Department of Biomaterial Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo, 113-8657, Japan.
Nanoscale. 2011 Jan;3(1):71-85. doi: 10.1039/c0nr00583e. Epub 2010 Oct 19.
Native wood celluloses can be converted to individual nanofibers 3-4 nm wide that are at least several microns in length, i.e. with aspect ratios>100, by TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl radical)-mediated oxidation and successive mild disintegration in water. Preparation methods and fundamental characteristics of TEMPO-oxidized cellulose nanofibers (TOCN) are reviewed in this paper. Significant amounts of C6 carboxylate groups are selectively formed on each cellulose microfibril surface by TEMPO-mediated oxidation without any changes to the original crystallinity (∼74%) or crystal width of wood celluloses. Electrostatic repulsion and/or osmotic effects working between anionically-charged cellulose microfibrils, the ζ-potentials of which are approximately -75 mV in water, cause the formation of completely individualized TOCN dispersed in water by gentle mechanical disintegration treatment of TEMPO-oxidized wood cellulose fibers. Self-standing TOCN films are transparent and flexible, with high tensile strengths of 200-300 MPa and elastic moduli of 6-7 GPa. Moreover, TOCN-coated poly(lactic acid) films have extremely low oxygen permeability. The new cellulose-based nanofibers formed by size reduction process of native cellulose fibers by TEMPO-mediated oxidation have potential application as environmentally friendly and new bio-based nanomaterials in high-tech fields.
天然木纤维素可通过 TEMPO(2,2,6,6-四甲基哌啶-1-氧自由基)介导的氧化和随后在水中的温和解聚,转化为 3-4nm 宽、至少几微米长的单个纳米纤维,即长宽比>100。本文综述了 TEMPO 氧化纤维素纳米纤维(TOCN)的制备方法和基本特性。TEMPO 介导的氧化在不改变原始结晶度(约 74%)或木材纤维素结晶宽度的情况下,选择性地在每个纤维素微原纤维表面形成大量 C6 羧酸盐基团。带负电荷的纤维素微原纤维之间的静电排斥和/或渗透效应,其 ζ-电位在水中约为-75mV,通过温和的机械解聚处理 TEMPO 氧化的木纤维素纤维,可导致完全个体化的 TOCN 在水中分散。自支撑的 TOCN 薄膜透明且柔韧,拉伸强度为 200-300MPa,弹性模量为 6-7GPa。此外,TOCN 涂覆的聚乳酸薄膜具有极低的氧气透过率。通过 TEMPO 介导的氧化对天然纤维素纤维进行尺寸减小处理形成的新型纤维素纳米纤维具有作为环保和新型生物基纳米材料在高科技领域应用的潜力。