105 resultados para pp collision


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Morphology, mechanical properties, and interfacial interaction of polyamide 1010/polypropylene (PA1010/ PP) blends compatibilized with polypropylene grafted with glycidyl methacrylate (PP-g-GMA) were studied. It was found that the size of the PP domains, tensile and impact strength of ternary blends, and adhesion fracture energy between two layers of PA1010 and PP were all significantly dependent on the PP-g-GMA contents in the PP layer. Correlations between morphology and related properties were sought. The improvements in properties have been attributed to chemical and physical interaction occurring between PA1010 and PP-g-GMA. (C) 1997 Elsevier Science Ltd.

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The modification of polypropylene (PP) was accomplished by melt grafting glycidyl methacrylate (GMA) on its molecular chains. The resulting PP-g-GMA was used to prepare binary blends of polyamide 1010 (PA1010) and PP-g-GMA. Different blend morphologies were observed by scanning electron microscopy (SEM) according to the nature and content of PA1010 used. Comparing the PA1010/PP-g-GMA and PA1010/PP binary blends, the size of the domains of PP-g-GMA were much smaller than that of PP at the same compositions. It was found that mechanical properties of PA1010/PP-g-GMA blends were obviously better than that of PA1010/PP blends, and the mechanical properties were significantly influenced by wetting conditions for uncompatibilized and compatibilized blends. A different dependence of the flexural modulus on water was found for PA1010/PP and PA1010/PP-g-GMA. These behaviors could be attributed to the chemical interactions between the two components and good dispersion in PA1010/PP-g-GMA blends. Thermal and rheological analyses were performed to confirm the possible chemical reactions taking place during the blending process. (C) 1997 John Wiley & Sons, Inc.

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The overall isothermal crystallization kinetics for neat polypropylene and grafted polypropylene systems were investigated. The rate constants were corrected assuming the heterogeneous nucleation and three dimensional growth of polypropylene spherulites. A semiempirical equation for the radial growth rate of polypropylene spherulites was developed as a function of temperature, and was used to determine the number of effective nuclei of different temperatures. The number of nuclei in grafted samples was estimated to be 10(2)-10(3) times larger than that of neat polypropylene. (C) 1997 John Wiley & Sons, Inc.

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The morphology of polyamidelOlO/polypropylene blends was found to significantly depend upon the concentration of the compatibilizer[polypropylene-grafted-acrylic acid (PP-g-AA)]. A significant reduction in phase size was observed because of the interaction that existed between the PP-g-AA and polyamide. These interactions have been confirmed by several methods. The tensile mechanical properties and impact behavior of the prepared blends were investigated and correlated with scanning electron microscope (SEM) analysis of the fracture surfaces. It was found that PP-g-AA as the compatibilizer has a profound effect upon the properties of the blends. This behavior is attributed to a series of chemical and physico-chemical interactions taking place between the two components.

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研究了在多官能团单体—三烯丙基异腈脲酸酯存在下,PP/LDPE共混物的辐射效应,并用SEM、DSC和动态力学性能对其形态结构和相容性进行了表征。结果表明:通过添加三烯丙基异腈脲酸酯,用辐射可以强化PP/LDPE共混物的相间结合力,改善共混物的相容性,从而提高共混物的力学性能。

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研究了在多官能团单体—三烯丙基异氰脲酸酯存在下PP/LDPE共混体系接受γ-辐射的效果。用溶解度参数和TEM技术评估了共混体系的相容性与多官能团单体在共混体系中的分布,并用SEM、DSC、动态力学等方法对共混体系相容性进行了表征。结果表明,PP/LDPE是不相容的共混体系,三烯丙基异氰脲酸酯主要分布在共混体系的相界面区域,辐照强化了共混体系的相间结合,增加了界面厚度,改善了共混体系的相容性。

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研究了在多官能团单体-三烯丙基异氰酸酯(TAIC)存在下,聚丙烯(PP)/乙烯-醋酸乙烯酯(EVA)共混体系的辐射交联、并应用凝胶量、力学性能等数据对其进行表征。结果表明,TAIC对PP/EVA共混体系的辐射交联的敏化作用显著,EVA对体系凝胶生成有正的协同作用,改善了TAIC在共混体系中的分布。敏化交联还改善了PP/EVA共混体系的相容性,增强了相间粘附,提高了其力学性能。

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本研究中采用三烯丙基异腈脲酸酯(TAIC)和三羟甲基丙烷三甲基丙烯酸酯(TMPTMA)为PP/PE共混体系的多官能团单体。研究了辐照剂量,多官能团单体种类和多官能团单体用量对共混物形态结构及力学性能的影响。发现TAIC及TMPTMA对PP/PE体系有较好的增容作用,共混物具有好的相容性,力学性能得到改善。

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Mechanical properties and morphology of blends of polypropylene (PP) with high molecular weight polyethylene (HMWPE) prepared by coprecipitation from xylene solution are investigated. Compared to blends of PP with commercial high-density polyethylene (HDPE), the mechanical properties of the blends of PP/HMWPE are much superior to those of PP/HDPE blends. Not only is the tensile strength stronger, but also the elongation at break is much higher than that of the PP/HDPE blends of the same composition. These differences increase with increasing HMWPE and HDPE content. Scanning electron microscopy of the fracture surface resulting from the tensile tests shows that the compatibility in PP/HMWPE blends is much better than that in PP/HDPE blends. This is most likely attributable to the enhanced chain entanglement of HMWPE with the PP in the amorphous phase due to the lower crystallinity, owing to the high molecular weight of the HMWPE, and a much more flexible chain. The thermal behavior and spherulite morphology of both blends are also investigated.

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Collision cross sections are calculated using the R-matrix method for excitations between the three lowest LS states for Na-like Cu ion. The complex resonance structures are investigated. The collision rate coefficients have been calculated assuming a Maxwellian distribution of electron-impact energies. The results of the collision cross sections are in good agreement with those of the other theory.

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用熔融接枝方法制备了聚丙烯-g-丙烯酸(PP-g-AA)。用光电子能谱,广角X射线衍射,红外光谱和化学滴定方法对接枝物进行了定性和定量表征。讨论了单体和引发剂浓度对接枝率的影响,确定了用红外光谱法测定接枝物含量的经验公式

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利用聚丙烯等离子体接枝甲基丙烯酸甲酯共聚物(PP-g-PMMA)作增容剂,研究了其在聚丙烯/聚偏氟乙烯(PVDF)共混体系中的作用。增容是通过PMMA与PVDF的偶极-偶极相互作用实现的。接枝共聚物使共混体系的抗张强度和模量均有提高,由不同等离子体处理时间所得的PP-g-PMMA,接枝率在7.7%~300%具有最好的增容效果;而由不同后聚合时间所得的共聚物,接枝率在30%~80%具有最好的增容效果。

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离子聚合物在Nylon-1010/PP共混物中的增容作用曲桂杰,刘景江(中国科学院长春应用化学研究所长春130022)关键词聚丙烯,Nylon-1010,离子聚合物,增容选择离子聚合物作为高聚物共混的增容剂,通过离子间的相互作用可达到增容效果[1]。...

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通过δ-TiCl_3-Et_2AICl催化淤浆聚合合成了不同嵌段长度的聚丙烯-乙丙橡胶嵌段共聚物(PP-EPR),作为乙丙橡胶(EPT)和PP的增容剂,明显改善PP的低温耐冲击性能。实验发现,当PP-EPR中PP段的聚合时间为5min,EPR段的聚合时间为30min时,PP-EPR的增容效果最好;PP-EPR加入量仅为4%,就可以显著地改善PP和EPT的相容性,使共混物PP/EPT/PP-EPR的拉伸强度只比PP降低22%,而-20℃和-40℃下的冲击强度分别为PP的9倍和8倍。