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Sol-Gel Transition in Di-(2-ethylhexyl) phthalate-Plasticized Poly(vinyl chloride)

机译:邻苯二甲酸二(2-乙基己基)酯增塑的聚氯乙烯中的溶胶-凝胶转变

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摘要

The gelation for di-(2-ethylhexyl) phthalate (DEHP)-plasticized poly(vinyl chloride) was studied by measuring time-resolved small-angle X-ray scattering (SAXS) and a flow of the solutions in test tube. It was found that for the gelation there were three regimes. At Regime I, the solution rapidly changed to a gel, and the SAXS intensity showed a peak and the peak intensity increased, keeping the peak angle constant. Applying the SAXS intensity to the kinetic analysis of the liquid-liquid phase separation, it was revealed that the spinodal decomposition proceeded to develop a periodic length of 29.9 nanometer in size, a hydrogen-bonding-type association in polymer rich phase followed, and then it induced fast gelation rate. At Regime II, the gelation slowly occurred and the SAXS intensity was not observed, suggesting that a homogeneous gel network was formed by a hydrogen-bonding. At regime III, the solution was a homogeneous sol.
机译:通过测量时间分辨小角X射线散射(SAXS)和溶液在试管中的流动,研究了邻苯二甲酸二(2-乙基己基)酯(DEHP)增塑的聚氯乙烯的胶凝作用。已经发现,对于凝胶化,存在三种方案。在条件I下,溶液迅速变成凝胶,SAXS强度显示一个峰,并且峰强度增加,保持峰角恒定。将SAXS强度应用于液-液相分离的动力学分析中,发现旋节线分解进行,形成了29.9纳米的周期长度,随后在聚合物富集相中发生了氢键型缔合,然后它诱导了快速的胶凝速度。在II型体系中,凝胶化缓慢发生,未观察到SAXS强度,表明通过氢键形成了均匀的凝胶网络。在方案III,溶液是均匀的溶胶。

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