Structural studies of electrospun cellulose nanofibers

被引:286
作者
Kim, Choo-Won
Kim, Dae-Sik
Kang, Seung-Yeon
Marquez, Manuel
Joo, Yong Lak [1 ]
机构
[1] Cornell Univ, Sch Chem & Biomol Engn, Ithaca, NY 14853 USA
[2] Philip Morris Inc, Richmond, VA 23234 USA
[3] Los Alamos Natl Lab, Chem Sci & Technol Div, Los Alamos, NM 87545 USA
关键词
cellulose; electrospinning; oxidation;
D O I
10.1016/j.polymer.2006.05.033
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Non-woven mats of submicron-sized cellulose fibers (250-750 mn in diameter) have been obtained by electrospinning of cellulose solutions. Cellulose are directly dissolved in two solvent systems: (a) lithium chloride (LiCl)/N,N-dimethyl acetamide (DMAc) and (b) N-methylmorpholine oxide (NMMO)/water, and the effects of (i) solvent system, (ii) the degree of polymerization of cellulose, (iii) spinning conditions, Lind (iv) postspinning treatment such as coagulation with water on the miscrostructure of electrospun fibers are investigated. The scanning electron microscope (SEM) images of electrospun cellulose fibers show that applying coagulation with water right after the collection of fibers is necessary to obtain submicron scale, dry and stable cellulose fibers for both solvent systems. X-ray diffraction studies reveal that cellulose fibers obtained from LiCI/DMAc are mostly amorphous, whereas the degree of crystallinity of cellulose fibers from NMMO/water can be controlled by various process conditions including spinning temperature, flow rate, and distance between the nozzle and collector. Finally, electrospun cellulose fibers are oxidized by HNO3/H3PO4 and NaNO2, and the degradation characteristics of oxidized cellulose fibers under physiological conditions are presented. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5097 / 5107
页数:11
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