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Urethane-Forming Reaction Kinetics of Natural Oil Polyols Versus Polyether Polyol

机译:天然油多元醇与聚醚多元醇形成氨基甲酸酯的反应动力学

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Urethane-forming reaction kinetics of isocyanate with natural oil polyols (NOPs) were compared to that of the petroleum based polyether polyol. NOPs in this study included a polyol synthesized from palm olein and castor oil, both containing pendant hydroxyls. Polyether polyol is a triol with ethylene oxide end groups, and therefore it contained a mixture of primary and secondary terminal hydroxyl groups. The non-catalyzed urethane forming kinetics study in toluene shows lower activation energy for both the synthesized NOP and naturally occurring castor oil compared to terminal hydroxyls of the polyether polyol. The kinetic results show higher reactivity of NOP with isocyanate in the non-catalyzed reaction in toluene at low temperatures, which was correlated with faster gel time in bulk polymerization. However, in toluene the reactivity of polyether polyol with isocyanate increases at a faster rate with temperature, and the polyether polyol showed higher response to organotin catalyst. The results indicate that the relative urethane-forming reactivities of NOPs compared to polyether polyols are not necessarily lower, and in fact under certain conditions can be higher, which needs to be taken into consideration during the incorporation of NOPs in polyurethane formulations.
机译:比较了异氰酸酯与天然油多元醇(NOP)形成氨基甲酸酯的反应动力学与石油基聚醚多元醇的动力学。这项研究中的NOP包括由棕榈油精和蓖麻油合成的多元醇,两者都含有侧链羟基。聚醚多元醇是具有环氧乙烷端基的三醇,因此它包含伯羟基和仲羟基的混合物。在甲苯中进行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NOP和天然存在的蓖麻油的活化能均较低。动力学结果表明,在低温下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,聚醚多元醇与异氰酸酯的反应性随温度以更快的速率增加,并且聚醚多元醇显示出对有机锡催化剂的更高响应。结果表明,与聚醚多元醇相比,NOP的相对形成氨基甲酸酯的反应性不一定较低,实际上在某些条件下可以更高,这在将NOP掺入聚氨酯配方时需要考虑。

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