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用于可解构、可回收聚氨酯热固性材料的可裂解添加剂。

Cleavable Additives for Deconstructable, Recyclable Polyurethane Thermosets.

作者信息

Ko Kwangwook, Lundberg David J, Lensch Valerie L, AlFaraj Yasmeen S, Husted Keith E L, Brutman Jacob P, Alsbaiee Alaaeddin, Hamilton Patrick N, Nguyen Suong T, Johnson Jeremiah A

机构信息

Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.

Department of Chemical Engineering, Massachusetts Institute of Technology, 25 Ames Street, Cambridge, Massachusetts 02139, United States.

出版信息

ACS Cent Sci. 2025 Jul 23;11(8):1355-1363. doi: 10.1021/acscentsci.5c00689. eCollection 2025 Aug 27.

Abstract

Polyurethane (PU) thermosets, particularly those derived from aliphatic components, are challenging to chemically deconstruct due to their permanent cross-linking. Current approaches to impart deconstructability typically rely on complete substitution of network precursors with cleavable analogs, limiting practicality. Cleavable additives (CAs) offer a potentially simple and cost-effective alternative, yet their application has been largely confined to chain-growth networks and remains unexplored in end-linked systems such as PUs. Here, we present a generalizable reverse gel-point theory that predicts the minimum CA loading required for deconstruction of end-linked networks. We validate this framework experimentally through the incorporation of two classes of silyl ether-based CAsbifunctional cleavable strands (BCSs) and trifunctional cleavable junctions (TCJs)into PU thermosets. Both additives enable selective PU dissolution at low loadings (5-12 wt %), with TCJs demonstrating enhanced efficiency. The combined use of BCSs and TCJs also allows fine-tuning of material properties. Furthermore, we show that polyol fragments generated from the deconstruction of TCJ-containing PUs can be chemically repolymerized to regenerate PU materials without loss of mechanical performance over multiple cycles. This work establishes CAs as a viable strategy for advancing PU circularity and offers a foundational framework for their broader application in end-linked polymer networks.

摘要

聚氨酯(PU)热固性材料,尤其是那些由脂肪族成分衍生而来的材料,由于其永久性交联,在化学解构方面具有挑战性。目前赋予可解构性的方法通常依赖于用可裂解类似物完全替代网络前体,这限制了实用性。可裂解添加剂(CAs)提供了一种潜在的简单且经济高效的替代方案,但其应用主要局限于链增长网络,在诸如PU等端交联体系中仍未得到探索。在此,我们提出了一种可推广的逆凝胶点理论,该理论预测了端交联网络解构所需的最低CA负载量。我们通过将两类基于硅醚的CAs——双功能可裂解链(BCSs)和三功能可裂解连接点(TCJs)——引入PU热固性材料中,对这一框架进行了实验验证。两种添加剂都能在低负载量(5 - 12 wt%)下实现PU的选择性溶解,其中TCJs表现出更高的效率。BCSs和TCJs的联合使用还能对材料性能进行微调。此外,我们表明,由含TCJ的PU解构产生的多元醇片段可以进行化学再聚合,以再生PU材料,且在多个循环中不会损失机械性能。这项工作将CAs确立为推进PU循环利用的可行策略,并为其在端交联聚合物网络中的更广泛应用提供了基础框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2379/12395304/a61ddcf891a2/oc5c00689_0001.jpg

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