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环氧热固性材料的溶解 温和醇解:机理与动力学研究

Dissolution of epoxy thermosets mild alcoholysis: the mechanism and kinetics study.

作者信息

Kuang Xiao, Shi Qian, Zhou Yunying, Zhao Zeang, Wang Tiejun, Qi H Jerry

机构信息

The George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology Atlanta GA 30332 USA

Renewable Bioproduct Institute, Georgia Institute of Technology Atlanta GA 30332 USA.

出版信息

RSC Adv. 2018 Jan 4;8(3):1493-1502. doi: 10.1039/c7ra12787a. eCollection 2018 Jan 2.

Abstract

Thermoset dissolution based on degradable bond or exchange reaction has been recently utilized to achieve thermosetting polymer dissolution and recycling. In this paper, an industrial grade epoxy thermoset was utilized as a model system to demonstrate the thermoset dissolution solvent assisted transesterification (or alcoholysis) with high efficiency under mild conditions. The anhydride-cured epoxy thermoset was depolymerized by selective ester bond cleavage in 1,5,7-triazabicyclo[4,4,0]dec-5-ene (TBD)-alcohol solution below 180 °C at ordinary pressure in less than two hours. The epoxy dissolution proceeded in a surface erosion mode transesterification that was coupled with catalyst-alcohol diffusion. Based on this observation, a surface layer model containing three layers, namely the gel layer, solid swollen layer and pure polymer layer was used to analyze the thermoset dissolution kinetics. The epoxy dissolution kinetics was derived from the surface layer model, which could be used to predict the dissolution rate during the diffusion-rate-controlled dissolution process well. The results show that alcohols with larger diffusivity and better solubility lead to a higher alcohol/catalyst concentration in the gel layer and promote faster erosion and dissolution of epoxy. This is the first work to show that it is possible to depolymerize industrial epoxy using the principle of dynamic bonds with fast dissolution rate at mild temperature under ordinary pressure.

摘要

基于可降解键或交换反应的热固性塑料溶解方法最近已被用于实现热固性聚合物的溶解和回收利用。在本文中,以一种工业级环氧热固性塑料作为模型体系,来展示在温和条件下通过溶剂辅助酯交换反应(或醇解反应)实现热固性塑料的高效溶解。在常压下,酸酐固化的环氧热固性塑料在180℃以下的1,5,7-三氮杂双环[4,4,0]癸-5-烯(TBD)-醇溶液中,通过选择性酯键断裂在不到两小时内发生解聚。环氧溶解以表面侵蚀模式进行,即酯交换反应与催化剂-醇扩散相耦合。基于这一观察结果,使用包含凝胶层、固体溶胀层和纯聚合物层的三层表面层模型来分析热固性塑料的溶解动力学。环氧溶解动力学由表面层模型推导得出,该模型可很好地用于预测扩散速率控制的溶解过程中的溶解速率。结果表明,具有较大扩散率和较好溶解性的醇会导致凝胶层中醇/催化剂浓度更高,并促进环氧的更快侵蚀和溶解。这是首次表明利用动态键原理在常压温和温度下以快速溶解速率使工业环氧解聚是可行的工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27ad/9077052/beec94089b47/c7ra12787a-s1.jpg

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