Real time SAXS/stress-strain studies of thermoplastic polyurethanes at large strains

被引:84
作者
Blundell, DJ
Eeckhaut, G
Fuller, W
Mahendrasingam, A [1 ]
Martin, C
机构
[1] Univ Keele, Dept Phys, Sch Chem & Phys, Keele ST5 5BG, Staffs, England
[2] Huntsman Polyurethanes R&D, B-3078 Everberg, Belgium
基金
英国工程与自然科学研究理事会;
关键词
small angle X-ray scattering; polyurethanes; stress-strain;
D O I
10.1016/S0032-3861(02)00386-5
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Simultaneous small angle X-ray scattering (SAXS) and force measurements have been recorded during tensile deformation of two contrasting polyurethane elastomers. The elastomers comprise the same hard and soft chemical segments; in Sample A, the length of the hard blocks is randomised while in Sample B the hard blocks are monodisperse. During deformation of Sample A, the SAXS halo from the mesophase structure deforms to an ellipse with intensification on the meridian. In Sample B, the halo transforms into a four point pattern. The ellipse patterns of A are interpreted in terms of a model based on particles located on a statistical lattice which is subjected to an affine deformation scheme. According to this model, the SAXS patterns of A are consistent with the hard phase regions behaving as embedded particles which separate from each other in an affine manner and which are not impeded by interconnections during the mechanical yield process. In B, the interconnection of the hard phase prevents affine deformation of the structure and involves the formation of a four point 'lattice' structure which then subsequently deforms in an affine manner. The differences in behaviour are linked with the segment sequencing which result in the phase regions of Sample A having a lower volume fraction and are consistent with variation in applied stress. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:5197 / 5207
页数:11
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