材料科学
极限抗拉强度
共聚物
小角X射线散射
高分子化学
环氧丙烷
聚合物
复合材料
环氧乙烷
物理
散射
光学
作者
S. Piril Ertem,Emel Yılgör,Cagla Kosak,Garth L. Wilkes,Mingqiang Zhang,İskender Yılgör
出处
期刊:Polymer
[Elsevier]
日期:2012-08-16
卷期号:53 (21): 4614-4622
被引量:67
标识
DOI:10.1016/j.polymer.2012.08.020
摘要
Influence of soft segment molecular weight and hard segment content on the morphology, thermomechanical and tensile properties of homologous polyurethaneurea copolymers based on narrow molecular weight poly(propylene oxide)glycol (PPG) oligomers were investigated. A series of polyurethaneureas with hard segment contents of 12–45% by weight and PPG number average molecular weights of 2000 to 11,800 g/mol were synthesized and characterized structurally by SAXS and mechanically by DMA and stress strain analysis. Bis(4-isocyanatocyclohexyl)methane and 2-methyl-1,5-diaminopentane were used as the diisocyanate and the chain extender respectively. All copolymers displayed microphase separation by SAXS and DMA. The critical entanglement molecular weight (Me) of PPG is reported to be around 7700 g/mol. Our mechanical results suggest that when copolymers possess similar hard segment contents and are compared to those based on soft segments with number average molecular weights (Mn) greater than Me, they generally displayed higher tensile strengths and particularly lower hysteresis and creep than those having soft segment molecular weights below Me. These results imply that soft segment entanglements in thermoplastic polyurethaneureas may provide a critical contribution to the tensile properties of these copolymers – particularly in the range where the soft segment content is dominant.
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