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Dynamical behavior of microgels of interpenetrated polymer networks

机译:互穿聚合物网络微凝胶的动力学行为

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摘要

Microgel suspensions of an interpenetrated Polymer Network (IPN) of PNIPAM and PAAc in D2O have been investigated through dynamic light scattering as a function of temperature, pH and concentration across the Volume Phase Transition (VPT). The dynamics of the system is slowed down under H/D isotopic substitution due to different balance states between polymer/polymer and polymer/solvent interactions suggesting the crucial role played by H-bonding. The swelling behavior, reduced with respect to PNIPAM and water, has been described by the Flory–Rehner theory, tested for PNIPAM microgel and successfully expanded to higher order for IPN microgels. Moreover the concentration dependence of the relaxation time at neutral pH has highlighted two different routes to approach the glass transition: Arrhenius and super-Arrhenius (Vogel Fulcher Tammann) respectively below and above the VPT and a fragility plot has been derived. Fragility can be tuned by changing temperature: across the VPT particles undergo a transition from soft-strong to stiff-fragile.
机译:PNIPAM和PAAc在D2O中互穿的聚合物网络(IPN)的微凝胶悬浮液已通过动态光散射作为温度,pH和整个体积相变(VPT)浓度的函数进行了研究。在H / D同位素取代下,由于聚合物/聚合物与聚合物/溶剂相互作用之间的平衡状态不同,系统的动力学变慢,这表明氢键起着至关重要的作用。相对于PNIPAM和水而言,这种溶胀行为有所降低,已由Flory-Rehner理论进行了描述,已针对PNIPAM微凝胶进行了测试,并成功地将其扩展至IPN微凝胶。此外,在中性pH值下弛豫时间对浓度的依赖性突出了接近玻璃化转变的两种不同途径:分别在VPT之上和之上的Arrhenius和super-Arrhenius(Vogel Fulcher Tammann),并得出了脆性图。可以通过改变温度来调节易碎性:整个VPT颗粒都经历了从软性到硬性的转变。

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