Huibin Chang

A comparative guide to controlled hydrophobization of cellulose nanocrystals via surface esterification

Surface esterification methods of cellulose nanocrystals (CNC) using acid anhydrides, acid chlorides, acid catalyzed carboxylic acids, and 1′1-carbonyldiimidazole (CDI) activated carboxylic acids were evaluated with acetyl-, hexanoyl-, dodecanoyl-, oleoyl-, and methacryloyl-functionalization. Their grafting efficiency was investigated using Fourier-transform infrared spectroscopy and 13C solid state NMR spectroscopy. Acid anhydride and CDI were found to be the most applicable reagents to graft short and long chain aliphatic carbons, respectively. The preservation of structural morphology and crystallinity of grafted CNCs were confirmed using transmission electron microscopy and X-ray diffraction. The hydrophobicity of grafted CNCs was evaluated by dispersing them in organic solvents with different Hansen’s solubility parameters. The dispersibility of grafted CNCs in organic solvents was improved by using never-dried CNCs as source materials and keep CNCs wet in their washing solvents after grafting, thus increasing the solvency range to disperse CNCs.

Individually Dispersed Wood-Based Cellulose Nanocrystals

Good dispersion of cellulose nanocrystals (CNCs) in the polymer matrix is one of the key factors to obtaining good properties in the resulting nanocomposites. However, the preparation of individually dispersed CNCs in solvents or in polymer matrices has been a challenge. In this study, individually dispersed wood-based CNCs have been successfully prepared in solvents, including dimethylformamide (DMF), H2O, and a mixture of H2O/DMF, by sonication of moisture-containing CNCs. The CNCs dispersions were characterized by dynamic light scattering (DLS). It is found that CNCs containing above about 3.8 wt % moisture is critical for achieving individually dispersed CNC in solvents. Hydrodynamic radius (Rh) of CNCs is smaller in H2O/DMF co-solvent mixture than that in pure DMF or in pure H2O under same sonication treatment conditions. Experimental results have been corroborated using molecular simulation study.

Post-sulfonation of cellulose nanofibrils with a one-step reaction to improve dispersibility

Cellulose nanofibrils (CNF) were sulfonated and the dispersion quality was compared to unfunctionalized and 2,2,6,6-tetramethylpiperdine-1-oxyl radical (TEMPO) post-oxidation treatment of existing CNF (mechanically fibrillated pulp). A post-sulfonation treatment on existing CNF in chlorosulfonic acid and dimethylformamide (DMF) resulted in sulfonated CNF that retained a fibril-like morphology. There was a small decrease in the cellulose crystallinity index for the sulfonated CNF, but this was much lower than the reported regioselective oxidative bisulfite pretreatment method used to make sulfonated CNF. The current approach was extremely quick, and 5min of reaction time was sufficient to result in significant improvements in dispersibility compared to unfunctionalized CNF. The sulfonated CNF and TEMPO oxidized CNF had better dispersibility compared to the unfunctionalized CNF when dispersed in DMF and water, and in many cases the sulfonated CNF had better dispersibility than the TEMPO CNF. It was found that when CNF was dispersed in DMF the TEMPO CNF formed carboxyl dimethylammonium groups, while the sulfonated CNF formed formate groups.