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Rheo-Kinetic Measurement of Thermoplastic Polyurethane Polymerization in a Measurement Kneader

机译:在测量捏合机中热塑性聚氨酯聚合的流变动力学测量

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The rheo-kinetics of thermoplastic polyurethane (TPU) formation was investigated in a measurement kneader at high temperatures.The TPU was made of a polyester polyol,methyl-propane-diol and a 50/50 mixture of 2,4'- and 4,4'-diphenylmethane diisocyanate (MDI).The reaction proceeded according to a second order reaction for which the kinetic constants were determined by size exclusion chromatography (SEC) analysis.The activation energy was found to be equal to 61.3 kJ/mol,and the pre-exponential factor was equal to 2.18e6 mol/kg K.For the temperature range under investigation,the flow activation energy was equal to 42.7 kJ/mol,which is comparable to that of a linear polymer.This indicates that the hard segments are completely dissolved at the temperatures investigated.The initial part of the reaction was much faster than anticipated from the kinetic measurements.Diffusion limitations at higher conversions probably cause this decrease in reaction velocity.At longer reaction times,the molecular weight leveled off because of depolymerization.Therefore,additional experiments are necessary to describe the complete polymerization of thermoplastic polyurethane.
机译:在高温捏合机中研究了热塑性聚氨酯(TPU)的流变动力学.TPU由聚酯多元醇,甲基丙烷二醇和2,4'-和4的50/50混合物制成4'-二苯基甲烷二异氰酸酯(MDI)。反应是通过二阶反应进行的,该反应通过尺寸排阻色谱(SEC)分析确定了动力学常数。发现活化能为61.3 kJ / mol,并且预指数因子等于2.18e6 mol / kg K.在研究的温度范围内,流动活化能等于42.7 kJ / mol,与线性聚合物相当,这表明硬链段是在起始温度下完全溶解。反应的起始部分比动力学测量的结果快得多。较高转化率下的扩散限制可能导致反应速度降低。在较长的反应时间下,分子由于解聚反应使重量失衡。因此,有必要进行额外的实验来描述热塑性聚氨酯的完全聚合。

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