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首页> 外文期刊>Polymer engineering and science >Layered Silicate Nanocomposites Based on Various High-Functionality Epoxy Resins.Part II:The Influence of an Organoclay on the Rheological Behavior of Epoxy Prepolymers
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Layered Silicate Nanocomposites Based on Various High-Functionality Epoxy Resins.Part II:The Influence of an Organoclay on the Rheological Behavior of Epoxy Prepolymers

机译:基于各种高功能环氧树脂的层状硅酸盐纳米复合材料。第二部分:有机粘土对环氧预聚物流变行为的影响

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The effect of an organically surface modified layered silicate on the viscosity of various epoxy resins of different structures and different functionalities was investigated.Steady and dynamic shear viscosities of the epoxy resins containing -10 wt% of the organoclay were determined using parallel plate rheology.Viscosity results were compared with those achieved through addition of a commonly used micron sized CaCO_3 filler.It was found that changes in viscosities due to the different fillers were of the same order,since the layered silicate was only dispersed on a micron-sized scale in the monomer (prior to reaction),as indicated by X-ray diffraction measurements.Flow activation energies at a low frequency were determined and did not show any significant changes due to the addition of organoclay or CaCO_3.Comparison between dynamic and steady shear experiments showed good agreement for low layered silicate concentrations below 7.5 wt%,i.e. the Cox-Merz rule can be applied.Deviations from the Cox-Merz rule appeared at and above 10 wt% although such deviations were only slightly above experimental error.Most resin organoclay blends were well predicted by the Power Law model,only concentrations of 10 wt% and above requiring the Herschel-Buckley (yield stress) model to achieve better fits.Wide-angle X-ray measurements have shown that the epxoy resin swells the layered silicate with an increase in the interlayer distance of approximately 15 A,and that the rheology behavior is due to the lateral,micron-size of these swollen tactoids.
机译:研究了有机表面改性的层状硅酸盐对不同结构和功能不同的各种环氧树脂的粘度的影响。采用平行板流变学方法测定了含有-10 wt%有机粘土的环氧树脂的稳态和动态剪切粘度。将结果与通过添加常用的微米级CaCO_3填料获得的结果进行了比较。发现由于不同填料而导致的粘度变化处于相同的数量级,因为层状硅酸盐仅以微米级规模分散。 X射线衍射测量表明,单体(反应之前)。测定了低频流动活化能,并且由于添加了有机粘土或CaCO_3而没有显示任何明显的变化。动态和稳态剪切实验之间的比较显示出良好的低于7.5 wt%的低层状硅酸盐浓度的协议,即Cox-Merz规则的偏差出现在10 wt%或以上,尽管这种偏差仅稍高于实验误差。大多数树脂有机粘土共混物均通过幂律模型很好地预测,浓度仅为10重量%及以上要求使用Herschel-Buckley模型(屈服应力)模型才能更好地拟合。广角X射线测量表明,epxoy树脂使层状硅酸盐溶胀,层间距离增加了约15A,并且流变行为是由于这些溶胀的类触针的侧面,微米大小所致。

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