doi:10.1016/j.carbpol.2006.06.010
Copyright © 2006 Elsevier Ltd All rights reserved.
Fabrication and characterization of poly (vinyl alcohol)/chitosan blend nanofibers produced by electrospinning method
Yong-Tang Jiaa, d, Jian Gongb, Xiao-Hua Gua, e, Hark-Yong Kimc, Jiong Dongd and Xin-Yuan Shena,
, 
aCollege of Material Science and Engineering, State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai 200051, China
bDepartment of Chemistry, Northeast Normal University, Changchun 130024, China
cDepartment of Textile Engineering, Chonbuk National University, Chonju 644-765, Republic of Korea
dDepartment of Textile Engineering, Liao Dong University, Dandong 118003, China
eQiqihar University, Qiqihar 161006, China
Received 17 April 2006;
revised 6 June 2006;
accepted 6 June 2006.
Available online 25 July 2006.
References and further reading may be available for this article. To view references and further reading you must
purchase this article.
Abstract
A series of poly (vinyl alcohol) (PVA)/chitosan (CS) blend nanofibrous membranes with different weight ratio of PVA to CS were fabricated by electrospinning method. The morphology, diameter, and structure of electrospun nanofibers were investigated by scanning electron microscopy (SEM), fourier transform infrared (FT-IR), X-ray diffraction (XRD) and differential scanning calorimetry (DSC). SEM images showed that the morphology and diameter of the nanofibers were mainly affected by concentration of the blend solution, weight ratio of the blend, respectively. FT-IR, XRD, and DSC demonstrated that there were strong intermolecular hydrogen bonds between the molecules of CS and PVA. The crystalline microstructure of the electrospun fibers was not well developed.
Keywords: Poly (vinyl alcohol)/chitosan blend; Nanofiber; Electrospinning
Fig. 1. SEM photographs of nanofiber mat with different weight ratio of PVA to CS (Concentration, 7.4 wt%; voltage, 15 kv; TCD, 15 cm).
Fig. 2. Average diameter and EW of the electrospun fibers as a function of the weight ratio (PVA/CS; voltage, 15 kv; TCD, 15 cm).
Fig. 3. SEM photographs of the electrospinning fibers as a function of the concentration (PVA/CS = 80/20; voltage, 15 kv; TCD, 15 cm).
Fig. 4. Average diameter of the electrospinning fibers as a function of the solution concentration. (PVA/CS = 80/20; voltage, 15 kv; TCD, 15 cm).
Fig. 5. The conductivity and [η] as a function of the solution concentration. (PVA/CS = 80/20; voltage, 15 kv; TCD, 15 cm).
Fig. 6. FT-IR spectra of the nanofibrous membranes with different weight ratio of PVA/CS (Concentration, 7.4 wt%; voltage, 15 kv; TCD, 15 cm).
Fig. 7. XRD patterns of the nanofibrous membranes with different weight ratio of CS/PVA (Concentration, 7.4 wt%; voltage, 15 kv; TCD, 15 cm).
Fig. 8. XRD patterns of the nanofibrous membrane and the corresponding film (PVA/CS = 80/20; Concentration, 7.4 wt%; voltage, 15 kv; TCD, 15 cm).
Fig. 9. DSC curves of the nanofibrous membranes with different weight ratio of PVA/CS (Concentration, 7.4 wt%; voltage, 15 kv; TCD, 15 cm).
Table 1.
DSC data obtained from the electrospun fibers of PVA/CS blend
