Seychal Guillem, Bron Pauline, Talon Olivier, Aramburu Nora, Raquez Jean-Marie
Laboratory of Polymeric and Composite Materials, Center of Innovation and Research in Materials and Polymers (CIRMAP), University of Mons, Place du Parc 23, 7000 Mons, Belgium.
POLYMAT and Department of Advanced Polymers and Materials: Physics, Chemistry, and Technology, Faculty of Chemistry, University of the Basque Country UPV/EHU, Paseo Manuel de Lardizabal 3, 20018 Donostia-San Sebastián, Spain.
ACS Sustain Chem Eng. 2025 Jul 15;13(29):11238-11253. doi: 10.1021/acssuschemeng.5c01260. eCollection 2025 Jul 28.
Covalent adaptable networks (CANs) and CO-derived polyhydroxyurethanes (PHUs) are often deemed as sustainable alternatives to conventional thermosets, particularly for composites made with epoxy (EP) matrices. However, the sustainability of CAN-based composites has never been assessed, nor has that of thermoset PHUs. Herein, we perform a life cycle assessment of PHUs, synergetic hybrid EP-PHU CANs, and EP in composite applications with either carbon or natural fibers (NFs) in order to address their syntheses, processes, and recycling. We demonstrate that producing cyclic carbonate monomers from epoxy and supercritical CO could be advantageous. PHUs provide potential environmental benefits to epoxy, but they are significantly limited by the energy inputs required for curing. Inversely, synergetic EP-PHU demonstrates noticeable environmental gain compared to EP and PHU-based composites and offers ideal recycling pathways. The chemical recovery of carbon fibers by oxidative depolymerization shows substantial benefits compared with virgin material production. When using NFs, mechanical recycling of CAN-based matrices is more suited due to the impacts of chemical recycling compared to virgin NF production, highlighting that the viability of a strategy strongly depends on raw materials and cannot be generalized easily. Strategies to further enhance the sustainability of composites are also proposed and discussed.
共价自适应网络(CANs)和一氧化碳衍生的聚羟基聚氨酯(PHUs)通常被视为传统热固性材料的可持续替代品,特别是对于由环氧(EP)基体制成的复合材料。然而,基于CAN的复合材料的可持续性从未被评估过,热固性PHUs的可持续性也未被评估过。在此,我们对PHUs、协同混合的EP-PHU CANs以及在与碳纤维或天然纤维(NFs)复合应用中的EP进行生命周期评估,以探讨它们的合成、加工和回收利用。我们证明,由环氧和超临界二氧化碳制备环状碳酸酯单体可能具有优势。PHUs对环氧具有潜在的环境效益,但它们受到固化所需能量输入的显著限制。相反,与基于EP和PHU的复合材料相比,协同的EP-PHU显示出显著的环境效益,并提供了理想的回收途径。通过氧化解聚对碳纤维进行化学回收与原始材料生产相比显示出显著的优势。当使用NFs时,由于化学回收与原始NF生产相比的影响,基于CAN的基体的机械回收更合适,这突出表明一种策略的可行性强烈依赖于原材料,不能轻易一概而论。还提出并讨论了进一步提高复合材料可持续性的策略。