首页> 外文期刊>Journal of Applied Polymer Science >Kinetic study of the aqueous free-radical polymerization of 2-acrylamido-2-methyl-1-propanesulfonic acid via an online proton nuclear magnetic resonance technique
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Kinetic study of the aqueous free-radical polymerization of 2-acrylamido-2-methyl-1-propanesulfonic acid via an online proton nuclear magnetic resonance technique

机译:在线质子核磁共振技术研究2-丙烯酰胺基-2-甲基-1-丙烷磺酸的水性自由基聚合

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摘要

The free-radical polymerization of 2-acrylamido-2-methyl-1-propane sulfonic acid (AMPS) in aqueous media and in the presence of potassium persulfate (KPS) as a thermal initiator was studied. The ~1H-NMR method was applied to record the reaction data in online gain. The effects of the monomer and initiator concentrations and also the reaction temperature were studied. The order of reaction with respect to the monomer was much greater than unity (1.94). None of the three theories describing an order of reaction higher than unity could predict the AMPS polymerization mechanism in this study. So, a new mechanism is presented. It is suggested that initiation took place through the formation of a complex between the initiator and monomer, and termination occurred not only by a bimolecular reaction but also by a monomolecular reaction. The order with respect to KPS was 0.49; this was consistent with classical kinetic theory. The determined activation energy at the overall rate of reaction was 92.7 kJ mol ~(-1) K ~(-1).
机译:研究了2-丙烯酰胺基-2-甲基-1-丙烷磺酸(AMPS)在水性介质中以及在过硫酸钾(KPS)作为热引发剂的条件下的自由基聚合。应用〜1H-NMR方法以在线增益记录反应数据。研究了单体和引发剂浓度以及反应温度的影响。相对于单体的反应顺序远大于1(1.94)。三种描述反应顺序高于整体的理论都无法预测AMPS聚合机理。因此,提出了一种新的机制。建议通过引发剂和单体之间的络合物的形成来引发,并且终止不仅通过双分子反应而且通过单分子反应发生。 KPS的顺序为0.49;这与经典动力学理论是一致的。在总反应速率下确定的活化能为92.7 kJ mol〜(-1)K〜(-1)。

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