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Urethane-forming reaction kinetics of natural oil polyols versus petroleum-based polyether polyol

机译:天然油多元醇与石油基聚醚多元醇形成氨基甲酸酯的反应动力学

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摘要

Urethane-forming reaction kinetics of isocyanate with natural oil polyols (NOPs) with pendant reactive hydroxyls was compared to that of the petroleum based polyether polyol with terminal hydroxyls. The non-catalyzed urethane forming kinetic study in toluene shows lower activation energy for pendant hydroxyls of the synthetic and naturally occurring NOP compared to terminal hydroxyls of the polyether polyol. At low temperatures in the non-catalyzed reaction in toluene, the NOPs showed higher reactivity with isocyanate, which was correlated with faster gel time in bulk polymerization. However, in toluene, the reactivity of polyether polyol increases at a faster rate with temperature, and in toluene and bulk reactions the polyether polyol shows higher response to dibutyltin dilaurate catalyst. The results indicate that relative reactivities of NOPs compared to polyether polyols are not necessarily lower in urethane forming reactions, and in fact under certain conditions can be higher, which needs to be taken into consideration during the incorporation of NOPs in polyurethanes.
机译:将异氰酸酯与具有侧链反应性羟基的天然油多元醇(NOP)形成氨基甲酸酯的反应动力学与具有末端羟基的石油基聚醚多元醇的动力学进行了比较。在甲苯中的非催化氨基甲酸酯形成动力学研究表明,与聚醚多元醇的末端羟基相比,合成的和天然存在的NOP的侧链羟基的活化能更低。在低温下,在甲苯中的非催化反应中,NOP与异氰酸酯的反应性更高,这与本体聚合中更快的凝胶时间有关。然而,在甲苯中,聚醚多元醇的反应性随温度以更快的速率增加,并且在甲苯和本体反应中,聚醚多元醇显示出对二月桂酸二丁基锡催化剂的更高的响应。结果表明,在聚氨基甲酸酯形成反应中,与聚醚多元醇相比,NOP的相对反应性不一定较低,实际上,在某些条件下可以更高,这在将NOP引入聚氨酯中时需要加以考虑。

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