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Crystallization and morphological and crystal structures of PP in an in situ microfibrillar composite of modified PA66 with PP

机译:改性PA66与PP的原位微原纤复合材料中PP的结晶,形态和晶体结构

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An in situ-profiled microfibril-reinforced composite of modified polyamide 66 (mPA66) with polypropylene (PP) was prepared using a non-conventional compatibilization technique. The scanning electron microscope morphological observations showed in situ-generated, profiled microfibrils with a non-uniform diameter distribution and very rough surfaces with many pits and knots. The pits and knots were confirmed by the compatibilizer diffusion determined by the energy dispersive spectrum analysis. The presence of the PA66-profiled microfibrils shows the significant nucleation ability of the PP crystallization. Differential scanning calorimetry observations illustrated that the profiled microfibrils can accelerate the crystallization rate and increase the crystallization temperature. Obvious trans crystallization layers were observed through a polarized optical microscope. The beta-crystalline phase of PP and larger, long period lamellar stacks were identified by small and wide-angle X-ray scattering measurements, respectively. These observations were very different from those of the simply blended samples of PP/PA66 in the presence or absence of the compatibilizer. Thus, the profiled microfibrils and improved interface adhesion may account for the powerful influence of PP on the crystallization and crystal structure. (C) 2017 Elsevier Ltd. All rights reserved.
机译:使用非常规增容技术制备了改性聚酰胺66(mPA66)与聚丙烯(PP)的原位异形微纤维增强复合材料。扫描电子显微镜的形态学观察结果表明,原位生成的异型微纤维直径分布不均匀,表面非常粗糙,具有许多凹坑和结。坑和结通过能量分散谱分析确定的增容剂扩散确定。 PA66轮廓微纤维的存在表明PP结晶具有明显的成核能力。差示扫描量热法观察表明,异型微纤丝可以加速结晶速率并提高结晶温度。通过偏振光学显微镜观察到明显的反结晶层。 PP和较大的,较长的层状叠层的β晶相分别通过小角度和广角X射线散射测量确定。这些观察结果与在存在或不存在增容剂的情况下简单混合的PP / PA66样品的观察结果完全不同。因此,异型微纤维和改善的界面粘附性可以解释PP对结晶和晶体结构的强大影响。 (C)2017 Elsevier Ltd.保留所有权利。

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