Elizalde Fermin, Pertici Vincent, Aguirresarobe Robert, Ximenis Marta, Vozzolo Giulia, Lezama Luis, Ruipérez Fernando, Gigmes Didier, Sardon Haritz
POLYMAT, University of the Basque Country UPV/EHU, Joxe Mari Korta Center, Avda. Tolosa 72, 20018 Donostia-San Sebastian, Spain.
Aix Marseille Univ, CNRS, ICR UMR 7273, 13397 Marseille, France.
ACS Appl Polym Mater. 2024 Jun 7;6(12):7057-7065. doi: 10.1021/acsapm.4c00840. eCollection 2024 Jun 28.
Recent studies have shown that the largest employed thermoset family, polyurethanes (PUs), has great potential to be reprocessed due to the dynamic behavior of carbamate linkage. However, it requires high temperatures, especially in the case of aliphatic PUs, which causes side reactions besides the desired exchange reaction. To facilitate the reprocessing of aliphatic PUs, in this work, we have explored the dynamic potential of alkoxyamine bonds in PU networks to facilitate the reprocessing under mild conditions considering their fast recombination ability. Taking advantage of the structural effect of the nitroxide and alkyl radicals on the dissociation energy, two different alkoxyamine-based diols have been designed and synthesized to generate PU networks. Our study shows that replacing 50 mol % of a nondynamic diol chain extender with these dynamic blocks boosts the relaxation times of the networks, enabling reprocessing at temperatures as low as 80 °C.
最近的研究表明,最大的热固性材料家族——聚氨酯(PU),由于其氨基甲酸酯键的动态特性,具有很大的再加工潜力。然而,这需要高温,尤其是对于脂肪族聚氨酯而言,除了所需的交换反应外,高温还会引发副反应。为了促进脂肪族聚氨酯的再加工,在这项工作中,我们考虑到烷氧基胺键快速重组的能力,探索了聚氨酯网络中烷氧基胺键在温和条件下促进再加工的动态潜力。利用氮氧化物和烷基自由基对解离能的结构效应,设计并合成了两种不同的基于烷氧基胺的二醇,以生成聚氨酯网络。我们的研究表明,用这些动态嵌段取代50摩尔%的非动态二醇扩链剂,可提高网络的弛豫时间,从而能够在低至80°C的温度下进行再加工。