Relationship between nanoscale deformation processes and elastic behavior of polyurethane elastomers

被引:141
作者
Christenson, EM
Anderson, JM
Hiltner, A [1 ]
Baer, E
机构
[1] Case Western Reserve Univ, Dept Macromol Sci, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Ctr Appl Polymer Res, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
polyurethanes; atomic force microscopy; elastomer;
D O I
10.1016/j.polymer.2005.08.083
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 cyclic deformation of two polyurethane elastomers that differed in soft segment content and molecular weight was investigated. The microphase-separated morphology of the polyurethane with higher soft segment content consisted of hard segment domains dispersed in a soft segment matrix. In the polyurethane with lower soft segment content, the hard segment domains appeared to be partially cocontinuous. Following an initial 'conditioning' cycle, both polyurethanes exhibited reversible elastomeric behavior. Structural changes that occurred during conditioning were investigated using atomic force microscopy and Fourier transform infrared dichroism. The results provided the basis of a structural model for the deformation behavior. Yielding and reorganization of hard domains resulted in a highly oriented microfibrous morphology. Subsequent unloading and reloading were associated with reversible relaxation and reformation of the microfibrous entities. The elastic behavior of the conditioned polyurethanes was satisfactorily described by classical rubber theory with inextensibility. The structural model proposed here extended previous efforts to describe the deformation processes Of polyurethanes during cyclic loading. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:11744 / 11754
页数:11
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