Lei Zepeng, Wang Zirui, Jiang Huan, Cahn Jackson R, Chen Hongxuan, Huang Shaofeng, Jin Yinghua, Wang Xiaohui, Yu Kai, Zhang Wei
Department of Chemistry, University of Colorado Boulder, Boulder, CO, 80309, USA.
Department of Mechanical Engineering, University of Colorado Denver, Denver, CO, 80217, USA.
Adv Mater. 2024 Nov;36(45):e2407854. doi: 10.1002/adma.202407854. Epub 2024 Sep 3.
Thermosets are well known for their advantages such as high stability and chemical resistance. However, developing sustainable thermosets with degradability and recyclability faces several principal challenges, including reconciling the desired characteristics during service with the recycling and reprocessing properties required at the end of life, establishing efficient methods for large-scale synthesis, and aligning with current manufacturing process. Here a general strategy is presented for the on-demand degradation and recycling of thermosets under mild conditions utilizing dynamic precursors with dual-factor-controlled reversibility. Specifically, dynamic triazine crosslinkers are introduced through dynamic nucleophilic aromatic substitution (SAr) into the precursor polyols used in polyurethane (PU) synthesis. Upon removal of the catalyst and alcohol, the reversibility of SAr is deactivated, allowing for the use of standard PU polymerization techniques such as injection molding, casting, and foaming. The resulting cyanurate-crosslinked PUs maintain high stability and diverse mechanical properties of traditional crosslinked PUs, yet offer the advantage of easy on-demand depolymerization for recycling by activating the reversibility of SAr under specific but mild conditions-a combination of base, alcohol, and mild heat. It is envisioned that this approach, involving the pre-installation of dual-factor-controlled dynamic crosslinkers, can be broadly applied to current thermosetting plastic manufacturing processes, introducing enhanced sustainability.
热固性材料因其诸如高稳定性和耐化学性等优点而广为人知。然而,开发具有可降解性和可回收性的可持续热固性材料面临着几个主要挑战,包括在使用过程中协调所需特性与使用寿命结束时所需的回收和再加工性能,建立大规模合成的有效方法,以及与当前制造工艺相匹配。本文提出了一种通用策略,利用具有双因素控制可逆性的动态前体,在温和条件下对热固性材料进行按需降解和回收。具体而言,通过动态亲核芳香取代反应(SAr)将动态三嗪交联剂引入聚氨酯(PU)合成中使用的前体多元醇中。去除催化剂和醇后,SAr的可逆性失活,从而可以使用标准的PU聚合技术,如注塑、浇铸和发泡。所得的氰尿酸酯交联PU保持了传统交联PU的高稳定性和多样的机械性能,但具有在特定但温和的条件(碱、醇和适度加热的组合)下激活SAr的可逆性以实现易于按需解聚进行回收的优点。据设想,这种涉及预安装双因素控制动态交联剂的方法可广泛应用于当前的热固性塑料制造工艺,从而提高可持续性。