Homogeneous Suspensions of Individualized Microfibrils from TEMPO-Catalyzed Oxidation of Native Cellulose

Tsuguyuki Saito, Yoshiharu Nishiyama, Jean‐Luc Putaux, Michel R. Vignon, Akira Isogai

Biomacromolecules · 2006 · 1.8K citations · 18 references

Concepts

TL;DR

The authors oxidized never‑dried native celluloses with TEMPO and then homogenized them mechanically to produce individual microfibrils. Oxidation with 3.6 mmol NaClO g⁻¹ followed by homogenization yielded transparent, highly viscous suspensions of long microfibrils (3–5 nm wide) from sulfite wood pulp and cotton; tunicin and bacterial cellulose required sonication, and a bulk oxidation degree of ~0.2 mol AGU⁻¹ was needed for smooth disintegration, with the limiting degree decreasing in the order sulfite wood pulp > cotton > bacterial cellulose > tunicin.

Abstract

Never-dried native celluloses (bleached sulfite wood pulp, cotton, tunicin, and bacterial cellulose) were disintegrated into individual microfibrils after oxidation mediated by the 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) radical followed by a homogenizing mechanical treatment. When oxidized with 3.6 mmol of NaClO per gram of cellulose, almost the totality of sulfite wood pulp and cotton were readily disintegrated into long individual microfibrils by a treatment with a Waring Blendor, yielding transparent and highly viscous suspensions. When observed by transmission electron microscopy, the wood pulp and cotton microfibrils exhibited a regular width of 3−5 nm. Tunicin and bacterial cellulose could be disintegrated by sonication. A bulk degree of oxidation of about 0.2 per one anhydroglucose unit of cellulose was necessary for a smooth disintegration of sulfite wood pulp, whereas only small amounts of independent microfibrils were obtained at lower oxidation levels. This limiting degree of oxidation decreased in the following order: sulfite wood pulp > cotton > bacterial cellulose, tunicin.

References

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