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首页> 外文期刊>Journal of Applied Polymer Science >Polymerization of methyl methalcrylate at high temperature with 1-butanethiol as chain transfer agent
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Polymerization of methyl methalcrylate at high temperature with 1-butanethiol as chain transfer agent

机译:以1-丁硫醇为链转移剂在高温下聚合甲基丙烯酸甲酯

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摘要

The free-radical polymerization of methyl methacrylate (MMA) at high temperature (120 to 180°C) has been studied in the presence of di-tertiobutyle peroxide as an initiator and 1-butanethiol as a chain transfer agent. No solvent was used, and the polymerization was run to high monomer conversion. Based on the experimental data collected with a dilatometric reactor, the features of the reaction have been pointed out. Working at high temperature with a chain transfer agent proved efficient to reduce the intensity of the gel effect and control the molecular weight obtained. At a temperature up to 170°C, however, the burn-out of the initiator limits the final conversion, and the increase of the polymerization rate during the gel effect has been more difficult to detect and quantify. An empirical expression of the termination rate constant has been adopted to describe the autoacceleration and predict the conversion versus time curves and the average molecular weight of the polymer obtained. The mathematical model includes two adjustable parameters that have been determined as a function of the temperature and the initial concentration of the chain transfer agent. The agreement between the predicted and experimental data on conversion and molecular weight was good, while the polydispersity index was often underestimated.
机译:在过氧化二叔丁基过氧化物作为引发剂和1-丁烷硫醇作为链转移剂的条件下,研究了甲基丙烯酸甲酯(MMA)在高温(120至180℃)下的自由基聚合。不使用溶剂,并且使聚合进行至高单体转化率。基于用膨胀反应器收集的实验数据,指出了反应的特征。事实证明,在高温下使用链转移剂可以有效降低凝胶效应的强度并控制所获得的分子量。然而,在高达170℃的温度下,引发剂的烧尽限制了最终转化率,并且在凝胶效应期间聚合速率的增加更难以检测和定量。已采用终止速率常数的经验表达式来描述自动加速并预测转化率与时间的关系曲线以及所得聚合物的平均分子量。该数学模型包括两个可调参数,这些参数已根据温度和链转移剂的初始浓度确定。预测和实验数据在转化率和分子量上的一致性很好,而多分散指数常常被低估了。

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