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Cellulose nanofibrils (CNFs) produced through processes involving oxidation (e.g. TEMPO oxidation) present reactive groups that allow for straightforward modification in aqueous suspension. CNFs fabricated through mechanical refinement alone can be challenging to modify for subsequent reactions due to only having hydroxyl groups present on the surface. To address these issues, CNFs with only hydroxyl groups present were functionalized with norbornene groups in their native aqueous suspension to achieve up to 10% functionalization per anhydroglucose unit. Since quantification of surface functionalizationof CNFs is challenging through most methods, a degradation and subsequent nuclear magnetic resonance analysis method was developed to quantify norbornene functionalization. The norbornene functionalized CNFs (nCNFs) were crosslinked through UV and thermally initiated thiol-eneclick reactions to create robust CNF hydrogels. By varying the reaction conditions, hydrogels made from nCNFs and a dithiol cross-linker could achieve compression modulus values up to 25 kPa. The materials were stable in aqueous suspensions and the cross-linked hydrogels still exhibited shear thinning behavior with high recovery, which demonstrated that even though effective cross-links were formed, a complete network was not. Through this study, thiolnorbornene crosslinking of CNFs could create robust hydrogels and improve aqueous stability that could have applications in sustainable materials and biomaterials.
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Biodegradation of Functionalized Nanocellulose
Nanocellulose has attracted widespread interest for applications in materials science and biomedical engineering due to its natural abundance, desirable physicochemical properties, and high intrinsic mineralizability (i.e., complete biodegradability). A common strategy to increase dispersibility in polymer matrices is to modify the hydroxyl groups on nanocellulose through covalent functionalization, but such modification strategies may affect the desirable biodegradation properties exhibited by pristine nanocellulose. In this study, cellulose nanofibrils (CNFs) functionalized with a range of esters, carboxylic acids, or ethers exhibited decreased rates and extents of mineralization by anaerobic and aerobic microbial communities compared to unmodified CNFs, with etherified CNFs exhibiting the highest level of recalcitrance. The decreased biodegradability of functionalized CNFs depended primarily on the degree of substitution at the surface of the material rather than within the bulk. This dependence on surface chemistry was attributed not only to the large surface area-to-volume ratio of nanocellulose but also to the prerequisite surface interaction by microorganisms necessary to achieve biodegradation. Results from this study highlight the need to quantify the type and coverage of surface substituents in order to anticipate their effects on the environmental persistence of functionalized nanocellulose.
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- Award ID(s):
- 2001611
- PAR ID:
- 10279401
- Date Published:
- Journal Name:
- Environmental Science & Technology
- ISSN:
- 0013-936X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1021/acs.est.0c07253
