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首页> 外文期刊>Journal of Applied Polymer Science >KINETIC STUDY OF THE REACTION BETWEEN HYDROXYL-TERMINATED POLYBUTADIENE AND ISOPHORONE DIISOCYANATE IN BULK BY QUANTITATIVE FTIR SPECTROSCOPY
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KINETIC STUDY OF THE REACTION BETWEEN HYDROXYL-TERMINATED POLYBUTADIENE AND ISOPHORONE DIISOCYANATE IN BULK BY QUANTITATIVE FTIR SPECTROSCOPY

机译:定量红外光谱法研究羟基封端的聚丁二烯与散装异氰酸二异氰酸酯的反应动力学

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摘要

A kinetic study of the reaction between a hydroxyl-terminated polybutadiene (HTPB) and isophorone diisocyanate (IPDI) was carried out in the bulk state by using quantitative Fourier transform infrared(FTIR) spectroscopy. The reaction is shown to obey a second-order rate law, being first order in both the HTPB and IPDI concentrations. The activation parameters obtained from the evaluation of kinetic data are Delta H-double dagger = 41.1 +/- 0.4 kJ mol, Delta S-double dagger = -198 +/- 2 J K-1 mol(-1) and E-a = 43.8 +/- 0.4 kJ mol(-1), which are quite different from the solution values. However, they are in agreement with the results obtained on propellants by torsional braid measurements. The large negative value of the activation entropy is indicative of an associative mechanism, which is in accord with the second-order rate law for the polyurethane formation. (C) 1997 John Wiley & Sons, Inc. [References: 14]
机译:通过使用定量傅里叶变换红外光谱(FTIR),对羟基封端的聚丁二烯(HTPB)和异佛尔酮二异氰酸酯(IPDI)之间的反应进行了动力学研究。已显示该反应服从二级速率定律,即HTPB和IPDI浓度均为一级。从动力学数据评估获得的激活参数为Delta H-双匕首= 41.1 +/- 0.4 kJ mol,Delta S-双匕首= -198 +/- 2 J K-1 mol(-1)和Ea = 43.8 +/- 0.4 kJ mol(-1),与溶液值完全不同。但是,它们与通过扭转编织测量得到的推进剂结果一致。活化熵的大负值表明缔合机理,这与聚氨酯形成的二级速率定律一致。 (C)1997 John Wiley&Sons,Inc. [参考:14]

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