Thermo-mechanical behavior of electrospun thermoplastic polyurethane nanofibers

被引:27
作者
Alhazov, Dmitriy [1 ]
Gradys, Arkadiusz [1 ,2 ]
Sajkiewicz, Pawel [2 ]
Arinstein, Arkadii [1 ]
Zussman, Eyal [1 ]
机构
[1] Technion Israel Inst Technol, Fac Mech Engn, IL-32000 Haifa, Israel
[2] Polish Acad Sci, Inst Fundamental Technol Res, PL-02106 Warsaw, Poland
基金
以色列科学基金会;
关键词
Block-copolymer; Electrospinning; Nanofibers; Thermo-mechanical properties; MULTIPLE MELTING ENDOTHERMS; BLOCK CONTENT POLYURETHANE; STYRENE TRIBLOCK COPOLYMER; POLYMER NANOFIBERS; THERMAL SHRINKAGE; THIN-FILMS; FIBERS; DEFORMATION; ORIGIN; NANOCOMPOSITES;
D O I
10.1016/j.eurpolymj.2013.09.028
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Analysis of the thermo-mechanical behavior of electrospun thermoplastic polyurethane (TPU) block co-polymer nanofibers (glass transition temperature similar to-50 degrees C) is presented. Upon heating, nanofibers began to massively contract, at similar to 70 degrees C, whereas TPU cast films started to expand. Radial wide-angle X-ray scattering (WAXS) profiles of the nanofibers and the films showed no diffraction peaks related to crystals, whereas their amorphous halo had an asymmetric shape, which can be approximated by two components, associated with hard and soft segments. During heating, noticeable changes in the contribution of these components were only observed in nanofibers. These changes, which were accompanied with an endothermic DSC peak, coinciding with the start of the nanofibers contraction, can be attributed to relaxation of an oriented stretched amorphous phase created during electrospinning. Such structure relaxation becomes possible when a portion of the hard segment clusters, forming an effective physical network, is destroyed upon heating. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3851 / 3856
页数:6
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