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MMA bulk polymerization and its influence on in situ resin viscosity comparing several chemorheological models

机译:比较几种化学流变模型的MMA本体聚合及其对原位树脂粘度的影响

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摘要

Earlier published rheological data of methyl methacrylate (MMA) heated and isothermally polymerized at temperatures between 50 and 80°C have been reanalyzed using three semiempirical models of viscosity advancement including a modified Boltzmann sigmoidal model, a microgel model for cure, and a first-order isothermal kinetic model. These alternative models possessed few fitting parameters and could be used without requiring more experiments to be run. For each dataset as a function of temperature, the analysis resolved time constants associated with both the induction time for polymerization and the rate of viscosity rise, which were inversely related to the polymerization temperature. We found the sigmoidal model the most robust to accommodate nonlinearities in viscosity advancement with radical polymerization of MMA.
机译:使用三个改进的Boltzmann乙状结肠模型,用于固化的微凝胶模型和一阶模型的粘度提高的三个半经验模型,重新分析了早先发布的在50至80°C之间加热和等温聚合的甲基丙烯酸甲酯(MMA)的流变数据。等温动力学模型。这些替代模型几乎没有拟合参数,可以在不进行更多实验的情况下使用。对于随温度变化的每个数据集,分析解析出的时间常数与聚合的诱导时间和粘度上升速率相关,这与聚合温度成反比。我们发现S型模型最能适应MMA自由基聚合在粘度增加中的非线性。

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