Mechanically Robust and Recyclable Diels–Alder Networks from a Degradable Cellulose-Based Matrix

IF 6.7 Q1 POLYMER SCIENCE
ACS polymers Au Pub Date : 2026-10-14 Epub Date: 2026-08-21 DOI:10.1021/acspolymersau.6c00135
Yazhou Su, Akihide Sugawara, Hiroshi Uyama
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引用次数: 0

Abstract

Designing sustainable polymer materials that combine mechanical robustness with recyclability remains a significant challenge. Here, we report a cellulose-based Diels–Alder (DA) cross-linked network that integrates structural strength, thermoreversible recyclability, and tunable biodegradability. Cellulose was functionalized with furfurylamine via carbamate formation to introduce furan moieties while minimizing perturbation of its π-electron system, yielding furfuryl carbamate cellulose (FC). By controlling the degree of substitution, FC was designed to enable efficient cross-linking through DA reactions while preserving the inherent biodegradability of cellulose. The DA cross-linked networks were prepared by reacting FC with 1,6-bis(maleimido)hexane (BMI) via solvent casting. The resulting films exhibited tunable mechanical properties with increasing BMI content, with Young’s modulus ranging from 0.4 to 3.1 GPa and maximum stress ranging from 20 to 56 MPa, while maintaining relatively high toughness. Chemical recycling was enabled through thermally induced retro-DA reactions in solution, followed by reformation from solution. Enzymatic degradation tests using cellulase showed that uncross-linked FC degraded rapidly, whereas cross-linked networks exhibited suppressed yet persistent degradation. This demonstrates that degradation behavior can be systematically controlled by cross-linking density. This work provides a molecular design strategy for constructing cellulose-based polymer networks that balance mechanical performance, recyclability, and controlled end-of-life behavior.

机械稳健性和可回收的diols - alder网络从可降解纤维素为基础的矩阵
设计可持续的高分子材料,结合机械坚固性和可回收性仍然是一个重大挑战。在这里,我们报道了一种基于纤维素的Diels-Alder (DA)交联网络,该网络集成了结构强度、热可逆可回收性和可调节的生物降解性。纤维素通过氨基甲酸酯形成糠胺,引入呋喃基团,同时将其π-电子系统的扰动降到最低,得到糠酰氨基甲酸酯纤维素(FC)。通过控制取代度,FC被设计成能够通过DA反应进行有效的交联,同时保持纤维素固有的生物降解性。用溶剂铸造法将FC与1,6-双(马来酰亚胺)己烷(BMI)反应制备DA交联网络。随着BMI含量的增加,薄膜的力学性能可调节,杨氏模量在0.4 ~ 3.1 GPa之间,最大应力在20 ~ 56 MPa之间,同时保持较高的韧性。化学循环是通过在溶液中热诱导的反da反应实现的,然后从溶液中进行重整。使用纤维素酶进行的酶降解测试表明,未交联的FC降解迅速,而交联的FC网络则表现出抑制但持续的降解。这表明降解行为可以通过交联密度系统地控制。这项工作为构建基于纤维素的聚合物网络提供了一种分子设计策略,可以平衡机械性能、可回收性和可控制的寿命终止行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.50
自引率
0.00%
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