and led to a remarkable improvement in the mechanical properties. For example, the toughness of the 10 wt% nanocomposite was found to increase by a factor of 150 times at 55 degrees C. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5103 / 5117
页数:15
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