AI Article Synopsis

  • Modifying cellulose nanofibrils (CNFs) with polymer functional groups in a water-based system is challenging due to limited accessible surface interactions.
  • A new scheme involves functionalizing CNFs with a methacrylate group followed by grafting-through polymerization, achieving up to 45 wt% polymer attachment with various types of (meth)acrylates.
  • The effectiveness of this method was validated through techniques like Soxhlet extraction and IR spectroscopy, revealing that high polymer modification levels do not significantly alter the overall morphology of the CNFs.

Article Abstract

Modifying the surface of cellulose nanofibrils (CNFs) produced by mechanical refinement with a variety of polymer functional groups in an entirely water-based system is challenging because only surface hydroxyl groups are accessible. To address this limitation, an entirely water-based, polymer modification scheme is developed. CNFs are functionalized with a reactive methacrylate functional group followed by subsequent grafting-through polymerization. This modification worked with a variety of water-soluble and water-insoluble (meth)acrylates and (meth)acrylamides, grafting up to 45 wt% polymer on to the CNFs. The reaction conditions introducing the methacrylate functional group are adjusted to vary the degree of functionality. Soxhlet extraction of modified samples demonstrates that the reactive methacrylate group is necessary to facilitate polymer grafting. The degree of functionalization of the polymers is studied via quantitative transmission IR spectroscopy and the morphology of the resulting cellulose nanofibrils is studied via a combination of optical, scanning electron, and atomic force microscopy. High levels of polymer modification do not significantly affect the micrometer-scale fibril morphology.

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http://dx.doi.org/10.1002/marc.202000531DOI Listing

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