Steffan K. Kristensen, Alexander Ahrens, Bjarke S. Donslund and Troels Skrydstrup,
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In this Perspective, depolymerization strategies for thermoset polymers are discussed with an emphasis on recent advancements within our group on recovering polymer building blocks from polyurethane (PU) and epoxy-based materials. While these two represent the largest thermoset polymer groups with respect to the production volumes, the recycling landscapes for these classes of materials are vastly different. For PU, increased collaboration between academia and industry has resulted in major advancements within solvolysis, acidolysis, aminolysis, and split-phase glycolysis for polyol recovery, where several processes are being evaluated for further scaling studies. For epoxy-based materials, the molecular skeleton has no obvious target for chemical scission. Nevertheless, we have recently demonstrated the possibility of the disassembly of the epoxy polymer in fiber-reinforced composites for bisphenol A (BPA) recovery through catalytic C–O bond cleavage. 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引用次数: 0
摘要
目前,大量的有机聚合物材料在使用结束后被送往垃圾填埋场或焚化炉焚烧,为了防止这种不可持续的废物处理方式,人们已经投入了大量的研究工作,为商用热固性聚合物的回收利用开发适当的解决方案。这种交联聚合物在固化后无法重新熔化,这意味着用于热塑性材料的机械回收工艺无法转化为热固性聚合物的回收工艺。此外,由于使用了不同的单体,这些材料的结构也各不相同,而且这些聚合物还可用于制造纤维增强聚合物复合材料,因此这些材料的回收利用工作极具挑战性。本视角将讨论热固性聚合物的解聚策略,重点介绍我们小组最近在从聚氨酯(PU)和环氧基材料中回收聚合物结构单元方面取得的进展。虽然就产量而言,这两种材料是最大的热固性聚合物,但这两类材料的回收情况却大相径庭。就聚氨酯而言,学术界和工业界加强合作,在多元醇回收的溶解、酸解、氨解和分相乙二醇分解方面取得了重大进展,目前正在对几种工艺进行评估,以进一步扩大研究范围。对于环氧基材料,分子骨架没有明显的化学裂解目标。不过,我们最近已经证明,通过催化 C-O 键裂解,可以分解纤维增强复合材料中的环氧聚合物,从而回收双酚 A(BPA)。此外,我们和其他人开发的碱促进裂解技术也显示出从环氧聚合物中回收双酚 A 的巨大潜力。要评估此类单体回收策略在工业规模的环氧材料中的适用性,仍需进一步努力。尽管如此,本文介绍的化学方法所展示的最新进展表明,热固性聚合物回收的未来可能包括以高效节能的方式进行单体回收以实现闭环回收的工艺。
Perspective on the Development of Monomer Recovery Technologies from Plastics Designed to Last
In order to prevent the current unsustainable waste handling of the enormous volumes of end-of-use organic polymer material sent to landfilling or incineration, extensive research efforts have been devoted toward the development of appropriate solutions for the recycling of commercial thermoset polymers. The inability of such cross-linked polymers to be remelted once cured implies that mechanical recycling processes used for thermoplastic materials do not translate to the recycling of thermoset polymers. Moreover, the structural diversity within the materials from the use of different monomers as well as the use of such polymers for the fabrication of fiber-reinforced polymer composites make recycling of these materials highly challenging. In this Perspective, depolymerization strategies for thermoset polymers are discussed with an emphasis on recent advancements within our group on recovering polymer building blocks from polyurethane (PU) and epoxy-based materials. While these two represent the largest thermoset polymer groups with respect to the production volumes, the recycling landscapes for these classes of materials are vastly different. For PU, increased collaboration between academia and industry has resulted in major advancements within solvolysis, acidolysis, aminolysis, and split-phase glycolysis for polyol recovery, where several processes are being evaluated for further scaling studies. For epoxy-based materials, the molecular skeleton has no obvious target for chemical scission. Nevertheless, we have recently demonstrated the possibility of the disassembly of the epoxy polymer in fiber-reinforced composites for bisphenol A (BPA) recovery through catalytic C–O bond cleavage. Furthermore, a base promoted cleavage developed by us and others shows tremendous potential for the recovery of BPA from epoxy polymers. Further efforts are still required for evaluating the suitability of such monomer recovery strategies for epoxy materials at an industrial scale. Nonetheless, recent advancements as illustrated with the presented chemistry suggest that the future of thermoset polymer recycling could include processes that emphasize monomer recovery in an energy efficient manner for closed-loop recycling.
期刊介绍:
ACS Organic & Inorganic Au is an open access journal that publishes original experimental and theoretical/computational studies on organic organometallic inorganic crystal growth and engineering and organic process chemistry. Short letters comprehensive articles reviews and perspectives are welcome on topics that include:Organic chemistry Organometallic chemistry Inorganic Chemistry and Organic Process Chemistry.