4.7 Article

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

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POLYMER
卷 46, 期 14, 页码 5103-5117

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ELSEVIER SCI LTD
DOI: 10.1016/j.polymer.2005.04.057

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ethylene-propylene elastomer; carbon nanofiber; nanocomposite

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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.

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