Single-step method for the isolation and surface functionalization of cellulosic nanowhiskers.

Biomacromolecules

PolyNew, Inc., Golden, Colorado 80401, USA.

Published: February 2009

AI Article Synopsis

  • The study presents a single-step method for surface modification of cellulosic nanowhiskers (CNW) by simultaneously hydrolyzing amorphous cellulose and esterifying hydroxyl groups using an acid mixture, which simplifies traditional multi-step processes.
  • The resulting CNW maintain similar sizes to those obtained through hydrochloric acid hydrolysis alone, but demonstrate narrower polydispersity indices, indicating improved individualization due to surface modifications.
  • Additionally, over half of the surface hydroxyl groups are substituted, enhancing the CNW's hydrophobic properties, making them more compatible with hydrophobic polymers for reinforcement purposes.

Article Abstract

Surface modification of cellulosic nanowhiskers (CNW) is of great interest, especially to facilitate their use as polymer reinforcements. Generally, alteration of the surface chemistry is performed using multiple reaction steps. In contrast, this study demonstrates that the needed hydrolysis of amorphous cellulose chains can be performed simultaneously with the esterification of accessible hydroxyl groups to produce surface functionalized CNW in a single step. The reaction is carried out in an acid mixture composed of hydrochloric and an organic acid (acetic and butyric are both demonstrated). Resulting CNW are of similar dimensions compared to those obtained by hydrochloric acid hydrolysis alone; sizes are verified by multiangle laser-light scattering and transmission electron microscopy. However, narrower diameter polydispersity indices indicate that surface groups aid the individualization of the nanowhiskers (Px = 2.5 and 2.1 for acetic and butyric acid, Px = 3.0 for hydrochloric acid). More than half of the hydroxyl groups located on the CNW surface are substituted under the employed reaction conditions as determined by quantitative Fourier-transform infrared-spectroscopy. The resulting surface modified CNW are dispersible in ethyl acetate and toluene indicating increased hydrophobicity and thus are presumably more compatible with hydrophobic polymers when used as a reinforcing phase.

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Source
http://dx.doi.org/10.1021/bm8011117DOI Listing

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