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Resistance-to-flow Analysis in Low Density Polyethylene/Plasticized Starch Blends Containing Compatibilizers with Attractive and Repulsive Interactions

机译:包含具有吸引和排斥相互作用的增容剂的低密度聚乙烯/增塑淀粉混合物的流阻分析

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Processing of polymer blends is mainly controlled by the behaviour of their components, interfacial area and strength. Therefore, many experimental and theoretical investigations have been devoted to elucidating their basic governing principles. Nonetheless, there are only limited data in the literature about the effect of compatibilizers on the rheological properties of blends. The resistance-to-flow of low density polyethylene/plasticized starch blend and their compatibilized versions with poly(ethylene-r-vinyl acetate), maleated poly(styrene-ethylene-butadiene-styrene) and maleated polyethylene was investigated with a capillary rheometer at different temperatures. Furthermore, the melt elasticity enhancement of the aforementioned alloys was compared with their non-compatibilized polyethylene/thermoplastic starch blend via rheomechanical spectroscopy at 190℃ and 500 Hz as an index of their interfacial strength. The results showed that by lowering the temperature of the melt alloys, the compatibilizer was directed toward interfacial localization and led to concomitant elasticity enhancement in comparison with their virgin blends. In addition, the resistance-to-flow of the blend and their alloys through capillary rheometer were enhanced and distinctively differentiated. This was attributed to the blend positive % parameter which pushes compatibilizers localization at the interface with different adsorption densities and conformational resistance against flow of the system. In other words, a quasi core/shell structure formation at the dispersed phase/matrix interface was proposed as the origin of resistive capillary flow, leading to a viscoelastic loss enhancement. In analogy with Gent-Schultz equation governing the joint adhesion energy of polymers, the energy loss during capillary flow of a multicomponent blend was correlated for the first time to their interfacial strength. Interestingly, the calculated energy loss for the investigated melt blend and its compatibilized alloys in capillary flow was proportional to the solid state deformation loss during peeling of a corresponding joint interfaces reported by our group.
机译:聚合物共混物的加工主要受其组分的行为,界面面积和强度控制。因此,许多实验和理论研究都致力于阐明其基本控制原理。但是,关于相容剂对共混物流变性能的影响,文献中仅有有限的数据。用毛细流变仪研究了低密度聚乙烯/增塑淀粉共混物及其与聚(乙烯-r-乙酸乙烯酯),马来酸化的聚(苯乙烯-乙烯-丁二烯-苯乙烯)和马来酸化聚乙烯的相容版本的抗流动性不同的温度。此外,通过流变力学在190℃和500 Hz下,将上述合金的熔体弹性增强与不相容的聚乙烯/热塑性淀粉共混物进行了比较,作为其界面强度的指标。结果表明,通过降低熔融合金的温度,相容剂与原始混合物相比,可直接用于界面局部化,并伴随着弹性的增强。此外,共混物及其合金通过毛细管流变仪的抗流动性得到增强,并与众不同。这归因于共混物的正百分比参数,它以不同的吸附密度和对系统流动的构象抵抗力推动相容剂在界面处的定位。换句话说,在分散相/基质界面处形成的准核/壳结构被认为是阻力毛细流动的起源,从而导致粘弹性损失的增加。与控制聚合物的接头粘合能的Gent-Schultz方程类似,多组分共混物在毛细流动过程中的能量损失首次与它们的界面强度相关。有趣的是,所研究的熔体混合物及其相容的合金在毛细管流动中计算出的能量损失与剥落过程中的固态变形损失成比例。

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