Yusuke Okita

Relationship between Length and Degree of Polymerization of TEMPO-Oxidized Cellulose Nanofibrils

The influence of 2,2,6,6-tetrametylpiperidine-1-oxyl (TEMPO)-mediated oxidation of wood cellulose and the mechanical disintegration of oxidized cellulose in water on degree of polymerization determined by viscosity measurement (DP(v)) and the apparent length of the TEMPO-oxidized cellulose nanofibrils (TOCNs) was investigated. DP(v) values decreased from 1270 to 500-600 with increasing addition of NaClO in the TEMPO-mediated oxidation stage. The DP(v) values were further decreased by mechanical fibrillation in water. There is a linear relationship between the average fibril length and DP(v); the lengths of TOCNs can be approximated from DP(v) using 0.5 M copper ethylenediamine as a solvent of both the cellulose and oxidized celluloses in TOCNs. Based on the cellulose fibril models and TEMPO oxidation mechanism, the depolymerization behavior of TOCNs is tentatively explained in terms of distribution of disordered regions in wood cellulose fibrils and formation of C6-aldehydes in cellulose fibrils during TEMPO-mediated oxidation.

TEMPO-mediated oxidation of softwood thermomechanical pulp.

Abstract A softwood thermomechanical pulp (TMP) was suspended in water and oxidized with sodium hypochlorite and catalytic amounts of sodium bromide and 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO) at pH 10. When the NaClO addition levels were 20–26 mmol g-1 of the TMP, the yields of water-insoluble TEMPO-oxidized TMPs fractions were approximately 40%. Sugar composition and other analyses revealed that most of the lignin and hemicellulose components in the TMP were removed as water-soluble fractions by the oxidation. Thus, almost pure TEMPO-oxidized celluloses can also be prepared from TMP, although the addition levels of NaClO are much higher than for the TEMPO-mediated oxidation of pure celluloses. The water-soluble fractions were analyzed by NMR, showing that polyuronic acids formed from glucomannan and cellulose by oxidation were the main compounds. The water-insoluble fractions of TEMPO-oxidized TMPs prepared with NaClO of 20–26 mmol g-1 had carboxylate contents of approximately 1.2 mmol g-1, and had the same cellulose I allomorph and the same crystal widths as in the original TMP. Transparent and highly viscous gels were obtained by disintegration of these TEMPO-oxidized TMPs in water, and the gels consisted of individual nanofibers 4–6 nm in width. Thus, TEMPO-oxidized cellulose nanofibers can also be prepared from TMP.

Different Conformations of Surface Cellulose Molecules in Native Cellulose Microfibrils Revealed by Layer-by-Layer Peeling

Layer-by-layer peeling of surface molecules of native cellulose microfibrils was performed using a repeated sequential process of 2,2,6,6-tetramethylpiperidine-1-oxyl radical-mediated oxidation followed by hot alkali extraction. Both highly crystalline algal and tunicate celluloses and low-crystalline cotton and wood celluloses were investigated. Initially, the C6-hydroxy groups of the outermost surface molecules of each algal cellulose microfibril facing the exterior had the gauche-gauche (gg) conformation, whereas those facing the interior had the gauche-trans (gt) conformation. All the other C6-hydroxy groups of the cellulose molecules inside the microfibrils contributing to crystalline cellulose I had the trans-gauche (tg) conformation. After surface peeling, the originally second-layer molecules from the microfibril surface became the outermost surface molecules, and the original tg conformation changed to gg and gt conformations. The plant cellulose microfibrils likely had disordered structures for both the outermost surface and second-layer molecules, as demonstrated using the same layer-by-layer peeling technique.