右旋糖酐分子量对功能聚合物共混体系动态力学性能的影响

S. Kavlak
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引用次数: 1

摘要

天然/合成聚合物的共混是获得具有理想性能(如热、机械和动态机械性能)的新材料的最实用的方法之一。动态力学分析(DMA)是研究这些聚合物共混体系的力学/粘弹性、热转变和相容性的有力方法。本研究采用溶剂铸造法制备了具有生物相容性的T10和T40葡聚糖(DEX)与聚甲基丙烯酸酰胺(PMAM)共混体系。研究了DEX/PMAM共混物在一定温度范围内的动态力学加载频率下的动态力学性能变化,包括存储模量(SM)、损耗模量(LM)和tan δ。从DMA测量结果中观察到热转变和弛豫。一般来说,在二元共混体系中可以观察到单玻璃化转变温度。研究发现,共混体系的动态力学性能和曲线的温度依赖表现出典型的行为,并且强烈依赖于分子量、氢键引起的分子内和分子间相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Molecular Weight of Dextran on Dynamic Mechanical Properties in Functional Polymer Blend Systems
Blending of natural/synthetic polymers is one of the most practical way to obtain a new material with desired properties such as thermal, mechanical and dynamic mechanical properties. Dynamic mechanical analysis (DMA) is a strong method to investigate the mechanical/viscoelastic properties, thermal transitions and compatibility in these polymer blend systems. In this study, biocompatible T10 and T40 dextran (DEX) and polymethacrylamide (PMAM) blend systems were prepared by solvent casting method. Variations of dynamic mechanical properties including storage modulus (SM), loss modulus (LM) and tan δ of the DEX/PMAM blends were investigated for all samples at a specific fixed frequency of dynamic mechanical loading in a certain temperature range. Thermal transitions and -relaxations were observed from results of DMA measurements. In general, a single glass transition temperature was observed in binary blend systems. It was found that temperature dependence of dynamic mechanical properties and curves exhibit typical behaviors and strongly depended on the molecular weight, intra- and intermolecular interactions due to the hydrogen bonding in these blend systems.
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