{"title":"Mechanically Robust and Recyclable Diels–Alder Networks from a Degradable Cellulose-Based Matrix","authors":"Yazhou Su, Akihide Sugawara, Hiroshi Uyama","doi":"10.1021/acspolymersau.6c00135","DOIUrl":null,"url":null,"abstract":"<p>Designing sustainable\r\npolymer materials that combine\r\nmechanical\r\nrobustness with recyclability remains a significant challenge. Here,\r\nwe report a cellulose-based Diels–Alder (DA) cross-linked network\r\nthat integrates structural strength, thermoreversible recyclability,\r\nand tunable biodegradability. Cellulose was functionalized with furfurylamine\r\nvia carbamate formation to introduce furan moieties while minimizing\r\nperturbation of its π-electron system, yielding furfuryl carbamate\r\ncellulose (FC). By controlling the degree of substitution, FC was\r\ndesigned to enable efficient cross-linking through DA reactions while\r\npreserving the inherent biodegradability of cellulose. The DA cross-linked\r\nnetworks were prepared by reacting FC with 1,6-bis(maleimido)hexane\r\n(BMI) via solvent casting. The resulting films exhibited tunable mechanical\r\nproperties with increasing BMI content, with Young’s modulus\r\nranging from 0.4 to 3.1 GPa and maximum stress ranging from 20 to\r\n56 MPa, while maintaining relatively high toughness. Chemical recycling\r\nwas enabled through thermally induced retro-DA reactions in solution,\r\nfollowed by reformation from solution. Enzymatic degradation tests\r\nusing cellulase showed that uncross-linked FC degraded rapidly, whereas\r\ncross-linked networks exhibited suppressed yet persistent degradation.\r\nThis demonstrates that degradation behavior can be systematically\r\ncontrolled by cross-linking density. This work provides a molecular\r\ndesign strategy for constructing cellulose-based polymer networks\r\nthat balance mechanical performance, recyclability, and controlled\r\nend-of-life behavior.</p>","PeriodicalId":72049,"journal":{"name":"ACS polymers Au","volume":"6 5","pages":"1455–1467"},"PeriodicalIF":6.7000,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS polymers Au","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acspolymersau.6c00135","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/21 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
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.