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Polyurethane Tri-block Copolymers-Synthesis, Mechanical, Elastic, and Rheological Properties

机译:聚氨酯三嵌段共聚物-合成,机械,弹性和流变性能

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摘要

A series of polyurethane tri-block copolymers were synthesized by reacting a 4,4'-methylenebis(phenyl isocyanate) (MDI)-endcapped poly(tetramethylene oxide) (PTMO, M^sub n^ = 2,000 g/mol) with a monoamine-diamide (6T6m) hard segment (HS). The concentration of the HS in the copolymer was varied between 9 and 33 wt % by changing the length of the soft mid-block segment. The structure of the copolymers was analyzed by nuclear magnetic resonance, the amide crystallinity was investigated by Fourier transform infra-red and the thermal properties were studied by differential scanning calorimetry. The mechanical and elastic properties of the tri-block copolymer were subsequently explored by dynamic mechanical analysis, compression set and tensile experiments, and the melt rheological behavior was studied by a parallel plate method. The amide end groups displayed a high crystallinity and the modulus of the tri-block copolymers was relatively high. The fracture strain increased strongly with the molecular weight and the copolymers demonstrated a ductile fracture behavior for molecular weights above 6000 g/mol. Good compression set values were obtained for the tri-block copolymers despite their low molecular weight. In the molten state, the tri-block polymers displayed a gelling effect at low frequencies, which was believed to be a result of a clustering of the end-segments. [PUBLICATION ABSTRACT]
机译:通过使4,4'-亚甲基双(异氰酸苯基酯)(MDI)封端的聚四亚甲基氧化物(PTMO,M ^ sub n = 2,000 g / mol)与单胺反应合成一系列聚氨酯三嵌段共聚物-二酰胺(6T6m)硬链段(HS)。通过改变软的中间嵌段的长度,共聚物中HS的浓度在9至33重量%之间变化。通过核磁共振分析共聚物的结构,通过傅立叶变换红外光谱研究酰胺的结晶度,并通过差示扫描量热法研究热性能。随后通过动态力学分析,压缩永久变形和拉伸实验探索了三嵌段共聚物的力学和弹性性能,并通过平行板法研究了熔体的流变行为。酰胺端基表现出高结晶度,并且三嵌段共聚物的模量相对较高。断裂应变随分子量的增加而强烈增加,并且共聚物在分子量超过6000 g / mol时表现出韧性的断裂行为。尽管三嵌段共聚物的分子量低,但仍获得了良好的压缩永久变形值。在熔融状态下,三嵌段聚合物在低频下显示出胶凝作用,这被认为是端段聚集的结果。 [出版物摘要]

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    《Polymer Engineering and Science》 |2010年第4期|p.747-755|共9页
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    Araichimani Arun,1,2 Kasper K.J. Baack,1 Reinoud J. Gaymans11 Polymer and Biomaterials Department, University of Twente, Enschede 7500AE, The Netherlands2 Dutch Polymer Institute, Eindhoven 5600 AX, The NetherlandsCorrespondence to: Reinoud J. Gaymans, e-mail: r.j.gaymans@ utwente.nlAraichimani Arun is currently at Department of Chemistry, Government Arts College, Tiruvannamalai, Tamil Nadu, India.Contract grant sponsor: Research Program of the Dutch Polymer Institute (DPI).DOI 10.1002/pen.21579Published online in Wiley InterScience (www.interscience.wiley.com).© 2009 Society of Plastics Engineers,;

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