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首页> 外文期刊>Journal of Polymer Science, Part B. Polymer Physics >Copolyester/layered silicate nanocomposites: The effect of the molecular size and molecular structure of the intercalant on the structure and viscoelastic properties of the nanocomposites
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Copolyester/layered silicate nanocomposites: The effect of the molecular size and molecular structure of the intercalant on the structure and viscoelastic properties of the nanocomposites

机译:共聚酯/层状硅酸盐纳米复合材料:嵌入剂的分子大小和分子结构对纳米复合材料的结构和粘弹性的影响

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The preparation of poly(ethylene glycol-co-cyclohexane-1,4-dimethanol terephthalate)/layered silicate nanocomposites via a melt-intercalation technique is reported. Layered silicates modified with different alkyl ammonium intercalants have been used for this purpose. A comparison is made between carefully chosen pairs of the nanocomposites, the choice depending on the cation-exchange capacity or the intercalant concentration of the organically modified montmorillonite, to study the effects of the molecular size and molecular structure of the intercalant. The structure of the nanocomposites is characterized with wide-angle X-ray diffraction. The presence of well-defined diffraction peaks and an observed increase in the interlayer spacing in the nanocomposites imply the formation of an intercalated hybrid. To investigate the viscoelastic behavior, these nanocomposites are also subjected to dynamic mechanical analysis. The dynamic mechanical properties show an increase in the storage modulus of the nanocomposites over the entire temperature range studied (except in the transition region from 68 to 78 degreesC) in comparison with that of the pristine polymer. The size of the intercalant molecule and the presence of functional groups capable of forming favorable interactions with the polymer govern the amount of polymer infiltrating the clay gallery space and control the increase in the modulus of the nanocomposite. The tan 5 peak signifying the glass-transition temperature shifts to lower temperatures in the nanocomposites. Interestingly, the nanocomposites show less damping than the pristine polymer. This behavior is understood in terms of the confinement of the polymer chains in the clay interlayer. (C) 2003 Wiley Periodicals, Inc. [References: 31]
机译:报道了通过熔融插层技术制备聚(乙二醇-共环己烷-1,4-二甲醇对苯二甲酸二乙酯)/层状硅酸盐纳米复合材料。为此目的已经使用了用不同的烷基铵嵌入剂改性的层状硅酸盐。在仔细选择的成对的纳米复合材料之间进行比较,该选择取决于阳离子交换能力或有机改性蒙脱土的插层剂浓度,以研究插层剂的分子大小和分子结构的影响。纳米复合材料的结构以广角X射线衍射为特征。明确定义的衍射峰的存在以及在纳米复合材料中观察到的层间间距的增加暗示了插层杂化体的形成。为了研究粘弹性行为,还对这些纳米复合材料进行了动态力学分析。动态力学性能显示,与原始聚合物相比,纳米复合材料在整个研究温度范围内的储能模量有所增加(在68至78摄氏度的过渡区域内除外)。嵌入剂分子的大小和能够与聚合物形成有利相互作用的官能团的存在控制着渗透到粘土通道空间中的聚合物的量,并控制了纳米复合材料模量的增加。 tan 5峰表示玻璃化转变温度移至纳米复合材料中的较低温度。有趣的是,纳米复合材料显示出比原始聚合物更少的阻尼。通过限制粘土中间层中的聚合物链可以理解这种行为。 (C)2003 Wiley Periodicals,Inc. [参考:31]

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