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Dynamic mechanical behavior and nanostructure morphology of hyperbranched-modified polypropylene blends

机译:超支化改性聚丙烯共混物的动态力学行为和纳米结构形态

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Polypropylene (PP) was modified utilizing two types of polyesteramide-based hyperbranched polymers (amphiphilic PS and hydrophilic PH). A maleicanhydride-modified PP (PM) was used as a reactive dispersing agent to enhance the modification by grafting the hyperbranched polymers onto the PP chains. Pure PP, two different non-reactively modified samples, i.e. excluding PM, and two different reactively modified samples, i.e. including PM, were studied. Investigating the morphology of the samples was performed by scanning electron microscopy. To follow the effect of the modification on the dynamic mechanical properties, dynamic mechanical analysis experiments both in the melt (rheometric mechanical spectrometry) and in solid state (dynamic mechanical thermal analysis) were carried out. In the next step, the nanocrystalline structure of the samples was studied by small angle X-ray scattering (SAXS) in two different modes, i.e. static and recrystallization. Hundreds of SAXS patterns were analyzed automatically using procedures written in PV-WAVE image-processing software. The chord distribution function (CDF) was calculated and the long period (/p) of the crystal lamellae was extracted from the COFs. The rheometric mechanical spectrometry results show that both hyperbranched polymers decrease complex viscosity rf and enhance liquid-like behavior. This happens more significantly when PM is included. The dynamic mechanical thermal analysis results reveal that Tg decreases when PS and PH are added. In the reactively modified samples this reduction is compensated most probably because of the crosslinked structure formed through the grafting reaction between the hyperbranched polymers and PM. Such structure is confirmed by SAXS data and calculated CDFs in the recrystallization mode. Static SAXS data also show enhancement in the crosshatched morphology of the crystalline lamellae of PP for reactively modified samples compared with non-reactively modified samples.
机译:利用两种类型的基于聚酯酰胺的超支化聚合物(两亲PS和亲水PH)对聚丙烯(PP)进行改性。使用马来酸酐改性的PP(PM)作为反应性分散剂,通过将超支化聚合物接枝到PP链上来增强改性。研究了纯PP,两个不同的非反应性改性样品(即不包括PM)和两个不同的反应性改性样品(即不包括PM)。通过扫描电子显微镜进行样品形态的研究。为了跟踪改性对动态力学性能的影响,进行了熔体(流变力学光谱)和固态(动态力学热分析)的动态力学分析实验。在下一步中,通过小角度X射线散射(SAXS)以两种不同的模式,即静态和重结晶,研究了样品的纳米晶体结构。使用PV-WAVE图像处理软件编写的程序自动分析了数百个SAXS模式。计算弦分布函数(CDF),并从COF中提取晶体薄片的长周期(/ p)。流变力学光谱分析结果表明,两种超支化聚合物均降低了复数粘度rf并增强了类似液体的行为。当包含PM时,这种情况会更加明显。动态机械热分析结果表明,当添加PS和PH时,Tg降低。在反应性改性的样品中,这种减少最有可能得到补偿,这是由于通过超支化聚合物与PM之间的接枝反应形成的交联结构。通过重结晶模式下的SAXS数据和计算出的CDF证实了这种结构。静态SAXS数据还显示,与未反应改性的样品相比,经反应改性的样品的PP结晶薄片的剖面线形态得到了增强。

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