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首页> 外文期刊>Macromolecules >Rheological behavior of POSS/polyurethane-urea nanocomposite films prepared by homogeneous solution polymerization in aqueous dispersions
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Rheological behavior of POSS/polyurethane-urea nanocomposite films prepared by homogeneous solution polymerization in aqueous dispersions

机译:水分散液中均相溶液聚合制备的POSS /聚氨酯-脲纳米复合膜的流变行为

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Reinforced polyurethane-urea nanocomposite with reactive polyhedral oligomeric silsesquioxanes (POSS) has been prepared via environmentally friendly aqueous dispersion with no organic solvent. Rheological behavior of this important class of materials has been investigated as a function of POSS concentration over a wide range of shear frequency and temperature (-100 to 230 degrees C). The functionalized diamino-POSS was reacted initially with isophorone diisocyanate (the urethane hard segments) before adding the polyester diol (the soft segments). The complete reaction of diamino-POSS with urethane segments was confirmed rheologically and morphologically (TEM). The molecular relaxations of the hard and soft segments of PU/POSS nanocomposites were investigated using the rectangular torsional mode in the glassy and rubbery states. It was found that the storage elastic modulus increased systematically only in the high-temperature range (i.e., the range of the T-g of the urethane segments) while the modulus did not significantly change at low temperatures corresponding to the range of the T-g of the polyester soft segments. In addition, the rheological behavior of the pure PU in the melt confirmed the existence of microphase separation of the hard and soft segments at 140 degrees C. The value of the microphase separation temperature (T-MPS) was found to be concentration independent when the POSS concentration is <= 6 wt %. For 10 wt % POSS the T-MPS shifted by 20 degrees C to a higher temperature. The viscoelastic material functions (G', G '', and eta* ) for pure PU film and samples with POSS <= 6 wt % were found to be well described by the time-temperature superposition (or WLF) principle in the low-temperature range studied (i.e., T < T-MPS (140 degrees C)); at higher temperatures the superposition principle failed to describe the experimental data. For 10 wt % POSS film, the validity of WLF principle was extended up to 160 degrees C due to the shift of T-MPS to higher temperature. The incorporation of POSS to the hard segments of PU produced a more homogeneous structure for the 10 wt % POSS as confirmed by TEM. In addition, the viscosity and activation energy of flow were increased dramatically by adding POSS to PU. The thermal stability of PU under a nitrogen atmosphere did not improve by adding POSS, but it improved slightly when tested in an oxygen atmosphere.
机译:已通过不使用有机溶剂的环保型水分散体制备了具有反应性多面体低聚倍半硅氧烷(POSS)的增强型聚氨酯-脲纳米复合材料。在很宽的剪切频率和温度范围内(-100至230摄氏度),已经研究了这一重要材料类别的流变行为与POSS浓度的关系。首先将官能化的二氨基-POSS与异佛尔酮二异氰酸酯(聚氨酯硬链段)反应,然后添加聚酯二醇(软链段)。流变学和形态学(TEM)证实了二氨基-POSS与氨基甲酸酯链段的完全反应。 PU / POSS纳米复合材料的硬链段和软链段的分子弛豫使用玻璃态和橡胶态的矩形扭转模式进行了研究。发现储能模量仅在高温范围内(即,氨基甲酸酯链段的Tg的范围)系统地增加,而在低温下对应于聚酯的Tg的范围的储能模量没有明显变化。软段。此外,纯PU在熔体中的流变行为证实了在140摄氏度下存在硬链段和软链段的微相分离。当温度升高时,微相分离温度(T-MPS)的值与浓度无关。 POSS浓度≤6重量%。对于10 wt%的POSS,T-MPS移20摄氏度至更高的温度。发现纯PU膜和POSS <= 6 wt%的样品的粘弹性材料功能(G',G”和eta *)在低温度下通过时间-温度叠加(或WLF)原理得到了很好的描述。研究的温度范围(即,T

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